SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs117962111 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422751 | TGTTCAGATCAGCCC[A/G]GATAAGAAGCTAAAA | 55626 |
rs118047697 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512467 | GACTACCTGTGGCCT[C/T]TCCAGGTTCCTCCTC | 55626 |
rs118075892 | snp | A/G | 3.38759e-05 | 0.00411544 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418077 | GGAAAAGAGGGAAAA[A/G]AAGAGAATGGGAGGA | 55626 |
rs118091841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529055 | CCTTTATTATTACAA[C/T]TTTCTACTCCTGCTC | 55626 |
rs137870297 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474676 | TACAAGCGTAAGCCA[C/T]GGCACCTGGCCTCTA | 55626 |
rs137890582 | snp | A/C | 0.00326836 | 0.0402927 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397603 | AGGGGAGGAAGAGGG[A/C]AGGGTTGGCTGGGTT | 55626 |
rs137923938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430159 | AAAGACTCCAGCACA[C/T]ACAGCTATTCAAGGG | 55626 |
rs137958075 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434649 | GTAACAGGGGCATGC[A/G]GTAGGACTCTAATGC | 55626 |
rs137996141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447146 | GGGCATGGTGGCTCA[C/G]GCCCATAACCCCAGC | 55626 |
rs138112582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410874 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACAAGGT | 55626 |
rs138137279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500015 | AGCTTAAAGCTACAA[A/G]AATCTGAGGTTATCT | 55626 |
rs138143902 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590033 | CAAAACAAAAGTTTT[A/G]TAAGTTTCCTAACAC | 55626 |
rs138179619 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409815 | CCCAGCGCTTTGTTC[C/T]AGTCTTCATTAGTGA | 55626 |
rs138188820 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514500 | TCTCTCTGGTTGAAA[C/G]ACTAAATCTTCAGTA | 55626 |
rs138191092 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460213 | TATTAGAATACTATG[A/T]AACAACAGAAATAAA | 55626 |
rs138207091 | snp | C/G/T | 3.30553e-05 | 0.00406531 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541898 | CTCAAGGAAATGATA[C/G/T]AAGGAGAAAAGCAAG | 55626 |
rs138218766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494259 | AGGAAGAATCATCCA[C/T]CAGCCCAAAAAGGAA | 55626 |
rs138238638 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464817 | TTTGCGAGGCCAAGG[A/C]AGTCGGATCACGAGG | 55626 |
rs138254477 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435320 | TACCGCTTGAGAGAT[C/T]AGATAAGGAAAAAGT | 55626 |
rs138259956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441067 | CAATCTGACAGAAGA[C/T]AGAAAAGCATGTTTA | 55626 |
rs138262595 | snp | A/G | 0.000249594 | 0.0111685 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397693 | CTCTGCCAGTTGCCC[A/G]GCCTCTGGGAGCAGT | 55626 |
rs138266103 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533429 | TATTAATTTTTCAAG[C/G]TCTCCCTTCCTCACA | 55626 |
rs138287735 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562325 | AACATGGCTGGAGCA[A/C]CACTAACAAGGAAGA | 55626 |
rs138306661 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450565 | CCACCTCAGCCTCCC[A/G]AGTAGCTGGGGCTAC | 55626 |
rs138330734 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487319 | CAAAAATAAAGTTAA[C/T]AATAATAACAAGTAA | 55626 |
rs138359469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429489 | AAGCACTAATCCTTA[C/T]TCTTGCTTTCTAGCT | 55626 |
rs138393774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471915 | ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCAGGAA | 55626 |
rs138395095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526633 | GACAAGGGAGAGAGA[C/T]CCAGTTTATTCTAAC | 55626 |
rs138402168 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584987 | TGAGGCAGGAGAAAC[A/G]CTTGAACCTGGGAGG | 55626 |
rs138444324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511047 | AAGTATGACACTTTC[C/T]GTGATAAAGATCACA | 55626 |
rs138457817 | in-del | -/AAAAAAAAAAAAC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566855 | CTTCTTAAAACTAAA[-/AAAAAAAAAAAAC]CCGCCATTGTAAAAC | 55626 |
rs138485807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522255 | ATACATTTGTAAGAT[A/G]ACTGGTTGGCACTAT | 55626 |
rs138526841 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445905 | TTAAGAGCTTATTCT[A/G]GGGGAAGGGATAAGA | 55626 |
rs138534531 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537510 | TTTAAAGGCCAAGGG[C/G]ACCCTACCGCAAGGA | 55626 |
rs138578536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475455 | TTCCACATGTATTAG[C/T]TTGCTGTATTCTTTG | 55626 |
rs138587262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401478 | ACTCCTGACCTTGTG[A/G]TCCACCCACTTGGAC | 55626 |
rs138598480 | snp | A/G | 0.000450349 | 0.0149991 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542854 | CGGCGGGTAGGACCC[A/G]GACTGAGGTTGCGGA | 55626 |
rs138616649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465987 | GGATCTAGACTAAAG[C/T]ACAGAGTCTTGAGAC | 55626 |
rs138640942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503339 | GAGAGATGGGGGAAT[C/T]GCCAGTGAGTGGAGC | 55626 |
rs138646165 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454218 | TTAATTTTTAGAGAC[A/G]GGGTCTTGCTGTGTT | 55626 |
rs138647850 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547684 | TTTCTTTCCCTTTCC[A/G]ACACGGGGCCAAAGT | 55626 |
rs138685076 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554641 | CCTGATATGCTCTTA[C/T]CAGCCACCTGAGAAG | 55626 |
rs138732313 | snp | C/T | 1.65326e-05 | 0.00287507 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542879 | TGCGGAGCGTGTTGC[C/T]GGCAGTGCTGCTCTG | 55626 |
rs138740618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548952 | GCTGAGATAGTGCCA[C/T]TGCACTCCAGTGCCT | 55626 |
rs138762925 | snp | A/G | 4.3448e-05 | 0.0046607 | intron-variant, synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543225 | TGAGGGGGTAGCAGA[A/G]TCTTGCACTGTGCTT | 55626 |
rs138803423 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589002 | CTCTTATAAGTAATA[A/T]ATGAAATAACACATG | 55626 |
rs138811342 | in-del | -/TTG | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487336 | ATAATAACAAGTAAA[-/TTG]TTGTTAACCAAAAAT | 55626 |
rs138816091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537977 | GGGACACCTTTTCTT[C/T]CCAGTCATCCTAACC | 55626 |
rs138827988 | in-del | -/TACAA | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516290 | TCAGTTCTTCATAGT[-/TACAA]TACGAGTACTATCTG | 55626 |
rs138850964 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446710 | GTCTCCAGACACTGC[C/T]GAATGTCCTCTGGGG | 55626 |
rs138854891 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410196 | CAGAGCCCTAGAGGG[C/T]GCTGCTTAAGAGCCC | 55626 |
rs138857882 | snp | A/C/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499812 | AGGCGCCCGCCACCA[A/C/G/T]GCCCAGCTAATTTTT | 55626 |
rs138871674 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481390 | GCTGAACACACTATT[A/T]TTGTTTTTGTTTTTG | 55626 |
rs138903464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416652 | CATCAAAAGGCAACA[C/T]GGACACTTCCGATAA | 55626 |
rs138905705 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414585 | TGGTTTATGAGGCCG[A/G]AAGTAAGCAAGCACC | 55626 |
rs138914941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470641 | GCACCATGGGCCTGC[A/G]GTCCTAGCTACTCAG | 55626 |
rs138923006 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559369 | CTAATTTCAGCCAGT[C/T]ATTTCATTACGCACA | 55626 |
rs138932121 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426682 | CCCCCTTTTCCTACA[A/G]TGTTCTGAAGAAAAG | 55626 |
rs138977915 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572590 | CTGCCTATCTTTGAT[A/G]TGGCAGAAGCTCTTA | 55626 |
rs138977968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516162 | TGTTGGCAACATTTG[C/T]TGCCCAGACAATATA | 55626 |
rs138982265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420874 | GGCCAGAGAAAGTAG[C/T]CTTACGAGGAGAATA | 55626 |
rs139006534 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488388 | TTGAACCCAAGAGGC[A/G]GAAGTTGCAGTGAGC | 55626 |
rs139063793 | snp | A/G/T | 0.0162398 | 0.0886349 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577722 | TTGGGAGGCCGAGGC[A/G/T]GGCAGATCACCTGAG | 55626 |
rs139067338 | snp | A/G | 0.0345262 | 0.126772 | intron-variant, utr-variant-5-prime | AMBRA1 | GRCh38.p7 | 11:46591239 | GTTGCTTTCTTCTCT[A/G]CATTCTTTCCTCTGA | 55626 |
rs139098516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447934 | TAGTGATGGCAAATA[C/T]TAAGTGTCTAATAAA | 55626 |
rs139101370 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539544 | CCTGGGCAACAAGAG[C/T]GAAACTCCATCTCAA | 55626 |
rs139120871 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490784 | TACAGGAAGGCAGGG[A/T]TCATAGTCTGTCTTA | 55626 |
rs139134180 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396959 | CAGTGGGGTAAGACG[A/G]CGAAGAGAGGCTGAA | 55626 |
rs139136938 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580536 | CCACCTTCATCTACC[C/G]AGATGCTCAGGCCAA | 55626 |
rs139155977 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573492 | ATAACTGCACTGCAC[A/G]TGTGGCTGTGTTATC | 55626 |
rs139209798 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534766 | GCAGCCTCAACCTTC[C/T]GAGCTCAAGCGATCC | 55626 |
rs139222125 | snp | A/C/G | 0.000230688 | 0.0107376 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542686 | GACAGCAAACTCACC[A/C/G]AAGAGGCACTGGTTC | 55626 |
rs139237554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476326 | GTGTGCACAAGTTAG[A/G]TGACTTGTCTTGAAG | 55626 |
rs139261712 | snp | C/T | 3.32701e-05 | 0.00407847 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46443557 | AGGTAGTATTGGCAA[C/T]GTTACTGGCCACAGC | 55626 |
rs139272811 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568579 | GGAGTTTGAGACCAG[C/T]CTGACCAACAGAGAC | 55626 |
rs139294318 | snp | C/G | 0.00245512 | 0.0349504 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543377 | CTGTTCCATCTATGG[C/G]GATCTCTGGTTCGTC | 55626 |
rs139332060 | snp | A/G | 0.000741088 | 0.0192353 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542280 | CCAGCGCAGGGTATC[A/G]TTGTTGAAGGTCAGG | 55626 |
rs139333130 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493358 | ATTAAGAAACAAATG[G/T]TTTAAACAAATAATT | 55626 |
rs139334786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435806 | CTGAGGGTGGAGGAA[C/T]GTCTGTTGGTGAGGA | 55626 |
rs139362284 | snp | C/T | 0.323908 | 0.238825 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585622 | AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 55626 |
rs139369669 | in-del | -/AAG | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489467 | TTTTTTATATTTAAA[-/AAG]AAGAAGAAGGAGTCA | 55626 |
rs139380522 | snp | C/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595534 | ACAGCAAGACTCCGT[C/T]TAAAAAAAAAAAAAA | 55626 |
rs139384613 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550824 | AGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55626 |
rs139398638 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438629 | AAGGCCTGTACAGAG[C/T]TCCAGATGACCCATA | 55626 |
rs139399285 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440904 | TCTTATAATATCATA[C/T]AGACAAGATAGAAAA | 55626 |
rs139400895 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427866 | ATACAAAAATTAGCC[A/G]GGAGTGGTGGCGAGT | 55626 |
rs139410825 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442405 | AACTCAGCCTCCTAA[A/C]GTGCTGAGATTACAG | 55626 |
rs139458730 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562104 | AAAGAAAATATGGCA[-/G]GGTGAAAGAAAACAA | 55626 |
rs139478917 | snp | C/G | 0.00173682 | 0.0294176 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443440 | TGAGTTCTGGCTCAC[C/G]AGCAAATATAACCCT | 55626 |
rs139523711 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496286 | TGTTCAGAGGCTGAG[A/G]CAGGAGAATCCCTTG | 55626 |
rs139525470 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586751 | ACAGATGAGGAGAGG[C/T]ACAGAGAGACTAAGT | 55626 |
rs139551376 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412821 | GGTAAATGGCCAGAA[C/G]TAACAGCAGAGGCCT | 55626 |
rs139552163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511770 | TCCCACCCTTGGTCC[G/T]TAGTTATCACCATCA | 55626 |
rs139553828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437433 | TGAAAATTGTAACAG[C/T]TTCTCCGGTAGCATA | 55626 |
rs139557421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501233 | GCCACTGTCTGAGTT[A/T]GCACACTTCCCCATG | 55626 |
rs139567439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503844 | AAATTGTGAATAAGA[A/G]ACTTCTGTGCCAGCA | 55626 |
rs139588449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529243 | TACTGCATAATCTGG[C/T]GTAATGGAGATCTGC | 55626 |
rs139592541 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565312 | CATTTTACTTCTGTT[C/T]TCCTTTTTTTTTAAA | 55626 |
rs139640359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579478 | ATAAATAAATTAAGT[A/C]AGTAAGTACATAAAA | 55626 |
rs139698070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574717 | TCATCCTTACTCTCA[C/T]GGCCAACTCTTGGGC | 55626 |
rs139706260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522798 | GTAAGCCTGTGAAGG[G/T]CTTAAAAAACATTTT | 55626 |
rs139721859 | in-del | -/AG | 0.0894459 | 0.191631 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421136 | AGACGCCAATATGAT[-/AG]AGATGAACCCAGCTT | 55626 |
rs139757774 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462324 | CCTTGGGGTATGGGA[A/C]ACCAGGAAATAATCT | 55626 |
rs139758427 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517707 | GGCCTGGTGGCACAC[A/G]CCTGTCCCAGCTACT | 55626 |
rs139763709 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467243 | TTTCAATTTCCGCTA[C/T]TATCTACTGATTTCC | 55626 |
rs139787433 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571273 | TCTCCAAAAATAACC[C/T]TGTAATTTTTAGAAA | 55626 |
rs139829780 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536161 | TGAAACCATAAGGAA[C/T]ATAATTTCAATTCTA | 55626 |
rs139858656 | snp | C/T | 0.000329625 | 0.0128337 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508213 | CCTCAAATTCCAAGT[C/T]GGTTCCCTCTACTGA | 55626 |
rs139896964 | snp | A/G | 0.000254257 | 0.0112723 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397907 | TGGATCCTGCTGAGC[A/G]CATCTTCTCCACTGG | 55626 |
rs139900800 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406862 | CACTCCAGCCTCTGC[A/G]ACAGAGTGAGACTCC | 55626 |
rs139968517 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432646 | CACTGAACCGAATTG[C/G]GTGGATTAAACACAT | 55626 |
rs139969342 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399317 | GACCTCAGGTAATCT[A/G]CCTGCCTCAGCCTCC | 55626 |
rs139970064 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485247 | CCGGCCTCAAGAAGC[C/T]CAAACTCTTAAACAT | 55626 |
rs139974491 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403305 | TACTGGTCTTCCAGC[C/T]CCTCCCTCTTCACAT | 55626 |
rs139974613 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523851 | GACAGTTCCTTGTGA[G/T]ATGTCATAGTTTTAT | 55626 |
rs139976066 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490505 | GCTTTCAGTCTCTTG[C/T]GGGAGGAAGTAGAAC | 55626 |
rs139977234 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472867 | AGGCAAACTCCACAC[A/G]TGCTCCAGGAAACAC | 55626 |
rs139982477 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506294 | GCTCCATTTGCCACA[C/T]CACTGCTACTTCAGG | 55626 |
rs139983280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436338 | CTTTCCCTGTGTGTT[A/G]CTAATGAGATGACAG | 55626 |
rs139987746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528133 | TTCAGCCTTTGAAAA[G/T]AAGGAAATTATGATA | 55626 |
rs140041392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557394 | GCCACAAAGCCCTGT[A/G]AACAGTCAGACAAAT | 55626 |
rs140128443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539825 | GGCCCTCAGTAACTG[A/G]TATCTCTTTTTTTCC | 55626 |
rs140133950 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524622 | CATTTGAGGGGAAAT[C/T]TCTTATTTCACATGG | 55626 |
rs140142328 | in-del | -/AAGGGCAGGG | 0.084728 | 0.187577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427095 | TTATAAGTTCAATTC[-/AAGGGCAGGG]AAGGAGAGAGTCATA | 55626 |
rs140176287 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419105 | TAAGATGGAGGGAGC[A/G/T]GAGCAGAGGGGAATC | 55626 |
rs140179377 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563286 | TGAAGTGTAGTGGCA[C/G]GATCTCAACTGAACT | 55626 |
rs140183115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424223 | GCTCTCTCCCAGCAG[A/G]AAAAAAGGGCAAACA | 55626 |
rs140248534 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434420 | AAACAAACAAACAAA[A/C]AAGTCTCAAGGCAAC | 55626 |
rs140259069 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411629 | GTGTGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 55626 |
rs140262651 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480329 | CTAAGATCATCCACA[C/T]CCAGCCAAGCTATTA | 55626 |
rs140270218 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572515 | GCAGTTTAAAAACGA[A/T]CTTCATCAAAAACGA | 55626 |
rs140295743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485970 | TAGGTAAAAGGCCCC[A/G]GGTGCTATAAGGCAA | 55626 |
rs140353106 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544818 | CTGATTAGTCAGCTG[C/T]TTAGAAAGCAGGAGG | 55626 |
rs140375378 | snp | A/G | 6.59587e-05 | 0.00574239 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418030 | TGGTCGGCAGGCATG[A/G]GATAAAGGACGTTGA | 55626 |
rs140391618 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455830 | TACTAGGTCATCCTT[C/T]CTTCCTCCCATGACA | 55626 |
rs140401992 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461103 | AAAAAATTAGCCAAG[C/T]ACGATGGTACACGCC | 55626 |
rs140403922 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408038 | GTGAGAGGAAGGGGC[C/T]GATGATAGGCCAGGC | 55626 |
rs140405133 | snp | A/G | 9.04069e-05 | 0.00672274 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397519 | ACCATCCAGAAGGTG[A/G]TTGTTATTGGTCAAC | 55626 |
rs140435768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541729 | AACCTTGAGCTTAGC[C/T]GAAATAGAGCTAGCG | 55626 |
rs140496136 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469277 | TCCAGCTCCTAATCT[A/T]CCCTTCCTCCAAAAT | 55626 |
rs140501340 | in-del | -/A | 0.202035 | 0.245356 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511934 | ATCTCTGCTCACTGC[-/A]ACCTCTGCCTTCCTA | 55626 |
rs140502323 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419834 | GAGGAAGGCAGGGAG[A/G]GATGATTGAGTCTGA | 55626 |
rs140520376 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538900 | TTATTTAAATTACTT[-/A]AAAAATTTAAAGATT | 55626 |
rs140549134 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457862 | AGTGAGTCGAGATTG[C/T]GCCACTGCACTCCAG | 55626 |
rs140568462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486963 | AATAAATACAAATAA[A/G]AGAGATGAGAGGGGC | 55626 |
rs140575040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502842 | GAAGTGGGCAGATCA[C/T]GAGGTCAGGAGTTCA | 55626 |
rs140613864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413803 | GCCTGAAACTCTTAG[C/T]TTTCAATACCCAGTG | 55626 |
rs140622888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536788 | GCAATTCCCCCATAA[A/G]AGTCTAAGAAACTTA | 55626 |
rs140623293 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506769 | CCAAATGTTCAATTT[C/G]ATACAGGCCATAAAA | 55626 |
rs140624115 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450544 | TTCTGGGCTCAGATG[A/G]TCCTCCCACCTCAGC | 55626 |
rs140625586 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523995 | TGCCTCAGCGTCCCA[C/G]GTAGCTGGGATTACA | 55626 |
rs140657013 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572641 | ATACCCACTGAAAAA[C/T]TGTCAGCATTATCAT | 55626 |
rs140687038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431923 | TTGTGATATCAAGAG[A/G]ACAGAATGACTTGTT | 55626 |
rs140689928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576573 | TGGAGAAGATACTTC[A/G]TAATATCCCTCGGTA | 55626 |
rs140742657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479889 | AAACAAGACAAATTT[A/C]TTATCTCTCAGTTCT | 55626 |
rs140744650 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571751 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCAAT | 55626 |
rs140796587 | snp | G/T | 3.29522e-05 | 0.00405894 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542390 | GGTGGGAAGGGCCTG[G/T]CCTCTCAGATTCAAT | 55626 |
rs140817330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478925 | CAATTTGTGCTGGAC[A/G]CAGTGGCTCACGCCA | 55626 |
rs140828830 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482940 | TTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 55626 |
rs140830491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428407 | AGGGGGAGCAAAACT[A/G]CATTCTATCCCAGAG | 55626 |
rs140835599 | snp | C/T | 8.27109e-05 | 0.00643029 | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433510 | ATGGGCCTGTTGCAG[C/T]CTGAAGACCTGGGCC | 55626 |
rs140839565 | in-del | -/TTC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513266 | TGCCTACGCTCTTTT[-/TTC]TTTTTTTTTTTTTTG | 55626 |
rs140864621 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581395 | AGGCAGATCACGAAG[C/T]CAGGAGATCGAGACC | 55626 |
rs140865165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554327 | ACTCAAGAGGAACAA[C/T]AAAATACAGGTCACA | 55626 |
rs140881427 | snp | C/G | 0.113334 | 0.209338 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429231 | AGCGGCCCCCTACCC[C/G]ATAAAATAAGCCTCC | 55626 |
rs140889307 | in-del | -/TATTTTATTATTTATATATAAATATG | 0.0295035 | 0.117819 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418307 | TAAATATATAATATA[-/TATTTTATTATTTATATATAAATATG]TATTTTATTATTTAT | 55626 |
rs140927539 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588605 | ACATGGTGAAAACCC[A/G]TCTCTACTAAAAAAA | 55626 |
rs140929886 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530762 | ACCAGCTATGAATGG[C/T]TTTCATATTTTTAAA | 55626 |
rs140954843 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446158 | TGGTGCCAGGGTGCT[A/G]AGGAGGAATGAAGCC | 55626 |
rs140958502 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549838 | TTTGGGGGGGGTGGG[A/G]GACAGAGTCTCACTC | 55626 |
rs140966222 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512457 | AGTATCCTATGACTA[C/T]CTGTGGCCTCTCCAG | 55626 |
rs141000470 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499227 | AAATCCACATTCCTA[C/T]TGTGCATTTTATGTT | 55626 |
rs141031041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582711 | GCTACATCAATAAAA[G/T]GAGAAGAATAAGAGT | 55626 |
rs141046683 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545319 | ACAAAAAAATGAGCC[A/G]GGCATGGTGGTGGGT | 55626 |
rs141063634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439879 | CAATCTTGTTTGTAA[C/T]ACAAAAAATACAAAT | 55626 |
rs141111628 | in-del | -/AACCCC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512416 | CCATCTGAATGACAA[-/AACCCC]CAGCCTCTCTGGCCA | 55626 |
rs141143617 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501079 | AGCCACACCTATCAA[C/T]AAAGCAATTCCCCAA | 55626 |
rs141144553 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590628 | AGAACTTTCTTACTA[A/C]AAGACAGAATTCAGT | 55626 |
rs141178615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559527 | CCTATTTGAAACACA[A/G]AATATTAAGAACAAA | 55626 |
rs141181296 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515820 | AGCTGGGATTAAAGG[C/T]ATGCGCCACCACACC | 55626 |
rs141214942 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466222 | CGTGCTGGCACACGC[C/T]TGTAGTCCCAGCTAC | 55626 |
rs141247514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414256 | TGGTGTCTCTGCAGC[A/G]CGGGAAAGAGCCAGC | 55626 |
rs141260598 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534199 | GCTGGCATTTAAATA[C/G]CACCTGGTGCCAGCC | 55626 |
rs141272368 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458680 | TTGCTCACTACAGCC[C/T]TGAATTCATGGCCTC | 55626 |
rs141275822 | snp | A/G | 0.00375017 | 0.0431395 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547290 | ATGGGTGGAGGCTAA[A/G]AGAGTCCTAGAAAAT | 55626 |
rs141278389 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410512 | AAACCAAGACCAGAG[C/T]TGCTGCCTCATCAGG | 55626 |
rs141282704 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442151 | AATTGTGTGTTTTTG[G/T]TTTTTTTTGGAGATA | 55626 |
rs141307244 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410163 | TCAAGGAGGTGCTGC[A/T]CTGGTTGAGGAGGGA | 55626 |
rs141307297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463219 | TCACTCCACTTGAGG[A/T]TGAGTTTAAAATTCA | 55626 |
rs141369547 | snp | A/T | 0.105214 | 0.203807 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459572 | AAAAAGTAGCTGGGC[A/T]TGGTGGCAGGTGCCT | 55626 |
rs141393191 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566287 | GCTGGCCATGGTGGC[A/G]GGCACCTGTAGTCCC | 55626 |
rs141397546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509826 | ACTTCCATAATGTTT[G/T]AATATAAAAGGAAAA | 55626 |
rs141439160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527782 | GTTAGGATGACCACT[A/G]TAAAAAGAAAAAAAA | 55626 |
rs141458487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513708 | GGAAGCAAGAGCATA[C/T]GTATTCAATGGAGAC | 55626 |
rs141552383 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475868 | AGGCAAAGAAAGCAG[A/G]CAGCTTCAAATAAAG | 55626 |
rs141587291 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426281 | CACACTTAGGAAGCA[A/G]ACGTTGCATGCCTCC | 55626 |
rs141588537 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494036 | AACAATGCCAGATGT[A/G]GACAATTCAAAGACC | 55626 |
rs141592653 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583038 | AAATGAATGACTGTC[A/G]CCAAGTCAATCCTAA | 55626 |
rs141620679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544347 | GAGTTCATCCTAACC[A/G]TAAAGCATAAAATGC | 55626 |
rs141663303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561173 | ATCACCTGAGGTCAG[A/G]AGTTCGAGACTAGCC | 55626 |
rs141694769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422121 | AAATTCTATTACACC[A/G]GACGTATTATCAGAA | 55626 |
rs141717528 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495204 | GAGCAGTTAATGAGC[A/G]GCTTAACCAACTCCA | 55626 |
rs141721301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548073 | GCTCTAAAGGAAAAA[G/T]ATATTTCTAGCACAT | 55626 |
rs141724027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503092 | AAAAAAAAAAAATGA[A/G]TTTTTGCTTTGTGTT | 55626 |
rs141736530 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579432 | ATTGCACTCCAGCCT[A/G]GGCAACAAGAGCAAA | 55626 |
rs141758483 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489927 | GGAAGACCCGGTTTA[A/G]AATTCCAGGTCAGCC | 55626 |
rs141780703 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401127 | CTCACTGTAGCCCCA[A/G]TGCTTTCTCAGAACT | 55626 |
rs141780771 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448693 | AATAAACAATAAACA[A/T]CTAGGTAGGCCAACT | 55626 |
rs141788039 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499845 | ATTTTTAGACAGATG[G/T]GGTTTCACCATCTTG | 55626 |
rs141794454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416202 | TGCTTATTAGATTTC[C/T]CTTATGAACTGTTAA | 55626 |
rs141813932 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588422 | TGGAAGTTAACAATT[C/G]AAGAGTACTTTATCC | 55626 |
rs141873717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445417 | TCTATTTGAGGTCCC[C/T]GTGGCGTATCATAAG | 55626 |
rs141874750 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407005 | ACAACATGGTGAAAC[C/T]CTGTCTCTACTAAAA | 55626 |
rs141966739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564087 | AGGCAGAGGTTGCAG[C/T]GAGCCGAGATGGCGC | 55626 |
rs141978653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | AMBRA1 | GRCh38.p7 | 11:46431069 | TCTGGTGCCTTTGGA[C/T]GTAAGGGGCAACCAA | 55626 |
rs141982771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522284 | ATGCTTAGCTCCTAT[A/G]TACCCTCAACACATT | 55626 |
rs142001347 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514579 | AGACACACTTTTCAC[A/C]TTTGAATGTGTCTGA | 55626 |
rs142012115 | snp | A/C/G/T | 4.95768e-05 | 0.00497859 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542871 | ACTGAGGTTGCGGAG[A/C/G/T]GTGTTGCCGGCAGTG | 55626 |
rs142052715 | snp | C/T | 0.00993945 | 0.0698483 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405058 | CATGCACCAGACATG[C/T]CATGAACACAAATTA | 55626 |
rs142055824 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502111 | ATTTTTTATGAAAAT[-/A]AAAAACTGCACAGGC | 55626 |
rs142069547 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575061 | GTGAACAAGTAAATG[C/G]TCCCATAGTTCAACT | 55626 |
rs142086699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447412 | TAGTGGTGTGTGCCT[A/G]TAGTCTCAGTTACTT | 55626 |
rs142195817 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521390 | CTCCTGGACTGTAAA[C/G/T]TGCCAAAAGAGACCC | 55626 |
rs142196448 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473823 | GCCCGGCTAACTTTT[A/T]GTATTTTTAGTGGAG | 55626 |
rs142200289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434030 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 55626 |
rs142223140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519781 | ATTTCTCATTCCTTT[C/T]GGATATACTATATGC | 55626 |
rs142249215 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595685 | AAAAATCTCCTCTAA[C/G]TCTTTGAAAATACTG | 55626 |
rs142263743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468409 | AGAGGAAGGAGGCCC[A/G]AGCATTACCCTTGGC | 55626 |
rs142288471 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470114 | TCCTTAGAGCTAAAG[A/G]AAACATGCCAAGTGC | 55626 |
rs142305607 | snp | A/C | 0.00874735 | 0.0655527 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396291 | AGGGGTCCACTGCAC[A/C]CCACTAGGAGAGCAC | 55626 |
rs142314527 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518779 | CATCAAAAATGAATA[C/T]TAAGCTCTGCTAAAA | 55626 |
rs142357580 | snp | G/T | 9.90197e-05 | 0.00703563 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542242 | CTAGCCTCGCCAGAG[G/T]AGTAGTTAGGTGTGG | 55626 |
rs142367481 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573664 | GCAGAATCCTTTTTC[-/T]TTTTTTTTTTTTTTA | 55626 |
rs142377530 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537602 | TAGTGAAGCAAAGGC[C/T]CACCACTCAAGTTGC | 55626 |
rs142396505 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462010 | CCCTAGTCAATGTTT[A/T]CTAAAATCCCCTTCA | 55626 |
rs142408752 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536766 | TCAGACTGTTCTAAG[A/C]TCCAAAGCAATTCCC | 55626 |
rs142425575 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397662 | CCCAGGAAGCTGTCC[A/G]GGGGCTTAGGCCTCG | 55626 |
rs142430348 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413533 | TTCATTCTTGTTGCC[C/G]AGGCTGGAGTGCAAT | 55626 |
rs142506605 | snp | A/G | 0.000381905 | 0.0138133 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408704 | CATGTGGCTCTGCTG[A/G]TTCTAGGGAGAGAAA | 55626 |
rs142513346 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495458 | TCAATACCAGGGATA[C/T]TGGAAGCTGATCCAT | 55626 |
rs142517316 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530506 | TTGCTTCAGGCCAGA[C/T]AGTACAAGAAACAAA | 55626 |
rs142532106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407634 | ACTTTGAAAATTCTC[A/T]GTTCATGGCATCGCA | 55626 |
rs142539782 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447221 | TGTAACCAGCCTGGA[C/G]AGAGTGAGACTCTTA | 55626 |
rs142541941 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538533 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTTGAGTGC | 55626 |
rs142575453 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497464 | AGCTAAATGTCATCT[C/G]AATACAAGGCAGAGC | 55626 |
rs142598266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540491 | GTTAATCCAGAACTG[A/G]TTTCAAGCATATGGG | 55626 |
rs142606909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403107 | ATTTAGAGTTCACAT[A/G]AGGTCTCTTCCTTGG | 55626 |
rs142606991 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450583 | TAGCTGGGGCTACAG[A/G]TGTGTGCCACCATGA | 55626 |
rs142609061 | snp | A/T | 6.59598e-05 | 0.00574243 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541938 | AGATAGGAAAGCGAC[A/T]GCTTACCTCCTGAGT | 55626 |
rs142633699 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590042 | AGTTTTATAAGTTTC[C/T]TAACACATATTGAAA | 55626 |
rs142646271 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405440 | AAAGGGCTGCCCAGC[C/T]GGGTGCAGTGCTTCA | 55626 |
rs142662742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479247 | AGAGTGTGCTAGCAG[A/G]CTACCTCAGATTTCA | 55626 |
rs142715609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416663 | AACACGGACACTTCC[A/G]ATAACCAGAGACCCT | 55626 |
rs142729064 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461780 | GTCACATAAACTTTG[G/T]ACCCCACAAAGGCAG | 55626 |
rs142738055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549104 | AGGAAAAAAAAAAAT[C/T]AGGCTCCTTTTCTCA | 55626 |
rs142772865 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424875 | GGTGTAGTGGCTCAT[A/G]CCTGTAATCCCAGCA | 55626 |
rs142821306 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406312 | CCCACCTCGGCCTCC[C/T]AAAGTTGCTAGAATT | 55626 |
rs142845246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421019 | AAAACAAGCCTCTGT[C/G]ACAAATTTACCTTTT | 55626 |
rs142886649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565086 | CATGGCAAAACCTCA[C/T]CTCTACAAAAAAATA | 55626 |
rs142929136 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492193 | CAGGAGATTGTGGTA[C/T]AGTCTGCTCTCCTGC | 55626 |
rs142929944 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582133 | AAAAAAAAAAAAATT[C/T]GAAAGCCTTGACATA | 55626 |
rs142936362 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472184 | CGCTTCTATTTAGTT[A/C]AACAAGAAGTATTTA | 55626 |
rs142938842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562552 | TTGTATTTGAGGTGT[A/G]AGAGAGAAATGAAGA | 55626 |
rs142976657 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488841 | AAATTCAACAACACA[C/T]TCCCAAAAAAGTAAT | 55626 |
rs142999403 | snp | C/G | 0.089084 | 0.191327 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423866 | CCTCCTGGGTTCAAG[C/G]GATTCTCCTGACTCA | 55626 |
rs143022875 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426118 | GAAATGAGTAAGATG[C/T]TCCCTATTTTCAGGA | 55626 |
rs143025759 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514793 | GGCAGGATTTTTTCA[C/T]GATTTCATAGGAACA | 55626 |
rs143045899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435988 | AGTGCCCACATCATG[A/G]GCCCGGGCAGAACAG | 55626 |
rs143065963 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438990 | TCATCAGTAAAACAC[A/G]GAATCAGGCTGGGCT | 55626 |
rs143074080 | snp | C/T | 0.000199309 | 0.00998072 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433596 | TTACATATCTGCCCA[C/T]TGGGGACAGGCTCAC | 55626 |
rs143077420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483707 | GAGTTGAAGACCAGC[C/T]TGACCAATATGGTGA | 55626 |
rs143090334 | in-del | -/AAAACAAAAACAAAAACA | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436638 | CCCAAGCCCTTTGCC[-/AAAACAAAAACAAAAACA]AAAACAAAAACAAAA | 55626 |
rs143096574 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567558 | TAGAGATGGGGTTTC[A/G]CCATGTTGGCCAAGC | 55626 |
rs143131306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509322 | ATTATATAATTTGAC[A/G]CTATGGACTGAAAAC | 55626 |
rs143136515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458886 | TGAGATAACAGGTCC[C/T]AGACGGCTTTTACTA | 55626 |
rs143166194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538821 | CTGGGTTTTAAATAA[C/G]CTACTTTATTAAGTG | 55626 |
rs143168231 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485383 | CACATTTGCAGAGCT[G/T]CTTCAAACTGTACGA | 55626 |
rs143178975 | snp | C/G | 9.04151e-05 | 0.00672305 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397493 | CCTGCAGCGTCCCCC[C/G]TGCTGCTGCCACCAT | 55626 |
rs143197722 | in-del | -/ATAA | 0.430583 | 0.172886 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486909 | AGACTCCATCTCAAC[-/ATAA]ATAAATAAATAAATA | 55626 |
rs143238548 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450424 | GGCAGAGACGAACAG[A/G]TGAGCACAAGATTTT | 55626 |
rs143247516 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541157 | AAGTCCCTAATAAAT[A/C]AAGATAGATGCGCAC | 55626 |
rs143267853 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440925 | AGATAGAAAAATGTC[A/G]TCCTCAGATATGAAC | 55626 |
rs143278456 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585222 | ACACTGCGGAAGGCC[A/G]CAGGGTCCTCTGCCT | 55626 |
rs143288318 | snp | A/G | 2.72379e-05 | 0.00369029 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494170 | ACATCCGGGCATTGC[A/G]TGGAGCTCGGTGCCT | 55626 |
rs143297246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530915 | TTGAGACGAATTCTC[A/G]CTCTGTAGCCCAGGC | 55626 |
rs143374983 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405898 | CACCATGCTCGGCTA[A/T]TTTTTTGTATATTTA | 55626 |
rs143394285 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510522 | CGATTCTGAAAAGTG[A/G]TAAGTACACTTACTT | 55626 |
rs143408711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435591 | TTTCTGGAACAGCTC[C/G]TTGCTAATACTAATC | 55626 |
rs143410359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527112 | CACATTTCAGCCCTG[A/G]GTGGCTCCCTTTCAA | 55626 |
rs143434903 | in-del | -/CTC | 0.111928 | 0.208413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444045 | TTTCAGACAAAGTAT[-/CTC]CTCCTTTATCACTTT | 55626 |
rs143441574 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403658 | AGAGTCAAATTCTGG[A/G]AGAAGTCAAACTCTT | 55626 |
rs143447460 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490536 | GGATCTTGATTTTCC[A/G]CAAACCCATTTTTGT | 55626 |
rs143460626 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460529 | AGGGTTTCACCGTGT[C/T]AGCCAAGATGGTCTT | 55626 |
rs143484768 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503918 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGGGCTCA | 55626 |
rs143509949 | snp | C/T | 0.000263809 | 0.0114819 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542582 | CTCCATCTGACTCAG[C/T]TGCCAACCCTGATGC | 55626 |
rs143516185 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520359 | GAGTGAAAAACACAA[A/G]GGATGTCTCAGCATT | 55626 |
rs143526215 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553988 | AACCCTGACAACTCA[C/T]AGATTAGGATCAGAA | 55626 |
rs143546176 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464240 | AAATGTCATCAGGAC[A/G]CCCTGTGAGCAGACT | 55626 |
rs143552325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415617 | TATGGTACCCTTACA[C/T]TTTGGGCCCTAAGGC | 55626 |
rs143576704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557741 | TGAGCCCAGGAGGTC[A/G]AGGCTGCAGTGAGCC | 55626 |
rs143591025 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506389 | CTTTTGCTTCTAAGA[G/T]CACAAATGCTAGTAG | 55626 |
rs143637805 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419462 | TGGGAGATTAAAAGA[A/G]ATGATGTATAAAATG | 55626 |
rs143652617 | snp | A/C | 0.000169374 | 0.00920099 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545805 | AATTCCAGATATTCT[A/C]AGGTTACAAGCTACC | 55626 |
rs143658619 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409560 | CTTCTGAAAACAGAC[C/T]CTTGCAGGTAGGGAG | 55626 |
rs143659757 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498933 | GGAGAGCACAGTGAT[C/G]TTGGTCAACTCATTT | 55626 |
rs143669055 | in-del | -/TATT | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425361 | GTGTGTAAGAAGTAG[-/TATT]TCTCTGTTCAGGACA | 55626 |
rs143680279 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465068 | AATAAAAAATAAAAA[A/T]AAATAAACACCAAGA | 55626 |
rs143810037 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477257 | AACCTCTAACTCTTA[C/T]CAGACAAAAAAGGAT | 55626 |
rs143832725 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481654 | AGGCATGATCTACCG[C/T]GCCCGGCCTATTTTT | 55626 |
rs143841871 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572703 | GTGTTTACTCTGAAC[C/T]AGGCACTTTACATGT | 55626 |
rs143851700 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548744 | ACGCCTGTAATCCCC[A/G]AACTTTGGGAAGCCA | 55626 |
rs143859340 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424319 | GCTGCCTTCAAGGCA[C/T]TTCTAGGCAACCTCC | 55626 |
rs143873452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511403 | GAAAAGGAACTAAGA[C/G]GATAATGAAGAATCT | 55626 |
rs143876835 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411493 | TTTTTTTCTGAGATG[C/G]AGTCTCACTCTGATG | 55626 |
rs143880001 | snp | A/G | 0.00480601 | 0.0487843 | synonymous-codon, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508349 | GATCATCCTCTGGGC[A/G]TAGTATGCAGCAGGA | 55626 |
rs143884253 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500498 | TTTAGGTCACCTTAA[C/G]CAATGCTATCAGAGT | 55626 |
rs143885481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482646 | CTTGTTCCTTTGTAC[C/T]CTGGACCAGTTAACT | 55626 |
rs143894911 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528722 | CAATAATGTGTACTG[C/T]ACACTTTTAAAATTA | 55626 |
rs143988647 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580946 | ACAGGTGTGAGCCAC[C/T]GCACCCAGCTAATTT | 55626 |
rs144054572 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494599 | TACTTGTTATCCAGA[C/T]GCCTGCTGTGGGAGG | 55626 |
rs144084225 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411115 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAG | 55626 |
rs144087679 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398064 | GGATAGAGAAAGACT[C/T]GCTCCATCACTGTGA | 55626 |
rs144090380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401755 | CTAACTGGGCTTCTT[A/G]CTTCCAGTCTCCTCC | 55626 |
rs144121544 | snp | A/G | 0.000395394 | 0.0140549 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545681 | CCAGAAGTGGATCTC[A/G]TTGGCAGTGGCAATC | 55626 |
rs144132836 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442912 | TTTTTAGTAGAGACA[A/G]GGTTTTACCATGTTG | 55626 |
rs144135818 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535540 | ATCAGTAGGAAAGAA[A/C]CTTCGCATTTAAATT | 55626 |
rs144140762 | snp | A/G | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542333 | GATTCAGGTGGCCAC[A/G]GGACAGGTTGGAGTT | 55626 |
rs144193451 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574934 | AAAACTCCCTATACA[C/G]GGTTCACATTCAAAA | 55626 |
rs144199233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511777 | CTTGGTCCTTAGTTA[C/T]CACCATCAGTGAAGG | 55626 |
rs144201971 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428320 | ATGGCCACAAAGAAA[A/G]AGCTTTCAATAAAAT | 55626 |
rs144204412 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462460 | TTTTTGATTGTCACT[A/T]ACCTGCTCTAAAGCT | 55626 |
rs144205496 | snp | A/G | 0.015999 | 0.0879972 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518307 | TGGTGGTGGGCTCCC[A/G]TAGTCCCAGCTACTT | 55626 |
rs144262882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408219 | AATGGCAGCTTGCAG[A/G]AGGGAGTCTCCCTTT | 55626 |
rs144286233 | snp | C/G | 1.65332e-05 | 0.00287512 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542110 | TGCGGACTAGCAGAG[C/G]TGCTCAACTCCAGCC | 55626 |
rs144313070 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511254 | TCCCTTATATTTAGG[A/G]TGTATAATCCTCAAA | 55626 |
rs144326018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412114 | TTCCAAAGGCCACCT[C/G]TTTAAAAAGCAGTAC | 55626 |
rs144388436 | snp | C/T | 3.31076e-05 | 0.0040685 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397746 | GTGAGGAGGTGTGGG[C/T]GGCACCAGGTTCAGT | 55626 |
rs144412383 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438131 | TTAAAGGCAAAAAAC[-/AA]ATATTGGAAAAAAAT | 55626 |
rs144417301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478934 | CTGGACGCAGTGGCT[A/C]ACGCCAGTAATCCTA | 55626 |
rs144450977 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454464 | AAATTGGCCAGGTGC[A/G]GTGGCTCACGCCTGT | 55626 |
rs144454005 | snp | A/G | 0.000131902 | 0.00811996 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46544014 | TGCTGTGAGTAAGTA[A/G]TGTCCAAGTGGATCA | 55626 |
rs144471103 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467337 | CCATGTTTGGGTTAA[C/T]GTAAATTATTTACAG | 55626 |
rs144515690 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563978 | GGAGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 55626 |
rs144560830 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538027 | GTGACACCTGCTGGA[A/G]AACTAGAAGCAAGGG | 55626 |
rs144597825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432228 | TGACAAGTACTGACA[G/T]GAGAATGTGTAAGAG | 55626 |
rs144598980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480043 | ACTGAGGTTCCCACT[C/T]GCTGCTAGCTGTTAG | 55626 |
rs144639588 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407508 | CCAGAGGCTCACAGC[A/G]GAGGTTGGCTGCTCC | 55626 |
rs144653135 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473422 | GAGGGTGATAACTTG[C/T]ATTTTTGTAACACAT | 55626 |
rs144676248 | in-del | -/ATTCACAGCATGCGAATAAGCAC | 0.310632 | 0.242536 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476531 | AATAGCCAGAAACTT[-/ATTCACAGCATGCGAATAAGCAC]ATTCACAGCATGTGC | 55626 |
rs144702743 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475420 | CATACATTTCTTTGA[C/G]GGGGTAGACTGGACC | 55626 |
rs144724685 | snp | C/T | 0.00296208 | 0.0383701 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542482 | TCCAGCTCCTGAAGC[C/T]GGTCATACTCCAGAA | 55626 |
rs144749594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402663 | GCCACTGGAGAAGCA[A/C]TTACATGTCTAGTTC | 55626 |
rs144750570 | snp | A/G | 3.35404e-05 | 0.00409501 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542950 | TCCTGCTGCGTTGAC[A/G]AGGCCTGCTCCGGGG | 55626 |
rs144751650 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489196 | ACATTAGGTATACCT[C/T]CTAATGCTATCCCTC | 55626 |
rs144763816 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556827 | GCTTCATTCTGTAAT[A/G]AAGAATTAGTATGAA | 55626 |
rs144779455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430606 | AGCAATTCATTTTCA[C/G]AAGAGTTTTCATATG | 55626 |
rs144792098 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547571 | GTGAGCTGTATCACA[C/T]AGGCAAATGATTGTT | 55626 |
rs144795392 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417883 | CTCGGCCCCAGTGAT[C/T]CCTCAACCCCCACAC | 55626 |
rs144815474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497480 | AATACAAGGCAGAGC[A/G]GATTTCAAATTCCAA | 55626 |
rs144827685 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444759 | TTTATTGCACTGCTA[C/T]TCCTGGTGTCCCTTT | 55626 |
rs144827765 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501316 | TGCACATTGGATGAA[A/C]TGGCATGCCTAGACT | 55626 |
rs144831832 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592107 | TGCGCCACCACGCCC[A/G]GCTAATTTTGAATTT | 55626 |
rs144877229 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567077 | TAGTGTTTGTTTGTT[C/T]GTTTGTTTGTTTGAG | 55626 |
rs144935576 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539713 | CACTTTCCTCAACTT[C/T]ATAAAATGGAAAATT | 55626 |
rs144968775 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491321 | TTCTACTTCTTAGCT[G/T]CATTACTCTGGGCAA | 55626 |
rs144971384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414288 | CCTGGCTCTTAGAGC[C/T]TCGCCTGAAAGATGT | 55626 |
rs144975864 | snp | G/T | 0.000704779 | 0.0187588 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433662 | GAGAAATATTTCCTA[G/T]GCTTCTGGCCATTCC | 55626 |
rs144977269 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502573 | ACAGAAGTCCTAGAA[A/C]TTCCCGGCTCAGAAG | 55626 |
rs144986385 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558344 | TCACGAGGTCAGGAG[G/T]GCGAGACCAGCCTGA | 55626 |
rs144994920 | in-del | -/TA | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528753 | TTAAGAGGGTAAATC[-/TA]TGTTATGTTTTCTAT | 55626 |
rs145003239 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455400 | TACTTTAGTTAGCCT[C/T]ATATAAGCAGAATCA | 55626 |
rs145040199 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410181 | GGTTGAGGAGGGACC[C/G]AGAGCCCTAGAGGGC | 55626 |
rs145087448 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567936 | GCGGATCACTTGACA[A/T]CAGGGGTCTGAAACC | 55626 |
rs145094928 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448111 | AAGAGAGAGAAGTGT[C/T]TAATCTGAAGATTAA | 55626 |
rs145121010 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572522 | AAAAACGAACTTCAT[C/T]AAAAACGAGCACACT | 55626 |
rs145136709 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485233 | GTGAGCCCCTATGCC[C/T]GGCCTCAAGAAGCCC | 55626 |
rs145195351 | snp | A/G | 0.000144506 | 0.00849895 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397537 | GTTATTGGTCAACTC[A/G]CAGTGGAGGGTTGGT | 55626 |
rs145221216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429088 | ATCCTTCTTGGCCAC[C/T]ATGACTCCCTCCTTA | 55626 |
rs145222869 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519078 | ACCCAGGCTGGAGTA[C/G]AGTGGCGCGATCTTG | 55626 |
rs145238098 | snp | C/T | 0.0008 | 0.019984 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523890 | TTATTTATTTTGAGA[C/T]AGAGTTTCGCTCTTG | 55626 |
rs145239522 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508499 | CATGAAAATTAAAGG[G/T]CATTTAACTCAACTC | 55626 |
rs145310960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571407 | TAGCCATATTACAGT[A/G]GTTCACTTCTGTAAT | 55626 |
rs145314974 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486084 | ACTTTCATCACTGGA[A/G]CAGAATGAAATGTAA | 55626 |
rs145316886 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429828 | TTTTGAGAATTCAGC[A/T]AAACTTCAGCTCAGC | 55626 |
rs145395542 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501868 | TATCAATTAGTCTAT[A/G]GTAAAATTAGTTTCA | 55626 |
rs145411370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589990 | ATGTTTGGATTTGAT[A/G]TTAATAAGCACCATA | 55626 |
rs145428157 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449052 | GTCTCTTCCAGAAAA[C/T]AGAAATATGAAATAC | 55626 |
rs145428746 | snp | A/C/T | 3.5747e-05 | 0.00422758 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397943 | TACTCTGAACCCTCA[A/C/T]CTGGCAGATACAAAG | 55626 |
rs145446546 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520269 | ACAAGCACACATTCA[A/G]TTAGCCATCAGGATG | 55626 |
rs145447326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499942 | CAGGCATGAGCCACC[A/G]CCCCCGGCTGACAGG | 55626 |
rs145466300 | snp | C/T | 0.00314384 | 0.0395226 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542503 | TACTCCAGAAAGAAG[C/T]GTCTCAGGTCACACT | 55626 |
rs145497295 | in-del | -/AATT | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562736 | GCCTGAGAAAATATG[-/AATT]AATTCAAGAGAAACT | 55626 |
rs145514359 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572162 | AAAAATTTGCTGGGC[A/G]TGGTGGCGCCAGCCT | 55626 |
rs145534913 | snp | C/T | 0.000182671 | 0.00955522 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46443550 | AGCCGGTAGGTAGTA[C/T]TGGCAATGTTACTGG | 55626 |
rs145536075 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536352 | AGTATCTAGTACACA[C/T]GCAACAAAGAAAAGG | 55626 |
rs145536763 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448710 | TAGGTAGGCCAACTA[A/C/T]GAAAAAAGAGAGAAG | 55626 |
rs145546060 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479044 | TCTCTACAAAAAATA[C/T]CAAAATTAGCCAGGC | 55626 |
rs145552896 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540181 | AGTTTATTTAAACCA[C/T]TCAGGAATTTCTCAG | 55626 |
rs145568995 | snp | G/T | 0.000439271 | 0.0148136 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46417915 | TTAAGCCACTTACTC[G/T]GGTCGGCAGATCACC | 55626 |
rs145582910 | snp | A/G | 1.65026e-05 | 0.00287246 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418036 | GCAGGCATGGGATAA[A/G]GGACGTTGAAAACTC | 55626 |
rs145601940 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455969 | GTTTTTATCACCATG[C/G]TATAGACTTGCCCTC | 55626 |
rs145634814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458535 | GTGTGATTTTTCCTT[C/T]TTCTTGAGATGGTGA | 55626 |
rs145674394 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530117 | ACTCTGAATAGATAC[A/G]GTAGAGAAGGGGATC | 55626 |
rs145698246 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593176 | AGTCTATATTCCTAG[C/G]AAAATTGGGATCACA | 55626 |
rs145723573 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450546 | CTGGGCTCAGATGAT[C/T]CTCCCACCTCAGCCT | 55626 |
rs145749616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463347 | AGTAGGTGCCTCTGA[C/T]AGCAAGAACACACAC | 55626 |
rs145761376 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434116 | TGAAACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 55626 |
rs145773879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465854 | ATTGTGCAACTGTCC[A/G]TGCTATATTCTATAA | 55626 |
rs145793822 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554619 | TAAAAGGATAAGGGA[C/T]TTCTCTCCTGATATG | 55626 |
rs145855535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457768 | TGAACCAGGTGTGGT[A/G]GTGCATGTCTATAAT | 55626 |
rs145859376 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545439 | TGCACTCCACCCTGG[G/T]TGACAGAGTGACACC | 55626 |
rs145888214 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409065 | GTAGCTGAGATCATG[A/G]GATAAAGAGTGAGCA | 55626 |
rs145903315 | in-del | -/A | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401947 | CCCTTATCATGCTGC[-/A]GACCTTCCTGCCCTG | 55626 |
rs145924379 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420722 | ACACCCAGAGTTAAG[A/G]AGGGATGAGGGTTAA | 55626 |
rs145999549 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453576 | GACTTAAGATAAATA[C/G]AATTATTTCCATTGT | 55626 |
rs145999852 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403163 | CAGAGGCCAGGGTAG[G/T]ATCAACAAGTTCCCA | 55626 |
rs146000898 | snp | C/T | 0.000614296 | 0.0175149 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547258 | TTCACCTCCGTAATA[C/T]AGATATTATGGTTCA | 55626 |
rs146002988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406569 | ATTTGCACATACATA[C/T]ATACATACTACAAAC | 55626 |
rs146023586 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590099 | AATGTATGGCCGAGC[A/G]AGGTGGCTCATGCCT | 55626 |
rs146024858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535643 | TAAGGAGAAAAAAAA[C/T]ACCAACAGCACTGAC | 55626 |
rs146041322 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447239 | AGTGAGACTCTTATC[A/G]CAAAAAAAAAAAAGG | 55626 |
rs146041780 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538563 | CAGTGGTGCAATCTC[A/G]GCTCACTGCAACCTC | 55626 |
rs146066841 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467608 | GGCTAGAGTGCACTG[A/G]CACGATCTCAGCTCA | 55626 |
rs146096425 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470326 | GGGCGCGGTGGCTCA[C/T]GCCTATAATCCCAGC | 55626 |
rs146096859 | in-del | -/TG | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452890 | ATGCCCAAATATATA[-/TG]TGTGTCTGTCTGTTT | 55626 |
rs146122101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475763 | TGGATACGAGAATCC[C/T]GTAATTTCTTGTCGC | 55626 |
rs146125819 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426297 | ACGTTGCATGCCTCC[C/T]GCAGCTAACTAAGCA | 55626 |
rs146162926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472547 | AGAGGTTAAATGACT[C/T]ACTCAAATTGTATAG | 55626 |
rs146165446 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562887 | CTCACTGCAATCTCC[A/G]CCTCCCAGGTTCAAG | 55626 |
rs146188250 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490677 | CTGCCAAATTTCCAA[C/G]CTTCATCCCTGCAAA | 55626 |
rs146234148 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559144 | GTCTCTACTAAAAAT[A/G]CAAAAATTAGATGGG | 55626 |
rs146241297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442242 | CTGCCACACAGGTTC[A/G]AGCAATTCTTGTGCC | 55626 |
rs146245372 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447037 | TTAATCTCTCTGAAC[C/T]TCAGTTTCCTTATCT | 55626 |
rs146267985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579992 | TGCTGGGATTACAGG[C/T]GTGAGTCACCACGCC | 55626 |
rs146273494 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537671 | TCCACTGCCCACAGG[C/G]AAAAGGAGACAAACC | 55626 |
rs146282346 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495386 | CAAGCCAGAAACAAA[A/T]GTCTATGATGGTTTT | 55626 |
rs146292312 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564455 | AAAACCAGGCATAAA[A/G]AGGCTAAATGATTTA | 55626 |
rs146361325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402308 | ACAGGGGCTCCAGAC[C/T]TAAGGATGCTTGGAA | 55626 |
rs146364394 | in-del | -/ATCTCTAG | 0.202035 | 0.245356 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419402 | CCACTACAAAACAAT[-/ATCTCTAG]ATCTCAACTTAGAAC | 55626 |
rs146369533 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471656 | TTTTTTTAGATGGAG[C/T]CTTGCTCTGTTGCCA | 55626 |
rs146387773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511588 | ACCTACACTGCTAAC[C/T]TGCCAACCCCACAAC | 55626 |
rs146402129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488228 | TGGGAAGCTGGGGCA[A/G]GTAGATCCCTTGACA | 55626 |
rs146408367 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438872 | AAACTTCTAAACACT[A/C]ATCTCAAATCTCAAG | 55626 |
rs146413309 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530722 | TATAAAGCAGGAGCT[A/G]GCAAACTATAACCTG | 55626 |
rs146415794 | snp | A/G | 8.27164e-05 | 0.0064305 | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433509 | CATGGGCCTGTTGCA[A/G]CCTGAAGACCTGGGC | 55626 |
rs146430502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443390 | ATAACAACTGCTCAA[C/T]AGGATGATGAAAAAC | 55626 |
rs146455320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525470 | TGTGTCAAGTCTGGG[C/T]GCGGTGGCTCATGCC | 55626 |
rs146455333 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581344 | CCAGGCGCAGTGGCT[C/T]ACACCTGTAATCCCA | 55626 |
rs146507289 | in-del | -/T | 0.0414363 | 0.137845 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536471 | CCCATCCAAAGAAAC[-/T]GGGAGAGATTAGATA | 55626 |
rs146518010 | in-del | -/AA | 0.0916144 | 0.193427 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563067 | CATCCCAATGTGCTG[-/AA]ACTACCGTGCCTGGC | 55626 |
rs146524676 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398488 | CTGAGAGTTATTTTT[A/C]TATTGATTGATTGAT | 55626 |
rs146529357 | snp | C/G/T | 0.000247096 | 0.0111129 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542341 | TGGCCACGGGACAGG[C/G/T]TGGAGTTGTTCTCAC | 55626 |
rs146535061 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463062 | TCTGGCCAATAATCC[C/T]CTTTTCTAAGAAGTC | 55626 |
rs146536124 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551688 | CCAGCCTGGCCAACA[C/T]GGCAAAACCTACTCT | 55626 |
rs146553727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413850 | AGCTAAAGAATGATC[C/T]CAACATGTCCTGGTG | 55626 |
rs146577669 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546111 | CACAATCTCAGCACA[C/T]TGCAACCTCTGCCTC | 55626 |
rs146592179 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458634 | CAAGATCTTGCTCTG[A/T]CGCCCAGGCTGGAGT | 55626 |
rs146645876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418831 | CTTCATTGCTTTTAA[A/G]TTAACTCCCTGGAAA | 55626 |
rs146652815 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485835 | AAGAAGCACAGGCAA[C/T]TCAGCTTAGAAACTG | 55626 |
rs146690240 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532129 | GTCTCAGAAATAAAT[A/T]AATTAATTAATTAAT | 55626 |
rs146708898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480242 | CCATGTAAAGTAACA[C/T]ATTCACAGGTTCTGG | 55626 |
rs146772605 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419691 | TGCCCCCAGGGTTGA[C/T]AGAAGGGGAAAAAAA | 55626 |
rs146791287 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424427 | GCTTTTTATTTTTCA[A/T]TTGGCCCGCTGCTTT | 55626 |
rs146811211 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553035 | ACTGCAACCTCTGCC[C/T]CCTGGGTTCAGGTAA | 55626 |
rs146850974 | in-del | -/C | 0.0799831 | 0.183287 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557559 | CACCTGTAATCCCTG[-/C]CCCTGGGAGGTTGAG | 55626 |
rs146862085 | in-del | -/TTAC | 0.0146672 | 0.084371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459357 | TTATATATTTTGGTA[-/TTAC]TTGAATTATTTACAG | 55626 |
rs146934022 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421796 | ATCCCAAACCATTTA[C/T]GGTTTTGGTCATCAG | 55626 |
rs146934554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566414 | CACAGCGAGACTACA[G/T]CTCAAGAAAAAAAAA | 55626 |
rs146977992 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577106 | TAGGACCTGCAATTC[C/T]ATTCCTACCTAGGTA | 55626 |
rs147016777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513793 | GCTAGAATATAGGCT[C/T]AGTATTGCTGGCTTT | 55626 |
rs147038545 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441044 | CCTGATTCACTACTT[C/T]TTGCTAACAATCTGA | 55626 |
rs147040384 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588428 | TTAACAATTGAAGAG[C/T]ACTTTATCCTTTTAA | 55626 |
rs147076863 | in-del | -/T | 0.284733 | 0.247575 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585808 | GGAAAATAACAATAA[-/T]TTTTTTTTTCTTTTG | 55626 |
rs147084075 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401284 | CTCGCTCTGTCGCCC[A/G]GACTGGAGTGCAGTG | 55626 |
rs147100074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405119 | ACTTGGTGCCATTTC[A/G]TGTGCTGAGACATGT | 55626 |
rs147106613 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445882 | ATTGAAAAAACAAAC[C/T]TCATATTTTAAGAGC | 55626 |
rs147123306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537003 | TTAGTGCTTCTAGGA[A/G]GAGATTGAGACCAAT | 55626 |
rs147138691 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460708 | ATATAAACCAAAGTC[A/T]TAAGAGCAGATGCCT | 55626 |
rs147175425 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455567 | GAGAATATAACCTCT[G/T]GATCTGTCATGGCCA | 55626 |
rs147206577 | in-del | -/AAAC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515474 | TGAGACTGCATCTCA[-/AAAC]AAACAAACAAACAAA | 55626 |
rs147211027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416555 | TGACCTAATTCAGCC[A/G]ATAAGGACTCAATCA | 55626 |
rs147244995 | snp | C/T | 0.00597247 | 0.0543191 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396129 | TGAATAGCCTTCTGT[C/T]GTTCCTTCCTACATA | 55626 |
rs147267009 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528797 | TACACGAAGATAAAA[A/C]GGGTTACATGTGCCA | 55626 |
rs147283716 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533672 | GTGTGCAGAGTTGGC[C/T]TAGCTTTAATTTACG | 55626 |
rs147283782 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478846 | AAGTTCTAAATCTGT[A/G]CCTTTATATCCTTTG | 55626 |
rs147340609 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503434 | CCCAAAACAATTACA[A/G]TTGATCACAGGTCAC | 55626 |
rs147352334 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416957 | CTCCATAAAGCCAGA[A/G]GAAGGGGAAGGGGTG | 55626 |
rs147373281 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549349 | AATGTTTTAAAAAAT[A/G]TAGGAAAGTTGAAAG | 55626 |
rs147385119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412715 | CCTTCCTCTTCTAAA[C/G]AGCCATTTTTGTGGG | 55626 |
rs147389778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501135 | ATGACCATGCATTTA[C/T]AGCTGGTACTCAAAT | 55626 |
rs147389841 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556593 | GTCAATATGTATAGT[C/T]ATATATATGGGCCCC | 55626 |
rs147444932 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528112 | TATACATAGAATGGA[A/G]TATTATTCAGCCTTT | 55626 |
rs147448508 | snp | C/T | 1.67652e-05 | 0.00289522 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397874 | ACGGCTGTCATGCCG[C/T]CCTCCGCCATCAGCC | 55626 |
rs147456627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436035 | AGACCAAGCTCATCA[A/G]GGCTTTGTCTCATGT | 55626 |
rs147477283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574715 | GCTCATCCTTACTCT[C/T]ATGGCCAACTCTTGG | 55626 |
rs147492804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432597 | TGCACAGCACTAAAT[A/G]AGGGACCTGAGGGAT | 55626 |
rs147493375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523697 | GCTTTACCCAGATGC[A/G]CTTTATTTAGAAAAA | 55626 |
rs147493674 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578750 | GCCAGGCATGGTGGC[A/G]GGCGTCTGTAGTCCC | 55626 |
rs147515391 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503996 | GAGCTGCCACACCCG[A/G]CTCTAGCAACAGTTT | 55626 |
rs147544015 | snp | C/T | 0.000942566 | 0.0216886 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494199 | CTGGATCTGTCACCA[C/T]TGTCCCTGAAAAAAA | 55626 |
rs147603362 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470088 | TTATATAAATAAGAC[C/T]TGTATTATCTTCCTT | 55626 |
rs147603787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523946 | TGATCTAGGCTCACC[A/G]CAACCTTCACCTCCT | 55626 |
rs147653649 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519184 | ATGCACCACCAAGCC[G/T]GGCTAATTTTTGTAT | 55626 |
rs147674814 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588538 | CCCAGCACTTTGGGA[C/G]GCCAAGGCAGGTGGA | 55626 |
rs147706967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405373 | CCTACTTGTCTTCAC[C/T]GCTTTTACCAAGTGG | 55626 |
rs147711241 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544951 | GTGAGGCCCCGCCCC[C/T]CAAATCTCTACGAAA | 55626 |
rs147722970 | snp | A/C | 0.00193233 | 0.031023 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408492 | CCTCTCCCACCCCCT[A/C]CAGCGCCACATGGCT | 55626 |
rs147746253 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540281 | AAACAGCAACTGCTT[G/T]GTTTCTTAGAGCAGT | 55626 |
rs147792882 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496981 | GCCAGACGTGATGGC[A/G]AGCGCCTGTAATCTC | 55626 |
rs147798253 | in-del | -/G | 0.0158469 | 0.0875917 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461539 | TGACCAACATAGTAT[-/G]GGGGAGGTCATAATT | 55626 |
rs147814350 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570193 | CTTGAACCTGGGAGC[C/G]AGAGGTTGCAGTGAG | 55626 |
rs147850414 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566136 | TTAAAAAGAGTGGAA[C/T]TGGTCAGGGCGCTAG | 55626 |
rs147863174 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474146 | TTTTACTGGTTCAGG[G/T]TGCTGCCCTGATTTA | 55626 |
rs147918734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501336 | ATGCCTAGACTACCT[C/T]AGTCTGAGTGAGTGT | 55626 |
rs147919508 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445269 | ACCGTTCTAGATAAA[C/T]GAATACCCACAAAAC | 55626 |
rs147920902 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592154 | TAGTCAGGCTGGTCT[C/T]GAATTTCCGACCTCA | 55626 |
rs147935667 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448613 | CATGAGCAGAAACCA[A/G]TGAAACTGAAAACAG | 55626 |
rs147954019 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582818 | TTCAATAAGGACTGG[C/T]TCTGATCAGAACCAA | 55626 |
rs147972448 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421840 | GAGACTGGGTGAGTT[G/T]TGAGTCCCCTTTTAG | 55626 |
rs147975599 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497827 | AGGCAGAAACAGTAA[C/G]TGATGACTCTCTAGA | 55626 |
rs148009276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471278 | AAAACCCCACCTCTG[C/T]TAAAAAATATAAAAA | 55626 |
rs148009412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560155 | AATTAAAATTATACA[C/T]AGTCCCTTTCTTTAT | 55626 |
rs148023039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415635 | TGGGCCCTAAGGCTT[A/G]AGGCATTTGCCAACC | 55626 |
rs148042064 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538099 | GAGGAAGAGGCAGAC[C/T]AGCACCTGTTTGTCT | 55626 |
rs148063286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554033 | CCAGGGTAGCCCTTC[A/G]GTCAAACTGCCACAT | 55626 |
rs148077172 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499032 | CAAGGGCTTTGATTT[C/G]TGGAAGGAAGGCACA | 55626 |
rs148102595 | in-del | -/TATAATCCACCCACTT | 0.106633 | 0.204807 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519259 | GATCTCCTGGCCTCA[-/TATAATCCACCCACTT]TGGCCTCCCAACATG | 55626 |
rs148111398 | snp | A/G | 0.106633 | 0.204807 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489242 | CCCACAACAGGCCCC[A/G]GTGTGTGATGTTCCC | 55626 |
rs148162271 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481927 | TGCTTGGAACAGTAC[C/T]TGGTATAGAACAAAT | 55626 |
rs148178878 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430816 | CAAAGCTCTAGGACA[C/G]GCCCATTACCCACTA | 55626 |
rs148209480 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527790 | GACCACTATAAAAAG[-/A]AAAAAAAAACAGGAA | 55626 |
rs148220827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514874 | ACAGGTAAGGGTAGT[A/G]AGAGATACAGAGTCT | 55626 |
rs148232432 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426166 | TGATTCAATTAGGGC[A/G]TACTGAGTAATGGGC | 55626 |
rs148274368 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509585 | ATAAATTATTAATAT[A/G]TCCATACAAAGAAAC | 55626 |
rs148287938 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450506 | GTGCAGTGGTGCAAT[C/G]ACGGCTCACGGAAGC | 55626 |
rs148324253 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533832 | TTAGAAGACCCTGCA[C/T]AATCTCATCCTTGTC | 55626 |
rs148362547 | in-del | -/C | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593095 | CTTTGAAAAGCAAAA[-/C]CAGCCAAGAAACCAC | 55626 |
rs148373547 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527407 | ATTGCTTGAACCCAG[A/G]AGGTGGAGGTTACAG | 55626 |
rs148377522 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475764 | GGATACGAGAATCCC[A/G]TAATTTCTTGTCGCA | 55626 |
rs148410207 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544160 | GTATCACTCAGGTAT[C/T]CACTTCATTCAAGAC | 55626 |
rs148413337 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457923 | AAAAAAAAAAAAAAA[-/G]ACATTCCACCCTACT | 55626 |
rs148477576 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407562 | GGCCCCAGCGAGGGG[C/T]TTCCACCAAGCACAA | 55626 |
rs148486014 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479148 | GGTTGCAGTGAGCTG[C/T]AATCAAACCACTGCA | 55626 |
rs148500124 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424852 | AAAAATTTTAAACAA[A/G]TAGGCCAGGTGTAGT | 55626 |
rs148506258 | in-del | -/ATTTGTGTGTGTGT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425308 | TCTTTTGCTTGATCC[-/ATTTGTGTGTGTGT]GTGTGTGTGTGTGTG | 55626 |
rs148530805 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402788 | TACCAGACACAAAGT[A/G]AGTGCTCAAAAAAGA | 55626 |
rs148535781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473464 | GATGAGTATTGTATT[A/G]ACATCTTTGGATAAA | 55626 |
rs148552959 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418771 | ATACTAGGGGACTCT[A/G]TGGCTCTAATAATGC | 55626 |
rs148619089 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500697 | TGTAAATCTCCTGTC[G/T]CTACGCTTTTGCTTA | 55626 |
rs148619372 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588885 | CACAGCTCTACTATA[-/C]CTACTGTGTGATCTT | 55626 |
rs148620140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590106 | GGCCGAGCGAGGTGG[C/T]TCATGCCTGTAATCC | 55626 |
rs148632674 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492575 | AGTCGGCAGTGGAGG[G/T]GGGAGGGAGGTAGGG | 55626 |
rs148678267 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575054 | CAGAGAAGTGAACAA[C/G]TAAATGCTCCCATAG | 55626 |
rs148724335 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400577 | GCTCACTGTAGCTTA[A/G]CCTCTTGGGTGCAAG | 55626 |
rs148731984 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569893 | TTGAACCCAGAAGGC[A/C/G]GAGGTTGCAGTGAGC | 55626 |
rs148732206 | snp | A/G | 1.69533e-05 | 0.00291142 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542156 | TTTGGCCCTCAGTCC[A/G]CTCGAGAGGTGGCAA | 55626 |
rs148755028 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396263 | ACCTGACCAGCTCTG[A/G]CGAAGGGGTCAGAGG | 55626 |
rs148775052 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520599 | TTTGTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs148778554 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461970 | TCTCATACTGCCCCC[C/G]ACTATCTAGACTCCT | 55626 |
rs148780911 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587195 | GATCTGCCTGGCCAA[C/T]ATGGTGAAACCCCAT | 55626 |
rs148784155 | in-del | -/T | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490403 | ACACTTTTCTCTTTA[-/T]TTTTTAATATTTTAA | 55626 |
rs148784670 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397860 | GCTCCCGCTGCACCA[C/T]GGCTGTCATGCCGCC | 55626 |
rs148801791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511366 | GTTCCCTGATCCTTA[A/G]GTTTGTCATTTCTAG | 55626 |
rs148818528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520297 | ATGATAGCCTCATTA[C/T]ATGTCATGGAGCCTC | 55626 |
rs148837512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536602 | ATTTTTAGGTTGCCG[A/G]CCCCCTTTTGTGGAC | 55626 |
rs148849778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443713 | GGAAAAACTAGACTA[C/T]GGCTGAAGAAAGCTA | 55626 |
rs148851141 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399817 | GAGTCAACTGACCAG[C/T]ACAGGACCCAGGTCT | 55626 |
rs148851799 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425840 | GCGAAACTCCGTCTC[-/A]AAAACAAAAAAAAAG | 55626 |
rs148885506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464162 | AACTCCAAGAAGAGA[A/G]GAGCAGGTGCCAGAG | 55626 |
rs148887354 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553597 | TAAAAATACAAAAAT[C/T]AGCCAGGCGTGGTAG | 55626 |
rs148939005 | snp | A/G | 0.000938196 | 0.0216383 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545785 | TGCCACCCTGTGAAT[A/G]AACCAATTCCAGATA | 55626 |
rs148954136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415128 | TGGGTGTGCCAGGGA[A/G]CTGTATCACCCAGGG | 55626 |
rs148994478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497882 | GATTCAGAGATAATG[A/G]GTTGGGGTGGGAAAA | 55626 |
rs148996554 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533053 | TTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 55626 |
rs149006799 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409276 | CGCAATCTCAGCTCA[C/T]TGCAACCTCTGCCTC | 55626 |
rs149047335 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491456 | ACACTCCCTAGTATA[C/T]AGCAAGTGCTCAATA | 55626 |
rs149064131 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438929 | AGCCTAACTCCAGGA[A/C]AAGGTTAAATGCAAT | 55626 |
rs149065218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474968 | GTCCGCATATATGTA[C/T]AACATGAGGAGGATG | 55626 |
rs149080572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558845 | AGCACAATGTCTAGC[A/G]TAGAAGAGCATGAGT | 55626 |
rs149092457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420222 | GACTCAACTCCAAAT[C/G]TAAGGAACTCGTTAA | 55626 |
rs149093532 | snp | A/C/T | 0.00341225 | 0.0411652 | synonymous-codon, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397492 | GCCTGCAGCGTCCCC[A/C/T]CTGCTGCTGCCACCA | 55626 |
rs149097092 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508970 | CTCCCTTAAGAATTA[A/G]TCATAGATATTTGTA | 55626 |
rs149114252 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433770 | TAGGACTGTAGTGAG[A/G]AGTATGATGAGAAGG | 55626 |
rs149147339 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502398 | TCCTAATATTAGAGT[C/T]TGTGGCTCATAAGAC | 55626 |
rs149151181 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595664 | AATAATGTATTGGCA[C/T]TTTACAAAAATCTCC | 55626 |
rs149208333 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577252 | AAATGTGATGTATAC[A/T]CACAATGGAATATTA | 55626 |
rs149216789 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449542 | ATAAAACTAAATTAG[A/C]GAGATATTCCATGTT | 55626 |
rs149257876 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503394 | AATTAAGCTTATTGT[C/T]TTATATGATTGTGGT | 55626 |
rs149298986 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589427 | GAGAATGAAACAAGA[A/G]TGACTGTGATTAAAG | 55626 |
rs149313662 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454235 | GGTCTTGCTGTGTTG[C/T]CCTAGCTGATCTCAA | 55626 |
rs149345604 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523142 | AAACAATCCACTGTT[A/G]GCCCTTGAGCTAACA | 55626 |
rs149364172 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446772 | GCTAGATAAACATAT[C/G]CTACATTTTAACTCC | 55626 |
rs149368788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538006 | CCTAGCAGCAGCAGC[C/T]CAACAGTGACACCTG | 55626 |
rs149370911 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542945 | CCTGGTCCTGCTGCG[C/T]TGACGAGGCCTGCTC | 55626 |
rs149417457 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466491 | CTAGGGCTTGAAGCA[C/T]GTGGAAAGGAGAATG | 55626 |
rs149436088 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481592 | GGTCTCGAACTCCCG[A/C]CTTCAGGTGATCGGC | 55626 |
rs149458497 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548732 | GCACAGTGGCTCACG[A/C]CTGTAATCCCCGAAC | 55626 |
rs149466841 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426079 | TCAAAATAAAAAAAA[A/T]AAAAAAAGAAAGAAA | 55626 |
rs149473793 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417338 | TACAGGCATGAGCCA[C/T]TGTGCCCAGCCCCAA | 55626 |
rs149523795 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411301 | CATCCCCAAGTGAGT[C/G]TATTATAGGATGCTG | 55626 |
rs149527723 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500212 | AGTCACTGCTGTTCT[A/C]AGAAGCAGTGATTGC | 55626 |
rs149577769 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494411 | TTTATGAGCATTTAC[C/G]AACAGCTCAGGAAAG | 55626 |
rs149593923 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441241 | AAGCTGGGCCGGGCA[C/T]GGTGGCTCACGCCTG | 55626 |
rs149608466 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526723 | TGAGCCCAGTCTACA[A/C]CCCACACACACAAAA | 55626 |
rs149624973 | snp | A/C/T | 1.66112e-05 | 0.00288189 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397712 | TCTGGGAGCAGTCCC[A/C/T]GAGAGGTGGAGGGCT | 55626 |
rs149646583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435445 | GAAAAAGATGATACA[A/G]GTAGAGCTTTCTTGG | 55626 |
rs149663069 | snp | C/T | 0.00328193 | 0.0403757 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443473 | CACTGATACCCCCAT[C/T]TGACATTGACTTACC | 55626 |
rs149699576 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587140 | ATCCCAACATGTTGG[A/G]AGGCCAAGGTGGGCA | 55626 |
rs149713300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437884 | CACCATTAGAAGTCT[C/T]TGTGGTGCTCCATAC | 55626 |
rs149716856 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529592 | AAAATTGGATTTAAG[C/T]AGGAAACATGACATC | 55626 |
rs149722154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512463 | CTATGACTACCTGTG[A/G]CCTCTCCAGGTTCCT | 55626 |
rs149730071 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400474 | AGTTCTTTCTATAGT[-/T]TTTTTTTTTTTTTTT | 55626 |
rs149732166 | snp | C/G | 1.65108e-05 | 0.00287317 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410286 | CATACCCAGGCCGCT[C/G]GCTGCTCCTGCTGTT | 55626 |
rs149747817 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583732 | TGAACAGACACTTCT[C/G]AAAAGAAGACATTTA | 55626 |
rs149752959 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579736 | GTTTTGTTTTGAGAT[A/G]GATTCTTGTTCTGTC | 55626 |
rs149784269 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472980 | CAACCTCAAATCAAC[A/C]TGATATTACAGTAAC | 55626 |
rs149818453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408935 | CCACAGAAACATCCA[A/G]TCTTGCAACCCTGGC | 55626 |
rs149841963 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457312 | CAGGCTAAGCTCCAA[C/G]GGCTAACAAATCCCA | 55626 |
rs149860106 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545325 | AAATGAGCCGGGCAT[A/G]GTGGTGGGTGCCTGC | 55626 |
rs149872449 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404716 | CCGCCTACTCTACTT[C/T]ACAGGAGGAGGGGAT | 55626 |
rs149897089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539681 | ATCTTTCACAAGAAA[C/T]TGACTTCCCTGAGCC | 55626 |
rs149928372 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574759 | ATACTTTGAAAAATA[C/G]TGGTTTAAAACTGAA | 55626 |
rs149931117 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469736 | GTGGTACGATCATTG[C/T]TCACTGCAGCCTCGA | 55626 |
rs149935573 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558317 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 55626 |
rs149943626 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433358 | AGCCCTTCCTTACTC[C/G]TTATGACTGTGTGAT | 55626 |
rs149985422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551468 | AAAATTATTTTAAAG[A/G]TGGGGTCTCGCTATG | 55626 |
rs149993395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428293 | CTCAACTCTTGGCTA[C/T]GGTTTTACCACATGG | 55626 |
rs150053199 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413808 | AAACTCTTAGCTTTC[A/C]ATACCCAGTGTCACT | 55626 |
rs150086782 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572130 | ACATGATGAAATGCC[A/G]TCTCTACCGAAAATA | 55626 |
rs150089869 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519868 | AATTATGAGGATCCC[A/G]GTGGCTCACGCCTGT | 55626 |
rs150189985 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446592 | AGGACAGATAATTAT[G/T]TGTGTGAAGAGTCTT | 55626 |
rs150212178 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463275 | TACAAGCCAAGTATA[C/T]CTGTTCTATTCCCAC | 55626 |
rs150226521 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499549 | TATTTTACAAATACA[C/T]TGAGGCTCGACAGGT | 55626 |
rs150234932 | snp | A/G | 3.34292e-05 | 0.00408821 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434895 | GTTATGGGGGGCCAG[A/G]GAGTACACTGCCAGG | 55626 |
rs150243113 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440313 | ACTGTAAAGAAAAAG[A/G]GCAGGAAGTACAGAC | 55626 |
rs150243808 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532581 | AGCTGGGACTACAGG[C/T]ACCCACCACCATGCC | 55626 |
rs150279592 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582725 | ATGAGAAGAATAAGA[A/G]TACTTACGTCATAAG | 55626 |
rs150296500 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524862 | AGGGGTACCTGAGCC[A/G]TGAGAATCACATGCA | 55626 |
rs150300312 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474640 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 55626 |
rs150383390 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459836 | TAATCTCCATTGTAT[G/T]TGACATATACATTTA | 55626 |
rs150385250 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548537 | TCAAAGAACGACTTC[C/T]GCAACGAGAAGCTTC | 55626 |
rs150402312 | snp | A/G | 0.00151222 | 0.0274559 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494110 | CCCTCTGTTGCTAGC[A/G]ACTCGGTTCTTACCT | 55626 |
rs150419558 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419888 | CAAACCAAGTGATAA[A/G]CAGCCCTGGATCTGA | 55626 |
rs150438990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541740 | TAGCCGAAATAGAGC[C/T]AGCGCAGCCAACTGA | 55626 |
rs150444112 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576789 | CATGTAAATGCAACA[C/T]GGCTTTATATGGGTC | 55626 |
rs150455671 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487008 | AACACCTGTAATCCC[A/T]GCACTTTGTGGGGCT | 55626 |
rs150461459 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561420 | CAGAAAAAAAAAAAA[C/G]CTTTGAGAACATTAA | 55626 |
rs150480293 | in-del | -/AA | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432825 | TTGAATCCCCTTGAC[-/AA]AAAACCCTGGCTAAA | 55626 |
rs150499438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495475 | GGAAGCTGATCCATT[C/G]AAAGTATTTGGTTTT | 55626 |
rs150508458 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407758 | GTGGCTTTTCCTCCC[A/G]TGGTCTCTTCTGGGC | 55626 |
rs150544334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510621 | CTAATGATAATAAGA[A/C]GACTGCCTTTTTATG | 55626 |
rs150548429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544788 | GCTGAAATGAACAAA[A/G]TGAATGTCTCCCAGC | 55626 |
rs150549602 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490101 | TAGGCACTCAGCTTC[A/G]TTTCCATCATTTCAG | 55626 |
rs150551491 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579470 | CTCAATAAATAAATA[A/C]ATTAAGTAAGTAAGT | 55626 |
rs150566579 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437242 | GACAAAAAGCATTTC[A/G]TCAGCCTCAAATCCA | 55626 |
rs150603729 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573170 | AGCACTTTGGGAGAC[G/T]GAGGTGGGCTGATCA | 55626 |
rs150605321 | snp | C/T | 3.3065e-05 | 0.00406588 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542873 | TGAGGTTGCGGAGCG[C/T]GTTGCCGGCAGTGCT | 55626 |
rs150619874 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431741 | GCAGAGACCAGCTTC[C/T]GCTTAAGAGAAGCAA | 55626 |
rs150620210 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522498 | GGCTTTTCACCAGAG[G/T]ATGAGTAAGACCAAA | 55626 |
rs150706946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447820 | AAATGGCCTTTAAAA[C/T]TATGTCTGTCATCTA | 55626 |
rs150708048 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539326 | ACTTTGGGAGGCCAA[A/G]GTGGGCAGATCACCT | 55626 |
rs150754946 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466278 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 55626 |
rs150757221 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590961 | AAGCTGAATGAACTT[C/G]TATCACAAAGCATGA | 55626 |
rs150768979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410536 | CATCAGGATGCTCAG[C/T]GCTGGATCAATTCAG | 55626 |
rs150773173 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396871 | CCCCTTACCCCACAG[C/T]AGTCCCCCATTAGTA | 55626 |
rs150777508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484450 | AGGAGCACACAACCA[C/T]GGGATTTAATAATCT | 55626 |
rs150828165 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476058 | AAAGGAAAAGGTGGA[A/G]AGCTGCACTCAGTGC | 55626 |
rs150858905 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583683 | AAAAAAAAAAAACAA[A/C]AAAACAACCCCATCA | 55626 |
rs150911921 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427567 | ACATGGCTGGGCCTC[C/G]CCCCCAGAGTTTCTG | 55626 |
rs150951218 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486185 | ACAGCCATCTTAATT[C/G]ATGTTGAGTTGGAAT | 55626 |
rs151005756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571454 | GCAAAGCAGAAGGAG[C/T]GTTTGAGCCCTAAAG | 55626 |
rs151059453 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565286 | AAAGGAAAAAGAACC[A/C]CATAATTTGTCATTT | 55626 |
rs151076522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457210 | CCTGCTGAACCCTCT[A/G]ATTCAAAGCCTGCTT | 55626 |
rs151081658 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582293 | CATACATGCTATTCC[C/T]TTCCCTTTCTATCCT | 55626 |
rs151108587 | in-del | -/AC/AT | 0.230603 | 0.249246 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459739 | AAAAAAAATACACAT[-/AC/AT]ACACACACACACACA | 55626 |
rs151127162 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504986 | TGACAAGCCCAAAAA[C/T]GGCAAAATGATCTAT | 55626 |
rs151135852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575207 | TCACACCTGTAATCC[C/T]GGCACTTTGGGAGGC | 55626 |
rs151147509 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403837 | ACTGACAGAAAAGGG[C/T]CAAGGGGAGTGGGGA | 55626 |
rs151148685 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434191 | ACATTTTAAAAAATT[A/G]TTAACATCCTGTAAT | 55626 |
rs151164174 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439873 | GGCATGCAATCTTGT[C/T]TGTAACACAAAAAAT | 55626 |
rs151187650 | snp | C/T | 0.00090694 | 0.0212755 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542245 | GCCTCGCCAGAGGAG[C/T]AGTTAGGTGTGGTTC | 55626 |
rs151203241 | in-del | -/TTG | 0.202651 | 0.245475 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533256 | TAACACACACACAAA[-/TTG]TTAATAGCAGATCTC | 55626 |
rs151218308 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524267 | TGCCCCCCAGAAATG[A/T]GGCAATGTCTGCTGA | 55626 |
rs151233267 | snp | A/C | 1.80847e-05 | 0.00300699 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397514 | CTGCCACCATCCAGA[A/C]GGTGGTTGTTATTGG | 55626 |
rs151241506 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541331 | CCACCTGGAAGGTCC[A/T]TTCAGAGAATCTCAA | 55626 |
rs151268102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518780 | ATCAAAAATGAATAT[G/T]AAGCTCTGCTAAAAT | 55626 |
rs151277299 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595914 | AAGAAAGAAAGAAAA[C/T]TCTCCTTCTTGGAGA | 55626 |
rs151284783 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468960 | ACCAGCCTGACCAAC[A/G]TGGCAAAACCCCGTC | 55626 |
rs151288780 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413555 | GAGTGCAATGGTGTG[A/C]TCTCGGCTCACTGCA | 55626 |
rs151291366 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536767 | CAGACTGTTCTAAGC[G/T]CCAAAGCAATTCCCC | 55626 |
rs151297112 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585499 | GGTGAAAGCCCGACT[C/T]TACTAAAAATACAAA | 55626 |
rs151304308 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400331 | TCCCCTAACCCCATC[C/T]ATCCCCTTCTCTCTG | 55626 |
rs151337271 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462201 | CACAAGTTAGGGATG[C/T]GCGTAAACAAGTGAG | 55626 |
rs180702309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428989 | CTTCACGTAGCCTCG[C/G]GACTTGAGAGACTGC | 55626 |
rs180716764 | snp | A/G | 0.0093968 | 0.0678977 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410414 | AGGTGAAAGGCATTA[A/G]AGAGGGAAGGATAAG | 55626 |
rs180784903 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563669 | ATGTAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 55626 |
rs180786712 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552000 | ACCACTGCACTCCGG[C/T]CTGGGTGACAGAGTG | 55626 |
rs180791454 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587236 | AATACAAAAATTAGC[C/T]GGACGTGGTGGCACA | 55626 |
rs180793305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570116 | AAATATAAAAAAATA[A/G]CTGGGCATGGTGGTG | 55626 |
rs180794278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525459 | AAAAACTTAGATGTG[C/T]CAAGTCTGGGCGCGG | 55626 |
rs180795428 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544257 | TATCACAAAAATAAC[A/G]ATTTCACATGAAAAA | 55626 |
rs180824108 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577120 | CCATTCCTACCTAGG[C/T]ATATTCCTAAAATAA | 55626 |
rs180832817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442964 | TGACCTCAAGTGATC[C/T]GCCTGCCTTGGCCTC | 55626 |
rs180839839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492055 | GCAGCAAGTTATTAT[C/T]TGCCAGTGAAAAAAG | 55626 |
rs180841475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483255 | TGGCTCTGGGGTGAC[A/T]CTCAACAGCTACCCA | 55626 |
rs180844174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472285 | ATCCTTTTCAGCCAC[C/T]TGAGCCTGTCTCTTA | 55626 |
rs180845432 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420511 | TGGCACCTTTATTCT[A/T]TCTCATGGAGGTTTT | 55626 |
rs180847266 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452178 | TCAATTTGTGAAGTA[A/G]AAAATGGTAATCCTA | 55626 |
rs180858790 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534927 | CATCTGCCCAACTTG[C/G]CTTCTCAGAGTGCTG | 55626 |
rs180861106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398920 | CTGGGATTACAGGCA[C/T]GCACCATCATACCTG | 55626 |
rs180875991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504431 | CCATTCTAGTAGGTG[G/T]TCTGGGCTTGAAAGC | 55626 |
rs180878139 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514891 | GAGATACAGAGTCTG[A/G]GAAAAAAGGAAAATC | 55626 |
rs180894177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463566 | CTTAACTAAAGAGTA[C/T]CTTGCACAAAAGCAC | 55626 |
rs180961314 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447261 | AAAAAAAGGCCACGC[A/G]CAGTAGCTCACACCT | 55626 |
rs180968567 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423619 | GATGGTCTTGATCTC[C/T]TGACCTTGTGATCTG | 55626 |
rs180980282 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401886 | GCAAAAGCCCTCACA[G/T]TAGTCAAAACTCCTT | 55626 |
rs181017080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437717 | AGGAAGAGATTTCTT[A/G]GATCTCAATTACTTG | 55626 |
rs181017237 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468707 | GTCCCCGTTACTCAG[A/G]AGGCTGAGGCAGGAG | 55626 |
rs181023118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459488 | AACCGACGCAAGTGG[A/C]TCACCTGAGGTCAGG | 55626 |
rs181029416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485669 | TTAAGGTGACAATAC[A/C]GAAAGGGCACACGGG | 55626 |
rs181034126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416105 | AAGAGGTCTTGGAGA[A/G]ACAGGGAAAGAAAGG | 55626 |
rs181040571 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573565 | TGTAATTTAGCCATC[A/T]TTTCAATCTTTAGAT | 55626 |
rs181064996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497208 | TTTTACCAACATTTT[A/T]AAAAACTGATGGAAA | 55626 |
rs181089178 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558824 | TCTGTCATAGTCCCA[A/G]TACCTAGCACAATGT | 55626 |
rs181096633 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519636 | AACTTTACAGCCTAG[C/T]TTTGATGTCTGGATG | 55626 |
rs181142357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548730 | AAGCACAGTGGCTCA[C/G]GCCTGTAATCCCCGA | 55626 |
rs181152433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479151 | TGCAGTGAGCTGTAA[C/T]CAAACCACTGCATTC | 55626 |
rs181155846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530047 | ATGCAAACAGAACCC[A/C]ATACACCTGGTGTTA | 55626 |
rs181158321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510016 | ACTGCTAGAGGAACA[C/T]AGGCTGCCTCTGAAA | 55626 |
rs181167061 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579863 | GATTACAGGTGTGCA[C/T]CACCACGCCTGGCTA | 55626 |
rs181179445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566606 | CCCGGGGGGTGAGGA[C/T]TGAGCTACCTAACCC | 55626 |
rs181201113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502826 | AGCACTTTGGGAGGC[C/T]GAAGTGGGCAGATCA | 55626 |
rs181228647 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562661 | TGTTTGCGGGTGGGG[A/G]AGCAGATTAAAGGGA | 55626 |
rs181236519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525108 | AGTTCGAGACCAGCT[C/T]GGGCAACCATAGGGA | 55626 |
rs181238175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473508 | ACAAAGTTAATTCTT[C/G]CTGTTACTTGTGGGG | 55626 |
rs181239163 | snp | C/T | 0.000586295 | 0.0171115 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493570 | ATCTGGCTCCTTGGC[C/T]CTTCACATTTTCAAA | 55626 |
rs181240482 | snp | C/T | 8.71103e-05 | 0.00659906 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543011 | AGGAAGGGGTAGTAG[C/T]TCTGGCAGAAGCAGG | 55626 |
rs181296184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462899 | GCTGGGATTACAGGC[A/G]TGCACCACCATGTCT | 55626 |
rs181322497 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577007 | TCTAAGCCCAGCCAA[C/T]AACTCTGAAATCACA | 55626 |
rs181354932 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419984 | GAAAAGACAGCAGCA[C/T]GTGTCCTCAATACAC | 55626 |
rs181386248 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482267 | AATGTTTTGGATAAT[G/T]GTAAATGCTGTTATA | 55626 |
rs181395358 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516159 | ATGTGTTGGCAACAT[A/T]TGCTGCCCAGACAAT | 55626 |
rs181414667 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396958 | TCAGTGGGGTAAGAC[A/G]ACGAAGAGAGGCTGA | 55626 |
rs181429263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570806 | GCACAAGTCATTTTC[C/T]AAATACATCTGCTGA | 55626 |
rs181436946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535719 | TAATATTACTGAGAT[A/G]CCAAGCCAAAGACCA | 55626 |
rs181475046 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442503 | TTGTCAGTGTGGTCT[A/G]TCATCAGAAGCAGTC | 55626 |
rs181502181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458500 | TGTGTACACTGAGCC[A/G]TCGATTTTCCATTGG | 55626 |
rs181509821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401306 | AGTGCAGTGACATGA[C/T]CTCAGCTCACTGCAA | 55626 |
rs181514806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436874 | AAAATAAAGAAATCA[C/T]AAATGTTAAGTAGTA | 55626 |
rs181539702 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415940 | GACTGTGACTGACAC[A/C]AAGTAGGCAGGCTGG | 55626 |
rs181546263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518866 | ACTATTTTTTCTTTC[C/T]CTGATTAATATTCTG | 55626 |
rs181547637 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550041 | CCAGGCTGGTCTTGA[A/G]CTCCTGACCTCAGGT | 55626 |
rs181548925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581648 | AAATACACAAATAAA[C/T]AATTACCCACATGTG | 55626 |
rs181551354 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497102 | GGTGACAGGGCAAGA[A/C]TCTGTCTCAAAAATA | 55626 |
rs181552203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478480 | ACAGAAATACAGGGC[A/T]ATATCCTAGAAAATA | 55626 |
rs181583916 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555685 | TAAAGTATGTTTATG[C/T]GGCAAAAATAATTCA | 55626 |
rs181591700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589491 | TGGGCAAAAAAATGC[A/G]GATTCCACTCCAAAA | 55626 |
rs181617448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461955 | AGACTTAATTTTAAG[C/T]CTCATACTGCCCCCC | 55626 |
rs181624952 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558146 | GGACCATCCAGACAA[A/G]TCCTGCCCAAATTCC | 55626 |
rs181629258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441407 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCGGG | 55626 |
rs181637249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419146 | AGGCACACAACTTGT[C/T]TCTAGCTTATATAAA | 55626 |
rs181644224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532051 | TTGAACCTGGGAGGC[A/G]GAAGTTGCAGTGAGC | 55626 |
rs181660499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481384 | TTCTGAGCTGAACAC[A/G]CTATTTTTGTTTTTG | 55626 |
rs181671053 | snp | A/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595191 | TGCGATGAGCCATGA[A/T]CACACCATTGCACTC | 55626 |
rs181721689 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573331 | ATCGCTGGAACCCGG[A/G]GGGCAGAGGTTGCAG | 55626 |
rs181751551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538562 | GCAGTGGTGCAATCT[C/T]GGCTCACTGCAACCT | 55626 |
rs181828135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570376 | CCAGAGGGAGAAGTA[C/T]GAAATTATATCTTTT | 55626 |
rs181835480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588504 | TGATGGGCCGGGCAC[A/G]GTGGCTCATACCTGT | 55626 |
rs181836376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552166 | TTGAGGTCAGGAATT[C/T]GGTATTAGCCTGGCC | 55626 |
rs181852986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473155 | TTAATACTTTAATGC[A/G]ACGTCACTGGAAAAT | 55626 |
rs181868895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429896 | TAACAAAAAGCCCTC[C/T]CTGGCTCAAGCAGAA | 55626 |
rs181925689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486538 | GTGAGACTAAAAAGT[C/T]CTCCTGAAAGTAATT | 55626 |
rs181929070 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469085 | GAGGCGGAGGTTGCA[A/G]TGAGCCGAAATCACG | 55626 |
rs181937991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447853 | CCACTCTCTGTGTGT[A/G]TTGCATCTACAGTTA | 55626 |
rs181944974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530783 | TATTTTTAAATGATT[A/G]AAAAACATCAAAAGC | 55626 |
rs181950186 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548848 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGCAGGC | 55626 |
rs181951803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510381 | GTTCTTATATCTGCC[C/T]AATATATAGAACTCT | 55626 |
rs181962033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515192 | AAAAACATCCTTCTT[A/G]GCTGGGCGTGGTGCC | 55626 |
rs182060323 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567153 | CTCGACTTACTGCAG[A/C]CTCCGCTTTCCGGAT | 55626 |
rs182083178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410903 | GTCACAAGATCAAGA[C/T]CATCCTGGCCAACAT | 55626 |
rs182118317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466744 | TACCTACCCATAATT[C/T]TTAAAGTTAGAAAGT | 55626 |
rs182122543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453216 | TTTCACTCAGCATAA[C/T]ATTTTCAAAGTTTAT | 55626 |
rs182134305 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538414 | TTTTAAATGGTTGAA[C/T]TTTAAACCACAATGC | 55626 |
rs182138918 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474801 | GCAGGTAAAGTTAAG[C/T]TCAAGGAAAGAAATA | 55626 |
rs182139777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555931 | TCCACTTCACTATGC[C/T]CATGTGGGCAAAGTC | 55626 |
rs182148924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571197 | TCCCCAGTGTTCTTC[C/T]ATACAAATCACTCAG | 55626 |
rs182151487 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496744 | CGTAGGTCACAAGCA[A/T]CTTTTTGTTGCTATT | 55626 |
rs182156798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536023 | ACTCTAAGTAATACC[A/G]TTTCATTTATTTAAC | 55626 |
rs182175643 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415373 | GTTACAAAAGTATGT[C/G]TGTGTTATTGTGGCA | 55626 |
rs182207178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457664 | CCAGCACTTTGGAAG[G/T]CCAAGGCAGGCAGAT | 55626 |
rs182248526 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535660 | CCAACAGCACTGACT[C/G]GCAGAGATAATAATA | 55626 |
rs182249442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590088 | TACAGTATAAAAATG[C/T]ATGGCCGAGCGAGGT | 55626 |
rs182261904 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493016 | ATCGTGCCACTGCAC[C/T]CCAGCCTGGGTGACA | 55626 |
rs182304105 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406526 | AAAAACAAAACAAAA[A/C]AAACAACACTCTCTT | 55626 |
rs182400729 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518123 | AAGAAAGAGATAGCC[A/G]TTTGTTTTCAGAAGA | 55626 |
rs182406879 | snp | C/G/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469895 | GTTGCCCAGACTGGT[C/G/T]TCGAACTCCTGGCCT | 55626 |
rs182408387 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449552 | ATTAGCGAGATATTC[C/T]ATGTTCATGAATAGG | 55626 |
rs182420314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425542 | ACTCACTGATATCGG[C/T]TAGAACTGTGGAAAT | 55626 |
rs182433187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487674 | CTGATAAAATACATT[C/G]AAAAATCAAAAAAGG | 55626 |
rs182464262 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477628 | GCTTGAGCCACTGTG[C/T]CCAGCCTCTTTGAGG | 55626 |
rs182476928 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402636 | CCCAAAGTGCTGGGA[C/T]TACAGGCATGAGCCA | 55626 |
rs182483666 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436268 | CTCTTTCAGAGGCCC[C/T]CAGGCTTATGTGATC | 55626 |
rs182498635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521698 | GTTTAAGTTATCCAA[C/T]GATAGGCATTCATCT | 55626 |
rs182503666 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540431 | GGCTCCTGATGAAGA[C/T]CAGTATGCCAGGCAC | 55626 |
rs182511719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527879 | TAAAATGGTTCAGCT[A/G]CTATGGAAAACAGTA | 55626 |
rs182521224 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576544 | CACCTGAATGATCCC[A/C]GAAAGATAGTCTTTG | 55626 |
rs182525218 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484896 | ATGATCCACCTGCCT[C/T]GGCCTCTGAAAGTGC | 55626 |
rs182534809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561093 | GCTACAGCAAGAATA[C/T]TGTTGGGCCAGGCGC | 55626 |
rs182535725 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453627 | AAGACTAATTCTGAG[A/T]GTATTATCTATAGCT | 55626 |
rs182541481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430395 | CCTAAAATGAAGAAA[A/T]CTTGTTTTAAAAATA | 55626 |
rs182551002 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454379 | AAAAAATTTTCTCAA[A/C]ACAACAATTCAAACC | 55626 |
rs182569158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411922 | TGAGCCACCATGCCC[A/G]GCCCAAATCTGTCTT | 55626 |
rs182572029 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581334 | AAAAATTAGGCCAGG[C/T]GCAGTGGCTCACACC | 55626 |
rs182595686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411547 | GATCTCAGCTCATTG[C/T]AACCTCTGCCTCCTG | 55626 |
rs182624002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564942 | TTATGTGCACCAAGA[A/G]TGTAGAGTGTGAGTA | 55626 |
rs182763381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506757 | AATCAAAATGAGCCA[A/C]ATGTTCAATTTGATA | 55626 |
rs182793391 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550256 | AACAGCAGGTTAGGT[C/G]TAAAACCTTCATTAG | 55626 |
rs182806534 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584819 | GCTAACACCTGTAAT[A/C/T]CCAACACTTTGGGAG | 55626 |
rs182837871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431674 | TATTCCACAATTAGG[C/T]CGGAAGGGTTAGAAG | 55626 |
rs182842946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545834 | CCAGCACACTGGGAA[A/G]TCAATTTCAAGAAAG | 55626 |
rs182847518 | snp | A/C/G | 0.00274364 | 0.0369368 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512696 | GGCCGCCCCTCCCCC[A/C/G]ACCTAGTGCCATTTC | 55626 |
rs182848041 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578016 | TGTACCTGTAATCCA[C/G]CTACTTGGGAGGCTA | 55626 |
rs182849941 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564610 | TGTCCTCACACCTAG[A/G]AAGTCATAATTAGAA | 55626 |
rs182912172 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578182 | CATTTCCCAGGAAAG[C/T]TACCATATAAAATTC | 55626 |
rs182914460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546328 | TACAGGCGTGAGCCA[C/T]CGCGCCCAGCCCACA | 55626 |
rs182956649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480350 | CAAGCTATTAATTGA[C/T]CACAGAGAAGAGCCA | 55626 |
rs182958182 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460559 | TGATCTCCTGACCTC[A/G]TGATCCGCCCACCTC | 55626 |
rs182972346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540073 | CTGACCTTAAGTGGT[C/T]TGCCCGACTCAGCCT | 55626 |
rs182983454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500144 | GGACTATTCCGTAGA[C/T]AATAGCTGTCAGGCT | 55626 |
rs182986254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520897 | GGCGTGAGCCACCGC[A/G]CCCGGCCCCTATAGC | 55626 |
rs183004888 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422124 | TTCTATTACACCGGA[C/T]GTATTATCAGAACAG | 55626 |
rs183020960 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439376 | AGAACAGAACAGAGA[A/G]TCCAGAAATATATCT | 55626 |
rs183026873 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417369 | ATTGAGCTTTTCAAT[A/C]TGCTTTCACTAGTAT | 55626 |
rs183043259 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465749 | CATCCATCCCCAAAA[C/T]AGTGATGCTCATGAT | 55626 |
rs183064431 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568286 | AACGTGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 55626 |
rs183086239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592486 | ACAAAACTGGGCGGG[C/T]GCGGTGGATGCCTGT | 55626 |
rs183097079 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571808 | GATTCTCCTGCCTCA[A/G]CCTCCTGAGTAGCTG | 55626 |
rs183124311 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572269 | TCGTGCAACTGCACT[C/T]CAGCCTGGTGATAGA | 55626 |
rs183148382 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421636 | AAGCACCCAGAGATG[C/T]AGTGTCTACCCCTTT | 55626 |
rs183156100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532495 | AGGCTGGAGTGCAGT[A/G]GTGCGATCTCAGCTC | 55626 |
rs183199896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506573 | GAGGGGGAGATGAGA[A/G]CTCTTAAGGCCCCAG | 55626 |
rs183257760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483733 | GGTGAAACCCCATCT[C/T]TACTACAAATACAAA | 55626 |
rs183267595 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412352 | GCAGTGGTGTGATCA[C/T]GGCTCACTACAGCCC | 55626 |
rs183268700 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465157 | CTACAGCCCAGACCC[A/T]GCCAAAATTATTCAA | 55626 |
rs183272185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444266 | GGCCATCTTTTATAA[A/T]ACCTACCCCCTAAGA | 55626 |
rs183279382 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545316 | AATACAAAAAAATGA[A/G]CCGGGCATGGTGGTG | 55626 |
rs183284319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505710 | GGTGGGCTGGGGGGA[A/G]CATAAGGAGGAGGCA | 55626 |
rs183288287 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525759 | CCGTCTCAAAAAAAA[A/C]AAAATTAGCCAGCAT | 55626 |
rs183300932 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484399 | TAGATTAGAGAGAAT[A/C]TTCAGCTGGCACCTT | 55626 |
rs183307646 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399593 | TGCTCTCGACCTCCT[A/G]ACTTCAGGCGATCCG | 55626 |
rs183309060 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444683 | CACCTAGTCTTCCTC[C/T]TCTGCACATCACTGC | 55626 |
rs183345152 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487329 | GTTAACAATAATAAC[A/G]AGTAAATTGTTGTTA | 55626 |
rs183380348 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585594 | TCGCTTGAACCAAGG[A/G]GGCGGAGGTTGCAGT | 55626 |
rs183381589 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416426 | CTTGCAGCTCCAAGA[A/G]CAGCCTGAGCAGGCT | 55626 |
rs183385135 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404078 | AGGCGTGGTGGCGTG[G/T]GCCAGGAGGCTGAGG | 55626 |
rs183386037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593025 | CAAAGTAGACAACAA[A/G]GTTATCAAGAAACAA | 55626 |
rs183422025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448669 | TAAAACCAAAAACTT[A/T]GAAAGATCAATAAAC | 55626 |
rs183426054 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513320 | ATATATAACTATAAT[A/G]TATCTATTAAAAATA | 55626 |
rs183429449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490009 | TCCCTACAGAATGGA[A/C]ATGCTACCACCTACC | 55626 |
rs183432074 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471095 | GGAAATTGAGGCTCA[C/G]ATCAAGATAAACCAT | 55626 |
rs183436853 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550853 | GCACTTTGGGAGGCC[A/G]AGACGGGCGGATCGC | 55626 |
rs183441453 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568484 | AAACAAAAAACAAAA[A/G]AAAAGTGGCCAGGTG | 55626 |
rs183446402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533456 | CACAGTTCGATAACA[C/T]GCCTTCTTGTTTGGA | 55626 |
rs183499885 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560379 | ACTATAATAAGGGGG[A/G]AGAAGTGAAGCACCA | 55626 |
rs183552853 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399146 | ATGATGCGATCTCAG[C/T]TCACTGCAACCTCCA | 55626 |
rs183566939 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422428 | GAGTAGAAGACAATG[A/T]TTGCTCCACTTCTGG | 55626 |
rs183586011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510978 | CAAGGAAAAATACTT[C/T]CTTTTCCAAAAAAAC | 55626 |
rs183606678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400033 | CCAGGCACTTGGTCA[A/G]CGGTGCCTGTTGTGA | 55626 |
rs183646881 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556214 | TTATTAATAGGACTT[A/T]CCTACGGCCATTTCA | 55626 |
rs183652198 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517240 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 55626 |
rs183659064 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469307 | TGAAATCATTGTTTT[C/T]ATAACAGAATTTTTT | 55626 |
rs183660233 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577682 | TCAGCCAGGCGCGGT[A/G]GCTCATGCCTATAAT | 55626 |
rs183677497 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425278 | ATTCACCTTGGATAA[A/G]ACAATGCTTCTGTAT | 55626 |
rs183699425 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433196 | AGATTAAAAGTTTCA[C/T]GTAGAAGTAAGGAAG | 55626 |
rs183744352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475075 | ATATCTTAAACTGAA[A/T]AACAGTCTTATCAAT | 55626 |
rs183746330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575785 | ATCCCAAAGTGCTGG[A/G]ATTATAGGCGTGAGC | 55626 |
rs183852504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538234 | ATGGTATACGACATC[C/T]TAGCTCATTTAAAAG | 55626 |
rs183855510 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496044 | AGGAGTTCAAGGTCA[C/G]CCTGGGCAACAAGAG | 55626 |
rs183860389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517935 | TCGTATATATATAGA[G/T]AGAGAGAGAACAAAA | 55626 |
rs183863743 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572610 | AGAAGCTCTTAGGCA[C/T]TGGAGGGAACTGTCA | 55626 |
rs183869811 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564013 | GCCAGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 55626 |
rs183876332 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594164 | CTGTCTGAGGCGTAA[A/G]TAAACAAACCCAGAT | 55626 |
rs183879263 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557061 | GAATCCCTTGAACCC[A/G]GGAGGTGGAAGTTGT | 55626 |
rs183921277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499084 | AGGGAATAGCTAATA[C/G]CATAGGTCTCCTGGA | 55626 |
rs183923088 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427223 | GCACTGGGCACTCAT[A/C]CTGACCCAGGATCTA | 55626 |
rs183932175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460054 | TATATAACTGAAGAT[A/G]AGCCAGAACAATTTC | 55626 |
rs183941105 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494794 | AAGAATATTAGAAAA[C/T]GTAATCCTATGTTAG | 55626 |
rs183948804 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456090 | CATTTTCAAAGAAAT[C/G]AGTATCATTACCTTT | 55626 |
rs183974907 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491750 | TTCTCAGATTTCACA[A/T]CTGTAAACAGCTGCC | 55626 |
rs183987694 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471855 | ATGGTCTCGATCTCC[C/T]GTCCTCATGATCCAC | 55626 |
rs183992549 | snp | C/T | 0.00648922 | 0.0565907 | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451904 | CAACTGAAAAACTTA[C/T]CAACTTTTCAAACAG | 55626 |
rs184006604 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514819 | GAACACATAAAATAA[C/T]GGCATGTCTTTGAGT | 55626 |
rs184044137 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428466 | GTGTCCTTAGTCATC[C/T]CTTCTGCCAATAAAA | 55626 |
rs184050449 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539314 | TGGAATCCCAGCACT[C/T]TGGGAGGCCAAGGTG | 55626 |
rs184051777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409255 | CTGTCACCCAGGCTG[C/T]AGTGGCGCAATCTCA | 55626 |
rs184055787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438357 | GCCCTAGCAGGGAAT[A/G]GGAGGGGTTAGAAAT | 55626 |
rs184074841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450559 | ATCCTCCCACCTCAG[C/T]CTCCCGAGTAGCTGG | 55626 |
rs184090851 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575384 | ATAGCTTGAACCCGG[A/G]AGGTGGAGGTTGTGG | 55626 |
rs184094160 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566106 | ACATCCAAACCATGA[A/T]ATACTGTGTAGCAAT | 55626 |
rs184094913 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479543 | CTCTACTAAAAATAC[A/C]AAAATTAGCCAGGTG | 55626 |
rs184097765 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407053 | GAGTGGTGGCACATG[C/G]CTGTAATCCCAGCTA | 55626 |
rs184107651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579777 | GAGTGCAGTGACATG[A/G]TATCAGCTCACTATA | 55626 |
rs184199284 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434797 | ACCTAGCAATGACCA[C/T]GCCAAGGCACCAGCG | 55626 |
rs184208934 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413786 | ATGAGCCACCATGCC[C/T]GGCCTGAAACTCTTA | 55626 |
rs184210057 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559247 | AGAGGTTGCAGTGAG[C/T]CGAGATCACGCCACT | 55626 |
rs184212587 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520852 | CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 55626 |
rs184222593 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414730 | AGAGGAGGAGGGAGC[A/G]CCTCAGTGCCAGGAA | 55626 |
rs184264236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457495 | ATTTTGAGATTTGTG[A/G]CATCAAGATAAAGCA | 55626 |
rs184276359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461975 | TACTGCCCCCCACTA[G/T]CTAGACTCCTTCCTC | 55626 |
rs184280873 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441520 | CTCTGTTTCAGAAAA[A/T]AAAAGATCAAGCTGT | 55626 |
rs184286482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419155 | ACTTGTTTCTAGCTT[A/C]TATAAATCACCGTTA | 55626 |
rs184313405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495258 | CTTGATTTGGGATAT[C/T]TTCTGAATTCTCCCT | 55626 |
rs184315056 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476262 | CCATCCAGTGGCAGC[C/T]CAAGAAATTCTATAA | 55626 |
rs184324151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456940 | CACATGACAAGAGAG[C/T]TAAAGCAAGAAAATA | 55626 |
rs184343636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517488 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTAAGTCT | 55626 |
rs184368219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566769 | TTGCCTTTAACTGCC[C/T]TTGGTCATTCCTGTG | 55626 |
rs184383345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501899 | TTATAGTAGTTTCGC[C/T]TAAGTTACAGTTTCC | 55626 |
rs184386444 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524110 | TGACCTCGGGTGATC[C/G/T]GCCCACCTCGGCCTC | 55626 |
rs184392463 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481671 | CCCGGCCTATTTTTG[C/T]TCTCTGAAGGTAAAG | 55626 |
rs184394187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477316 | TTGTCTCTTTAAAGA[G/T]ACTTCTTTTTTTTTT | 55626 |
rs184404102 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585934 | CCTCAGCCTCCCGAG[C/T]AGCTGAGATTACAGG | 55626 |
rs184404274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562267 | CAAGTACTAAGGTCC[C/G]TAACAGGTAAGCTTA | 55626 |
rs184413380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568891 | AGCTCACTGCAACCT[A/C]CGCCTCCCAGGTTCA | 55626 |
rs184422129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435803 | GATCTGAGGGTGGAG[A/G]AATGTCTGTTGGTGA | 55626 |
rs184500330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579869 | AGGTGTGCACCACCA[C/T]GCCTGGCTAACTTTA | 55626 |
rs184531236 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485181 | GACCTCAGGTGATCC[A/G]CCCGCCTTGGCCTCC | 55626 |
rs184531425 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436559 | AACCCACCATCTGGT[C/T]TAGCCTGTAAGGCTA | 55626 |
rs184537349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468355 | GAACAGCCTGGGCAA[C/T]ATAGTGAGACCTCAT | 55626 |
rs184547749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565231 | CCATTGCACTCCAAG[C/T]CTGGGAGACAGAGAA | 55626 |
rs184557151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529219 | TAGTCCAAAAGAAGG[C/T]TGCTCTCATACTGCA | 55626 |
rs184561645 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547599 | GTTATTGAGAAACTT[G/T]CCAAGTTTTGATCCT | 55626 |
rs184562854 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548740 | GCTCACGCCTGTAAT[C/T]CCCGAACTTTGGGAA | 55626 |
rs184583777 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551997 | CGCACCACTGCACTC[A/C/T]GGCCTGGGTGACAGA | 55626 |
rs184594383 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445620 | TAGTTACAAGGTCTA[C/T]CACTTCCCTGGAAGG | 55626 |
rs184628646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481180 | AGCACGGTGCAATTA[C/T]ACCCAAACAGCTCTG | 55626 |
rs184643150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439697 | TCAGCAAAGTCAAAA[C/T]TCGAATGACAAGTAG | 55626 |
rs184695054 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500675 | TTCAGGGTCCCTGAA[A/T]AAGCCCTGTAAATCT | 55626 |
rs184711854 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534792 | GATCCTCCCACCTCA[A/G]CCCCACGAGTAGCTG | 55626 |
rs184726084 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587206 | CCAACATGGTGAAAC[C/T]CCATCTCTACTCAAA | 55626 |
rs184734143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417647 | CACTAGGAAACCAGA[C/G]AACAAGGGAAAACAA | 55626 |
rs184776580 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460986 | GGTGGTGCACACTTA[C/T]AATCCCAGCACTTTG | 55626 |
rs184844599 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461536 | CCTTGACCAACATAG[C/T]ATGGGGGAGGTCATA | 55626 |
rs184845699 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441212 | ATACAAATCTGTTTT[C/T]GTTATTAAAAGATAA | 55626 |
rs184853345 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569473 | TATATATAAAGTGCC[A/C]AGCAAGATGGCAGGT | 55626 |
rs184853925 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418786 | ATGGCTCTAATAATG[C/T]GCTCTCCTTAGAGCC | 55626 |
rs184936787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423336 | AAACCTTTATATTCT[A/G]TGTTGGAATTCAGAA | 55626 |
rs184950031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537839 | TCTTCTACTATAAGG[C/T]CAATGAACAAAACTT | 55626 |
rs184958286 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509362 | ACAATAACAGAAAAA[C/T]GTTTTCTATGATAAT | 55626 |
rs184960562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590289 | AGGCTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 55626 |
rs184972806 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468525 | AGGCCAGGGCCAGGC[A/G]CAGTGACTCACGCCT | 55626 |
rs185013924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535143 | TTGCCTGTATCACAA[A/G]TGAAATTCTCACAGT | 55626 |
rs185030347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492729 | CCTCACAGCCGAAAA[A/C]CATCTGTCACTAAGC | 55626 |
rs185032176 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514966 | AGTACTTATTTATCA[A/T]TTAACAAACCAGTTC | 55626 |
rs185039341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446143 | GGTGCTCTCTGCCAA[C/T]GGTGCCAGGGTGCTG | 55626 |
rs185048597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552037 | CATCTCCAAAAAAAA[A/T]TTAACCAATTAATTA | 55626 |
rs185053812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587686 | TCAGCCCTTGTTTAT[C/T]TCCTTCAGAATACTT | 55626 |
rs185054792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401386 | GCTGGGACTACAGGC[A/C]TGTGCCACCATACCC | 55626 |
rs185060526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570252 | GGGCAACACAGTGAG[A/G]CCATGTCTCAAAAAA | 55626 |
rs185067758 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485397 | TTCTTCAAACTGTAC[A/G]AAAGACAAACTGGAC | 55626 |
rs185070087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556527 | ACTCTAGATGGAGAA[C/G]TCATGAGTGATATTT | 55626 |
rs185074699 | snp | C/G | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451328 | CCCAGAATGTGTCTA[C/G]GGATAAAATCATAAT | 55626 |
rs185086592 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558848 | ACAATGTCTAGCGTA[C/G]AAGAGCATGAGTATG | 55626 |
rs185089612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408109 | GTGAGAGGTCCTCCC[A/G]TGGGGCAGTCCCAAA | 55626 |
rs185096189 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520100 | CCCAAGATGGCGCCA[C/T]TGCACTCCAGCCTGG | 55626 |
rs185102570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538773 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACTG | 55626 |
rs185104427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491181 | GAAAAACACTGAAGT[C/T]CCCTGGGAGCTCTCT | 55626 |
rs185118927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574622 | CTTTTTCTAAAGGAA[A/G]TCTTATGTGAAAACA | 55626 |
rs185196222 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427602 | AGCAGATCTTAAGTG[A/G]GGCTGAGAATCTGCA | 55626 |
rs185225312 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471642 | GTTTTGTTTTGTTTT[G/T]TTTTTAGATGGAGTC | 55626 |
rs185244647 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534483 | CTGGGCAAGAAGAGC[A/G]AAACTCCATCTCAAA | 55626 |
rs185249239 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423680 | ACAGGCGTGAGCCAC[C/T]GTGCCCGGCCAATTT | 55626 |
rs185255577 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401910 | ACTCCTTAGCTTGAC[A/C]TTTGAGGGCTCTCTG | 55626 |
rs185296135 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576788 | TCATGTAAATGCAAC[A/G]TGGCTTTATATGGGT | 55626 |
rs185304081 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454184 | GAAAAGAAATAGCTA[C/T]GAAATTTTTTTTTAA | 55626 |
rs185307961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430860 | TGGTCAGAGCTTGAC[A/G]TTAGAGATGGAGACA | 55626 |
rs185318968 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411630 | TGTGCCACCACGCCC[A/G]GCTAATTTTTGTATT | 55626 |
rs185336844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551213 | AAGAAAAACTAATGG[G/T]AACACGCTGGGGACT | 55626 |
rs185351695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514315 | GACATAGCAAAGGCC[C/G]TAACAACCTGGCTTG | 55626 |
rs185363474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485875 | TTCTCAATAAGCACA[C/T]TTCTCACTAGTGGTA | 55626 |
rs185371151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477647 | GCCTCTTTGAGGACA[C/T]GTCTTTATTGTACAT | 55626 |
rs185379925 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468747 | AACCTGGGAGGCGGA[A/G]CTTGCAGTGAGCCGA | 55626 |
rs185385770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447679 | TGCACCACTGCACTA[A/C]AGCCTGGGTTACAGA | 55626 |
rs185390527 | snp | C/T | 0.00119737 | 0.0244387 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518167 | AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55626 |
rs185413717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400946 | GGAGAGAAAACCTGA[A/C]GGGCTCTCAGAGTAC | 55626 |
rs185424742 | snp | A/G | 0.000256937 | 0.0113315 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543208 | GGGGGAGGCGGTGGG[A/G]GTGAGGGGGTAGCAG | 55626 |
rs185428989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563341 | GTGATCTTCCCATCT[C/T]GGCCTCCCCAGAAGC | 55626 |
rs185432945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516165 | TGGCAACATTTGCTG[A/C]CCAGACAATATAGTG | 55626 |
rs185441245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493977 | GGCTAACCATCATCC[A/G]TCAAGAGTTTAGACA | 55626 |
rs185442984 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474355 | GAACAGGTCTATTCA[C/T]ATACTTCTCAACATA | 55626 |
rs185453316 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577023 | AACTCTGAAATCACA[C/T]ACTCTGGAGAAGCTG | 55626 |
rs185459279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535977 | GAGGTCACCGGAGCT[C/T]AAGTTTTGGAAGGTG | 55626 |
rs185500349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457863 | GTGAGTCGAGATTGC[A/G]CCACTGCACTCCAGC | 55626 |
rs185516077 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578986 | CAAGTGAATGAATAA[A/C]GAGGTTAACCAAGCA | 55626 |
rs185529732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557593 | GGAGGATTGTTTGAG[A/T]CCAGGAATTCAAGAT | 55626 |
rs185535652 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496812 | CCTTCATTTAAAAAA[A/G]AAAAAAAAAGGGAAG | 55626 |
rs185540637 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594486 | AACAAAATGAACAGT[A/C]TACGTAAAAGCTCCA | 55626 |
rs185577391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422988 | AGAAAGGAACTGTGA[A/G]GAGGAAAGATGCCTT | 55626 |
rs185581674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519213 | ATTTTTAGTAGAGAC[A/G]GGATTTCACCATGTT | 55626 |
rs185594246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478703 | CTTGTTGCCCAGGCT[A/G]GAGTGCAATGGCGCA | 55626 |
rs185611541 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538637 | GTAGCTAGGACTACA[A/G]GCATGCACCACCATG | 55626 |
rs185642910 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572966 | TGTGGTGGTGGACGC[C/T]TGTAATCCCAGCTAC | 55626 |
rs185645820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458767 | ATGACCAGAACCTCA[C/T]ATTTTAGATACTGTC | 55626 |
rs185650188 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404749 | TGGGGCGAGGAACCA[C/G]GTCTTGCCTCCTAAA | 55626 |
rs185653258 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538486 | AAAAATTATGGTACA[C/T]CCTTAATAGTTTCTG | 55626 |
rs185658787 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437338 | TGCCCTCTCCCCTGA[C/G]TCCACCCAACTTCAT | 55626 |
rs185661600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576719 | TGCTTAACACCACCT[A/G]AACAATATCCCTCCA | 55626 |
rs185665042 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415988 | CCTTTATGAGGCCAC[A/G]ACAAACTGGGTGTAG | 55626 |
rs185671791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541162 | CCTAATAAATCAAGA[C/T]AGATGCGCACATAGC | 55626 |
rs185749226 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501205 | GAGGGAAAAAAATCA[A/G]TTCCTGGCCATGGCC | 55626 |
rs185797949 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410918 | CCATCCTGGCCAACA[C/T]TGTGAAACCCTGTCT | 55626 |
rs185806063 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577178 | TTCAAAGCAACACTA[C/T]TCACAAGAGCAGAAG | 55626 |
rs185809689 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561690 | CTTGGCTGACTAAAA[C/T]AGGGAAAGAAAAAAT | 55626 |
rs185871906 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522452 | CTCACAGACCACAGA[C/G]TTTTTTTTTAACCCA | 55626 |
rs185882242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481324 | AGGGGAAAGGATCTG[C/T]GACAAGGATATAAGA | 55626 |
rs185933784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429960 | AGAGAGTAGCATATC[A/C]AGTCTGGAGGAATCG | 55626 |
rs185947847 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567610 | AAGTGATTCGCCCGC[C/G]TCAGCCTCCCAAAGT | 55626 |
rs185948254 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563812 | CACCACTGTACTCCA[C/G]GCTAGTCTGGCAACA | 55626 |
rs185961781 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581661 | AATAATTACCCACAT[A/G]TGGTGGCACGTGCCT | 55626 |
rs186021435 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416241 | ATAAGACAATCAGCA[C/T]CATGTGCTTTGGGGA | 55626 |
rs186031501 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497288 | GATTAGTGGGGGATA[C/T]ATAAAGGAAAACAAG | 55626 |
rs186050158 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530529 | GAAACAAATTCTTTA[G/T]GCATTTATGCCTGCT | 55626 |
rs186050363 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459899 | TCAGAAAAACTCCTT[A/G]GTCTTGGATTTACCA | 55626 |
rs186097569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526194 | CTGGGCAACAAGAGC[A/G]AAACATCGGCTCAAA | 55626 |
rs186106348 | snp | C/G | 0.00709967 | 0.059156 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545591 | GACAATGCAGATGGG[C/G]CAGCGCACTCACCGG | 55626 |
rs186108210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505771 | AGGGGAGAGAGAGAG[A/G]AGGTGGTAGCAGGAG | 55626 |
rs186108238 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588993 | TCTAAAGGACTCTTA[C/T]AAGTAATAAATGAAA | 55626 |
rs186136415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415381 | AGTATGTGTGTGTTA[C/T]TGTGGCATATTTTTC | 55626 |
rs186140994 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577730 | CCGAGGCGGGCAGAT[A/C]ACCTGAGGTCGGGAG | 55626 |
rs186141855 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437854 | TATAGCCGAAGACAC[C/T]GGCTATAGCTTACAC | 55626 |
rs186156474 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442773 | ATATCTTAATTATTT[A/C/T]AAGGCAACTGGCAAA | 55626 |
rs186171662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484135 | CCATGCACAAGGGGC[C/T]CAAGGTAGGGGATAT | 55626 |
rs186174302 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479280 | GCCTACTTAGTTGTG[A/G/T]CAGCATGTTACAGTA | 55626 |
rs186176035 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465175 | CAAAATTATTCAAAC[C/T]GATCCAATCCTAAAC | 55626 |
rs186176480 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510270 | TCAACTGGAGGAACT[G/T]TCATTATCTGTTTGG | 55626 |
rs186179549 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397121 | ACTCTCTGGAGGCTC[C/T]CTGTCCAGGGCTGAG | 55626 |
rs186196154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482690 | AAGGAATCTTTTTGG[C/T]TTCTACTTTACCAGC | 55626 |
rs186262139 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589644 | TTTTTTTTTGAGACA[C/G]AGTCTCCCTCTGTCG | 55626 |
rs186299174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486598 | CTAAGACCAGAGTAC[C/T]GGTGTTTTTAAAAGA | 55626 |
rs186300256 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469138 | ACAACAGGGAAACTC[C/G]ACCTCAAAAAAAGAA | 55626 |
rs186314956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420151 | TTCAGGTTTGAGGCA[C/T]GGCACTGACTGCCCT | 55626 |
rs186316800 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525151 | ACAAGAAATTTAAAA[A/C]TTATCTGGGCATGGT | 55626 |
rs186337937 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502925 | AATTAGCTGGGCGTG[G/T]TGGCAGGCACCTGTA | 55626 |
rs186346503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555693 | GTTTATGTGGCAAAA[A/G]TAATTCATTGTGATT | 55626 |
rs186348471 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463222 | CTCCACTTGAGGATG[A/G]GTTTAAAATTCAGCC | 55626 |
rs186399245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531531 | CCCAGCCAATATGGC[A/G]AAACCCTGTCTCTAC | 55626 |
rs186407834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548887 | TCCCAGCTACTCATC[A/G]GACTGAAGCAGGAGA | 55626 |
rs186420206 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510508 | CTTTTATTTGGAACC[A/G]ATTCTGAAAAGTGAT | 55626 |
rs186434803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581336 | AAATTAGGCCAGGCG[C/T]AGTGGCTCACACCTG | 55626 |
rs186434975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567459 | GCATTCTCCACCACC[C/T]GAGTTCAAGCAGTCC | 55626 |
rs186471887 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469713 | CTGTTGCCCCAGGGT[G/T]GAGTGCAGTGGTACG | 55626 |
rs186487455 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425493 | ACTGGGAACCTCTCA[A/T]CATGTCTCAGTGCTG | 55626 |
rs186494354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573451 | CCATGCATTTTTCCT[G/T]CTGTACCACACTCCC | 55626 |
rs186500642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511776 | CCTTGGTCCTTAGTT[A/G]TCACCATCAGTGAAG | 55626 |
rs186523892 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506963 | AAGGTCAAGAGATGG[A/T]GACCATCCTGGCTAA | 55626 |
rs186524670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483453 | AAAGAAAGGAAATTA[A/G]CAACCACAGGTTGGC | 55626 |
rs186527276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464263 | AGCAGACTTGATGCA[A/G]CAATTAGAGAATGCA | 55626 |
rs186528054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556141 | CTGCCCCAGTACTCT[C/T]TGGAAACTCCATATG | 55626 |
rs186530235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570999 | TGTAACCATAACCAC[C/T]GTACTGAAATGTGGC | 55626 |
rs186550404 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536163 | AAACCATAAGGAACA[A/T]AATTTCAATTCTACT | 55626 |
rs186550611 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484960 | TTTTTTTTTTAAGAC[A/G]AAATCTCACTCTTGT | 55626 |
rs186560013 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398994 | GGCCAGGCTGGTTTC[A/G]AGCTCCTGACCTCAG | 55626 |
rs186562020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571370 | GACTTAGGGATCATT[C/T]TGAACATAAAATCTT | 55626 |
rs186576722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443269 | AGTGATGTTAATTAA[A/G]CTCGATTAATCCAGA | 55626 |
rs186587569 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420622 | ACACTAAAAGGACAA[C/T]GTGGGTGTGATGAGA | 55626 |
rs186603235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550066 | TCAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 55626 |
rs186657859 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512922 | CCCTTTTGCAGCCAG[C/T]TAACGCCTGTTATCT | 55626 |
rs186666929 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488795 | AATAAGAGAACAACA[A/G]AAGGAAATTTGGGAA | 55626 |
rs186689788 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448980 | AAGAACTGGGCCCAG[A/G]TGGTTTCACTAAATT | 55626 |
rs186698179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558345 | CACGAGGTCAGGAGT[A/G]CGAGACCAGCCTGAT | 55626 |
rs186698509 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406710 | ACATGGCGAAACCCC[A/G]TCTCTACTAAAAAAT | 55626 |
rs186705956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532306 | CAGAGAACAAATGTA[A/C]ACTAACACCTCAAGG | 55626 |
rs186714229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487336 | ATAATAACAAGTAAA[C/T]TGTTGTTAACCAAAA | 55626 |
rs186722119 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470360 | TTGGGAGTCCGAGAC[A/G/T]GGCGGATCACGAGGT | 55626 |
rs186730761 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46449876 | CCAGCCTGACCAACA[C/T]AGTGAAATCCCATCT | 55626 |
rs186733805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426217 | TGAGCAGGGTGCACA[C/T]GCGTGGACATGCAGA | 55626 |
rs186761235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570598 | CCCATTTTACAGACA[A/G]AACCCTAGCTCAACG | 55626 |
rs186810532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453236 | TCAAAGTTTATCCAC[A/G]CTTATTGCATGTTTC | 55626 |
rs186823312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540665 | ATAAAAAGGTCTTGC[C/T]CTCTCCAAATCCTAT | 55626 |
rs186831283 | snp | C/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595936 | TCTTGGAGAGGCTTG[C/T]GGAGCATAGCTATAG | 55626 |
rs186841544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399669 | CGTGCCTGGTCAGAA[A/G]CTGAGAGTTTTAACT | 55626 |
rs186851778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535664 | CAGCACTGACTGGCA[A/G]AGATAATAATATTAC | 55626 |
rs186869834 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493256 | AATTAAATCACAGGA[A/T]CTGGCTCATGAGTAT | 55626 |
rs186942403 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576649 | AATCTACATCCTTTA[C/T]GTTGCAATTAAAACA | 55626 |
rs186955609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561499 | AAATAAGAAAAACAA[A/C]ACCTGGAAGAGGTTA | 55626 |
rs186989510 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552432 | GTAGCTCACACCTGT[A/T]ATCCCAGCACTTTGG | 55626 |
rs186991777 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402644 | GCTGGGATTACAGGC[A/G]TGAGCCACTGGAGAA | 55626 |
rs187022604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473157 | AATACTTTAATGCAA[C/T]GTCACTGGAAAATAA | 55626 |
rs187025739 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447881 | TTACAGCCTGGGTGA[C/T]ACAGCCAGACCATCT | 55626 |
rs187045933 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515343 | CCAGGCGTGGTGGTG[C/T]GTGCCTATAATCCCA | 55626 |
rs187073851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537847 | TATAAGGCCAATGAA[C/T]AAAACTTTCTCCTTT | 55626 |
rs187088042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578051 | AGGAGGAAAGCTTGA[A/G]TTCAAGGCTACAGTG | 55626 |
rs187088162 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495425 | GGTAGAATTGGCTGC[C/T]GAGCATTAAATGACA | 55626 |
rs187092578 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517572 | GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55626 |
rs187092808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564796 | GTTAACTATTATTTG[C/T]CTCCTAGTGGGCTAT | 55626 |
rs187108305 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556622 | CCGCAGTCAGAATGG[C/T]TGATTGAATTCCAGC | 55626 |
rs187118599 | snp | A/G | 1.69453e-05 | 0.00291073 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434937 | AGGAAAGCCCCTCTG[A/G]CTGCTGGGGATGAAA | 55626 |
rs187140812 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476524 | TAGATTAGAATAGCC[A/G]GAAACTTATTCACAG | 55626 |
rs187145027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457228 | TCAAAGCCTGCTTCA[C/T]TCAGGCTAAGGACAG | 55626 |
rs187170163 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559567 | CAGTGGATATTCTGA[G/T]AGCAGAGATGAGAAT | 55626 |
rs187177887 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424753 | GCTGAGGTGGGAGGA[C/T]TGCTTGAGCCCAGTT | 55626 |
rs187180702 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520856 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGT | 55626 |
rs187287599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575675 | GTGCACGCCACCACG[C/T]CCAACTAATTTTTGT | 55626 |
rs187290598 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480453 | ATTTGGGGGTGGTTT[A/G]TTCAGCAGCAAAAGC | 55626 |
rs187307266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460587 | CTCAGCCTCCCAAAG[A/T]GCTGGCATTACAGGC | 55626 |
rs187309778 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439548 | TCCTAGTGAATCAAA[G/T]ACTTAACTATTAAAA | 55626 |
rs187350003 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544339 | AAATACAAGAGTTCA[C/T]CCTAACCGTAAAGCA | 55626 |
rs187359462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505071 | TGAAGTGCTGAGAAG[A/G]TGAGGATACCAAACA | 55626 |
rs187365592 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539567 | CATCTCAAAAAAATA[A/T]AAATGTTATATTAAG | 55626 |
rs187374375 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429209 | CCTCGGACAATCTTC[A/G]CCTACCAGCGGCCCC | 55626 |
rs187398859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540210 | AGAATAGCACATGAA[C/G]AGGTACTACTAAAGC | 55626 |
rs187403799 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500283 | AAAAAAGGACTTAGC[A/G]TTTTTTTTTTAGACA | 55626 |
rs187407678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520974 | ATGTCTTGTCTTTGC[C/T]ACATGAAAACAGGTA | 55626 |
rs187410185 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576292 | AAAATGCCAGAGACA[C/T]TGGTGTTGCTGTTGT | 55626 |
rs187410785 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472317 | CATTGAGGTGTTCTT[A/G]TCACTGGAACATCTA | 55626 |
rs187423898 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560916 | AATGACTTTGGCAAC[A/G]ATATACCTTTCATCC | 55626 |
rs187509618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578539 | TTTATTATTATCATA[C/T]AAATATGGCTAATTA | 55626 |
rs187509993 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565587 | TGGCATGTACCTGCG[G/T]TCCCAGTTACTTAGG | 55626 |
rs187515677 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546836 | AGCACTTTGGGAGGC[A/C/T]GAGGCAGGCAGACCA | 55626 |
rs187526070 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579476 | AAATAAATAAATTAA[G/T]TAAGTAAGTACATAA | 55626 |
rs187530035 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456364 | ATACATTCCCCACAA[A/C]CTGACACTGCCAATA | 55626 |
rs187585724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433844 | AATAAGGCTGAACGC[A/G]GTGGCTCATGCCTGT | 55626 |
rs187593741 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412916 | CTGGCTGCCAGGAAG[A/C]CTGATTTACAAACTT | 55626 |
rs187600988 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461149 | TTAGGAGGCTGAGGT[A/G]GAAGGATCTCTTGAA | 55626 |
rs187620311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568296 | AACCCCGTCTCTACT[A/G]AAAATACAAAAATTA | 55626 |
rs187628629 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525683 | TTGAATCCGGGAGGC[A/G]GAAGTTGCAGTGACC | 55626 |
rs187629888 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532879 | AACGCTCATACTCTT[A/G]GGCACTAGCAATTCC | 55626 |
rs187636259 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500701 | AATCTCCTGTCTCTA[C/T]GCTTTTGCTTAAGCT | 55626 |
rs187640975 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410869 | GCACTTTGGGAGGCC[A/C/G]AGGCGGGCAGATCAC | 55626 |
rs187648601 | snp | C/G/T | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550866 | CCGAGACGGGCGGAT[C/G/T]GCGAGGTCAGGAGAT | 55626 |
rs187661004 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418142 | GGAGAAACAAATTAG[A/G]AGGAGGAAAGGAGGT | 55626 |
rs187666136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452397 | TATGTTGCCCGGCTT[A/G]CCTTGAACTCCTGGC | 55626 |
rs187679540 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568584 | TTGAGACCAGCCTGA[C/T]CAACAGAGACACCCC | 55626 |
rs187682466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533674 | GTGCAGAGTTGGCCT[A/T]GCTTTAATTTACGCT | 55626 |
rs187698160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585897 | CACAACCTCCGCCTC[C/T]GGGGTTCAAGCTATT | 55626 |
rs187717410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438534 | AAATGCATTAGATAC[C/T]GATTTGGAAAACCCA | 55626 |
rs187722443 | snp | C/G/T | 0.00358891 | 0.0422285 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417212 | ACGTGCCACTATGCC[C/G/T]GGCTAATTTTTTGTA | 55626 |
rs187735050 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528623 | TGGTGGCTGCCAGGG[G/T]CTTGTGGGAGGGTGA | 55626 |
rs187744411 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490205 | TCCCACAATTTTACC[A/T]GGTAGAGCTGCAATA | 55626 |
rs187744795 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513652 | CTCCAAAATGCCTCA[A/C]ATCTCTATTTTGTAC | 55626 |
rs187751765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564979 | AAATAAATCATGGCC[A/G]GGTGCAAAGGCTCAT | 55626 |
rs187859389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400177 | AAGGCTCTGAGGCTG[C/T]GAGGGATGGCTCCAC | 55626 |
rs187868663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460083 | TCATCTCTGTGTAAA[C/T]ATCTTAGAGAAGACA | 55626 |
rs187871539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481296 | TATAATTCTTCTACA[C/G]GGCCCTCTTTCTAGG | 55626 |
rs187884272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466911 | ATGTTTCTTTTTTTC[G/T]TTTCTTTTTTCTTTT | 55626 |
rs187886217 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516564 | GCCTCCCAAGTAGCT[A/G]GGACTACAGGCACCT | 55626 |
rs187887056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439700 | GCAAAGTCAAAACTC[A/G]AATGACAAGTAGGAA | 55626 |
rs187890630 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445127 | TTCCCCTCCAAAGCA[A/T]CAGAGTATATAAATA | 55626 |
rs187891251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521787 | AGCAGAGACTGGCAG[G/T]CAATTCCTGCCCCTG | 55626 |
rs187898864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422845 | GCAGTGGTGGCCAGA[A/G]GTCAAGTGCAGTTGG | 55626 |
rs187914850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550296 | TTTTGGTGACAGTGC[A/G]TCACAGTTGATGTGC | 55626 |
rs187923875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593394 | AGAAGAGCCAGAGGG[C/T]CTTGTTCCATAAGCC | 55626 |
rs187948081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444776 | CCTGGTGTCCCTTTC[C/T]TTCCCCAAATGATCA | 55626 |
rs187958487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526763 | GAAAAATAACTGAAT[C/T]GGTTTTAAGTCACTA | 55626 |
rs187974687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484461 | ACCATGGGATTTAAT[A/C]ATCTTTGAGATCATT | 55626 |
rs188026258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585003 | CTTGAACCTGGGAGG[C/T]AGAGGTTGCTGAGAT | 55626 |
rs188090574 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422192 | TGATTCATGATTGAC[A/C/G]AGTCCTGGTTTCACC | 55626 |
rs188092868 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572919 | ACCTGGTGAAACTCC[A/G]TCTCTACTAAAAATA | 55626 |
rs188093071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530614 | AAACTAGAGAGAGAG[A/C]AAGTGCAGGAGTCCC | 55626 |
rs188101538 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594319 | ACACTTGTTGTGTAA[C/T]TATAGTCCCCCAACT | 55626 |
rs188105279 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510359 | CAGAAGTCGATGTTC[C/G]TGCACTGTTCTTATA | 55626 |
rs188109664 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557124 | CTGGGCAACAAGAGC[A/G]AAACTCCATCTCAAA | 55626 |
rs188145127 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423706 | AATTTTTATTATTTT[A/T]AAATTTTTACTGTTC | 55626 |
rs188164179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485990 | CTATAAGGCAACTGG[A/G]AAGGCTGAGTTCTCT | 55626 |
rs188170049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538325 | AGTTATTTGTATATT[C/T]TAAAAGAAAATGAGC | 55626 |
rs188177395 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586745 | TATTTTACAGATGAG[G/T]AGAGGCACAGAGAGA | 55626 |
rs188177969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468931 | GGTGGATCACCTGAA[A/G]TCAGGAATTCGAGAC | 55626 |
rs188178492 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545871 | TTAAGGTAAAATGAC[A/T]ATGTCTAGGGACTAC | 55626 |
rs188187299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447798 | TGGCAAATACTAAGT[A/G]CATAATAAATGGCCT | 55626 |
rs188211503 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572281 | ACTCCAGCCTGGTGA[C/T]AGAGCGAGATTCCAT | 55626 |
rs188223060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465769 | ATGCTCATGATAAAT[C/T]AGCACTTCTCATAAG | 55626 |
rs188257057 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577025 | CTCTGAAATCACATA[C/T]TCTGGAGAAGCTGCA | 55626 |
rs188259751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551608 | AGGCGCGATGGCTCA[C/T]GCCTGTAATCCCAGA | 55626 |
rs188259996 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506688 | GGAAGAAATAATGCT[C/T]AACCGCCCTTCTCTC | 55626 |
rs188267793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514530 | AACATCACTGTGGTT[C/T]AAATGTGGCAGAAAT | 55626 |
rs188290494 | snp | A/C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428707 | TCTAAACTGGAATTC[A/C/G]GTTGCTGACCCAGCC | 55626 |
rs188297852 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409434 | CCATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC | 55626 |
rs188314644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491761 | CACATCTGTAAACAG[C/G]TGCCCACTGCAACAC | 55626 |
rs188319029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471905 | TGCCAGGATTACAGG[C/T]GTGAGCCACCGTGCC | 55626 |
rs188333082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451938 | GACAGTTGCTTTGGG[C/T]TGGAGGGATGTGAGA | 55626 |
rs188368571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417398 | ATAAGCTAGAGCTCC[A/G]AGCAGAAAGGAAAAC | 55626 |
rs188387893 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494804 | GAAAACGTAATCCTA[C/T]GTTAGGTCATTTGAA | 55626 |
rs188404440 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537262 | ACATGAGCAACAGAG[A/G]TTTTGACAAAGAAAA | 55626 |
rs188431671 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421655 | GTCTACCCCTTTCCC[A/G]GGCCAAAGCTGAACA | 55626 |
rs188435638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534807 | GCCCCACGAGTAGCT[A/G]GGACTACAGGCACAT | 55626 |
rs188439233 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551998 | GCACCACTGCACTCC[A/G]GCCTGGGTGACAGAG | 55626 |
rs188453443 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514843 | TTTGAGTCTTTTAAA[A/C]TACAGAATGTGTGGG | 55626 |
rs188477621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569074 | GGCCTCCCAAAGTGC[C/T]AGGATTATAGTTGTG | 55626 |
rs188542439 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572045 | TGGTAGCTCACGCCT[A/G]TAATCCCAGGACTTT | 55626 |
rs188597606 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579798 | GCTCACTATATCCCC[C/T]GCCTCCCCAGTTCAA | 55626 |
rs188599525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558717 | GTAACCAAAGATATC[C/T]CAAAATAAATTTATT | 55626 |
rs188607449 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573557 | GGCAGTTATGTAATT[C/T]AGCCATCTTTTCAAT | 55626 |
rs188615701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538650 | CAGGCATGCACCACC[A/G]TGCCTGGCTAATTTT | 55626 |
rs188661331 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423581 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTAT | 55626 |
rs188671935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401643 | GCTTTCCCAGGCTCT[G/T]CGGGAGGCCCTGCTG | 55626 |
rs188678084 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475309 | ATGACATTTGCTAAC[A/G]TTCAACGTTTAAGAA | 55626 |
rs188692347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556312 | CCTGACTCCATACAG[A/C]TCTTGTGTGACTCTT | 55626 |
rs188699307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517320 | ACCCAGCTGATTTTT[C/G]TATTTTTAGTAAAAA | 55626 |
rs188726334 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450753 | CAGCCACAAGGAGAT[A/T]TTTTAAGCAGTAAAG | 55626 |
rs188732305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479960 | AAAGGTGTTGGCTGG[C/G]CTGTGTTCGGGTCTG | 55626 |
rs188745961 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399364 | TAGGCATGAGCCACC[A/G]TGCCCAGCCTTTGTT | 55626 |
rs188746804 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562298 | GCGCATGTGAAGGCC[A/G]GAAATAAGGCCAACA | 55626 |
rs188747178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407254 | AGGGGCTGCCTAAGA[A/G]AATGGCCCACTTCTC | 55626 |
rs188752551 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444362 | TGTATGACATTTTTT[C/T]CCTTGGTAACCAATT | 55626 |
rs188757660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524702 | TAAACAGCCATTACT[A/G]TTTTTTTCTTCCTTA | 55626 |
rs188767698 | snp | A/G | 0.000231355 | 0.0107529 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542874 | GAGGTTGCGGAGCGT[A/G]TTGCCGGCAGTGCTG | 55626 |
rs188778515 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576941 | TGCAAATAATAAAAC[C/T]AGTATGTTAGAACTC | 55626 |
rs188796901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462735 | TCCCCATTCAAGTAC[C/T]TTCTCAAATAATTCA | 55626 |
rs188805954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427965 | AGTGAGCCAAGGTTG[C/T]GCCACTGCACTCCTG | 55626 |
rs188814882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408402 | GGCTCTTAATGCCAC[C/T]AGGTGGGCATCACCC | 55626 |
rs188818733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501901 | ATAGTAGTTTCGCTT[A/C]AGTTACAGTTTCCAA | 55626 |
rs188829581 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592825 | CCCAGAAAGCAGACC[C/T]TCACAGGACAAGCGT | 55626 |
rs188831219 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481996 | ATTCCAAAGTCCTCA[C/T]GTTTTGCAAGTTTTG | 55626 |
rs188888096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431851 | ATGACATCTCCTATT[C/T]ACCCAATGTCAAATA | 55626 |
rs188914590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474864 | ATCAGAGCCAGAACA[A/G]TGAAAAAAAACAAAA | 55626 |
rs188973074 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458174 | AAAAAGATAGCTAAT[G/T]TGAAATAGCTTCTAA | 55626 |
rs188973281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508859 | AAGAAGGTATCCACA[C/G]GTATCTTCACCAGGA | 55626 |
rs188978838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485188 | GGTGATCCGCCCGCC[C/T]TGGCCTCCCAACATG | 55626 |
rs188979448 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548821 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAATAC | 55626 |
rs188980485 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436673 | AACAAAAACAAAACA[C/T]GGCAATATCCCTCTC | 55626 |
rs189013346 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499350 | CAAGCACAATCCAGA[C/T]GTGTTCCATTTTCTT | 55626 |
rs189019573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427442 | AGCAAGAACAAAAGC[A/G]GAAAGGATCAAGATA | 55626 |
rs189022914 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581225 | CACCTGTAATCCCGG[G/T]ACTTTGGGAGGCCAA | 55626 |
rs189027088 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477592 | ATCCTCCCACCTTGG[C/T]CTACTGTGCTGGGAT | 55626 |
rs189042705 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435956 | GTGGCTTACCCTTGA[C/G/T]GTGAGCATAGAACAA | 55626 |
rs189050871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518029 | GGAATCCTCTATACG[C/T]TTTCTGCAAGTTTGA | 55626 |
rs189055804 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471447 | GCTGGGCATGGTGGC[A/G]GGCGCCTGCAGTCCC | 55626 |
rs189097176 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529469 | GCGGGTACTGCAATG[A/C]CCAGTGACTCCCCCT | 55626 |
rs189101577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477815 | GCATAGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 55626 |
rs189105489 | snp | A/G | 2.08588e-05 | 0.00322939 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547849 | CAATAAGAAGGTAGA[A/G]CGTGGACTATCCGGC | 55626 |
rs189160964 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454552 | CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC | 55626 |
rs189176204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412136 | AAGCAGTACAGTTGT[A/C]CCTTGGTATCTTTGG | 55626 |
rs189184647 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494746 | AATGCACAAGAAAAA[C/G]ACAGTACCTTCTTTT | 55626 |
rs189250939 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481375 | GTAGCAGTCTTCTGA[C/G]CTGAACACACTATTT | 55626 |
rs189301982 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567003 | CATGGGCAACAGAGT[A/G]AGCCCTGTCTCAAGA | 55626 |
rs189302927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461660 | ATAAAAGATTATGCC[A/C]ACAGAAACATGTCCT | 55626 |
rs189313451 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441406 | GTAGTCCCAGCTACT[C/G]GGGAGGCTGAGGCGG | 55626 |
rs189316003 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457597 | TGGATTTGGTGGTGA[C/T]GGTTGCTTATAAGAT | 55626 |
rs189321482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419095 | AAAGGTGCATTAAGA[C/T]GGAGGGAGCGGAGCA | 55626 |
rs189332073 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502947 | GCACCTGTAGTCTCA[A/G]CTACTCAGGAGGCTG | 55626 |
rs189346362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496730 | GTGGGCCCGTACAAC[A/G]TAGGTCACAAGCATC | 55626 |
rs189349757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544184 | TCAAGACTTCCAAAA[C/T]TTTCAAAGAGATTAA | 55626 |
rs189367487 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569623 | GAGATCTGCAAAAAT[A/G]CAAGGTCTGCCTGAG | 55626 |
rs189402502 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535227 | TCAGAAGTTAGAAAG[C/T]GTTTACTGTATAGTA | 55626 |
rs189412300 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515062 | ACCTAGAAGCTTGTT[C/T]CACCCTAAAGTGCTC | 55626 |
rs189479489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485444 | AAGCCCAGGCTTACA[C/T]CCCACCTCCCTTAGC | 55626 |
rs189516152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570338 | CCCACTCTAAGTCTC[C/T]TCCATGGAACTATCC | 55626 |
rs189518992 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530014 | GGCTGGGACCAATTA[C/T]AATAAGCAAAATATG | 55626 |
rs189530121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587854 | GAACAAACATCTTCA[C/T]AGGTAAGGGTTGAAA | 55626 |
rs189531383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414119 | GCTCCCTCAGTGTCA[C/T]GATGCTCTCTTCACA | 55626 |
rs189532036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552135 | GCACTTTGGAAGGCC[A/G]AGGCAGGCAGATCAC | 55626 |
rs189548212 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447085 | AGTACCTACAACTTA[C/T]AGGATTGTTGGAAGA | 55626 |
rs189551034 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559161 | AAAAATTAGATGGGC[A/G]TGGTGGCACGCCCCT | 55626 |
rs189613609 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482882 | GGCGTGGTGGCATGC[A/G]CCTGTAGTTCCAGCT | 55626 |
rs189641012 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563642 | GTCAGGAGTTTGAGA[A/C]CAGCCTGGCCAATGT | 55626 |
rs189644760 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525271 | ATACCACTGCATTCC[A/G]GCCTGGGCAACCGAT | 55626 |
rs189645553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566486 | AGAGAATTATGCTGA[C/G]TGAAAAAGGCCAATC | 55626 |
rs189651929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587217 | AAACCCCATCTCTAC[G/T]CAAAATACAAAAATT | 55626 |
rs189682426 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574893 | TTTACAGGTTTGTTA[A/C]AAATATTACATGGAA | 55626 |
rs189684894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533185 | AAAAAAAAAAGGAAA[A/C]GAATTAAAATAAATG | 55626 |
rs189688915 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550852 | AGCACTTTGGGAGGC[C/T]GAGACGGGCGGATCG | 55626 |
rs189715562 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402597 | TCTCGAACTCCTGAC[C/T]TTGTGATCTGCCTGC | 55626 |
rs189754758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509883 | GAAATCAGAAAAAAA[C/T]TGATTAAGAACAGAA | 55626 |
rs189761107 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468583 | GTGGGTGCATCACAA[A/G]GTCAGGAGATCGAGA | 55626 |
rs189777217 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548561 | AAGCTTCTAATTGCA[A/C]ATACAATTCTAGCTC | 55626 |
rs189815083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555867 | ACCTGCAAGAAGCTG[C/T]TAAAATGGAGTCCAA | 55626 |
rs189821297 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571132 | TCTGGCTTCAATTCC[A/G]CTGATATTCTATAAA | 55626 |
rs189826076 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535985 | CGGAGCTCAAGTTTT[G/T]GAAGGTGTGACTTCC | 55626 |
rs189847540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441800 | ATCTAAGGAGGTTTG[A/C]CCTTTCAACAAAGAT | 55626 |
rs189850362 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398420 | CTGCTTCATTACAAT[A/G]CTGTCTTCCTTCAGC | 55626 |
rs189855979 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471689 | CTGGAGTGCAGTAGC[A/G]TGATCTCGGCACACT | 55626 |
rs189865526 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454221 | ATTTTTAGAGACGGG[G/T]TCTTGCTGTGTTGCC | 55626 |
rs189877854 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431655 | TCTTAATGATTTAAA[A/C/T]GATTATTCCACAATT | 55626 |
rs189896584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516287 | ACATCAGTTCTTCAT[A/G]GTTACAATACGAGTA | 55626 |
rs189905929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494037 | ACAATGCCAGATGTG[A/G]ACAATTCAAAGACCA | 55626 |
rs189908445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474762 | GAAAGGATTAGTACT[C/T]ATTCTGGATTTTCCC | 55626 |
rs190001242 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423179 | AATGCACATATCCTA[C/G]AGTGGCAGTGGGAGA | 55626 |
rs190014132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405492 | GGGAGGCCAAGAAGG[A/G]AGGCTTGCTTGAAGC | 55626 |
rs190015835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459477 | CTAGATTGGGAAACC[A/G]ACGCAAGTGGATCAC | 55626 |
rs190032290 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468377 | AGACCTCATCTCTTG[A/C]AAAAAAAGAAAAAAG | 55626 |
rs190036929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497161 | AAAAATAAAGGGAAG[A/G]GGTTAAGATGATAAA | 55626 |
rs190041206 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519444 | TATAACCTGAAGATA[C/T]TCTTTTAACTGGTTG | 55626 |
rs190041283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449121 | ACTTTCCCCCTAAGA[C/T]CAGGAACAAGGCAAG | 55626 |
rs190050421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425525 | AACTAGAACCTGGAG[A/C]AACTCACTGATATCG | 55626 |
rs190054583 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478893 | CTCAGTATATGTAAG[A/G]ACACTTTTAAAAAAA | 55626 |
rs190104996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491519 | TTGGAATTTTCTCAA[A/G]AGAAGAAAACAAATG | 55626 |
rs190111119 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419311 | GAAGCAACTTAATCA[A/G]AGATAGGGGCAGGTC | 55626 |
rs190115046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451676 | ATCTGTTTAACTTGA[A/G]ACTTTCTAATTCAGA | 55626 |
rs190158707 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496973 | AAAAATTAGCCAGAC[A/G]TGATGGCGAGCGCCT | 55626 |
rs190169043 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573011 | GAGGCTGAGGCAGGC[A/G]AATCGCTTGAACCTG | 55626 |
rs190180931 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538504 | TTAATAGTTTCTGGG[G/T]TTTTTTTTAGACGGA | 55626 |
rs190249017 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445648 | AGGAATTATTCCATT[G/T]CATTCTGATCCAGGC | 55626 |
rs190263530 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401002 | AAAGCCTTCTAACAG[C/T]GGGGCAGAAGGTAAG | 55626 |
rs190297764 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523342 | CTACTGAAATAATTT[A/C]TCCACCATTTCCCTC | 55626 |
rs190303726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452661 | AGCTTCATTCAAATG[C/T]AGTCTTAAAATCTGT | 55626 |
rs190311755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561715 | AAAAATTTCCCTCGA[A/G]GCTTCAAGAAAAGAA | 55626 |
rs190333225 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492829 | CTGAGGCAGGCAGAT[C/T]ACGAAGTGAGGAGAT | 55626 |
rs190344995 | snp | A/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595068 | AGTCTCTATAAAAAA[A/T]AAATAAATAAATACA | 55626 |
rs190353966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411192 | TGGGGCGGCCTGAGC[A/G]GAGGAAGACAAACTT | 55626 |
rs190368871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410885 | AGGCGGGCAGATCAC[A/G]AGGTCACAAGATCAA | 55626 |
rs190382492 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453272 | TTCACTTTTTTTTTT[C/T]TCTTCCCCAAAGAGA | 55626 |
rs190389643 | snp | A/G | 0.000798403 | 0.0199641 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518331 | GCTACTTGGGAAGCT[A/G]AGGCAGGAGAATGGC | 55626 |
rs190392642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430387 | GGCAGACACCTAAAA[G/T]GAAGAAATCTTGTTT | 55626 |
rs190431378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557721 | GCTGAGGTGGGAGGA[C/T]AGCCTGAGCCCAGGA | 55626 |
rs190446876 | snp | G/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484330 | CAAAGCACATACTAA[G/T]CATAACCTAAGAAGA | 55626 |
rs190471179 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526667 | GCCTCCAGATGACTC[C/T]AGAGAAAACCCAAGG | 55626 |
rs190476058 | snp | G/T | 3.29549e-05 | 0.00405911 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545675 | CCAGTCCCAGAAGTG[G/T]ATCTCATTGGCAGTG | 55626 |
rs190489737 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506227 | ACAAGCTGACAGTCA[A/G]AAGGTAGCTCTGCTC | 55626 |
rs190538002 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472607 | CTGTCAACTTCTAGT[G/T]TATTTTCTAAAACAC | 55626 |
rs190555776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501309 | AAAGATGTGCACATT[A/G]GATGAACTGGCATGC | 55626 |
rs190559478 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429795 | TGAAAGCCGAGAGGG[A/C]ACACAGGCAGTTTAG | 55626 |
rs190571218 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576730 | ACCTGAACAATATCC[A/C]TCCAAGAGATTATAA | 55626 |
rs190578116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541748 | ATAGAGCTAGCGCAG[C/T]CAACTGACTCATACT | 55626 |
rs190601057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479421 | AACATGACATAAGGA[C/G]AGATTCAAAAAGTGC | 55626 |
rs190608730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564388 | TTATCTCACTTTTTC[C/T]TCACAATGATACTAT | 55626 |
rs190623552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520275 | ACACATTCAATTAGC[C/T]ATCAGGATGATAGCC | 55626 |
rs190667912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438131 | CTTAAAGGCAAAAAA[C/G]ATATTGGAAAAAAAT | 55626 |
rs190750276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549302 | ATATACAGTGTTATC[C/T]ACTGTGACATTGTTT | 55626 |
rs190752613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581593 | CCTGGGTGACAGTGC[A/G]AGACTTCCTCTCAAA | 55626 |
rs190756632 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567506 | AAATAGCTGGGAGTA[C/G]ATGCAGGCACCACCA | 55626 |
rs190765766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415280 | GATCCTCTCTCATTT[C/T]CACCTGCATCCATGC | 55626 |
rs190766278 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585160 | GAAGGCAGCATGCTC[A/G]TTAAGAGTCATCACC | 55626 |
rs190785281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439035 | CAGTACTACGGGAGG[C/G]CAAGGCAGGGTAATC | 55626 |
rs190795657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417244 | TTTAGTAGAGACGGG[A/G]TTTTACCACGTTGAC | 55626 |
rs190812587 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531651 | GGAGTTGGAGGTTGG[A/G]GTGAGCAGAGATCTG | 55626 |
rs190816784 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499477 | CTAAGCAATATTACA[C/T]GTTTTTAAGCAATAA | 55626 |
rs190818379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420403 | TGCTATTCTCACTCA[A/G]CCTCACTGTCTGAAC | 55626 |
rs190820827 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480008 | GTTGCTGGCAGAATT[C/T]AGTTCCTTGCAGATG | 55626 |
rs190825158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460169 | AAATGTTCATCAATC[A/G]GGAACAGACAACAAG | 55626 |
rs190833078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510665 | ATTCCCCAAGCTATG[A/C]AACTGTAGATTAATG | 55626 |
rs190846948 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498706 | TGACCAGACAGTCAG[A/G]TTGTCATTGCTCCTC | 55626 |
rs190855150 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459977 | AGAATAATACCCTGA[A/G]ATGCCTTTCACATGT | 55626 |
rs190882918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539168 | AAGTCAGGTTATAGG[C/T]GTATGGAAGCTCAGT | 55626 |
rs190895335 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590658 | TCACATTCTGAACCC[G/T]TCCAGTTTTTAAAGG | 55626 |
rs190904835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571457 | AAGCAGAAGGAGTGT[C/T]TGAGCCCTAAAGTCC | 55626 |
rs190919930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578084 | CTACAATCACCACTG[C/T]AGTCTAGCCTGGAAG | 55626 |
rs190924970 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416424 | TTCTTGCAGCTCCAA[C/G]AGCAGCCTGAGCAGG | 55626 |
rs190944962 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421491 | GAGGGAGATGAGGGC[A/G]TGGAGGGTGCAGAAT | 55626 |
rs190951597 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463421 | GAAGGTATGCAGTAA[C/G]TCCATATTAATTAAA | 55626 |
rs190965656 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399013 | TCCTGACCTCAGGTG[A/G]TCCACCCTCCTCGGC | 55626 |
rs190969014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556142 | TGCCCCAGTACTCTT[C/T]GGAAACTCCATATGG | 55626 |
rs190971805 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483571 | ATAGGAAAAGGAAAC[A/G]AGAAAGAAAAGCTGA | 55626 |
rs190974105 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465118 | ATCACCCCAGGGCCA[A/C]GTATGGACAACTAGT | 55626 |
rs190980302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443311 | TTAAGTGTATGGTAT[A/G]GTTGATATCTGGTTA | 55626 |
rs190988471 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568315 | ATACAAAAATTAGCC[A/G]GGAGTGGTGGCAGGC | 55626 |
rs191057615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442817 | ACACAGACAAGATAG[A/G]AAAATTTCAGCTTCA | 55626 |
rs191086617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418475 | TTACATATGTATACA[C/T]GTGCCACGTTGGTGT | 55626 |
rs191096799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46449881 | CTGACCAACATAGTG[A/G]AATCCCATCTCTACT | 55626 |
rs191099691 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416027 | TGCAAGGGAGAGGAC[C/T]AGAAATTTGGCTGGG | 55626 |
rs191100239 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505369 | GAGGGAGGTGGGCAG[A/G]GAAGGAGACAGAGAA | 55626 |
rs191102321 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525699 | GAAGTTGCAGTGACC[C/T]GAGATCGTGCCACTG | 55626 |
rs191104792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426941 | TTTGGTATTTGCCAC[C/T]CCCAAGTCCAGACAA | 55626 |
rs191113167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513072 | AACAAGTGCTTCAGA[G/T]ACATGATCTTCTTTC | 55626 |
rs191127680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489564 | ATGACCTGTGGCTAG[A/G]AGCAAGAAAACCCTG | 55626 |
rs191131467 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470488 | CAGCTACTGAGGAGG[C/T]TGAGGCAGGAGAATG | 55626 |
rs191158106 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589720 | CGCCTACCGGGTTCA[C/T]GCCATTCTCCTGCCT | 55626 |
rs191199053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411921 | GTGAGCCACCATGCC[C/T]GGCCCAAATCTGTCT | 55626 |
rs191240741 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532347 | TAGAATAAAACAAAA[G/T]TTTTTCTCAAAAACT | 55626 |
rs191262174 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567876 | AGCTGGGGCTGGGCG[C/T]GGTGGCTCACACCTG | 55626 |
rs191334198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437444 | ACAGCTTCTCCGGTA[A/G]CATATTCAGTTTCAG | 55626 |
rs191350539 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469750 | GCTCACTGCAGCCTC[A/G]AACTCCTGGGCTCAA | 55626 |
rs191383649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516082 | ATATGAAGCTTTGTT[G/T]CTGGAGAGTCTCTGA | 55626 |
rs191401348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444489 | GCATTTCATACACAA[C/T]CACCCTCCTTCTGAT | 55626 |
rs191409357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576679 | ACATTCCCTCTTGTC[C/T]TGTCCTCTATGGAAA | 55626 |
rs191425784 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554701 | AAGGGAGCTAAGTCA[A/C]ACTGAAGTCACACAG | 55626 |
rs191443934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399430 | GAAGTGCAGTGGCAC[A/C]ATCTTGGCTCACTGC | 55626 |
rs191462679 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473158 | ATACTTTAATGCAAC[A/G]TCACTGGAAAATAAG | 55626 |
rs191472160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399795 | TGATGCCATATTTCC[C/T]GGAAAAGAGTCAACT | 55626 |
rs191475945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512423 | GAATGACAACAGCCT[C/T]TCTGGCCAACAGAAA | 55626 |
rs191478515 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422384 | AATAGGGAATGAGTC[C/T]GGTTGCCAAGATCTT | 55626 |
rs191510613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582634 | TTGGACGCGAATCCT[A/G]GTTCTGCCATTTGCT | 55626 |
rs191518621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550095 | AAGTGCTGGGATTAC[A/G]GGTGTGAGCTACTGC | 55626 |
rs191535949 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477073 | CCGAGATTGCGCCAC[C/T]GCACTCCAGCCTGGG | 55626 |
rs191537856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457360 | AGGTGAGGTTAGATC[A/G]GAAAATGGACTCCTA | 55626 |
rs191541459 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589458 | GAACCTAAGTTTTTT[G/T]GGGGTAAACCAAACC | 55626 |
rs191559196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537885 | AATCACCTTTTATGA[A/G]CTCCACTCACTCAGG | 55626 |
rs191565531 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495764 | TATTTTTCAAATATA[C/T]TACTGTTGTGATAAA | 55626 |
rs191568133 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517931 | ATATTCGTATATATA[G/T]AGAGAGAGAGAGAAC | 55626 |
rs191608174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425059 | GAATTGCTTGAACCC[A/G]GGCGGCAGAGGTTGC | 55626 |
rs191634819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465700 | TTGCAGTGTAAGGGA[A/T]CATCAGTGTAAGGAG | 55626 |
rs191637433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535704 | AAGCCAAAGACCTAA[C/T]AATATTACTGAGATG | 55626 |
rs191642168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493546 | ATAGGTAAAGGAGGG[A/G]GAAGCTTTATCTGGC | 55626 |
rs191659996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570651 | GAACAGTAATTTGAT[G/T]GCTGTTAATATTTTT | 55626 |
rs191664009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556865 | ATAAGGGCTGGTTGC[A/G]GTGGCTCATGCCTGT | 55626 |
rs191665644 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593626 | AACCACACCGGGAAG[C/T]CCCAGCAACTCTCCC | 55626 |
rs191672722 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572286 | AGCCTGGTGATAGAG[C/T]GAGATTCCATCTCAA | 55626 |
rs191695314 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539873 | GTCTTGCTCCATCAC[C/G]CAGGCTGGAGTGCAG | 55626 |
rs191714193 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422120 | CAAATTCTATTACAC[A/C/T]GGACGTATTATCAGA | 55626 |
rs191733181 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575684 | ACCACGCCCAACTAA[G/T]TTTTGTATTTTTAGT | 55626 |
rs191749680 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469301 | CCAAAATGAAATCAT[C/T]GTTTTTATAACAGAA | 55626 |
rs191782258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576499 | TCAGCAAGTCATCTC[C/T]GTCACCTCCCTCATT | 55626 |
rs191827023 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480675 | TTGCTGAAGTTTAAC[A/C]AAAGTCAGCCTTATT | 55626 |
rs191833019 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428294 | TCAACTCTTGGCTAC[G/T]GTTTTACCACATGGC | 55626 |
rs191837315 | snp | A/C/G/T | 0.000161311 | 0.0089797 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408465 | AAGTGGCACTCACTC[A/C/G/T]GTCTTAGGGTCCCTC | 55626 |
rs191846378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521688 | AGCAATTATCGTTTA[A/C]GTTATCCAACGATAG | 55626 |
rs191848472 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540330 | TACAGAGATCTTTAA[C/T]AAACTTTTAAAGTGC | 55626 |
rs191854481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500646 | AACACTCCATAGCTC[C/T]AGCCACAGATCTATT | 55626 |
rs191857671 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471808 | AATTTTTTGTATTTT[A/C]GTAGAGATGGGGTTT | 55626 |
rs191858972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451743 | AATAAGAATGGGGTT[A/G]GGGATGTAAACACTC | 55626 |
rs191906270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455428 | TCATTTACTATTGGT[A/G]TCTTTTAACATGCTT | 55626 |
rs191910327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402764 | TTGAATTCATGGTGC[C/T]GAACACAATACCAGA | 55626 |
rs191959935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434626 | CTCCTCCCTTATTCC[C/T]GACCGTCGTAACAGG | 55626 |
rs191966642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413163 | TGGCCAAAAGGTCCC[C/T]TCGAATGCTTTCCAT | 55626 |
rs191988539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475513 | ATCCCCTCCCATCAC[A/G]GACTATCCAATGAAA | 55626 |
rs191994903 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579647 | ACAAAAAATGGAAAG[A/G]TACAGCTCCTATCTT | 55626 |
rs192004419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456696 | GAGGGTCTTTGGCTC[A/G]TCAGCAGCAGGAGGG | 55626 |
rs192006218 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494756 | AAAAAGACAGTACCT[A/T]CTTTTACAGACTGTC | 55626 |
rs192007698 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520895 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCCCTATA | 55626 |
rs192022612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560160 | AAATTATACACAGTC[C/T]CTTTCTTTATAAGAA | 55626 |
rs192035995 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563919 | GGAGGCTGGGGTGTG[C/T]GGATCACCTGAAGTC | 55626 |
rs192039109 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536289 | AGGGAGCTCACTGAC[A/G]GAAAGGTAAACAAAT | 55626 |
rs192053365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448396 | AGAGAGATTTAAAAA[C/T]ATTTTGGATTAAATG | 55626 |
rs192071734 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548148 | AACTCTCCCACACAA[C/G]ATAAATATATCCCAA | 55626 |
rs192080569 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565664 | ATGAACTGAGATCAC[A/G]CCACCATACTCCAAC | 55626 |
rs192081499 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486952 | ATAAATAAATAAATA[A/C]ATACAAATAAAAGAG | 55626 |
rs192084108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529746 | CCCGAATTGATATGG[A/G]AAAAAAACATCCAAA | 55626 |
rs192175996 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440004 | AATCAGGCACTCTCA[A/T]GAACTCCAAGTGGAA | 55626 |
rs192202461 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406977 | CGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGACA | 55626 |
rs192230197 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501471 | CAGAATGGGAATAAG[C/G]AGGTTGGAAAATAAA | 55626 |
rs192230221 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551211 | AGAAGAAAAACTAAT[G/T]GTAACACGCTGGGGA | 55626 |
rs192230777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523347 | GAAATAATTTCTCCA[C/G]CATTTCCCTCTGTCT | 55626 |
rs192235356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568867 | GCTGGAGAGCAGTGG[C/T]GCCATCTCAGCTCAC | 55626 |
rs192247459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534225 | CAGCCAGGTGCGGTG[A/G]CTCAGGCCTATAATC | 55626 |
rs192270149 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521812 | CCCCTGATGTGAGGT[A/G]GGCCAAGGCAAGGTA | 55626 |
rs192285578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481315 | CCTCTTTCTAGGGGA[A/G]AGGATCTGCGACAAG | 55626 |
rs192316966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561644 | ACTGTGTTCAGTGTT[C/T]TCCAATCTTATAGTC | 55626 |
rs192352386 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585929 | TCCTGCCTCAGCCTC[C/T]CGAGTAGCTGAGATT | 55626 |
rs192355981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544430 | CAAGAAGCATGAATC[C/T]TGGTGGCAATGAACA | 55626 |
rs192361520 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474874 | GAACAGTGAAAAAAA[A/C]CAAAAAGCAAGATAG | 55626 |
rs192372808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577374 | ACAAAAGATCACATA[C/T]TGTATGATGCCATTT | 55626 |
rs192391980 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517216 | GCAATGGTGCAATCT[C/T]GGCTCACTGCAACCT | 55626 |
rs192423601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400902 | CCCACTTCCTCCTGG[C/G]ACACCCGGCTCCAGC | 55626 |
rs192437377 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506718 | CTCTCTTGCTTTTAT[C/G]TTTGACAATACCAAA | 55626 |
rs192445083 | snp | A/C | 3.72141e-05 | 0.00431343 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435068 | AAAGAAAAGAGGATA[A/C]GAAACTTTGGAGTTG | 55626 |
rs192463088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546185 | GGACCACAGGCGCAT[A/G]GCACCATGCTCAGCT | 55626 |
rs192502305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466024 | AGAATAAAGAATAGT[C/G]ATCTCAAAACAGAAA | 55626 |
rs192512446 | snp | C/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528814 | GGTTACATGTGCCAA[C/G/T]AGAACAAAGAAAAGA | 55626 |
rs192516690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547367 | TTATCAACTTTGGAC[A/G]ACATAGAATATTGAT | 55626 |
rs192542913 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572921 | CTGGTGAAACTCCGT[C/G]TCTACTAAAAATAAA | 55626 |
rs192554384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468079 | TTCCAGGGCATAGGA[C/T]GGTGACAGGTATATT | 55626 |
rs192557837 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461414 | TCTGGGCATATGTTT[G/T]CAAGTATTTTTAAAA | 55626 |
rs192563473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445257 | AGGCTAAAACAAACC[A/G]TTCTAGATAAATGAA | 55626 |
rs192578373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507958 | CAATCTGGCCTGGGG[A/C]CCAATGGGAGGTCTC | 55626 |
rs192592506 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484966 | TTTTAAGACAAAATC[G/T]CACTCTTGTCCCCCA | 55626 |
rs192648753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417510 | ATACCTATTTCCAAT[C/T]CTTTTTAAGTTAAAG | 55626 |
rs192658741 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594436 | GGGAATTAAAAATCA[C/T]AGAGACAGAAAACGA | 55626 |
rs192700570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501148 | TACAGCTGGTACTCA[A/G]ATAATGTTGTTTCAT | 55626 |
rs192708825 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540728 | CTTGGATGATACTTC[C/T]CTCTCTCTGAGACTA | 55626 |
rs192719048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534652 | CATCCAGGAAGCAGT[A/C]CTTGTGCATACTCCT | 55626 |
rs192730035 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569201 | ATCAAAATGGGATTA[C/T]ATATACCACACTCTA | 55626 |
rs192738041 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460623 | CCACCGCGTCCAGCA[A/T]AAACACAACTCTTAA | 55626 |
rs192743102 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491698 | AGGGAGTCTAGAGTT[A/C]CTTCTCCTAATGGCA | 55626 |
rs192770392 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527014 | TTGTAAAGCATAAGG[A/C]CCCTGTATTAGTCAG | 55626 |
rs192776293 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484847 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGA | 55626 |
rs192778488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564825 | ATGAATATTAATTAG[C/T]ATTTGTAATATATAC | 55626 |
rs192806354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414582 | GGCTGGTTTATGAGG[C/G]CGGAAGTAAGCAAGC | 55626 |
rs192809278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444862 | TCTCTGCACTCTTCC[A/G]GTTGCTGCTGGCCAC | 55626 |
rs192818727 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445827 | TTTTCTCAGTACATG[A/T]TGAACAAAATGCTAG | 55626 |
rs192884725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556474 | TATCTATTGTGTGCA[A/G]AAGATATCCAAGGAT | 55626 |
rs192885019 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517483 | AGGTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTA | 55626 |
rs192887770 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485225 | TTACAGGCGTGAGCC[A/C]CTATGCCCGGCCTCA | 55626 |
rs192900739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592897 | TCTAACCACAAACAC[C/G]ATAGTTATAAGATTT | 55626 |
rs192916106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551627 | TGTAATCCCAGAACT[C/T]TGGGAGGCCAAGGTG | 55626 |
rs192920052 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514659 | TTTTTTTTTTTGATA[C/G]AGACAGAGTCTGGCT | 55626 |
rs192949720 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439669 | AAAATAAGTTCTATG[A/T]CAAAAATAACCTTCA | 55626 |
rs192956184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513880 | TTAAATTTTAGCTAC[A/G]ACTTTTTTTTTTTTT | 55626 |
rs192964372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471577 | AGTAATATTCCTTTA[A/C]GAGTATTTTGGCATT | 55626 |
rs192994989 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427520 | GTTCTTAACTTAGCG[C/T]GCAGAGTCATCAGGA | 55626 |
rs193027982 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494999 | AGCGGACGAAAGACC[A/C/G]GAGAGGTAAATACCA | 55626 |
rs193029814 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423266 | TTATTGAGTTTCTTC[C/G]ACCCTAGGAAAGCCT | 55626 |
rs193032656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576760 | AAATATAGGAAGCCC[A/G]TTTCAAATAGCTTCA | 55626 |
rs193073080 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412191 | GGATACCAAAATCTA[C/T]GGTTGCTCAAGTCCC | 55626 |
rs193086909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537422 | ATCAGAGAGAGACTA[G/T]ACTACAAAAGTTCTA | 55626 |
rs193089758 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509206 | AGATCTACATTCTTC[A/C]AACTACGGCTTTAAT | 55626 |
rs193098355 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565070 | AGACCAGCCTGGGCA[A/T]CATGGCAAAACCTCA | 55626 |
rs193108892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468483 | TCAGCCTCCTAGTAG[C/T]ACAAGCATCACTCTT | 55626 |
rs193153165 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572055 | CGCCTATAATCCCAG[C/G]ACTTTGCGAGGCCGA | 55626 |
rs193181587 | snp | A/C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490360 | GGCACCAAGATAAGG[A/C/G]AGAAGAGATGAATAA | 55626 |
rs193199475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450967 | GGGTGTAAGGGGAGG[A/G]AGTATATGGGAACTG | 55626 |
rs193203022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407984 | TGAGGCTGGCACAGA[A/G]AGTCAGGGCCGAGTG | 55626 |
rs193216957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562213 | AACCTTGAGAAAAGA[A/G]GCAGGTGAAAAAAAT | 55626 |
rs193236796 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432060 | TTTTTTTTGAGATTC[C/T]CTTTCATTCATTCAT | 55626 |
rs193262400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578659 | GAGGCCGAGGTGGGC[A/G]GATCACGAGGTCAGG | 55626 |
rs193264343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557446 | TAGGCAAAATGAGAC[C/T]GTCCACTGTAGAGGT | 55626 |
rs199521879 | snp | C/T | 6.64352e-05 | 0.00576309 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542913 | TGTACTGAAGGCAGA[C/T]GGCCGGTTCAGGAGG | 55626 |
rs199528432 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410260 | CAGCTGCTCCCTGCC[C/T]ACTTCCCAAACATAC | 55626 |
rs199551192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541861 | CCCAGACACTCCAGA[C/T]ACAGCCACAACATCT | 55626 |
rs199573787 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546624 | TGCTTAAGCTATTGC[-/A]AAAAAAAAAAAAAGG | 55626 |
rs199600009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568183 | AATCCAGCTGGATGC[C/T]GCAGTGGCACACACC | 55626 |
rs199607275 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568785 | TCAAAAAAAAAAAAA[-/A]GGAACCCTCAACCCT | 55626 |
rs199674607 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465062 | AATAAAAATAAAAAA[-/T]AAAAAAAAATAAACA | 55626 |
rs199706022 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569440 | GATTAAAAAAAAAAA[A/T]ATATATATATATATA | 55626 |
rs199744367 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565715 | TGTCTCAAAAAAAAA[A/C]GTGTATAAAAATGTT | 55626 |
rs199750404 | snp | G/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593091 | ACAGACTTTGAAAAG[G/T]AAAACAGCCAAGAAA | 55626 |
rs199765942 | snp | A/C | 1.65064e-05 | 0.00287279 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46544041 | ATCAAATCTCACCAG[A/C]CTAAAATCACAGAAG | 55626 |
rs199780113 | in-del | -/CTGTGCTCT | 0.0429648 | 0.14013 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585050 | CTCCAGCCTGGGCGA[-/CTGTGCTCT]CTGTGCTCTCTGAAA | 55626 |
rs199819879 | in-del | -/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592768 | CTTAAAAAAAAAAAA[-/G]AAAAAAGAGAGACAG | 55626 |
rs199820988 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493864 | TCCTTCCGCAGATTT[A/G]TATCTATCTTTTTCT | 55626 |
rs199828767 | snp | A/C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441970 | CAAAAAAAAAAAAAA[A/C/T]TTTTTTTTTTTTTTT | 55626 |
rs199831320 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584087 | ATGTATGTTTATTGC[A/G]GCACTATTCACAATA | 55626 |
rs199835892 | in-del | -/TCTAGATC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419405 | CTACAAAACAATATC[-/TCTAGATC]TCAACTTAGAACAAA | 55626 |
rs199878517 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454188 | GAAATAGCTATGAAA[-/T]TTTTTTTTTAATTTT | 55626 |
rs199915642 | in-del | -/AG | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552661 | TCCAGCCTGGGCAAC[-/AG]AGCGAGATTCTGTCT | 55626 |
rs199920145 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418596 | TGATGTTCTCCTTCC[C/T]GTGTCCAAGTGTTCT | 55626 |
rs199949664 | snp | A/G | 0.000199392 | 0.00998279 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548235 | ATGTGAAATATAGCC[A/G]TTTTCCTTACCTTGC | 55626 |
rs199959227 | in-del | -/A | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589262 | TAATTTTAGCTGTGC[-/A]AAAAAAAAATTGATC | 55626 |
rs199965992 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585697 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 55626 |
rs199967437 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409619 | GCCAATGCTAGCATC[C/T]CCCTTCCTTGGGCAT | 55626 |
rs199969795 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424940 | AGGAGTTCAAGACCA[G/T]CCTGACCAAGATGGT | 55626 |
rs199970253 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501672 | TTACCTCACCCCACA[C/T]TGACCACTGTCACTC | 55626 |
rs200024990 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483020 | TCTCAAAAAAAAAAA[A/G]AAAAAAAAAAAAGAG | 55626 |
rs200038782 | snp | C/G | 1.65146e-05 | 0.0028735 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410281 | CCAAACATACCCAGG[C/G]CGCTCGCTGCTCCTG | 55626 |
rs200047750 | in-del | -/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450449 | ATTTTTTTTTTTTTT[-/T]CTTTTCTTGAGAGAG | 55626 |
rs200063825 | snp | A/G | 0.000796899 | 0.0199453 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443639 | CACATTATATTATTT[A/G]TCCACGTTTCCACTG | 55626 |
rs200094704 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563241 | CATAGACCTCATCTC[-/T]TTTTTTTTGTTTGTT | 55626 |
rs200121822 | in-del | -/TCTC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413493 | CTTTCTTTCTTTCTT[-/TCTC]TATTTTTTTCTGAGA | 55626 |
rs200177176 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574114 | TATTGTGAATAGTGC[C/T]GCAATAAACATACAT | 55626 |
rs200180277 | snp | C/T | 0.000441087 | 0.0148442 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547799 | ACAAATCTTAAGTTA[C/T]AGATAAATACTGAGT | 55626 |
rs200188506 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546033 | ACACAGTTCCTATTT[C/T]TTTTTTTTTTTTTTT | 55626 |
rs200196528 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442150 | AATTGTGTGTTTTTG[-/T]TTTTTTTTTGGAGAT | 55626 |
rs200223766 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568813 | CTACCTTTTTTTTTT[-/C]TTTTTTTTTTTTTGA | 55626 |
rs200226243 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579044 | ACCACAAGAAAGCAA[-/T]TAAAAAAAAAAAAAA | 55626 |
rs200247498 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492583 | GTGGAGGTGGGAGGG[C/T]GGTAGGGAAAGACTG | 55626 |
rs200249207 | snp | C/T | 0.27008 | 0.249192 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583731 | ATGAACAGACACTTC[C/T]GAAAAGAAGACATTT | 55626 |
rs200264033 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564158 | TCAAAAAAAAAAAAA[A/C]AAAAAACGTAAGAGC | 55626 |
rs200296421 | snp | A/G | 3.29712e-05 | 0.00406011 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542599 | GCCAACCCTGATGCC[A/G]GAAAACCCCTCCCTT | 55626 |
rs200309915 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529754 | GATATGGAAAAAAAA[-/C]ATCCAAATTTTTAGA | 55626 |
rs200401176 | in-del | -/AG | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531253 | TTGAGTAATTGCAAC[-/AG]AGACTGTACAGCCTC | 55626 |
rs200417273 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462225 | AAGTGAGCACGGCGG[A/C]GTAAGCACACACCTT | 55626 |
rs200433904 | snp | A/C/T | 8.39051e-05 | 0.0064766 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397879 | TGTCATGCCGCCCTC[A/C/T]GCCATCAGCCTCTGG | 55626 |
rs200440284 | in-del | -/C | 0.0333695 | 0.124785 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396476 | TTAGCTGTAGACTAT[-/C]CCCCTCTCCTCCCAC | 55626 |
rs200443575 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562219 | GAGAAAAGAGGCAGG[G/T]GAAAAAAATATTTCA | 55626 |
rs200466391 | in-del | -/A | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548033 | GAGAGAGATAAACCT[-/A]AATTACCTTCAGGAA | 55626 |
rs200478769 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590928 | AAAAAAAAAAAAAAA[C/G/T]AAAAACAAAAAGAAA | 55626 |
rs200517459 | snp | A/T | 0.000148926 | 0.00862792 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543443 | GTAGAGCAAGGCAGT[A/T]AGGTAGAACCTCCAA | 55626 |
rs200566712 | snp | A/G | 0.00199806 | 0.0315442 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508389 | AGAGAGACAGAGATG[A/G]ACAAACACAAACTAG | 55626 |
rs200606172 | in-del | -/A | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595061 | GACTCCAGTCTCTAT[-/A]AAAAAAAAAATAAAT | 55626 |
rs200608002 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585703 | AAAAAAAAATATATA[A/T]ATATATATATATATA | 55626 |
rs200615140 | snp | A/G | 0.00199802 | 0.0315439 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397961 | GGCAGATACAAAGCA[A/G]AAGAGAGAGCGAATT | 55626 |
rs200619916 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498644 | CTCGGAGAGAGGCTG[A/C]AATTTGAAGGAATGA | 55626 |
rs200668615 | in-del | -/AAAT | 0.0185938 | 0.0946107 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525303 | GAAACCCTGTTTCAA[-/AAAT]AAATAAATAAATAGG | 55626 |
rs200729255 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461296 | GCAAAACAACTCAAT[C/T]TGTTGAGGCAAATAG | 55626 |
rs200757787 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562109 | AAAATATGGCAGGTG[C/T]AAGAAAACAACACAC | 55626 |
rs200804417 | snp | A/G | 5.06624e-05 | 0.00503276 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408592 | ATTCTGCAGCTGAAG[A/G]GCCAGAGTCTGGGTG | 55626 |
rs200826059 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585375 | TAAATAAATAATTCC[-/A]AAAAAAAAAACGCTG | 55626 |
rs200828505 | in-del | -/TT | 0.343254 | 0.231956 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562804 | ATGCAACATTGGTTC[-/TT]TTTTTTTTTTTTGAG | 55626 |
rs200836549 | in-del | -/TAGATAGATAGATAGATAGA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447709 | AGCCAGACCATCTTG[-/TAGATAGATAGATAGATAGA]TAGATAGATAGATAG | 55626 |
rs200841087 | snp | A/G | 8.29924e-05 | 0.00644122 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397713 | CTGGGAGCAGTCCCC[A/G]AGAGGTGGAGGGCTG | 55626 |
rs200869869 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405785 | CTTCCAGGCTGGAGT[G/T]CAGTGGCATATCACA | 55626 |
rs200875374 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570262 | GTGAGACCATGTCTC[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAAGC | 55626 |
rs200898027 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424941 | GGAGTTCAAGACCAG[C/T]CTGACCAAGATGGTG | 55626 |
rs200899627 | in-del | -/GG | 0.0123036 | 0.0774623 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570898 | CCCTACTCCAAGAAA[-/GG]GATAGAGAACTGGAA | 55626 |
rs200903618 | in-del | -/TT | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562835 | GAAGGAGTTTCACTC[-/TT]GTTGCCCACGCTGGA | 55626 |
rs200904856 | snp | C/T | 1.80814e-05 | 0.00300672 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397520 | CCATCCAGAAGGTGG[C/T]TGTTATTGGTCAACT | 55626 |
rs200914758 | snp | A/G | 6.9371e-05 | 0.00588903 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397607 | GAGGAAGAGGGCAGG[A/G]TTGGCTGGGTTGGCT | 55626 |
rs200917347 | in-del | -/T | 0.0952156 | 0.196321 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411785 | AATCTGTCTTTTTAA[-/T]TTTTTTTTTTATTTT | 55626 |
rs200921586 | snp | C/T | 0.00145049 | 0.0268913 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541934 | CAGAAGATAGGAAAG[C/T]GACTGCTTACCTCCT | 55626 |
rs200936140 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542732 | ATTCCGCCTCAGAGC[A/G]GGAGTTCAGACTGAG | 55626 |
rs200949868 | snp | C/T | 3.29761e-05 | 0.00406041 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548337 | GCACCCCGTTCTCGC[C/T]CCCAGAGTATCCGGA | 55626 |
rs200963271 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564574 | AAAATACAGAAAAAG[-/A]AAAAAAAAAAGCTCT | 55626 |
rs200967246 | in-del | -/AAAGACCCC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417832 | GACATTTCCCTTCTA[-/AAAGACCCC]AGTTGGTGAATACTG | 55626 |
rs200994445 | snp | A/G | 0.000424365 | 0.0145603 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434940 | AAAGCCCCTCTGGCT[A/G]CTGGGGATGAAAGCT | 55626 |
rs200996700 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525754 | AGACTCCGTCTCAAA[A/G]AAAAAAAAATTAGCC | 55626 |
rs201008226 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538686 | TATTTTTAATAGAGA[C/T]GCGGTTTTACCATGT | 55626 |
rs201023525 | snp | G/T | 0.00245048 | 0.0349175 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433435 | CTTCCAAGCCTAGGG[G/T]AGCTGCCATACAGTG | 55626 |
rs201030293 | in-del | -/A | 0.366679 | 0.221102 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588776 | GCGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs201061717 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584547 | AAAAAGAAAAAAAAC[-/A]AAAAAAAACAAATGA | 55626 |
rs201160414 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449152 | GAAGCCCCTTCTTAC[A/C]AATACTTTTCAACAT | 55626 |
rs201166954 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484404 | TAGAGAGAATCTTCA[G/T]CTGGCACCTTCAAAA | 55626 |
rs201174857 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548992 | AGCAAGACTCCATCT[G/T]AAAAAAAAAAAGATT | 55626 |
rs201193906 | in-del | -/TGTT | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452902 | ATATGTGTGTCTGTC[-/TGTT]TAAAATTATAGCTTT | 55626 |
rs201203187 | snp | A/G | 1.66474e-05 | 0.00288503 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548222 | CAGCACAAATCCTAT[A/G]TGAAATATAGCCATT | 55626 |
rs201208538 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559047 | GCTCACTCCTGTAAT[-/C]CCAGCACTTTGGGAG | 55626 |
rs201218346 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487925 | CCAGATACACATTTC[A/G]GATTCAAAGAGCTAA | 55626 |
rs201268663 | snp | A/C | 0.00199792 | 0.0315431 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493717 | GAAACGCCTACAAGA[A/C]GGAATCACATGTGAA | 55626 |
rs201285627 | in-del | -/CAAAA | 0.02016 | 0.0983543 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590018 | ATAAAGCTACATGAT[-/CAAAA]CAAAAGTTTTATAAG | 55626 |
rs201354368 | snp | A/G | 3.30857e-05 | 0.00406716 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397779 | CCGTCTGAGAGCTGC[A/G]GTGAATGCGGTGGCT | 55626 |
rs201399145 | snp | A/G | 6.68717e-05 | 0.00578199 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542944 | CCCTGGTCCTGCTGC[A/G]TTGACGAGGCCTGCT | 55626 |
rs201405311 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411130 | GAAAAAAAAAAAAAA[C/T]AAAAGCAGAGGCCTC | 55626 |
rs201421498 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549825 | TTTTCTTTCTTTTTT[-/G]GGGGGGGGTGGGGGA | 55626 |
rs201499075 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547884 | CTACTCTCTGGGAGA[A/C]AAAAAAAAAAAAAAA | 55626 |
rs201504923 | snp | C/T | 3.2987e-05 | 0.00406108 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417901 | TCAACCCCCACACTT[C/T]AAGCCACTTACTCTG | 55626 |
rs201509997 | snp | C/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542680 | AGCACAGACAGCAAA[C/G]TCACCGAAGAGGCAC | 55626 |
rs201519408 | in-del | -/ATTG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406055 | TGTCTTTATTTATTT[-/ATTG]TATTATTATTTTTGA | 55626 |
rs201535679 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542281 | CAGCGCAGGGTATCG[C/T]TGTTGAAGGTCAGGA | 55626 |
rs201542637 | in-del | -/TAAC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589748 | CCTCAGTCTCCCAAG[-/TAAC]TGGGACTACAGGCGC | 55626 |
rs201578105 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494724 | AGTGACAGGTAAAAG[-/A]AAAAAAAATGCACAA | 55626 |
rs201599930 | snp | A/G | 0.00199799 | 0.0315437 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547087 | TAGAACACCAAAAGA[A/G]AAGGGTATCTTAAGG | 55626 |
rs201603918 | in-del | -/TAGATAGATAGATAGA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447709 | AGCCAGACCATCTTG[-/TAGATAGATAGATAGA]TAGATAGATAGATAG | 55626 |
rs201653590 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585807 | TGGAAAATAACAATA[A/T]TTTTTTTTTTCTTTT | 55626 |
rs201687485 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583672 | AAAAAAAAAAAAAAA[A/C]AAAAAAACAACAAAA | 55626 |
rs201687974 | snp | A/G | 0.000261673 | 0.0114354 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547073 | CAAAAAAAAAAAATT[A/G]GAACACCAAAAGAAA | 55626 |
rs201748454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475088 | AAAAACAGTCTTATC[A/G]ATAGAAAAAAAATTA | 55626 |
rs201767064 | snp | C/T | 9.5996e-05 | 0.00692739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397975 | AGAAGAGAGAGCGAA[C/T]TGGCTGCTGGCCTGG | 55626 |
rs201784560 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565715 | TGTCTCAAAAAAAAA[-/C]GTGTATAAAAATGTT | 55626 |
rs201816639 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445085 | ACAAAAAAAAAAAAA[G/T]AAAAAAAAACTTAGT | 55626 |
rs201819276 | in-del | -/A | 0.236724 | 0.249647 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450057 | GAGCGAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs201825460 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413829 | CAGTGTCACTGACTG[A/T]CTGTGAGCTAAAGAA | 55626 |
rs201837751 | in-del | -/C | 0.307919 | 0.243198 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428592 | CTTCTTCTTCTTCTT[-/C]TTTTTTTTTTAAGGT | 55626 |
rs201880316 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515472 | AGTGAGACTGCATCT[C/T]AAAACAAACAAACAA | 55626 |
rs201940168 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565777 | TTATAAAAATTCAGA[-/T]TTTTTTTTTTCAGAA | 55626 |
rs201959219 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416726 | CAGAACACTCTGGGA[-/AA]AGACTCTGCACCAAG | 55626 |
rs201961029 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498645 | TCGGAGAGAGGCTGT[C/T]ATTTGAAGGAATGAA | 55626 |
rs201973374 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488903 | CGTTCAGTAAAAAGG[-/T]TTTTTTGTTTTTTTG | 55626 |
rs202000950 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579045 | ACCACAAGAAAGCAA[A/T]AAAAAAAAAAAAAAA | 55626 |
rs202001744 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517831 | GACAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs202029338 | snp | C/G/T | 0.000184742 | 0.00960954 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494144 | GACAAAGCGTCCAAG[C/G/T]GAAGGTGCAGACATC | 55626 |
rs202034039 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587642 | TCCCTGTAAATACCC[A/C]GGGCTCGCCTCACTC | 55626 |
rs202037773 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418559 | TCCCCACTCCCCCTA[C/T]CCCACAACAGGCCCC | 55626 |
rs202076417 | snp | A/G | 8.24396e-05 | 0.00641973 | splice-donor-variant | AMBRA1 | GRCh38.p7 | 11:46541943 | GGAAAGCGACTGCTT[A/G]CCTCCTGAGTGAATC | 55626 |
rs202077633 | in-del | -/GTCCCAGGAG | 0.0279526 | 0.114869 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411390 | AAGACGAGGGACTGT[-/GTCCCAGGAG]GTCCCAGGAGGTCCC | 55626 |
rs202108742 | snp | A/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397759 | GGCGGCACCAGGTTC[A/T]GTGCCCGTCTGAGAG | 55626 |
rs202122492 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426087 | AAAAAAAAAAAAAAA[C/T]AAAGAAAACATTGTG | 55626 |
rs202149587 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582500 | AATCTCCATACAGGC[A/T]TGGACATCTATTTTT | 55626 |
rs202150389 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545163 | AAAAAAAAAAGCCGG[-/C]GGGGGGGGGGGTGGT | 55626 |
rs202161574 | in-del | -/ATAAATAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486909 | AGACTCCATCTCAAC[-/ATAAATAA]ATAAATAAATAAATA | 55626 |
rs202199737 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533258 | ACACACACACAAATT[A/G]TTAATAGCAGATCTC | 55626 |
rs202203753 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513903 | TTTTTTTTTTTTAAA[A/C]AACAAGGGCCAGTCA | 55626 |
rs202220170 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484287 | TTTCTAGATCATTGC[A/T]TTTGTTCTGAGGGGT | 55626 |
rs367572501 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581016 | CCATGCTGGTCTCAA[A/G]CTCCTGAGCTCAAGC | 55626 |
rs367574443 | in-del | -/CT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537397 | AATCATTTACTCTCT[-/CT]GTTTTGTCATCAGAG | 55626 |
rs367575756 | snp | A/C | 1.77071e-05 | 0.00297544 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433651 | CCAACAAAACAGAGA[A/C]ATATTTCCTAGGCTT | 55626 |
rs367581553 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539399 | TCCGTCTCTACTAAA[A/G]ATACAAAATTAGCCA | 55626 |
rs367590170 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444392 | AAAATGGATTTTTTT[-/T]AACAGGGTGACACTT | 55626 |
rs367678351 | snp | A/C/G | 3.30689e-05 | 0.00406615 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543425 | ACCAGCATGGGGCAG[A/C/G]GGGTAGAGCAAGGCA | 55626 |
rs367679091 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559809 | ACAAATCATATCCTC[A/G]CTGAATTTCAAGTTT | 55626 |
rs367760647 | snp | A/C | 1.65411e-05 | 0.00287581 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397773 | CAGTGCCCGTCTGAG[A/C]GCTGCGGTGAATGCG | 55626 |
rs367763157 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579681 | GGATCTTACTGTCTT[A/G]GAGTATACTTCTTAT | 55626 |
rs367774947 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400510 | TTTTTTTTTTTTTTT[G/T]AGACCAGGTCTCGCT | 55626 |
rs367780816 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499800 | AGCTGGGTTTACAGG[C/T]GCCCGCCACCACGCC | 55626 |
rs367782685 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422227 | TCCACTGCAGCTCTT[C/T]CCTGGTATATGACGA | 55626 |
rs367786785 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468020 | GAATAGTGAGAAGAG[A/C]TCCTGGAATCTTCAG | 55626 |
rs367790068 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486266 | CAGAAAGATAAAGGG[A/C]GATCAAAGAGATAAA | 55626 |
rs367807066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552117 | CTCACGCCTATAATC[C/T]CAGCACTTTGGAAGG | 55626 |
rs367819076 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553537 | AGATCACAAGGTCAG[A/G]AGTTCGAGACCAGCC | 55626 |
rs367826994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450564 | CCCACCTCAGCCTCC[C/T]GAGTAGCTGGGGCTA | 55626 |
rs367829480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517597 | CCCAGCACTTTGGGA[C/G]GCTGAGGCAGGTGGA | 55626 |
rs367860213 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431646 | GATTCTGTCTCTTAA[A/T]GATTTAAACGATTAT | 55626 |
rs367866774 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429774 | TGCCTGGTTCCAATT[-/A]GAAAATGAAAGCCGA | 55626 |
rs367876540 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508950 | CTCTTGGAACCTCTT[C/T]TTCTCTCCCTTAAGA | 55626 |
rs367881438 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593687 | GCCCCTCCGGCCGCG[A/C]CCCTCAACGCAGTCC | 55626 |
rs367885435 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552521 | GAAACCCCGTCTCTA[A/C]TAAAAATACAAAAGT | 55626 |
rs367913738 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469111 | TCACGCCACTGAACT[C/G]CAGCCTGCGTGACAA | 55626 |
rs367921911 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533675 | TGCAGAGTTGGCCTA[C/G]CTTTAATTTACGCTA | 55626 |
rs367938170 | snp | A/G | 6.7974e-05 | 0.00582944 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434874 | GGTGTAGAGCATTTC[A/G]CCCAGGTTATGGGGG | 55626 |
rs367942465 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582224 | GTATTCCAACCATAT[A/C]AACCTTCTTCCAGTT | 55626 |
rs367956338 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432713 | CAAGTACATCCAACT[A/G]TAAATGGTACAGATT | 55626 |
rs367975954 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500603 | CCATCCAGAGTTCGG[A/G]GCTTTCTGATATCTC | 55626 |
rs367983946 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541190 | AGCCATACATGGAAC[A/G]TATGGTGGGCGATCA | 55626 |
rs368063703 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459144 | GCAGATCTAGATACA[C/G/T]GGACAGACAGAAATC | 55626 |
rs368081970 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411043 | AGACAGAGGTTGCAG[C/T]GAGCTGAGATCGCGC | 55626 |
rs368132450 | snp | G/T | 2.84459e-05 | 0.00377122 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494181 | TTGCGTGGAGCTCGG[G/T]GCCTGGATCTGTCAC | 55626 |
rs368178943 | snp | C/T | 3.2963e-05 | 0.00405961 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508269 | GAGGAGGTGGAAGAA[C/T]GGAGACGGTTCTGTT | 55626 |
rs368190678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441997 | TTTTTTTGAGACAGG[A/G]TCTTGCTTTGTTGCC | 55626 |
rs368208385 | snp | A/G | 8.39102e-05 | 0.00647673 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397880 | GTCATGCCGCCCTCC[A/G]CCATCAGCCTCTGGA | 55626 |
rs368227658 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571638 | CATGGTTTGTGTCAC[C/T]GCACTCTAGCCTAGG | 55626 |
rs368249344 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554951 | ACATAAGACAAATGC[C/T]GGTCAGGCATGGTGG | 55626 |
rs368253837 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551421 | GGGCTCAAGCAATCC[C/T]CCTGCCTCAGCCTCC | 55626 |
rs368255467 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432970 | CCTTAGACAAGACAG[G/T]GTCCTAGACAGGACC | 55626 |
rs368255546 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466727 | TATTTTTATCAAAGT[A/G]CTACCTACCCATAAT | 55626 |
rs368255560 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517441 | GGCGTAAGCCACCGC[G/T]CCCGGCTAGAAAGCA | 55626 |
rs368265608 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579349 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 55626 |
rs368330733 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468814 | GTGAGGCTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 55626 |
rs368343912 | snp | A/C/T | 0.000153988 | 0.00877328 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408464 | GAAGTGGCACTCACT[A/C/T]GGTCTTAGGGTCCCT | 55626 |
rs368344517 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441458 | GTGCGGAGATTGCAG[G/T]ACACCGAGATCATGC | 55626 |
rs368351007 | snp | A/C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534799 | CCACCTCAGCCCCAC[A/C/G]AGTAGCTGGGACTAC | 55626 |
rs368357456 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454577 | CATCTCCACTAAAAA[-/T]ACAAAAAAAAAAAAA | 55626 |
rs368371852 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561003 | CTTTCTATTCTCTGC[A/G]TAGTCTTTGAGAAAG | 55626 |
rs368382340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587096 | AAAGAAACACAACTT[C/T]AGGTCAGGCACAGTG | 55626 |
rs368397049 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412861 | AACTCATCTCTGTTT[C/T]TGGTGAGCAAATCCT | 55626 |
rs368407716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511258 | TTATATTTAGGGTGT[A/G]TAATCCTCAAACATC | 55626 |
rs368409184 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543874 | CTGGAAAGATAAGAC[C/T]TGGGTATTGAGAATT | 55626 |
rs368412913 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573830 | CTCCCCCCACCCCAC[A/C]ACAGTCCCCAGAGTG | 55626 |
rs368431114 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527432 | TTACAGTGAGCCGAG[A/G]TCATGCCACTGTATT | 55626 |
rs368436605 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396939 | GGCCCGATCCCTGTT[C/G]GTTTCAGTGGGGTAA | 55626 |
rs368447760 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509032 | CAGTAAAATATACTT[A/G]GGAGAACAGAAAATC | 55626 |
rs368451272 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567923 | GAGGCCGAGGCAGGC[A/G]GATCACTTGACATCA | 55626 |
rs368452938 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442312 | CACACTCAGCTAATT[A/T]TTGTATTTTTAGTAG | 55626 |
rs368462191 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461784 | CATAAACTTTGTACC[C/T]CACAAAGGCAGAGAC | 55626 |
rs368462461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497561 | GGAAAATGTGAAACA[C/T]AATAAACACAATATG | 55626 |
rs368472478 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565254 | ACAGAGAAAAATTCC[A/C]TCTAAAAAAAAAACG | 55626 |
rs368536116 | snp | A/G | 3.33311e-05 | 0.00408221 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543269 | GGATGCCAGAAGAGC[A/G]GGAGGACAGCATGTG | 55626 |
rs368549192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448537 | AAAATCTGTAATTTA[A/G]GCACCTACCATAAGA | 55626 |
rs368559941 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405305 | AACAATTATCAGTTT[A/T]GGTGCCCATCTCCCT | 55626 |
rs368567106 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466163 | GCCTACAATCCAGTT[A/G]GGAAGATAGGACTTC | 55626 |
rs368581507 | in-del | -/ATAG | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450720 | GTGTTGGGATTATAG[-/ATAG]GCATGAGCCACCATG | 55626 |
rs368584188 | snp | C/T | 1.65581e-05 | 0.00287728 | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548394 | ATGGCGCTCAGTAGC[C/T]ACTGTCACACCAGGC | 55626 |
rs368611258 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427941 | TTGAACCCAGGTGGC[A/G]GAGGTTGCAGTGAGC | 55626 |
rs368621730 | snp | C/G | | | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46541978 | TCAGAGCTCTCCTCA[C/G]GCATATCCTGATGTA | 55626 |
rs368728859 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444339 | ACTTTCTCTGAGATA[C/T]ATTCTTCTGTATGAC | 55626 |
rs368729337 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414167 | CTTCCCAACTTCTTG[C/G]GACCATTCCCTTGGA | 55626 |
rs368732790 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457805 | TACTTAGAAGGCTGA[A/G]GCATGAAAATCACTT | 55626 |
rs368751462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574576 | TATTAGCCCTTTGTC[A/G]GATGAGTAGGTTGCG | 55626 |
rs368778782 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399838 | ACCCAGGTCTAGGGA[A/G]GGAGAGAAGGATCTG | 55626 |
rs368786073 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465006 | CTGCGATCGCGCCAC[A/C]GCACTCCAGCCTGGC | 55626 |
rs368792469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497649 | CCAAACCAGCTCAAA[A/C]ATTTACTGAGCAGGT | 55626 |
rs368857637 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434138 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGTACTTAA | 55626 |
rs368857938 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568380 | GAAGAATTGCTTGAA[C/T]CCAGGAGGCAGAGGT | 55626 |
rs368877578 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576469 | AACAATTATGTCCCA[G/T]GGTTATCAGGGACCT | 55626 |
rs368898575 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490123 | TCATTTCAGTTGCTG[C/T]GACTACACAGAGCTA | 55626 |
rs368936055 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443717 | AAACTAGACTATGGC[C/T]GAAGAAAGCTAATGA | 55626 |
rs368948402 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433812 | TGAGTGTAGTGTTTG[A/G]CATATAGAAAGCACA | 55626 |
rs368961450 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471307 | AATTCGTCTGGGCAC[A/G]GTGGCTCATACCTGT | 55626 |
rs368964576 | in-del | -/AGG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577884 | GAACCCAGGAGGAGG[-/AGG]TTGCAGTGAGCCGAT | 55626 |
rs368966869 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414873 | ATTTTTGAAGGCCTT[A/G]GTCTACTGCCAAGTG | 55626 |
rs368975252 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480713 | AACAACCAGAGAGAG[A/G]CTCTTTGCTCTACAA | 55626 |
rs368977701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401524 | GAGGCATGAGCCACC[A/G]CACCCAGCTCAGCTC | 55626 |
rs368993355 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545288 | AACATGGTGAAACCC[A/T]ATCTTTATTAAAAAT | 55626 |
rs369008392 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516500 | CAGTGGCACGATCTC[A/G]GCTCACTGCAAGCTC | 55626 |
rs369043833 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520899 | CGTGAGCCACCGCGC[C/T]CGGCCCCTATAGCAT | 55626 |
rs369058163 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517146 | GGATTACTCAAAAGC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs369133624 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443725 | CTATGGCTGAAGAAA[C/G]CTAATGAGTCCCATC | 55626 |
rs369135951 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574912 | TATTACATGGAAGAA[-/T]AAATGTAAAACTCCC | 55626 |
rs369144082 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512486 | AGGTTCCTCCTCTAG[C/T]ACCACACTTGCGGAA | 55626 |
rs369150751 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574366 | TGCCATTCTAACTGG[C/T]GTGAGATGGTATCTC | 55626 |
rs369161543 | snp | A/G | 5.33789e-05 | 0.00516591 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443645 | ATATTATTTATCCAC[A/G]TTTCCACTGCAAAAC | 55626 |
rs369166236 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504771 | CTCCACAGCAAGCTC[G/T]TGGAAAGGCTCAAAA | 55626 |
rs369206519 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490033 | ACCTACCTCACAGGG[A/T]TGTTGCAAAGATGAA | 55626 |
rs369292170 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473682 | TTTGAGACGGAGTCT[C/G/T]GCACTGTCGCCCAGG | 55626 |
rs369313452 | snp | A/G | 6.6177e-05 | 0.00575188 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417871 | ATTACCCCAGTCCTC[A/G]GCCCCAGTGATCCCT | 55626 |
rs369353560 | snp | C/G | 3.29592e-05 | 0.00405938 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46541976 | CCTCAGAGCTCTCCT[C/G]AGGCATATCCTGATG | 55626 |
rs369391832 | snp | A/G | 1.66504e-05 | 0.0028853 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544092 | AGAGAGATTATGTTA[A/G]CTGAGAAGAGGAAAC | 55626 |
rs369458881 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505730 | AGGAGGAGGCAGTCT[A/G]ACACAGGAAAATCGA | 55626 |
rs369462195 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580441 | TCTCACAATTAGCAT[G/T]ACTAAAACTGAGGTC | 55626 |
rs369464689 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404663 | CTGCCTGCTGCTCCC[A/G]CTGACCAGAGCCTCA | 55626 |
rs369475210 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555439 | TCTCATAACAACCCT[A/G]TGAAGCAGACATTGT | 55626 |
rs369476815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558761 | GATCCTTTCTTAGGA[C/T]TCGTTCTTCCTAAGT | 55626 |
rs369482687 | snp | C/T | 8.84427e-05 | 0.00664933 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408480 | GGTCTTAGGGTCCCT[C/T]TCCCACCCCCTCCAG | 55626 |
rs369527019 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472835 | AGCTGTTCTCCCTGC[C/T]CTGTCACCTGCTCAC | 55626 |
rs369531553 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520510 | TATTACTGTCTGTAA[A/C]AAGCCTTCAAAGCTC | 55626 |
rs369532212 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427177 | AGAGCCTATATTTGT[A/G]AAGTTATATAAATTC | 55626 |
rs369537379 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541717 | GGCTAAAGCCAGAAC[-/C]TTGAGCTTAGCCGAA | 55626 |
rs369572491 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484662 | TTGGCTTTTTTTTTT[-/T]CTGAGATGGAGTCTC | 55626 |
rs369577015 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481343 | AAGGATATAAGAGCA[C/T]AGTAGCCCCCTCCCC | 55626 |
rs369583834 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590293 | TGCAGTGAGCCAAGA[C/T]TGCGCCACTGCCTGC | 55626 |
rs369586410 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568237 | CCGAGGCAGGAAGAT[C/G]TCCTGAGGTCAAGAG | 55626 |
rs369594191 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526546 | AAAAAAAAATTAAAA[-/T]TAAAAAAAAAAAAAA | 55626 |
rs369630690 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415765 | TGTCCAGTGCTAATG[C/T]CATCTTACTCAGGGA | 55626 |
rs369653074 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563629 | CAGATCACTTGAAGT[C/G/T]AGGAGTTTGAGACCA | 55626 |
rs369655473 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533071 | GGGAGGCTGAGGCAC[A/G]AGAATCGCTTGAGCC | 55626 |
rs369656772 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574856 | TTCACTTTTTCAAAC[A/G]ATGTTTCACTTTCTC | 55626 |
rs369659711 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542317 | TGGCAAGCACGACAG[C/T]GATTCAGGTGGCCAC | 55626 |
rs369675096 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460471 | GGACTACAGGTGCCC[A/G]CCACCATGCCCGGCT | 55626 |
rs369707508 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482478 | AACTATATCAATATG[A/G]TAGATTCTGGAGACA | 55626 |
rs369720931 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549225 | GATTAAAGAACAAAT[C/T]GTGGTCTATACAATG | 55626 |
rs369721020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514609 | AGGTTGGGGTGTATT[C/T]TACAGTTGTGTGACA | 55626 |
rs369730873 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502524 | CTTGGGTACAAGTTA[C/T]ATATTTGTTATTAGA | 55626 |
rs369760084 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445625 | ACAAGGTCTACCACT[C/T]CCCTGGAAGGAATTA | 55626 |
rs369763086 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405709 | CCAGCCTGAGTGACA[C/G]AGTGAGACTCTATCT | 55626 |
rs369765248 | snp | G/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452286 | GTATCTTTTAGATGG[G/T]CTACTAGTGTCTTAT | 55626 |
rs369767213 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496802 | TCAGTTTATCCCTTC[A/C]TTTAAAAAAAAAAAA | 55626 |
rs369798860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556406 | TAAACAACACATTCC[C/T]GAAGGCAAACACACC | 55626 |
rs369798957 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449004 | CTAAATTCTACCAAA[C/T]ATTTAAGGAAGAAAT | 55626 |
rs369827441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428657 | CCTCTCCAATTTTAC[C/T]GAGGTGGCTGACCAC | 55626 |
rs369837961 | snp | A/G | 1.85896e-05 | 0.00304868 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408721 | TCTAGGGAGAGAAAG[A/G]CAGACTAAAGTCAGA | 55626 |
rs369840871 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547589 | GCAAATGATTGTTAT[C/T]GAGAAACTTTCCAAG | 55626 |
rs369856494 | snp | C/T | 1.64985e-05 | 0.0028721 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541926 | AAGGGATGCAGAAGA[C/T]AGGAAAGCGACTGCT | 55626 |
rs369928404 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545589 | CAGACAATGCAGATG[C/G]GGCAGCGCACTCACC | 55626 |
rs369971064 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470928 | AGGGAGGAGGAGAAA[A/G]AACTAATAAGTTCAC | 55626 |
rs370014086 | snp | C/T | 2.3849e-05 | 0.0034531 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435041 | CATTCACGGAAGCTG[C/T]ATCAGACAAAGAAAG | 55626 |
rs370039241 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593061 | AACTGTCATTGCTAC[A/G]CTAGTTAAAATGATA | 55626 |
rs370067551 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577170 | CATGCATGTTCAAAG[C/T]AACACTATTCACAAG | 55626 |
rs370069704 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428589 | CTTCTTCTTCTTCTT[-/C]TTCTTTTTTTTTTAA | 55626 |
rs370073097 | snp | A/G/T | 9.04108e-05 | 0.00672296 | missense, synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397486 | CCTAGGGCCTGCAGC[A/G/T]TCCCCCCTGCTGCTG | 55626 |
rs370089540 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499861 | GGTTTCACCATCTTG[C/G]CCAGGCTAGTCTTGA | 55626 |
rs370093434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468577 | GCTGAGGTGGGTGCA[C/T]CACAAGGTCAGGAGA | 55626 |
rs370109451 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424425 | AAGCTTTTTATTTTT[C/T]AATTGGCCCGCTGCT | 55626 |
rs370148584 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571430 | TCTGTAATCCCAGTG[A/G]TTTGGGAGGCAAAGC | 55626 |
rs370149848 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549943 | CCTGCCTCAGCCTCC[A/G]GAGTAGCTGGGATTA | 55626 |
rs370167428 | snp | C/T | 9.96777e-05 | 0.00705896 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397709 | GCCTCTGGGAGCAGT[C/T]CCCGAGAGGTGGAGG | 55626 |
rs370198312 | snp | A/C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438643 | GCTCCAGATGACCCA[A/C/T]AAACACTCCCTGAAG | 55626 |
rs370200700 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418257 | TATAATATATATTTT[A/G]TTATTTATATATAAT | 55626 |
rs370203853 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426070 | GACTCCATCTCAAAA[A/T]AAAAAAAAAAAAAAA | 55626 |
rs370210352 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524933 | CTACCAATCTATGTG[C/G/T]TGGTCCATCCAACCG | 55626 |
rs370213779 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474338 | AGGTATATGATCAAT[A/C]CGAACAGGTCTATTC | 55626 |
rs370219601 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507105 | TGGCATGAACCTGGG[A/G]GGCGGAGCTTGCAGT | 55626 |
rs370223309 | in-del | -/AATT | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440546 | TCAATTTCAGATGAC[-/AATT]AAAGAAAGAAAGTGA | 55626 |
rs370242228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410567 | ACAAATCTCTAATAG[C/T]CTAAATGCCTGGAAT | 55626 |
rs370285082 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408056 | TGATAGGCCAGGCTG[C/T]AGCCAAAATGTCAAC | 55626 |
rs370320087 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404453 | GTGCCTCAGAGCAAG[C/G]CTCCTTGCCCTAGGA | 55626 |
rs370326350 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445854 | CTAGTTGCTAAGAGA[A/G]GGTAGAAAATAAATT | 55626 |
rs370326543 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515654 | GGTTTGCATTAGGTA[A/G]CTTCAGTTTTAATGA | 55626 |
rs370342164 | snp | C/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545172 | AAGCCGGGGGGGGGG[C/G/T]GGTGGTGGTGGGCAT | 55626 |
rs370409176 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493753 | GACTAAAGACTACCA[C/T]GAAACAGATACTAAC | 55626 |
rs370418476 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559771 | TAACTGATTTTTATC[A/G]CTGGCTTGTTATATA | 55626 |
rs370446035 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570098 | AAATCCTGTCGCTAC[C/T]AAAAATATAAAAAAA | 55626 |
rs370495397 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454532 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 55626 |
rs370513705 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491013 | TTACATGATCACAAG[A/T]AAGTTTAATAAAAAG | 55626 |
rs370519442 | snp | A/G | 3.21652e-05 | 0.00401018 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494115 | TGTTGCTAGCAACTC[A/G]GTTCTTACCTTGGGA | 55626 |
rs370575516 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532577 | AAATAGCTGGGACTA[A/C]AGGCACCCACCACCA | 55626 |
rs370609166 | in-del | -/GA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421139 | CGCCAATATGATAGA[-/GA]TGAACCCAGCTTAGG | 55626 |
rs370614262 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411191 | CTGGGGCGGCCTGAG[C/T]GGAGGAAGACAAACT | 55626 |
rs370631116 | snp | C/G/T | 9.92835e-05 | 0.00704499 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508180 | AGAAAGCAAGCTGAG[C/G/T]ATGTACTTACTCAAA | 55626 |
rs370651158 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418040 | GCATGGGATAAAGGA[C/T]GTTGAAAACTCTCTA | 55626 |
rs370668853 | snp | C/G/T | 3.34086e-05 | 0.00408698 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542941 | AGGCCCTGGTCCTGC[C/G/T]GCGTTGACGAGGCCT | 55626 |
rs370705896 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589824 | AGAAGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 55626 |
rs370705966 | snp | A/C | 1.6766e-05 | 0.00289529 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547118 | AAATACTCACGTGTA[A/C]ATCCCAAATCCTAAC | 55626 |
rs370716892 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409976 | CAGACTTCATGGGGC[A/G]GCATCCTTCTCCAGG | 55626 |
rs370745575 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436189 | ATCTACTGCAGTAAT[A/C]CAAAAAAAGTCAAGG | 55626 |
rs370782218 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557095 | GAGCAGAGATCGTGC[C/T]ATTGTACTCCAGCCT | 55626 |
rs370784769 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521872 | AAAAAATAGACATAC[A/T]ACAAAAAGACACCAC | 55626 |
rs370796261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582733 | AATAAGAGTACTTAC[A/G]TCATAAGGTTGTTAG | 55626 |
rs370811093 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578150 | AGGAGAACTAAAAAG[A/G]ACAATGTCCATATAA | 55626 |
rs370857114 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465527 | AGATTAAAAACTAGT[A/G]ACCTAAATATTTCAG | 55626 |
rs370884989 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474998 | GACATTATGTTCCCA[C/T]AGGATCAACCTGAGT | 55626 |
rs370888636 | snp | C/T | 0.000100271 | 0.00707992 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542943 | GCCCTGGTCCTGCTG[C/T]GTTGACGAGGCCTGC | 55626 |
rs370908342 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400798 | AGCCCCAGTCTTAGA[C/T]GATCTTCCTCAGCAT | 55626 |
rs370911278 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540070 | CTCCTGACCTTAAGT[A/G]GTCTGCCCGACTCAG | 55626 |
rs370934421 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558864 | AAGAGCATGAGTATG[C/T]GTATTTACTTATATT | 55626 |
rs370981235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465242 | CAATAAAGGCTCATG[C/T]TCCTCCCTGCCCTCC | 55626 |
rs370999448 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506546 | CTAGCCATTCAGTTA[A/T]GGAAGAAAGCTGAGG | 55626 |
rs371017810 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420152 | TCAGGTTTGAGGCAC[A/G]GCACTGACTGCCCTG | 55626 |
rs371042964 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485180 | TGACCTCAGGTGATC[C/T]GCCCGCCTTGGCCTC | 55626 |
rs371081938 | snp | A/G | 3.29881e-05 | 0.00406115 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548320 | GAGCTCCCATGGCCC[A/G]AGCACCCCGTTCTCG | 55626 |
rs371102155 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456239 | AAAAAAACCCCAAAC[A/G]CAAACATCTAGCATT | 55626 |
rs371104625 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523137 | ACCCCAAACAATCCA[C/T]TGTTAGCCCTTGAGC | 55626 |
rs371129735 | snp | A/C/G | 0.000361699 | 0.0134433 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493712 | AGCAAGAAACGCCTA[A/C/G]AAGAAGGAATCACAT | 55626 |
rs371215239 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498897 | CAGACAACAGAAGGC[C/G]TAGCTGGTATTCCTG | 55626 |
rs371220768 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456769 | CCTAAAATCTGCAAT[A/G]AAGGGAAATGGAAAT | 55626 |
rs371225226 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561850 | ACCTAGTTATTTAAA[C/T]CTGAGTAGAAGCTGG | 55626 |
rs371249875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497723 | TATACTACAAAAGGA[C/T]GAGTTCGACAGGAAG | 55626 |
rs371266546 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422711 | CAATAAAACTCAGAC[A/G]AGTAGTTCAAGCAGC | 55626 |
rs371270050 | in-del | -/TCTTTCT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516418 | AACCTCAAAGAAAGA[-/TCTTTCT]TTTTTTTTTTTTTTT | 55626 |
rs371294102 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486681 | GAGGCCAAGGTGGGC[A/G]GATGACCTGAGGTCA | 55626 |
rs371296509 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552134 | AGCACTTTGGAAGGC[C/T]GAGGCAGGCAGATCA | 55626 |
rs371309322 | in-del | -/CT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399929 | GGCTCAAATCTCAGC[-/CT]TGTCACTTGCTTGCT | 55626 |
rs371411237 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414311 | AAAGATGTGGTTTCC[A/G]TGGCAATTTTGGCTC | 55626 |
rs371421065 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478936 | GGACGCAGTGGCTCA[C/T]GCCAGTAATCCTAAC | 55626 |
rs371432446 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517559 | TACTAAACAGGCCGG[A/G]TGCAGTGGCTCACGC | 55626 |
rs371439180 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551747 | AAAGACAAAAATTAG[G/T]CCAGGTGCAGTGGCT | 55626 |
rs371441233 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579406 | AGGTTGTGGTGAGCC[A/G]AGATCACGCCATTGC | 55626 |
rs371494186 | snp | C/T | 5.15079e-05 | 0.00507457 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433455 | GCCATACAGTGAAGG[C/T]ACAAGCAATGGCACT | 55626 |
rs371496041 | snp | C/T | 3.29625e-05 | 0.00405958 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542614 | GGAAAACCCCTCCCT[C/T]CTGTGGCTGAAGTGT | 55626 |
rs371515045 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471569 | GGCAACAGAGTAATA[C/T]TCCTTTAAGAGTATT | 55626 |
rs371521715 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503940 | CTGGGCTCAAGCAAT[A/C]CTCTTGCTTCAACCT | 55626 |
rs371523816 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535775 | TATTCAATAGGAATG[C/G]GGTACCAAAAAGATA | 55626 |
rs371586805 | in-del | -/GCAGGGAAGG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427099 | AAGTTCAATTCAAGG[-/GCAGGGAAGG]AGAGAGTCATAATGA | 55626 |
rs371597594 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580170 | ATCCAACAATGTACA[C/G]TGATTACTCCCTTCC | 55626 |
rs371640113 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46591087 | ATTTCCTGCAGAAAC[A/G]TAATAAAATATTCCT | 55626 |
rs371659593 | in-del | -/AG | 0.00398722 | 0.0444715 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523891 | TATTTATTTTGAGAT[-/AG]AGTTTCGCTCTTGTT | 55626 |
rs371672704 | snp | A/G | 3.29843e-05 | 0.00406092 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46544021 | AGTAAGTAGTGTCCA[A/G]GTGGATCAAATCTCA | 55626 |
rs371687372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573911 | ATGAGTGAGAATATG[C/T]GGTGTTTGGTTTTTT | 55626 |
rs371705661 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499400 | CTTAACAAATATTCA[A/T]ATGTATTTTACTTGC | 55626 |
rs371710597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520864 | CCCGCCTCGGCCTCC[C/T]AAAGTGTTGGGATTA | 55626 |
rs371712829 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585924 | TATTCTCCTGCCTCA[C/G]CCTCCCGAGTAGCTG | 55626 |
rs371759806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494788 | ATGGTGAAGAATATT[A/G]GAAAACGTAATCCTA | 55626 |
rs371775634 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527057 | TCATTTAGAAAGACT[G/T]GCACTCTCTCCTATC | 55626 |
rs371776782 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512498 | TAGCACCACACTTGC[A/G]GAAATGAGTCCCAAA | 55626 |
rs371799005 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442862 | AGCCCTATGGGATTA[C/T]AGGTGCATGCCATCA | 55626 |
rs371813110 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501807 | TTAGATGCTTGGTGA[C/T]GTTTTTGTAGCCAGA | 55626 |
rs371844397 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482581 | AGGAACAAGGAGAAA[A/C]CCTTGTTCCCAATGG | 55626 |
rs371847168 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587238 | TACAAAAATTAGCCG[A/G]ACGTGGTGGCACACA | 55626 |
rs371851157 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443895 | TACATGGTCTGGTAG[A/G]CTCAACATCTAAAAG | 55626 |
rs371855137 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565316 | TTACTTCTGTTTTCC[C/T]TTTTTTTTAAATTAA | 55626 |
rs371877353 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547617 | AAGTTTTGATCCTCT[-/CA]GTTTCCTTTGCTTGT | 55626 |
rs371914852 | snp | G/T | 1.67761e-05 | 0.00289617 | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433618 | CAGGCTCACCGAAAT[G/T]GCATTGGGACCTGAG | 55626 |
rs371932809 | snp | C/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450986 | ATATGGGAACTGTCT[C/G]TATTTTCCACTCAAC | 55626 |
rs371938280 | snp | C/G | 1.827e-05 | 0.00302236 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397954 | CTCACCTGGCAGATA[C/G]AAAGCAGAAGAGAGA | 55626 |
rs371945158 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595179 | GGAGGTGGAGGCTGC[A/G]ATGAGCCATGATCAC | 55626 |
rs371949641 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488948 | GAGTCTTGCTCTGTC[A/G]CCCAAGTGCGGGGGC | 55626 |
rs371951737 | snp | A/G | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594160 | GCTCCTGTCTGAGGC[A/G]TAAATAAACAAACCC | 55626 |
rs371957379 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552947 | CCAAACCTCATCACT[C/T]ACTTTTTTTCTTTTT | 55626 |
rs371988729 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555454 | TAGGGTTGTTATGAG[A/G]CTCCAAATAAGAAAA | 55626 |
rs371998429 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469130 | CCTGCGTGACAACAG[C/G]GAAACTCCACCTCAA | 55626 |
rs372010309 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534361 | TTAGCCAGGCGTGGT[A/G]GCAGGCGCCTGTAAT | 55626 |
rs372075885 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408473 | CTCACTCGGTCTTAG[A/G]GTCCCTCTCCCACCC | 55626 |
rs372268716 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480902 | AGGGGTTTGGGGCAC[A/G]GCCTCTTAAAGAGGG | 55626 |
rs372279233 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480909 | TGGGGCACAGCCTCT[G/T]AAAGAGGGATCTCTA | 55626 |
rs372318397 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413312 | TGCCTCCCCATCCCA[A/G]TCCTTTCTGCTCCCC | 55626 |
rs372329991 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527861 | GCACTGTTGGTAGGA[C/T]TGTAAAATGGTTCAG | 55626 |
rs372331322 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441652 | AGGGTAAGCTAATAG[C/T]GTCTGAAGCACCACT | 55626 |
rs372340158 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509720 | CACTAATACATATAC[C/T]AAAATATGTTGCTGT | 55626 |
rs372414170 | in-del | AT/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494253 | TCACTAAGGAAGAAT[AT/C]ATCCACCAGCCCAAA | 55626 |
rs372458103 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502164 | GGCTCACTGCAATCT[C/T]CGCCTCCTAGGTTCA | 55626 |
rs372464770 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489051 | GGGACTACAGGCGCC[C/T]GCAACCGCCCGGTTA | 55626 |
rs372466818 | in-del | -/ATTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425308 | TCTTTTGCTTGATCC[-/ATTT]GTGTGTGTGTGTGTG | 55626 |
rs372469642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567694 | GACTTTTGCACTTCT[A/G]ATGACAAGATGACCC | 55626 |
rs372496804 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434166 | TAATAAATGCTAACC[A/G]TTGTTATCAACATTT | 55626 |
rs372634377 | snp | A/G | 1.65663e-05 | 0.002878 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543449 | CAAGGCAGTTAGGTA[A/G]AACCTCCAAGTAAAT | 55626 |
rs372642036 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417847 | AAAGACCCCAGTTGG[C/T]GAATACTGATTACCC | 55626 |
rs372708312 | snp | G/T | 3.32712e-05 | 0.00407854 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410403 | GGTAAAGAAGAAGGT[G/T]AAAGGCATTAGAGAG | 55626 |
rs372718912 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542015 | CCTGTGACACAGTTC[C/T]AGATCTGCTGGACTG | 55626 |
rs372725542 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413487 | TCTTAGCTTTCTTTC[C/T]TTCTTTCTCTATTTT | 55626 |
rs372885426 | snp | C/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594775 | AGCACAAATATGGAT[C/T]AATATGTACATCCTA | 55626 |
rs372916033 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577809 | TACAAAATGTGCCGG[G/T]CATCGTGGTGCATGC | 55626 |
rs372919095 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46443551 | GCCGGTAGGTAGTAT[C/T]GGCAATGTTACTGGC | 55626 |
rs372945300 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582017 | GCTACTTGGGAAGCC[A/G]AGGTGGGAGGATCCT | 55626 |
rs372965312 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433081 | CCCACAGAAAAAAAA[A/C]ATTTCATGGCATACT | 55626 |
rs372998425 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400685 | GCAGAGACGGTTTCG[C/T]CGTGTTGCCCAGGCT | 55626 |
rs372998797 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521396 | GACTGTAAATTGCCA[A/T]AAGAGACCCCCACAG | 55626 |
rs373020619 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416863 | TTCACACTCTCCACC[C/T]GGCTGAGGCTGGAAA | 55626 |
rs373032722 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445385 | TGTGCTGTCAGTGAG[C/T]CCACTGACCTCAAAT | 55626 |
rs373041461 | snp | A/C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514240 | AGGTATAGTCCTGTG[A/C/T]GGTCACTTTATTCCA | 55626 |
rs373046842 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481564 | GATAGGGTTTCTCCA[C/T]GTTGGTCAGGCTGGT | 55626 |
rs373090100 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453133 | AGCCCTAGGCAATCA[C/T]TAATTGCTTCTCCTG | 55626 |
rs373151442 | in-del | -/TTTTG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579727 | TTTTGTTTTGTTTTG[-/TTTTG]AGATGGATTCTTGTT | 55626 |
rs373169093 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472333 | TCACTGGAACATCTA[A/G]AGTTGGCAGTCCCAG | 55626 |
rs373223606 | snp | C/T | 5.42795e-05 | 0.0052093 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397432 | GTTCGAGGGGAGGCA[C/T]CAGTGCAACGTTTGT | 55626 |
rs373231503 | snp | C/T | 0.000495311 | 0.0157293 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417885 | CGGCCCCAGTGATCC[C/T]TCAACCCCCACACTT | 55626 |
rs373279928 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429183 | CGCACTGGCTTCATC[C/T]TCCCCCTCTCCCTCG | 55626 |
rs373280576 | snp | A/C/T | 0.000781183 | 0.0197494 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545560 | GAATGTTCTCTATCA[A/C/T]GTCAGTCCTGTGCCA | 55626 |
rs373293957 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497354 | GACTGAAGGTTACAC[A/G]AGGCACTATAAAAGA | 55626 |
rs373325160 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505352 | GCATTCAGTTTACTG[C/T]AGAGGGAGGTGGGCA | 55626 |
rs373330808 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569630 | GCAAAAATGCAAGGT[C/G]TGCCTGAGCATAGTG | 55626 |
rs373386086 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488257 | CATCAGGAGCTTAAG[A/C]CCAGCCTGGCCAATA | 55626 |
rs373392743 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482641 | TTTCCCTTGTTCCTT[A/T]GTACCCTGGACCAGT | 55626 |
rs373423843 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576913 | CTGTGCTTCAATTAT[C/T]CCATCAGTAAAATGC | 55626 |
rs373429644 | snp | A/G | 3.29565e-05 | 0.00405921 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542707 | GCACTGGTTCTGGGC[A/G]GGGGCATGGATTCCG | 55626 |
rs373463340 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571136 | GCTTCAATTCCGCTG[A/G]TATTCTATAAATGAC | 55626 |
rs373484455 | in-del | -/ATAATCCACCCACTTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519260 | ATCTCCTGGCCTCAT[-/ATAATCCACCCACTTT]GGCCTCCCAACATGC | 55626 |
rs373486110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549942 | TCCTGCCTCAGCCTC[C/T]GGAGTAGCTGGGATT | 55626 |
rs373491912 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531696 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTTAAA | 55626 |
rs373502308 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520716 | TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 55626 |
rs373518901 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409806 | TATCAACAACCCAGC[A/G]CTTTGTTCCAGTCTT | 55626 |
rs373531128 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437846 | AAGTAAAATATAGCC[A/G]AAGACACCGGCTATA | 55626 |
rs373535279 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506344 | ACATTTACATCTTTC[C/T]CAGACAAATAAACCT | 55626 |
rs373535301 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556402 | ACAGTAAACAACACA[C/T]TCCCGAAGGCAAACA | 55626 |
rs373537064 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580574 | GAATCATACTTGACA[A/C]CTTCTTCTTCCCACA | 55626 |
rs373549035 | in-del | -/CGAATAAGCACATTCACAGCATG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476543 | CTTATTCACAGCATG[-/CGAATAAGCACATTCACAGCATG]TGCTCCTAAACTGTC | 55626 |
rs373563903 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445071 | CAAAAAAAAGAAAAA[-/C]AAAAAAAAAAAAACA | 55626 |
rs373565996 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465542 | GACCTAAATATTTCA[A/G]GTAACTTTGGGGCTC | 55626 |
rs373583556 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559808 | GACAAATCATATCCT[C/T]GCTGAATTTCAAGTT | 55626 |
rs373590747 | snp | C/G | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542490 | CTGAAGCCGGTCATA[C/G]TCCAGAAAGAAGCGT | 55626 |
rs373600164 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458842 | CAAGGAATGTCACCA[C/T]TGGCCTTAGAAACTG | 55626 |
rs373603626 | snp | A/G | 0.000242807 | 0.0110156 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418091 | AAAAGAGAATGGGAG[A/G]AGAAACAATTTGTTA | 55626 |
rs373616230 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438831 | AAAGCAATTTCAAAA[C/T]TATTTATGCATGAGG | 55626 |
rs373646906 | snp | A/C | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595885 | AGCTACTCGGGACTA[A/C]AAAAAAAAAAAAAAA | 55626 |
rs373689052 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454976 | CCTCAACCTTCTGGG[C/T]TCAAGTGATTCTCCT | 55626 |
rs373712599 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491229 | AAGAAAAAGAATGAC[A/C]TTTTAATGTTTTGTC | 55626 |
rs373752274 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557830 | AAACAAACATAGCCC[A/G]GCATGGTGATGCATG | 55626 |
rs373758426 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428589 | CTTCTTCTTCTTCTT[C/T]TTCTTTTTTTTTTAA | 55626 |
rs373766435 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583590 | TGGGAGAAAATTTTC[A/G]CAACCTACTCATCTG | 55626 |
rs373805812 | snp | C/G | 3.47536e-05 | 0.0041684 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433640 | GGACCTGAGGGCCAA[C/G]AAAACAGAGAAATAT | 55626 |
rs373882287 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562147 | CCTGGGGTGGCCAGA[A/G]AAAGCCTCTCTGAGA | 55626 |
rs373894964 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563785 | GACGGTAGTTGCAGT[A/G]AGCCAAGATCACACC | 55626 |
rs373897378 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431331 | AGCTCCAGTCACCAA[C/G]CATGCAGCTGCTGGC | 55626 |
rs373905132 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541388 | GTATCTCTGAAAAAA[A/T]TGGAATTTTTCTTGA | 55626 |
rs373931417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590051 | AGTTTCCTAACACAT[A/G]TTGAAAATATTGTGA | 55626 |
rs373934857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567641 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC | 55626 |
rs373948026 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525363 | TTGGGAGGTCAAGGC[A/G]GGTGGATCACCTGAG | 55626 |
rs373970515 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475864 | AAGAAGGCAAAGAAA[A/G]CAGGCAGCTTCAAAT | 55626 |
rs374000194 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489388 | TGACCTCATGATCCA[C/T]CTGCCTCGGCCTCCC | 55626 |
rs374008826 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404978 | GTCACCTTCAGGCTG[-/A]AGGCCTCACTCCCAG | 55626 |
rs374027659 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571175 | ATTCTTATGCCTGGG[C/T]AAAAGGTCCCCAGTG | 55626 |
rs374034791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468680 | AGCCGGGTGTGGTGG[C/T]GGGCGCCTGTAGTCC | 55626 |
rs374048994 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500165 | CTGTCAGGCTGTGGG[A/G]CCAGCAGGCATTGAC | 55626 |
rs374058086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533632 | TGGTTCTCAACACAG[A/T]CTCAAGACACAAATC | 55626 |
rs374067398 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593350 | CAGTTTACCCACCCA[C/G]AAAAAGGCGAGAACA | 55626 |
rs374078838 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404673 | CTCCCGCTGACCAGA[A/G]CCTCAGCTTAGCTGG | 55626 |
rs374080626 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560109 | ACCTGACAAATTGAA[A/G]ACAAATAATTCAACA | 55626 |
rs374086952 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516498 | TGCAGTGGCACGATC[C/T]CGGCTCACTGCAAGC | 55626 |
rs374092166 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518536 | GGTAAACTACAGGCC[C/T]CAGGTCAGCTGTCTT | 55626 |
rs374098590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423826 | TAGAGTGCAGTGGCA[C/T]GATATCAGCTCACCA | 55626 |
rs374116919 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474556 | ACCACGCCTGGCTGA[C/T]TTCGTATTTTTAGTA | 55626 |
rs374131837 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532588 | ACTACAGGCACCCAC[A/C]ACCATGCCCAGCTAA | 55626 |
rs374162754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524963 | GGTGATTCAAACAAA[C/T]ACTGAGTGCCTTCTG | 55626 |
rs374249850 | snp | C/G | 5.34278e-05 | 0.00516827 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433427 | TCATTACCCTTCCAA[C/G]CCTAGGGGAGCTGCC | 55626 |
rs374268276 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564936 | AATAAGTTATGTGCA[C/T]CAAGAATGTAGAGTG | 55626 |
rs374284299 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507781 | CAAGTATTTCAGAAC[A/G]AAGACAACATCTCCA | 55626 |
rs374289799 | snp | A/C/G | 0.000104789 | 0.00723771 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397600 | GACAGGGGAGGAAGA[A/C/G]GGCAGGGTTGGCTGG | 55626 |
rs374335602 | snp | C/T | 0.000116018 | 0.00761548 | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548426 | CAGGAAATGAAGGAG[C/T]AAGTAACAGCTCCAA | 55626 |
rs374387714 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397755 | TGTGGGCGGCACCAG[C/G]TTCAGTGCCCGTCTG | 55626 |
rs374390115 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567922 | AGAGGCCGAGGCAGG[C/T]GGATCACTTGACATC | 55626 |
rs374464407 | snp | C/T | 0.000629817 | 0.0177345 | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548383 | GGACAACCTTCATGG[C/T]GCTCAGTAGCCACTG | 55626 |
rs374478868 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584592 | CACACTCTGCTATAA[C/T]CACTAGAAAGAATTT | 55626 |
rs374479542 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478671 | TTTTTTTTTTTTTTT[G/T]GAGATGGAGTTTCGC | 55626 |
rs374509648 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403937 | GCATGTGGCGGCTCA[A/C]GCCTATAATCCCAGT | 55626 |
rs374512755 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591652 | ACGAGGTCAGGGGTT[C/T]AAGACCAGCCTGGCC | 55626 |
rs374517793 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551899 | CAGGCGTGGTGGCAG[C/G]CACCAGTAATCCCAG | 55626 |
rs374520924 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431103 | CTGGAAAACCAGAAA[C/G]CTTTCTGTAGCATGG | 55626 |
rs374522097 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499496 | TTTAAGCAATAAATC[A/G]AAGTCCTCAGTAAGA | 55626 |
rs374534180 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532074 | CAGTGAGCTGAGATC[A/G]GGCCACTGCACTCTA | 55626 |
rs374623134 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483032 | AAGAAAAAAAAAAAA[-/A]GAGTAAAAACCATGA | 55626 |
rs374635899 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524006 | CCCACGTAGCTGGGA[C/T]TACAGGGATGCACCA | 55626 |
rs374652271 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399138 | GGAGTGCAATGATGC[A/G]ATCTCAGCTCACTGC | 55626 |
rs374707063 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558614 | TATCTAGCTGACAAA[-/T]TATCAAGAATTTTCT | 55626 |
rs374715898 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456739 | TTGCTGCAAAGAGGA[A/T]GCAGATTTCAAAAGC | 55626 |
rs374736699 | snp | A/C/G | 0.000593594 | 0.0172178 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541935 | AGAAGATAGGAAAGC[A/C/G]ACTGCTTACCTCCTG | 55626 |
rs374739492 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508418 | AGCACTAATGTGGGG[A/G]ATACTATGAAAGGCA | 55626 |
rs374788441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443321 | GGTATGGTTGATATC[C/T]GGTTAATGGACCTGA | 55626 |
rs374899572 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494925 | CAAAGGTTATTGATA[A/T]GTTATCCCATTTAAT | 55626 |
rs374901824 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460601 | GTGCTGGCATTACAG[A/G]CGTGAGCCACCGCGT | 55626 |
rs374902813 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472818 | ACTGAGTCACTGAGC[A/G]GAGCTGTTCTCCCTG | 55626 |
rs374911385 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560644 | AGTGTGCTGAGAACA[C/T]AAGAACTCCTAAAAA | 55626 |
rs374922085 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485089 | ATTACAGGCACCTGC[C/T]ACCACGCCCGGCTAA | 55626 |
rs374978681 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568308 | CTAAAAATACAAAAA[-/A]TTAGCCGGGAGTGGT | 55626 |
rs374984058 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450674 | TCTCCAACTCCTGAA[C/T]TCAAGAGATCCACCT | 55626 |
rs375020123 | snp | C/T | 4.96833e-05 | 0.00498389 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544076 | AGACAAAGACACACA[C/T]AGAGAGATTATGTTA | 55626 |
rs375025155 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418351 | TTTATTATTTATATA[A/T]ATATATATTTTATTA | 55626 |
rs375078081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451340 | CTAGGGATAAAATCA[C/T]AATAATCATCACAGT | 55626 |
rs375079158 | in-del | -/TGAT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491533 | AGAGAAGAAAACAAA[-/TGAT]ACAACTGCCAATAGA | 55626 |
rs375091868 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562297 | AGCGCATGTGAAGGC[C/T]GGAAATAAGGCCAAC | 55626 |
rs375093036 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410840 | GGCGCCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55626 |
rs375104316 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579774 | CTGGAGTGCAGTGAC[A/T]TGATATCAGCTCACT | 55626 |
rs375107127 | snp | G/T | 1.88131e-05 | 0.00306695 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434833 | CTGTCATTAGGTTGG[G/T]CTTCCTATCCCTTAC | 55626 |
rs375149264 | snp | C/T | 5.48211e-05 | 0.00523522 | intron-variant, synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543240 | ATCTTGCACTGTGCT[C/T]TGCTCTCCCACCTGG | 55626 |
rs375152769 | snp | C/T | 3.31131e-05 | 0.00406884 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543281 | AGCGGGAGGACAGCA[C/T]GTGCAGGAAATTGTG | 55626 |
rs375214917 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481168 | ACTGATAAGAGCAGC[A/G]CGGTGCAATTACACC | 55626 |
rs375218074 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546839 | ACTTTGGGAGGCCGA[A/G]GCAGGCAGACCACTT | 55626 |
rs375228913 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556367 | ACAGAGAATGTGGGG[A/G]AAAACATCATAAATT | 55626 |
rs375237098 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424572 | ATTATACTCGCTGGG[C/T]GTGATGGCTCCTGCC | 55626 |
rs375254461 | in-del | -/CA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540891 | CCACAGTGCCTAGCA[-/CA]GTGTTAGAAAATTTG | 55626 |
rs375268432 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580271 | GGTCTTCTCCTCCTA[C/T]TCTATACTTGTTCTC | 55626 |
rs375321882 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518026 | ATGGGAATCCTCTAT[A/G]CGTTTTCTGCAAGTT | 55626 |
rs375323283 | in-del | -/GAC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401261 | TCAGCTCTTTTCGAG[-/GAC]ACAGAGTCTCGCTCT | 55626 |
rs375334640 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471778 | GACTACAGGCACGCG[G/T]CACCATGCCCAGCTA | 55626 |
rs375346909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534719 | CACTCTGTTGCCCAG[A/G]CTGCAGTGCAGAGGC | 55626 |
rs375352143 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418995 | GGAGGTGATAGGGGG[A/G]CGGGAGGGGGTGATA | 55626 |
rs375369842 | snp | A/C | 0.021333 | 0.101051 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446267 | TACTGTTACCAGGTT[A/C]TTTTCTTCAAGAACT | 55626 |
rs375373111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456222 | AAGGAAAAATGGGGG[A/G]AAAAAAAACCCCAAA | 55626 |
rs375435986 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493730 | GAAGGAATCACATGT[C/G]AAAAGCTGACTAAAG | 55626 |
rs375443026 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575432 | ATTGCACTCTAGCCT[C/G]GGCAACAAGAGCAAA | 55626 |
rs375474419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587304 | AGAATCGCTTGAACC[A/C]GGGAGGTGGAGGCTG | 55626 |
rs375493009 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550982 | GGAGACTGTAGTCCC[A/T]GCTACTCAGGAGGCT | 55626 |
rs375505244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579161 | ACATAGCAAATTTTA[A/G]AAGTACATAAAAAGG | 55626 |
rs375552551 | snp | A/C | 2.23481e-05 | 0.00334269 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408477 | CTCGGTCTTAGGGTC[A/C]CTCTCCCACCCCCTC | 55626 |
rs375558035 | snp | A/G | 0.000115862 | 0.00761037 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542235 | AGAGGAACTAGCCTC[A/G]CCAGAGGAGTAGTTA | 55626 |
rs375574290 | snp | A/G | 1.7117e-05 | 0.00292544 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433633 | GGCATTGGGACCTGA[A/G]GGCCAACAAAACAGA | 55626 |
rs375574414 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559444 | CTAATCCATCACTAC[C/T]TCAACTATAAGTAGG | 55626 |
rs375670328 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571987 | GCCACTGCGCCCTGC[A/C]CAATCAATCAATATC | 55626 |
rs375708123 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412622 | TTCACTGTTTTTTTT[A/T]CCCCAAAATGTTTTT | 55626 |
rs375730870 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414792 | ATGGCTTTGTAGAGG[C/G]GCTGACTGGCCAGTT | 55626 |
rs375752162 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556839 | AATGAAGAATTAGTA[C/T]GAAAATGGTAATAAG | 55626 |
rs375775001 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566439 | AAAAAAAAAGAGTGG[A/C]GCTATTGATAATATA | 55626 |
rs375775082 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528204 | TGGAGATGGAGTGTC[A/G]CTTTGTCACCCAGGT | 55626 |
rs375775094 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591751 | TCCCAGCTACTCAGG[A/G]GGCTGAGGCAGAGAA | 55626 |
rs375782200 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441228 | GTTATTAAAAGATAA[A/G]CTGGGCCGGGCACGG | 55626 |
rs375784286 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46493610 | AACATTTCCTTACCT[C/G]CCAGGACCCTGTTAA | 55626 |
rs375792318 | snp | C/T | 1.65603e-05 | 0.00287747 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397806 | GGCTGACGATGATGT[C/T]GTTGCCGAAGCCGCC | 55626 |
rs375805810 | snp | A/C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489535 | TCTTGCTCAAGACAC[A/C/T]GGACCAGGCCGTAAT | 55626 |
rs375810743 | in-del | -/GG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546792 | ATACCAAAAGAAGCC[-/GG]GGGCATGGTGGCTCA | 55626 |
rs375823976 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464878 | GGTGAAACCCCGTCT[C/G]TACTAAAAATACAAA | 55626 |
rs375835873 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428082 | CCTGTTTAGGGTGAG[C/G]GGGAGGCATATTGCT | 55626 |
rs375868004 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587534 | TGAAGACTGAAGACT[C/T]AGATGGCAGCAAGGA | 55626 |
rs375911943 | snp | C/T | 0.00286018 | 0.0377082 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397691 | CGCTCTGCCAGTTGC[C/T]CGGCCTCTGGGAGCA | 55626 |
rs375922653 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528401 | GTCTCGAACACCTGA[C/T]CTCAAGTGCTCTGCC | 55626 |
rs375952910 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550861 | GGAGGCCGAGACGGG[C/T]GGATCGCGAGGTCAG | 55626 |
rs375975707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507283 | AGGAGATCAAGACCA[C/T]CCTGGCTAACATGGT | 55626 |
rs375977019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589392 | CTGAAAGCTCTCTCT[C/G]AGTTTATGAGGAACA | 55626 |
rs375994932 | in-del | -/AC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486946 | AATAAATAAATAAAT[-/AC]AAATAAATACAAATA | 55626 |
rs376008193 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574502 | TCCTTCGCCCACTTT[C/T]TGATGGGGTTGTTTG | 55626 |
rs376026098 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478008 | GTGAAGAAGCACAGG[G/T]TAGTTTACTGGTGAA | 55626 |
rs376063036 | in-del | -/CAAC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583680 | AAAAAAAAAAAAAAA[-/CAAC]AAAACAACCCCATCA | 55626 |
rs376138719 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504310 | TGTAGGCCTTAGCAA[A/C]TACGGGCCATAGCAC | 55626 |
rs376142258 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539207 | TCTCTTCGTTTTTAT[A/G]TATGTTTGAAGATTT | 55626 |
rs376172728 | snp | C/G | 3.50085e-05 | 0.00418366 | intron-variant, synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543015 | AGGGGTAGTAGCTCT[C/G]GCAGAAGCAGGGGGG | 55626 |
rs376172943 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441684 | TACTATGTATTCGAC[A/G]GCTCACATCTAGAGT | 55626 |
rs376188754 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510843 | GAGGAAAAAGAAACT[A/G]AACAACCAGCAATGA | 55626 |
rs376190464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477847 | TTGGGAGGCTGAGAC[A/G]GGCAGATCGCTTGAG | 55626 |
rs376197572 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583946 | TAAACTAGTTCAACC[A/G]TTGTGGAAGTCAGTG | 55626 |
rs376197996 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434648 | CGTAACAGGGGCATG[C/T]GGTAGGACTCTAATG | 55626 |
rs376203986 | snp | C/T | 8.35708e-05 | 0.00646362 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46493612 | CATTTCCTTACCTGC[C/T]AGGACCCTGTTAACA | 55626 |
rs376215684 | snp | C/T | 0.000735204 | 0.0191588 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543175 | GCGGAAGTCCTGGGG[C/T]GCTCCGTGGAGGGCT | 55626 |
rs376218287 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573737 | TAGTTACATATGTAT[A/G]CATGTGCCATGCTGG | 55626 |
rs376256898 | in-del | -/C | 0.0017001 | 0.029106 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547884 | CTACTCTCTGGGAGA[-/C]AAAAAAAAAAAAAAA | 55626 |
rs376262629 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577219 | CCCAAATGTTCTTCA[A/G]TGGATGAATGGATAA | 55626 |
rs376263821 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419996 | CACGTGTCCTCAATA[-/C]ACACACACACACACA | 55626 |
rs376271468 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46417919 | GCCACTTACTCTGGT[C/T]GGCAGATCACCAGGT | 55626 |
rs376275885 | snp | C/G | 2.88488e-05 | 0.00379784 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547912 | AAAGTTAAAATACAT[C/G]ATTTGTAGACCATGG | 55626 |
rs376283962 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413404 | ACAATGAGCTCATGG[A/G]TTTGGTTTCAATTCC | 55626 |
rs376305643 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409326 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 55626 |
rs376313985 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435789 | TGGTAAGGTGGCAAG[A/T]TCTGAGGGTGGAGGA | 55626 |
rs376328588 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445733 | ACACCCTCCTTTGAC[C/T]ACTAGTCTCTCAAAT | 55626 |
rs376339329 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423548 | AGGCGCCTGCCACCA[C/T]GCCCGGCTAGTTTTT | 55626 |
rs376356071 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414255 | CTGGTGTCTCTGCAG[C/T]GCGGGAAAGAGCCAG | 55626 |
rs376362160 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506878 | GCAATAAGATTGGCT[A/G]GCTTAGGCTGGGCGT | 55626 |
rs376371225 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571233 | ATGACAGAAGTTTGC[A/C]AGCTCAAGTCAGCAC | 55626 |
rs376388429 | in-del | -/AATAC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516293 | GTTCTTCATAGTTAC[-/AATAC]GAGTACTATCTGGAG | 55626 |
rs376440249 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481605 | CGACTTCAGGTGATC[A/G]GCCTGCCTCGGCCTC | 55626 |
rs376440291 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403701 | CATGCAAAAAAGCTG[A/G]CGCGTGCAAATACCC | 55626 |
rs376449730 | snp | A/G | 1.67747e-05 | 0.00289605 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545585 | GTGCCAGACAATGCA[A/G]ATGGGGCAGCGCACT | 55626 |
rs376461092 | in-del | -/CT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590567 | GTGATATACATAACT[-/CT]GTTCCAGCTTAAGTT | 55626 |
rs376477879 | snp | A/C | 1.80863e-05 | 0.00300713 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397448 | CAGTGCAACGTTTGT[A/C]TCTACCTGTTCCGTG | 55626 |
rs376528949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474891 | AAAAAGCAAGATAGT[C/T]GAAAGAGAAAGAACA | 55626 |
rs376539830 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582517 | GGACATCTATTTTTC[A/C]ACTCTAGTCTCACTA | 55626 |
rs376621837 | snp | A/G | 1.72113e-05 | 0.00293348 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547088 | AGAACACCAAAAGAA[A/G]AGGGTATCTTAAGGA | 55626 |
rs376636604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432231 | CAAGTACTGACATGA[C/G]AATGTGTAAGAGGTA | 55626 |
rs376646331 | in-del | -/GGTA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486230 | TCTGCCTGGCTACTG[-/GGTA]GGTACCAGATGGGTA | 55626 |
rs376649753 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580816 | GTTGTTTTGGAGACA[C/G]AGCCTTGCTCTGTCA | 55626 |
rs376652783 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512858 | CCCTGTCAATTACCA[A/G]CTCAGAGGTCATTCA | 55626 |
rs376655048 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524262 | TGGAATGCCCCCCAG[A/G]AATGTGGCAATGTCT | 55626 |
rs376679597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464995 | GTTGCAGTGAGCTGC[A/G]ATCGCGCCACCGCAC | 55626 |
rs376689965 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520788 | TTTTTTTTTTTTTTA[G/T]TAGAGACGGGGTTTC | 55626 |
rs376691998 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573934 | GGTTTTTTGTTCTTG[C/T]GATAGTTTACTGAGA | 55626 |
rs376701333 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529456 | GTGGGGTGGTGGTGC[A/G]GGTACTGCAATGACC | 55626 |
rs376719558 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590866 | TGCAGTGAACTGAGA[C/T]CGTGCCACTGCACTC | 55626 |
rs376733491 | in-del | -/CGGGGGCTGACACCTACAG | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436405 | GCTATTGTGCCAACT[-/CGGGGGCTGACACCTACAG]CACCATTACACATAA | 55626 |
rs376735100 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561252 | TGGGCGTGGTGTCAC[A/G]CGCCTGTAATCCCAG | 55626 |
rs376788694 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495818 | ATTGAATTCATGATA[A/G]CTTTTCATTATCGTA | 55626 |
rs376839489 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505523 | AAAGAAAGGCAAACA[C/T]CCCAGAAGGGACTTT | 55626 |
rs376850157 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569898 | CCCAGAAGGCGGAGG[C/T]TGCAGTGAGCCAAGA | 55626 |
rs376940915 | in-del | -/GG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545162 | AAAAAAAAAAAAGCC[-/GG]GGGGGGGGGGGTGGT | 55626 |
rs376985111 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531752 | CCTCCTTCACTCTAT[A/C]CTCATTCCCATATTG | 55626 |
rs377046241 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549857 | AGAGTCTCACTCTGT[A/G]GCCCCAGTTGGAGTG | 55626 |
rs377069728 | snp | C/T | 0.000150371 | 0.00866966 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46435032 | GCACCAGCACATTCA[C/T]GGAAGCTGCATCAGA | 55626 |
rs377082551 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418233 | TTTTATTATTTATAT[A/G]TAAATATATATAATA | 55626 |
rs377122079 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516837 | ACATTCTGCTGTGAC[C/T]ACCACAAACTTGACT | 55626 |
rs377153459 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465488 | TTTTTACCATATTTT[C/G]TCAGAGAGTTCACTG | 55626 |
rs377181876 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440586 | AACAAAACAAAATAA[C/G/T]TTTAAATAAATTATG | 55626 |
rs377194979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507942 | AGCCACCATCCTCTC[A/G]CAATCTGGCCTGGGG | 55626 |
rs377208384 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471020 | GAAAATGTTGCATGG[A/C/T]GATTTCTGATAGGGT | 55626 |
rs377209167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535498 | CAAATTTAATGAATG[C/T]CTTCCACAGAAACTT | 55626 |
rs377215311 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568260 | GTCAAGAGTGCAAGA[C/G]CAGCCTGGCCAACGT | 55626 |
rs377235227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406215 | CCCACCACCATGCCC[A/G]GCTAATTTTTGTGTT | 55626 |
rs377239407 | in-del | -/TGGGTACTAGTC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519371 | GAGGTGCAGAAAGTC[-/TGGGTACTAGTC]CATATGGAATAAACA | 55626 |
rs377257005 | snp | A/G | 3.30077e-05 | 0.00406236 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548302 | GCTCCTGCAGAAGCC[A/G]CTGAGCTCCCATGGC | 55626 |
rs377259278 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590139 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC | 55626 |
rs377292527 | snp | A/G | 7.29395e-05 | 0.00603858 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408532 | ACCAGGACCTGAGGC[A/G]GCTGTCCCTGGCTCC | 55626 |
rs377330437 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445071 | CAAAAAAAAGAAAAA[A/C]AAAAAAAAAAAAACA | 55626 |
rs377334045 | snp | A/T | 1.65674e-05 | 0.00287809 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542869 | AGACTGAGGTTGCGG[A/T]GCGTGTTGCCGGCAG | 55626 |
rs377349516 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509910 | AGAAACAGGAATAGT[C/T]ATATCCAAATGGTAC | 55626 |
rs377414027 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536765 | TTCAGACTGTTCTAA[A/G]CTCCAAAGCAATTCC | 55626 |
rs377430582 | snp | C/T | 0.000149919 | 0.00865661 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397692 | GCTCTGCCAGTTGCC[C/T]GGCCTCTGGGAGCAG | 55626 |
rs377436639 | snp | C/T | 6.5912e-05 | 0.00574035 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545683 | AGAAGTGGATCTCAT[C/T]GGCAGTGGCAATCAG | 55626 |
rs377447735 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418326 | TTATTATTTATATAT[-/A]AATATGTATTTTATT | 55626 |
rs377471088 | snp | C/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452862 | CTCATTTATGATTCT[C/G]ACATTGAGAAAAATG | 55626 |
rs377496805 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531135 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 55626 |
rs377503864 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485098 | ACCTGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 55626 |
rs377512695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498857 | ATTTTTGTTTCCCTA[C/T]GCTGCTCTGTTTCTA | 55626 |
rs377517877 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564975 | CTACAAATAAATCAT[A/G]GCCAGGTGCAAAGGC | 55626 |
rs377532521 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419442 | ACACATACATTCAAA[C/T]AATTTGGGAGATTAA | 55626 |
rs377534311 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498471 | ATTTGGGAAGGAGTA[G/T]GGGGAAAAATACTTT | 55626 |
rs377566518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490867 | TGTCTGCTAAATGTA[A/G]TTGTTCTGGGACCAT | 55626 |
rs377670476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558597 | CTACCTAGTATCTAC[G/T]AATATCTAGCTGACA | 55626 |
rs377685001 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491541 | AAACAAATGATACAA[C/T]TGCCAATAGAATCTG | 55626 |
rs386753211 | multinucleotide-polymorphism | CA/TG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435929 | CACCGTGTGATTCCC[CA/TG]CCAGGAAGAAGTGGC | 55626 |
rs386753212 | multinucleotide-polymorphism | CCA/TCC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500754 | TCGCTATACCCATCA[CCA/TCC]ATATCAATTCCTCTC | 55626 |
rs386753213 | multinucleotide-polymorphism | AA/GG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514891 | GAGATACAGAGTCTG[AA/GG]AAAAAAGGAAAATCA | 55626 |
rs386753214 | multinucleotide-polymorphism | AAC/TAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543968 | TGGAACTGCTGGACT[AAC/TAA]TTACCTGTTGATTAG | 55626 |
rs397729057 | in-del | -/TTTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551314 | GTTTGTGGGGACTTT[-/TTTT]ATTTTTATTTTTTAA | 55626 |
rs397753464 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559309 | TCTCAAAAAAAAAAA[-/A]GAAAGAAAAGAAAAG | 55626 |
rs397767525 | in-del | -/CT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399930 | GCTCAAATCTCAGCT[-/CT]GTCACTTGCTTGCTG | 55626 |
rs397841537 | in-del | -/A | | | intron-variant, frameshift-variant | AMBRA1 | GRCh38.p7 | 11:46431084 | CGTAAGGGGCAACCA[-/A]GACCTGGAAAACCAG | 55626 |
rs397847968 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460339 | CTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 55626 |
rs397848852 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526743 | ACACACAAAAAAAAA[-/A]CCATGAAAAATAACT | 55626 |
rs397849176 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503063 | GAGACTCTGTCTCAA[-/A]AAAAAAAAAAAAAAA | 55626 |
rs397955311 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507197 | AAAAAAAAAAAAAAA[-/A]GGCTTGGCACGGTGG | 55626 |
rs398015946 | in-del | -/A | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466936 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAGA | 55626 |
rs398015947 | in-del | -/A | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478670 | CGAAACTCCATCTCC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs398045181 | in-del | -/A | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457922 | AAAAAAAAAAAAAAA[-/A]GACATTCCACCCTAC | 55626 |
rs527254335 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429302 | GAGAGAGGCCCCCTG[C/T]CCGCATCCTGGGGAG | 55626 |
rs527259976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437697 | TTTGATGAGTTAATT[C/T]ATACAGGAAGAGATT | 55626 |
rs527274363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541040 | AATTTCAGTTGCTTC[A/G]ACAGAGGATGTAATG | 55626 |
rs527297158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533589 | TAAGGCCTCTCTTAT[C/T]TTGACAGAACAAGTC | 55626 |
rs527309028 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464415 | AATTCACTATGCACC[A/T]TCCTGAGATGGTCTA | 55626 |
rs527312141 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424477 | ATTAGGATCAAAGCA[C/G]AGAGATTACTTCAGC | 55626 |
rs527350356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534409 | CTGAGGCAAAAGAAT[A/C]ACTTGAACCCGGGAG | 55626 |
rs527375520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579504 | TAAAAAGTAGATAAA[A/C]CCTTAAGGCCAACAT | 55626 |
rs527389893 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478757 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 55626 |
rs527440983 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460191 | GACAACAAGACATAC[A/G]AATGACTATTAGAAT | 55626 |
rs527461497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452332 | CTTTGTTATTTTAAG[A/G]TTTTTTGTTGTTGTT | 55626 |
rs527477753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508964 | TTTTCTCTCCCTTAA[C/G]AATTAGTCATAGATA | 55626 |
rs527500096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444943 | GTCTCATTTTCAATT[G/T]GTAAGGAAAAGTACA | 55626 |
rs527501073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557245 | CACAGAGGTTGCAGT[A/G]AGCCGAGATCACGCC | 55626 |
rs527501787 | snp | A/G | 3.31526e-05 | 0.00407127 | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548384 | GACAACCTTCATGGC[A/G]CTCAGTAGCCACTGT | 55626 |
rs527507420 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413394 | GAGCTGGACTACAAT[A/G]AGCTCATGGATTTGG | 55626 |
rs527520262 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399262 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 55626 |
rs527538702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500627 | ATATCTCTCTCATAT[C/T]ACAAACACTCCATAG | 55626 |
rs527541241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492226 | GGCCAGAGCCTATGA[A/G]GTCCTGGTGTCTGAC | 55626 |
rs527603459 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577206 | AAGGCAGAAACAGCC[C/T]AAATGTTCTTCAATG | 55626 |
rs527604694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492843 | TCACGAAGTGAGGAG[A/T]TTGAGATCATCCTGG | 55626 |
rs527604770 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484686 | GAGTCTCACTCTGTC[A/G/T]CCCAGGCTGGAGTGC | 55626 |
rs527612227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513127 | AATAGAAGGTTCGGA[C/T]CAACACAGGAGTGAA | 55626 |
rs527650616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468209 | ATGCAGCAAGCAGTG[C/T]GTGGTGGGACCAATC | 55626 |
rs527668060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524157 | ACAGGTGTGAGCCAC[C/T]GCACCCGGCCTAATG | 55626 |
rs527675436 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421941 | CTGGTCTTCATGTAC[A/C]GACACCCTAAAAACA | 55626 |
rs527729752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524935 | ACCAATCTATGTGTT[A/G]GTCCATCCAACCGGT | 55626 |
rs527734291 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523235 | TGACATTTGATTTCA[C/T]TGATTCGCCTCTGGG | 55626 |
rs527739812 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508110 | CAAGAACATCCACCA[C/T]TGTAGCTCCAACAGT | 55626 |
rs527747705 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414749 | CAGTGCCAGGAAGGG[C/T]GGGATGACTGCGCTA | 55626 |
rs527749456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405878 | CTGGGACTACAGATG[C/T]GTGCCACCATGCTCG | 55626 |
rs527755794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517084 | CATTGGACAGCAAGG[C/G]GGAAATATTACAACT | 55626 |
rs527759424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414414 | GGGACAGAGCTGGGG[C/T]CTTGTCAGGAGCCCC | 55626 |
rs527766689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571633 | TAAGCCATGGTTTGT[A/G]TCACTGCACTCTAGC | 55626 |
rs527767331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564044 | AACTACTTGGGAGGC[C/T]GAGGCAGGAGAATCG | 55626 |
rs527799147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406908 | AAAACAGGCCAGGCA[C/T]GGTGGCTCACGCCTT | 55626 |
rs527812925 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46451156 | TTGAGGCTTAGAGCA[A/G]AAGAAGAAATAAAGA | 55626 |
rs527830979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564856 | ACAGATCATCAGATG[A/C]GACAAGGAAAACTAT | 55626 |
rs527856887 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532285 | GTTTTTCTCATACAA[C/G]GGTGTCAGAGAACAA | 55626 |
rs527859707 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435252 | AGCAGGAAACTATAG[A/G]ATAGTCAACACCACC | 55626 |
rs527876195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547499 | ACACTGTCCCCAAAT[C/G]ACACATGCCACATTC | 55626 |
rs527881249 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538689 | TTTTAATAGAGACGC[A/G]GTTTTACCATGTTAG | 55626 |
rs527894629 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428465 | GGTGTCCTTAGTCAT[C/T]CCTTCTGCCAATAAA | 55626 |
rs527895334 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595496 | GAGCAGAGATCGTGC[C/T]ACTGCACTCCAGCCT | 55626 |
rs527896075 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534661 | AGCAGTCCTTGTGCA[C/T]ACTCCTCAGTTCCCT | 55626 |
rs527913093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585735 | ATATTCCTAGCTTCC[C/T]AAATTGCTGGGTTTA | 55626 |
rs527924700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491400 | ACCTATCTCATATGA[C/T]TACTGCAAGACAGAA | 55626 |
rs527939159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421125 | ACAAAACCCTCAAGA[C/T]GCCAATATGATAGAT | 55626 |
rs527973932 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586741 | ATGGTATTTTACAGA[C/T]GAGGAGAGGCACAGA | 55626 |
rs527987183 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475855 | TTCACAAGAAAGAAG[A/G]CAAAGAAAGCAGGCA | 55626 |
rs528039564 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464412 | AATAATTCACTATGC[A/G]CCTTCCTGAGATGGT | 55626 |
rs528049335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472792 | TATCTGGTGGCCTTC[A/G]GAACTATGTCACTGA | 55626 |
rs528078297 | snp | A/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46417943 | ACCAGGTCTCCTTTG[A/T]TAGTACCATAGGCCA | 55626 |
rs528117239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410453 | AAACTCCTGGCTTTG[C/T]GGACTGTGGCTGCCC | 55626 |
rs528134023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521184 | GCCCAAAACCTCACA[A/C]TAAAACTCCTGAAGG | 55626 |
rs528146148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513401 | ATATAATCTAGCCCA[A/G]TAACAAACTCAACTG | 55626 |
rs528152875 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399539 | GGCTAATTTTTTGTA[-/T]TTTTTAGTAGAGATG | 55626 |
rs528157913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567913 | CAGCATTTGAGAGGC[C/T]GAGGCAGGCGGATCA | 55626 |
rs528158703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560095 | ATCTCTAATTAACCA[C/T]CTGACAAATTGAAAA | 55626 |
rs528163341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434518 | TCTGATTATTTCCTT[A/G]AAAGCTGGATTGCCA | 55626 |
rs528197750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457729 | AACATAGTAAAACCC[C/T]GTCTCTACTAAAAAT | 55626 |
rs528209287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505313 | AGCACGTGGACACTC[A/G]GAGGACAGGAGCAAC | 55626 |
rs528254408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440023 | CTCCAAGTGGAATAA[A/T]AATTTGGCACGAGCT | 55626 |
rs528259887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479342 | CCATGGCCTTAGAGA[A/G]TCTTCTTCCTGGTTT | 55626 |
rs528274320 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516558 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGACTACAG | 55626 |
rs528287664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425192 | CATCTCTGGGCACAG[A/G]GCACAACACAAGTTC | 55626 |
rs528298165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536065 | GAGCCAATGACTCTC[C/T]GTAAGACCAAATGAT | 55626 |
rs528306749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480186 | ATAATCTTCCCACCT[C/T]AAGATCTATAATCTT | 55626 |
rs528308324 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591565 | TCTGCACCCTTAAAA[C/G/T]CACTCTCTTAGCCGG | 55626 |
rs528313305 | in-del | -/AGTCTGGGTACT | 0.0134861 | 0.0810011 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519367 | AGTTGAGGTGCAGAA[-/AGTCTGGGTACT]AGTCCATATGGAATA | 55626 |
rs528320442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425835 | CAAGAGCGAAACTCC[A/G]TCTCAAAAACAAAAA | 55626 |
rs528349221 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499658 | CAGGGGAAATTTTTC[-/T]TTTTTTTCTTTTTTT | 55626 |
rs528388180 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567604 | GGCCTCAAGTGATTC[A/G]CCCGCCTCAGCCTCC | 55626 |
rs528391952 | in-del | -/C/T/TT | 0.469128 | 0.131323 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428589 | TTCTTCTTCTTCTTC[-/C/T/TT]TTCTTTTTTTTTTAA | 55626 |
rs528397417 | in-del | -/ATTT | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511079 | TAGGATAAATAACAG[-/ATTT]ATTATATAAAAGGAG | 55626 |
rs528417094 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552483 | CAAGTTCAAGAGATC[A/G]AGACCATCCTGGCCA | 55626 |
rs528458883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456137 | TTATTTAAGACAAAA[A/G]CAAATAAGCTCACAA | 55626 |
rs528477749 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438705 | ACACCACTCATCCGC[C/T]GGGTTTCTTAAGGCC | 55626 |
rs528504287 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494063 | GACCAGAAAGTAGGT[C/T]TAAAACTAAATCCTA | 55626 |
rs528576703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494624 | GGGAGGAGGTCTTAA[A/T]GGAAGAAAAATTCCC | 55626 |
rs528598365 | snp | C/G/T | 0.000145482 | 0.00852779 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543193 | TCCGTGGAGGGCTGA[C/G/T]GGGGAGGCGGTGGGG | 55626 |
rs528640676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517929 | CCATATTCGTATATA[C/T]ATAGAGAGAGAGAGA | 55626 |
rs528658167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470422 | GTGAAACCCTATCTC[C/T]ACTAAAAATACAAAA | 55626 |
rs528658836 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503089 | AAAAAAAAAAAAAAA[A/T]GAATTTTTGCTTTGT | 55626 |
rs528665417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573275 | CCAGGTGTGGTGGCA[C/T]GCACCTGTAATCCCA | 55626 |
rs528686906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407995 | CAGAGAGTCAGGGCC[A/G]AGTGTGGCAGAGCCA | 55626 |
rs528700576 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437107 | CCTCAAAACTCATCA[C/T]CAACACACAAAAAAG | 55626 |
rs528703185 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518425 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 55626 |
rs528709099 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445147 | GTATATAAATAGATA[A/C]ACATTGTATCTGTGA | 55626 |
rs528713379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511064 | TGATAAAGATCACAG[C/T]AGGATAAATAACAGA | 55626 |
rs528728344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532733 | AGCCACAGTGCCCGG[C/T]CTTAAGAGTTCTAAT | 55626 |
rs528763642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566247 | AACACGGTGAAACCC[A/G]TCTCTACTAAAAATA | 55626 |
rs528776615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511654 | ATGTGCTCTAGTATT[G/T]CTTAAATAATGTGCC | 55626 |
rs528782067 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409222 | CTCTTTTTTTTTTTT[C/T]GGTGAGACAGTCTCG | 55626 |
rs528798698 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502625 | AAGGACAGGTGGCTA[C/G]AATTCTAGTCAGGAG | 55626 |
rs528822475 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455061 | TAATTAAAAAAAAAT[G/T]TGTTTTTGTAGATAT | 55626 |
rs528826208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566656 | ATCTTCTGGGCAAAG[C/G]TTCATTGCAACTTTA | 55626 |
rs528831916 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581651 | TACACAAATAAATAA[C/T]TACCCACATGTGGTG | 55626 |
rs528857981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574579 | TAGCCCTTTGTCAGA[C/T]GAGTAGGTTGCGAAA | 55626 |
rs528879647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425046 | GGCTGAGGCAGGAGA[A/C]TTGCTTGAACCCGGG | 55626 |
rs528886232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438504 | GGGAGCAATTAGCAG[C/T]TGCAGTGCCTTTGCA | 55626 |
rs528891544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527745 | GCAAAGCAAAACCAC[A/G]TTTATTTATCGCCTC | 55626 |
rs528904567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519553 | TGCTAGAACTCTCTG[A/G]CCTCTACTGTTAGGG | 55626 |
rs528929103 | in-del | -/TT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399401 | GATGGAGTTTTGCTC[-/TT]GTCACTCAGGCTGAA | 55626 |
rs528948279 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469349 | TGTTTTAGAAACAGA[C/G]TACCTTGGGAATGAT | 55626 |
rs528948322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463477 | CTGACTTGGACTATT[C/T]GACTGTCAGCTCCTT | 55626 |
rs528951704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511959 | TTCCTAGTTCAAGTG[A/G]TTCTCCTGCCTCAGC | 55626 |
rs528957601 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432663 | TGGATTAAACACATA[C/T]GCTACACAGCTAAAG | 55626 |
rs528970107 | in-del | -/ATC | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538862 | TTTTAGATGTATAAT[-/ATC]ATAGCCATTAGTCAC | 55626 |
rs528970212 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409409 | TTCACCATGTTGGCC[A/C]GGATGGTCTCCATCT | 55626 |
rs528999960 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401515 | AAGTTCTGGGAGGCA[C/T]GAGCCACCGCACCCA | 55626 |
rs529007574 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585555 | CCTGTAGTCCCAGCT[A/T]CTCAGGAGGCTGAGG | 55626 |
rs529008297 | snp | A/G | 1.65236e-05 | 0.00287429 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410335 | CGTCTCGTTCAGCTG[A/G]TCCCAGTAGTACTCA | 55626 |
rs529008591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550742 | AGTGTCCATCTAAAG[A/G]GTACTGGATGACTAA | 55626 |
rs529009384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456277 | ACCAGGCAGGGATTT[C/T]CTCAAAGCCTCTACC | 55626 |
rs529035577 | snp | A/G | 6.70084e-05 | 0.00578789 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542140 | CTGCTGGAGCTGGGC[A/G]TTTGGCCCTCAGTCC | 55626 |
rs529038215 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438662 | CACTCCCTGAAGGCA[C/T]TATATCCCCTGTGGT | 55626 |
rs529070738 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547979 | TTAGCATTCACAGTG[C/T]AGGCTTAAAAACTGG | 55626 |
rs529074059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439158 | ATGTGCCTGTAGGCC[A/G]AGTTACTTGGAAGGC | 55626 |
rs529076116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense | AMBRA1 | GRCh38.p7 | 11:46431005 | TATCCAAAAAAGCTG[C/G]TGTCTTCCCTTCCAC | 55626 |
rs529094820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534514 | ATAAAGTAAAATAAA[C/T]AGCACCTGAAATCCA | 55626 |
rs529103848 | snp | A/G | 2.80619e-05 | 0.00374569 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543080 | GAGTGCCAGAGCAGC[A/G]GCTGCAAAGGCACAG | 55626 |
rs529104179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590354 | AAAAAAAAATTAATT[C/T]AAAAAAATGTAAGCC | 55626 |
rs529108635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485616 | ATACCCAAAGTGTTC[C/T]GGAAAATACTAAGCA | 55626 |
rs529112605 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432047 | TTTATTTATTTATTT[A/T]TTTTTGAGATTCTCT | 55626 |
rs529135038 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424503 | TCAGCTGAGGAATCT[A/G]CTTCTGTGCTAAAAG | 55626 |
rs529161752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581136 | AAGGTCATGATACTC[A/T]TGCTTAAAACCTTCA | 55626 |
rs529170735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478924 | GCAATTTGTGCTGGA[C/T]GCAGTGGCTCACGCC | 55626 |
rs529215464 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578293 | GGAGTTCGAGACCAG[A/C]TGGGTCAACATGGAG | 55626 |
rs529215623 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557536 | AAACCAGCCAGGCAC[A/T]GTGGCTCACACCTGT | 55626 |
rs529218028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535481 | AAAATCCTACTTCTA[A/C]GCAAATTTAATGAAT | 55626 |
rs529244743 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537140 | TTTCTCCTAGAAGCA[C/T]TGTGTTAGTTACCAT | 55626 |
rs529253246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566146 | TGGAATTGGTCAGGG[C/T]GCTAGCTCACACCTT | 55626 |
rs529275153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462744 | AAGTACTTTCTCAAA[C/T]AATTCACCCCCCTCC | 55626 |
rs529275776 | in-del | -/A | 0.404559 | 0.196498 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406373 | CTCTATCTTTAAATT[-/A]AAAAAAAAAAAAAAA | 55626 |
rs529311306 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399857 | GAGAAGGATCTGTCC[A/G]CCACTCCCTCTGCAG | 55626 |
rs529326124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558096 | CCAGCTGAAAGCAGA[C/T]GCACAAAGCACAACT | 55626 |
rs529366547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400523 | TTGAGACCAGGTCTC[A/G]CTATGTCACCTAAAC | 55626 |
rs529368889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502543 | TTTGTTATTAGAGAG[C/T]AGTCACTGATTCCTA | 55626 |
rs529426504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494015 | TGGGCTATGGGCCCA[A/C]TAGGAAACAATGCCA | 55626 |
rs529434799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446448 | TACATACGAGGCACT[G/T]AGCCTCAGAAACCAA | 55626 |
rs529438210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533465 | ATAACACGCCTTCTT[A/G]TTTGGAGGTTGGGGA | 55626 |
rs529449844 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507749 | CTAAGATAGAAAATC[C/T]GCCTCTTAGGGAAAT | 55626 |
rs529455501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525734 | CCAGCCTGGGCAACA[A/G]AGCAAGACTCCGTCT | 55626 |
rs529460213 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477610 | ACTGTGCTGGGATTA[C/T]AGGCTTGAGCCACTG | 55626 |
rs529481642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414729 | CAGAGGAGGAGGGAG[C/T]GCCTCAGTGCCAGGA | 55626 |
rs529489898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429922 | CAGAAGGGAATCAGA[C/G]AGAAAATAAGATTCT | 55626 |
rs529497731 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465252 | TCATGCTCCTCCCTG[A/C]CCTCCTTCTGCCTCC | 55626 |
rs529528150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423564 | GCCCGGCTAGTTTTT[A/T]GTATTTTTAGTAGAG | 55626 |
rs529531872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517708 | GCCTGGTGGCACACG[C/T]CTGTCCCAGCTACTT | 55626 |
rs529543909 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540101 | CCTCCCAAAGTTCTT[A/C/G]GATGACAGGCGTGAG | 55626 |
rs529552787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407946 | CTCTGCTGCTGGGAA[A/G]TGCTAATTGGTTTTT | 55626 |
rs529562752 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565554 | TCTACATAAACCAAA[A/T]AAATTAGCCGGGTGT | 55626 |
rs529592859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573087 | GCCTGGGCAACAAGA[A/G]CAAAACTCTGTCTCA | 55626 |
rs529593363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469704 | GATCTCACTCTGTTG[C/T]CCCAGGGTGGAGTGC | 55626 |
rs529639961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515199 | TCCTTCTTGGCTGGG[C/T]GTGGTGCCTCACGCC | 55626 |
rs529645602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462109 | ACAAGAGATATCTGA[C/T]GAGATTAAAATGTAT | 55626 |
rs529661312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554672 | AGATTTTACTCTGTT[C/T]CCTGTAAAGAACAAA | 55626 |
rs529662879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450508 | GCAGTGGTGCAATCA[C/T]GGCTCACGGAAGCCT | 55626 |
rs529676169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506396 | TTCTAAGAGCACAAA[C/T]GCTAGTAGTGTGTTT | 55626 |
rs529680638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459462 | TAAAAAATTTATATC[C/T]TAGATTGGGAAACCG | 55626 |
rs529698577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442275 | AGCCACCCGAGTAGC[G/T]GGGAAAACAGGCATG | 55626 |
rs529723260 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448844 | AATTTGAAAACCTAC[A/C]TGCAATGGACTAACT | 55626 |
rs529772516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498475 | GGGAAGGAGTAGGGG[G/T]AAAAATACTTTCTTA | 55626 |
rs529773503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546404 | GGTGCAAGACAACCC[A/G]CTAGCCAGTTACTAG | 55626 |
rs529791715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443121 | AAAACAAAGATTTCT[C/T]TGCTCTGAAGAGTTT | 55626 |
rs529808872 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423476 | GGTTCACTGCAAGCT[-/C]CACCTCCTGGGTTCA | 55626 |
rs529820252 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474036 | GACCTACCTAGCACA[C/T]AGTAGCACTCAAGAA | 55626 |
rs529825352 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594634 | AAAGGCCTAGAGCCA[C/T]AGGTGTGCTTCTTAC | 55626 |
rs529833060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521561 | GAGATGACAAGCCCT[C/T]ATTCTTTGTAAAAAA | 55626 |
rs529838546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490617 | CTACAGTACTGGTCA[C/T]ACCCCCTAAAACTGC | 55626 |
rs529867844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465132 | AAGTATGGACAACTA[C/G]TGCCCACACCTACAG | 55626 |
rs529884454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419885 | ATGCAAACCAAGTGA[C/T]AAGCAGCCCTGGATC | 55626 |
rs529911624 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412073 | GCTCCTTTTAAGGGG[A/C]CTGTCAGGCTGTGGA | 55626 |
rs529920120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46453934 | GACTTCAATGGTTAC[A/G]TGTCTTATTTGTAGG | 55626 |
rs529939942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404143 | GCAGTGAGCCGTGTT[C/T]GTGTCACTGTACTCC | 55626 |
rs529988691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568633 | TAAAATAAGCCGGGC[A/G]TGGTGGCACATGCCT | 55626 |
rs529993253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569390 | CATTACCCTGCAGCC[C/T]ACCTTTTTCACCTAT | 55626 |
rs530045979 | snp | A/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458583 | ATCAACTTTTCCTTC[A/C]TATAATATTTTTTAA | 55626 |
rs530083025 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564545 | GCTCTAACCATTATA[C/T]AATACTGCTTCTATA | 55626 |
rs530091894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593392 | TCAGAAGAGCCAGAG[G/T]GCCTTGTTCCATAAG | 55626 |
rs530095602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441095 | TTATTGAATTAGTAG[A/C]CAATGGAATACTGAG | 55626 |
rs530122174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592589 | ATGATGAAACCCCGT[C/T]TTTACTACAAATACA | 55626 |
rs530124352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537215 | TTTCTTACAATAAGA[A/G]TTAACTGAAAAGTTC | 55626 |
rs530141692 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46593870 | CAGTCCAGCGAACGG[A/G]CTGAGCCACAGGGAA | 55626 |
rs530142008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456464 | CTCATCATTATGCAA[C/T]GCAGCTGCTTAAGGG | 55626 |
rs530144114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481552 | ATTTTTAGCAGAGAT[A/G]GGGTTTCTCCATGTT | 55626 |
rs530166465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537895 | TATGAACTCCACTCA[C/G]TCAGGAACAACAGTC | 55626 |
rs530169644 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426963 | TCCAGACAAGATTAA[C/G]AAAAGGCTCAGTTTC | 55626 |
rs530184703 | snp | A/C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462219 | GTAAACAAGTGAGCA[A/C/T]GGCGGTGTAAGCACA | 55626 |
rs530207198 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480859 | CACTGCCATCCAACT[A/C/G]TCTCTCCTTTACGTA | 55626 |
rs530216368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583139 | AACAGCATGGTACTG[C/G]TACCAAAACAGAGAT | 55626 |
rs530225479 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408055 | ATGATAGGCCAGGCT[G/T]CAGCCAAAATGTCAA | 55626 |
rs530227061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584492 | ACTAACCTGCACATT[A/G]TGCACATGTACCCTA | 55626 |
rs530228870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575804 | ATAGGCGTGAGCCTC[C/T]GTGCCCAGCCAGGCT | 55626 |
rs530246072 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569442 | TTAAAAAAAAAAAAA[-/T]ATATATATATATATA | 55626 |
rs530263723 | in-del | -/CTGT | 0.0146672 | 0.084371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413826 | ACCCAGTGTCACTGA[-/CTGT]CTGTGAGCTAAAGAA | 55626 |
rs530283886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457171 | AGGCCTGCTCCCAGC[A/G]AAGAAAGGTGAAGAG | 55626 |
rs530291761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495512 | CCCAAAAGAGAAAGC[A/G]TACACTGTGTTCCTT | 55626 |
rs530296495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512491 | CCTCCTCTAGCACCA[C/T]ACTTGCGGAAATGAG | 55626 |
rs530319512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447964 | ATGGCCTTTAAAGTT[A/G]TATCTGTCATCTACT | 55626 |
rs530345534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496440 | AGCATCATGGGTCAA[A/G]TCTAATTATTCCACA | 55626 |
rs530350812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488068 | TACTAGACAGAGAGG[A/G]ACAATGGTAAAATAG | 55626 |
rs530360661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544119 | AAACTTGTGTTTGAA[G/T]TTATAGCAATCATTA | 55626 |
rs530361898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504113 | ACTGTCATTAGCAAA[A/G]CCTTTGCTACAGTAT | 55626 |
rs530379252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465594 | GAGGAAGCCTCTCTA[A/G]GGAACATGCAAAGCC | 55626 |
rs530412733 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522114 | AATGTATACATAGTG[C/T]GCAATCATGTATCTA | 55626 |
rs530436774 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558241 | TTTTGTACATCAATA[A/G]ATAACTAAAACACTA | 55626 |
rs530452016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552479 | GTAACAAGTTCAAGA[A/G]ATCGAGACCATCCTG | 55626 |
rs530458312 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440426 | ATTTCTGAAAAGATA[C/T]ATAAGGAACTGCTAA | 55626 |
rs530497190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561747 | TCAAATTATTAAACA[C/T]AGAGTTCTTATGCTA | 55626 |
rs530497688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457793 | TATAATCCCAACTAC[C/T]TAGAAGGCTGAGGCA | 55626 |
rs530500254 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553969 | AGGAAATCATCTCCT[C/T]AGTAACCCTGACAAC | 55626 |
rs530503589 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404058 | CAAAATAAACAAAAT[G/T]AGCCAGGCGTGGTGG | 55626 |
rs530546166 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591742 | CGCCTGTAATCCCAG[A/C]TACTCAGGAGGCTGA | 55626 |
rs530571172 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403294 | ACCTCTGGGAGTACT[C/G]GTCTTCCAGCCCCTC | 55626 |
rs530607091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537029 | CCAATTTTTATCTCT[C/T]TCAGTTGCTGGAATT | 55626 |
rs530609019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528768 | TATGTTATGTTTTCT[A/G]TCACAGACACACGTA | 55626 |
rs530620811 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529275 | CACTAGTGAGCCTCA[A/T]CCAGCAAATAAGCTT | 55626 |
rs530634808 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480070 | TTAGCAGAGGCCATT[C/T]CCATCTTTGATCATT | 55626 |
rs530652009 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426382 | CATGGACGCACTACA[A/G]AGGAAGGGACTAGGT | 55626 |
rs530652424 | snp | A/G | 1.68374e-05 | 0.00290145 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418071 | GGTAGAGGAAAAGAG[A/G]GAAAAAAAGAGAATG | 55626 |
rs530691819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472272 | TAAACTGAGATGGAT[C/T]CTTTTCAGCCACCTG | 55626 |
rs530691920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480572 | ATCAACATGTGTACC[G/T]TAAAAGCAACTGGCA | 55626 |
rs530715238 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568035 | TGCCTGTAATTCCAG[A/C]TACTTGGCAGGCTGA | 55626 |
rs530721597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411047 | AGAGGTTGCAGTGAG[C/T]TGAGATCGCGCCACT | 55626 |
rs530726976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425892 | TGTCTCACGCCTGTA[A/G]TCCCAGCACTTTGGG | 55626 |
rs530760679 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583081 | AAGCTGGAGGCATCA[C/T]GCTACCTGACTTCAA | 55626 |
rs530761683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519888 | CTCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 55626 |
rs530791020 | in-del | -/G | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520737 | GTAGCTGGGACTACA[-/G]GGCGCCCACCACCAA | 55626 |
rs530914477 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488741 | AAATTAAAATGAATA[A/C]AATCACACAAAGTAT | 55626 |
rs530915608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439589 | TAAAAGTTATAAATG[A/G]TCTCCCTAATGATGA | 55626 |
rs530936981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544670 | CCAAACTTCTTTCAG[G/T]TTTTCCCAAAGAAGT | 55626 |
rs530952455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440247 | GTAGGCAGTCATAAA[A/G]AAGAACAAATAAGCT | 55626 |
rs530961435 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552887 | ATAGGCAAGTTTCTA[-/T]TTTTTTTTCACTTTT | 55626 |
rs530998345 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442761 | CACAGACATAGAATA[C/T]CTTAATTATTTTAAG | 55626 |
rs531025511 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487974 | GATGGAAAATGATAT[A/C]TCATGTAATCAACAA | 55626 |
rs531042674 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402351 | AACTGCCCATTGTGG[A/G]AGAAGCATTTATTTT | 55626 |
rs531051405 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495059 | AGGATTCAAGGAAGA[C/T]TGGACTTTGAAGTCC | 55626 |
rs531051636 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555145 | ACACACATACTCCCA[C/T]TCCCAATAACATGAC | 55626 |
rs531059988 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478888 | CTTTCCTCAGTATAT[C/G]TAAGGACACTTTTAA | 55626 |
rs531109519 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519222 | AGAGACGGGATTTCA[C/T]CATGTTGTCCAGGCT | 55626 |
rs531124609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504035 | CTGAATGTAATTATC[C/T]AGTGGCTAGTATATA | 55626 |
rs531126046 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399731 | TTCCCTTTACCCCCC[A/C]GTCTTCACAAGCTAT | 55626 |
rs531146208 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456230 | ATGGGGGAAAAAAAA[A/C]CCCCAAACACAAACA | 55626 |
rs531155524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457001 | AACTTTCCTTACAGG[C/T]CACCTACACGTGAAT | 55626 |
rs531165970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409262 | CCAGGCTGTAGTGGC[A/G]CAATCTCAGCTCACT | 55626 |
rs531174448 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474392 | GGCCCAATTTCTAAC[C/T]TTGTTCTATTTTTTG | 55626 |
rs531187421 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438304 | CAGACTCTGCAATGT[A/C]ATCTCCTCCCAATTA | 55626 |
rs531211923 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559008 | TCAAATACCTTAAAA[A/T]GAAAAACCTAAGCCG | 55626 |
rs531229375 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459667 | AATGAGCTGAGATCA[C/T]ACCACTGCACTCCAG | 55626 |
rs531238973 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494778 | CAGACTGTCAATGGT[A/G]AAGAATATTAGAAAA | 55626 |
rs531269431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429270 | TCGCTACTCAGAAAT[C/T]GGTGTGTGGGGAGTG | 55626 |
rs531281555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447359 | GACCAACATGGTGAA[A/G]CCCTACCTCTACTAA | 55626 |
rs531282354 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577788 | AAACCCTGTCTCTAC[C/T]AAAAGTACAAAATGT | 55626 |
rs531303468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484526 | TAAAGTACAAATAAA[C/T]AGTGGCGCCTCAATC | 55626 |
rs531313740 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414683 | CAGCCAGAGGCACAG[C/T]AGCAGCTTGGGCAGA | 55626 |
rs531316568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436103 | CTTATTTGAAGGAGA[C/T]GTCCACTGTCAGAGG | 55626 |
rs531334206 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532859 | AATTTTCATTTACCA[C/G]TAACAACGCTCATAC | 55626 |
rs531355230 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491919 | CAGCTGTTCCCCCAA[A/C]GCTAAATGCCAAGGA | 55626 |
rs531375105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460299 | TGATCCATATGCATA[C/T]GACCCCATTTATATA | 55626 |
rs531389561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516126 | GAACACGCATCCCCT[A/G]TGCCTACTTACTACG | 55626 |
rs531399943 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424098 | TGATTATTTAAAAAC[C/T]CAAATCACAGCTTTG | 55626 |
rs531412095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46451007 | TCCACTCAACTTTTA[A/T]TAAACCTAAAAAAGA | 55626 |
rs531433325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587563 | GAAACTTAAATTTAC[A/G]CAATTATGATTCGTG | 55626 |
rs531441364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476472 | GCTGGTACTGCTTCT[A/G]TCCCATAGGACCTTC | 55626 |
rs531444114 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519385 | CTGGGTACTAGTCCA[C/T]ATGGAATAAACAAAC | 55626 |
rs531445808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588379 | AAGAACTTAAATAAC[A/G]TCTGTTCATTGTTGT | 55626 |
rs531450929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507991 | TCCTCGCGCGCCAGT[C/G]AATCAGCAAAGCAAC | 55626 |
rs531452021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405565 | CTCTAAAAAAAAATA[A/G]TGATTAAAAAAATAG | 55626 |
rs531465362 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540927 | CATTCAACTAATACT[A/T]ATTGACTGAGTGACT | 55626 |
rs531485118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398208 | TGGCCCAGAAGGCAG[C/G]AGGTTGGCCTCAATG | 55626 |
rs531498751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563847 | GAGACTGTCTCAAAA[A/C]AAAAAAAAAAAAAAA | 55626 |
rs531508433 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436382 | AGGCATTAGAATACA[C/T]TGATTAGGCTATTGT | 55626 |
rs531523499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500531 | GCTGCCTAAAATATA[C/T]ATTGGATGATGGCTG | 55626 |
rs531566067 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474957 | AGCCTGACAAAGTCC[A/G]CATATATGTATAACA | 55626 |
rs531594664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508850 | AGATGATTAAAGAAG[C/G]TATCCACAGGTATCT | 55626 |
rs531598559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412019 | CACAGCCAAACAAAA[A/G]TGCTCTTCTTTTCAC | 55626 |
rs531613454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564774 | GAAGGAGCGAACCTC[A/T]CTGGAGGTTAACTAT | 55626 |
rs531655400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491550 | ATACAACTGCCAATA[A/G]AATCTGGAGGGACAT | 55626 |
rs531674634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547588 | GGCAAATGATTGTTA[C/T]TGAGAAACTTTCCAA | 55626 |
rs531674782 | snp | A/C/G | 0.00239393 | 0.0345281 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467011 | AAACCTTCACCTCCC[A/C/G]GATCCAGGCGATTCT | 55626 |
rs531678878 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452168 | TAAATGTCTATCAAT[C/T]TGTGAAGTAAAAAAT | 55626 |
rs531684129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443883 | AGGTACTGTACATAC[A/G]TGGTCTGGTAGGCTC | 55626 |
rs531758623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577174 | CATGTTCAAAGCAAC[A/G]CTATTCACAAGAGCA | 55626 |
rs531791190 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450418 | CAGGGAGGCAGAGAC[A/G]AACAGGTGAGCACAA | 55626 |
rs531805185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515428 | CAGTGAGCTGAGATC[A/G]CACTACTGCACTCCA | 55626 |
rs531810450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413070 | TGTACTTCCTGACCC[A/G]GAACCTTCCTTCCTA | 55626 |
rs531822047 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569688 | TTTGGGAGGCTAAGG[A/T]GGGTGTATCACTTGA | 55626 |
rs531822984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529295 | CAAATAAGCTTGGAA[A/C]CTCCATTTTCCCCCT | 55626 |
rs531851776 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413796 | ATGCCCGGCCTGAAA[C/T]TCTTAGCTTTCAATA | 55626 |
rs531865640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459542 | ATGGTGAAACCCCGT[C/T]TCTACTAAAAATACA | 55626 |
rs531915837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482704 | GCTTCTACTTTACCA[C/G]CTATGAGCCACAAGA | 55626 |
rs531932777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546559 | CAACGGGCTGAAGGA[A/G]GCAAAAGTAGATGTT | 55626 |
rs531951906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434511 | ATAGTTTTCTGATTA[C/T]TTCCTTAAAAGCTGG | 55626 |
rs531954315 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570093 | TGGTGAAATCCTGTC[A/G]CTACTAAAAATATAA | 55626 |
rs531960970 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528828 | ACAGAACAAAGAAAA[G/T]ATAAACGCCACCTTG | 55626 |
rs531966261 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489687 | AGATTATGCAGGACA[G/T]ACAGCTAATACCCCA | 55626 |
rs531969093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498380 | CTTTGAGCCAGCAGG[A/G]TAGAAGCTGGCTGGG | 55626 |
rs531971913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555808 | TCATACCCCAAATCT[C/T]CCCCTTCCTATTGCA | 55626 |
rs531993587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427763 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCAGAGG | 55626 |
rs531996999 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491397 | CGCACCTATCTCATA[C/T]GATTACTGCAAGACA | 55626 |
rs532014203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443806 | TTCAATGTGGAAATA[C/T]AATCCCATTCATCAG | 55626 |
rs532027072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398053 | GACTAAACGCAGGAT[A/T]GAGAAAGACTCGCTC | 55626 |
rs532042409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499629 | ACTTTTCATTATTGT[A/G]CCTCTGCCTACTACA | 55626 |
rs532097054 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491505 | CTATATTATTATTAT[G/T]GGAATTTTCTCAAGA | 55626 |
rs532110145 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450954 | TGGGGAAGCCTGTGG[C/G]TGTAAGGGGAGGGAG | 55626 |
rs532112105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539653 | AAATTCTCACTCAGA[A/G]ACCTATTATATGATC | 55626 |
rs532181301 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498144 | AAGATATTTGCCAGA[G/T]GAAAAGTGAGAGAAA | 55626 |
rs532187601 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428169 | TCTTAGGTCAAGAAA[-/G]GAAGAAAGAAGAAGG | 55626 |
rs532214512 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515334 | AAAAAGTAGCCAGGC[A/C/G]TGGTGGTGCGTGCCT | 55626 |
rs532224960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507351 | AGGCGCGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 55626 |
rs532230786 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494944 | ATCCCATTTAATTCT[C/T]CTGGCTAGGCCACGA | 55626 |
rs532246278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483868 | GCACTCCAGCCTGGG[C/T]AACAAAGTGAGACTC | 55626 |
rs532262945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454333 | CATGCCTGGCAAACT[A/G]TGAAATATTCCTATG | 55626 |
rs532272723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404843 | AGGAACTTATAATTG[A/G]CTAGAAGCCAGAAAT | 55626 |
rs532283905 | snp | A/G | 3.61644e-05 | 0.00425216 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397461 | GTCTCTACCTGTTCC[A/G]TGGTTCTCCCCTAGG | 55626 |
rs532313340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569595 | CTGTGTACTATAGAA[A/T]TAGCATTCCAAAGAG | 55626 |
rs532340145 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420930 | AAGTTGCTGTGCTGC[A/G]TTTTTTAAATGGGGG | 55626 |
rs532359190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459513 | GTCAGGAGTTCGAGA[A/C]CAGCCTGGCCAACAT | 55626 |
rs532362698 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419930 | CATGTGCCTTGGGTA[A/C/T]GTATCTGAAAGGCCT | 55626 |
rs532382268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434393 | CCCACCCCACCCTCC[C/T]GCAAAACAAACAAAC | 55626 |
rs532394426 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447894 | GACACAGCCAGACCA[C/T]CTTGTAAATAAATAC | 55626 |
rs532414337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562989 | TTTTAGTGGAAACAG[A/G]GTTTCACCATGTTAG | 55626 |
rs532472745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530755 | GGCCAAAACCAGCTA[A/T]GAATGGTTTTCATAT | 55626 |
rs532477251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554859 | GTCTTTGTGATACCG[C/T]CACACAGTCCCCAAA | 55626 |
rs532494789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563740 | AGCAACTCGGGAGGC[C/T]GAGACAGGAGAATTC | 55626 |
rs532501128 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506236 | CAGTCAGAAGGTAGC[A/T]CTGCTCTTCTCCTGC | 55626 |
rs532567675 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450070 | TCAAAAAAAAAAAAA[A/C]AAACAACTAATGTCC | 55626 |
rs532568463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427679 | CACATTGAGAACTGC[C/T]GTGCAATCAGATTTG | 55626 |
rs532569650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584731 | CTCCTGCCTCAGCCT[C/G]GCAAGCAGCTGGAAA | 55626 |
rs532570840 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562484 | AATATAAGAGATGAA[C/T]AGTCATACTCAGAAT | 55626 |
rs532612932 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474210 | GGTGGTAAAATCAGT[A/C]AGTTTGATATTTTTC | 55626 |
rs532620680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553551 | GAAGTTCGAGACCAG[C/T]CTGGCCAACATAGTG | 55626 |
rs532648680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536180 | ATTTCAATTCTACTT[A/G]TTCAATTCAACTAAC | 55626 |
rs532656081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488959 | TGTCGCCCAAGTGCG[A/G]GGGCGAGATCTTGGC | 55626 |
rs532657637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577070 | TCTCTAACATGTCAG[A/C]AGATCATTAATATAT | 55626 |
rs532667644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481044 | TTAATGTCCTCTTGG[C/G]TCTTTTGGCTGACTT | 55626 |
rs532668064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489545 | GACACTGGACCAGGC[C/T]GTAATGACCTGTGGC | 55626 |
rs532689598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592762 | GCCTGTCTTAAAAAA[A/G]AAAAAGAAAAAAGAG | 55626 |
rs532817518 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490813 | TATTCACTCTGGTAA[A/C]CTAGAACACTGCCTG | 55626 |
rs532837681 | in-del | -/T | 0.321292 | 0.23962 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573663 | GCAGAATCCTTTTTC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs532841642 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396282 | AGGGGTCAGAGGGGT[A/C]CACTGCACCCCACTA | 55626 |
rs532842665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470493 | ACTGAGGAGGCTGAG[A/G]CAGGAGAATGGCGTG | 55626 |
rs532871943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534456 | GCCCAGATCGCACCA[C/T]TGCACTCCAGCCTGG | 55626 |
rs532874168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593424 | CTCCACCTACTCAAA[A/G]GTCCCTTCAAAGGCT | 55626 |
rs532875754 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573369 | AGATCAAGCCACTAC[A/C]CTCCAGCCTGGGCGA | 55626 |
rs532882457 | snp | G/T | 1.66283e-05 | 0.00288338 | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433600 | ATATCTGCCCATTGG[G/T]GACAGGCTCACCGAA | 55626 |
rs532892264 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408701 | CTCCATGTGGCTCTG[C/T]TGGTTCTAGGGAGAG | 55626 |
rs532893250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537292 | ACTGCTGTTTGAAGG[C/T]ACTTATTTCAAATGA | 55626 |
rs532906879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470833 | GTTTACTCATCAGAC[A/G]AATATTTGAGTATCT | 55626 |
rs532936744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549170 | GAAATTAAAATTCTA[C/T]TAAAATGGCAACTAG | 55626 |
rs532945761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534454 | GAGCCCAGATCGCAC[C/T]ATTGCACTCCAGCCT | 55626 |
rs532970225 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535215 | ACTAAGAAGAACTCA[A/G]AAGTTAGAAAGCGTT | 55626 |
rs532983537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446352 | ATTAAAACAACCCCA[A/G]CCATTTAGTAGGCCT | 55626 |
rs533002829 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437744 | CTTGTTTATTTAGGC[A/C]ACAGGAAAGTAATGT | 55626 |
rs533007755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527543 | ATATTTGCTAACCAT[A/G]TATCAGATAAATGTT | 55626 |
rs533008784 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464807 | ATCCAAGCACTTTGC[G/T]AGGCCAAGGCAGTCG | 55626 |
rs533010260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492967 | GGCAGGAGAATTGCT[C/T]GAACCCGGGAGGTGG | 55626 |
rs533012759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424916 | CCGAGGTGGGTGAAT[A/C]ACGAGGTCAGGAGTT | 55626 |
rs533036365 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430085 | CAGAGAAGGGAAAGA[G/T]CAAAAGGACCCTAGA | 55626 |
rs533037465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580985 | TTTTTGTAGAGATGG[A/G]ATCTTACCATGTCAC | 55626 |
rs533069956 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530626 | GAGCAAGTGCAGGAG[G/T]CCCCTAACAACCTCT | 55626 |
rs533073423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589672 | TCGCCCAGGCTGGAG[C/T]GCAGTGGTGCTAACT | 55626 |
rs533146711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461147 | ATTTAGGAGGCTGAG[A/G]TGGAAGGATCTCTTG | 55626 |
rs533165407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452371 | TGTTTGTTTTTTAGA[C/T]GGGGCCTCACTATGT | 55626 |
rs533167045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414630 | TGGCACTTCACACCC[C/T]CCATGGTTATCAGTG | 55626 |
rs533184014 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415235 | GACCACTCATCTGTA[A/G]ACCGCTCAAAAGACA | 55626 |
rs533187962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502499 | ACTTGCCAAAAGTTA[C/T]CCCCTCTTCCTTGGG | 55626 |
rs533200982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406972 | GATCACGAGGTCAGG[A/G]GTTCGAGACCAGCCT | 55626 |
rs533231187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565392 | ATTTATCCAGAAAAA[C/T]GATAACTTATGTTCA | 55626 |
rs533263068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485486 | GACTGGTAGTTAAAG[C/T]CTCAGGGGAATTAGT | 55626 |
rs533270172 | in-del | -/AAC | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404199 | GTCTCAAAAAATAAA[-/AAC]AAAATAAATAAATCT | 55626 |
rs533308768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469528 | TATATGTGTAATATA[C/T]ATGAAAACTGTATGA | 55626 |
rs533328941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428864 | GTCTCTGGACGGCTA[C/T]GGCGTAGGATGGCAG | 55626 |
rs533340869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539545 | CTGGGCAACAAGAGC[A/G]AAACTCCATCTCAAA | 55626 |
rs533364330 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574880 | CTTTCTCTCATCCTT[C/T]ACAGGTTTGTTACAA | 55626 |
rs533365506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429218 | ATCTTCGCCTACCAG[C/T]GGCCCCCTACCCCAT | 55626 |
rs533390467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587367 | CCTGGGCCACAGAGT[A/G]AGACCCTGCCACAAA | 55626 |
rs533405516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509108 | GAGCATCAGAGGCTG[C/T]GTGGGCACTGGGCAA | 55626 |
rs533422372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525098 | TGAGCCCAGGAGTTC[A/G]AGACCAGCTCGGGCA | 55626 |
rs533478947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501349 | CTTAGTCTGAGTGAG[C/T]GTGGGTGTGTGCATG | 55626 |
rs533495061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468820 | GCTCCGTCTCAAAAA[A/G]AAAAAAAAGAAAAAA | 55626 |
rs533546191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516672 | TCTCCTGACCTCATG[A/T]TCCGCCCACCTCGGC | 55626 |
rs533546969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436621 | TACTTACTACTCAGG[A/G]TCCCAAGCCCTTTGC | 55626 |
rs533548194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525286 | AGCCTGGGCAACCGA[C/T]TGAAACCCTGTTTCA | 55626 |
rs533572298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531847 | TGCCAGCTGGGAGAG[A/G]TGGCTCACGCCTGTA | 55626 |
rs533579186 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503048 | CCTGGGTGACAGAGC[A/G]AGACTCTGTCTCAAA | 55626 |
rs533596308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406461 | GTGGGAGGATCACTT[A/G]ATCCCAGGAGTTCAA | 55626 |
rs533603597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577879 | CACTTGAACCCAGGA[C/G]GAGGAGGTTGCAGTG | 55626 |
rs533645868 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476409 | GTGGCTTGTGGTTAG[A/T]TAATAGTGGTGGGGA | 55626 |
rs533685592 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559213 | ACTGAGGTGGGAGAA[G/T]TGCTTGAACTCGGGA | 55626 |
rs533714994 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575577 | GCTGGAGTACAATGG[C/T]ATGATCTCGGCTCAC | 55626 |
rs533720646 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536137 | GCCAAACAGGACTTA[C/T]ATTGCATATGAAACC | 55626 |
rs533741535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537303 | AAGGCACTTATTTCA[A/T]ATGAAACGGAGGAAA | 55626 |
rs533743539 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497929 | GGATATTTAGTGGAA[A/G]AACTGAAGGGAGAGG | 55626 |
rs533765505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491644 | TAGTTTAATGGTGAA[G/T]GAAAACCATCTGCTA | 55626 |
rs533765572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483557 | GAGGCTGCTTGGAGA[C/T]AGGAAAAGGAAACGA | 55626 |
rs533779819 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532989 | CCAACATGGTGAAAC[C/G]CTGTCTCTACTAAAA | 55626 |
rs533824908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484120 | CACTGCAGCTTTGTG[C/T]CATGCACAAGGGGCC | 55626 |
rs533835993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414750 | AGTGCCAGGAAGGGC[A/G]GGATGACTGCGCTAT | 55626 |
rs533868699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572080 | GGCCGAGGTGGGTGG[A/G]TCACAAGGTCAAGAG | 55626 |
rs533873723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460612 | ACAGGCGTGAGCCAC[C/T]GCGTCCAGCATAAAC | 55626 |
rs533883683 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565482 | GAAGGTGAGGTGGGC[A/G]GATTGCTTGAGCCCA | 55626 |
rs533884828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459633 | GGAGAATTGCTCGGA[C/G]CTGGGAGGTGGAGGT | 55626 |
rs533885687 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469120 | TGAACTCCAGCCTGC[A/C/G]TGACAACAGGGAAAC | 55626 |
rs533886114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461353 | TTGGTTGTGGAAGCA[A/C]AAATGCATGTCATAT | 55626 |
rs533891025 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409643 | GGGCATCTCCCAGGC[-/A]ACTGCCTTGGAATAG | 55626 |
rs533910818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563322 | CTTGACTTCCCAGGA[A/G]TAAGTGATCTTCCCA | 55626 |
rs533936663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547704 | GGGGCCAAAGTGCTG[C/T]TCATACAGTACTTCA | 55626 |
rs533952387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444247 | ATCAGAATATTTTTA[C/T]TAAGGCCATCTTTTA | 55626 |
rs533959062 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595022 | TGAGCCCTGGAGTTC[A/C]AGACCAGCCTGGGCA | 55626 |
rs533981603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428742 | CCTCGGCTTTCTTGT[C/T]GGCACCAGGTGGCAC | 55626 |
rs534024834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450654 | CACCATGTTGCCCAG[C/T]CTTGTCTCCAACTCC | 55626 |
rs534042835 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491044 | CAAAACATCTGTATC[C/G]AGGAGGGCAAGAAGG | 55626 |
rs534098099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578100 | AGTCTAGCCTGGAAG[A/G]AAGTGTGTCTCAAAT | 55626 |
rs534103289 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427892 | CGAGTGCCTGTAGAC[A/C]CAGCTAATCAGGAGG | 55626 |
rs534111284 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452748 | TCTAATCTGAAATCA[A/C]AGTCAATGTATCCTA | 55626 |
rs534114333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587677 | TTCCCTCTGTCAGCC[C/T]TTGTTTATTTCCTTC | 55626 |
rs534124404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428977 | GGCAAACTGTTCCTT[A/C]ACGTAGCCTCGGGAC | 55626 |
rs534125955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530283 | GTATACAAAGCACAC[A/C]GCACGCTCTACACCA | 55626 |
rs534144701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420233 | AAATGTAAGGAACTC[A/G]TTAAGGCTCCTTAAA | 55626 |
rs534165376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474511 | CTCCTGCCTCAGCCT[A/C]CCGAGTAGCTGGGAC | 55626 |
rs534165964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515437 | GAGATCGCACTACTG[A/C]ACTCCAGACTGGGTG | 55626 |
rs534177602 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506828 | ATGAATGGCTAGAAA[A/G]GTCAGAAGCAGCAGA | 55626 |
rs534179905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412444 | CGTGCCTCACCACGC[C/T]TGGCTAATTTTTTTT | 55626 |
rs534180367 | in-del | -/GTGA | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557545 | GGCACAGTGGCTCAC[-/GTGA]ACCTGTAATCCCTGC | 55626 |
rs534186134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413235 | CTTGGCTACTGACTG[A/G]AGAGGTCCACTGCCA | 55626 |
rs534190629 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526671 | CAGATGACTCTAGAG[-/A]AAAACCCAAGGAAGA | 55626 |
rs534216972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577255 | TGTGATGTATACACA[C/T]AATGGAATATTATTC | 55626 |
rs534235144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458942 | GAATTATACAGAACC[A/G]AATCATAATTTAAAG | 55626 |
rs534272527 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555124 | AAGATTCCATCCCAT[C/T]TCCACACACACATAC | 55626 |
rs534294309 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456380 | CTGACACTGCCAATA[C/G]TTAATCCCAGCAACA | 55626 |
rs534296709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446921 | CCAATGGGATCTTAC[A/G]GCTTGTTTTTTGTTT | 55626 |
rs534315258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409462 | CTCAGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 55626 |
rs534316498 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499965 | CTGACAGGGGAAATT[C/T]TTCTAAGATAGTTAA | 55626 |
rs534317128 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561571 | AGGATTTGAATTCAG[G/T]CTTTTCCTTCAGATA | 55626 |
rs534339427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546918 | TCTACTAAAAACACA[A/G]AAATGAGCCAGGCAT | 55626 |
rs534380712 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419448 | ACATTCAAATAATTT[C/G]GGAGATTAAAAGAGA | 55626 |
rs534396563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522624 | AAGAGGCAGTGTATC[C/T]TAATTCACTGATTTC | 55626 |
rs534421470 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455338 | ATTCCTCTTTCCCTC[C/T]CTCCCCAGTCCCTGG | 55626 |
rs534424881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487094 | AAAACCCCATCTCTA[C/T]GAAAAGTACAAAAAT | 55626 |
rs534440809 | in-del | -/AGA | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568364 | TCAGAAGGCTGAGGG[-/AGA]AGAATTGCTTGAACC | 55626 |
rs534454770 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583668 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAAACAAC | 55626 |
rs534466171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551983 | TAGTGAGCCAAGATC[A/G]CACCACTGCACTCCG | 55626 |
rs534484943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521863 | ACCTCAGGAAAAAAA[C/T]AGACATACTACAAAA | 55626 |
rs534497599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415712 | ACTAGTTTTCTTAGT[C/T]CAACACAACTTGGTC | 55626 |
rs534503294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568967 | ATGTGCGACCAAGAC[C/T]AGCTAATTTTTGTAT | 55626 |
rs534535661 | in-del | -/AAAT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439435 | TGAAGATGACATCCC[-/AAAT]AAATGGAGATAAATG | 55626 |
rs534537439 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573668 | AATCCTTTTTCTTTT[C/T]TTTTTTTTTTATTAT | 55626 |
rs534539886 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529731 | AACAGAATCCAGATA[A/C]CCGAATTGATATGGA | 55626 |
rs534546599 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418142 | GGAGAAACAAATTAG[-/A]AGGAGGAAAGGAGGT | 55626 |
rs534553731 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546895 | GGCCAACATAGTGAA[A/T]CCCCGTCTCTACTAA | 55626 |
rs534576689 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559192 | GTAATCCCAGCTACT[C/T]GGGAGACTGAGGTGG | 55626 |
rs534576951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512045 | ATTTTTAGTAGAGAC[A/G]GGGTTTTGCCATGTT | 55626 |
rs534597813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401013 | ACAGTGGGGCAGAAG[G/T]TAAGAAGAAAAAAGT | 55626 |
rs534603041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463061 | GTCTGGCCAATAATC[C/T]CCTTTTCTAAGAAGT | 55626 |
rs534604721 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548788 | GCTTGAGGTCAGGAG[G/T]TTGAGACAGCCTGGC | 55626 |
rs534605502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566450 | GTGGAGCTATTGATA[A/T]TATAACTTGGATGAA | 55626 |
rs534607382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567008 | GCAACAGAGTGAGCC[C/T]TGTCTCAAGAAAATA | 55626 |
rs534615751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558588 | AACCACTACCTACCT[A/C]GTATCTACTAATATC | 55626 |
rs534622373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447673 | TGAGACTGCACCACT[A/G]CACTACAGCCTGGGT | 55626 |
rs534637492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455524 | AGAATAATATTCAAC[A/T]CTACAGGAAAGTAGT | 55626 |
rs534637982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401544 | CAGCTCAGCTCTTCT[C/T]AAGTAGATTACCAGG | 55626 |
rs534648033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463606 | ACTCAATTTGTTAAC[C/T]AGGACTCAAAGTATC | 55626 |
rs534651646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503502 | CTGCAAGAATTACCA[A/G]TGTGACAGACAGACA | 55626 |
rs534661034 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490229 | TGCAATAGCTTTAAA[G/T]GTACTTACAGCTCTT | 55626 |
rs534662657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541461 | TTGTCAAACTGCAGT[A/G]TTCCAAAAGATAAGG | 55626 |
rs534670880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494957 | CTTCTGGCTAGGCCA[C/T]GAAGTATTATTACTA | 55626 |
rs534677429 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504253 | AGTAAGGGGGCAAGC[A/G]TAGCTGGAATAATTG | 55626 |
rs534701209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430350 | GACCTGAGACTGACT[C/T]TGCCTTGCTGAGGAG | 55626 |
rs534725989 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465834 | TTGCTTAAACATTCA[C/T]AGAAATTGTGCAACT | 55626 |
rs534735244 | in-del | -/T | 0.0107246 | 0.0724382 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541428 | ATATACATATATGTA[-/T]TTTTTTTTCTTTTCC | 55626 |
rs534750428 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588786 | ATCTCAAAAAAAAAA[A/G]AAAAAAAGTATTATG | 55626 |
rs534759177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543621 | GCATATCTGAATGAG[C/T]GCAGCTGACAAACCA | 55626 |
rs534778845 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438249 | GGGGCAGCTCCGGAG[A/G]GAGAAAAAACAATGC | 55626 |
rs534779494 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470907 | TTCATGGAAATTACA[C/T]TCTAGAGGGAGGAGG | 55626 |
rs534794691 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524861 | CAGGGGTACCTGAGC[C/T]GTGAGAATCACATGC | 55626 |
rs534797958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478350 | TCACTTACAGCAAAT[C/T]AGTAAGTGCTTGCAC | 55626 |
rs534808895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470283 | CCATATCTACAAAAA[A/T]TTTTTTAAAAAATCA | 55626 |
rs534814623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518938 | ATCACTAGGAATACA[A/G]TTTTTAAAATAGTCA | 55626 |
rs534815852 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495598 | AAAGAGATAAGACTA[C/T]ATGGAATGTAAAAGG | 55626 |
rs534833117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431266 | CTTGGTGGCAGATGG[C/T]ACCTACTGAGAATCA | 55626 |
rs534878873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556908 | TTGGGAGGCTGAGGC[A/G]GGTGGATCACCTGAG | 55626 |
rs534879700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519744 | CTCAGCAGGGCATTT[G/T]GTATTCAAGCTTTGC | 55626 |
rs534921987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399566 | GATGGGGTTCCACCA[C/T]GTTGGCCAGGCTGCT | 55626 |
rs534949220 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501000 | TCCTTTGCAAGGCAC[A/G/T]CAAGACAAAGATCTA | 55626 |
rs534980900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437934 | ACACAAACTTTAACA[C/T]GTATCAAACTCACCA | 55626 |
rs534997690 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462917 | CACCACCATGTCTGG[C/T]TAATTTTTGTATTTT | 55626 |
rs535030967 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425438 | ATTTTCCAATTCTTG[-/A]AAAAAAAGGATGTTT | 55626 |
rs535035109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437284 | TTGCATTTGTATTAT[A/G]TGATGACGATTCCAA | 55626 |
rs535038467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462990 | AACTCCTGGCCTCAA[A/G]TGATCCACCTACCTT | 55626 |
rs535051158 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423921 | GGCATGGGCCACCAC[A/G]CCTGGTTAATTTTGT | 55626 |
rs535057831 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462197 | CTATCACAAGTTAGG[C/G]ATGCGCGTAAACAAG | 55626 |
rs535069039 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578285 | TGAGCTCAGGAGTTC[A/G]AGACCAGCTGGGTCA | 55626 |
rs535101138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510388 | TATCTGCCCAATATA[C/T]AGAACTCTTCTAGCA | 55626 |
rs535112621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485784 | GAACAGAAAAGTTCA[C/T]TGACAAGGCCCAGTA | 55626 |
rs535122825 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475935 | CAGGAATTCTAAACC[C/T]TAACAGCTATTCTCC | 55626 |
rs535189279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565681 | CACCATACTCCAACC[C/T]GGGCTCAGAGCCAGA | 55626 |
rs535267124 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510171 | CGAGTCAATATTATA[A/G]TATCTGTGTATAGCA | 55626 |
rs535279900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501762 | CTCACATTTATTTCA[A/G]TGTTTAATATAAGAA | 55626 |
rs535286269 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492663 | TTCCTTCTCTAGAGA[A/C]TGACCAGAAGCAATA | 55626 |
rs535297812 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471217 | GAGGCTCGGGCGGGC[A/G]GATCACTTGAAATCA | 55626 |
rs535312809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557712 | ACTCGGAAGGCTGAG[C/G]TGGGAGGATAGCCTG | 55626 |
rs535323692 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453796 | AGTAAGGCACTTGGT[C/G]TATCATGTTTAGGCA | 55626 |
rs535353138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493173 | CCTTCCTCAGAAGAT[A/T]CCACACTGCCTGGAA | 55626 |
rs535358241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470106 | TATTATCTTCCTTAG[A/C]GCTAAAGAAAACATG | 55626 |
rs535358462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580171 | TCCAACAATGTACAG[C/T]GATTACTCCCTTCCT | 55626 |
rs535384395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572871 | GGCTGAAGTGGATCA[C/T]CTGAGATCAGGAGTT | 55626 |
rs535396816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565861 | CACTGCACCCTCCAC[C/T]TCCCAGGCTCAAGTG | 55626 |
rs535442314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416525 | AAGAACCAGTTTTCC[C/T]TTCTCCTAGGCCACT | 55626 |
rs535469646 | in-del | -/ATA | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535667 | CACTGACTGGCAGAG[-/ATA]ATAATATTACTGAGG | 55626 |
rs535478958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408847 | GTGCTCCTGCAACTA[C/T]ATCTTGATGGTGGTT | 55626 |
rs535497036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400971 | GAGTACTGGGTCAAC[C/T]CCATCTTCAGGTTTT | 55626 |
rs535525850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558401 | TAAAAATACCAAAAT[C/T]AGCTGGGCATGGTGG | 55626 |
rs535567920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446786 | TCCTACATTTTAACT[C/T]CAGGGTAGGTGCTCT | 55626 |
rs535574743 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530208 | GACGTCACTGTAGTC[C/T]CCAAGTGCTCCAAGA | 55626 |
rs535589649 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550468 | TACAATTAGCAATCT[A/G]TGGCAATTATTTGGC | 55626 |
rs535594205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559094 | CACCTGAGGTCAGGA[A/G]TTCGAGACCAGCCTG | 55626 |
rs535599594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437867 | ACCGGCTATAGCTTA[C/T]ACACCATTAGAAGTC | 55626 |
rs535600658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533939 | CAGAGATTTTGCATT[C/T]GCCCTTTCCTCTGTC | 55626 |
rs535630422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460583 | CCACCTCAGCCTCCC[A/G]AAGTGCTGGCATTAC | 55626 |
rs535650590 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414247 | AAAGATGCCTGGTGT[C/G]TCTGCAGCGCGGGAA | 55626 |
rs535662322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423754 | CTCACAGGCAGTGCA[C/T]CCATTTTTTTTTTTT | 55626 |
rs535665937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525933 | GAAATAGGCTAGGTG[A/C]GGTGGCTCACACCTG | 55626 |
rs535679004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508487 | GAACTCTGGAGACAT[G/T]AAAATTAAAGGGCAT | 55626 |
rs535702063 | in-del | -/AG | 0.00159617 | 0.0282053 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396138 | TCTGTCGTTCCTTCC[-/AG]TACATACTCACCCTG | 55626 |
rs535709655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415513 | AGGAGGCCTCAGAGG[A/C]GTCTTAACTTCCTTA | 55626 |
rs535732007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564981 | ATAAATCATGGCCAG[A/G]TGCAAAGGCTCATGC | 55626 |
rs535752215 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402112 | GGATGCTCCTTCTCT[A/G]GGACCTCACAGTGCT | 55626 |
rs535773142 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505653 | GGAAATGTAAATTCA[-/G]GTCATGCTAAAGCCA | 55626 |
rs535774598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444477 | TCCTTCTGAGGTGCA[C/T]TTCATACACAACCAC | 55626 |
rs535780068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526897 | CATGAGGTTAGTTTA[C/T]AGCCAAAATCACATC | 55626 |
rs535803359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545068 | TGAGGTCAAGGCTGC[A/G]GTAACTTGGGCCCAT | 55626 |
rs535831748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500835 | TCTCACCTCTCCCCA[A/C]ATACTCTCTCCCTTT | 55626 |
rs535842805 | snp | A/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481325 | GGGGAAAGGATCTGC[A/G/T]ACAAGGATATAAGAG | 55626 |
rs535856984 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460687 | TATAAAAGATAAAGT[A/G]CAACCATATAAACCA | 55626 |
rs535900899 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492613 | GTGACAGGGAAACAA[C/G]CTTTGCCACATATAA | 55626 |
rs535901329 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583673 | AAAAAAAAAAAAAAA[A/C]AAAAAACAACAAAAC | 55626 |
rs535907295 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493044 | ACAGGGCGAGACTCT[G/T]TCTCAAAAATAAATA | 55626 |
rs535936844 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554047 | CGGTCAAACTGCCAC[A/G]TAAGTGATTAATTAC | 55626 |
rs535957891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593758 | CTGCCCACCCGCCGG[C/G]GCCAAGGTCTTCTCA | 55626 |
rs535977674 | snp | A/C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532807 | ATAAGAAATACTTTA[A/C/T]ATATCTTACATTAGT | 55626 |
rs535981172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427284 | AAGTCTGGATCCCAA[C/G]TTTTTTCTATGGTTC | 55626 |
rs535985035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533153 | GGGCTACAAAGCGAG[A/T]CTCTGTCTCAAAAGA | 55626 |
rs535985197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434630 | TCCCTTATTCCTGAC[C/T]GTCGTAACAGGGGCA | 55626 |
rs535988125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541314 | CACCCCAAGGTGAAA[C/G]TCCACCTGGAAGGTC | 55626 |
rs535998001 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538235 | TGGTATACGACATCC[C/T]AGCTCATTTAAAAGT | 55626 |
rs536034349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568127 | CACTCCAGCCTGGGA[C/G]ACAGAGTGAGACTCT | 55626 |
rs536054396 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517326 | CTGATTTTTGTATTT[C/T]TAGTAAAAACAGGGT | 55626 |
rs536079391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402632 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCATGA | 55626 |
rs536104063 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403443 | CCATGGTGCTCTCCA[A/T]ATAGTGGGGCACAGC | 55626 |
rs536116222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509213 | CATTCTTCAAACTAC[A/G]GCTTTAATATCTTGC | 55626 |
rs536125455 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500183 | AGCAGGCATTGACAA[A/G]TGATCTCAATGCCAG | 55626 |
rs536137682 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481071 | ACTTCCCTGTGCCTG[A/G]GTCTTGACTATTAAT | 55626 |
rs536140536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461333 | ATGTCAATAACTATT[A/C]AATTTTGGTTGTGGA | 55626 |
rs536143326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561270 | CCTGTAATCCCAGCT[A/G]CTCGGAAGGCTGAGG | 55626 |
rs536157422 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46395924 | TTTCGGCCACTGTAG[A/G]GAAGACACAGTCAAG | 55626 |
rs536166811 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440969 | GTGGTAATTCATAAA[C/T]CAAAATCAACACAGA | 55626 |
rs536177310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452509 | AACTTTTCTCTTATG[G/T]ATTATCTGAGCTCTC | 55626 |
rs536189786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553103 | GCCTGCCACCACACC[C/T]GGCTAATTTTTGTAT | 55626 |
rs536203549 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462760 | AATTCACCCCCCTCC[-/T]TTTTTTTTTGAGACA | 55626 |
rs536203672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422334 | ATATGCTAGAAAGAA[G/T]AAATTTCTTAGAGTT | 55626 |
rs536212107 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539075 | CTAGTGGTTACAGAC[A/G]AAATTATCTGATATC | 55626 |
rs536238245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496983 | CAGACGTGATGGCGA[C/G]CGCCTGTAATCTCAG | 55626 |
rs536250766 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592969 | CAATGTAGACAACAA[C/G]GTTATCAGGAAACAA | 55626 |
rs536253212 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484922 | AGTGCTGGGATTACA[G/T]GTGTGAGCCACTGTG | 55626 |
rs536265382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537524 | GCACCCTACCGCAAG[A/G]AGCCACAATACCCTG | 55626 |
rs536265617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425964 | ATTCTGGCTAACACG[A/G]TGAAACCCCGTCTCT | 55626 |
rs536295064 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578547 | TATCATATAAATATG[A/G]CTAATTAGACTCTGG | 55626 |
rs536297660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409992 | GCATCCTTCTCCAGG[C/G]CCTATCTTCTCTCCT | 55626 |
rs536301295 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410135 | TTTCTCAAATGAAAC[-/TG]TACACAAAAGATCAA | 55626 |
rs536313448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489921 | GAGTCAGGAAGACCC[C/G]GTTTAAAATTCCAGG | 55626 |
rs536315794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520841 | CGATTTCCTGACCTC[A/G]TGATCCGCCCGCCTC | 55626 |
rs536345047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472385 | ACCGCAAATAACCTG[A/G]GTGCTAGGACATATA | 55626 |
rs536348042 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553068 | CTGTTTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 55626 |
rs536380308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529695 | GCTGACTGTTAGGTG[A/G]GAATGTGAGCCTGTT | 55626 |
rs536404231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457391 | AATACAACACTCAGT[C/T]CAACTTCACATTCAC | 55626 |
rs536405127 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591873 | AAAAACACACACACA[A/C]AAAAACGCTCTCTTA | 55626 |
rs536411814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447489 | GCAATGAGATGAGAT[C/T]GCACCACCACACTGC | 55626 |
rs536415307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560357 | TGAGTAAATTCTAAT[G/T]ACTGTAACTATAATA | 55626 |
rs536434964 | snp | C/T | 3.91321e-05 | 0.00442318 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494221 | TGAAAAAAATAAAAA[C/T]ACTACACATAAGAGA | 55626 |
rs536436060 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409455 | CGCCCGCCTCAGCCT[A/C]CCAAAGTGCTGGGAT | 55626 |
rs536487824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504649 | AGGAGAGGAAGCCTG[C/T]CCAGGAAGATGGTCA | 55626 |
rs536504812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495917 | TGAAGTTAAAAAGGA[A/T]CCTAAGCGGGGGAAA | 55626 |
rs536543098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457902 | CAGGGCAAGACTCCG[G/T]TGCAAAAAAAAAAAA | 55626 |
rs536579222 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588954 | ATGGAAAAATAGTAT[C/T]TCTATGGGGAAATTA | 55626 |
rs536655403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440894 | ACTGGCAAAGTCTTA[C/T]AATATCATACAGACA | 55626 |
rs536678361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574992 | TGTTAATAGTTGTTG[C/T]CAATTCAAGAAAGCT | 55626 |
rs536678416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582611 | AGGGGAATGTGGAGC[C/G]AGGTTGTTTGGACGC | 55626 |
rs536680328 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471720 | GCAACCTCCACCTCC[A/G]AGGTTCAAGCAATTC | 55626 |
rs536728154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553019 | GGGGCGATCTCGGCT[C/T]ACTGCAACCTCTGCC | 55626 |
rs536740815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575381 | AGCATAGCTTGAACC[C/T]GGAAGGTGGAGGTTG | 55626 |
rs536758009 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567647 | ATTACAGGCGTGAGC[C/T]ACCGTGCCCAGCCTT | 55626 |
rs536768726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489090 | TTTTATTACACTTTA[A/C]GTTTTAGGGTACATG | 55626 |
rs536769458 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480306 | CATTATTTTACCTAC[A/T]AAACCATCTAAGATC | 55626 |
rs536775655 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592920 | TAAGATTTCCAAAGA[C/G]GCTGGGGAGAAGGAG | 55626 |
rs536782121 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549191 | TGGCAACTAGCAGCA[C/T]AATACACACAAGTGT | 55626 |
rs536794554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441343 | ATATGGCAAAACCCC[A/G]TCTCTGCTAAAAATA | 55626 |
rs536857778 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514797 | GGATTTTTTCATGAT[C/T]TCATAGGAACACATA | 55626 |
rs536863364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520627 | TTGAGACGGAGTCTC[A/G]CTCTGTCACCAAGGC | 55626 |
rs536872224 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403381 | CGACCATCTTCACCA[C/G]ACAAAACAGAGGCTC | 55626 |
rs536872763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543466 | ACCTCCAAGTAAATC[A/G]AGAAAAACTAACCAC | 55626 |
rs536873606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567141 | CAGTGGTCCCATCTC[A/G]ACTTACTGCAGCCTC | 55626 |
rs536921196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512984 | AGAGACACAAATAAA[C/T]GAAGAGCTGCAAAAC | 55626 |
rs536936985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559225 | GAATTGCTTGAACTC[A/G]GGAGGCAGAGGTTGC | 55626 |
rs536941553 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464751 | ACTACCTCCTTTATT[A/G]AACACCGAGACAAGG | 55626 |
rs536949158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560233 | CCTCTACTGCACACA[A/G]GCAGCAGCATTAGTT | 55626 |
rs536952041 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572918 | AACCTGGTGAAACTC[C/T]GTCTCTACTAAAAAT | 55626 |
rs536952928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523489 | CATGTCAATCAATAC[C/T]ACCCTGAGGAGGATT | 55626 |
rs536966809 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581434 | TAACACATGAAACCC[A/C/T]GTCTCTACTAAAAAT | 55626 |
rs536974683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479610 | GCTGAGGCAGGAGAA[C/T]CACTTGAACCCAGGA | 55626 |
rs536982376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447721 | TTGTAGATAGATAGA[C/T]AGATAGATAGATAGA | 55626 |
rs536984927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535765 | GAGCAAGCTGTATTC[A/G]ATAGGAATGGGGTAC | 55626 |
rs536985197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432407 | AAGCTTGAAAAGTGG[C/T]TCAGTGTAGTTGGAC | 55626 |
rs537000756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534734 | GCTGCAGTGCAGAGG[C/T]GCAATCATGGCTCAC | 55626 |
rs537004762 | in-del | -/A | 0.34303 | 0.232046 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568772 | GCAAAACTCCATCTC[-/A]AAAAAAAAAAAAAGG | 55626 |
rs537006928 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538615 | TTCTCCTGCCTCAGC[C/T]TCCCACGTAGCTAGG | 55626 |
rs537028877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504475 | TGTCATGGGCAGCCA[C/T]ACCTTTACCCTGCTT | 55626 |
rs537053542 | in-del | -/CTCA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477536 | TTGTAGAGATGAGCT[-/CTCA]CTATGTTGCCCAGGC | 55626 |
rs537062035 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517408 | CCCGCCTCGGCCTCC[C/G]AAAGTGCTAGGATTA | 55626 |
rs537064787 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433120 | TACAGCTTGTTCCCT[-/CA]CACACACACACACAA | 55626 |
rs537067063 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424731 | TCTAATCCTAGCTAC[C/T]TGGGAGGCTGAGGTG | 55626 |
rs537080671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486925 | TAAATAAATAAATAA[A/G]TAAATAAATAAATAA | 55626 |
rs537089845 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495804 | CATTTAAAAGTACAA[C/T]TGAATTCATGATAGC | 55626 |
rs537092716 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410012 | TCTTCTCTCCTCACC[A/C]CAAGTGTGCCCAGGC | 55626 |
rs537106314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416866 | ACACTCTCCACCTGG[C/G]TGAGGCTGGAAACTG | 55626 |
rs537108908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488264 | AGCTTAAGACCAGCC[C/T]GGCCAATATGGTGAA | 55626 |
rs537130163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544318 | ACCTTAAGCACACCT[C/T]TGCTCAAATACAAGA | 55626 |
rs537170409 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427566 | CACATGGCTGGGCCT[C/T]GCCCCCAGAGTTTCT | 55626 |
rs537183762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536570 | GTAGTCAGGCTAAGA[A/G]GACTGCTACTTTCCT | 55626 |
rs537184033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527896 | TATGGAAAACAGTAT[A/G]GAGGTTCCTCAAACA | 55626 |
rs537199226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433158 | TAAAAATAAGCATTT[A/C]ATTGGGTCCTTTATG | 55626 |
rs537200498 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584538 | AATAATAATAAAAAG[-/A]AAAAAAAACAAAAAA | 55626 |
rs537207885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463749 | ACATAGCACAGTACT[C/T]GGGGCCCTAAGAAAT | 55626 |
rs537215381 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549600 | AACCACAATAACAAT[A/G]CTATACCAATTATCA | 55626 |
rs537234459 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511105 | AAAAGGAGGATAAAT[A/C/G]ATGGTCGTTAAGTAT | 55626 |
rs537251038 | in-del | -/AAAC | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515473 | TGAGACTGCATCTCA[-/AAAC]AAACAAACAAACAAA | 55626 |
rs537289787 | snp | A/G | | | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430648 | GAGATCATCTCTTGG[A/G]GAGAGATGTCACTTA | 55626 |
rs537294641 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502827 | GCACTTTGGGAGGCC[A/G]AAGTGGGCAGATCAC | 55626 |
rs537315590 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503714 | GCAAATTAATTAGAA[C/T]AGTTAAGAAAATAAA | 55626 |
rs537318065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401622 | CCCCCAGAGAGCCCC[A/G]GATGGGCTTTCCCAG | 55626 |
rs537346926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456651 | AGCTTTTATTGTTTG[C/G]TGGAAGCACAAGCGA | 55626 |
rs537387168 | snp | C/T | 3.29728e-05 | 0.00406021 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542598 | TGCCAACCCTGATGC[C/T]GGAAAACCCCTCCCT | 55626 |
rs537391533 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440815 | TTTTCCTTGTCCAAT[A/G]AAGATACCAAGACTG | 55626 |
rs537391544 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480828 | AGCTAAAGCTGCTGA[C/T]AGAAGAGGAAAATTT | 55626 |
rs537428938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428645 | ATGCAAAAGAATCCT[C/T]TCCAATTTTACTGAG | 55626 |
rs537433853 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454644 | CAGTCCCAGCTACTT[A/G]GGAGGCTGAGGCAGG | 55626 |
rs537465334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421440 | GATCCTGATAAGCAC[C/T]TGCTTGCTTAGCACA | 55626 |
rs537468724 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416207 | ATTAGATTTCTCTTA[A/T]GAACTGTTAAGAAAA | 55626 |
rs537509290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413433 | CCAGACACTGTACCA[A/G]GGAATAGAGTTGAAG | 55626 |
rs537512076 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458159 | AACAGCACTTGTCAT[-/A]AAAAGATAGCTAATT | 55626 |
rs537534508 | in-del | -/A | 0.208169 | 0.246476 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483020 | CTCAAAAAAAAAAAG[-/A]AAAAAAAAAAAAGAG | 55626 |
rs537535554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471161 | GAAATTTGAATTCAC[A/G]CCAGATGCAGTGGCT | 55626 |
rs537543038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578037 | TGGGAGGCTAAAGCA[A/G]GAGGAAAGCTTGAGT | 55626 |
rs537553249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571102 | AATCTCTCACATTTG[C/T]CTCCTTACAATGGTT | 55626 |
rs537563066 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507883 | AGCTTTCCACGGTCA[A/C]TGGACATGCAAAAGG | 55626 |
rs537565780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574757 | GAATACTTTGAAAAA[C/T]ACTGGTTTAAAACTG | 55626 |
rs537582290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524472 | TCTGAGACTAACCAA[A/G]AAAACTCTGAGTAAC | 55626 |
rs537595669 | in-del | -/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594192 | ATCATAAGCCACGGG[-/T]TTAAAAAAGAGCCTG | 55626 |
rs537598419 | snp | C/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452094 | ACTTTAAATAGGTGG[C/T]CTGTATGGTAGGTGA | 55626 |
rs537606919 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568903 | CCTCCGCCTCCCAGG[C/T]TCAATCGATTCTCCT | 55626 |
rs537611464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445998 | AAATGGGAACACAAA[C/T]GATTAAGACTCCCAA | 55626 |
rs537613272 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455210 | CTTTTTCTTTTTTTT[A/T]AATTGTGCTAAAAAG | 55626 |
rs537625241 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454815 | ATTAAAGACACAGCA[A/G]TAGATAGAGCCTTCT | 55626 |
rs537637749 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507469 | GAGCGAAAGAGCGAG[A/G]CTCCGTCTCAAAAAA | 55626 |
rs537649605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446709 | TGTCTCCAGACACTG[C/T]CGAATGTCCTCTGGG | 55626 |
rs537702870 | snp | C/T | 0.00112878 | 0.02373 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494176 | GGGCATTGCGTGGAG[C/T]TCGGTGCCTGGATCT | 55626 |
rs537706584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490762 | GCTAACCACCTAGAC[C/T]TGGAGCTACAGGAAG | 55626 |
rs537751028 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463166 | GTTACAGTTCTTCTG[C/T]TCAATTTCCTGCCCT | 55626 |
rs537755672 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436672 | AAACAAAAACAAAAC[A/T]CGGCAATATCCCTCT | 55626 |
rs537769427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483325 | CCCAGTCACCTATTT[C/G]CAGGAGTTTCTTTCC | 55626 |
rs537793965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538832 | ATAACCTACTTTATT[A/G]AGTGATTAATAATAT | 55626 |
rs537808952 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587494 | AAATATCAGACACAT[-/A]TTACATGTAGCAATC | 55626 |
rs537816748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465997 | TAAAGTACAGAGTCT[G/T]GAGACATGCCTAGAA | 55626 |
rs537872238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428888 | ATGGCAGGCACAATC[C/T]CTGGGGGCAGATGAA | 55626 |
rs537876205 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586823 | ATTTGAACCAGGCTG[C/T]TTGGCTCCAGGACTC | 55626 |
rs537880801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483952 | ATGGGTTATTAACTT[A/C]CAGCATTCATACTGC | 55626 |
rs537882583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577604 | AGATGGCTAAATTTA[C/T]GTGAAGTGAATTTCA | 55626 |
rs537890980 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397322 | ATCTTCCTCTCCACC[A/C]TGACCCTCTTCCTCC | 55626 |
rs537918481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404382 | AAATCTGGGCTCAAA[A/G]AGAGCCCTGATCCCT | 55626 |
rs537933447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475957 | CTATTCTCCAGGTGT[C/T]GGAAAAGAACACTGT | 55626 |
rs537948310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458789 | GATACTGTCCAGCCA[C/T]GGGATTAGAATATTC | 55626 |
rs538006189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554970 | CAGGCATGGTGGGAG[A/G]CCAAGGTGGGAAGGT | 55626 |
rs538011588 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545910 | CATCCTCTGTAAAAA[C/G]ATGTAGAAGATCAGC | 55626 |
rs538038407 | in-del | -/G | 0.00159617 | 0.0282053 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396139 | CTGTCGTTCCTTCCT[-/G]ACATACTCACCCTGG | 55626 |
rs538047214 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434680 | TCAGATGCTTCTGCA[A/G]TGTTACTAGCCAGCA | 55626 |
rs538047301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443370 | GGTGCAGAAATGGCA[G/T]GTAGATAACAACTGC | 55626 |
rs538079085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427169 | AAGTCAAAAGAGCCT[A/G]TATTTGTGAAGTTAT | 55626 |
rs538085538 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458635 | AAGATCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 55626 |
rs538086550 | snp | C/G | 0.0471551 | 0.14613 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583397 | TAAAACCATAAAAAC[C/G]CTAGAAGAAAACCTA | 55626 |
rs538088691 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481174 | AAGAGCAGCACGGTG[C/T]AATTACACCCAAACA | 55626 |
rs538099496 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584908 | GAAACCCTGTCTCTA[C/T]TAAAAATACAAAAAT | 55626 |
rs538126992 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594918 | AGAGGAAGGGTGTAA[A/G]AAGGAAACAAGATAG | 55626 |
rs538160361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585991 | GTATTTTTAGCAGAG[A/G]CAGGGTTTCTCCACG | 55626 |
rs538168307 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595821 | GAACCCCGTCTCTAC[C/T]AAAAATACAAAAAAT | 55626 |
rs538189061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435613 | ATACTAATCTCTAAC[C/T]CTACCAAGAGAGGAA | 55626 |
rs538194602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458105 | CTCTGAAACTTGAGA[A/T]GTCCCCAGAACCAGG | 55626 |
rs538224352 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488374 | GGCAGGAGAATCGCT[C/T]GAACCCAAGAGGCGG | 55626 |
rs538231904 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449105 | TGGTGAGGAACTAGA[C/T]ACTTTCCCCCTAAGA | 55626 |
rs538233393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514093 | CAGCATCTTGCCTGC[C/T]TTTCCTAGGAACAGG | 55626 |
rs538238319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420172 | TGACTGCCCTGTGGC[A/G]GCTGCATTAGGAACC | 55626 |
rs538241363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434634 | TTATTCCTGACCGTC[A/G]TAACAGGGGCATGCG | 55626 |
rs538266224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403648 | AGCTTGCTGTAGAGT[C/T]AAATTCTGGGAGAAG | 55626 |
rs538269348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427994 | TGCCTGGGCGACAGA[C/G]GGAGACTCCATGTCA | 55626 |
rs538274090 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410240 | GGAAGGGATGGGCCT[C/T]CAGCCAGCTGCTCCC | 55626 |
rs538276952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412304 | ATAGTTATTATACTG[C/T]ATTGCATCTCACTCT | 55626 |
rs538298573 | in-del | -/T | 0.0554779 | 0.157039 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423758 | CAGGCAGTGCACCCA[-/T]TTTTTTTTTTTTTTT | 55626 |
rs538306149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428584 | TTCCACTTCTTCTTC[C/T]TCTTCTTCTTTTTTT | 55626 |
rs538344574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563110 | TCTTAAATAATTATA[C/T]ATAACATTTGAGAGT | 55626 |
rs538380405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530934 | TGTAGCCCAGGCTGG[A/G]GTGCAGTGGCATGAT | 55626 |
rs538406943 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526034 | AACATGGAGAAACCC[C/T]ATCTCTACTAAAAAT | 55626 |
rs538422684 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505703 | GCGCACAGGTGGGCT[C/G]GGGGGAGCATAAGGA | 55626 |
rs538437911 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576640 | CTAACATGTAATCTA[C/T]ATCCTTTATGTTGCA | 55626 |
rs538445644 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488856 | CTCCCAAAAAAGTAA[C/T]AGGTCAAAGAAGTCG | 55626 |
rs538450449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403512 | CTCATTAATTCCATG[C/T]TTGCCCTGAATGCCC | 55626 |
rs538457087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529617 | GACATCAGCCTAGCA[C/T]AGACTAAGGCATCAA | 55626 |
rs538501323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419271 | TGGCCTCACAGTCTC[C/T]TTCACCACTCTCTGA | 55626 |
rs538507728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497771 | GTTTTAGTACTGGTA[C/T]ACAGAAATCCTGGAC | 55626 |
rs538508787 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470206 | CGAGCACTTTGGAGG[A/C]CAAGCTGGGAGGATC | 55626 |
rs538514202 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480560 | TCTTTGCTCTAGATC[-/A]ACATGTGTACCTTAA | 55626 |
rs538518081 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396723 | ACTGACACCCACAGG[C/T]GCTGCTCTGAGGGCC | 55626 |
rs538529735 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576046 | TCTCAAATCACACAC[A/T]CTATGGAAGCTGCAG | 55626 |
rs538534148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553938 | TCCTGAATAGGCTAA[A/G]GATGAACTAACTGGA | 55626 |
rs538567211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530195 | CAGCACACATACAGA[C/T]GTCACTGTAGTCCCC | 55626 |
rs538573527 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564484 | TACCTAAGTGAAGGA[G/T]AGATTCAAAATCAAA | 55626 |
rs538587489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545870 | TTTAAGGTAAAATGA[C/T]TATGTCTAGGGACTA | 55626 |
rs538603154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442341 | AGAGACGAGGTTTCA[C/T]CATGTTGGCCAGGCT | 55626 |
rs538610443 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46593982 | GGACAACTCAGCCCT[C/T]GACCCGGCGCCGCCG | 55626 |
rs538647351 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594683 | TTTGGGTTCAGAACC[C/T]GATAAAGTGTTGACA | 55626 |
rs538649836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435386 | TGTTATTGTCCCAGA[A/G]ATCAAAACCAAGATA | 55626 |
rs538656844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521629 | TCCAAATTGACATCT[C/T]TGCTCTAATGCAGAG | 55626 |
rs538659286 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445056 | TTGGTTCAAAGGGGC[-/A]AAAAAAAAGAAAAAC | 55626 |
rs538668158 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585125 | GGCGGTGCAAGATGT[C/G]CTTTGTTAAACAGAT | 55626 |
rs538696831 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400683 | TTGCAGAGACGGTTT[C/T]GCCGTGTTGCCCAGG | 55626 |
rs538697001 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439028 | GTAATCCCAGTACTA[C/G]GGGAGGCCAAGGCAG | 55626 |
rs538706008 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517970 | ATAATAAAGCCAATG[C/T]GGCAAAATGTTAACA | 55626 |
rs538729808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474648 | CCACCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 55626 |
rs538729902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482950 | GGAGGCGGAGGTTGC[A/G]GTGAGCCGAGACCAT | 55626 |
rs538734566 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465159 | ACAGCCCAGACCCTG[A/C]CAAAATTATTCAAAC | 55626 |
rs538743007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475228 | AATGCAAAGTATTAA[C/T]TATGAATAAGAGAAG | 55626 |
rs538746657 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554446 | AAGAAAAAAATCAAA[A/G]GATCAGGATTACCAA | 55626 |
rs538763147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522664 | TTTATTGAATTCCAT[A/G]ATGTTGAATTCTTAG | 55626 |
rs538792077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553199 | CCACCCGCCTCAGCC[C/T]CCCAAAGTGCTGGGA | 55626 |
rs538814010 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517989 | AAAATGTTAACATTT[A/G]GGGAATGTGGGTAAA | 55626 |
rs538817964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535937 | CCATTCACAAGTTAG[C/G]AACATAGCACACAGT | 55626 |
rs538821968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440750 | AGCACTTAGAAATAG[A/G]TGGTTGCTGCTGAAG | 55626 |
rs538828202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46591101 | CATAATAAAATATTC[C/T]TAAGATTGCTTCATG | 55626 |
rs538837219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441452 | CTGGGGGTGCGGAGA[G/T]TGCAGTACACCGAGA | 55626 |
rs538848048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46449919 | CAAAAATTAGCGGGG[C/T]GTGGTGGCGCATATC | 55626 |
rs538850349 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520721 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 55626 |
rs538859919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404227 | AATCTTGGTGCCTGT[A/G]GCAGGTGTGAGTACA | 55626 |
rs538862340 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433135 | TCACACACACACACA[A/C]AAAGCTTTAAAAATA | 55626 |
rs538874321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479719 | ACCCTGAGACACTAT[A/G]TGAAGAAGCACAGGT | 55626 |
rs538880815 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489251 | GGCCCCGGTGTGTGA[C/T]GTTCCCCTTCCTGTG | 55626 |
rs538936055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480226 | TGCAAAGTCCTTTCT[G/T]CCATGTAAAGTAACA | 55626 |
rs538963197 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593089 | ATACAGACTTTGAAA[A/C]GCAAAACAGCCAAGA | 55626 |
rs538979848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583195 | CCTCAGAAATAATGC[C/T]GCATATCTACAACTA | 55626 |
rs538983498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464836 | CGGATCACGAGGTCA[A/G]GAGTTTGAGACCATC | 55626 |
rs539003789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418459 | ACAACGTGCAGGTTT[C/G]TTACATATGTATACA | 55626 |
rs539010016 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476522 | CATAGATTAGAATAG[A/C]CAGAAACTTATTCAC | 55626 |
rs539012074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520857 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGTT | 55626 |
rs539013131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427102 | TTCAATTCAAGGGCA[A/G]GGAAGGAGAGAGTCA | 55626 |
rs539022607 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461459 | AAGGAAGGAAGCAAA[C/T]GAAAGCAAACAACTG | 55626 |
rs539040614 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410706 | TATTCTTCAGACACA[A/G]AGAAAGGAACTAAGA | 55626 |
rs539053844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419156 | CTTGTTTCTAGCTTA[C/T]ATAAATCACCGTTAA | 55626 |
rs539061033 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500566 | GAGACAAAGTCCAAA[C/T]TTCTCAGCCAGGCAT | 55626 |
rs539061626 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517439 | CAGGCGTAAGCCACC[A/G]CGCCCGGCTAGAAAG | 55626 |
rs539063974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575945 | TCTATTATTAATAAC[A/G]TGTTCCCATTTCTTC | 55626 |
rs539066221 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567707 | CTGATGACAAGATGA[C/T]CCCACCCCAACCAGC | 55626 |
rs539086451 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465135 | TATGGACAACTAGTG[C/T]CCACACCTACAGCCC | 55626 |
rs539119790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510336 | CAGAATCCTAAATTT[C/T]CAACCAACAGAAGTC | 55626 |
rs539148350 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401844 | GAGCTCTGGTTAAGT[C/G]TGCACCCTGTTCAAA | 55626 |
rs539148460 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469099 | AGTGAGCCGAAATCA[C/T]GCCACTGAACTCCAG | 55626 |
rs539165191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557752 | GGTCGAGGCTGCAGT[A/G]AGCCCTGATCATGCC | 55626 |
rs539170464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458044 | TCAGGAGCAAAAATA[A/G]GTGAGAGAGAGCATG | 55626 |
rs539188069 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559694 | AGGAGTATCAGTCAA[A/G]TTTATAACAAGAATC | 55626 |
rs539219796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501380 | AGTGCACCCTGTGAC[A/G]GAATGGCATCCTGTC | 55626 |
rs539230286 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591919 | TTGGAAACTTATCCA[A/G]CCCAGAATGACCTCA | 55626 |
rs539231183 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540551 | TCTTTCACATCTAGT[C/T]AAGTCTCCCTCTGCT | 55626 |
rs539239816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425678 | ATCCCTGTCTCTACT[A/T]AAAATACAGAAATTA | 55626 |
rs539259490 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505443 | AGAAGACCTGGACTA[A/C]TAATGTTGAGGTGAC | 55626 |
rs539277140 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484770 | CTCCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 55626 |
rs539300996 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588568 | ATCACCTGAAGTCAG[C/G]AGTTCGAGACCAGCC | 55626 |
rs539307661 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579093 | ACTTTAAAAGCCAGT[A/C]ATACCAAAATACAAA | 55626 |
rs539322492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472518 | AGTACCACACCCTCA[A/C]CTGTCAAGTGGACAG | 55626 |
rs539339866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476926 | AGCCTGGTCAAGATG[C/G]TAAAACCTTGTCTCT | 55626 |
rs539352226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477793 | AAAGATTGATTGGTG[A/G]GGCCAGGCATAGTGG | 55626 |
rs539355479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528834 | CAAAGAAAAGATAAA[C/T]GCCACCTTGCTGAGG | 55626 |
rs539356060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469229 | CTAACGTATTTTCAT[C/T]GAATATGGTAAAATG | 55626 |
rs539356898 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575472 | AAAAAAAAAAAAAAC[C/T]AGGTAGCTTATAAAC | 55626 |
rs539376425 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579571 | AAATATCTTCATACC[C/G]TCACCCTTTTCTCTC | 55626 |
rs539383254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426042 | GTCCCAGCTACTCGG[A/G]AGGCTGAGGCGAGAC | 55626 |
rs539386031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469898 | GCCCAGACTGGTCTC[A/G]AACTCCTGGCCTCGG | 55626 |
rs539403851 | snp | A/G | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594783 | TATGGATTAATATGT[A/G]CATCCTAGATGTGAT | 55626 |
rs539414960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556221 | TAGGACTTTCCTACG[A/G]CCATTTCAGGATACT | 55626 |
rs539418100 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525868 | AGTGAGCAGAGATCA[C/T]GCCATTGCACTCCAG | 55626 |
rs539421610 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451332 | GAATGTGTCTAGGGA[C/T]AAAATCATAATAATC | 55626 |
rs539435082 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414885 | CTTAGTCTACTGCCA[A/C]GTGGGTTTTAGTACC | 55626 |
rs539437106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423733 | GTTCTGACAGAGCAG[A/G]ACTAACTCACAGGCA | 55626 |
rs539450003 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532595 | GCACCCACCACCATG[C/T]CCAGCTAATTTTTGT | 55626 |
rs539490006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408051 | GCTGATGATAGGCCA[A/G]GCTGCAGCCAAAATG | 55626 |
rs539503097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491727 | CATTCTGCATCCTTT[G/T]ATAGATTTTCTCAGA | 55626 |
rs539525525 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538117 | CACCTGTTTGTCTTA[A/G]TGATTTACATCAGAA | 55626 |
rs539526470 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400115 | CAGCTTTCTGCTCAG[C/T]TCTTGGTAGGGTGAG | 55626 |
rs539528871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565766 | TAGCCAAAAAATTTA[C/T]AAAAATTCAGATTTT | 55626 |
rs539532994 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46596032 | TCGCTCTGTCGCCCA[G/T]GCTGGAGTGCAGTGG | 55626 |
rs539540207 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566394 | CGGCACTCCAGCCTG[A/G]GTGACACAGCGAGAC | 55626 |
rs539561805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484141 | ACAAGGGGCCCAAGG[C/T]AGGGGATATCTAATC | 55626 |
rs539593705 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445083 | AAACAAAAAAAAAAA[A/C]ACAAAAAAAAACTTA | 55626 |
rs539606648 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437042 | TACATAGATCCAGCT[C/T]GTGTGTGTTAACGTT | 55626 |
rs539631684 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407111 | TTGAACTCGGGAAGC[A/G]GTGGTTGCAGTGAGC | 55626 |
rs539640926 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421209 | ATGTTGAGACCCCCG[A/G]GTTGTTGCTAGCCAC | 55626 |
rs539644174 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523696 | CGCTTTACCCAGATG[A/C]GCTTTATTTAGAAAA | 55626 |
rs539657855 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533094 | CTTGAGCCCCAGAGG[G/T]GGAGGATGCAGTGAG | 55626 |
rs539663457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413330 | CTTTCTGCTCCCCAC[A/G]AACAGGTCTAATTCT | 55626 |
rs539686259 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481852 | TTTAGCCTCAGTTTC[C/G]TCATCTGTAAAAATG | 55626 |
rs539700924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405166 | CCACCACCCTACTTC[A/C]CCTGACTCCTATTCA | 55626 |
rs539718837 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576494 | GGACCTCAGCAAGTC[A/G]TCTCTGTCACCTCCC | 55626 |
rs539741757 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459774 | CACACACACACACAC[A/C]CCCTGGAATACCACA | 55626 |
rs539750709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564118 | CATTGCACTCCACTC[G/T]GGGCAACAAGAGCAA | 55626 |
rs539754509 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444210 | GTAACACAATAAAAA[C/T]TTATGAGCCTCACTT | 55626 |
rs539756180 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572151 | ACCGAAAATACAAAA[A/C]TTTGCTGGGCGTGGT | 55626 |
rs539757401 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537738 | CACTGAAATACACAC[A/T]GTATGCTTATCAATA | 55626 |
rs539799754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499317 | ATTCTTTCCTGCTGT[A/C]TTTTCCCATTCTAAG | 55626 |
rs539820276 | snp | A/G | 0.000263696 | 0.0114795 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508273 | AGGTGGAAGAACGGA[A/G]ACGGTTCTGTTGGTA | 55626 |
rs539844431 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493157 | GGCGTCTCCCTCTTT[G/T]CCTTCCTCAGAAGAT | 55626 |
rs539851539 | in-del | -/G | 0.0023933 | 0.0345097 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396063 | GGGATCCAGGTTTCT[-/G]GCCAGTTACATCACT | 55626 |
rs539858261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405414 | GTAAAAGCTCAGTGA[A/G]ATCAAATCAGAAAGG | 55626 |
rs539898097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556806 | AATGCTTATAGTAGA[A/G]TAATAGCTTCATTCT | 55626 |
rs539900531 | snp | C/T | 3.63808e-05 | 0.00426487 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397952 | CCCTCACCTGGCAGA[C/T]ACAAAGCAGAAGAGA | 55626 |
rs539935928 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532675 | CTCCTGACCTTGTGA[C/T]CCGCCCACCTTGGCC | 55626 |
rs539939743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492460 | GATTCTCCAAAACAG[A/G]ATGTCATTTTAAAAC | 55626 |
rs539948029 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568560 | GGTGGATCACCTGAG[C/G]TCAGGAGTTTGAGAC | 55626 |
rs539960389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548566 | TCTAATTGCAAATAC[A/G]ATTCTAGCTCAAAAG | 55626 |
rs539989846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443682 | CAATACTGGGATTAG[C/T]AGTGGGGAGAGAAGA | 55626 |
rs540023812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524254 | AAGGGGAGTGGAATG[C/G]CCCCCAGAAATGTGG | 55626 |
rs540033034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585345 | CACCCAAGAATGATC[A/C]ATAAAAATAAATAAA | 55626 |
rs540053289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523067 | AGCTCATATCTGTCC[A/G]TGGAATGAGGTTTCT | 55626 |
rs540060383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420817 | CAACAAAGTCTCCCC[G/T]GAAACTACAATGATT | 55626 |
rs540074108 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426247 | AGAAACCCAGGGCAC[A/T]TGAGATTTCAAAGTA | 55626 |
rs540102387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516323 | TGGAGTAAAAATAGG[C/T]TTCTCCAATTGGTGT | 55626 |
rs540102613 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507659 | TTAAGGTTCCTGAAT[A/C/G]GGGGGTAAGAGTAGG | 55626 |
rs540103189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468340 | AGTCCAGGAGTTTGA[G/T]AACAGCCTGGGCAAT | 55626 |
rs540164291 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523945 | ATGATCTAGGCTCAC[C/T]GCAACCTTCACCTCC | 55626 |
rs540164343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515200 | CCTTCTTGGCTGGGC[A/G]TGGTGCCTCACGCCT | 55626 |
rs540176526 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496985 | GACGTGATGGCGAGC[A/G]CCTGTAATCTCAGCT | 55626 |
rs540183642 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491028 | TAAGTTTAATAAAAA[A/G]CAAAACATCTGTATC | 55626 |
rs540213570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441877 | TTGAAAGAAGCATTA[C/T]GAGATTTATACTATG | 55626 |
rs540233171 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483069 | TTACCAGGCATCCCT[A/G]AAGAATGTAGCCCCA | 55626 |
rs540281844 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490376 | AGAAGAGATGAATAA[C/T]AGACTATCAAAACAC | 55626 |
rs540291386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508568 | ATCACCAGTGTTTCT[G/T]TTCTGAGATAAGGCA | 55626 |
rs540336613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497540 | GGAGAGGACCCAGCA[C/T]GACCAGGAAAATGTG | 55626 |
rs540344187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451774 | ATCATCCTGGAGACA[C/T]AATTACTATCTTTCT | 55626 |
rs540345063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482465 | AGCCACTGGCACTAA[C/T]TATATCAATATGGTA | 55626 |
rs540389730 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514597 | TGAATGTGTCTGAGG[-/T]TGGGGTGTATTTTAC | 55626 |
rs540427999 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457797 | ATCCCAACTACTTAG[-/AA]GGCTGAGGCATGAAA | 55626 |
rs540431998 | in-del | -/AAATA | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526232 | AAAAACAATAATAAT[-/AAATA]AAATAAAATAAAATA | 55626 |
rs540441766 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413915 | TGTTTGCTCTGGGTT[C/G]TTCCTGGGAACTACA | 55626 |
rs540444542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531380 | GCTCAAACAGAGTGA[A/C]CTTCTTGGGCAGGTG | 55626 |
rs540501551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458221 | AAACATTAACACCAG[G/T]AACACAGTGGAAAAG | 55626 |
rs540521682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466688 | TGAGTAAGTAAATTA[A/C]ACAGTGGATAGCTTT | 55626 |
rs540522269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467695 | CACACCACCATACCC[A/G]GCTAATTTTTGTAGT | 55626 |
rs540531385 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561295 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTAGGAG | 55626 |
rs540540317 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454463 | GAAATTGGCCAGGTG[C/T]GGTGGCTCACGCCTG | 55626 |
rs540563352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421654 | TGTCTACCCCTTTCC[C/T]GGGCCAAAGCTGAAC | 55626 |
rs540604854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554234 | ACCATTTATAATCTT[A/G]CAAGGTGTGGTGGAA | 55626 |
rs540627726 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486195 | TAATTGATGTTGAGT[G/T]GGAATGTGCCACTCA | 55626 |
rs540664618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498035 | CTGCCACTCACTTCC[A/G]TGCTGATACAAGGTC | 55626 |
rs540671339 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468761 | AGCTTGCAGTGAGCC[A/G]AGATCACACCACTGC | 55626 |
rs540672783 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481571 | TTTCTCCATGTTGGT[C/T]AGGCTGGTCTCGAAC | 55626 |
rs540673028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589593 | TATTCCTTTAAGAGT[A/G]AGATAAATTGGAAGT | 55626 |
rs540680127 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478764 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC | 55626 |
rs540686348 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469596 | TACTATAAACTAGGC[A/G]CAATTTAAATATGTT | 55626 |
rs540713932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494325 | GACCCCACATAAATT[A/G]GTCATCTGGCTGCTC | 55626 |
rs540718107 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546092 | CCAGGCTGGAGTGCA[A/G]TGGCACAATCTCAGC | 55626 |
rs540722236 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434335 | CTCTTAAAAAAAAAA[A/C]AAAAAACACTTAAAT | 55626 |
rs540722292 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556907 | CTTGGGAGGCTGAGG[C/T]GGGTGGATCACCTGA | 55626 |
rs540744124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479128 | ACTTGAGCCCAGGAG[C/G]CAGAGGTTGCAGTGA | 55626 |
rs540745793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534433 | CCGGGAGGCGGAGGT[C/T]ACAGTGAGCCCAGAT | 55626 |
rs540750141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490197 | GTATGTTCTCCCACA[A/G]TTTTACCTGGTAGAG | 55626 |
rs540787280 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453279 | TTTTTTTTTTCTTCC[C/G]CAAAGAGACAAGGTC | 55626 |
rs540812943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513336 | TATCTATTAAAAATA[A/T]AAATATATATAAGAG | 55626 |
rs540826964 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505090 | GGATACCAAACAAAG[C/G]AACAACTGTCTTAAT | 55626 |
rs540840309 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398613 | CCTCGGCCTCCTGAG[C/T]AACTACAGGTGCCCG | 55626 |
rs540844981 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411670 | GATGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 55626 |
rs540851175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402968 | AAGAGAAAAAATACC[A/G]GGGCTAGAGGGAAAT | 55626 |
rs540855751 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561028 | AGAAAGAATCCAACT[A/C]CTTCCTGGGAGCACC | 55626 |
rs540884910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408383 | ACCATGTCGCTGCTG[A/G]GGAGGCTCTTAATGC | 55626 |
rs540889726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403824 | CCCTTTGGTGCTAAC[C/T]GACAGAAAAGGGCCA | 55626 |
rs540894984 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557372 | TTTCTAAAAATAAAA[A/C]GTTTAGGCCACAAAG | 55626 |
rs540898473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448649 | CACCTATAGAGAAAA[A/G]TCAATAAAACCAAAA | 55626 |
rs540924187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484709 | TGGAGTGCAGTGGTG[C/T]GATCTCTGGCTCACT | 55626 |
rs540938883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553517 | TTTGGGAGGCCAAGG[C/T]GGGCAGATCACAAGG | 55626 |
rs540945378 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579611 | CATCCTGGCAAGATA[A/C]CAAGCTAAGCAGCCA | 55626 |
rs540966614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445574 | ACTTTCTTGATTTTT[C/T]TATGCCTCTTTGATA | 55626 |
rs540969219 | in-del | -/A | 0.0529228 | 0.15382 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557301 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs540984627 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464481 | CTCCCAGGACCCAAT[G/T]TGGGTTTTGTACCTT | 55626 |
rs540990080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541865 | GACACTCCAGATACA[A/G]CCACAACATCTATAG | 55626 |
rs540991952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550562 | CTCTCTTGTACTTTT[C/T]TAATGGGGGGAGATG | 55626 |
rs540992096 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506984 | TCCTGGCTAACAAAG[G/T]GAAACCCCATCTCTA | 55626 |
rs540993747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429751 | TGCAGTTCTCTGTTA[C/T]AATACTGTGCCTGGT | 55626 |
rs540994630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438531 | TGCAAATGCATTAGA[C/T]ACCGATTTGGAAAAC | 55626 |
rs541000946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493776 | ATACTAACTACCTAC[A/G]CTGAAAAATCTGGGC | 55626 |
rs541005376 | snp | A/G | | | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430531 | ACCACAGTTTGAGAA[A/G]CACTGATCCAGAAGT | 55626 |
rs541006012 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578537 | TGTTTATTATTATCA[C/T]ATAAATATGGCTAAT | 55626 |
rs541030443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423361 | TCAGAATTCACAAAA[C/T]GTTGATGTAATTTTT | 55626 |
rs541067297 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579357 | AGCTACTCGGGAGGC[A/T]GAGGCAGAAGAATCA | 55626 |
rs541083337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572492 | ACATCCATGAGTAAA[C/T]AATCATAGCAGTTTA | 55626 |
rs541149758 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590241 | CTGGGTGCGGTGGTG[C/T]GCACCTGTAGTCCAC | 55626 |
rs541173906 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431815 | TCTAGATAAGAAAAT[A/T]GACTTGATGAACATC | 55626 |
rs541183401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565325 | TTTTCCTTTTTTTTT[A/T]AATTAAAAAAATCAA | 55626 |
rs541199617 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548042 | AAACCTAAATTACCT[A/T]CAGGAAAACTGTCTA | 55626 |
rs541200970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407670 | CCACGCAATACCCTG[C/T]TGGGGACTGCGGTGT | 55626 |
rs541217054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509855 | AAGGGCATAGATTTT[C/T]GGTTTTTTAATGGAA | 55626 |
rs541217097 | snp | A/G | 0.000798403 | 0.0199641 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518158 | CTCACGGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 55626 |
rs541217951 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577210 | CAGAAACAGCCCAAA[A/T]GTTCTTCAATGGATG | 55626 |
rs541247656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399730 | TTTCCCTTTACCCCC[A/C]AGTCTTCACAAGCTA | 55626 |
rs541266582 | in-del | -/A | 0.00319959 | 0.0398693 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494252 | TCACTAAGGAAGAAT[-/A]CATCCACCAGCCCAA | 55626 |
rs541286303 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400260 | GGGTTTTGATGGTGA[G/T]TTTTCTTTCCTTTTG | 55626 |
rs541308259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557950 | ACACTCCAGCCTGGG[C/T]GACTGAGCAAGACTC | 55626 |
rs541312735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540105 | CCAAAGTTCTTGGAT[A/G]ACAGGCGTGAGCCAC | 55626 |
rs541351842 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539108 | GGTGCCGGGAGCAGA[C/T]GGAATATAGATTAAA | 55626 |
rs541353564 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429208 | CCCTCGGACAATCTT[C/T]GCCTACCAGCGGCCC | 55626 |
rs541374034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540755 | ACTACATCCAATCTC[A/G]GTACCATACAATGAA | 55626 |
rs541375042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476389 | TAGATGGTGTATTTT[C/T]AGGGGTGGCTTGTGG | 55626 |
rs541378165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533224 | TGTTTTGATTAGCAT[A/G]GAAAAAATTCTGGAG | 55626 |
rs541382210 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46453947 | ACGTGTCTTATTTGT[A/T]GGAATTAGGCCCCCA | 55626 |
rs541394807 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588121 | GCAGATGACTTGAGG[C/T]CAGGGGTTCAAGACC | 55626 |
rs541414072 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432266 | GATAGCACAAGGAAC[A/G]AGTGATCAATTCTAT | 55626 |
rs541429358 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525675 | AGAATCATTTGAATC[C/T]GGGAGGCGGAAGTTG | 55626 |
rs541434994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492823 | GGGAGGCTGAGGCAG[A/G]CAGATCACGAAGTGA | 55626 |
rs541534047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485062 | CCTGCCTTGGCCTCC[C/T]GAATAGCTGGGATTA | 55626 |
rs541544258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540997 | CATAATTCATATTCC[C/T]ACCCTTGTTAGAAGC | 55626 |
rs541557773 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415220 | TCATTTGAGACTGGA[A/G]ACCACTCATCTGTAG | 55626 |
rs541563315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517561 | CTAAACAGGCCGGGT[A/G]CAGTGGCTCACGCCT | 55626 |
rs541565878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444548 | TAGAACATTCTTGTA[C/T]GCTAGCTAACCTAAA | 55626 |
rs541589696 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535303 | AACTATTCACACTCC[A/G]CATAATTAGAGGTAA | 55626 |
rs541594873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500299 | TTTTTTTTTTAGACA[A/G]GAAAAGTAAGATGGC | 55626 |
rs541596723 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426532 | ACTGTCAGAGTTGGT[C/G]AATCTGTCATGGAAA | 55626 |
rs541601154 | in-del | -/A | 0.132409 | 0.220618 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488462 | AAAACAAAACAAAAC[-/A]AAAAAAAAAACTGAC | 55626 |
rs541620360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491443 | TAAAGCACGTAAAAC[A/G]CTCCCTAGTATATAG | 55626 |
rs541633315 | snp | A/C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430063 | CTGGGAGGACTAGCA[A/C/T]GATAAACAGAGAAGG | 55626 |
rs541651443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517048 | CCAAGTGAGGTATAC[A/G]AGGGGTTGTGCTATT | 55626 |
rs541662227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460844 | GTAATCCCAACACTT[C/T]GAGAGGCCAGGGTGG | 55626 |
rs541684290 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491949 | AAACAGAGATCTGCC[A/G]GCAGTAGAGAAGCAG | 55626 |
rs541700541 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436518 | TCACTGCTATCACCA[C/T]TAGGCCTTTCTACTG | 55626 |
rs541721653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399222 | GGGATTACAGGTGCC[C/T]GCCACCACACCCAGC | 55626 |
rs541724669 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573756 | GTGCCATGCTGGTGC[A/G]CTGCACCCACTAACT | 55626 |
rs541754411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502532 | CAAGTTATATATTTG[C/T]TATTAGAGAGTAGTC | 55626 |
rs541763893 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445421 | TTTGAGGTCCCTGTG[A/G]CGTATCATAAGATGA | 55626 |
rs541776068 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499557 | AAATACATTGAGGCT[C/T]GACAGGTACCATATA | 55626 |
rs541787764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436441 | CCATTACACATAAAA[C/T]CGAAGAGGGACCACA | 55626 |
rs541804851 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538470 | AAAAAATACTTAAAC[-/A]AAAAATTATGGTACA | 55626 |
rs541808746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399672 | GCCTGGTCAGAAGCT[A/G]AGAGTTTTAACTGTT | 55626 |
rs541815395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557870 | ACAGCTACTGGAGAG[A/G]CCGAGGCAAGAGAAT | 55626 |
rs541822193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428814 | TGAGTCTCGCAGGTC[A/G]CTCACCCTCCAGACC | 55626 |
rs541844681 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483720 | GCCTGACCAATATGG[C/T]GAAACCCCATCTCTA | 55626 |
rs541860901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421853 | TTGTGAGTCCCCTTT[C/T]AGATTTCCACGGGGA | 55626 |
rs541867284 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587237 | ATACAAAAATTAGCC[A/G]GACGTGGTGGCACAC | 55626 |
rs541879845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578330 | TGTCTCCACTAAAAA[C/T]ACAAAAATTAGCCAG | 55626 |
rs541929713 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549826 | TTTTCTTTCTTTTTT[G/T]GGGGGGGTGGGGGAC | 55626 |
rs541939284 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534259 | GAACTTTGGGAGGCC[C/G]AGGCGGGCGGAGCAC | 55626 |
rs541939872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437524 | TGGTGGCATAGAGTG[A/G]TTTGGTAGCTCCATT | 55626 |
rs541939946 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573704 | AAGTTTTAGGGTACA[G/T]GTGCATATTGTGCAG | 55626 |
rs541940979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579192 | GCCGGGCATGGTGGC[C/T]CACGCCTGTAATCCC | 55626 |
rs541943038 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468664 | ATACAAAAAAAAAAA[A/T]AGCCGGGTGTGGTGG | 55626 |
rs541972448 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429946 | AGATTCTGAGTCATA[C/G]AGAGTAGCATATCCA | 55626 |
rs541975748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442968 | CTCAAGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 55626 |
rs541976894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438419 | TTCCTATCAGCTCCA[C/T]AAATTATAAACAAAC | 55626 |
rs541987582 | in-del | -/A | 0.247053 | 0.249983 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526548 | AAAAAAATTAAAATT[-/A]AAAAAAAAAAAAAAA | 55626 |
rs541989923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555543 | AGGTTCACTATGGTT[C/T]CCCTCACCAAACAAT | 55626 |
rs542016866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405244 | AACCCCACAGGCTGG[G/T]CAAAGCCCCTCCTCC | 55626 |
rs542040012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525569 | CAGCCTGACCAACAC[A/G]GTGAAACCCTGTCCC | 55626 |
rs542058716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406861 | GCACTCCAGCCTCTG[C/T]GACAGAGTGAGACTC | 55626 |
rs542121474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453228 | TAACATTTTCAAAGT[C/T]TATCCACGCTTATTG | 55626 |
rs542146833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435877 | GCACTGTGCCTATAG[G/T]CCTTGTTTCGGTTTT | 55626 |
rs542160605 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411765 | TGAACCACTGCGCCC[A/G]GCCCAAATCTGTCTT | 55626 |
rs542164171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539981 | GGACTACAGGCCTGC[A/G]CCACCAAGCCCGGCT | 55626 |
rs542182171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411056 | AGTGAGCTGAGATCG[C/T]GCCACTGTACTCCAG | 55626 |
rs542197846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581947 | CATAGTGAGGCTTTG[C/T]CTCTACAAATAATCA | 55626 |
rs542204775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539418 | CAAAATTAGCCAGGC[A/G]TGGTGGCGCATGCCT | 55626 |
rs542209177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429137 | GCAATCCGGTTCTTC[G/T]TAGGCATCAACATCT | 55626 |
rs542227330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592319 | TAACAGACTTAGTCC[C/G]CAGACTTTCCAAGCT | 55626 |
rs542256078 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419084 | AAGGAAACCTAAAAG[A/G]TGCATTAAGATGGAG | 55626 |
rs542259008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582898 | ATCACAATCAAGAAA[C/T]AGTTGTAAAAGGCCT | 55626 |
rs542263749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426197 | TGTTACAGTGATAGT[A/G]GTGGTGAGCAGGGTG | 55626 |
rs542264349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532529 | GCAACCTCTGCCTCC[C/T]GGCTTCAAGCGATTC | 55626 |
rs542284460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480386 | GCAGACCAGGCAAAC[C/T]GCAATTGGACTCGCA | 55626 |
rs542314197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464923 | GGTGGTGGGTGCCTG[C/T]AATCCCAGCTACTCA | 55626 |
rs542319354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472714 | CAAAAGACTCAGAGA[A/G]CAGTAAAGTCAGCAA | 55626 |
rs542334257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576123 | TTACACAGCTAAGAA[A/G]AGAGTCATTTAAGAT | 55626 |
rs542349352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422676 | CAAGATGGTCGTATT[C/T]TTTTTCCCCTACTGC | 55626 |
rs542363467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450863 | GAACCCTAATGTAAA[C/T]GCATACTTTGAGTGA | 55626 |
rs542365038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439174 | AGTTACTTGGAAGGC[C/T]GAGGCAGGAGGATCA | 55626 |
rs542369593 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403532 | CCTGAATGCCCACTG[A/C]AAGCTAGGGAGGCAC | 55626 |
rs542375066 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453553 | TGGAAAACCAGCAAT[C/T]ATAAAAGGACTTAAG | 55626 |
rs542396909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418685 | GACTCTTAACTCATG[A/C]CTGAGAACTTGGGGC | 55626 |
rs542397459 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570989 | TGCAATATACTGTAA[C/T]CATAACCACTGTACT | 55626 |
rs542404686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507772 | AGGGAAATCCAAGTA[C/T]TTCAGAACGAAGACA | 55626 |
rs542438160 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498469 | GTATTTGGGAAGGAG[A/T]AGGGGGAAAAATACT | 55626 |
rs542501855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440001 | TGAAATCAGGCACTC[C/T]CATGAACTCCAAGTG | 55626 |
rs542513916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491381 | CTGTTAATTAGGTAA[C/T]CGCACCTATCTCATA | 55626 |
rs542555990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547960 | GCACATTAACCATTC[C/T]AGATTAGCATTCACA | 55626 |
rs542561441 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544379 | CTCATACTCTGCCAC[A/C]GAATCAGTTCTTCCC | 55626 |
rs542571442 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581569 | CGAGATCGCACCACT[C/G]CACTCCTGCCTGGGT | 55626 |
rs542578715 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590768 | TACAAAAAATTAGCC[A/G]GGCATGGTGGCACAC | 55626 |
rs542602932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519120 | CTTCTGCTTCCTGTG[C/T]TTAAGCAATTCTCTT | 55626 |
rs542604443 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528663 | ATTCAAAGGATACAG[A/C]GTTTCAGTCACGCAA | 55626 |
rs542611648 | snp | C/T | 0.000280493 | 0.0118393 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417893 | GTGATCCCTCAACCC[C/T]CACACTTTAAGCCAC | 55626 |
rs542622743 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399469 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 55626 |
rs542624934 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559023 | AGAAAAACCTAAGCC[C/G]GGTGCAGTGGCTCAC | 55626 |
rs542625380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409135 | TCCAACTGTATGCTC[A/G]TAAGATTCCACTTTG | 55626 |
rs542633702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471921 | GTGAGCCACCGTGCC[C/T]GGCCAGGAATAACTT | 55626 |
rs542634328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416931 | GAATGGATGCCTGGA[C/G]AAACTCTGACCTCCA | 55626 |
rs542711054 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558764 | CCTTTCTTAGGACTC[A/C/G]TTCTTCCTAAGTAGA | 55626 |
rs542722116 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512358 | GTTTAATCTATACAT[A/C]ATTTCCCTATAAATT | 55626 |
rs542728004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567875 | TAGCTGGGGCTGGGC[A/G]CGGTGGCTCACACCT | 55626 |
rs542739023 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490800 | TCATAGTCTGTCTTA[C/T]TCACTCTGGTAACCT | 55626 |
rs542748934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567172 | CGCTTTCCGGATTCA[A/G]GCTATTCTCATGCCT | 55626 |
rs542771130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456870 | GCAGAAATGAAGATA[A/T]ATGCTTTCAGCAGCA | 55626 |
rs542772075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521137 | TGGTTGCCCCTCACT[A/G]GCGACAAGACTCTCA | 55626 |
rs542798249 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552056 | ACCAATTAATTAATC[-/A]AAAAAATAAATTAAA | 55626 |
rs542800546 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496366 | CAGCCTGGGCGACAA[A/G]AGTAAAACTCTGTCT | 55626 |
rs542820948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494600 | ACTTGTTATCCAGAC[A/G]CCTGCTGTGGGAGGA | 55626 |
rs542829572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526473 | TGTCACTTTTGGAAA[C/G]CTTAAGCTGCTATGT | 55626 |
rs542857284 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472903 | TGCTCTTTGGTACCA[C/G]TCCCTTACCTCTTGC | 55626 |
rs542889476 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591511 | TAGTGGGAGAATGTG[A/G]CCTTGTACAGTTTCC | 55626 |
rs542909187 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585449 | GAGGCAGGTGGACCA[A/C/T]GAGGTCAGGAGATCG | 55626 |
rs542915167 | in-del | -/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396788 | GCTGGCCAGCCTACA[-/C]CCCCCACTCCTGAGT | 55626 |
rs542944017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527368 | ACCTGTAATCCCAAC[C/T]ACTTGGGAAGCTGAA | 55626 |
rs542944025 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546332 | GGCGTGAGCCACCGC[A/G]CCCAGCCCACAGTTC | 55626 |
rs542956756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536022 | AACTCTAAGTAATAC[C/T]GTTTCATTTATTTAA | 55626 |
rs542984974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439900 | AAATACAAATTTAAA[A/T]TGCCCACATACTACT | 55626 |
rs542989931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424770 | GCTTGAGCCCAGTTA[C/T]TAAAATTTACAGTGG | 55626 |
rs543016757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543765 | AGGGTTACTTCTAAT[A/G]AGGCAATCACTGGAG | 55626 |
rs543033090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495020 | GTAAATACCATGGTC[A/G]CATAACTAGTAAGTG | 55626 |
rs543040548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566596 | ACAGACGGGACCCGG[C/G]GGGTGAGGATTGAGC | 55626 |
rs543072888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479829 | AAACTATCTGTTATC[A/G]GTTTTCTATAACTGC | 55626 |
rs543098215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581046 | CAATCCACCCGCCTC[A/C]GCCTCCCAAAGTGCT | 55626 |
rs543120377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447147 | GGCATGGTGGCTCAC[A/G]CCCATAACCCCAGCA | 55626 |
rs543134359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471884 | ACCCACCTCGGCCTC[C/G]CAAAGTGCCAGGATT | 55626 |
rs543164833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534404 | AGAGGCTGAGGCAAA[A/G]GAATCACTTGAACCC | 55626 |
rs543168265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446436 | CTAGAAAGTATTTAC[A/G]TACGAGGCACTTAGC | 55626 |
rs543193530 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467257 | ATTATCTACTGATTT[C/T]CTATGATGGGAGATG | 55626 |
rs543200605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425731 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 55626 |
rs543210721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455653 | GGGCTCATGCCATCC[A/G]GCCTGGTGAGCCTCA | 55626 |
rs543226441 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589438 | AAGAATGACTGTGAT[G/T]AAAGGAACCTAAGTT | 55626 |
rs543254922 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479984 | GGGTCTGTCTCCTTG[C/T]CCATTTCGGTTGCTG | 55626 |
rs543300400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580681 | ACAGTCTAATCCAAA[C/T]CATCATCGCCTTTTG | 55626 |
rs543304488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470395 | AGATCGAGACCAATC[C/T]TGGCTAACACGGTGA | 55626 |
rs543324351 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573755 | TGTGCCATGCTGGTG[C/T]GCTGCACCCACTAAC | 55626 |
rs543336571 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507829 | AGAAAAAACACCAAC[C/T]CTCCAGCCTCCCTGA | 55626 |
rs543345090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462754 | TCAAATAATTCACCC[C/T]CCTCCTTTTTTTTTT | 55626 |
rs543346137 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529229 | GAAGGTTGCTCTCAT[A/G]CTGCATAATCTGGCG | 55626 |
rs543346374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439143 | GCCAGATATGGTGGC[A/G]TGTGCCTGTAGGCCG | 55626 |
rs543348146 | snp | A/G | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595715 | GCCCAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 55626 |
rs543356102 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551473 | TATTTTAAAGATGGG[G/T]TCTCGCTATGTTGCC | 55626 |
rs543356751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531444 | GCTGGGCGCGGTGGC[G/T]CACGCCTGTAATCCC | 55626 |
rs543367097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471216 | GGAGGCTCGGGCGGG[C/T]GGATCACTTGAAATC | 55626 |
rs543378088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431981 | ATGTTATGTTACCCA[A/T]CATTGGTTCTGCTAG | 55626 |
rs543388325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486287 | AAGAGATAAAGGACC[A/C]AACACCAGAAATATT | 55626 |
rs543397503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424017 | ATCCACCCGCCTCAG[A/C]CTCCCAAAGTGTTGG | 55626 |
rs543411158 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476844 | AAGGCTGGGTGTGGT[A/G]CCTCACGCCTGTAAT | 55626 |
rs543416744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424966 | ATGGTGAAACCCCAT[C/T]TCTACTAAAAATACA | 55626 |
rs543418082 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472455 | CAAATGAAGTTAGAG[A/C]ACTTTACCAATTTTT | 55626 |
rs543465777 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581613 | TTCCTCTCAAAAAAT[A/T]AATAAATAAATACAT | 55626 |
rs543519434 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557977 | ACTCAGAGAGGACCT[A/G]CATGATAAGATACCA | 55626 |
rs543525544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566524 | TTACATTCTATATAA[C/T]TCCATTTATACAACA | 55626 |
rs543538907 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510653 | AGGGACATAGGAATT[C/T]CCCAAGCTATGAAAC | 55626 |
rs543575430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540905 | ACAGTGTTAGAAAAT[C/T]TGTAACCATTCAACT | 55626 |
rs543578790 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469100 | GTGAGCCGAAATCAC[A/G]CCACTGAACTCCAGC | 55626 |
rs543584935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528378 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCGAA | 55626 |
rs543586146 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401178 | AGCATGGTCTGGGGC[A/G]TGCTGTGGCTGGCCT | 55626 |
rs543593978 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400395 | CAGTTTCACAGCTTG[G/T]TGGCATCTAAGGCCC | 55626 |
rs543598843 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425826 | CCTGTGCAACAAGAG[C/T]GAAACTCCGTCTCAA | 55626 |
rs543612785 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541781 | TAGGCCCTATCCTAT[C/T]TCTGCCACCAGAGCA | 55626 |
rs543624832 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562639 | AAGGGTTCTACTATA[-/TG]TGTTATGTTTGCGGG | 55626 |
rs543641549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511447 | TCAGAAAGAATGCTC[A/G]GTGTCATGACATAAC | 55626 |
rs543654004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503047 | GCCTGGGTGACAGAG[C/T]GAGACTCTGTCTCAA | 55626 |
rs543684477 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586904 | CTGTTTTCAGTGGTC[A/G]CCTAGAATAAAATAC | 55626 |
rs543687210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541716 | AGGCTAAAGCCAGAA[A/C]CTTGAGCTTAGCCGA | 55626 |
rs543693766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550669 | CCCTTAAAAATTGGT[A/G]CAGAGTAGTTACTAC | 55626 |
rs543705689 | snp | A/C/G | 0.000599232 | 0.0172996 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542979 | GGGATGGAAGGGCTC[A/C/G]GTCTGTACAAAAGAA | 55626 |
rs543715324 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485363 | ACTCAAAAGATGAAC[A/G]GGGACACATTTGCAG | 55626 |
rs543722608 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580917 | CACCTTAGCCTCTTG[-/T]AGTAGCTGTAAGCAC | 55626 |
rs543747360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534301 | AGTTCAAGACCAGTC[C/T]GGCCAACATGGTGAA | 55626 |
rs543755026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423441 | CTGTCACCCAGGCTG[C/G]AGTGCAGTGGTGCGA | 55626 |
rs543760300 | in-del | -/T | 0.425123 | 0.178415 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571688 | CTCAATCAATCAATC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs543782122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572569 | GTGCATACAGTAGGT[A/T]AAGAACTGCCTATCT | 55626 |
rs543791673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420693 | CTCCAAAGGTCAGAT[A/G]GTGTGAGCAGAGCAC | 55626 |
rs543812052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430425 | ACTAATCCTGGGTCC[C/G]TCTGACTCCCATTCT | 55626 |
rs543828279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412705 | AACTGTTTATCCTTC[C/T]TCTTCTAAACAGCCA | 55626 |
rs543840702 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410937 | GAAACCCTGTCTCTA[A/C]TAAAAATACAAAAAT | 55626 |
rs543858659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408431 | CCAGACATGGGAGGG[A/G]GTATGCATCCTGAGT | 55626 |
rs543884757 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515137 | GTGGTCGTTTAGTAA[C/G]CTGAGGCCCTTTGGC | 55626 |
rs543903565 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562816 | TTCTTTTTTTTTTTT[C/T]TGAGAAGGAGTTTCA | 55626 |
rs543904703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569334 | TGTATGCATATAATA[A/G]TTTTTGTTTCCTGTA | 55626 |
rs543914763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563633 | TCACTTGAAGTCAGG[A/C]GTTTGAGACCAGCCT | 55626 |
rs543915264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454688 | CCCGGAAGGCGGAGC[C/T]TGCAGCGAGCCGAGA | 55626 |
rs543949962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459232 | GATGTATAAATATAC[A/G]TATGTTTTTTATTAC | 55626 |
rs543965638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437398 | CAGAGATATGCAAAG[A/G]ACAAACGAAAAGAGA | 55626 |
rs543966887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510713 | GCCACAATTATTAAA[C/T]ACAAGTATATCCTAG | 55626 |
rs543988624 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450486 | ACTCCATTGCCCAGG[C/G]TGGAGTGCAGTGGTG | 55626 |
rs544005553 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429832 | GAGAATTCAGCAAAA[C/T]TTCAGCTCAGCAGTC | 55626 |
rs544020876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529988 | AGGATGCTACCTGCA[C/T]AGTTCTAATGGGCTG | 55626 |
rs544041568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485001 | GGAGTGCAATGGCGC[A/G]ATCTCAGCTCACTGC | 55626 |
rs544042700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434131 | AAAAAAAAAAAAAAA[A/G]AAAAAAGAAAGAAAG | 55626 |
rs544063327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489395 | ATGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 55626 |
rs544079372 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427502 | CCCTACAGCCCATGG[A/T]TCGTTCTTAACTTAG | 55626 |
rs544083969 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562877 | ATGATCTCGACTCAC[C/T]GCAATCTCCGCCTCC | 55626 |
rs544090913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589027 | CACATGTAAAGAACA[C/T]GACACAGTAAATGCT | 55626 |
rs544118609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579988 | AAAGTGCTGGGATTA[A/C]AGGCGTGAGTCACCA | 55626 |
rs544119605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566052 | CACCATGCCCAGCCA[A/G]ATGTCTTTCAATGGG | 55626 |
rs544126236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481487 | TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGGATT | 55626 |
rs544139695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419737 | CATGTGGTTTAGACA[A/G]TAATATTCATAAAAT | 55626 |
rs544143767 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530555 | CTGCTCTTAACCATC[A/C]AAGAATCCCACAAGA | 55626 |
rs544147511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478536 | CCCTGATATCCTATG[C/T]CTAGGAAACCAGGGT | 55626 |
rs544194854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504931 | ATGGGCTCTGAGTAA[C/T]GGCTCCCTTGGTTTT | 55626 |
rs544199890 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524150 | TGGGATTACAGGTGT[A/G]AGCCACCGCACCCGG | 55626 |
rs544206800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496352 | GCGCCTTTGCACTCC[A/G]GCCTGGGCGACAAGA | 55626 |
rs544269333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402765 | TGAATTCATGGTGCC[A/G]AACACAATACCAGAC | 55626 |
rs544270442 | in-del | -/T | 0.450357 | 0.149522 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460325 | ATATAAACACAACTC[-/T]TTTTTTTTTTTTTTG | 55626 |
rs544295961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570216 | GCAGTGAGCAGAGAT[C/T]GCACCATTGAACTCC | 55626 |
rs544326245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515779 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 55626 |
rs544338461 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410944 | TGTCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG | 55626 |
rs544351920 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527998 | ATCTTGAAGAGATAT[C/T]TGCACACCCATGTTC | 55626 |
rs544368757 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446320 | TTGGAAACAACAGGA[A/G]GAAAAAGCCTGATGT | 55626 |
rs544380196 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561407 | AAAGAATATTGTCAG[-/A]AAAAAAAAAAAAGCT | 55626 |
rs544398662 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588255 | GGGAATCACTTGAAC[C/T]TGGGAGGCGCAGGTT | 55626 |
rs544413366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449433 | CCACCACTTACATTA[C/G]CATCAAAAAAATAAA | 55626 |
rs544422476 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46594041 | GGCGCAAAAGATCAC[C/T]GAATACAAGAACGCC | 55626 |
rs544425000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545354 | GCAATCCCAGCTACT[C/G]TGGAGGCTGAGGCAC | 55626 |
rs544426209 | in-del | -/AAAC | 0.300035 | 0.244942 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515482 | CATCTCAAAACAAAC[-/AAAC]AAACAAACAAACAAA | 55626 |
rs544452150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482243 | CCTCTGCAGTTCAGC[A/G]TGATGGGCAATGTTT | 55626 |
rs544453904 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576504 | AAGTCATCTCTGTCA[C/G]CTCCCTCATTTCTAA | 55626 |
rs544516748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575603 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 55626 |
rs544539785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522146 | CATTACAAAAGTCTC[A/G]TCTGAGAAGTCAGCC | 55626 |
rs544558003 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403016 | ATCCAGGCACAGTGG[C/T]AGACAGGGGGTTAAT | 55626 |
rs544558071 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464860 | GACCATCCTGGCCAA[A/C]AGGGTGAAACCCCGT | 55626 |
rs544571148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448587 | TAAACCCAAAGTAAG[C/G]AGAAGAAAAACATGA | 55626 |
rs544579808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575737 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCGT | 55626 |
rs544588177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418811 | AGAGCCTTTTAGCTA[A/G]CTAACTTCATTGCTT | 55626 |
rs544589513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561546 | TCACAGATGAGTCTG[C/G]AGCCAAAGCAGGATT | 55626 |
rs544596790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457625 | GATGGGCTGGGCCAG[G/T]CGCAGTGGCTCACGC | 55626 |
rs544612930 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513275 | TCTTTTTTCTTTTTT[C/T]TTTTTTTGTGAGAAT | 55626 |
rs544622960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419528 | ATTATTGCAACCAGG[A/G]ACCTGTATCTCAGTC | 55626 |
rs544629522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529752 | TTGATATGGAAAAAA[A/G]ACATCCAAATTTTTA | 55626 |
rs544655296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568381 | AAGAATTGCTTGAAC[C/T]CAGGAGGCAGAGGTT | 55626 |
rs544658425 | snp | A/C | 0.00159617 | 0.0282053 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396140 | CTGTCGTTCCTTCCT[A/C]CATACTCACCCTGGC | 55626 |
rs544676912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544681 | TCAGGTTTTCCCAAA[A/G]AAGTACTATCCAAAA | 55626 |
rs544701892 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553445 | TCAGAAAGATTTCAC[A/T]GCAAGAAAACACCAA | 55626 |
rs544702831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522021 | ATTCCTCAGTGCCTC[C/T]GGGCAGTGAGCGATA | 55626 |
rs544707098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473791 | AAGTAGCTGGCACTA[C/T]GGACACCCACCACCA | 55626 |
rs544716979 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569082 | AAAGTGCTAGGATTA[C/T]AGTTGTGAGCCACCA | 55626 |
rs544719294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576347 | TGCCAAGGCAGGTCT[C/T]GAACTCCTGGGCTCA | 55626 |
rs544719817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433394 | TGGTCCTGGCTGGGA[A/G]GTCACACCACTGTCC | 55626 |
rs544724840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458342 | TTTAAAACCCCACCT[C/T]CTCCCAGAAGCTTTC | 55626 |
rs544735664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411785 | AAATCTGTCTTTTTA[A/T]TTTTTTTTTTATTTT | 55626 |
rs544735672 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528786 | ACAGACACACGTACA[C/T]GAAGATAAAAAGGGT | 55626 |
rs544738042 | in-del | -/AAAAAAAAAAAAAA | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595570 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAA]GTCCCAGCCTTTGAA | 55626 |
rs544746774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441795 | AAGGAATCTAAGGAG[A/G]TTTGACCTTTCAACA | 55626 |
rs544748519 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520258 | AATTTTAATACACAA[G/T]CACACATTCAATTAG | 55626 |
rs544768686 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544469 | ATTAAGTGACATAGC[C/T]GAAACCAGAAAATTG | 55626 |
rs544770571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528949 | GCAAAAAGAGTCACA[C/T]GTACCCTCTGATGCA | 55626 |
rs544806403 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417754 | AGCTAATCCTACCAG[C/G]CCCTGTGGGAAGAGG | 55626 |
rs544818372 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402140 | GCTTCACAACTCCCC[A/G]TAGCTGTGGCATCTC | 55626 |
rs544841863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402241 | GGGTTTACACTGGGC[A/G]TGTATTTGTCAAATA | 55626 |
rs544842366 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418574 | CCCCACAACAGGCCC[C/T]GGTGTGTGATGTTCT | 55626 |
rs544850910 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441019 | CTACAAGGTTTGGTG[A/C]AATGCCCTGCCTGAT | 55626 |
rs544853256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496171 | CTAGGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 55626 |
rs544856751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567448 | CTTGGCTCAATGCAT[C/T]CTCCACCACCCGAGT | 55626 |
rs544868545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457033 | ATTGCTCTATGAGCC[C/T]ACATTCACATTAGGG | 55626 |
rs544880481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536922 | TAAATTCTCAGAAGA[C/T]GCTCAGTCTTACTAA | 55626 |
rs544881080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410762 | CCCACTGGAGAGATA[A/C]AGAGCCATGGACAGC | 55626 |
rs544907827 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397173 | GGAGAAAGTGGGGTG[C/T]CTGGCAGAGATACCC | 55626 |
rs544918953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567754 | CTAGCCAGAAGCAGA[C/T]TCAGTACATAAGGAC | 55626 |
rs544950634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521231 | ACTGCTTACATCACC[G/T]TCATCCCCTCTGGTC | 55626 |
rs544969365 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405781 | CTGTCTTCCAGGCTG[A/G]AGTGCAGTGGCATAT | 55626 |
rs544985375 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492831 | GAGGCAGGCAGATCA[C/T]GAAGTGAGGAGATTG | 55626 |
rs544996064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401333 | GCAACCTCCACTTCC[C/T]GGGTTCATGCAATTC | 55626 |
rs545008028 | in-del | -/ACG | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555364 | CCACCTTCTAGCTAT[-/ACG]ACTTTGGGGATACTT | 55626 |
rs545020668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402055 | ATGCTCTCGTCCCAT[C/T]TCCTCTGCCACCCAC | 55626 |
rs545025314 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547058 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAATTA | 55626 |
rs545033959 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465009 | CGATCGCGCCACCGC[A/C]CTCCAGCCTGGCGAC | 55626 |
rs545036710 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549826 | TTTTCTTTCTTTTTT[-/G]GGGGGGGTGGGGGAC | 55626 |
rs545101179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561713 | GAAAAAATTTCCCTC[A/G]AGGCTTCAAGAAAAG | 55626 |
rs545127557 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446060 | ATGTCTCAAGAAACA[A/T]CTTCTGGAGAACAGC | 55626 |
rs545137364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504810 | ACATCATTTTCAAAG[G/T]TTTTTAAATCAGCAG | 55626 |
rs545158101 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432952 | CAATATAAGAGAGAC[A/G]TGCCTTAGACAAGAC | 55626 |
rs545161295 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514490 | ATAAAATACATCTCT[C/G]TGGTTGAAAGACTAA | 55626 |
rs545162940 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478742 | TCACTGCAACCTCCA[C/T]CTCCCGGGTTCAAGC | 55626 |
rs545204044 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487811 | GCAGACAAAAACCCA[A/G]CTATATCAATGATAA | 55626 |
rs545237952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592463 | GACCAAACTACTAAT[A/C]AAATACAACAAAACT | 55626 |
rs545265547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488608 | ATTGACCAAGTAGAT[C/T]TAACCGACATCTACA | 55626 |
rs545284658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528235 | TGGAGTGCAGTGGCA[C/T]GATCCCGGCTCGCTG | 55626 |
rs545305577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472814 | TGTCACTGAGTCACT[A/G]AGCAGAGCTGTTCTC | 55626 |
rs545305640 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490535 | CGGATCTTGATTTTC[C/T]GCAAACCCATTTTTG | 55626 |
rs545317934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581529 | GGAGAATGACGTGAG[C/T]CCGGAGGCAGAGCTT | 55626 |
rs545318912 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515328 | AATACAAAAAAGTAG[-/C]CAGGCGTGGTGGTGC | 55626 |
rs545320615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520096 | GTGACCCAAGATGGC[A/G]CCATTGCACTCCAGC | 55626 |
rs545329141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511697 | GAACAGAATCCGTAA[A/G]TCTGGCTGTGACAAC | 55626 |
rs545368910 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498326 | CTTTTCAGGGAAACA[C/G]CAGAGAAACCCTCAT | 55626 |
rs545382464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456946 | ACAAGAGAGTTAAAG[C/T]AAGAAAATAAATCAG | 55626 |
rs545388546 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503994 | GTGAGCTGCCACACC[C/T]GGCTCTAGCAACAGT | 55626 |
rs545395298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508839 | TGGTAAGCCTCAGAT[A/G]ATTAAAGAAGGTATC | 55626 |
rs545405421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509374 | AAATGTTTTCTATGA[C/T]AATATTAAATGGATT | 55626 |
rs545420332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417695 | CTTTAGATTCAAGAA[A/G]ACATGATCACTAAAT | 55626 |
rs545443384 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572988 | CCCAGCTACTCGGGA[A/G]GCTGCAGGAGGCTGA | 55626 |
rs545450933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495422 | CTTGGTAGAATTGGC[G/T]GCCGAGCATTAAATG | 55626 |
rs545459366 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582156 | TTGACATAGTCCTGC[C/T]TAAGTCTCTATCCTC | 55626 |
rs545510527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556535 | TGGAGAAGTCATGAG[G/T]GATATTTATTTTATT | 55626 |
rs545517443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447850 | ACTCCACTCTCTGTG[G/T]GTATTGCATCTACAG | 55626 |
rs545521966 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440047 | ACGAGCTGTATAGAG[A/T]GTGGTATGGCAATAA | 55626 |
rs545546412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527448 | TCATGCCACTGTATT[C/G]CAGCCTAGGTGACAA | 55626 |
rs545548973 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399623 | GCCCACCTAGGCCTC[C/G]CAAAGTGTTGGGATT | 55626 |
rs545550987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492071 | TGCCAGTGAAAAAAG[C/T]TTTAACGTGCCTTCG | 55626 |
rs545561075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580831 | GAGCCTTGCTCTGTC[A/G]CCCGGCCTGGAGTGC | 55626 |
rs545566269 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461380 | ATATATATGCCTGTA[C/T]AGATACTACTCTAAA | 55626 |
rs545571669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548191 | AACCCATTCTAAGGT[C/T]TCATTCTACCATCAC | 55626 |
rs545603719 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417098 | CACTCTGTCGCTAGG[G/T]TGGCGTGCAATGGCA | 55626 |
rs545612746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436636 | GTCCCAAGCCCTTTG[A/C]CAAAACAAAAACAAA | 55626 |
rs545655694 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577717 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 55626 |
rs545656566 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573914 | AGTGAGAATATGCGG[C/T]GTTTGGTTTTTTGTT | 55626 |
rs545686542 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589068 | CATTAACCTTCCCTA[C/T]AGCCTCCTTAAATAA | 55626 |
rs545700375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413632 | AGTAGCTGGGATTAC[A/G]GGTGTGTGCCACCAT | 55626 |
rs545702441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516000 | TTTTACAATCCTAAA[A/T]GTCTATTTCCCACCT | 55626 |
rs545710506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467908 | CCAGAAGTCTAGGGC[C/T]ACATACTGGCAAGTA | 55626 |
rs545727722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507983 | GGTCTCTGTCCTCGC[A/G]CGCCAGTGAATCAGC | 55626 |
rs545734073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567383 | GGCCTTATTTATTTT[C/T]TGAGACAGAGTCTTG | 55626 |
rs545736439 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456195 | GAACAGTATTCCAAA[A/C]AACGTAGTGTTAAGG | 55626 |
rs545744671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530906 | TTCATTTATTTGAGA[C/T]GAATTCTCGCTCTGT | 55626 |
rs545766312 | snp | C/G/T | 0.000299483 | 0.0122334 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443479 | TACCCCCATTTGACA[C/G/T]TGACTTACCATTACT | 55626 |
rs545772892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451968 | AGAGGGAAAGGGGAA[C/G]TGACTGCTGATGTGT | 55626 |
rs545798439 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465670 | CTTTATTTACTTTTG[G/T]TTTTTCCTGGCTCTT | 55626 |
rs545812498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399065 | AGGCGTGAGCCACCA[C/T]GCCTGGCCATATTTA | 55626 |
rs545842482 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595163 | GGATATCCTGAGCCC[A/G]GGAGGTGGAGGCTGC | 55626 |
rs545846832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483610 | CAGGGTTTTAAAAAG[C/G]AGGAGGCTGGCAGGC | 55626 |
rs545849797 | snp | C/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450095 | ATGTCCACACAAACA[C/G]CTACACATGGATATT | 55626 |
rs545906420 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569766 | GAAATGACCAGCCAA[C/T]ATGGCTGGTCATGAG | 55626 |
rs545910099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475717 | CTGTAAAATGTCAAA[C/T]AGTCAACTTGCAACC | 55626 |
rs545941424 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586313 | ACTCGGGAGGCTGAG[G/T]CACAAGAATCGCTTG | 55626 |
rs545949617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449628 | CAGATTCAACACAAT[C/G]CCAATCAAAATCCTG | 55626 |
rs546001893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524755 | GCAGGGAATATGATG[A/C]CCTCTGTCCACTCAA | 55626 |
rs546016368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578197 | TTACCATATAAAATT[C/G]CAGGTAGGGCCGGAC | 55626 |
rs546034847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436141 | GTAATTTTTTAAAAG[C/T]CAAGCTCAGCTGCCC | 55626 |
rs546040175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422618 | GGAAACCTTCTTCTC[C/T]ATCCTTTTAAAATGA | 55626 |
rs546060049 | in-del | -/AG/GAGAATG | 1.70217e-05 | 0.00291729 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418079 | AAAGAGGGAAAAAAA[-/AG/GAGAATG]GAGAATGGGAGGAGA | 55626 |
rs546060584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570377 | CAGAGGGAGAAGTAC[A/G]AAATTATATCTTTTC | 55626 |
rs546072448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571392 | TAAAATCTTGAAAAG[C/T]AGCCATATTACAGTG | 55626 |
rs546072529 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563796 | CAGTGAGCCAAGATC[A/T]CACCACTGTACTCCA | 55626 |
rs546078698 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414286 | CACCTGGCTCTTAGA[G/T]CCTCGCCTGAAAGAT | 55626 |
rs546084193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450417 | GCAGGGAGGCAGAGA[C/T]GAACAGGTGAGCACA | 55626 |
rs546098071 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460716 | CAAAGTCATAAGAGC[A/G]GATGCCTGTGAAGTG | 55626 |
rs546112516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516725 | GGCGTGACCCACTGC[A/G]CCCGGCCAAAAGATC | 55626 |
rs546141864 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524767 | ATGCCCTCTGTCCAC[C/T]CAAGTCACTATGCCT | 55626 |
rs546142956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547032 | GCCAAGATCACACCA[C/T]TGGGCAACAGAGCGA | 55626 |
rs546170555 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396590 | CCACTAGAAACTACA[C/T]GTACAGTTAAGAGTC | 55626 |
rs546185250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546150 | AAGCAATCCTCGCAC[A/C]TCAGCCTCCCAAGTA | 55626 |
rs546186291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538568 | GTGCAATCTCGGCTC[A/T]CTGCAACCTCCGCCT | 55626 |
rs546211991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442894 | GCCTAGCTAGTTTTT[A/G]TATTTTTAGTAGAGA | 55626 |
rs546220110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491264 | AAAACAACTACGAGG[A/C]GGCGGATCGGGAAGG | 55626 |
rs546228406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585495 | ACATGGTGAAAGCCC[A/G]ACTCTACTAAAAATA | 55626 |
rs546231797 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484950 | GTGCCCAGGCTTTTT[G/T]TTTTAAGACAAAATC | 55626 |
rs546265522 | in-del | -/A | 0.212425 | 0.24716 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559298 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAGAAA | 55626 |
rs546288037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434631 | CCCTTATTCCTGACC[A/G]TCGTAACAGGGGCAT | 55626 |
rs546302281 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520617 | TTTTTTTTTTTTGAG[A/G]CGGAGTCTCGCTCTG | 55626 |
rs546304196 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563974 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 55626 |
rs546322406 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428799 | CAGCTTCCCCTCTTG[A/T]GAGTCTCGCAGGTCG | 55626 |
rs546359945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531451 | GCGGTGGCTCACGCC[C/T]GTAATCCCAGCACTT | 55626 |
rs546368289 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420931 | AGTTGCTGTGCTGCG[C/T]TTTTTAAATGGGGGT | 55626 |
rs546371599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412621 | TTTCACTGTTTTTTT[C/T]TCCCCAAAATGTTTT | 55626 |
rs546396446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403497 | CTCAGCTCAGCTAAA[C/T]TCATTAATTCCATGC | 55626 |
rs546401401 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594641 | TAGAGCCACAGGTGT[A/G]CTTCTTACATAATAA | 55626 |
rs546407976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553552 | AAGTTCGAGACCAGC[C/G]TGGCCAACATAGTGA | 55626 |
rs546408225 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404632 | AGGCAGAAGCAGCCA[A/G]CTGCCCGGTCTCACT | 55626 |
rs546419217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515057 | AGAATACCTAGAAGC[C/T]TGTTCCACCCTAAAG | 55626 |
rs546446566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411183 | TCTCGCCCCTGGGGC[A/G]GCCTGAGCGGAGGAA | 55626 |
rs546450234 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396290 | GAGGGGTCCACTGCA[A/C]CCCACTAGGAGAGCA | 55626 |
rs546469734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442119 | GGGACTACAGATGTA[C/T]GCCACCATGCTCAAT | 55626 |
rs546487016 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397038 | CTGCCCACCCAACAG[G/T]TGGACAGGGCAAAGC | 55626 |
rs546502877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553867 | TCATGATACAGCTCT[C/T]ATCACTTATTAGTGC | 55626 |
rs546535324 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404176 | CCTGGATGGAAGAGC[A/G]AGATCTTGTCTCAAA | 55626 |
rs546537140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450510 | AGTGGTGCAATCACG[A/G]CTCACGGAAGCCTCA | 55626 |
rs546548615 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570631 | ATGTTACTTGCCCCC[A/C]CATTGAACAGTAATT | 55626 |
rs546565835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488859 | CCAAAAAAGTAATAG[A/G]TCAAAGAAGTCGTAC | 55626 |
rs546588791 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402585 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTTG | 55626 |
rs546599909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46449915 | AATACAAAAATTAGC[A/G]GGGCGTGGTGGCGCA | 55626 |
rs546601006 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399084 | GGCCATATTTATTTA[-/T]TTTTTTTGAAATGGA | 55626 |
rs546605899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506439 | AGGAAGGCAAATTGG[C/T]ACAAAGGTTGTTCTC | 55626 |
rs546636602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592683 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 55626 |
rs546671880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443174 | AAAACCTAAAGTTTA[C/G]GTGGAACTGAAAAGA | 55626 |
rs546683555 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551376 | GGAGTGCGATGGTGC[A/T]ATCATGGCTCACTGC | 55626 |
rs546715069 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439063 | ATCACTTGAGGTCAG[A/G]AGCTCGAGACCAGCC | 55626 |
rs546716348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480991 | CTGATACTTAAAGGT[C/T]TGGAAAACTTCAGTA | 55626 |
rs546727404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521581 | TTTGTAAAAAATAAT[G/T]GTGTGTTCTGAAACG | 55626 |
rs546754441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568141 | AGACAGAGTGAGACT[C/T]TGTCTTAAAAAAATA | 55626 |
rs546765426 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529448 | CAGGATGGGTGGGGT[A/G]GTGGTGCGGGTACTG | 55626 |
rs546767347 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476042 | GAGACACTAATATCA[C/T]AAAGGAAAAGGTGGA | 55626 |
rs546796489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495564 | CTGAAATTGTGCAGA[C/T]GAAAGGAGGGGCAAG | 55626 |
rs546814640 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511658 | GCTCTAGTATTGCTT[A/C]AATAATGTGCCTTTT | 55626 |
rs546843928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465805 | CAGAACTTCTGAAAT[A/G]TATACATACAATCTT | 55626 |
rs546857784 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488099 | TTAATTCATCAGGAA[A/C/T]ACATATCAGTCGTAG | 55626 |
rs546857927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496569 | GAATCTATCTCTCGT[C/T]AGAAGGGCTGAAGAG | 55626 |
rs546867330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504130 | CTTTGCTACAGTATC[C/T]CTTTGCCTCAGAAAG | 55626 |
rs546889745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562945 | AGCTGGGATTACAGG[C/T]ACATGCCACCACACC | 55626 |
rs546899737 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450606 | CACCATGACCAGCTG[A/G]TTTTTTTTGTATTTT | 55626 |
rs546927569 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408147 | CACTGGTAGGGGGAC[A/G]ACAAGCTAGGCTGTG | 55626 |
rs546968113 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485184 | CTCAGGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 55626 |
rs546986827 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439231 | GTGAGATATGATCAC[A/G]CCACTGTACTCCAGC | 55626 |
rs546987215 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425981 | GAAACCCCGTCTCTA[A/C/T]TAAAAATACAAAAAA | 55626 |
rs546990112 | snp | C/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592697 | CGGGAGGCAGAGGTT[C/G]CAGTGAGCCAAGATC | 55626 |
rs547020240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583157 | CCAAAACAGAGATAT[A/T]GATCAATGGAACAGA | 55626 |
rs547059475 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476767 | TTTTATAAGCTCTCA[C/G]TTAGCTCCTGTGTTA | 55626 |
rs547083153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584521 | TAAAACTTGAAGTAT[A/G]ATAATAATAATAAAA | 55626 |
rs547097107 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500247 | TTATAAATTTAGTTC[A/G]AAACTGGATCCAGTA | 55626 |
rs547107716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427082 | GATTAGGACTATATT[A/G]TAAGTTCAATTCAAG | 55626 |
rs547107788 | in-del | -/AT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516196 | GAACTGGCAAGCCAC[-/AT]ATATATGTCACTTTA | 55626 |
rs547141687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580055 | GACCATCTCCACTTC[A/G]TCCCTTCCCATGCCT | 55626 |
rs547141831 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571346 | CATGGATATACAGAG[-/T]TTAAAAGTGACTTAG | 55626 |
rs547170594 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533971 | AAAATGTCCTTCCCC[C/T]AGTGTCGACGGGGTT | 55626 |
rs547192582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470477 | GCCTGTAGTCCCAGC[G/T]ACTGAGGAGGCTGAG | 55626 |
rs547193849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492241 | AGTCCTGGTGTCTGA[C/G]AGAGAAACCACTGAG | 55626 |
rs547199817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402312 | GGGCTCCAGACTTAA[A/G]GATGCTTGGAAAACC | 55626 |
rs547203066 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525968 | TTCAGCACTTTGGGA[G/T]GTCAAGGCGGACAGA | 55626 |
rs547203154 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462164 | CTGCATGCATCTCCC[-/A]AGAAAACCCTGGACC | 55626 |
rs547242739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551920 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCTG | 55626 |
rs547271991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536320 | AATTTTCTGTCATGG[A/G]TGCAATATCACAAAG | 55626 |
rs547294225 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591871 | CAAAAAACACACACA[A/C]AAAAAAACGCTCTCT | 55626 |
rs547310994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552514 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 55626 |
rs547315027 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579312 | AAAATACAAAATTAG[C/T]CGTGTGTGGTGGTGC | 55626 |
rs547327538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544770 | TGAGGCCAATAAGGG[A/G]AAGCTGAAATGAACA | 55626 |
rs547342553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492844 | CACGAAGTGAGGAGA[C/T]TGAGATCATCCTGGC | 55626 |
rs547351940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433093 | AAACATTTCATGGCA[C/T]ACTATTACTTTTTAC | 55626 |
rs547362820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570703 | ACTGTAGGTTAATGA[C/T]ACAACACTGGGTTTT | 55626 |
rs547369528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579576 | TCTTCATACCCTCAC[A/C]CTTTTCTCTCTTAAT | 55626 |
rs547383640 | in-del | -/T | 0.359787 | 0.224604 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469839 | CCAGCTAACTTAAAC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs547411218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437703 | GAGTTAATTCATACA[G/T]GAAGAGATTTCTTGG | 55626 |
rs547424593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469759 | AGCCTCGAACTCCTG[C/G]GCTCAAGCAATCCTC | 55626 |
rs547454776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525809 | CCCAGCTACTTGTGA[A/G]GCTGAGGCAGGAGAA | 55626 |
rs547468656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46451162 | CTTAGAGCAAAAGAA[G/T]AAATAAAGATTATTC | 55626 |
rs547496739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508120 | CACCATTGTAGCTCC[A/T]ACAGTGGCCAACTTG | 55626 |
rs547497820 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421529 | TAATCACTGATCCAT[A/G]GGCTGAGAGGTCATC | 55626 |
rs547511661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564079 | AACCCAGGAGGCAGA[C/G]GTTGCAGTGAGCCGA | 55626 |
rs547516043 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415376 | ACAAAAGTATGTGTG[C/T]GTTATTGTGGCATAT | 55626 |
rs547555887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428505 | GAGAAAAGCAAACTA[C/T]GCCTGGTGAGATTCA | 55626 |
rs547588038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577298 | GTATGAAGTACTGAT[A/T]AATATTCCAATGGAG | 55626 |
rs547594149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428846 | TTAGGCCGAGGCCTG[A/C]CAGTCTCTGGACGGC | 55626 |
rs547595451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399293 | TAGCCAGGCCAGTCT[C/T]GAACTCCTGACCTCA | 55626 |
rs547637868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530914 | TTTGAGACGAATTCT[C/T]GCTCTGTAGCCCAGG | 55626 |
rs547649517 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577863 | GCTGAGGCAGGAGAA[A/T]CACTTGAACCCAGGA | 55626 |
rs547680194 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576018 | TGCCGGTCCCAATCT[A/T]AGCCCAGTCAACTCT | 55626 |
rs547682608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421133 | CTCAAGACGCCAATA[G/T]GATAGATGAACCCAG | 55626 |
rs547702801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549108 | AAAAAAAAAATCAGG[A/C]TCCTTTTCTCATCTA | 55626 |
rs547717314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541055 | GACAGAGGATGTAAT[A/G]CAGCGCAATATGCTG | 55626 |
rs547720125 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424530 | AAAGAAATACTGAGG[C/T]ACTCACGGCTTCTGG | 55626 |
rs547745890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429305 | AGAGGCCCCCTGCCC[A/G]CATCCTGGGGAGGAG | 55626 |
rs547749391 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572061 | TAATCCCAGGACTTT[G/T]CGAGGCCGAGGTGGG | 55626 |
rs547752914 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413885 | CTTGGGTCTCAGTGA[G/T]GGTGAATGAGTCACT | 55626 |
rs547761040 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492208 | TAGTCTGCTCTCCTG[A/C]CAGGCCAGAGCCTAT | 55626 |
rs547772724 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433207 | TTCACGTAGAAGTAA[-/G]GAAGTATTCAGTTTA | 55626 |
rs547774195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516286 | AACATCAGTTCTTCA[C/T]AGTTACAATACGAGT | 55626 |
rs547784475 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421136 | AAGACGCCAATATGA[C/T]AGATGAACCCAGCTT | 55626 |
rs547819134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413242 | ACTGACTGAAGAGGT[C/T]CACTGCCAACAGAAC | 55626 |
rs547825808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564884 | TATACATTATTATTT[A/C]TTCGATATCTACAGC | 55626 |
rs547826226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517124 | TAATATATAATCATA[A/G]CACACATGGATTACT | 55626 |
rs547829504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428892 | CAGGCACAATCTCTG[C/G]GGGCAGATGAAGGTA | 55626 |
rs547855105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484046 | CTCACCCTGTAAAGA[C/T]AGTCTCTCATGTTAT | 55626 |
rs547882482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556741 | TGTGACTATTGATAG[G/T]ATGTATATCACAGGG | 55626 |
rs547922291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525167 | TTATCTGGGCATGGT[A/G]GCACATGCCTATAGT | 55626 |
rs547954081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406909 | AAACAGGCCAGGCAC[A/G]GTGGCTCACGCCTTT | 55626 |
rs547964030 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496722 | GGGAAAATGTGGGCC[C/T]GTACAACGTAGGTCA | 55626 |
rs547982140 | in-del | -/AGG | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577875 | GAATCACTTGAACCC[-/AGG]AGGAGGAGGTTGCAG | 55626 |
rs547986925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499934 | TGGGATTACAGGCAT[A/G]AGCCACCGCCCCCGG | 55626 |
rs547991653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482938 | CATTTGAACCTGGGA[A/G]GCGGAGGTTGCAGTG | 55626 |
rs548008317 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414369 | TCCCTGGGTGATGAT[-/A]ACTTGACTATAATTA | 55626 |
rs548008792 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495612 | ATATGGAATGTAAAA[-/G]GGGGGTTAAAGAGAA | 55626 |
rs548025200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533467 | AACACGCCTTCTTGT[A/T]TGGAGGTTGGGGAAG | 55626 |
rs548045257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531759 | CACTCTATCCTCATT[C/T]CCATATTGCCAAAGA | 55626 |
rs548045757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491563 | TAGAATCTGGAGGGA[C/T]ATCAAAATATCAACG | 55626 |
rs548046159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500585 | TCAGCCAGGCATTCC[A/G]GGCCATCCAGAGTTC | 55626 |
rs548052590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483735 | TGAAACCCCATCTCT[A/G]CTACAAATACAAAAA | 55626 |
rs548085714 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468248 | AAAAAAAAGTGGGGA[C/G]GGGTGGCGGGCAGCA | 55626 |
rs548096843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523548 | TTCCCTGCTTGCTAA[A/G]AATTATGCATTTTCC | 55626 |
rs548096903 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529733 | CAGAATCCAGATACC[C/T]GAATTGATATGGAAA | 55626 |
rs548135263 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481513 | GGATTACAGGCATGC[G/T]TCACCATGCCTGGCT | 55626 |
rs548142040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540290 | CTGCTTGGTTTCTTA[A/G]AGCAGTAACTGAAGA | 55626 |
rs548159175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524158 | CAGGTGTGAGCCACC[A/G]CACCCGGCCTAATGT | 55626 |
rs548159524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436725 | ATCCAGCTGGGGATA[C/T]AGAACCAAAGGAACT | 55626 |
rs548166169 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566036 | GAACACAGGTGTGAG[C/T]CACCATGCCCAGCCA | 55626 |
rs548187168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547655 | GATTTTTCAGGTTAG[C/T]ACTGCTCATCTACTT | 55626 |
rs548197790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539732 | AAATGGAAAATTGAA[C/T]ACCTGACTTGCATAG | 55626 |
rs548207878 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595865 | TGGCAGGAGCCTGTA[A/G]TCCCAGCTACTCGGG | 55626 |
rs548208375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484630 | TCCACTGCATCCCTG[C/T]CACCACCTATACTTC | 55626 |
rs548213600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587564 | AAACTTAAATTTACG[C/T]AATTATGATTCGTGA | 55626 |
rs548237153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468128 | GTTGAATGAAGAAAT[A/G]GCCAAACAACAGCTG | 55626 |
rs548276133 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578811 | GTGTGAACCCGGGAG[A/G]TGGAGCTTGCAGTGA | 55626 |
rs548276414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588394 | ATCTGTTCATTGTTG[C/T]TGTAAAATAGCATGG | 55626 |
rs548296182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422964 | TGCAAAGCAAGGGGG[C/T]TTTGAGGAAGAAAGG | 55626 |
rs548308887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515430 | GTGAGCTGAGATCGC[A/G]CTACTGCACTCCAGA | 55626 |
rs548331113 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564101 | GTGAGCCGAGATGGC[A/G]CCATTGCACTCCACT | 55626 |
rs548338948 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569723 | AGCAGTTCGAGACCA[G/T]CCTGGCCAACATGGC | 55626 |
rs548357950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508039 | CTCTGGGCATCTTAA[C/T]CCTCTGTCCCTCACC | 55626 |
rs548380619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584929 | ATACAAAAATTAGCT[A/G]GATGAGGTGGTGGGT | 55626 |
rs548387979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398217 | AGGCAGCAGGTTGGC[C/T]TCAATGAGTTCTCTC | 55626 |
rs548406041 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46451008 | CCACTCAACTTTTAA[A/T]AAACCTAAAAAAGAG | 55626 |
rs548424843 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507473 | GAAAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 55626 |
rs548440534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555934 | ACTTCACTATGCCCA[C/T]GTGGGCAAAGTCTAA | 55626 |
rs548443441 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585634 | TCACGCCACTGCACT[A/C]CAGCCTGGGTGACAG | 55626 |
rs548464561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538220 | AGCTGTCAGCCCTTA[C/T]GGTATACGACATCCT | 55626 |
rs548465924 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435109 | AATTCTGGGGCCAAG[A/G]AACTTTAGGGACTTC | 55626 |
rs548480530 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443976 | AAGACACCATTAACA[C/T]AGAAAAGCCAGCAGC | 55626 |
rs548494696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489708 | TAATACCCCACATTA[C/G]CCAGGCCCCTATTCC | 55626 |
rs548502393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556632 | AATGGTTGATTGAAT[G/T]CCAGCTCCATCCTTT | 55626 |
rs548508791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481659 | TGATCTACCGCGCCC[A/G]GCCTATTTTTGTTCT | 55626 |
rs548516772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444877 | GGTTGCTGCTGGCCA[C/G]TGTGTCAGAAGACTG | 55626 |
rs548530409 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506824 | CACAATGAATGGCTA[C/G]AAAGGTCAGAAGCAG | 55626 |
rs548550427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574591 | AGATGAGTAGGTTGC[A/G]AAAGTTTGCAGAATC | 55626 |
rs548557164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523437 | TTCCACTCTCCTCCC[A/C]CGTTCCCAAAAAGAT | 55626 |
rs548605432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413079 | TGACCCGGAACCTTC[C/T]TTCCTACCTCAGAAA | 55626 |
rs548610275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575185 | AAAACCACTCAGGCA[C/T]GATGGCTCACACCTG | 55626 |
rs548619945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524065 | TAGAGACAGGGTTTC[A/C]CTATGCTGGCCAGGC | 55626 |
rs548655117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464298 | TATCCCTCTTGGCAC[A/C]AAATACCCACAAATA | 55626 |
rs548655253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456335 | GAGTATTAAGAATTA[C/T]TCTACCTCCACTAAT | 55626 |
rs548665654 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460355 | GAGACGGAGTCTCGC[G/T]CTGTTGCCCAGGCTG | 55626 |
rs548719361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529352 | TTGTTGCTATTTAAA[A/C]ATCAGGCAGCTTCTC | 55626 |
rs548733503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546320 | GCTAGGAATACAGGC[A/G]TGAGCCACCGCGCCC | 55626 |
rs548735419 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412404 | ATTCTCCTACCTCAG[C/T]CTCCCGAGTAGCTGG | 55626 |
rs548739407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404962 | CCCAGAGCCCCAGCA[G/T]GTCACCTTCAGGCTG | 55626 |
rs548774968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490532 | GAACGGATCTTGATT[C/T]TCCGCAAACCCATTT | 55626 |
rs548817095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470775 | CAAAAAAATAAAATA[A/G]AAAGCTCCCATTCTA | 55626 |
rs548820696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559822 | TCGCTGAATTTCAAG[C/T]TTTCCTCCAATATGT | 55626 |
rs548830957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512591 | CCCCATCACCTGAAC[A/C]ACCTGTCTCAAAACT | 55626 |
rs548833251 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581201 | AAGCTGGCCAGGTAC[A/G]GTGGCTCACACCTGT | 55626 |
rs548889697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428419 | ACTGCATTCTATCCC[A/G]GAGCTTCCTCCTCAA | 55626 |
rs548893227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539276 | AAAAATGAAGTTATC[A/G]GCCAGGCGCAGTGGC | 55626 |
rs548945753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530843 | AATCAAATTTATCTC[C/T]ATAAATAGTTTTTTT | 55626 |
rs548951385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590442 | TGAGTCCAGCCTGAG[A/C]AACATAGGGAGACCT | 55626 |
rs548957364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479332 | CCTTCTGTATCCATG[A/G]CCTTAGAGAGTCTTC | 55626 |
rs548972504 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480157 | TCAGATGAGGCCCAC[C/G]CAGATAAATCAGGAT | 55626 |
rs548975651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511974 | ATTCTCCTGCCTCAG[C/T]CTCCCAAGTAGCTGG | 55626 |
rs548989152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400582 | CTGTAGCTTAGCCTC[C/T]TGGGTGCAAGTGATC | 55626 |
rs549001506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558166 | GCCCAAATTCCTAAC[C/G]TGAGTAATTATGAGA | 55626 |
rs549004006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566947 | TATGAACCCAGGAGG[C/T]GGAGGGTGCAGTGAT | 55626 |
rs549021024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471509 | GGTAAACCTGGGAGA[C/T]GGAGGTTGCAGTGAG | 55626 |
rs549047823 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583055 | CAAGTCAATCCTAAG[C/G]CAAAAGAACAAAGCT | 55626 |
rs549062857 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550119 | CTACTGCACCCAGCC[A/G]ACACTAGCTTTTCTA | 55626 |
rs549080996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438681 | ATCCCCTGTGGTATC[A/G]CCTGCCCCACACCAC | 55626 |
rs549083022 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537263 | CATGAGCAACAGAGG[G/T]TTTGACAAAGAAAAC | 55626 |
rs549084269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447596 | CGTGTACCTGTAGTC[C/T]CAGCTACCCAGGAGA | 55626 |
rs549087137 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578622 | GGCACAGTGGTTCAC[A/G]CCTGTAATCCCAGCA | 55626 |
rs549088398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503456 | ACAGGTCACCATAAC[A/C]GATCTAATAATAATG | 55626 |
rs549102092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510987 | ATACTTCCTTTTCCA[A/G]AAAAACCTATTTTGT | 55626 |
rs549119222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589779 | CGCCCACCACCATTC[C/G]CCGCTAATTTTTTTT | 55626 |
rs549119879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525745 | AACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 55626 |
rs549140079 | snp | C/T | 1.66363e-05 | 0.00288407 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410402 | GGGTAAAGAAGAAGG[C/T]GAAAGGCATTAGAGA | 55626 |
rs549147030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455046 | CACCCCACACCCAGC[C/T]AATTAAAAAAAAATT | 55626 |
rs549168882 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415292 | TTTCCACCTGCATCC[A/G]TGCCTGACCTGCTGA | 55626 |
rs549169084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407134 | CAGTGAGCTGAGATC[A/G]CAGAGGCTGAAGTGA | 55626 |
rs549175356 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495203 | AGAGCAGTTAATGAG[C/T]GGCTTAACCAACTCC | 55626 |
rs549181588 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517806 | ACTGCACTCCAGCCT[G/T]GGCAACAGGGACAGA | 55626 |
rs549186128 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446485 | AGAGACTGCTAAGGG[A/T]TTTCTAAGGTTTCAA | 55626 |
rs549239904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486548 | AAAGTCCTCCTGAAA[A/G]TAATTCCCTAAGGAA | 55626 |
rs549263506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517349 | AACAGGGTTGCACCA[G/T]GTTGGCTGGAGCTGG | 55626 |
rs549275053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526990 | AGCAAGTGTAAACTT[G/T]CTCACTGTTTGTAAA | 55626 |
rs549290366 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572041 | GGCGTGGTAGCTCAC[A/G]CCTATAATCCCAGGA | 55626 |
rs549306266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407953 | GCTGGGAAGTGCTAA[C/T]TGGTTTTTAAAAGTG | 55626 |
rs549315040 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500908 | CTATCTTTTTAGATA[C/T]TTATGTAAAACTTGA | 55626 |
rs549338065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527756 | CCACATTTATTTATC[A/G]CCTCACACCTGTTAG | 55626 |
rs549343801 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400010 | GAGAAAAGGAGCTAA[C/T]GCACAGCCCAGGCAC | 55626 |
rs549349065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478887 | GCTTTCCTCAGTATA[C/T]GTAAGGACACTTTTA | 55626 |
rs549350905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469974 | TGAGCCACTGTGCCC[A/C]GCCTATTTCATTTTA | 55626 |
rs549392003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501577 | AAGTCTCAGGGCACT[A/G]ACCATATTTGTTCCT | 55626 |
rs549397085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445843 | TGAACAAAATGCTAG[C/T]TGCTAAGAGAGGGTA | 55626 |
rs549399833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493116 | CCCATTTTCTGTTCT[A/G]TGGAGATTTCTGAGC | 55626 |
rs549404789 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503820 | ATCCAAAGTACAGCC[C/T]GTGTGTCAAAATTGT | 55626 |
rs549415937 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419932 | TGTGCCTTGGGTACG[C/T]ATCTGAAAGGCCTCT | 55626 |
rs549424291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471368 | AGGATCACAAGGTCA[A/G]GAGATCGAGACCACC | 55626 |
rs549440818 | in-del | -/AAG | 0.0123036 | 0.0774623 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468390 | TGAAAAAAAAGAAAA[-/AAG]AAGAGGAAGGAGGCC | 55626 |
rs549441070 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465534 | AAACTAGTGACCTAA[A/G]TATTTCAGGTAACTT | 55626 |
rs549468592 | snp | C/T | 1.67579e-05 | 0.00289459 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542142 | GCTGGAGCTGGGCGT[C/T]TGGCCCTCAGTCCGC | 55626 |
rs549483331 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436694 | TATCCCTCTCCTTTT[C/T]TGGATCAACACATGA | 55626 |
rs549484103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424439 | TCAATTGGCCCGCTG[C/T]TTTCCAAAGGCCACC | 55626 |
rs549575105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588574 | TGAAGTCAGGAGTTC[A/G]AGACCAGCCTGACCA | 55626 |
rs549588411 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474847 | GAGGGCAGCTAACCC[A/G]TATCAGAGCCAGAAC | 55626 |
rs549614781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463404 | ATAGATGCTCTGCTG[G/T]AGAAGGTATGCAGTA | 55626 |
rs549636893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477800 | GATTGGTGAGGCCAG[C/G]CATAGTGGCTCACGC | 55626 |
rs549647884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461334 | TGTCAATAACTATTA[A/G]ATTTTGGTTGTGGAA | 55626 |
rs549649903 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497526 | AAGGAGAAATGACAG[A/G]AGAGGACCCAGCACG | 55626 |
rs549652646 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453649 | TCTATAGCTGAAATA[G/T]AGTCTTCACTGTTTC | 55626 |
rs549653662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519342 | TCACTTCAAATTCAA[C/T]AGATATCAGAGTTGA | 55626 |
rs549655252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438621 | TTCAGAATAAGGCCT[A/G]TACAGAGCTCCAGAT | 55626 |
rs549660325 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462110 | CAAGAGATATCTGAC[A/G]AGATTAAAATGTATT | 55626 |
rs549669888 | in-del | -/A/AA | 0.0183124 | 0.0940286 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557301 | TGAGACTCCATCTCA[-/A/AA]AAAAAAAAAAAAAAA | 55626 |
rs549681129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510156 | TGCAGTGAACACCAA[C/T]GAGTCAATATTATAA | 55626 |
rs549736205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580138 | GCTATAATCATCAAT[A/G]ATCTCTGTGCTGACA | 55626 |
rs549754375 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544768 | GATGAGGCCAATAAG[A/G]GAAAGCTGAAATGAA | 55626 |
rs549756593 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414493 | TCTGCCATGAGTCCC[-/CT]GATTCTGTCCTTTGA | 55626 |
rs549776804 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485519 | ATTTTTAGTGGCAGG[A/G]CTAAAACAAAACATA | 55626 |
rs549778561 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579624 | TACCAAGCTAAGCAG[C/G]CAAGAATACAAAAAA | 55626 |
rs549797429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573407 | AGACTCTGTCTCAGA[A/G]AAACAAAACAAAAAA | 55626 |
rs549798734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565431 | CTTGTTATCAGCTGG[A/G]TGCAGTGGCTCACAC | 55626 |
rs549803414 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405299 | CACTAAAACAATTAT[C/T]AGTTTAGGTGCCCAT | 55626 |
rs549814308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416365 | GGATGCTCCAGAGAT[A/G]GTGAAAGATGGTCTC | 55626 |
rs549842074 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | AMBRA1 | GRCh38.p7 | 11:46430912 | AAAGAGGGAGATGCT[A/G]TACTGTCCCATTAAA | 55626 |
rs549846922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424799 | GGGCTATGATAGTGC[C/T]ACTGTACTCCACCGT | 55626 |
rs549850309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525873 | GCAGAGATCACGCCA[C/T]TGCACTCCAGCCTGG | 55626 |
rs549852652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455285 | AGTTCAGTAGAACTG[A/T]ATGTATGTAACAAAT | 55626 |
rs549863728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566397 | CACTCCAGCCTGGGT[A/G]ACACAGCGAGACTAC | 55626 |
rs549880208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445726 | ATGGTTGACACCCTC[C/G]TTTGACCACTAGTCT | 55626 |
rs549884057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527601 | TACAACTCAATAACC[A/G]AAAAACCCCACAAAT | 55626 |
rs549896406 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464842 | ACGAGGTCAAGAGTT[G/T]GAGACCATCCTGGCC | 55626 |
rs549918210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541180 | ATGCGCACATAGCCA[C/T]ACATGGAACATATGG | 55626 |
rs549926965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566777 | AACTGCCCTTGGTCA[C/T]TCCTGTGCGTAGGAC | 55626 |
rs549929601 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532698 | CCTTGGCCTTCCAAA[C/G]TGCTGGGATTACAGG | 55626 |
rs549930038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407777 | TCTCTTCTGGGCAAA[C/T]GGCTCAACACAGACT | 55626 |
rs549935461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422235 | AGCTCTTCCCTGGTA[C/T]ATGACGAATGCTGAC | 55626 |
rs549940188 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556823 | AATAGCTTCATTCTG[A/T]AATGAAGAATTAGTA | 55626 |
rs549947091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493004 | CAGTGAGCCAAGATC[A/G]TGCCACTGCACTCCA | 55626 |
rs549950326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462079 | AGAAAGGCCTGTGGC[A/C]AATTTCTAGCTTTTA | 55626 |
rs549951546 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417195 | TAGCTGGGACTACAG[A/G]CACGTGCCACTATGC | 55626 |
rs549959121 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485194 | CCGCCCGCCTTGGCC[A/T]CCCAACATGCTGGGA | 55626 |
rs549974479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414120 | CTCCCTCAGTGTCAC[A/G]ATGCTCTCTTCACAG | 55626 |
rs549987227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453497 | CATAGGTTCATATGA[G/T]AATTAAATAGTAGTT | 55626 |
rs550003540 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548693 | CATAGCTCAACCTTG[A/T]AGCTAAAGAAAGGAT | 55626 |
rs550010754 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570902 | ACTCCAAGAAAGGGA[G/T]AGAGAACTGGAAAAA | 55626 |
rs550023919 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437043 | ACATAGATCCAGCTC[A/C/G]TGTGTGTTAACGTTT | 55626 |
rs550042510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492565 | TAAATTTATAAGTCG[G/T]CAGTGGAGGTGGGAG | 55626 |
rs550069288 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579597 | CTCTCTTAATACAAC[A/G]TCCTGGCAAGATACC | 55626 |
rs550081648 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533721 | TATTCTCAACCAGCA[A/G]CCACAGTTATCTTTT | 55626 |
rs550089304 | snp | C/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592480 | AATACAACAAAACTG[C/G]GCGGGCGCGGTGGAT | 55626 |
rs550091941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577977 | GAAACAAAACAAAAA[C/T]GCTAGAAGCTGAGTG | 55626 |
rs550108681 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414689 | GAGGCACAGCAGCAG[C/G]TTGGGCAGAGTGCAG | 55626 |
rs550126313 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423735 | TCTGACAGAGCAGGA[C/T]TAACTCACAGGCAGT | 55626 |
rs550162667 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399321 | TCAGGTAATCTGCCT[A/G]CCTCAGCCTCCCAAA | 55626 |
rs550173931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460556 | TCTTGATCTCCTGAC[C/G]TCGTGATCCGCCCAC | 55626 |
rs550189864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516413 | CTAGGAACCTCAAAG[A/G]AAGATCTTTCTTTTT | 55626 |
rs550195144 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532746 | GGCCTTAAGAGTTCT[A/G]ATCTATGAAATCTAT | 55626 |
rs550198658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561803 | GCCAATCACATTTCT[C/T]AGCCAATCAAAAGAA | 55626 |
rs550237415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441369 | AAATACAAAAATTAG[C/T]TGGGTGTGGTGGCGT | 55626 |
rs550243593 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591767 | GGCTGAGGCAGAGAA[C/T]TGCTTGAACCTGGGA | 55626 |
rs550256010 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553700 | CAGTGAGCTGAGACC[A/G]TGCCATTGTACTTCA | 55626 |
rs550256457 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572469 | TTCTCATTTAATCAA[C/T]CATAGATACATCCAT | 55626 |
rs550256461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549224 | TGATTAAAGAACAAA[C/T]TGTGGTCTATACAAT | 55626 |
rs550332139 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502050 | GGAAAATAAGAGAGG[-/T]TTTTTGTCTCTCTCC | 55626 |
rs550354499 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462691 | CCTGCCCTAGTCAAT[C/G]TTTACTAAAATCCCC | 55626 |
rs550362312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418994 | TGGAGGTGATAGGGG[A/G]GCGGGAGGGGGTGAT | 55626 |
rs550381282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475890 | CAAATAAAGGATATA[A/C]TAAAATATCAAGACT | 55626 |
rs550383261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587462 | TGACTATGTAAAACC[C/T]AGTATTATCATACAT | 55626 |
rs550406896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468843 | AGAAAAAAGAAAAAG[A/G]GAGAAAGAAAAGGAG | 55626 |
rs550408933 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571810 | TTCTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 55626 |
rs550412246 | snp | C/T | 0.000148293 | 0.00860957 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545682 | CAGAAGTGGATCTCA[C/T]TGGCAGTGGCAATCA | 55626 |
rs550422568 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553976 | CATCTCCTTAGTAAC[C/T]CTGACAACTCATAGA | 55626 |
rs550444344 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476427 | ATAGTGGTGGGGAGA[C/T]ACGTAAAGAGTCCCA | 55626 |
rs550461560 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487670 | GATCCTGATAAAATA[A/C]ATTCAAAAATCAAAA | 55626 |
rs550481223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561179 | TGAGGTCAGGAGTTC[A/G]AGACTAGCCTGGCCA | 55626 |
rs550497063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517274 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 55626 |
rs550508624 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434114 | GAGTGAAACTCCGTC[-/T]CAAAAAAAAAAAAAA | 55626 |
rs550518163 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475541 | AAAAATGAAAATGAG[A/C]GACAGAGGAATCCTA | 55626 |
rs550543678 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531057 | TCAGCTAATTTTTGT[A/C]TTTTTAGTGGAGATG | 55626 |
rs550547398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575799 | GGATTATAGGCGTGA[G/T]CCTCCGTGCCCAGCC | 55626 |
rs550562764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404066 | ACAAAATTAGCCAGG[C/T]GTGGTGGCGTGTGCC | 55626 |
rs550601541 | snp | A/T | 0.000798403 | 0.0199641 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396341 | ACCTGGGCCTGGCCC[A/T]GTTCAATGCCCCTCA | 55626 |
rs550617550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506363 | ACAAATAAACCTCCC[A/C]CTTAGTTTTCCTTTT | 55626 |
rs550629740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449782 | AGACTTAATATAGGC[C/T]GGGCGCAGTGGCTCA | 55626 |
rs550631126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513589 | ATCACTCTGTGGCAC[A/G]TAACTATTAAGAGAT | 55626 |
rs550642760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536247 | CTAGGTAGACAAGGG[A/G]TATATACAGACATGA | 55626 |
rs550682799 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470970 | TTAAATTATGGTAAG[A/C]TCCATGGAGAAATAT | 55626 |
rs550696078 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46449979 | CAGGAGAATCGCTTG[-/A]ACACAGTAGGTGGAG | 55626 |
rs550706404 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528769 | ATGTTATGTTTTCTA[A/T]CACAGACACACGTAC | 55626 |
rs550706564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520697 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 55626 |
rs550707989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537120 | GGCAAATAACTAAAA[C/T]AGCATTTCTCCTAGA | 55626 |
rs550735417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575288 | CATGGTGTAATCCCA[A/T]CTCTACTAAAAACAC | 55626 |
rs550752657 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536412 | TTTCCCAAGGGACAC[A/G]GTGACAGCTGTGCTG | 55626 |
rs550754313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448513 | TGTATAAGAAAAGAC[A/G]AAAGATCTAAAATCT | 55626 |
rs550769194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480084 | TCCCATCTTTGATCA[C/T]TGCAGCACCTTGACT | 55626 |
rs550778889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583082 | AGCTGGAGGCATCAC[A/G]CTACCTGACTTCAAA | 55626 |
rs550779166 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509680 | AAATCTTAAGTGGGA[G/T]AAAAATTGAAGAATG | 55626 |
rs550782054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503400 | GCTTATTGTCTTATA[C/T]GATTGTGGTTCACAG | 55626 |
rs550821206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464762 | TATTAAACACCGAGA[A/C]AAGGCCGGGCGCAGT | 55626 |
rs550824062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425895 | CTCACGCCTGTAATC[C/G]CAGCACTTTGGGAGG | 55626 |
rs550841566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473050 | TATTGGCATACAAGA[A/G]TGCTAGATCATGTTA | 55626 |
rs550859784 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465078 | AAAAAAAAATAAACA[A/C]CAAGACAATATTCCC | 55626 |
rs550934531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456256 | AAACATCTAGCATTC[A/G]CTCCCACCAGGCAGG | 55626 |
rs550946166 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521471 | CAAATAAACTTGAAC[A/G]CACTGTGGCTTTCTT | 55626 |
rs550949743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590942 | AGAAAAACAAAAAGA[A/G]AAAAAGCTGAATGAA | 55626 |
rs550964842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479570 | GGTGTAGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 55626 |
rs551000011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551774 | GGCTCATGCCTGTAA[C/T]CTCAGCACTTTGGGA | 55626 |
rs551006522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457275 | TGCAATCACTGCCAC[A/G]TTACCATTACCCAGC | 55626 |
rs551026704 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399915 | AACAGAAAAGACTTC[A/G]GCTCAAATCTCAGCT | 55626 |
rs551035952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591830 | CCACTGCACTCCAGC[C/T]TGGGGGACAAAGCAA | 55626 |
rs551043542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457738 | AAACCCCGTCTCTAC[G/T]AAAAATACAAAAAAT | 55626 |
rs551045476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448256 | GAATAATACATATTA[C/T]ACTTGCAGACTACAA | 55626 |
rs551057161 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530738 | GCAAACTATAACCTG[C/T]GGGCCAAAACCAGCT | 55626 |
rs551066222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582386 | AGGTTCCCCTACTAT[A/C]ATCTCTTTTTATTCT | 55626 |
rs551069223 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562653 | ATGTGTTATGTTTGC[A/G]GGTGGGGGAGCAGAT | 55626 |
rs551072795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592523 | AGCACTTTGAGAGGC[C/T]GACGTGGACGAATCA | 55626 |
rs551073733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410472 | CTGTGGCTGCCCATC[C/T]TTTCTCTCTCCTGGG | 55626 |
rs551106426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402411 | CTGTTGCCCAGGCTG[A/G]AGTGCGGTGGCGAGA | 55626 |
rs551114988 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423547 | CAGGCGCCTGCCACC[A/T]CGCCCGGCTAGTTTT | 55626 |
rs551125302 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536152 | TATTGCATATGAAAC[C/T]ATAAGGAACATAATT | 55626 |
rs551130194 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400909 | CCTCCTGGGACACCC[A/G/T]GCTCCAGCTCCCAGG | 55626 |
rs551131294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425227 | ACTTCTGTGTCTTTC[C/T]ACATCTCAAAGGAAA | 55626 |
rs551141187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561106 | TATTGTTGGGCCAGG[C/T]GCAGTAGCTCACACC | 55626 |
rs551168307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425844 | AACTCCGTCTCAAAA[A/G]CAAAAAAAAAGAAAA | 55626 |
rs551198774 | in-del | -/AAAT | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407205 | GAGACTCTGTCTCAA[-/AAAT]AAATAAATAAATAAA | 55626 |
rs551216678 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473919 | CTTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 55626 |
rs551249449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591608 | ATACCTGTAATCCCA[C/G]CACTTTGGGAGGCCA | 55626 |
rs551251773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551244 | GGAGGGACTAGATAA[A/G]TGGAAACAAAAATGG | 55626 |
rs551266028 | snp | A/C | 3.29832e-05 | 0.00406085 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543338 | GTGATTGCAGGAGGG[A/C]ACGCTGACGGTAGTG | 55626 |
rs551293995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559630 | CTAAATACAAAACCT[G/T]CATCCTAATTTACTC | 55626 |
rs551307770 | snp | C/G | 0.000148516 | 0.00861603 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418037 | CAGGCATGGGATAAA[C/G]GACGTTGAAAACTCT | 55626 |
rs551372041 | in-del | -/AATT | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532125 | TATGTCTCAGAAATA[-/AATT]AATTAATTAATTAAT | 55626 |
rs551394287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464466 | TTCAAAGGCACAGAG[C/T]TCCCAGGACCCAATT | 55626 |
rs551418493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513423 | ACTCAACTGATCATA[C/T]GTGATACGTACATTT | 55626 |
rs551420402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504377 | CAAAGGGATGGCAAA[C/T]ATGAAAATGGAAGTC | 55626 |
rs551433395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520570 | ACCCTCTCTTCCCCA[C/G]TGCCCCACAGCATTT | 55626 |
rs551446798 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540321 | CAGTCCTTTTACAGA[C/G]ATCTTTAATAAACTT | 55626 |
rs551460944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431338 | GTCACCAAGCATGCA[A/G]CTGCTGGCTAGCTGC | 55626 |
rs551464633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535556 | CTTCGCATTTAAATT[A/G]GATTATCCACATGTA | 55626 |
rs551474647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440751 | GCACTTAGAAATAGA[C/T]GGTTGCTGCTGAAGT | 55626 |
rs551482370 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503263 | GTCACTATAGGGATA[C/T]TAAATGGCCTAATTT | 55626 |
rs551486820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495685 | GGGAGCCCACAAATT[A/G]TACATGTACACAGAG | 55626 |
rs551494492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494732 | GTAAAAGAAAAAAAA[A/T]TGCACAAGAAAAAGA | 55626 |
rs551515024 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550882 | GCGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 55626 |
rs551522578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518546 | AGGCCCCAGGTCAGC[C/T]GTCTTCTTTTGTAAA | 55626 |
rs551525031 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549495 | TTTTTTTGTATAATT[C/T]TGGAATTATTTCAGT | 55626 |
rs551560292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417254 | ACGGGGTTTTACCAC[A/G]TTGACCAGGATGGTC | 55626 |
rs551567699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541518 | AGCAATACAATCAGC[A/G]AAGAGCCAATATACT | 55626 |
rs551579253 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439405 | CTAAATACAGAAAAG[A/T]AATTAATAGTATGAT | 55626 |
rs551581900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511089 | AACAGATTTATTATA[C/T]AAAAGGAGGATAAAT | 55626 |
rs551638348 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519747 | AGCAGGGCATTTGGT[A/T]TTCAAGCTTTGCAGC | 55626 |
rs551638373 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552558 | GGCGTGATGGTACGC[A/G]CCTGTAATCCCAGCT | 55626 |
rs551653929 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488385 | CGCTTGAACCCAAGA[G/T]GCGGAAGTTGCAGTG | 55626 |
rs551687101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513192 | TAACATTTATCTTGT[C/T]GTTTGGTTCCTCCAT | 55626 |
rs551703052 | snp | C/T | 1.80873e-05 | 0.00300721 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408538 | ACCTGAGGCGGCTGT[C/T]CCTGGCTCCGGCACC | 55626 |
rs551709672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438761 | CAATTCCATTCACCC[A/G]GTAAGAGTTCACTCT | 55626 |
rs551711423 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466116 | AAGATGTACATAAAA[C/T]GGTAGTAAGATGTAC | 55626 |
rs551717130 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451504 | CTCTAAGATTTGTTC[C/T]AGGAGAAGGGAAATG | 55626 |
rs551722394 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516943 | TCACTGAAGCTGAAG[-/A]AAAAAAAAAATACAA | 55626 |
rs551734110 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462861 | GGTTCAAGCGATTCT[C/G]CTTGCTTCAAAACTC | 55626 |
rs551757420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447264 | AAAAGGCCACGCGCA[A/G]TAGCTCACACCTGTA | 55626 |
rs551785265 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470456 | TAGCCGGGCGTGGTG[A/G]TGGGTGCCTGTAGTC | 55626 |
rs551820386 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471181 | ATGCAGTGGCTCATG[A/C]CTGTAATCCCAGCAC | 55626 |
rs551822130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433063 | CTTCCATCATAATTA[C/T]AACCCACAGAAAAAA | 55626 |
rs551876096 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488517 | TTCAATAATAATAGA[A/G]ATTTCAATACCCACT | 55626 |
rs551876488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486624 | AAAGAGACAAGAGGA[A/G]GCTAGGTGCAGTGGC | 55626 |
rs551879162 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490706 | AAAAGCCATTCACCA[C/T]GCAAAAGTTCCACTT | 55626 |
rs551910651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506644 | TGACTGACAGGCTGT[A/C]CTCTTTCACAAATGC | 55626 |
rs551916326 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437561 | GGTTCTGTTTACAAT[A/T]TCATTCTCACATTTG | 55626 |
rs551934419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408037 | GGTGAGAGGAAGGGG[C/T]TGATGATAGGCCAGG | 55626 |
rs551958786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586784 | CTTGCCCAAGTTGTA[C/T]AGCTAGTAAGCAGGG | 55626 |
rs551967800 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396742 | GCTCTGAGGGCCTTG[C/T]GGGGAGAAGACTGGT | 55626 |
rs551971017 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567368 | TGAGCCACCAAGCAC[G/T]GCCTTATTTATTTTT | 55626 |
rs551977860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507403 | AGAATGGCGTGAACT[C/T]GGGAGGCGGAGCTTG | 55626 |
rs551980528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565707 | CCAGATCATGTCTCA[A/C]AAAAAAACGTGTATA | 55626 |
rs552004219 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445869 | GGGTAGAAAATAAAT[C/T]GAAAAAACAAACTTC | 55626 |
rs552006252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558273 | TAACCTAATATCACC[A/G]GGCGCAGTCGCTCAC | 55626 |
rs552009725 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528896 | AAGGCAGTAGAAGCT[A/G]GGCTACCTCTGTGTA | 55626 |
rs552043088 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435925 | GTCCCACCGTGTGAT[A/T]CCCTGCCAGGAAGAA | 55626 |
rs552050141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453800 | AGGCACTTGGTCTAT[A/C]ATGTTTAGGCAGTTT | 55626 |
rs552051723 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454551 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 55626 |
rs552056667 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420134 | TACAGACATGGAACT[A/G]GTTCAGGTTTGAGGC | 55626 |
rs552064741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404335 | GCTCTGGTTTTGTCA[A/G]TACAAAACCTGCCAG | 55626 |
rs552069284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550253 | GTAAACAGCAGGTTA[C/G]GTCTAAAACCTTCAT | 55626 |
rs552069761 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446602 | ATTATTTGTGTGAAG[A/T]GTCTTGTGCATCGCA | 55626 |
rs552081386 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414095 | CAAGGGCTCCCTGAA[C/G]AGACCTGAGCTCCCT | 55626 |
rs552087084 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455072 | AAATTTGTTTTTGTA[A/G]ATATGGGATCTCAGT | 55626 |
rs552088208 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502673 | TCATCAGGTCTATCA[C/T]CTGATAAGAATGGTA | 55626 |
rs552134922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473457 | CTGATAGGATGAGTA[C/T]TGTATTGACATCTTT | 55626 |
rs552136945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481623 | CTGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 55626 |
rs552140711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554922 | TAGAAGCAAAAGACA[C/T]GGCTAGGATATGTAC | 55626 |
rs552149841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499818 | CCGCCACCACGCCCA[A/G]CTAATTTTTATATTT | 55626 |
rs552158018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491516 | TTATTGGAATTTTCT[C/G]AAGAGAAGAAAACAA | 55626 |
rs552180213 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547573 | GAGCTGTATCACACA[A/G]GCAAATGATTGTTAT | 55626 |
rs552198300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474214 | GTAAAATCAGTCAGT[C/T]TGATATTTTTCCTGG | 55626 |
rs552205790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546633 | TATTGCAAAAAAAAA[A/C]AAAAGGAATGGAAGA | 55626 |
rs552209598 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483154 | AGTGAACTGGGCCTA[C/T]GATAAACCCAGGGAC | 55626 |
rs552242111 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595767 | CGAGGCGGGCGGTTC[A/C]TGAGGTCAGGAGATT | 55626 |
rs552242426 | in-del | -/TAAGA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576133 | AAGAAAAGAGTCATT[-/TAAGA]TAAGGAAGACATCCC | 55626 |
rs552245777 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436054 | TTTGTCTCATGTAGA[A/T]ATACCTCAAGCAAAA | 55626 |
rs552255070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530165 | GTACACGGGAAATTA[C/T]TCCCAACGTATTTGC | 55626 |
rs552271001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483885 | ACAAAGTGAGACTCT[C/G]TCTCGAAAAGAAAAA | 55626 |
rs552298572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514794 | GCAGGATTTTTTCAT[G/T]ATTTCATAGGAACAC | 55626 |
rs552346881 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465944 | TGGCCTTCAACCTCA[C/T]TAAGGCTGACAAAGA | 55626 |
rs552370954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404864 | AGCCAGAAATGGGCT[A/G]CATGCTAACCAAGAA | 55626 |
rs552373740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522395 | CATGGACATCTTTAC[C/T]TAGTATCCAAATCCA | 55626 |
rs552388081 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444380 | TTGGTAACCAATTAA[A/G]TAAAAAATGGATTTT | 55626 |
rs552396248 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458763 | CACCATGACCAGAAC[C/G]TCACATTTTAGATAC | 55626 |
rs552425174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481093 | ACTATTAATTGAATG[C/T]TGTTCAGATTCCATC | 55626 |
rs552437145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412224 | ATACACAAACTATCC[A/G]TATCCTTTTGTATAC | 55626 |
rs552442429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562999 | AACAGGGTTTCACCA[C/T]GTTAGCCAAGCTGGT | 55626 |
rs552444028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46449930 | GGGGCGTGGTGGCGC[A/G]TATCTGTAATCCCAG | 55626 |
rs552453788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441251 | GGGCACGGTGGCTCA[A/C]GCCTGTAATCCCAGC | 55626 |
rs552477301 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415957 | AGTAGGCAGGCTGGG[A/G]TTTCAGACATAAAAA | 55626 |
rs552494675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496861 | TCATGCCTGTAATCC[C/T]GGCACTTTGGGAGGC | 55626 |
rs552504950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489031 | CCTCAGCCTCCAGAG[C/T]AGCTGGGACTACAGG | 55626 |
rs552509419 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433843 | TAATAAGGCTGAACG[C/T]GGTGGCTCATGCCTG | 55626 |
rs552514303 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408983 | TCAACAACAGGCCCC[C/T]GTCGGGGAGTGGGGA | 55626 |
rs552528697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457297 | TTACCCAGCGACAGA[C/T]AGGCTAAGCTCCAAG | 55626 |
rs552559219 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399435 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAACCT | 55626 |
rs552577381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419212 | TAATATTTTCTGAGC[A/G]GCATATTTTCTAAGT | 55626 |
rs552593017 | snp | G/T | 1.68286e-05 | 0.0029007 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433622 | CTCACCGAAATGGCA[G/T]TGGGACCTGAGGGCC | 55626 |
rs552615050 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419952 | GAAAGGCCTCTGACA[A/G]GACAGCCTCCAGAAT | 55626 |
rs552626513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517666 | GGTGAAACCATGTCT[C/G]TACTAAAAATACAAA | 55626 |
rs552644782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427329 | GATCAGCAGCAGCAG[C/G]AGCAGCAGCCATCAT | 55626 |
rs552664364 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568892 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 55626 |
rs552675010 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448088 | GGCCCAAATAGTGTG[C/T]CAGGGCCAAGAGAGA | 55626 |
rs552701223 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484236 | GGGTTTTGACCTCAC[A/G]TTTGGCCTTCTCTTT | 55626 |
rs552708713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583685 | AAAAAAAAAACAACA[A/C]AACAACCCCATCAAA | 55626 |
rs552727606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562285 | ACAGGTAAGCTTAGC[A/G]CATGTGAAGGCCGGA | 55626 |
rs552761911 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473683 | TTGAGACGGAGTCTC[A/G]CACTGTCGCCCAGGC | 55626 |
rs552770116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478552 | CTAGGAAACCAGGGT[C/T]CAGCTTTTTATTTGA | 55626 |
rs552782442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529702 | GTTAGGTGGGAATGT[A/G]AGCCTGTTTTTTCAA | 55626 |
rs552783807 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564165 | AAAAAAAAAAAAAAA[C/T]GTAAGAGCAATCTTA | 55626 |
rs552799833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553144 | GATAGGGTTTCACCA[C/T]ATTGGTCAGGCTGGT | 55626 |
rs552799843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544399 | CAGTTCTTCCCTCAT[A/G]TGGCAGCTACACCGG | 55626 |
rs552810271 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583197 | TCAGAAATAATGCCG[A/C]ATATCTACAACTATC | 55626 |
rs552835860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544909 | ATCACTGAAGGCCAG[C/T]AGTTCGAGACTAGCC | 55626 |
rs552837762 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525231 | CCTTGGGCCATGGAC[G/T]TTGAGGCTGCAGTGA | 55626 |
rs552845523 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504728 | CCTCCAAAGCCACCC[G/T]CCCAAGAGATAAATC | 55626 |
rs552861276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545087 | ACTTGGGCCCATGAG[G/T]TCATGACTGCACAAC | 55626 |
rs552885576 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445474 | AACCTTCACAGAAAA[C/T]TCCCCTTTAATAATT | 55626 |
rs552892483 | snp | A/C/G | 0.00358891 | 0.0422285 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46395928 | GGCCACTGTAGGGAA[A/C/G]ACACAGTCAAGGGAG | 55626 |
rs552897462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545566 | TCTCTATCACGTCAG[C/T]CCTGTGCCAGACAAT | 55626 |
rs552922867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520064 | GAATCGCTTGAACCC[A/C]GGAGGCAGAGGTTGC | 55626 |
rs552939979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448519 | AGAAAAGACGAAAGA[C/T]CTAAAATCTGTAATT | 55626 |
rs552940526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427122 | GGAGAGAGTCATAAT[C/G]AAGTTTGTAGATTGA | 55626 |
rs552955661 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410136 | TTCTCAAATGAAACT[A/G]TACACAAAAGATCAA | 55626 |
rs552978794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441007 | CACAGTAATGTACTA[C/G]AAGGTTTGGTGCAAT | 55626 |
rs552982493 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448818 | ATACTATGAACAACC[A/G]TATGCCTACAAATTT | 55626 |
rs553020594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538237 | GTATACGACATCCTA[C/G]CTCATTTAAAAGTGA | 55626 |
rs553040136 | in-del | -/TTTTTTTTTTTTTTTTTTTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400490 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTTT]GAGACCAGGTCTCGC | 55626 |
rs553062376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417515 | TATTTCCAATTCTTT[C/T]TAAGTTAAAGTCTAC | 55626 |
rs553070572 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471770 | GTAACTGGGACTACA[C/G]GCACGCGTCACCATG | 55626 |
rs553073074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481885 | AGTGTATCATAGCAA[C/T]GCTGCTGGTGATTAA | 55626 |
rs553082131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410634 | AACCGGCTCCTCCTC[A/G]GAGCTAAGAGACAGC | 55626 |
rs553090404 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513124 | ACAAATAGAAGGTTC[A/G]GATCAACACAGGAGT | 55626 |
rs553114226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521887 | TACAAAAAGACACCA[C/T]AGTGCCTACAGTGTA | 55626 |
rs553140992 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548024 | CTACAAATTGAGAGA[C/G]ATAAACCTAAATTAC | 55626 |
rs553147120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505577 | TCCATTGTTACTAAC[A/C]AGGGAGCAATATAAG | 55626 |
rs553157760 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487015 | GTAATCCCAGCACTT[C/T]GTGGGGCTGAGTGGG | 55626 |
rs553175849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561274 | TAATCCCAGCTACTC[A/G]GAAGGCTGAGGCAGG | 55626 |
rs553188559 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554498 | AGGGACCTAAACACA[A/C]TAACAGCTCAAACAA | 55626 |
rs553252073 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550577 | TTAATGGGGGGAGAT[A/G]CTGAAAATATTCATT | 55626 |
rs553259677 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497033 | ACAAGAATCGCTTGA[A/C]CCAGGAGGCGGAGGT | 55626 |
rs553264071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528188 | TTATTTATTTATTTT[C/T]TGGAGATGGAGTGTC | 55626 |
rs553288239 | snp | C/T | | | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397726 | CCGAGAGGTGGAGGG[C/T]TGGGGTGAGGAGGTG | 55626 |
rs553297913 | in-del | -/TGTTT | 0.00399838 | 0.0445332 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579710 | ATGAGGAAACAGACA[-/TGTTT]TGTTTTGTTTTGTTT | 55626 |
rs553323780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516690 | CGCCCACCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 55626 |
rs553333305 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567268 | GTAGAAACGTGGTTT[C/T]ACCATTTTGGCCAGA | 55626 |
rs553339501 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418215 | TCTATATCTATCTAT[C/T]TATTTTATTATTTAT | 55626 |
rs553352207 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515757 | CTTGGCTCACTGCAA[A/C]CTCCGCCTCCTGGGT | 55626 |
rs553357313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479633 | ACCCAGGAGGCGGAG[A/G]TTGCAGTGAGCTGAG | 55626 |
rs553377821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535797 | AAAAAGATAAAAAAA[A/G]GGAAGGCTGCATATG | 55626 |
rs553393414 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575025 | ATAAATATATCTGAA[A/G]ATATTCTTGGCAGCA | 55626 |
rs553400750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476095 | ACAATGACTGATGAG[C/T]CCACACAAACCAAAC | 55626 |
rs553410104 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463939 | GCTCTTGCCTTGGGG[C/T]CAACAGGATTAGCAC | 55626 |
rs553417126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512403 | CCCCTGTTGGCTGTC[C/T]ATCTGAATGACAACA | 55626 |
rs553422797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425570 | AATGAGGCTGGGCGC[A/G]GTAGCTCACGCCTGT | 55626 |
rs553435909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517401 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 55626 |
rs553437762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508571 | ACCAGTGTTTCTGTT[C/T]TGAGATAAGGCAAAC | 55626 |
rs553438321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463999 | AGGAGAGATAGGGAG[C/G]TTTTCACTCTAGGAA | 55626 |
rs553498166 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414782 | AGCCCCTGGGATGGC[C/T]TTGTAGAGGGGCTGA | 55626 |
rs553501131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509323 | TTATATAATTTGACG[C/T]TATGGACTGAAAACA | 55626 |
rs553514193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457476 | AGGTTCAAGGAAAAT[A/G]TTAATTTTGAGATTT | 55626 |
rs553563072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431744 | GAGACCAGCTTCTGC[C/T]TAAGAGAAGCAAAAG | 55626 |
rs553565233 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439709 | AAACTCGAATGACAA[A/G]TAGGAAGCTCCTATT | 55626 |
rs553625229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424793 | TACAGTGGGCTATGA[C/T]AGTGCCACTGTACTC | 55626 |
rs553631418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543532 | GGAAACAACTCTCTA[C/T]CCCTGAAGCACTGAC | 55626 |
rs553632217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407318 | CTCTGAGAGGTTTGC[C/G]TCCTACTGAGAGGGC | 55626 |
rs553648485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436283 | CCAGGCTTATGTGAT[C/T]TGATACTTAAGAGTG | 55626 |
rs553673525 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520771 | GGCTAATTTTTTGTA[-/T]TTTTTTTTTTTTTTT | 55626 |
rs553685081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586148 | GCACTGGCTCACACC[C/T]GTAATTCCAGCACTT | 55626 |
rs553691618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475524 | TCACAGACTATCCAA[C/T]GAAAAATGAAAATGA | 55626 |
rs553699137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432435 | GACAGAGGATATCTG[C/T]AGGAGACAGGAGGGA | 55626 |
rs553700412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414277 | AAGAGCCAGCACCTG[A/G]CTCTTAGAGCCTCGC | 55626 |
rs553709072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468536 | AGGCGCAGTGACTCA[C/T]GCCTGTAATCCCAGC | 55626 |
rs553712046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531436 | AGAATGAGGCTGGGC[A/G]CGGTGGCTCACGCCT | 55626 |
rs553731586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581449 | CGTCTCTACTAAAAA[C/T]ACAAAAAATTAGCCT | 55626 |
rs553764208 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569481 | AAGTGCCAAGCAAGA[C/T]GGCAGGTACAGAATA | 55626 |
rs553794623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565130 | GGCATGGTGGCATTC[A/G]CCTGTAGTTCCAGTT | 55626 |
rs553796085 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450683 | CCTGAACTCAAGAGA[A/T]CCACCTGCCTTGGCC | 55626 |
rs553805401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572129 | AACATGATGAAATGC[C/T]GTCTCTACCGAAAAT | 55626 |
rs553842475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498127 | GAATATGAGTGAATT[C/G]GAAGATATTTGCCAG | 55626 |
rs553861035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554293 | AAAATAAAAAAAACC[A/G]ACCTTCCGACCTCCT | 55626 |
rs553906277 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414193 | TTGGATAACATTCTT[C/T]TTTCATTTATCAGTG | 55626 |
rs553911705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452672 | AATGCAGTCTTAAAA[C/T]CTGTCCTAAGAAAGG | 55626 |
rs553923211 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442835 | AATTTCAGCTTCAGA[A/T]ATGAACAACTAAGCC | 55626 |
rs553927807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465480 | GGTCTAAGTTTTTAC[C/T]ATATTTTCTCAGAGA | 55626 |
rs553932452 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595943 | GAGGCTTGTGGAGCA[C/T]AGCTATAGCCCTCAT | 55626 |
rs553935446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576778 | TCAAATAGCTTCATG[C/T]AAATGCAACATGGCT | 55626 |
rs553945610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569073 | TGGCCTCCCAAAGTG[A/C]TAGGATTATAGTTGT | 55626 |
rs553971162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428788 | GGTATCTCTGTCAGC[G/T]TCCCCTCTTGTGAGT | 55626 |
rs553986842 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595042 | CAGCCTGGGCAACAT[A/G]GTGAGACTCCAGTCT | 55626 |
rs554008215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569999 | AGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55626 |
rs554014634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459085 | GTGACCAAATTATGT[C/T]CAACTACACCATGGA | 55626 |
rs554018574 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402831 | TTTTAAAATGTACAA[A/G]CAAATGGCTCCCCCA | 55626 |
rs554043727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524722 | TTTCTTCCTTAGATT[A/G]CAGCTCCCAAAATAT | 55626 |
rs554043908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411762 | GCATGAACCACTGCG[C/T]CCAGCCCAAATCTGT | 55626 |
rs554096666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507547 | CCCTGCTCCTTTAGC[A/G]CATCCTCCCATGGCT | 55626 |
rs554108503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523898 | TTTGAGATAGAGTTT[C/T]GCTCTTGTTGCCCAG | 55626 |
rs554116809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532063 | GGCGGAAGTTGCAGT[A/G]AGCTGAGATCGGGCC | 55626 |
rs554140284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422564 | TTTCTTGTTCAAAGA[C/T]AGACAGGAAAAGAAT | 55626 |
rs554159932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499163 | TTACCATTTACAAAT[G/T]CCTCTCCTCCCTTAT | 55626 |
rs554182360 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555141 | CCACACACACATACT[C/T]CCACTCCCAATAACA | 55626 |
rs554191038 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405065 | CAGACATGCCATGAA[C/T]ACAAATTAGTGGTCC | 55626 |
rs554226184 | snp | C/T | 3.32524e-05 | 0.00407739 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397697 | GCCAGTTGCCCGGCC[C/T]CTGGGAGCAGTCCCC | 55626 |
rs554237041 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452339 | ATTTTAAGGTTTTTT[G/T]TTGTTGTTGTTGTTG | 55626 |
rs554256688 | in-del | -/A | 0.199873 | 0.244923 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526734 | ACACCCCACACACAC[-/A]AAAAAAAAACCATGA | 55626 |
rs554260251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435784 | CAGCCTGGTAAGGTG[A/G]CAAGATCTGAGGGTG | 55626 |
rs554262990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546977 | TTGGGAGGCTGAAGC[A/G]GAAGTATCACTTGAA | 55626 |
rs554271434 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570217 | CAGTGAGCAGAGATC[A/G]CACCATTGAACTCCA | 55626 |
rs554281331 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562138 | ACCCTTTTACCTGGG[G/T]TGGCCAGAGAAAGCC | 55626 |
rs554284823 | snp | A/C | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594563 | AATTATGTAGCCTGA[A/C]CTTAAGGCAGGGGGA | 55626 |
rs554306179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475968 | GTGTCGGAAAAGAAC[A/G]CTGTTCCCCTCCATA | 55626 |
rs554319934 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565258 | AGAAAAATTCCCTCT[-/A]AAAAAAAAACGAAAA | 55626 |
rs554320027 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522959 | TCAGAAAGGCAAAGC[A/G]AGTTAGTACGTGAAG | 55626 |
rs554351988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412548 | GCCTACCTCAGCCTC[C/T]CAAAGTACTGGGATT | 55626 |
rs554383816 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590912 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs554386958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466153 | CTTGTTTGGAGCCTA[C/T]AATCCAGTTGGGAAG | 55626 |
rs554445644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569269 | AAAAAAGTAACCCTC[C/T]AACCCTACCCTCTTG | 55626 |
rs554454008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531203 | TCACTCATTTAGATA[A/T]TGTTTGTGATTGCTT | 55626 |
rs554463493 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46594044 | GCAAAAGATCACCGA[A/G]TACAAGAACGCCCCA | 55626 |
rs554467830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482260 | GATGGGCAATGTTTT[A/G]GATAATTGTAAATGC | 55626 |
rs554470608 | snp | A/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452833 | CTTAGAAGTGTCCCA[A/T]GTTTCTCTGAGTTCT | 55626 |
rs554532555 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420880 | AGAAAGTAGCCTTAC[A/G]AGGAGAATAATAAGA | 55626 |
rs554547323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428108 | TTGCTAGCGCTCTAG[A/G]GGGAGAAGGGGTATA | 55626 |
rs554548689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404469 | CTCCTTGCCCTAGGA[C/G]GGACAAGGCTGGAGA | 55626 |
rs554554828 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515464 | GGTGACAGAGTGAGA[C/G]TGCATCTCAAAACAA | 55626 |
rs554562267 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497151 | AATAAAATAAAAAAA[A/T]AAAGGGAAGGGGTTA | 55626 |
rs554603500 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487386 | TATTAACAAGTTAAT[-/AA]AGTTAGATGAAAATA | 55626 |
rs554615805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571127 | ATGGTTCTGGCTTCA[A/G]TTCCGCTGATATTCT | 55626 |
rs554616409 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579214 | TGTAATCCCAGCACT[A/T]TGGGAGGCTGAGGCA | 55626 |
rs554622926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505928 | CGCAGTCTCCCAGGC[A/G]TGCATGGAAAGAGGG | 55626 |
rs554643658 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467612 | AGAGTGCACTGGCAC[A/G]ATCTCAGCTCACTGC | 55626 |
rs554675853 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396177 | AGGTGGCCCCAGTCT[A/G]TAGCAGGCCCTGGGG | 55626 |
rs554680035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460012 | GAAGTAAGAGTGTTA[C/T]AGCTTTAGTAGCCAA | 55626 |
rs554689449 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516583 | CTACAGGCACCTGCC[A/T]CCATGCCTGGCTAAT | 55626 |
rs554717676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472653 | CAATCTTTTTGTGTT[C/G]ACAACATACATTTGA | 55626 |
rs554735978 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583442 | GGACATAGGCATGGG[A/C]AAGGACTTCATGTCT | 55626 |
rs554769927 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501722 | AATAATTATATTTTT[A/G]TTAATCTTTTAGATG | 55626 |
rs554776038 | in-del | -/C | 0.0337553 | 0.125452 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584482 | TACATATGTAACTAA[-/C]CTGCACATTGTGCAC | 55626 |
rs554779003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464862 | CCATCCTGGCCAACA[C/G]GGTGAAACCCCGTCT | 55626 |
rs554780913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473609 | AATAGCAATAATAAG[C/T]ATTGAAAAGGCAGAA | 55626 |
rs554782167 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594934 | AAGGAAACAAGATAG[A/T]CCCAGTTTGTCGGGC | 55626 |
rs554783977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546837 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGACCAC | 55626 |
rs554793030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465251 | CTCATGCTCCTCCCT[A/G]CCCTCCTTCTGCCTC | 55626 |
rs554806924 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496471 | CCCATGAGAGAGAGC[C/T]GGCCTTCCCAGAATC | 55626 |
rs554811991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483403 | TGGCATGAGGACCCA[C/G]GGGAAGAGCTGGCCT | 55626 |
rs554821214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585211 | CAGGGACACAAACAC[C/T]GCGGAAGGCCGCAGG | 55626 |
rs554843825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434711 | CTCCTGCAAAGCAAT[C/T]TTTCTCTGGCCTGTG | 55626 |
rs554843895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443373 | GCAGAAATGGCATGT[A/G]GATAACAACTGCTCA | 55626 |
rs554848624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539011 | GCACAGATAGAGAAC[A/T]TTTCCATCAGTGTAA | 55626 |
rs554869747 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576081 | TGGCTTTGATCACTA[C/T]GATTCAGGAAGAATC | 55626 |
rs554880603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435641 | GAAACAGAACAAAGC[C/G]CAGCTGCGGCTGGAT | 55626 |
rs554931743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568953 | CTGAGACTACAGGCA[C/T]GTGCGACCAAGACCA | 55626 |
rs554932632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586018 | CACGTTGGTCAGGCT[A/G]GTCATGAACTCCCAA | 55626 |
rs554979761 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526191 | AGTCTGGGCAACAAG[A/G]GCGAAACATCGGCTC | 55626 |
rs554987259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561565 | CAAAGCAGGATTTGA[A/G]TTCAGGCTTTTCCTT | 55626 |
rs555010888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450045 | GCCTGGGCAACAGAG[C/T]GAGACTGTCTCAAAA | 55626 |
rs555013765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404399 | GAGCCCTGATCCCTG[G/T]GCTCCCCTGAAGAGT | 55626 |
rs555043274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566417 | AGCGAGACTACATCT[C/G]AAGAAAAAAAAAAAA | 55626 |
rs555047745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562420 | TACTATTAGAGGATT[G/T]TAGCTAAGGAAATGA | 55626 |
rs555049006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553447 | AGAAAGATTTCACAG[C/G]AAGAAAACACCAAGT | 55626 |
rs555060826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554085 | GAAAGTGCCAAAAAT[A/G]CAGTTCCTATTAGTT | 55626 |
rs555073518 | snp | C/T | 0.0032664 | 0.0402806 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494253 | TCACTAAGGAAGAAT[C/T]ATCCACCAGCCCAAA | 55626 |
rs555098138 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430077 | ACGATAAACAGAGAA[G/T]GGAAAGATCAAAAGG | 55626 |
rs555101982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442732 | GATACGAAAACTGGC[A/G]TATCAGGAAATGCCA | 55626 |
rs555117060 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455442 | TATCTTTTAACATGC[C/G/T]TTGAAAGAGGAGATG | 55626 |
rs555119845 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568131 | CCAGCCTGGGAGACA[C/G]AGTGAGACTCTGTCT | 55626 |
rs555124183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555016 | GGTCAAGACTACAGT[A/G]AGCCATGATTGCACC | 55626 |
rs555153399 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480143 | AATAGCTCATGTAAT[C/T]AGATGAGGCCCACCC | 55626 |
rs555154058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446797 | AACTCCAGGGTAGGT[A/G]CTCTTAGCACCACTA | 55626 |
rs555154954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418604 | TCCTTCCTGTGTCCA[A/T]GTGTTCTCATTGTTC | 55626 |
rs555173274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529630 | CATAGACTAAGGCAT[C/G]AAGAAAGTCCATGCC | 55626 |
rs555214637 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523651 | GAATGCCTGCTAAAT[C/T]GATACCTGTGTAAAA | 55626 |
rs555225453 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423803 | AGTTCCGCTCTTGCT[G/T]CCCAGGCTAGAGTGC | 55626 |
rs555248134 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477940 | AATTAGCCAGAGCTA[A/T]TTTTTGTATTTTAAA | 55626 |
rs555253460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463034 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGTCT | 55626 |
rs555260912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485890 | CTTCTCACTAGTGGT[A/G]TAAGATAAGGTAAAG | 55626 |
rs555295438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502220 | GAGTAGCTGGGACTA[C/T]AGGTGGAGAAGTTTT | 55626 |
rs555301347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437181 | AGTAAGATTTTCCTT[C/T]TTCTGGAAAGCTTGG | 55626 |
rs555342959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522532 | ATGGGAAAAAAAAAG[A/G]TCCACAGCTAGTTTT | 55626 |
rs555356495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587955 | GGTACCAAAACAACA[C/T]ACAATGAAGAAAAAA | 55626 |
rs555369613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408875 | GTTAACTTGTCTGTG[C/T]CCATTCTCCCCCAAG | 55626 |
rs555410244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400991 | CTTCAGGTTTTAAAG[A/C]CTTCTAACAGTGGGG | 55626 |
rs555419745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429695 | TGGTTACAACCAAAG[G/T]TATTATACTGTGCAA | 55626 |
rs555425419 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460871 | GTGGGAAGATCACTG[A/G]AGGCCAGGAATGCAA | 55626 |
rs555440976 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541140 | TACAAAATTACAGAA[A/G]GAAGTCCCTAATAAA | 55626 |
rs555441183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558410 | CAAAATTAGCTGGGC[A/G]TGGTGGCACATGCCT | 55626 |
rs555455240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550512 | CCTATTACTTCTCAA[C/T]TTTTTACTTAATGGG | 55626 |
rs555469464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588672 | CCCAGCTACCAGGGA[C/G]GCTGAGGCAGGAGAA | 55626 |
rs555469473 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579223 | AGCACTTTGGGAGGC[C/T]GAGGCAGGAGTATCA | 55626 |
rs555470799 | in-del | -/ATAG | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450716 | CAAAGTGTTGGGATT[-/ATAG]ATAGGCATGAGCCAC | 55626 |
rs555493407 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415168 | TGCCTATGAGACACA[A/C]AAGAACCCTGAGCTC | 55626 |
rs555544108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572877 | AGTGGATCACCTGAG[A/G]TCAGGAGTTCAAGAC | 55626 |
rs555563494 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526112 | CCAGAGGCTGAGGCA[C/G]GAGAATCACTTGAAC | 55626 |
rs555592363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547981 | AGCATTCACAGTGTA[C/G]GCTTAAAAACTGGAG | 55626 |
rs555592721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533961 | TCCTCTGTCTAAAAT[A/G]TCCTTCCCCTAGTGT | 55626 |
rs555594178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556861 | GGTAATAAGGGCTGG[C/T]TGCGGTGGCTCATGC | 55626 |
rs555603557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565890 | TGATCCTCCCACCTC[A/G]GCCACCCAAGTAGCT | 55626 |
rs555629717 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426008 | AAAAATTAGCTGGGC[A/G]TGGTGGCGGGCTCCT | 55626 |
rs555648772 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510198 | AGCAAGTAGGCATAG[A/G]AGGCACAGATGCCTT | 55626 |
rs555662076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436448 | ACATAAAACCGAAGA[C/G]GGACCACAAGGATGG | 55626 |
rs555675720 | snp | C/T | 0.000399281 | 0.0141238 | stop-gained, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518150 | AAGAATTACTCACGG[C/T]CAGGCGCGGTGGCTC | 55626 |
rs555693238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509431 | TGCCCCAGGCACACT[C/T]GACTCAATAATTCTA | 55626 |
rs555696556 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509284 | ATTGCCTTCTCAAGT[A/T]TTCCTCCATCTCTCA | 55626 |
rs555730132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408338 | TGGTGGGAGTTGAGG[C/T]GAGCTGCAAGAGTGA | 55626 |
rs555756594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501144 | CATTTACAGCTGGTA[C/G]TCAAATAATGTTGTT | 55626 |
rs555771993 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452529 | TCTGAGCTCTCTGTA[A/C]ATAAATACACTGGCT | 55626 |
rs555791687 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492636 | ACATATAAAAATGGA[A/T]TTCTGCTTTACTTCC | 55626 |
rs555796054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477295 | AGTTTTCATTAGGGA[A/G]AGTCTTTGTCTCTTT | 55626 |
rs555808999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445176 | GATATTAAAATTTCA[C/T]GGGAGGAGAGACAAG | 55626 |
rs555863086 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429193 | TCATCCTCCCCCTCT[A/C]CCTCGGACAATCTTC | 55626 |
rs555868048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572815 | ATAAGTATTCTGAGC[C/T]GGGTATGGTGGCTCA | 55626 |
rs555868886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501950 | GCCTTTCTCCTAAGT[A/G]TACCTAAATAAAGAC | 55626 |
rs555874043 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399631 | AGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 55626 |
rs555893564 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463286 | TATACCTGTTCTATT[C/T]CCACTCAACACTTTC | 55626 |
rs555897959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525642 | TGTAGTCCCAGCTAC[C/T]CTGGTGGCTGAGGCA | 55626 |
rs555907402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564215 | GCAGAAAAATCCCAG[C/T]ATTAAAAAAAAAAAA | 55626 |
rs555914730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462220 | TAAACAAGTGAGCAC[A/G]GCGGTGTAAGCACAC | 55626 |
rs555924542 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460615 | GGCGTGAGCCACCGC[A/G]TCCAGCATAAACACA | 55626 |
rs555936012 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398843 | CAGTGGTGTGATCTT[C/G]GCTCACTGCAACCTC | 55626 |
rs555936196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587873 | TAAGGGTTGAAACAC[A/C]CAGTCACAATCAAGA | 55626 |
rs555939768 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431633 | GCTACCAACATCAGA[C/T]TCTGTCTCTTAATGA | 55626 |
rs556010132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500276 | TAAGAGTAAAAAAGG[A/T]CTTAGCATTTTTTTT | 55626 |
rs556011349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444482 | CTGAGGTGCATTTCA[C/T]ACACAACCACCCTCC | 55626 |
rs556019422 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462768 | CCCCTCCTTTTTTTT[G/T]TGAGACAGGGTATCA | 55626 |
rs556035233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400123 | TGCTCAGCTCTTGGT[A/G]GGGTGAGAACCAGGC | 55626 |
rs556037307 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429625 | GGAAGAATGTGGTAT[A/G]TGACTCTTTCTGGTT | 55626 |
rs556078516 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578198 | TACCATATAAAATTC[A/C]AGGTAGGGCCGGACG | 55626 |
rs556083806 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422424 | AAGAGAGTAGAAGAC[A/C]ATGATTGCTCCACTT | 55626 |
rs556087712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407437 | CAGCTCAGAGTCCAC[A/C]GAAACCTGCAAAAAA | 55626 |
rs556120860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500895 | AACTTATTACAGTCT[A/G]TCTTTTTAGATACTT | 55626 |
rs556126876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491768 | GTAAACAGCTGCCCA[C/T]TGCAACACAGCCCCT | 55626 |
rs556168862 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46596033 | CGCTCTGTCGCCCAG[A/G]CTGGAGTGCAGTGGA | 55626 |
rs556178042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565233 | ATTGCACTCCAAGCC[C/T]GGGAGACAGAGAAAA | 55626 |
rs556181215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444462 | GTCATTTCCTCCTCC[G/T]CCTTCTGAGGTGCAT | 55626 |
rs556217284 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470760 | AGGTGAGACTGTCTC[-/A]AAAAAAATAAAATAA | 55626 |
rs556235402 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554199 | GCAATATAAAGGCAC[-/T]TTCAAAGAAATACAC | 55626 |
rs556238800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565815 | CCCTCTGTCGCCCAG[A/G]CTGGAGTGGGTAGCA | 55626 |
rs556243969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491312 | GCTCCATTCTTCTAC[A/T]TCTTAGCTGCATTAC | 55626 |
rs556260288 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398514 | TTGATTGATGGAGTC[C/T]CACTCTTTCACCCAG | 55626 |
rs556312109 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413335 | TGCTCCCCACAAACA[C/G]GTCTAATTCTAAGCC | 55626 |
rs556325986 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570192 | GCTTGAACCTGGGAG[A/C]CAGAGGTTGCAGTGA | 55626 |
rs556333160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579142 | GTGAAAAAAGAAAGG[C/T]TAAACATAGCAAATT | 55626 |
rs556344905 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422634 | ATCCTTTTAAAATGA[A/G]GAGGAAAAAGGTATT | 55626 |
rs556368120 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505498 | AAGATTCTAGTCTAC[A/G]TCAGCCCAAAAAGAA | 55626 |
rs556388950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530070 | TGGTGTTACTGTCTT[A/G]GAAAAGCCTCCAAAG | 55626 |
rs556389905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563611 | TTAGGAAACAGAGGC[A/G]GCCAGATCACTTGAA | 55626 |
rs556400412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564139 | ACAAGAGCAAAACTC[C/T]GTCTCAAAAAAAAAA | 55626 |
rs556403018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525522 | GGCCAAGGCAGGTAG[A/G]TCAAGATCACTTGAG | 55626 |
rs556443000 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421909 | CAGTACTGACAAAGA[C/G]AGTATAAGAGATGGC | 55626 |
rs556455486 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404655 | GTCTCACTCTGCCTG[C/T]TGCTCCCGCTGACCA | 55626 |
rs556464353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517440 | AGGCGTAAGCCACCG[C/T]GCCCGGCTAGAAAGC | 55626 |
rs556469911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459196 | ATCCCCACTACAAAA[C/T]AAAATGATGAAAACT | 55626 |
rs556487639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423174 | TGAGAAATGCACATA[C/T]CCTAGAGTGGCAGTG | 55626 |
rs556522419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415094 | CCAGCTGGCTGGCTG[G/T]ATCCTGTGCCCTTGG | 55626 |
rs556537087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555314 | ATTTAGAGGTTCCTT[G/T]TGCAATCTGATTATC | 55626 |
rs556543878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491738 | CTTTGATAGATTTTC[C/T]CAGATTTCACATCTG | 55626 |
rs556555116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500169 | CAGGCTGTGGGGCCA[C/G]CAGGCATTGACAAGT | 55626 |
rs556631808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429121 | AAGGAGTTCATAAAT[A/G]GCAATCCGGTTCTTC | 55626 |
rs556652318 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484175 | AAGAAAGTTTGAAAT[A/G]TAAAGAAATATAACA | 55626 |
rs556656004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592924 | ATTTCCAAAGAGGCT[A/G]GGGAGAAGGAGGATA | 55626 |
rs556685947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488274 | CAGCCTGGCCAATAT[A/G]GTGAAACCCCATCTC | 55626 |
rs556687049 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515668 | AACTTCAGTTTTAAT[G/T]ACTCCATTTTTATTT | 55626 |
rs556691574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539954 | CTCCTGCCTCAGCTT[C/T]CCAAGCAGATGGGAC | 55626 |
rs556701327 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467492 | GCTTTTTCCCATTCT[A/C]TTTTTACAATGAATA | 55626 |
rs556701637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540495 | ATCCAGAACTGGTTT[C/T]AAGCATATGGGCAGA | 55626 |
rs556703106 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465688 | TTTCCTGGCTCTTTG[C/T]AGTGTAAGGGATCAT | 55626 |
rs556703650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532393 | TGAAAACCCGTAGTA[A/G]GAGAATTTACTACTG | 55626 |
rs556759470 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511030 | AAAATACCAACACCA[C/T]GAAGTATGACACTTT | 55626 |
rs556761529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433165 | AAGCATTTCATTGGG[C/T]CCTTTATGCATCTCC | 55626 |
rs556794844 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560293 | CCTCTGTATAGGATA[G/T]ATCACAAATGGGCTA | 55626 |
rs556798332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426176 | AGGGCGTACTGAGTA[A/G]TGGGCTGTTACAGTG | 55626 |
rs556802965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447770 | GATAGATAGATAGAT[A/G]GATAGATAGTGATGG | 55626 |
rs556835031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512293 | GGAGCTTGACTTCTG[A/C]CTTTTGATATTCTAA | 55626 |
rs556836224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556259 | ACATCATATAGAACC[A/G]AAGTTCAAACTGTAA | 55626 |
rs556837891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439911 | TAAAATGCCCACATA[C/T]TACTTTTTTTTTTTA | 55626 |
rs556865964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463846 | TGCAAGTTGGTAAAA[C/T]GTAACAAAAAAATTC | 55626 |
rs556877518 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497182 | AGATGATAAATTTTA[C/T]GTTATGTGTATTTTA | 55626 |
rs556879376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507671 | AATGGGGGGTAAGAG[C/T]AGGGAGACCAAAAAA | 55626 |
rs556879556 | in-del | -/ATT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456121 | ATTCCACCCACAAAC[-/ATT]ATTTAAGACAAAAAC | 55626 |
rs556885445 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578312 | GTCAACATGGAGAAA[-/C]CCTGTCTCCACTAAA | 55626 |
rs556894977 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433698 | AACAACTTTCACTCT[G/T]ACTCTTGTCTTTTTC | 55626 |
rs556916276 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460483 | CCCGCCACCATGCCC[A/G]GCTAATTTTTTTTGT | 55626 |
rs556943084 | snp | A/G | 3.30404e-05 | 0.00406437 | synonymous-codon, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508310 | GGAGCGCTGGCGAAT[A/G]CTGTCTCTCCGTGAG | 55626 |
rs556958971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432672 | CACATACGCTACACA[A/G]CTAAAGAAGACAAAA | 55626 |
rs556983759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489147 | TGTATACATGTGCCA[C/T]GCTGGTGTGCTGCAC | 55626 |
rs557000852 | in-del | -/GAC | 0.378962 | 0.21417 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401260 | CTCAGCTCTTTTCGA[-/GAC]GACAGAGTCTCGCTC | 55626 |
rs557005439 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566535 | ATAATTCCATTTATA[A/C]AACATTCTTAAAATG | 55626 |
rs557015330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528091 | ATGGATAAAGAAAAT[A/G]TGGTATATACATAGA | 55626 |
rs557018430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545018 | TGTAGTCCCAGATAC[C/T]CATAAGACTGAGGTG | 55626 |
rs557025149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424751 | AGGCTGAGGTGGGAG[G/T]ATTGCTTGAGCCCAG | 55626 |
rs557025512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416878 | TGGCTGAGGCTGGAA[A/G]CTGATGACAGACCTG | 55626 |
rs557028998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537480 | GAAACCATTTTCTTT[C/T]TCCTAGTACCAGTTT | 55626 |
rs557056211 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429522 | AAATGCCCTAGCTTC[A/G]TCCTCATGTCCCTGA | 55626 |
rs557056685 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556502 | GATATGGCAAAGTGC[C/T]AACTGGTTAACTCTA | 55626 |
rs557060639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417382 | ATCTGCTTTCACTAG[C/T]ATAAGCTAGAGCTCC | 55626 |
rs557084276 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403645 | GAAAGCTTGCTGTAG[A/T]GTCAAATTCTGGGAG | 55626 |
rs557092496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401160 | GTGCACTGAAGCCCT[C/T]GCAGCATGGTCTGGG | 55626 |
rs557102062 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528977 | GCAGCAAAGGAAAAG[A/G]GCACAATGTTAACAA | 55626 |
rs557106955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455772 | TGCCATCCAGAGTTC[A/G]GCAATGAGTTACCAC | 55626 |
rs557124189 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577677 | AAAATTCAGCCAGGC[A/G]CGGTGGCTCATGCCT | 55626 |
rs557177116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588582 | GGAGTTCGAGACCAG[A/C]CTGACCAACATGGTG | 55626 |
rs557180653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551574 | ATCAAAAATTTTCTT[C/T]AAAATATTAAACGAC | 55626 |
rs557186611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457359 | AAGGTGAGGTTAGAT[C/T]GGAAAATGGACTCCT | 55626 |
rs557193286 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560875 | CCCAGAAACGGAAAC[C/T]GAAACCAGCTGCCTC | 55626 |
rs557212027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503823 | CAAAGTACAGCCCGT[G/T]TGTCAAAATTGTGAA | 55626 |
rs557214965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519827 | TACAAACTTTTTGCT[C/T]CCAGGACTCCTTTAA | 55626 |
rs557218260 | snp | A/C/T | 0.00398731 | 0.0445001 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547503 | TGTCCCCAAATGACA[A/C/T]ATGCCACATTCGGAA | 55626 |
rs557221609 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448400 | AGATTTAAAAATATT[C/T]TGGATTAAATGTAAA | 55626 |
rs557229969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534312 | AGTCCGGCCAACATG[A/G]TGAAACCCCGTCTTT | 55626 |
rs557240277 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585101 | CCACTCAGGGTTAAA[C/T]GGATTAAGGGCGGTG | 55626 |
rs557247906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543776 | TAATGAGGCAATCAC[C/T]GGAGGGTTTCAGAAT | 55626 |
rs557268251 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495830 | ATAGCTTTTCATTAT[C/T]GTATATTTCACTTAT | 55626 |
rs557272330 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402572 | GGTTTCACCACATTG[C/G]CCAGGCTGGTCTCGA | 55626 |
rs557284028 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480888 | TATAGAGACCAATGA[C/G]GGGTTTGGGGCACAG | 55626 |
rs557304604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550426 | TTAAGAGCCAGACCT[C/T]TCTTTATAAAGGAAT | 55626 |
rs557313458 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546236 | ATAATATTTTTGGTA[C/T]AATATCCTGCCCAGG | 55626 |
rs557318698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495100 | CACTACATTTCACTG[C/G]TTCCTACAAGAGAAG | 55626 |
rs557320686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504616 | TCTCAATCCTTGCTG[C/T]AGACAGAGATGAATG | 55626 |
rs557333251 | snp | A/C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439091 | GCCTGGGCAACACAG[A/C/T]GAGATCTCATCTCTA | 55626 |
rs557391888 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478979 | CAAGGTGGTAGGATC[A/G]CTTGAGCCCAAGAGT | 55626 |
rs557403849 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471184 | CAGTGGCTCATGCCT[C/G]TAATCCCAGCACTTT | 55626 |
rs557415616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425512 | GTCTCAGTGCTGGAA[C/T]TAGAACCTGGAGAAA | 55626 |
rs557445999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559193 | TAATCCCAGCTACTC[A/G]GGAGACTGAGGTGGG | 55626 |
rs557465108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471696 | GCAGTAGCGTGATCT[C/T]GGCACACTGCAACCT | 55626 |
rs557472697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511562 | GAGCAAAGTTCATTT[G/T]GCTTTACCTAACCTA | 55626 |
rs557488455 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494991 | TACAGAGAAGCGGAC[G/T]AAAGACCAGAGAGGT | 55626 |
rs557509197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551441 | CCTCAGCCTCCAGAG[C/T]AGCTAACTTTTAAAA | 55626 |
rs557539872 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541609 | AAGTAGTCCTGCACA[A/T]ACAATGTCTCGACAA | 55626 |
rs557590406 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432614 | GGGACCTGAGGGATA[A/T]CCCTCTAAGGAGCTT | 55626 |
rs557595984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567057 | AAAAATGTAAGCATA[C/T]TAAGTAGTGTTTGTT | 55626 |
rs557613489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430513 | ACTGTAAGTTGTCCA[A/G]GAACCACAGTTTGAG | 55626 |
rs557624932 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398867 | CAACCTCCGCCTCCC[C/G]GGTTCAAGCAATTAT | 55626 |
rs557626110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438325 | CTCCCAATTAGAAAT[G/T]ATTTCCAAGTGAAAA | 55626 |
rs557631766 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398046 | GATTCTTGACTAAAC[A/G]CAGGATAGAGAAAGA | 55626 |
rs557641356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416711 | ACACTCTGTGATCTG[C/T]AGAACACTCTGGGAA | 55626 |
rs557648136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424162 | CACCTAACTCTCCCC[A/C]TTTGAAGCAGGAACA | 55626 |
rs557678134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408943 | ACATCCAATCTTGCA[A/G]CCCTGGCTCACTCAG | 55626 |
rs557699025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494330 | CACATAAATTAGTCA[C/T]CTGGCTGCTCACTAA | 55626 |
rs557705711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590050 | AAGTTTCCTAACACA[C/T]ATTGAAAATATTGTG | 55626 |
rs557765096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401613 | GCAGCCAAGCCCCCA[C/G]AGAGCCCCGGATGGG | 55626 |
rs557776199 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439115 | ATCTCTATAAAAAAA[A/T]ATTTAAAAATCAGCC | 55626 |
rs557797415 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478553 | TAGGAAACCAGGGTC[C/T]AGCTTTTTATTTGAA | 55626 |
rs557840854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543638 | CAGCTGACAAACCAA[C/T]TGTCTTACAAAAGAC | 55626 |
rs557849888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46591109 | AATATTCCTAAGATT[C/G]CTTCATGACACTCAC | 55626 |
rs557866011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424626 | CCGAGATAGGAAGAT[C/G]ACCTGGCACCAGGAG | 55626 |
rs557894110 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506989 | GCTAACAAAGTGAAA[C/T]CCCATCTCTACTAAA | 55626 |
rs557895100 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440300 | AACACTGAGCTATAC[C/T]GTAAAGAAAAAGGGC | 55626 |
rs557902321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544278 | ACATGAAAAACACCT[A/G]GAGTTGCCATCCCAG | 55626 |
rs557904194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535953 | AACATAGCACACAGT[A/G]AAACATCAGAGGTCA | 55626 |
rs557926374 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462652 | TTCTGCTCATACTGC[C/G]CCCACTATCTAGACT | 55626 |
rs557945603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580360 | AGATTTCTCTCCAGC[A/G]CTACTTTTGTGAATC | 55626 |
rs557955174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518979 | TGGAAAAGAAAAAAA[C/G]TGGTCGGAGCAGATC | 55626 |
rs557970545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548807 | AGACAGCCTGGCCAA[C/T]ATGGTGAAACCCCGT | 55626 |
rs557980069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527056 | TTCATTTAGAAAGAC[C/T]TGCACTCTCTCCTAT | 55626 |
rs557985032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549475 | GGTTACATTGAGGTT[A/G]GTGTTTTTTTTGTAT | 55626 |
rs557985115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540809 | AAAAATTTCGTTGTC[C/T]TGCCTCCACAATAAC | 55626 |
rs557991429 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558595 | ACCTACCTAGTATCT[A/G]CTAATATCTAGCTGA | 55626 |
rs557992725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462935 | ATTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 55626 |
rs557999947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466503 | GCATGTGGAAAGGAG[A/G]ATGGTTCAGGATAGA | 55626 |
rs558013795 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476017 | AAAATGGTCACTCTT[C/T]CATATAGGGGAGACA | 55626 |
rs558053425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550569 | GTACTTTTTTAATGG[A/G]GGGAGATGCTGAAAA | 55626 |
rs558060793 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427413 | TGTTTATTTTCAGAG[A/C]TAGTAAGAGACAGAG | 55626 |
rs558077628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502987 | AATGGCATGAACCTG[A/G]GAGGCGGAGCATGCA | 55626 |
rs558097616 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580359 | CAGATTTCTCTCCAG[C/T]GCTACTTTTGTGAAT | 55626 |
rs558109048 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476790 | CTGTGTTAGCTCTAT[C/T]AGTTCTGCCTTAAAG | 55626 |
rs558125202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401102 | GAGGTCCCCTGGGGC[C/T]CTCCCTGTGCTCACT | 55626 |
rs558131160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588892 | CTACTATACCTACTG[G/T]GTGATCTTGGTTAAA | 55626 |
rs558133359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512104 | CAAGTGATTTGCCCG[A/C]CTCAGCCTCCCAAAG | 55626 |
rs558180334 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485282 | CTATACTGTCTCTCA[C/G]ACAGAGTATACCATA | 55626 |
rs558187680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438042 | ATGTTGCCGGACTGG[A/G]ACTACACCTGAGAAA | 55626 |
rs558199980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493266 | CAGGATCTGGCTCAT[A/G]AGTATCTCACCAACC | 55626 |
rs558202520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470311 | TCAGCCAGGTTGGCC[A/G]GGCGCGGTGGCTCAC | 55626 |
rs558213669 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485218 | CTGGGATTACAGGCG[-/T]TGAGCCCCTATGCCC | 55626 |
rs558218871 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461254 | ACTGGAAAAATAAAA[C/T]ATAATAAACTTGTTG | 55626 |
rs558219878 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420644 | GTGATGAGACAATTG[C/T]GGCTGGGATCACTTA | 55626 |
rs558253980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478975 | AGGCCAAGGTGGTAG[C/G]ATCGCTTGAGCCCAA | 55626 |
rs558261657 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407133 | GCAGTGAGCTGAGAT[C/G]GCAGAGGCTGAAGTG | 55626 |
rs558265922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415811 | TGGTGGGTAAGAGAG[C/T]TCCCCAGGCAGCCCA | 55626 |
rs558266848 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421401 | GAAGCCAGAAAATGC[C/T]GCACAAAGATCAGCA | 55626 |
rs558292407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501076 | TCTAGCCACACCTAT[A/C]AACAAAGCAATTCCC | 55626 |
rs558293357 | in-del | -/AAGTT | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474793 | TATGGCTAGCAGGTA[-/AAGTT]AAGTTCAAGGAAAGA | 55626 |
rs558310669 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556918 | GAGGCGGGTGGATCA[A/C]CTGAGGTCAGGAGTT | 55626 |
rs558339924 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481901 | GCTGCTGGTGATTAA[C/T]ATGTGAGAAGTGCTT | 55626 |
rs558341168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466331 | TAGCCTGGGCAACAG[A/G]GCAAGACTCTGTCTA | 55626 |
rs558349470 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522797 | AGTAAGCCTGTGAAG[C/G]TCTTAAAAAACATTT | 55626 |
rs558351398 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446136 | CTGGGGAGGTGCTCT[C/G]TGCCAATGGTGCCAG | 55626 |
rs558395470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412627 | TGTTTTTTTTTCCCC[A/G]AAATGTTTTTGATTT | 55626 |
rs558410205 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565716 | GTCTCAAAAAAAAAC[A/G]TGTATAAAAATGTTA | 55626 |
rs558412954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437370 | ACTCTTCCTGGCTAC[C/T]GCAATGAGCTCACAG | 55626 |
rs558423180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537762 | ATCAATACCCTCACT[A/T]TTTGCAAACACTATT | 55626 |
rs558423883 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428886 | GGATGGCAGGCACAA[C/T]CTCTGGGGGCAGATG | 55626 |
rs558424483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497110 | GGCAAGACTCTGTCT[C/T]AAAAATAAATAAATA | 55626 |
rs558435699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538337 | ATTTTAAAAGAAAAT[A/G]AGCATAAATATAAAA | 55626 |
rs558450574 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415771 | TGCTAATGCCATCTT[-/A]ACTCAGGGAAGAGGC | 55626 |
rs558480768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428069 | CTGCTGCCTGGGACC[A/T]GTTTAGGGTGAGGGG | 55626 |
rs558491453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513225 | CATCATCATCCACAT[C/T]TACTTCCTGTCTATC | 55626 |
rs558495036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489344 | AGAGATGAGGTTTCA[C/T]CACGTTAGCCAGGAT | 55626 |
rs558520100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484999 | CTGGAGTGCAATGGC[A/G]CGATCTCAGCTCACT | 55626 |
rs558563860 | in-del | -/CAT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455996 | CTCCCTCCTTCAATA[-/CAT]CATATGTCCTAATGA | 55626 |
rs558567148 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413618 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGATTACAG | 55626 |
rs558585699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482021 | GTTTTGGTTACTACA[A/T]CCTTGTAGTATAATT | 55626 |
rs558594259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577382 | TCACATATTGTATGA[C/T]GCCATTTACATGAAA | 55626 |
rs558597398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474667 | TGCTGGGATTACAAG[C/T]GTAAGCCACGGCACC | 55626 |
rs558610403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504881 | TCTAACCTTAGACAT[A/G]TCTGATTTGGTCAAA | 55626 |
rs558610480 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513969 | GGTTTGCATGTCTGA[A/C]ATGGTGCTTCCCAAC | 55626 |
rs558654208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410729 | AACTAAGATGGCAAA[C/T]GTGAGGCTGGAGTGA | 55626 |
rs558672561 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464840 | TCACGAGGTCAAGAG[A/T]TTGAGACCATCCTGG | 55626 |
rs558672694 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589935 | TCTAAAAATTGTCAA[C/T]TTAAACAGACAACAT | 55626 |
rs558677945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592043 | CTCCGCCTCCCGAGT[G/T]CAAGTGATTCTCCTG | 55626 |
rs558682769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402691 | TTCTCTCTGGACTTG[C/G]TCTTTGAGGGAAGAG | 55626 |
rs558721859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479750 | TAGTTTACTGGTGAA[C/T]AGAAAGGAGACAAGT | 55626 |
rs558749138 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565778 | TTATAAAAATTCAGA[-/T]TTTTTTTTTCAGAAG | 55626 |
rs558753139 | snp | G/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452757 | AAATCACAGTCAATG[G/T]ATCCTATAGCCTGGT | 55626 |
rs558770650 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482374 | ATGTCATTCCTTTAT[C/G]TTACCAGTCCAACGG | 55626 |
rs558772652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520923 | ATAGCATTTTGTACC[C/T]CTCTTAAGAGGCCTT | 55626 |
rs558803695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553306 | ACAATAATTGGCTCT[C/T]TACATTTCACAAAAG | 55626 |
rs558816388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593212 | TCAAACAATAACTCA[C/T]TGTTTTCATAACTTG | 55626 |
rs558830073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434642 | GACCGTCGTAACAGG[G/T]GCATGCGGTAGGACT | 55626 |
rs558833153 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518122 | AAAGAAAGAGATAGC[C/T]ATTTGTTTTCAGAAG | 55626 |
rs558871321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442378 | GAACTCCTGGGATCA[C/T]GTGATCCTCCCAACT | 55626 |
rs558872588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582934 | GGATATTTCATAACT[C/G]AAAAAAAAAAAAGCC | 55626 |
rs558898632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576009 | GAAAGAGATTGCCGG[C/T]CCCAATCTAAGCCCA | 55626 |
rs558906424 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46593993 | CCCTCGACCCGGCGC[C/T]GCCGCCGCTCAGGAG | 55626 |
rs558921121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411380 | GCAGGGCCTGGAAGA[C/T]GAGGGACTGTGTCCC | 55626 |
rs558936013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575719 | ATGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 55626 |
rs558939498 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46593983 | GACAACTCAGCCCTC[A/G]ACCCGGCGCCGCCGC | 55626 |
rs558942450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464397 | CATTTCCCTGGATTT[A/C]ATAATTCACTATGCA | 55626 |
rs558951262 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580879 | TAACTGCAGTCTCAA[A/C]CTCCGCAGATCAGAT | 55626 |
rs558955592 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465160 | CAGCCCAGACCCTGC[C/G]AAAATTATTCAAACC | 55626 |
rs558957548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575553 | ACAGAGTCTCACTCC[A/G]TCACCCAGGCTGGAG | 55626 |
rs558959627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560727 | ATTTTTTGGTTTCAA[A/G]CTATCAAAAGAATCA | 55626 |
rs558978464 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567723 | CCCACCCCAACCAGC[A/C/G]ATTCCTCTGTAGCCC | 55626 |
rs558978653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458068 | GAGCATGGTGAATGG[A/G]TCTGTTTCACAGCAT | 55626 |
rs558979432 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464968 | GAGAATCACTTGAAC[A/C/T]GGGAGGTGGAGGTTG | 55626 |
rs558979760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528913 | GCTACCTCTGTGTAG[A/G]GGAGGAAAAAAGCAG | 55626 |
rs559021051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457606 | TGGTGACGGTTGCTT[A/G]TAAGATGGGCTGGGC | 55626 |
rs559040503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568200 | CAGTGGCACACACCT[A/G]TAATCCCAGCACTCT | 55626 |
rs559047965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403626 | CTCTTGGCCAGCAGG[A/G]TAGGAAAGCTTGCTG | 55626 |
rs559053906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561437 | TTTGAGAACATTAAC[C/T]CAGGAATCTTCACAA | 55626 |
rs559062037 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437708 | AATTCATACAGGAAG[-/A]GATTTCTTGGATCTC | 55626 |
rs559063130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448543 | TGTAATTTAAGCACC[A/T]ACCATAAGAAAGAAG | 55626 |
rs559069493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433139 | ACACACACACAAAAA[C/G]CTTTAAAAATAAGCA | 55626 |
rs559081370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471924 | AGCCACCGTGCCTGG[C/T]CAGGAATAACTTTCT | 55626 |
rs559089662 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469810 | GCTAGGATTACAGGC[C/T]CAAACTACCATGCCC | 55626 |
rs559097376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449205 | GCAATCAGAAACCAC[A/C]CCCCACCGCAAAACA | 55626 |
rs559100541 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488193 | AGATGCAGTGGCTCA[C/T]GCCTGTAACTCCAGC | 55626 |
rs559100859 | snp | A/G | 0.000114038 | 0.00755023 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543181 | GTCCTGGGGCGCTCC[A/G]TGGAGGGCTGAGGGG | 55626 |
rs559104397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581532 | GAATGACGTGAGCCC[A/G]GAGGCAGAGCTTGCA | 55626 |
rs559137427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528241 | GCAGTGGCACGATCC[C/T]GGCTCGCTGCAACCT | 55626 |
rs559155968 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425692 | TAAAAATACAGAAAT[C/T]AGCCGGGGTGGTGGC | 55626 |
rs559164835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543877 | GAAAGATAAGACTTG[G/T]GTATTGAGAATTAAA | 55626 |
rs559171064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432097 | TCTACTAAGTGTCAG[A/G]TTCCGCATGAAGTTC | 55626 |
rs559174691 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556211 | TTTTTATTAATAGGA[C/T]TTTCCTACGGCCATT | 55626 |
rs559198182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441383 | GCTGGGTGTGGTGGC[A/G]TGCACCTGTAGTCCC | 55626 |
rs559209709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432863 | CTATGGGATGTGGGA[C/T]GTTCACTCAGGCACG | 55626 |
rs559225240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536486 | TGGGAGAGATTAGAT[A/G]TCGAAACTCTTTAGA | 55626 |
rs559246981 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425827 | CTGTGCAACAAGAGC[A/G]AAACTCCGTCTCAAA | 55626 |
rs559259360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581999 | TGGGTGCCTGTAGTC[C/T]CAGCTACTTGGGAAG | 55626 |
rs559273034 | snp | A/G | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595600 | TCCCAGCCTTTGAAG[A/G]CTTTAATTAAACTCA | 55626 |
rs559292638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417728 | GTCTCTGGATGAAAT[A/G]TGAAATGGGGAGCTA | 55626 |
rs559293296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409153 | AGATTCCACTTTGAA[C/T]TCTTGAATTTGCAAG | 55626 |
rs559327419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529179 | GCAGGCATTCTTCTC[C/T]AAGATTTTACATAGT | 55626 |
rs559328181 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427078 | AGATGATTAGGACTA[C/T]ATTATAAGTTCAATT | 55626 |
rs559372461 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578951 | TATACATTCAGTACA[C/T]AGAAATAAGAGCCAA | 55626 |
rs559380067 | in-del | -/CACACAGCACGCTCTACA | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530278 | AGGATGTATACAAAG[-/CACACAGCACGCTCTACA]CCATTCAGCCCCAGA | 55626 |
rs559383363 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490687 | TCCAAGCTTCATCCC[C/G/T]GCAAAAAGCCATTCA | 55626 |
rs559383598 | in-del | -/AAAACA | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436637 | CCCAAGCCCTTTGCC[-/AAAACA]AAAACAAAAACAAAA | 55626 |
rs559424003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520344 | CTTGTGAAAGAATGA[A/G]AGTGAAAAACACAAA | 55626 |
rs559460246 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511629 | CCTTTTCTTTTGGCA[A/C]AGCCTCCTAATGTGC | 55626 |
rs559487344 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521153 | GCGACAAGACTCTCA[A/G]ACAAGGTTGCTAGAT | 55626 |
rs559492925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558819 | ACATGTCTGTCATAG[C/T]CCCAGTACCTAGCAC | 55626 |
rs559501394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513363 | AGAGTACTCCATAGG[C/T]TTTCAACTGACAACG | 55626 |
rs559511810 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399470 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 55626 |
rs559548184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486587 | GTGGGGAACATCTAA[C/G]ACCAGAGTACTGGTG | 55626 |
rs559579465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503151 | GACTAGCTTCTGGCC[C/T]ATCTCAAGTTTCAAC | 55626 |
rs559599179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439230 | AGTGAGATATGATCA[C/T]GCCACTGTACTCCAG | 55626 |
rs559611232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592340 | TTTCCAAGCTGGGAA[C/G]GAAAAGGGAACCACA | 55626 |
rs559617296 | snp | A/G | 0.00159617 | 0.0282053 | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518387 | GTGAGCCAAGATAGC[A/G]CCGCTGTACTCCAGC | 55626 |
rs559617700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527385 | CTTGGGAAGCTGAAG[C/T]AGGAGAATTGCTTGA | 55626 |
rs559622296 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516379 | TGAGTAAACATCCTA[C/G]GAATGTTTACCACCA | 55626 |
rs559632132 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511918 | GGAGTGCAGTGGTGC[A/G]ATCTCTGCTCACTGC | 55626 |
rs559632271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519124 | TGCTTCCTGTGCTTA[A/G]GCAATTCTCTTGCCT | 55626 |
rs559652881 | snp | G/T | 1.8581e-05 | 0.00304797 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408521 | CTCCTACCTTCACCA[G/T]GACCTGAGGCGGCTG | 55626 |
rs559683074 | snp | A/C/G | 0.000144771 | 0.00850685 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397421 | TCTGCTTGGCGGTTC[A/C/G]AGGGGAGGCACCAGT | 55626 |
rs559685449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478723 | GCAATGGCGCAATCT[C/T]GGCTCACTGCAACCT | 55626 |
rs559688089 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581994 | GGTGGTGGGTGCCTG[C/T]AGTCCCAGCTACTTG | 55626 |
rs559689092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507945 | CACCATCCTCTCGCA[A/G]TCTGGCCTGGGGCCC | 55626 |
rs559691214 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405429 | AATCAAATCAGAAAG[C/G]GCTGCCCAGCCGGGT | 55626 |
rs559703215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470406 | AATCCTGGCTAACAC[A/G]GTGAAACCCTATCTC | 55626 |
rs559720171 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454045 | GCAAATCATGAACTT[C/T]AGGGGCAGACCTGAG | 55626 |
rs559761164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559410 | CACGAGAGGGCCAGG[A/C]AAGAGAGTAAGCAAA | 55626 |
rs559769971 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507879 | GAGAAGCTTTCCACG[G/T]TCACTGGACATGCAA | 55626 |
rs559777150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455047 | ACCCCACACCCAGCT[A/G]ATTAAAAAAAAATTT | 55626 |
rs559779069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463278 | AAGCCAAGTATACCT[A/G]TTCTATTCCCACTCA | 55626 |
rs559791800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416066 | TAGTGGTGGAAGCCA[C/T]AGACAAAACAACACT | 55626 |
rs559845067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503871 | AGCAACAGTCTTTTA[C/T]TTGTTTAATACATAT | 55626 |
rs559890657 | in-del | -/AC | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566996 | ACTCTGGCATGGGCA[-/AC]AGAGTGAGCCCTGTC | 55626 |
rs559932382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494609 | CCAGACGCCTGCTGT[A/G]GGAGGAGGTCTTAAA | 55626 |
rs559936590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580044 | CAAAATACACAGACC[A/G]TCTCCACTTCGTCCC | 55626 |
rs559944889 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473295 | AAGGAAGCTAAAGCT[A/G]GAAAGACACTGCAAT | 55626 |
rs559958417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556492 | GATATCCAAGGATAT[A/G]GCAAAGTGCTAACTG | 55626 |
rs559963385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471243 | AATCAGGAGTTTAAG[A/G]CCAGCCTGGCCAACA | 55626 |
rs559985757 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491054 | GTATCCAGGAGGGCA[A/T]GAAGGCTCAGGAAAA | 55626 |
rs559988167 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530654 | TCTTTGGGGCCCTCA[C/T]TGTCATAATGCCTTC | 55626 |
rs560010713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515251 | GGCCAGATGGGTGAA[C/T]TGCCTGAGCTCAGGA | 55626 |
rs560021393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566235 | ACTGGTCTGCCCAAC[A/G]CGGTGAAACCCGTCT | 55626 |
rs560039186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500321 | TAAGATGGCTGTGCT[C/T]TCAGGAAGCTCGTTC | 55626 |
rs560046509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462811 | GGCTAAAGTGCAGTG[A/G]TGCGATCCCAGCTCA | 55626 |
rs560050536 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404816 | CTGTCCCCATCCCCC[C/T]AAAAGAATGAAAGGA | 55626 |
rs560072815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489540 | CTCAAGACACTGGAC[C/T]AGGCCGTAATGACCT | 55626 |
rs560079750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563707 | TAGCTGGGTATAGTG[A/G]TGCACACCTGTAATC | 55626 |
rs560117542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573889 | TCTCATTGTTCAATT[C/T]CCACCTATGAGTGAG | 55626 |
rs560133519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481585 | TCAGGCTGGTCTCGA[A/G]CTCCCGACTTCAGGT | 55626 |
rs560135493 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490386 | AATAATAGACTATCA[A/T]AACACTTTTCTCTTT | 55626 |
rs560139165 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457826 | AAAATCACTTGAGCC[A/T]AGGAGGGAGGTGGAG | 55626 |
rs560140261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555801 | TAATAATTCATACCC[C/T]AAATCTTCCCCTTCC | 55626 |
rs560157097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467789 | TCCTCCCAAAGTGCT[A/G]GGATTATAGGTGTGA | 55626 |
rs560174210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499613 | CCCTTACTTTTCTGA[C/G]ACTTTTCATTATTGT | 55626 |
rs560183267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450516 | GCAATCACGGCTCAC[A/G]GAAGCCTCAATTTTC | 55626 |
rs560195782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507340 | AAAAATTAGCCAGGC[A/G]CGGTGGCGGGCGCCT | 55626 |
rs560220146 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450932 | TGTACCACACTGGTG[C/T]GGACAGTGGGGAAGC | 55626 |
rs560223498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413581 | CTGCAACCTCAGCCT[C/T]CCAGATTCGAGTGAT | 55626 |
rs560247498 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482479 | ACTATATCAATATGG[C/T]AGATTCTGGAGACAA | 55626 |
rs560264118 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552404 | AAAAAAAAAAAAAAA[-/AA]GGCCAGGCACGGTAG | 55626 |
rs560276978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593423 | CCTCCACCTACTCAA[A/G]GGTCCCTTCAAAGGC | 55626 |
rs560286257 | in-del | -/CCT | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530441 | CCCAACCAGGGCAAG[-/CCT]CCTCATTTGCACACG | 55626 |
rs560309178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584561 | ACAAAAAAAACAAAT[G/T]AATGACTGAAAAATA | 55626 |
rs560309706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457693 | ATCACCTGAGGTCAG[A/G]AGTTCAAGACCAGCC | 55626 |
rs560332017 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486339 | TCTAAGTAATATCAC[A/G]ATGGCCCTTAACTGC | 55626 |
rs560347148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458226 | TTAACACCAGGAACA[C/T]AGTGGAAAAGCAATA | 55626 |
rs560396112 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408333 | GTACTTGGTGGGAGT[G/T]GAGGCGAGCTGCAAG | 55626 |
rs560398804 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569438 | GAGATTAAAAAAAAA[A/T]AAATATATATATATA | 55626 |
rs560415660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474181 | GAAAAAAAAAAAAGA[A/G]TAGCAATAAATGTGG | 55626 |
rs560433256 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411623 | GCAGATGTGTGCCAC[C/T]ACGCCCGGCTAATTT | 55626 |
rs560460609 | in-del | -/TATTT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452946 | AACTTACAATTCACC[-/TATTT]TAAAGTATACAATTC | 55626 |
rs560461538 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413060 | CAACAAACCATGTAC[C/T]TCCTGACCCGGAACC | 55626 |
rs560476796 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435964 | CCCTTGATGTGAGCA[A/T]AGAACAAGAGTGCCC | 55626 |
rs560485027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545475 | TCAAAAAAAAAATAG[A/G]AGGAGCTATGAGGAT | 55626 |
rs560485689 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462413 | TACTCTCCTCACGTC[C/T]GTCTTCAATGCCAGA | 55626 |
rs560539550 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561913 | ACTTAAAGATGGGGA[A/T]GGATGTAAAAGCACT | 55626 |
rs560575335 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563041 | GACCTCAGGTGATCT[A/G]CCTGCCTTGCCATCC | 55626 |
rs560609155 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450016 | GTGAGTCGAGATCAC[A/G]CCACTGCACTCCAGC | 55626 |
rs560611140 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466189 | ACTTCCATCAAAAGC[A/G]TTATAAATGAGGCCA | 55626 |
rs560614715 | in-del | -/AC | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475077 | ATCTTAAACTGAAAA[-/AC]AGTCTTATCAATAGA | 55626 |
rs560635818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402974 | AAAAATACCAGGGCT[A/G]GAGGGAAATGGCAGT | 55626 |
rs560638556 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411192 | TGGGGCGGCCTGAGC[-/G]GAGGAAGACAAACTT | 55626 |
rs560644639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404735 | GGAGGAGGGGATAGT[A/G]GGGCGAGGAACCAGG | 55626 |
rs560647236 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483760 | CAAAAATTAGCTGGG[C/T]GTGGTGGTGTACGCC | 55626 |
rs560661207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442969 | TCAAGTGATCCGCCT[A/G]CCTTGGCCTCCCAAA | 55626 |
rs560671831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585397 | AAAACGCTGGGCATG[A/G]TGCCTCACACTTGTA | 55626 |
rs560671982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552556 | TAGGCGTGATGGTAC[A/G]CGCCTGTAATCCCAG | 55626 |
rs560719527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458565 | AACTCCTTGAGAGAA[A/G]GGATCAACTTTTCCT | 55626 |
rs560808427 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396270 | CAGCTCTGGCGAAGG[A/G]GTCAGAGGGGTCCAC | 55626 |
rs560813467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566232 | GAGACTGGTCTGCCC[A/G]ACACGGTGAAACCCG | 55626 |
rs560848865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441891 | ACGAGATTTATACTA[C/T]GGAGGTTCAGAGACA | 55626 |
rs560849778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522969 | AAAGCGAGTTAGTAC[A/G]TGAAGCCTCAAGAGA | 55626 |
rs560858044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507880 | AGAAGCTTTCCACGG[G/T]CACTGGACATGCAAA | 55626 |
rs560867762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412037 | CTCTTCTTTTCACTG[C/T]GCTGTAGTAAACCTC | 55626 |
rs560898718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496419 | AGAAAATAAAGCTAG[A/C]AAAGAAGCATCATGG | 55626 |
rs560945021 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562869 | GCAATGGCATGATCT[C/T]GACTCACTGCAATCT | 55626 |
rs560962613 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490637 | CCTAAAACTGCAGGT[G/T]TGTGTCTGCTTTGTC | 55626 |
rs560973954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459458 | TTAATAAAAAATTTA[C/T]ATCCTAGATTGGGAA | 55626 |
rs561004116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498474 | TGGGAAGGAGTAGGG[A/G]GAAAAATACTTTCTT | 55626 |
rs561020023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584490 | TAACTAACCTGCACA[A/T]TGTGCACATGTACCC | 55626 |
rs561055356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473134 | CAACTTGAATTTAGT[A/G]GTTAATTAATACTTT | 55626 |
rs561065201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473934 | GGATTACAGGCGTGA[G/T]CCACCGCACCCGGAC | 55626 |
rs561069881 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397284 | AGGCCTTGCCCATTT[A/G]ACTGTCTTGTGCCCA | 55626 |
rs561096457 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407359 | GCTCCATTGAGAAGC[C/T]CGTGGTGGTTCCCTT | 55626 |
rs561125542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481512 | GGGATTACAGGCATG[C/T]GTCACCATGCCTGGC | 55626 |
rs561126937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503832 | GCCCGTGTGTCAAAA[C/T]TGTGAATAAGAGACT | 55626 |
rs561145313 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464255 | GCCCTGTGAGCAGAC[G/T]TGATGCAGCAATTAG | 55626 |
rs561165325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544690 | CCCAAAGAAGTACTA[C/T]CCAAAACAGTTAGCT | 55626 |
rs561177358 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537177 | CAAAAATAATAATTA[A/C]AAATTATCTAACAGA | 55626 |
rs561221669 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443012 | CAGGCGTGAGCCACC[A/G]CACCCAGCCTGTAAC | 55626 |
rs561223344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504108 | GTCTGACTGTCATTA[C/G]CAAAGCCTTTGCTAC | 55626 |
rs561244541 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552417 | AAAAGGCCAGGCACG[A/G]TAGCTCACACCTGTA | 55626 |
rs561255318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480813 | ACTACCTTTTGACAG[A/G]GCTAAAGCTGCTGAT | 55626 |
rs561264611 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446618 | GTCTTGTGCATCGCA[A/G]AACATTTAGCATCCC | 55626 |
rs561287970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512474 | TGTGGCCTCTCCAGG[C/T]TCCTCCTCTAGCACC | 55626 |
rs561332279 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551753 | AAAAATTAGGCCAGG[A/T]GCAGTGGCTCATGCC | 55626 |
rs561340167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592560 | GCCAGGAGTTCAAGA[C/T]CAGCCTGGCCAACAT | 55626 |
rs561352372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433413 | ACACCACTGTCCCCT[C/T]ATTACCCTTCCAAGC | 55626 |
rs561359982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457091 | CCTGTCAAATCAGCA[C/T]CTGTACATTTCAGGG | 55626 |
rs561389791 | in-del | -/TGTT/TGTTTGTT | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567064 | AAGCATATTAAGTAG[-/TGTT/TGTTTGTT]TGTTTGTTTGTTTGT | 55626 |
rs561393876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545401 | TAGGAGGCAGAGGTC[A/G]CAGTGAGACAAGACT | 55626 |
rs561419649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402301 | GCTCCTCACAGGGGC[C/T]CCAGACTTAAGGATG | 55626 |
rs561421424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410213 | CTGCTTAAGAGCCCA[C/T]CAAAAGCAGGAGGAA | 55626 |
rs561433112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438074 | GCGACCTTGTCAAAT[A/G]ATCCTTAGTCTGGGA | 55626 |
rs561436600 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515877 | GATGGGGTTTCACCA[C/T]GTTGGTCAGGCTGGT | 55626 |
rs561442846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593357 | CCCACCCAGAAAAAG[G/T]CGAGAACATAACACT | 55626 |
rs561458687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489396 | TGATCCACCTGCCTC[G/T]GCCTCCCAAAGTGCT | 55626 |
rs561494583 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467547 | TGTTACTCTATGTTA[C/T]TCTTTTTTTTTTTTT | 55626 |
rs561530137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551888 | CAAAAATTAGCCAGG[C/T]GTGGTGGCAGGCACC | 55626 |
rs561537111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567770 | TCAGTACATAAGGAC[C/T]ATTTCACATGTGCCT | 55626 |
rs561552185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532301 | GGTGTCAGAGAACAA[A/G]TGTACACTAACACCT | 55626 |
rs561556678 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410834 | TGGCCAGGCGCCAGT[A/G]GCTCACGCCTGTAAT | 55626 |
rs561559324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525375 | GGCGGGTGGATCACC[G/T]GAGGTCAGGAGTTCA | 55626 |
rs561579014 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440361 | TACCATTTGGGTTAA[A/G]TAAAAGGCAGAAAAA | 55626 |
rs561582070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541750 | AGAGCTAGCGCAGCC[A/G]ACTGACTCATACTGC | 55626 |
rs561582619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461865 | AGATGAAGCATGCAA[A/G]CACATGCCCAGGCCC | 55626 |
rs561600635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457627 | TGGGCTGGGCCAGGC[A/G]CAGTGGCTCACGCCT | 55626 |
rs561604615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513314 | CCTCAGATATATAAC[C/T]ATAATATATCTATTA | 55626 |
rs561618009 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559702 | CAGTCAAGTTTATAA[A/C]AAGAATCAGTGATTT | 55626 |
rs561624323 | in-del | -/ACAAAAACAAAAACAAAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436653 | AAAACAAAAACAAAA[-/ACAAAAACAAAAACAAAA]CACGGCAATATCCCT | 55626 |
rs561627696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424294 | TGCCCTTTGTTACTA[C/T]TGACAATGTGCTGCC | 55626 |
rs561630883 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499804 | GGGTTTACAGGCGCC[A/C]GCCACCACGCCCAGC | 55626 |
rs561643226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534408 | GCTGAGGCAAAAGAA[C/T]CACTTGAACCCGGGA | 55626 |
rs561700207 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587241 | AAAAATTAGCCGGAC[A/G]TGGTGGCACACACCT | 55626 |
rs561706458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429191 | CTTCATCCTCCCCCT[C/G]TCCCTCGGACAATCT | 55626 |
rs561715275 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437573 | AATTTCATTCTCACA[C/T]TTGCTGTTTGTTGTC | 55626 |
rs561747932 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429956 | TCATAGAGAGTAGCA[C/T]ATCCAGTCTGGAGGA | 55626 |
rs561761517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578348 | AAAAATTAGCCAGGC[A/G]TGGTCATGTGCGCTT | 55626 |
rs561763269 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502799 | GATGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55626 |
rs561775531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533507 | GCTTTGTTGCAGGTA[A/C]TATGCCTGCTGAGAT | 55626 |
rs561805160 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579487 | TTAAGTAAGTAAGTA[C/G]ATAAAAAGTAGATAA | 55626 |
rs561807728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453235 | TTCAAAGTTTATCCA[A/C]GCTTATTGCATGTTT | 55626 |
rs561851097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477633 | AGCCACTGTGCCCAG[A/C]CTCTTTGAGGACACG | 55626 |
rs561871361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556651 | GCTCCATCCTTTTCC[A/T]GGTATATGATGGTAT | 55626 |
rs561894918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508938 | CCTTAGCATGATCTC[C/T]TGGAACCTCTTTTTC | 55626 |
rs561923955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555663 | TAAAAAGTGCTCAGG[C/G]AGAAAATAAAGTATG | 55626 |
rs561925317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399255 | ATTTTTGTATTTTTA[C/G]TAGAGACGGGGTTTC | 55626 |
rs561932618 | snp | C/G | 0.000214361 | 0.0103506 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548342 | CCGTTCTCGCCCCCA[C/G]AGTATCCGGACAGCA | 55626 |
rs561942662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476337 | TTAGGTGACTTGTCT[G/T]GAAGCTGCCGGCAGA | 55626 |
rs561950933 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452284 | GTGTATCTTTTAGAT[A/G]GTCTACTAGTGTCTT | 55626 |
rs561958158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407556 | GGTCATGGCCCCAGC[A/G]AGGGGCTTCCACCAA | 55626 |
rs561965207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532564 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGACTACAG | 55626 |
rs561984153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547419 | GAAAGAAACTAAGCT[A/T]TGTATGTTAGGCAGT | 55626 |
rs561986976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444928 | GACAGTCTTGTCTTT[A/G]TCTCATTTTCAATTT | 55626 |
rs561993198 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463445 | AATTAAAGAAACAAA[C/G]GGCCACTTGAATATA | 55626 |
rs561994044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435249 | CTTAGCAGGAAACTA[C/T]AGGATAGTCAACACC | 55626 |
rs561994760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399718 | TTCCTTCTCTTCTTT[C/T]CCTTTACCCCCCAGT | 55626 |
rs562030826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435929 | CACCGTGTGATTCCC[C/T]GCCAGGAAGAAGTGG | 55626 |
rs562038530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422710 | CCAATAAAACTCAGA[C/T]GAGTAGTTCAAGCAG | 55626 |
rs562072590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421920 | AAGACAGTATAAGAG[A/G]TGGCTCTGGTCTTCA | 55626 |
rs562073411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414366 | CCCCTCCCTGGGTGA[C/T]GATACTTGACTATAA | 55626 |
rs562074843 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411027 | AATCACTTGAACCAG[A/G]AGACAGAGGTTGCAG | 55626 |
rs562078264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422811 | TTGGGAATCTCATCA[C/T]CTGTAAAGCTAAAAC | 55626 |
rs562084055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586524 | GGGGAAAGAGGGACA[A/G]ATATGCTGTTTTAAC | 55626 |
rs562104972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475841 | AGGAAACTGTGGCAT[C/T]CACAAGAAAGAAGGC | 55626 |
rs562159273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482881 | AGGCGTGGTGGCATG[C/T]GCCTGTAGTTCCAGC | 55626 |
rs562175128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517064 | AGGGGTTGTGCTATT[C/T]GATCCATTGGACAGC | 55626 |
rs562176929 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456570 | AGAGAAAGAAAAAGA[C/G]AGCGACTGACTCAAA | 55626 |
rs562181299 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414676 | TGGCAGGCAGCCAGA[G/T]GCACAGCAGCAGCTT | 55626 |
rs562183918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538657 | GCACCACCATGCCTG[G/T]CTAATTTTTTTTGTA | 55626 |
rs562191904 | snp | C/T | 7.85248e-05 | 0.00626548 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443644 | TATATTATTTATCCA[C/T]GTTTCCACTGCAAAA | 55626 |
rs562266571 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571235 | GACAGAAGTTTGCCA[C/G]CTCAAGTCAGCACAA | 55626 |
rs562285963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491383 | GTTAATTAGGTAATC[A/G]CACCTATCTCATATG | 55626 |
rs562293933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573722 | GCATATTGTGCAGGT[G/T]AGTTACATATGTATA | 55626 |
rs562304975 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532093 | CACTGCACTCTAGCC[C/T]GGGTGACAGAGCAAG | 55626 |
rs562318867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399130 | CCCAGGCTGGAGTGC[A/G]ATGATGCGATCTCAG | 55626 |
rs562328621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448640 | ACAGGAAATCACCTA[C/T]AGAGAAAAATCAATA | 55626 |
rs562379055 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595452 | TGAGGCAGGAGAATC[G/T]CTTGAACCCAGGAGG | 55626 |
rs562385291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450928 | CAAATGTACCACACT[A/G]GTGTGGACAGTGGGG | 55626 |
rs562405843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548920 | TGCTTGAACCCAGGA[C/T]GCAGAAGTTGCAGAG | 55626 |
rs562418018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531686 | TGCACTCCAGCCTGG[G/T]TGACAGAGCGAGACT | 55626 |
rs562421369 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499089 | ATAGCTAATAGCATA[A/G]GTCTCCTGGAACTAC | 55626 |
rs562421397 | snp | A/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458503 | GTACACTGAGCCATC[A/G/T]ATTTTCCATTGGTAC | 55626 |
rs562423468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507984 | GTCTCTGTCCTCGCG[C/T]GCCAGTGAATCAGCA | 55626 |
rs562425867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428837 | TCCAGACCTTTAGGC[C/T]GAGGCCTGCCAGTCT | 55626 |
rs562436097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483730 | TATGGTGAAACCCCA[C/T]CTCTACTACAAATAC | 55626 |
rs562448997 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531010 | TGCCTCAGCCTCCCA[A/G]GTAGTTGGGAAAACA | 55626 |
rs562453781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556569 | ATTATCCATAACATC[C/G]AAATTACAGTCAATA | 55626 |
rs562467763 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540920 | TTGTAACCATTCAAC[A/T]AATACTTATTGACTG | 55626 |
rs562482914 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508846 | CCTCAGATGATTAAA[G/T]AAGGTATCCACAGGT | 55626 |
rs562496444 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423621 | TGGTCTTGATCTCCT[A/G]ACCTTGTGATCTGCC | 55626 |
rs562518841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492086 | CTTTAACGTGCCTTC[A/G]GTTAAGCCACACAGA | 55626 |
rs562562421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586338 | CGCTTGAACCCAGGA[A/G]GCAGAGGCTGCAATG | 55626 |
rs562566529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474915 | AAGAACACAGTGTGC[A/G]CTTGAGAAATGGACA | 55626 |
rs562569892 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528972 | CTGATGCAGCAAAGG[A/G]AAAGGGCACAATGTT | 55626 |
rs562593505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460733 | ATGCCTGTGAAGTGG[C/T]AAAGATAATCAAAGG | 55626 |
rs562608354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429236 | CCCCCTACCCCATAA[A/G]ATAAGCCTCCAGCCC | 55626 |
rs562613515 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555928 | TCTTCCACTTCACTA[C/T]GCCCATGTGGGCAAA | 55626 |
rs562615905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587473 | AACCCAGTATTATCA[C/T]ACATTAAATATCAGA | 55626 |
rs562621660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516919 | AGCTTGTTCAGGTTC[A/G]AAGCTGCTATCACTG | 55626 |
rs562627308 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563677 | AAACCCCGTCTCTAC[C/T]AAAAATATGAAAATT | 55626 |
rs562630865 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484463 | CATGGGATTTAATAA[A/T]CTTTGAGATCATTTT | 55626 |
rs562657324 | in-del | -/T | 0.00199481 | 0.0315187 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46395918 | AGGCCTTTCGGCCAC[-/T]TGTAGGGAAGACACA | 55626 |
rs562666649 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406807 | AGAATCACTTGAACC[C/T]GGGAGGCAGAGGTTG | 55626 |
rs562680369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475755 | CTTTGCTCTGGATAC[A/G]AGAATCCCGTAATTT | 55626 |
rs562682710 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590854 | GGAAGTGGAGGTTGC[A/G]GTGAACTGAGATCGT | 55626 |
rs562700186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570408 | AGCAGAAAATGACAA[A/G]TGGAGATAATTCTCC | 55626 |
rs562702381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467969 | ACAACCAGGCAGGAA[A/G]CTGCTACGAAAGCAT | 55626 |
rs562716868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460240 | TAAATCAATCAAACT[A/G]TATCAACATGGACTT | 55626 |
rs562722535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450971 | GTAAGGGGAGGGAGT[A/G]TATGGGAACTGTCTG | 55626 |
rs562723591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562720 | TTTTTCTATGAATAT[A/G]AGCCTGAGAAAATAT | 55626 |
rs562731758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449693 | AGTTTATATGAAAGG[C/G]CAAAAGACCCAGAAT | 55626 |
rs562742556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564767 | ATCTAAAGAAGGAGC[A/G]AACCTCACTGGAGGT | 55626 |
rs562763709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483672 | TGGGAGACCAAGGTG[G/T]GTGGATCACCTGAAG | 55626 |
rs562815811 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420200 | ACCTCCTACACCCTT[A/C]CTGTAGGACTCAACT | 55626 |
rs562816473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428806 | CCCTCTTGTGAGTCT[C/T]GCAGGTCGCTCACCC | 55626 |
rs562832757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523367 | TCCCTCTGTCTAGAC[A/T]ACATGAAATTGTCAT | 55626 |
rs562878989 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466960 | GTCTCGCTCTGTTGC[C/T]AGGCTGGAGTGCAGT | 55626 |
rs562898683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581090 | TGAGCCACCGCGCCC[A/G]GCCCCAGAGTAACGT | 55626 |
rs562904350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530781 | CATATTTTTAAATGA[C/T]TGAAAAACATCAAAA | 55626 |
rs562916662 | snp | C/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453149 | TAATTGCTTCTCCTG[C/G]ACATTTCATGTAATG | 55626 |
rs562927797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553555 | TTCGAGACCAGCCTG[A/G]CCAACATAGTGAAAC | 55626 |
rs562938683 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428380 | AAAGACCACAATACT[A/G]TTCCATGGAGAAGGG | 55626 |
rs562939675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | AMBRA1 | GRCh38.p7 | 11:46591261 | TTCCTCTGATATACA[C/T]TCTCTTCTACCATAA | 55626 |
rs562941104 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487000 | CCATGGCTAACACCT[A/G]TAATCCCAGCACTTT | 55626 |
rs562947147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420933 | TTGCTGTGCTGCGTT[C/T]TTTAAATGGGGGTCT | 55626 |
rs562947498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471425 | CTACTAAAAATACAA[A/C]AAATTAGCTGGGCAT | 55626 |
rs562948651 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411867 | CTGGGCTCAAATGAT[C/T]TTCCCACCTCGGCCT | 55626 |
rs562956225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489626 | AATTAAGTATATCAG[G/T]TCCACATCTGCTAGG | 55626 |
rs562965754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531454 | GTGGCTCACGCCTGT[A/G]ATCCCAGCACTTTGG | 55626 |
rs563024608 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414310 | GAAAGATGTGGTTTC[C/T]GTGGCAATTTTGGCT | 55626 |
rs563025966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506941 | GAGGCCAAGGCAGGC[A/G]GATCACAAGGTCAAG | 55626 |
rs563031085 | in-del | -/ATTACC | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499147 | GTAATACAAGAGATA[-/ATTACC]ATTTACAAATTCCTC | 55626 |
rs563084892 | in-del | -/AAT | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476132 | CACACAGTACCCAGA[-/AAT]AATAACAGAGAAGAG | 55626 |
rs563085273 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397049 | ACAGGTGGACAGGGC[A/G]AAGCTGCCTCGCGGG | 55626 |
rs563088983 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396462 | TTGGTGTTTCCCTCA[G/T]TAGCTGTAGACTATC | 55626 |
rs563126577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567428 | TGGGAGTGCAGTGGC[A/G]CCATCTTGGCTCAAT | 55626 |
rs563131761 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446440 | AAAGTATTTACATAC[A/C/G]AGGCACTTAGCCTCA | 55626 |
rs563155077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546184 | GGGACCACAGGCGCA[C/T]GGCACCATGCTCAGC | 55626 |
rs563170561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447131 | AAATACAAAGTGGTC[A/G]GGCATGGTGGCTCAC | 55626 |
rs563177978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425015 | GGCAGGTGCCTGTAA[A/T]CCCAGCTACCTGGGA | 55626 |
rs563181508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498350 | CCCTCATCAATTCCA[A/G]CAGCCTGAAGCTGAC | 55626 |
rs563195728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538579 | GCTCACTGCAACCTC[C/T]GCCTCCCCGGGTCCA | 55626 |
rs563206729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439157 | CATGTGCCTGTAGGC[C/T]GAGTTACTTGGAAGG | 55626 |
rs563270073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575122 | AAAAGTACCAGTGGT[A/G]TCAGTAACTCCCTCT | 55626 |
rs563295148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415990 | TTTATGAGGCCACAA[A/C]AAACTGGGTGTAGAT | 55626 |
rs563296049 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479835 | TCTGTTATCAGTTTT[C/T]TATAACTGCCATAAC | 55626 |
rs563296427 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530103 | CCCTTTAGAGCACTA[C/T]TCTGAATAGATACAG | 55626 |
rs563298754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527733 | CATTAGGGAAATGCA[A/T]AGCAAAACCACATTT | 55626 |
rs563307142 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535996 | TTTTGGAAGGTGTGA[C/T]TTCCTTGTACAACTC | 55626 |
rs563333876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565498 | GATTGCTTGAGCCCA[A/G]GAGTTCAAGACCAGC | 55626 |
rs563335441 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539494 | CCCAGGAGATGGAGG[C/T]TGTGGTGAGCCGAGA | 55626 |
rs563353895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417206 | ACAGGCACGTGCCAC[C/T]ATGCCCGGCTAATTT | 55626 |
rs563370391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528390 | TGGCCAGGCTGGTCT[C/T]GAACACCTGACCTCA | 55626 |
rs563377868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425756 | AGGCAGGAAAATCAC[C/T]TGAACGCAGAAGGCA | 55626 |
rs563388544 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417842 | TTCTAAAAGACCCCA[G/T]TTGGTGAATACTGAT | 55626 |
rs563390638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409362 | TACACCACCATGCTC[A/G]GCTAATTTTTGTATT | 55626 |
rs563460243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486512 | TCTAGATGCCCACCC[C/T]AGTTGACTAAGTGAG | 55626 |
rs563471003 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587213 | GGTGAAACCCCATCT[A/C]TACTCAAAATACAAA | 55626 |
rs563486027 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494429 | CAGCTCAGGAAAGAG[A/G]AGGATTTTTCTTGAG | 55626 |
rs563500778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547955 | CAAAAGCACATTAAC[C/T]ATTCTAGATTAGCAT | 55626 |
rs563512254 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485531 | AGGGCTAAAACAAAA[C/T]ATAGATATTGGGCTA | 55626 |
rs563529102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573015 | CTGAGGCAGGCGAAT[C/T]GCTTGAACCTGGGAG | 55626 |
rs563537938 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554991 | GTGGGAAGGTTGCTT[G/T]AGTCCAGGAGGTCAA | 55626 |
rs563547277 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542104 | TCCTCCTGCGGACTA[C/G]CAGAGCTGCTCAACT | 55626 |
rs563565424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | AMBRA1 | GRCh38.p7 | 11:46430917 | GGGAGATGCTGTACT[A/G]TCCCATTAAACCCTT | 55626 |
rs563583090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422933 | GGCTAGAAGAGCTGT[A/G]GAAAAAGGTGCAAGG | 55626 |
rs563589780 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399363 | ATAGGCATGAGCCAC[C/T]GTGCCCAGCCTTTGT | 55626 |
rs563596004 | in-del | -/A | 0.0763149 | 0.179815 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564145 | GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs563597948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535451 | AGATGAGAGCACACA[C/T]TTTCTCAAACCCTAA | 55626 |
rs563611300 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581085 | AAGCATGAGCCACCG[C/T]GCCCGGCCCCAGAGT | 55626 |
rs563630242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525700 | AAGTTGCAGTGACCC[A/G]AGATCGTGCCACTGC | 55626 |
rs563642167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526335 | CCTTGTGTGGTCCCC[C/T]CCCACACTGAATCTA | 55626 |
rs563653591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407826 | GGAGGCTGCTTTGTT[A/T]GGAGCTAGGATCAGC | 55626 |
rs563656415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415262 | GACATGAATGCGCTC[A/G]CTGATCCTCTCTCAT | 55626 |
rs563663324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510024 | AGGAACATAGGCTGC[C/G]TCTGAAATGCCTGTC | 55626 |
rs563667466 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400471 | TTCTAGTTCTTTCTA[C/T]AGTTTTTTTTTTTTT | 55626 |
rs563699539 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485460 | CCCACCTCCCTTAGC[A/T]AATCTATCAAGACTG | 55626 |
rs563699963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462086 | CCTGTGGCAAATTTC[C/T]AGCTTTTACAAGAGA | 55626 |
rs563720682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485031 | CAACCTTTGCCTCCC[A/G]GGTTCAAGCGATTCT | 55626 |
rs563762601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478779 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 55626 |
rs563808415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423552 | GCCTGCCACCACGCC[C/T]GGCTAGTTTTTTGTA | 55626 |
rs563815821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502536 | TTATATATTTGTTAT[G/T]AGAGAGTAGTCACTG | 55626 |
rs563828540 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588283 | GTTGCAATGAGCCAA[A/G]ATAGCGCAGCTGCAC | 55626 |
rs563832262 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503471 | AGATCTAATAATAAT[A/G/T]AAAACATCTGAAATA | 55626 |
rs563860041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476452 | GTCCCAAGCCAACCC[A/G]TGGTGCTGGTACTGC | 55626 |
rs563866846 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493481 | TGAATATCAAACCAG[A/G]ACCCCAAAATAGAAT | 55626 |
rs563924435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566008 | TGCCAGCCTCAGCCT[C/T]CCAAAGTGCTGGGAA | 55626 |
rs563924689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579473 | AATAAATAAATAAAT[A/T]AAGTAAGTAAGTACA | 55626 |
rs563938734 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582627 | AGGTTGTTTGGACGC[A/G]AATCCTGGTTCTGCC | 55626 |
rs563949119 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507458 | CACTCCAGCCTGAGC[A/G]AAAGAGCGAGACTCC | 55626 |
rs563954348 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590231 | AAAAAATTAGCTGGG[A/T]GCGGTGGTGCGCACC | 55626 |
rs563974866 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427698 | CAATCAGATTTGGGT[A/G]GGATGTAGGTCTATA | 55626 |
rs564006256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446284 | TTTCTTCAAGAACTG[C/T]AGGCCAACTGAGCCT | 55626 |
rs564032190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527457 | TGTATTCCAGCCTAG[C/G]TGACAAAGTGAGACT | 55626 |
rs564098633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423426 | ACATGGAGTCTCGCT[C/T]TGTCACCCAGGCTGG | 55626 |
rs564102832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534450 | CAGTGAGCCCAGATC[A/G]CACCATTGCACTCCA | 55626 |
rs564115289 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468925 | AAGGCAGGTGGATCA[C/T]CTGAAGTCAGGAATT | 55626 |
rs564126531 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436250 | AAACAAAACAAGGAA[C/T]TGCTCTTTCAGAGGC | 55626 |
rs564129967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580064 | CACTTCGTCCCTTCC[C/T]ATGCCTTAAACCCAA | 55626 |
rs564139862 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502948 | CACCTGTAGTCTCAG[C/T]TACTCAGGAGGCTGA | 55626 |
rs564144975 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582169 | GCCTAAGTCTCTATC[C/T]TCATTCTATGCCTCT | 55626 |
rs564147822 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424381 | TATTCATTTGTTCCT[A/G]AAGGAGACCCCAAAG | 55626 |
rs564171694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557955 | CCAGCCTGGGCGACT[A/G]AGCAAGACTCAGAGA | 55626 |
rs564185134 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416162 | AGAATCATAGTCCAG[A/T]ATTCTGTGCCAGTTT | 55626 |
rs564185646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550025 | GGTTTTGCCATGTTG[G/T]CCAGGCTGGTCTTGA | 55626 |
rs564199873 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439490 | AGTGAGTAGCCATAT[-/G]GGGGGGAAATTGGAT | 55626 |
rs564201277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526682 | TAGAGAAAACCCAAG[A/G]AAGATCAGCAGAAGA | 55626 |
rs564207791 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502485 | TCTCTGACGATTTTA[A/C]TTGCCAAAAGTTACC | 55626 |
rs564216881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565355 | ATATACATCACATGA[A/G]TCAGCAACTGCATGC | 55626 |
rs564244799 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414342 | CCTTTTGATTCGGAG[A/G]CATGCTTTCCCCTCC | 55626 |
rs564271931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493830 | ATGCCCAGAAAGAAA[C/T]AAAATCTCCCAAGAT | 55626 |
rs564319911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539610 | AAGGGCAGCTTGCAC[A/G]AATCTTTAGTCATGA | 55626 |
rs564320790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579382 | GAATCACTTGAACCC[A/G]GGAGGCAGAGGTTGT | 55626 |
rs564331183 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469516 | ATGTACACCTATTAT[A/G]TGTGTAATATATATG | 55626 |
rs564352781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549139 | CCACAAGACTTACAA[A/G]GAGAAAACTTCATCA | 55626 |
rs564382518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540127 | GTGAGCCACCGTGCC[C/T]GGCAGTAACTGGTAT | 55626 |
rs564387655 | snp | G/T | | | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430535 | CAGTTTGAGAAGCAC[G/T]GATCCAGAAGTCTGA | 55626 |
rs564391873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492865 | TCATCCTGGCTAACA[C/T]GTTGAAACCCCCTCT | 55626 |
rs564392583 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541878 | CAGCCACAACATCTA[C/T]AGGACTCAAGGAAAT | 55626 |
rs564423002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415231 | TGGAGACCACTCATC[C/T]GTAGACCGCTCAAAA | 55626 |
rs564457139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405206 | ACTAGGCTCAGGGCC[A/G]CCTCCTCCAGGAGTC | 55626 |
rs564459635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407680 | CCCTGTTGGGGACTG[C/T]GGTGTAGAAAGCCAT | 55626 |
rs564469127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477458 | GAGTAGCTGGAACTG[C/T]GGAACTACATGCACA | 55626 |
rs564479941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492003 | GGCAGATGTCTGGAA[C/T]AAAGAAGGGTGGAGA | 55626 |
rs564491436 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419582 | CTATGAAAACGACAG[A/G]AAGCTGAAACTCTAT | 55626 |
rs564525987 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528950 | CAAAAAGAGTCACAC[A/G]TACCCTCTGATGCAG | 55626 |
rs564533074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567973 | GCCAACCTGGTGAAA[C/T]CCCATCTCTACTAAA | 55626 |
rs564534711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591528 | CTTGTACAGTTTCCA[C/T]TCAAGGACTAGGAAC | 55626 |
rs564581963 | in-del | -/TTGT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574511 | CACTTTTTGATGGGG[-/TTGT]TTGTTTTTTTCTTGT | 55626 |
rs564603479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406947 | GCACTTTGGGAGTCC[A/G]AGGTAGGCGGATCAC | 55626 |
rs564628323 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483817 | ACAGGAGAATTGCTT[C/G]AATCTGGGAGGTGGA | 55626 |
rs564661794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588125 | ATGACTTGAGGTCAG[A/G]GGTTCAAGACCAGCC | 55626 |
rs564664607 | in-del | -/TTTGTTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536005 | TGTGACTTCCTTGTA[-/TTTGTTT]CAACTCTAAGTAATA | 55626 |
rs564677866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410946 | TCTCTACTAAAAATA[C/T]AAAAATTAGCTGGCC | 55626 |
rs564701334 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499892 | ACTCCTGACCTTGTG[A/G]TCCATCTGCCTCGGC | 55626 |
rs564703861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465037 | GACACAGTGAGATTC[C/T]CTCTCAAAAAATAAA | 55626 |
rs564724979 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587333 | TGCAGTGAGCCAAGA[C/T]TGCACCACTGCACTC | 55626 |
rs564803605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476398 | TATTTTTAGGGGTGG[C/T]TTGTGGTTAGATAAT | 55626 |
rs564820757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524973 | ACAAATACTGAGTGC[A/C]TTCTGTTAGTTATAT | 55626 |
rs564828222 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403258 | AGGCTCAGAGAGTCA[A/C]AGGAGGAGCTGCCCT | 55626 |
rs564847798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418817 | TTTTAGCTAACTAAC[C/T]TCATTGCTTTTAAAT | 55626 |
rs564864656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522113 | GAATGTATACATAGT[A/G]TGCAATCATGTATCT | 55626 |
rs564871053 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473812 | CCCACCACCACGCCC[A/G]GCTAACTTTTTGTAT | 55626 |
rs564893207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576375 | TCAAGAGATCCTCCC[A/G]CCTCAGACTCCCAAA | 55626 |
rs564907248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465510 | AGTTCACTGTTCTCT[A/G]AAGATTAAAAACTAG | 55626 |
rs564916869 | snp | A/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493412 | GAAAGTGGGAATAGG[A/G/T]TAAGAGAAACATTTT | 55626 |
rs564930423 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551146 | ATATATTGTCGAGAG[-/A]AAAAAAGCAAGGTAC | 55626 |
rs564947271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458401 | CACTATTAGCTGTTT[C/T]TCATAACACAAAACT | 55626 |
rs564953845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583076 | GAACAAAGCTGGAGG[C/T]ATCACGCTACCTGAC | 55626 |
rs564970670 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512231 | CATTTACTCCTTCTT[C/T]GGTCGTCTCTTCCTT | 55626 |
rs564995250 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46544005 | GTTAACAATTGCTGT[A/G]AGTAAGTAGTGTCCA | 55626 |
rs565028118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403930 | TGTGGCTGCATGTGG[C/T]GGCTCACGCCTATAA | 55626 |
rs565029314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529244 | ACTGCATAATCTGGC[A/G]TAATGGAGATCTGCT | 55626 |
rs565039542 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521313 | TGCAGTCTGGTCCCT[A/G]GGAGGCTCATTAAAT | 55626 |
rs565066175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592467 | AAACTACTAATCAAA[C/T]ACAACAAAACTGGGC | 55626 |
rs565067610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575750 | TCGAACTCCTGACCT[C/T]GTGATCTGCCTGCCA | 55626 |
rs565097695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480477 | CAAAAGCTAAATGAC[A/G]TAATGGCCAAAGCTA | 55626 |
rs565121226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559555 | AAAGTACAGAGACAG[C/T]GGATATTCTGATAGC | 55626 |
rs565125793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433328 | AGCCTGCTGGTCATG[C/G]ATGGGCTTGACTACA | 55626 |
rs565156035 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558237 | TGGTTTTTGTACATC[A/G]ATAGATAACTAAAAC | 55626 |
rs565190682 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543955 | GTTTAGCTGGAATTG[C/G]AACTGCTGGACTAAC | 55626 |
rs565202528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440089 | TCCCCCCTGCAATTC[A/C]ATTTCTAGAAATGTA | 55626 |
rs565207355 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515387 | CTGAGGCACGAGAAT[A/C]ACTTGAACCTGGGAG | 55626 |
rs565209503 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474085 | ACACAAACTTGAAAA[C/T]AGGACTATATTACTC | 55626 |
rs565216798 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584083 | GCACATGTATGTTTA[C/T]TGCGGCACTATTCAC | 55626 |
rs565270892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457000 | AAACTTTCCTTACAG[A/G]CCACCTACACGTGAA | 55626 |
rs565277217 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562209 | TAGAAACCTTGAGAA[A/C]AGAGGCAGGTGAAAA | 55626 |
rs565279708 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534655 | CCAGGAAGCAGTCCT[C/T]GTGCATACTCCTCAG | 55626 |
rs565283803 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487970 | AAAGGATGGAAAATG[A/G]TATCTCATGTAATCA | 55626 |
rs565318676 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454485 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 55626 |
rs565335071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471280 | AACCCCACCTCTGCT[A/G]AAAAATATAAAAATT | 55626 |
rs565336118 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586208 | AGCCAGAGTTCAACA[C/T]AAGCCTGGCCAACAT | 55626 |
rs565337937 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506067 | AACTGCTTCCCTGAA[G/T]AGACCCTGGTGCTGG | 55626 |
rs565338042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552229 | CAAAAATTAGCCGGG[C/T]GTGGTGGTGCACACC | 55626 |
rs565353545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463396 | TAAAATATATAGATG[C/T]TCTGCTGTAGAAGGT | 55626 |
rs565383757 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591685 | GATGGTAAAACACCA[A/T]CTCTACTAAAAATAC | 55626 |
rs565391850 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565241 | CCAAGCCTGGGAGAC[-/AG]AGAAAAATTCCCTCT | 55626 |
rs565423444 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496276 | TAATCTCAGCTGTTC[A/G]GAGGCTGAGGCAGGA | 55626 |
rs565430915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417103 | TGTCGCTAGGTTGGC[A/G]TGCAATGGCATGATG | 55626 |
rs565438989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409257 | GTCACCCAGGCTGTA[C/G]TGGCGCAATCTCAGC | 55626 |
rs565448417 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438035 | GTCTCTGATGTTGCC[A/G]GACTGGGACTACACC | 55626 |
rs565464927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401334 | CAACCTCCACTTCCC[A/G]GGTTCATGCAATTCT | 55626 |
rs565476810 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574437 | ATGAGCATTTTTTCA[C/T]GTGTTTTTTGGCTGC | 55626 |
rs565479991 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561591 | TCCTTCAGATAGTAC[C/T]AGAGCTACACTCCCA | 55626 |
rs565489469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575079 | CCATAGTTCAACTAG[C/T]ATAAACAAACCTAAT | 55626 |
rs565491346 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566765 | CATCTTGCCTTTAAC[A/T]GCCCTTGGTCATTCC | 55626 |
rs565500155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580321 | CCCTTGGTTGTAAAT[A/G]CCATCTATATACTAA | 55626 |
rs565526889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464183 | GGTGCCAGAGAATCA[A/G]CACTAGATGTTTTCA | 55626 |
rs565538411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566971 | CAGTGATCAGAGATC[A/G]CACCACTGCACTCTG | 55626 |
rs565547394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558890 | ATATTCAGAGTTGTG[A/G]AAAGATCCCAAATGA | 55626 |
rs565550589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559182 | GCACGCCCCTGTAAT[A/C]CCAGCTACTCGGGAG | 55626 |
rs565552181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567412 | TGCTCTGTCTCCCAG[A/G]TGGGAGTGCAGTGGC | 55626 |
rs565564009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581203 | GCTGGCCAGGTACGG[C/T]GGCTCACACCTGTAA | 55626 |
rs565567629 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520134 | ACAAGAGTGAAACTC[C/T]GCCTCGAAAAAAAAA | 55626 |
rs565593129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447623 | GAGACTGAGGTGGGA[G/T]AGCTTGAGTCTGGAA | 55626 |
rs565608605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410177 | CTCTGGTTGAGGAGG[A/G]ACCCAGAGCCCTAGA | 55626 |
rs565625513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425092 | TTAGCCGAGATCACG[C/T]CACTGCACTCCAGCC | 55626 |
rs565638811 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409439 | TCCTGACCTCGTGAT[C/G]CGCCCGCCTCAGCCT | 55626 |
rs565649988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494893 | GCCATTTATTAAGTA[C/T]CTGCTAGGTTCCAAT | 55626 |
rs565650131 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583115 | ATACTACAAGGCTAC[A/G]GTAACCAAAACAGCA | 55626 |
rs565666786 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525977 | TTGGGAGGTCAAGGC[A/G]GACAGATCACCTGAG | 55626 |
rs565680388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463046 | GGCGTGAGCCACCAC[A/G]TCTGGCCAATAATCC | 55626 |
rs565701748 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545324 | AAAATGAGCCGGGCA[C/T]GGTGGTGGGTGCCTG | 55626 |
rs565703745 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586231 | GCCAACATGGCAAAA[C/T]TCTGACTCTACTAAA | 55626 |
rs565711999 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512044 | TATTTTTAGTAGAGA[C/T]GGGGTTTTGCCATGT | 55626 |
rs565727519 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549314 | ATCCACTGTGACATT[A/G]TTTCTTTAGCTCCAC | 55626 |
rs565733794 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539901 | CAGTGGCGTGATCTT[C/G]GCTCACCGCAACCTC | 55626 |
rs565752534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551377 | GAGTGCGATGGTGCA[A/G]TCATGGCTCACTGCA | 55626 |
rs565763007 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397053 | GTGGACAGGGCAAAG[C/G]TGCCTCGCGGGCCTC | 55626 |
rs565770354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437932 | GCACACAAACTTTAA[A/C]ACGTATCAAACTCAC | 55626 |
rs565770948 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401525 | AGGCATGAGCCACCG[A/C]ACCCAGCTCAGCTCT | 55626 |
rs565778382 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504286 | ATAAAGCATACACAC[C/T]ACCTCTTTTGTAGGC | 55626 |
rs565781789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526991 | GCAAGTGTAAACTTG[C/T]TCACTGTTTGTAAAG | 55626 |
rs565795163 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537297 | TGTTTGAAGGCACTT[A/T]TTTCAAATGAAACGG | 55626 |
rs565796378 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559934 | TTCAAGACAAGATTA[C/T]TACTTTTCAAAGTAA | 55626 |
rs565807008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438682 | TCCCCTGTGGTATCG[C/T]CTGCCCCACACCACT | 55626 |
rs565809364 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430286 | ACTGTGCCTGCAACA[G/T]AATTAGCAAAGAATC | 55626 |
rs565809586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402313 | GGCTCCAGACTTAAG[A/G]ATGCTTGGAAAACCG | 55626 |
rs565848942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431114 | GAAACCTTTCTGTAG[C/T]ATGGGGGTTTAAAGT | 55626 |
rs565855839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590527 | CAATTGTTTTCTAAC[A/G]ATATACAAAACTAAT | 55626 |
rs565879471 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513009 | CAAAACTCCCACACT[C/G]GACATGACCACTGCA | 55626 |
rs565886144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479335 | TCTGTATCCATGGCC[C/T]TAGAGAGTCTTCTTC | 55626 |
rs565909717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535524 | AACTTAAAGAAAAAG[C/T]ATCAGTAGGAAAGAA | 55626 |
rs565936230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445862 | TAAGAGAGGGTAGAA[A/T]ATAAATTGAAAAAAC | 55626 |
rs565939606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518877 | TTTCCCTGATTAATA[G/T]TCTGAGTTATGTGCA | 55626 |
rs565969113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517857 | AAAAAAAATGCCAAA[C/T]ACTTAAAGAATAGGA | 55626 |
rs565976772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462814 | TAAAGTGCAGTGGTG[C/T]GATCCCAGCTCACTG | 55626 |
rs565988544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417223 | TGCCCGGCTAATTTT[G/T]TGTATTTTAGTAGAG | 55626 |
rs566000786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566448 | GAGTGGAGCTATTGA[A/T]AATATAACTTGGATG | 55626 |
rs566002581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408907 | TTAGTCTATACCCTA[C/G]AACAATGAAAGGCCA | 55626 |
rs566012826 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425090 | AGTTAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 55626 |
rs566024801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399517 | GATTACAGGCTCCCA[C/T]CACACCTGGCTAATT | 55626 |
rs566034601 | in-del | -/TTT | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516045 | AATTAGGAAGACTTC[-/TTT]AAGTTGGAATAGACC | 55626 |
rs566039646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502579 | GTCCTAGAAATTCCC[A/G]GCTCAGAAGAGAGCA | 55626 |
rs566061675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400020 | GCTAACGCACAGCCC[A/G]GGCACTTGGTCAACG | 55626 |
rs566070580 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541420 | ATACATATATATACA[A/T]ATATGTATTTTTTTT | 55626 |
rs566095167 | in-del | -/TG | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513491 | ACTGAGCACTTCATA[-/TG]TATTTGTTTAAACCT | 55626 |
rs566099148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446494 | TAAGGGATTTCTAAG[C/G]TTTCAAGGTTCTCCC | 55626 |
rs566103080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504051 | AGTGGCTAGTATATA[C/T]GATGCAGATATTTGC | 55626 |
rs566131956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534163 | TTATTGTCTTTCTCC[C/T]ATTAGAATGAGAGAA | 55626 |
rs566137429 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540703 | TCAAGACTTGATTTT[A/G]CAAAGCCTTCTTGGA | 55626 |
rs566160692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485234 | TGAGCCCCTATGCCC[A/G]GCCTCAAGAAGCCCA | 55626 |
rs566163392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488155 | CACAAAATACATTAA[C/T]CAAAAATTGACAAAA | 55626 |
rs566173880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538308 | TTACAATGAGAACCC[C/T]GAGTTATTTGTATAT | 55626 |
rs566175875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546457 | TGATCATGATCGGAG[G/T]ACAGGAATATCTGTA | 55626 |
rs566189951 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520703 | CGGGTTCACGCCATT[C/G]TCCTGCCTCAGCCTC | 55626 |
rs566194328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427987 | GCACTCCTGCCTGGG[C/T]GACAGAGGGAGACTC | 55626 |
rs566198774 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453744 | CCCAAAAAAGCACCA[C/T]GTGGCTGTCTATAAT | 55626 |
rs566223513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415367 | TAAAGAGTTACAAAA[A/G]TATGTGTGTGTTATT | 55626 |
rs566224305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485737 | TGGGGAAAAGAGAGA[C/T]AAAAGCACAGAAAAA | 55626 |
rs566230337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572681 | GACAATCAGCTAGTA[C/T]TTTGGGGTGTTTACT | 55626 |
rs566232826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428549 | TCTAGGATCTGCAGC[A/G]ATTAGGCAATGAGGA | 55626 |
rs566254887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501683 | CACATTGACCACTGT[C/T]ACTCACTGATTCACC | 55626 |
rs566257289 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469749 | TGCTCACTGCAGCCT[C/G]GAACTCCTGGGCTCA | 55626 |
rs566257402 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481551 | TATTTTTAGCAGAGA[C/T]AGGGTTTCTCCATGT | 55626 |
rs566258603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461345 | ATTAAATTTTGGTTG[C/T]GGAAGCACAAATGCA | 55626 |
rs566273636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557623 | TCAGCCTGGTCAACA[C/T]AGTGAGACCCCTGTC | 55626 |
rs566282260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403504 | CAGCTAAACTCATTA[A/G]TTCCATGCTTGCCCT | 55626 |
rs566283425 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452658 | GAAAGCTTCATTCAA[A/C]TGCAGTCTTAAAATC | 55626 |
rs566295457 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462148 | TTCCTTTTCTGTCAG[A/G]GCTGCATGCATCTCC | 55626 |
rs566295657 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538095 | GGCAGAGGAAGAGGC[A/G]GACCAGCACCTGTTT | 55626 |
rs566299678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509321 | TATTATATAATTTGA[C/T]GCTATGGACTGAAAA | 55626 |
rs566322172 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445244 | AATAATGGAATAAAG[A/G]CTAAAACAAACCGTT | 55626 |
rs566322962 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, splice-donor-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46593931 | GGTCCGTTCTACCGA[C/T]CGGCAGGAGAAGGCG | 55626 |
rs566328886 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554711 | AGTCAAACTGAAGTC[A/T]CACAGGGCTGCTGAT | 55626 |
rs566363000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500926 | ATGTAAAACTTGATG[C/T]TATTCCATAACTTAA | 55626 |
rs566363813 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514738 | CCTCGGCCTCCCAAA[C/G]TCCCAGGATTACAGC | 55626 |
rs566374507 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443215 | AAGGGAGTGTAGGAT[A/C]CAAGAGCTAAACCTT | 55626 |
rs566404254 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444194 | TCTGGACCCCTGGCA[C/T]GTAACACAATAAAAA | 55626 |
rs566411330 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435331 | AGATTAGATAAGGAA[A/G]AAGTTATTAAAAATT | 55626 |
rs566418884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404210 | TAAAAACAAAATAAA[C/T]AAATCTTGGTGCCTG | 55626 |
rs566453397 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442290 | TGGGAAAACAGGCAT[A/G]CACCACCACACTCAG | 55626 |
rs566457670 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396722 | TACTGACACCCACAG[A/G]CGCTGCTCTGAGGGC | 55626 |
rs566487785 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567546 | TCATATTTTTAGTAG[A/G]GATGGGGTTTCGCCA | 55626 |
rs566491728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434633 | CTTATTCCTGACCGT[C/T]GTAACAGGGGCATGC | 55626 |
rs566544183 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465827 | TACAATCTTGCTTAA[A/T]CATTCACAGAAATTG | 55626 |
rs566548194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561330 | AAGTTGCAGTGAGCC[A/G]AGATCATGCCATTGC | 55626 |
rs566560760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490685 | TTTCCAAGCTTCATC[C/T]CTGCAAAAAGCCATT | 55626 |
rs566583993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505601 | ATATAAGACCCCCTG[A/G]GAAAAAACAGTAAGT | 55626 |
rs566607680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585898 | ACAACCTCCGCCTCC[A/G]GGGTTCAAGCTATTC | 55626 |
rs566623397 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450857 | AAGCATGAACCCTAA[G/T]GTAAACGCATACTTT | 55626 |
rs566632322 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400420 | AGGCCCCAAGAGATC[C/T]CTCACCCTTCTTGTT | 55626 |
rs566644064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513797 | GAATATAGGCTCAGT[A/G]TTGCTGGCTTTTCCT | 55626 |
rs566650751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457974 | CTTTAGATTCTAAAA[C/T]GGAAAAAAGATTTCA | 55626 |
rs566670326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568869 | TGGAGAGCAGTGGCG[C/T]CATCTCAGCTCACTG | 55626 |
rs566690756 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458636 | AGATCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 55626 |
rs566690906 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449130 | CTAAGACCAGGAACA[A/T]GGCAAGGAAGCCCCT | 55626 |
rs566702637 | snp | A/C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415369 | AAGAGTTACAAAAGT[A/C/T]TGTGTGTGTTATTGT | 55626 |
rs566712204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472464 | TTAGAGCACTTTACC[A/C]ATTTTTCCTACTTAA | 55626 |
rs566728103 | snp | C/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451595 | TCAGAAAAGCTAATT[C/T]GGGGAAGGTAAAAAA | 55626 |
rs566728305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46449917 | TACAAAAATTAGCGG[A/G]GCGTGGTGGCGCATA | 55626 |
rs566729866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553909 | CTGAAAATATCAACA[C/T]TTTCAGGCCAACTTC | 55626 |
rs566766059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497755 | GGGGAAAAGGCCATC[A/G]GTTTTAGTACTGGTA | 55626 |
rs566795538 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593183 | ATTCCTAGGAAAATT[-/G]GGATCACAGACGATC | 55626 |
rs566800800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418292 | TTTATTATTTATATA[C/T]AAATATATAATATAT | 55626 |
rs566805485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488150 | AAAGTCACAAAATAC[A/G]TTAATCAAAAATTGA | 55626 |
rs566818685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583174 | ATCAATGGAACAGAA[C/T]AGAGCCCTCAGAAAT | 55626 |
rs566868782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488931 | TTGTGTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 55626 |
rs566868838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480211 | AATCTTAATCATAAC[A/T]GCAAAGTCCTTTCTG | 55626 |
rs566911417 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558901 | TGTGAAAAGATCCCA[A/G]ATGAACCCAAAACTA | 55626 |
rs566911551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553066 | TTCTGTTTCAGCCTC[C/T]CGAGTAGCTGGGACT | 55626 |
rs566918348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427085 | TAGGACTATATTATA[A/G]GTTCAATTCAAGGGC | 55626 |
rs566923328 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553761 | AAAAAAAAACACAAA[A/C]ACAAAAACAAAAAAA | 55626 |
rs566931204 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439325 | CAAAGATTAAACTCA[C/T]GTGGAACTTTCAAAT | 55626 |
rs566943186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439811 | AAATTGGTAAAGCAC[A/G]TGGACAGGTCAAGAG | 55626 |
rs566972073 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559678 | TGCAATCTGGGGATA[C/T]AGGAGTATCAGTCAA | 55626 |
rs566984273 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553979 | CTCCTTAGTAACCCT[A/G]ACAACTCATAGATTA | 55626 |
rs566992111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433798 | AGGCATATACATACT[A/G]AGTGTAGTGTTTGAC | 55626 |
rs566995847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442268 | GTGCCTCAGCCACCC[A/G]AGTAGCTGGGAAAAC | 55626 |
rs567007816 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568162 | TAAAAAAATAAAATA[A/T]AATAAAATCCAGCTG | 55626 |
rs567011834 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398712 | TGATCTCCTGATCTC[A/G]TGATCTGCCCACCTC | 55626 |
rs567050032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448146 | AACTGTCTAGGCCCT[A/G]TACTATTTGGCAACT | 55626 |
rs567078349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410622 | CCTGACAAGCCTAAC[C/T]GGCTCCTCCTCGGAG | 55626 |
rs567088144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440609 | AAATTATGGCCAACT[G/T]TAAATAAATTATGGA | 55626 |
rs567099362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582670 | TATACCTTGGGCAAA[C/T]TGCTTAATTTCTCTG | 55626 |
rs567133684 | in-del | -/T | 0.0205511 | 0.0992634 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444391 | TAAATAAAAAATGGA[-/T]TTTTTTTAACAGGGT | 55626 |
rs567142060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433133 | CCTCACACACACACA[A/C]AAAAAGCTTTAAAAA | 55626 |
rs567155822 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592750 | GCGACAGAGCTAGCC[C/T]GTCTTAAAAAAAAAA | 55626 |
rs567156653 | in-del | -/ATC | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551348 | ACAGGGTATCACTCT[-/ATC]ATCACCCAGGCTGGA | 55626 |
rs567160841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521479 | CTTGAACGCACTGTG[A/G]CTTTCTTCATTTCTG | 55626 |
rs567181824 | snp | A/T | 1.66125e-05 | 0.00288201 | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433597 | TACATATCTGCCCAT[A/T]GGGGACAGGCTCACC | 55626 |
rs567196602 | in-del | -/CCATCCT | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592859 | CCTTCAAAGTCTTGA[-/CCATCCT]CTACTAGACTCTAAC | 55626 |
rs567198362 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571687 | TCTCAATCAATCAAT[-/C]TTTTTTTTTTTTTTT | 55626 |
rs567211735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592957 | TCAACCAGGAAACAA[C/T]GTAGACAACAAGGTT | 55626 |
rs567218070 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411078 | GTACTCCAGCCTGGG[A/T]GACAGTGCAAGACTC | 55626 |
rs567220123 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544495 | AATTGGCCTGTATTC[A/G/T]ACTGGAAATCCAAGA | 55626 |
rs567231250 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424009 | CTCAGGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 55626 |
rs567244406 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396423 | CCTGGCGAGGGGCAT[A/G]TCATCATTTTAATGA | 55626 |
rs567248653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561239 | TACAAAAATTAGCTG[A/G]GCGTGGTGTCACGCG | 55626 |
rs567254708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403367 | TGCTGCTGGTCTACC[A/G]ACCATCTTCACCAGA | 55626 |
rs567348793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489153 | CATGTGCCATGCTGG[C/T]GTGCTGCACCCATTA | 55626 |
rs567361566 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438860 | GGCCTTATTCATAAA[C/T]TTCTAAACACTAATC | 55626 |
rs567373838 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528780 | TCTATCACAGACACA[C/T]GTACACGAAGATAAA | 55626 |
rs567378052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495593 | AGGAGAAAGAGATAA[A/G]ACTATATGGAATGTA | 55626 |
rs567388076 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471209 | CACTTTGGGAGGCTC[G/T]GGCGGGCGGATCACT | 55626 |
rs567403812 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593737 | GTGTCACGGCGGCCG[A/G]CCAGCCTGCCCACCC | 55626 |
rs567405282 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448442 | ACATGACTTCTCAAA[A/T]TTCGTGAAATGTAGT | 55626 |
rs567405858 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575801 | ATTATAGGCGTGAGC[A/C]TCCGTGCCCAGCCAG | 55626 |
rs567410137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489742 | GAAGTTTTTTGTTCT[C/T]CCAGTAATTACCAGG | 55626 |
rs567413167 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484917 | CTGAAAGTGCTGGGA[A/T]TACAGGTGTGAGCCA | 55626 |
rs567421239 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475583 | TTTGTCAAATTCAGA[A/C]GGCCCAAGGACTCAA | 55626 |
rs567423066 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433783 | AGGAGTATGATGAGA[A/G]GGCATATACATACTG | 55626 |
rs567445334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520756 | GCCCACCACCAAGCC[C/T]GGCTAATTTTTTGTA | 55626 |
rs567446249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504647 | GCAGGAGAGGAAGCC[C/T]GCCCAGGAAGATGGT | 55626 |
rs567452944 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464790 | AGTGGCTCACACCTG[C/T]AATCCAAGCACTTTG | 55626 |
rs567466688 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568108 | AGCTGAGATCCTGCC[A/G]CTGCACTCCAGCCTG | 55626 |
rs567501913 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479598 | GCTACTAGGGAGGCT[C/G]AGGCAGGAGAATCAC | 55626 |
rs567509171 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409427 | ATGGTCTCCATCTCC[C/T]GACCTCGTGATCCGC | 55626 |
rs567532833 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591850 | GGACAAAGCAAGACT[C/G]CGTCTCAAAAAACAC | 55626 |
rs567545053 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549931 | TCATGCAATTCTCCT[C/G]CCTCAGCCTCCGGAG | 55626 |
rs567561219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505475 | AATCCACAGCTGCTA[C/T]TAAAAACAAGATTCT | 55626 |
rs567569682 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448598 | TAAGCAGAAGAAAAA[C/T]ATGAGCAGAAACCAA | 55626 |
rs567628601 | snp | A/C | 1.65767e-05 | 0.00287891 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544081 | AAGACACACATAGAG[A/C]GATTATGTTAACTGA | 55626 |
rs567629097 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581419 | CGAGACCATCCTGGC[C/T]AACACATGAAACCCC | 55626 |
rs567637668 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402396 | AGACGGAGTCTTGCT[C/G]TGTTGCCCAGGCTGG | 55626 |
rs567649949 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591836 | CACTCCAGCCTGGGG[G/T]ACAAAGCAAGACTCC | 55626 |
rs567664810 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489655 | GAGCAGATGCTCATT[-/G]AGGATGAAAGTCAAA | 55626 |
rs567667310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480137 | ACTTTTAATAGCTCA[C/T]GTAATCAGATGAGGC | 55626 |
rs567674579 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400178 | AGGCTCTGAGGCTGC[A/G]AGGGATGGCTCCACT | 55626 |
rs567679691 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471719 | TGCAACCTCCACCTC[C/T]GAGGTTCAAGCAATT | 55626 |
rs567693573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575327 | CCCAGCGTGGTGGCA[C/T]GTGCCTGTAATCCCA | 55626 |
rs567709971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433073 | AATTATAACCCACAG[A/G]AAAAAAACATTTCAT | 55626 |
rs567711303 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578258 | TTAGGAAGCCGAGGC[A/G]GGTGGATCACCTGAG | 55626 |
rs567740145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582535 | TCTAGTCTCACTATA[C/T]TGACCTAGTGTTTTA | 55626 |
rs567743287 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420838 | TACAATGATTTATAA[C/T]TGTAGGGAATGGGGC | 55626 |
rs567753122 | in-del | -/AAAAAAAAAAAAAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411102 | AAGACTCTGTCTCAA[-/AAAAAAAAAAAAAG]AAAAAAAAAAAAAAG | 55626 |
rs567758635 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461570 | GGCTAAAGTTAAATA[C/T]TTGGGGATGTGGAGT | 55626 |
rs567763571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421203 | AATGAAATGTTGAGA[C/G]CCCCGGGTTGTTGCT | 55626 |
rs567766915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418133 | AAAATCCAGGGAGAA[A/G]CAAATTAGAAGGAGG | 55626 |
rs567790441 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472295 | GCCACCTGAGCCTGT[A/C]TCTTAGCATTGAGGT | 55626 |
rs567805719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401511 | CCCAAAGTTCTGGGA[A/G]GCATGAGCCACCGCA | 55626 |
rs567817075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474898 | AAGATAGTCGAAAGA[A/G]AAAGAACACAGTGTG | 55626 |
rs567823781 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416621 | TACATCCTTTAGGAG[-/AA]ACTATCAAGGATCCC | 55626 |
rs567836243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550467 | TTACAATTAGCAATC[G/T]GTGGCAATTATTTGG | 55626 |
rs567846465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456263 | TAGCATTCGCTCCCA[C/T]CAGGCAGGGATTTCC | 55626 |
rs567851871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559081 | GAGTCGGGTGGATCA[C/T]CTGAGGTCAGGAGTT | 55626 |
rs567860130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551302 | GGAATTTTAGTTAGT[G/T]TGTGGGGACTTTATT | 55626 |
rs567872518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432327 | TGCAGGTAGCTGGAG[A/G]TAGGGGACAGGAGGG | 55626 |
rs567877859 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501769 | TTATTTCAATGTTTA[A/C]TATAAGAAGTGTTTT | 55626 |
rs567885641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447443 | GGGATGCTGAGGCAT[A/G]AGAATTGCTTGAACC | 55626 |
rs567888794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467403 | TAGTATAATAAATTC[A/G]TATTTCCTTTCACAT | 55626 |
rs567894434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438957 | AATTCACATAAATCA[A/G]CTTGGTGGTTGCTGA | 55626 |
rs567922585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484662 | TTGGCTTTTTTTTTT[C/T]CTGAGATGGAGTCTC | 55626 |
rs567937381 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575568 | GTCACCCAGGCTGGA[A/G]TACAATGGTATGATC | 55626 |
rs567943194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540326 | CTTTTACAGAGATCT[C/T]TAATAAACTTTTAAA | 55626 |
rs567998775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491577 | ACATCAAAATATCAA[C/T]GAATGATAAATAAAT | 55626 |
rs568004461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532936 | CACTTAAGTACACAA[A/C]GATCCTGCAACACTG | 55626 |
rs568008114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590954 | AGAAAAAAAGCTGAA[G/T]GAACTTCTATCACAA | 55626 |
rs568061039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492219 | CCTGCCAGGCCAGAG[C/G]CTATGAAGTCCTGGT | 55626 |
rs568082701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468487 | CCTCCTAGTAGCACA[A/G]GCATCACTCTTAAAG | 55626 |
rs568083094 | in-del | -/TCTAT | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587016 | TATATATACCTGTGA[-/TCTAT]TCTAGAGAGTAGAAA | 55626 |
rs568096560 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422466 | GACAATCTCTTGTAC[C/T]GCTTGCCTCTCTACC | 55626 |
rs568111487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429287 | GTGTGTGGGGAGTGG[A/G]AGAGAGGCCCCCTGC | 55626 |
rs568120934 | in-del | -/C | 0.00755907 | 0.0610114 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595247 | ATCTTAAATTTTTTT[-/C]TTTTTTAAATGCCGG | 55626 |
rs568121129 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495668 | GCAGACTGCAGTTAC[C/T]GGGGAGCCCACAAAT | 55626 |
rs568136551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459631 | CAGGAGAATTGCTCG[A/G]ACCTGGGAGGTGGAG | 55626 |
rs568137486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578829 | GAGCTTGCAGTGAGC[C/T]GAGATTGCACCACTG | 55626 |
rs568139934 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400548 | CTAAACTGGAGTGCA[A/G]TGGTACAAACATGGC | 55626 |
rs568157479 | in-del | -/ACACATACACACACACAC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459734 | AAAGAAAAAAAAAAT[-/ACACATACACACACACAC]ACACACACACACACA | 55626 |
rs568158432 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46451111 | TCATGGTAGTTCATA[C/T]CTATCATATAACCAC | 55626 |
rs568175074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460371 | CTGTTGCCCAGGCTG[C/G]AGCACAGTGGCGCAA | 55626 |
rs568192536 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469075 | TTGAACCTGGGAGGC[A/C/G]GAGGTTGCAGTGAGC | 55626 |
rs568193699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444185 | TTCATCTCTTCTGGA[C/G]CCCTGGCACGTAACA | 55626 |
rs568278479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584986 | CTGAGGCAGGAGAAA[C/G]GCTTGAACCTGGGAG | 55626 |
rs568294268 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435649 | ACAAAGCCCAGCTGC[A/G]GCTGGATGGCCAGGG | 55626 |
rs568369555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436804 | TGACAATGCTCAGAA[A/G]AATAAACAGAAACTA | 55626 |
rs568375638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428898 | CAATCTCTGGGGGCA[C/G]ATGAAGGTAATCACG | 55626 |
rs568389589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576748 | CAAGAGATTATAAAA[C/T]ATAGGAAGCCCATTT | 55626 |
rs568389608 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484103 | TTATCATAGGCTCAG[C/T]TCACTGCAGCTTTGT | 55626 |
rs568391313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585644 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 55626 |
rs568415126 | in-del | -/GG | 0.0310518 | 0.120672 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441374 | AAAAATTAGCTGGGT[-/GG]GTGGTGGCGTGCACC | 55626 |
rs568419290 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404419 | CCCTGAAGAGTCTGA[C/T]AGCACAATAGTGGTG | 55626 |
rs568444686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466127 | AAAATGGTAGTAAGA[A/T]GTACTTCTTGCTTGT | 55626 |
rs568471589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508091 | ATAATTGAGGAGTTG[C/G]GAGCAAGAACATCCA | 55626 |
rs568479449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515431 | TGAGCTGAGATCGCA[A/C]TACTGCACTCCAGAC | 55626 |
rs568537764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507529 | TCTAGAGCCTGGGGC[C/T]GACCCTGCTCCTTTA | 55626 |
rs568555437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454562 | AACACGGTGAAACCC[C/G]ATCTCCACTAAAAAT | 55626 |
rs568561701 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531134 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 55626 |
rs568561781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539705 | CTGAGCCTCACTTTC[C/T]TCAACTTTATAAAAT | 55626 |
rs568573879 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532050 | CTTGAACCTGGGAGG[C/T]GGAAGTTGCAGTGAG | 55626 |
rs568580073 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488532 | GATTTCAATACCCAC[C/T]CTCAATAACTGACAA | 55626 |
rs568595408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492675 | AGACTGACCAGAAGC[A/T]ATAGCACACACAACG | 55626 |
rs568598473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555031 | GAGCCATGATTGCAC[C/T]GCTGCACTCTTCAGC | 55626 |
rs568600465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405813 | ACAGCTCACTGCAGT[C/T]GCCACCTTCCAGGCT | 55626 |
rs568615478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422276 | CTTCCCAAAGTAGAT[G/T]GTTCTCATTTCTGTC | 55626 |
rs568617524 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491813 | CCATAAGTGTAATTA[A/G]GCCATTTGGGGTCAG | 55626 |
rs568617612 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451974 | AAAGGGGAAGTGACT[A/G/T]CTGATGTGTATGGGG | 55626 |
rs568641897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428455 | GTCAAATGAAGGTGT[C/G]CTTAGTCATCCCTTC | 55626 |
rs568657465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474428 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 55626 |
rs568663741 | snp | G/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592910 | ACCATAGTTATAAGA[G/T]TTCCAAAGAGGCTGG | 55626 |
rs568664535 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531063 | AATTTTTGTATTTTT[A/G]GTGGAGATGTGGTTT | 55626 |
rs568670747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529429 | CCCCTGTGGGTGAAT[C/T]AGGCAGGATGGGTGG | 55626 |
rs568673477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497846 | TGACTCTCTAGATTC[A/T]ATAGTTTAGAAAGAG | 55626 |
rs568677745 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507457 | GCACTCCAGCCTGAG[C/T]GAAAGAGCGAGACTC | 55626 |
rs568678628 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421061 | CTGTACAGGGATTAA[C/T]AGGCAAATATTATCT | 55626 |
rs568681521 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427875 | TTAGCCGGGAGTGGT[G/T]GCGAGTGCCTGTAGA | 55626 |
rs568709827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530203 | ATACAGACGTCACTG[C/T]AGTCCCCAAGTGCTC | 55626 |
rs568725094 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568742 | TCACCATTGCACTCC[A/T]GCTTGGGCAACAAGA | 55626 |
rs568731972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522618 | GAATTTAAGAGGCAG[G/T]GTATCCTAATTCACT | 55626 |
rs568745134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547582 | CACACAGGCAAATGA[C/T]TGTTATTGAGAAACT | 55626 |
rs568773444 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483889 | AGTGAGACTCTGTCT[C/T]GAAAAGAAAAAAAAA | 55626 |
rs568787695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436056 | TGTCTCATGTAGATA[C/T]ACCTCAAGCAAAAAA | 55626 |
rs568790990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412430 | GCTGGTACTACAGGC[A/G]TGCCTCACCACGCCT | 55626 |
rs568792398 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498801 | CCACTGTCCTCTTGA[C/G]AGTATACAGTTGACT | 55626 |
rs568793125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523444 | CTCCTCCCCCGTTCC[A/C]AAAAAGATTCGCACA | 55626 |
rs568837262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585957 | ATTACAGGCATGCAC[A/C]ACCACACCCAGCTAA | 55626 |
rs568853864 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595803 | CATCCTGGCTAATGC[A/G]GTGAACCCCGTCTCT | 55626 |
rs568863082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428617 | TAAGGTTTTTTGGCT[A/G]TAAGTTTATTCAATG | 55626 |
rs568866275 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582935 | GATATTTCATAACTC[-/A]AAAAAAAAAAAGCCA | 55626 |
rs568872659 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522657 | CCTGGAATTTATTGA[A/G]TTCCATAATGTTGAA | 55626 |
rs568873166 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413773 | TGGGATTACAGGCAT[A/G]AGCCACCATGCCCGG | 55626 |
rs568885008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475376 | ACAGTTTAATGTCCA[A/G]GTTCCAGGTTGGAAA | 55626 |
rs568912544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404870 | AAATGGGCTGCATGC[C/T]AACCAAGAAAACAGC | 55626 |
rs568933081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538720 | CCAGGCTGGTCTCGA[A/G]CTCCTGACCTCAGGC | 55626 |
rs568934502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459540 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 55626 |
rs568953044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586805 | GTAAGCAGGGGTGCT[A/G]GAATTTGAACCAGGC | 55626 |
rs568973359 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578213 | CAGGTAGGGCCGGAC[A/G]TGGTGGCTCACACCT | 55626 |
rs568992638 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396863 | GCAGGCGCCCCCTTA[C/T]CCCACAGTAGTCCCC | 55626 |
rs569007918 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476964 | ATACAAAAAAATTAG[-/T]TGGGCATGGTGGCGC | 55626 |
rs569034078 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415979 | ACATAAAAACCTTTA[C/T]GAGGCCACAACAAAC | 55626 |
rs569069845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563008 | TCACCATGTTAGCCA[A/G]GCTGGTCTCAAACTC | 55626 |
rs569072032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46449949 | CTGTAATCCCAGCTA[C/T]TCAGGAGGCTGAAGC | 55626 |
rs569091791 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592904 | ACAAACACCATAGTT[A/G]TAAGATTTCCAAAGA | 55626 |
rs569107069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546754 | AATTAAAAAACCAAT[A/G]GTAAACAAGTCTCTG | 55626 |
rs569122847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481156 | TGCCGTCCCCAGACT[A/G]ATAAGAGCAGCACGG | 55626 |
rs569177800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593573 | CCATTTTCGCCACAC[A/T]CTGGGGGTGCCCTAG | 55626 |
rs569236562 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481647 | GGATTACAGGCATGA[A/T]CTACCGCGCCCGGCC | 55626 |
rs569257038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515427 | GCAGTGAGCTGAGAT[C/T]GCACTACTGCACTCC | 55626 |
rs569290709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568893 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAT | 55626 |
rs569301255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470664 | CTACTCAGAAGGCTA[A/G]AGTGAGAGGATTGCT | 55626 |
rs569310888 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403347 | TGGCCCAGGGCCCAG[A/G]CTACTGCTGCTGGTC | 55626 |
rs569324760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514841 | TCTTTGAGTCTTTTA[A/G]AATACAGAATGTGTG | 55626 |
rs569326481 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461775 | ATATGGTCACATAAA[-/C]TTTGTACCCCACAAA | 55626 |
rs569343799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433149 | AAAAAGCTTTAAAAA[A/T]AAGCATTTCATTGGG | 55626 |
rs569355190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404379 | GGGAAATCTGGGCTC[A/C]AAGAGAGCCCTGATC | 55626 |
rs569380255 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525706 | CAGTGACCCGAGATC[A/G]TGCCACTGCACTCCA | 55626 |
rs569408622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569668 | GATATTTGTAATCCC[A/G]GCACTTTGGGAGGCT | 55626 |
rs569420625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544915 | GAAGGCCAGTAGTTC[A/G]AGACTAGCCTGGGTA | 55626 |
rs569422705 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521768 | AGCATGTGATGCAGT[C/T]GCCAGCAGAGACTGG | 55626 |
rs569429735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583354 | CAAAAATTAATTCAA[A/G]ATGGATTAAAGACTT | 55626 |
rs569465301 | snp | G/T | 0.000617072 | 0.0175543 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433649 | GGCCAACAAAACAGA[G/T]AAATATTTCCTAGGC | 55626 |
rs569492762 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576045 | CTCTCAAATCACACA[A/C]TCTATGGAAGCTGCA | 55626 |
rs569502639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427139 | AGTTTGTAGATTGAA[A/G]AATAAAGCTGGGACA | 55626 |
rs569519934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537306 | GCACTTATTTCAAAT[A/G]AAACGGAGGAAAGGG | 55626 |
rs569568833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566405 | CCTGGGTGACACAGC[A/G]AGACTACATCTCAAG | 55626 |
rs569572795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462957 | CGGGGTTTCACCATA[C/T]TGGCCAGGCTGGTCT | 55626 |
rs569576598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584889 | CCAGACTGGCCAACA[A/T]GGTGAAACCCTGTCT | 55626 |
rs569592477 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589706 | CTAACTGCAAGCTCC[A/G]CCTACCGGGTTCACG | 55626 |
rs569593671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530181 | TCCCAACGTATTTGC[A/G]GCACACATACAGACG | 55626 |
rs569618674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462300 | AACCTGCAAGCTTCT[C/G]TATATGCCCCTTGGG | 55626 |
rs569640364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511206 | TCTCTATCTCAGTGC[C/T]TCAAAGTAATTGATT | 55626 |
rs569656720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580164 | TGACAAATCCAACAA[C/T]GTACAGTGATTACTC | 55626 |
rs569692964 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579781 | GCAGTGACATGATAT[C/T]AGCTCACTATATCCC | 55626 |
rs569707148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485217 | TGCTGGGATTACAGG[C/T]GTGAGCCCCTATGCC | 55626 |
rs569710818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416430 | CAGCTCCAAGAGCAG[C/G]CTGAGCAGGCTAGGC | 55626 |
rs569717885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557506 | CCACTGTCACCTTTT[C/T]AAAAACAAAAAATAA | 55626 |
rs569727742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541274 | GTATGGAGAGTCTTT[C/T]CTTCCATGAATTATT | 55626 |
rs569735004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511906 | GTCACCCAGGCTGGA[C/G]TGCAGTGGTGCGATC | 55626 |
rs569739382 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505558 | GGAGTATGAGAGAAA[C/T]CAGTCCATTGTTACT | 55626 |
rs569748327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408812 | GTGTGGGCCAGGCCC[C/T]GCAGGCTAAGAGAAG | 55626 |
rs569763321 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566786 | TGGTCATTCCTGTGC[A/G]TAGGACAAGCTAACT | 55626 |
rs569766714 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541779 | GCTAGGCCCTATCCT[A/G]TCTCTGCCACCAGAG | 55626 |
rs569787525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437157 | ACAAGGTGTGCAGAG[C/G]AGAGTACAAGTAAGA | 55626 |
rs569801137 | in-del | -/CA | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540889 | TCCCACAGTGCCTAG[-/CA]CAGTGTTAGAAAATT | 55626 |
rs569833926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423741 | AGAGCAGGACTAACT[A/C]ACAGGCAGTGCACCC | 55626 |
rs569910860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579721 | GACATGTTTTGTTTT[A/G]TTTTGTTTTGAGATG | 55626 |
rs569927662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525918 | CTCTGTCTCAAAAAA[A/G]AAATAGGCTAGGTGC | 55626 |
rs569941149 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532772 | TCTATGAAATAATGT[G/T]CAGTTAAATAAAACA | 55626 |
rs569946454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518118 | CTGAAAAGAAAGAGA[C/T]AGCCATTTGTTTTCA | 55626 |
rs569958532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414216 | TATCAGTGACACGAC[A/G]GGAGAGGATCAGACC | 55626 |
rs569987048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415492 | ATTCTAGTTCTGTCA[C/T]CTGTTAGGAGGCCTC | 55626 |
rs569992458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414708 | GGCAGAGTGCAGGTG[A/G]GGGAGCAGAGGAGGA | 55626 |
rs570017876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549284 | TCAAAAGAATATCTA[C/T]ATATATACAGTGTTA | 55626 |
rs570030197 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500815 | AGCTCAAATCCATGA[A/C]GCTTTCTCACCTCTC | 55626 |
rs570060061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536556 | GACCCCTTTCTATAG[C/T]AGTCAGGCTAAGAAG | 55626 |
rs570073674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477746 | CCCATCAGCGACTGA[A/G]GTGGTTCTAAAAGTA | 55626 |
rs570097343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540574 | CCTCTGCTTCCTACC[C/G]AGGGCCCTTAGTAAC | 55626 |
rs570106756 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578695 | GAGACCATCCTGGCT[A/C]ACACGGTGAAACCCT | 55626 |
rs570116295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492566 | AAATTTATAAGTCGG[A/C]AGTGGAGGTGGGAGG | 55626 |
rs570170961 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452928 | ATAGCTTTACTGAGA[C/T]ATAACTTACAATTCA | 55626 |
rs570171152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571931 | CTGACCTCGTGATCC[A/G]CCTGCCTCAGCCTCC | 55626 |
rs570174789 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484867 | AGCCAGGATGATCTC[A/G]ATCTCCTGACCTCAT | 55626 |
rs570181559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525110 | TTCGAGACCAGCTCG[A/G]GCAACCATAGGGAGA | 55626 |
rs570186137 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572659 | TCAGCATTATCATCA[A/T]CATCTTGACAATCAG | 55626 |
rs570222993 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565901 | CCTCAGCCACCCAAG[C/T]AGCTGCGCCCACAGG | 55626 |
rs570264183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468921 | GGCCAAGGCAGGTGG[A/C]TCACCTGAAGTCAGG | 55626 |
rs570289360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451423 | CTTTGCTTCTCTCAG[A/G]AACTCTTCTCTTCTG | 55626 |
rs570306946 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471673 | TTGCTCTGTTGCCAG[A/G]CTGGAGTGCAGTAGC | 55626 |
rs570309196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406246 | TTTAGTAGAGACAGC[A/G]TTTCACCATGTTGGC | 55626 |
rs570328180 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460662 | ACAATATTTTACTAA[C/T]ATATTAAGCTATAAA | 55626 |
rs570348523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398698 | AACCAGGATGTTCTT[G/T]ATCTCCTGATCTCGT | 55626 |
rs570382799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525858 | TGGAGGTTGCAGTGA[C/G]CAGAGATCACGCCAT | 55626 |
rs570387565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469179 | TAATAAAATATTAGA[C/T]TTAGTTAGTTTAGGC | 55626 |
rs570398148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484740 | GCAAGCTCCGCCTCC[C/T]GGATTCACATCATTC | 55626 |
rs570428863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415377 | CAAAAGTATGTGTGT[A/G]TTATTGTGGCATATT | 55626 |
rs570462093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476909 | GCCAGGAGTTCGAAA[C/G]CAGCCTGGTCAAGAT | 55626 |
rs570466763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414864 | AGATGGAGGATTTTT[A/G]AAGGCCTTAGTCTAC | 55626 |
rs570492442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460513 | TATTTTTAGTAGAGA[C/T]AGGGTTTCACCGTGT | 55626 |
rs570497190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462215 | GCGCGTAAACAAGTG[A/T]GCACGGCGGTGTAAG | 55626 |
rs570502019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423710 | TTTATTATTTTTAAA[C/T]TTTTACTGTTCTGAC | 55626 |
rs570522898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564886 | TACATTATTATTTCT[C/T]CGATATCTACAGCAA | 55626 |
rs570527687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492300 | GGATCAAACATACTA[C/T]TTAGGAAAGGCCAGA | 55626 |
rs570528929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46451282 | CCAAGTCTCATTCCA[C/G]AGTCAGGTCTTCAAC | 55626 |
rs570531653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518637 | AAAATACCTACTGCC[G/T]AGCCCTTTACAGAAG | 55626 |
rs570548265 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445076 | AAAAGAAAAACAAAA[A/C]AAAAAAAACAAAAAA | 55626 |
rs570552285 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458502 | TGTACACTGAGCCAT[C/T]GATTTTCCATTGGTA | 55626 |
rs570584913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436902 | GTACATGAACCTAAA[C/T]AGGAAAGGAGATGAG | 55626 |
rs570593359 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573332 | TCGCTGGAACCCGGA[A/G]GGCAGAGGTTGCAGT | 55626 |
rs570593438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565717 | TCTCAAAAAAAAACG[C/T]GTATAAAAATGTTAA | 55626 |
rs570610556 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576320 | TGTTTTGTAGACGGG[A/G]TCTCCGTATGTTGCC | 55626 |
rs570670285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577338 | CCTCCAAAACATTAC[A/G]CTAAGTCAAAGAAGC | 55626 |
rs570683890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533077 | CTGAGGCACGAGAAT[C/T]GCTTGAGCCCCAGAG | 55626 |
rs570706051 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540463 | ATATTCCAAAACCAG[G/T]AATTGAGGAGCTGTT | 55626 |
rs570722761 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429383 | GAACTCCACAGAAAA[A/C]CCTTTTCCACTTCTT | 55626 |
rs570734394 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577867 | AGGCAGGAGAATCAC[C/T]TGAACCCAGGAGGAG | 55626 |
rs570737643 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568287 | ACGTGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 55626 |
rs570759459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423100 | TCAATAGAAAGCAGA[C/T]GCTAAGAGACAGCTG | 55626 |
rs570827262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556790 | TATTTACCATATGAA[A/G]AATGCTTATAGTAGA | 55626 |
rs570832331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556219 | AATAGGACTTTCCTA[C/T]GGCCATTTCAGGATA | 55626 |
rs570846126 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570755 | ATATTAACACATGAC[A/G]ACAGAAAAAATTCAA | 55626 |
rs570850150 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459773 | ACACACACACACACA[C/T]ACCCTGGAATACCAC | 55626 |
rs570879237 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529829 | ATCTTGGTTAATGTA[A/T]CAATAGGCCCACCCA | 55626 |
rs570891809 | snp | C/T | 8.40739e-05 | 0.00648304 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508145 | AACTTGGAAGCACTC[C/T]AAGCTTGAGAGGAGA | 55626 |
rs570917099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586750 | TACAGATGAGGAGAG[G/T]CACAGAGAGACTAAG | 55626 |
rs570918706 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561166 | CAGGTGGATCACCTG[A/T]GGTCAGGAGTTCGAG | 55626 |
rs570919992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500056 | TACACATCAGACACT[A/G]AGGCCTAGGATGGGA | 55626 |
rs570928512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547729 | ACTTCAGAGAGACTT[C/T]AGGGACTGACTTGGA | 55626 |
rs570946664 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398450 | CGTAGTTTTGTGTTA[C/T]CTCCTCAAAGCCCCT | 55626 |
rs570959901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448711 | AGGTAGGCCAACTAC[A/G]AAAAAAGAGAGAAGA | 55626 |
rs570961844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440757 | AGAAATAGATGGTTG[C/T]TGCTGAAGTTTCATT | 55626 |
rs570983858 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399305 | TCTCGAACTCCTGAC[C/G]TCAGGTAATCTGCCT | 55626 |
rs570985363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475224 | TTGGAATGCAAAGTA[C/T]TAATTATGAATAAGA | 55626 |
rs570990619 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460297 | GATGATCCATATGCA[C/T]ACGACCCCATTTATA | 55626 |
rs571000975 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531771 | ATTCCCATATTGCCA[A/C]AGAGAAAATGGGTTG | 55626 |
rs571013476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524164 | TGAGCCACCGCACCC[A/G]GCCTAATGTCATATT | 55626 |
rs571053315 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496756 | GCATCTTTTTGTTGC[G/T]ATTAAAACCTAAATA | 55626 |
rs571057097 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523648 | TCTGAATGCCTGCTA[A/C]ATCGATACCTGTGTA | 55626 |
rs571081481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413963 | GAGGAAGGCTAGGAG[G/T]TCCAATCAGGGCCAG | 55626 |
rs571093329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468256 | GTGGGGAGGGGTGGC[A/G]GGCAGCATGGTGGCT | 55626 |
rs571102157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413289 | GTCTCAGATGTGTTG[C/T]TCCACTATGCCTCCC | 55626 |
rs571115273 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493035 | GCCTGGGTGACAGGG[C/T]GAGACTCTGTCTCAA | 55626 |
rs571163757 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539677 | ATGATCTTTCACAAG[-/A]AAACTGACTTCCCTG | 55626 |
rs571185222 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553272 | TAAAAAGTAATAACT[A/G]TTTATTGTAAAAAGC | 55626 |
rs571185950 | snp | A/C/G | 8.39051e-05 | 0.0064766 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418068 | CTAGGTAGAGGAAAA[A/C/G]AGGGAAAAAAAGAGA | 55626 |
rs571226909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544304 | CCCAGGAAACAGCTA[C/T]CTTAAGCACACCTTT | 55626 |
rs571246807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456634 | ATTGCTGAGACTCCC[A/G]CAGCTTTTATTGTTT | 55626 |
rs571295353 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552959 | ACTCACTTTTTTTCT[C/T]TTTTGAGACAGAGTC | 55626 |
rs571302582 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508423 | TAATGTGGGGAATAC[C/T]ATGAAAGGCAGTTAA | 55626 |
rs571341222 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470621 | AAAAAAATTAGCCAG[A/G]TGTGGCACCATGGGC | 55626 |
rs571343891 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505382 | AGGGAAGGAGACAGA[A/G]AAAGAATAAACAGTC | 55626 |
rs571354122 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463696 | ATCTTTTGTCTGATT[C/T]CTGCAACTCCAGGAA | 55626 |
rs571361838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496862 | CATGCCTGTAATCCC[A/G]GCACTTTGGGAGGCT | 55626 |
rs571374187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505387 | AGGAGACAGAGAAAG[A/G]ATAAACAGTCAGTTT | 55626 |
rs571408528 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425239 | TTCTACATCTCAAAG[G/T]AAATGGTCTAATGAG | 55626 |
rs571429668 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409563 | CTGAAAACAGACCCT[G/T]GCAGGTAGGGAGCAC | 55626 |
rs571431575 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575805 | TAGGCGTGAGCCTCC[A/G]TGCCCAGCCAGGCTT | 55626 |
rs571458986 | snp | A/T | 0.0001359 | 0.00824205 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542971 | TGCTCCGGGGGATGG[A/T]AGGGCTCGGTCTGTA | 55626 |
rs571461793 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445082 | AAAACAAAAAAAAAA[A/C]AACAAAAAAAAACTT | 55626 |
rs571469444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400035 | AGGCACTTGGTCAAC[A/G]GTGCCTGTTGTGATT | 55626 |
rs571472959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401621 | GCCCCCAGAGAGCCC[C/T]GGATGGGCTTTCCCA | 55626 |
rs571473925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511097 | TATTATATAAAAGGA[A/G]GATAAATCATGGTCG | 55626 |
rs571494469 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551599 | AACGACACCAGGCGC[A/G]ATGGCTCACGCCTGT | 55626 |
rs571510932 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520613 | CTTTTTTTTTTTTTT[A/T]GAGACGGAGTCTCGC | 55626 |
rs571528394 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46449837 | AGGCCAAGGCAGGTG[A/C/G]ATCATGAGGTCAGGA | 55626 |
rs571534603 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477372 | ACTCAGACTGGAGTG[C/T]AGTGATGTGATCTCT | 55626 |
rs571568899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480399 | ACTGCAATTGGACTC[A/G]CAGAATTGTGAGAAA | 55626 |
rs571571094 | snp | A/C/G | 0.00239393 | 0.0345281 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476303 | GGGTTGGCAGGTGAA[A/C/G]GAGTAGGGTGTGCAC | 55626 |
rs571583461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431580 | AGGAGCTGGGCAAGA[A/G]CCCTGGCTTATGAAA | 55626 |
rs571598615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551075 | GCACTCCAGCCTGGG[C/T]GACGGAGTGAGACTC | 55626 |
rs571608478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400779 | TGGGTGAGTCACTGC[C/G]CCCAGCCCCAGTCTT | 55626 |
rs571620898 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485873 | TGTTCTCAATAAGCA[C/T]ACTTCTCACTAGTGG | 55626 |
rs571646237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439539 | GACTAAATTTCCTAG[C/T]GAATCAAAGACTTAA | 55626 |
rs571647388 | in-del | -/A | 0.145305 | 0.227022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552679 | GCGAGATTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs571649669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590041 | AAGTTTTATAAGTTT[A/C]CTAACACATATTGAA | 55626 |
rs571650741 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495756 | CATACTATTATTTTT[C/T]AAATATACTACTGTT | 55626 |
rs571666349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527890 | AGCTGCTATGGAAAA[C/T]AGTATGGAGGTTCCT | 55626 |
rs571682279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478977 | GCCAAGGTGGTAGGA[C/T]CGCTTGAGCCCAAGA | 55626 |
rs571687937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455472 | GCATAACTAGGTAGC[A/G]TGCACACAAAGACAT | 55626 |
rs571695485 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515675 | GTTTTAATGACTCCA[C/T]TTTTATTTTTTATTT | 55626 |
rs571699664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486666 | ATCCTAGCACTTTGG[A/G]AGGCCAAGGTGGGCG | 55626 |
rs571743691 | snp | C/T | 0.000199475 | 0.00998487 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46493651 | AGTAGCCAAGCCAGG[C/T]TGTCCACGTTCATGA | 55626 |
rs571760700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558288 | GGGCGCAGTCGCTCA[A/C]ACCTGTAATCCCAGC | 55626 |
rs571769164 | in-del | -/ATA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584519 | CCTAAAACTTGAAGT[-/ATA]ATAATAATAATAAAA | 55626 |
rs571818635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479482 | CTTTTCAGAACTCTG[A/G]GGTCAGGAGTTTGAG | 55626 |
rs571821031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486038 | TACTTCTCTGTTTCC[C/T]AGGCAACAAAGCCAG | 55626 |
rs571847416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453829 | TTAATAACTACTCTA[A/C]CAGTCATTTAATCTG | 55626 |
rs571863702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566380 | CCGAGATTGAGCCAC[A/G]GCACTCCAGCCTGGG | 55626 |
rs571880740 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433067 | CATCATAATTATAAC[A/C]CACAGAAAAAAAACA | 55626 |
rs571883383 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445982 | AGTACTGTGGATCTG[A/C]AAATGGGAACACAAA | 55626 |
rs571883608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455151 | CTTGGCCTCCCAAAT[C/T]GCTGGGATTATGGGC | 55626 |
rs571920382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446635 | ACATTTAGCATCCCT[A/G]GCCTCTACCCACTAG | 55626 |
rs571928023 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446160 | GTGCCAGGGTGCTGA[C/G]GAGGAATGAAGCCTG | 55626 |
rs572003640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558487 | CCGGGAGGTGGAGGT[G/T]GCAATGAGCTGAGAT | 55626 |
rs572023555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446847 | CAAGTGATGCTGTTA[C/T]AGTCATGGAAAGAAA | 55626 |
rs572062238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439022 | ACACCTGTAATCCCA[C/G]TACTACGGGAGGCCA | 55626 |
rs572080201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550553 | TTGATGATTCTCTCT[C/T]GTACTTTTTTAATGG | 55626 |
rs572087175 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579930 | GTTGGCCAGGCTGGT[C/T]TTGAACTCCTGACCT | 55626 |
rs572092624 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506895 | CTTAGGCTGGGCGTG[A/C/G]TTGCTCACACCTATT | 55626 |
rs572104506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437196 | CTTCTGGAAAGCTTG[C/G]CTCTAAAACCCCTTA | 55626 |
rs572122617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430660 | TGGGGAGAGATGTCA[C/T]TTAGTGCCATCTTAA | 55626 |
rs572142191 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471500 | GGAGAATGGGGTAAA[C/T]CTGGGAGATGGAGGT | 55626 |
rs572142483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429701 | CAACCAAAGTTATTA[C/T]ACTGTGCAAGTTGCC | 55626 |
rs572164214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470240 | TGAGCCAGGAGTTCA[A/G]GACCAGCCTGAGCAA | 55626 |
rs572168188 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565324 | GTTTTCCTTTTTTTT[A/T]AAATTAAAAAAATCA | 55626 |
rs572170869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565955 | TTTTTTTGTATTTTT[C/T]GTAAAGACAGATTGC | 55626 |
rs572193556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579315 | ATACAAAATTAGCCG[G/T]GTGTGGTGGTGCATG | 55626 |
rs572204951 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430215 | TAGAAAAGATGGGAG[A/G]TGAGGCGCAGACAGC | 55626 |
rs572214845 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539106 | TAGGTGCCGGGAGCA[A/G]ACGGAATATAGATTA | 55626 |
rs572235919 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436122 | CACTGTCAGAGGCAT[C/T]GTGGTAATTTTTTAA | 55626 |
rs572252070 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526193 | TCTGGGCAACAAGAG[C/T]GAAACATCGGCTCAA | 55626 |
rs572255412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572476 | TTAATCAATCATAGA[C/T]ACATCCATGAGTAAA | 55626 |
rs572261204 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468744 | GTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 55626 |
rs572270995 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502392 | TTGCACTCCTAATAT[G/T]AGAGTCTGTGGCTCA | 55626 |
rs572313550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548016 | TGATCAAGCTACAAA[C/T]TGAGAGAGATAAACC | 55626 |
rs572314719 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518155 | TTACTCACGGCCAGG[C/T]GCGGTGGCTCACGCC | 55626 |
rs572322157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588071 | GGTGCTGTGGCTCAT[A/G]CATGTAATCACAGAA | 55626 |
rs572323523 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406458 | AAGGTGGGAGGATCA[C/T]TTGATCCCAGGAGTT | 55626 |
rs572346394 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399725 | TCTTCTTTCCCTTTA[A/C]CCCCCAGTCTTCACA | 55626 |
rs572356049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533213 | ATGGAAAAATGTGTT[C/T]TGATTAGCATAGAAA | 55626 |
rs572356738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408347 | TTGAGGCGAGCTGCA[A/G]GAGTGACCCAGCTCA | 55626 |
rs572357226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436483 | GTTTGCTAACTAATA[A/C]AATAATGATATCCAA | 55626 |
rs572383456 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400187 | GGCTGCGAGGGATGG[C/T]TCCACTGAACTGCTG | 55626 |
rs572386099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532565 | CCTCAGCCTCCCAAA[C/T]AGCTGGGACTACAGG | 55626 |
rs572403802 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461050 | GAGCTCGAGACCAGC[C/T]TCAGCAATCTAATGA | 55626 |
rs572407099 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457416 | ATTCACCTTGGAAGG[A/G]GGGAAAAATTTAACG | 55626 |
rs572430048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422716 | AAACTCAGACGAGTA[A/G]TTCAAGCAGCAAACG | 55626 |
rs572432643 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477298 | TTTCATTAGGGAGAG[A/T]CTTTGTCTCTTTAAA | 55626 |
rs572465339 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497576 | TAATAAACACAATAT[A/G]AGATGCTGCCTATGG | 55626 |
rs572493302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469317 | GTTTTTATAACAGAA[C/T]TTTTTATTTCTCTGA | 55626 |
rs572531478 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427341 | CAGCAGCAGCAGCCA[A/T]CATTAGTCTCTGTAA | 55626 |
rs572541382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525674 | AAGAATCATTTGAAT[A/C]CGGGAGGCGGAAGTT | 55626 |
rs572544121 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471136 | TCTCCAGGTTACCAA[C/G]AGTTTAGACGAAATT | 55626 |
rs572605397 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420420 | CTCACTGTCTGAACG[A/G]GCACAGATATGGTAA | 55626 |
rs572657672 | in-del | -/CTC | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507470 | AGCGAAAGAGCGAGA[-/CTC]CGTCTCAAAAAAAAA | 55626 |
rs572703679 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579255 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 55626 |
rs572708580 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587288 | GGGAGGCTGAGGCAC[A/G]AGAATCGCTTGAACC | 55626 |
rs572752617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433272 | CACATATTCTAGGGT[A/G]TGAGGAAAGGCCTTT | 55626 |
rs572768031 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583688 | AAAAAAACAACAAAA[A/C]AACCCCATCAAAAAG | 55626 |
rs572776670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491859 | GTAGGAAACAGGAAA[C/T]TGAAGTAAGGAGGTC | 55626 |
rs572783003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492647 | TGGAATTCTGCTTTA[C/T]TTCCTTCTCTAGAGA | 55626 |
rs572788830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484383 | TTATACTGAGTCATT[A/C]TAGATTAGAGAGAAT | 55626 |
rs572808828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530377 | CCTGCACTGGGAGAA[G/T]GGCTGCCTGCCAAGC | 55626 |
rs572830773 | in-del | -/AAACAAACAAAC | 0.00390528 | 0.0440158 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515474 | TGAGACTGCATCTCA[-/AAACAAACAAAC]AAACAAACAAACAAA | 55626 |
rs572835323 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585039 | CACTCACTGCACTCC[A/T]GCCTGGGCGACTGTG | 55626 |
rs572847897 | in-del | -/T | 0.171704 | 0.237423 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517147 | GGATTACTCAAAAGC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs572853643 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441420 | TCGGGAGGCTGAGGC[A/G]GGAGAATCGCATGAA | 55626 |
rs572860042 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553996 | CAACTCATAGATTAG[A/G]ATCAGAAATCTAGAC | 55626 |
rs572861517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419526 | CTATTATTGCAACCA[A/G]GAACCTGTATCTCAG | 55626 |
rs572867538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558689 | CTGAAAATATGGAAA[C/T]TAATAAATTTAGGTA | 55626 |
rs572868425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522661 | GAATTTATTGAATTC[C/T]ATAATGTTGAATTCT | 55626 |
rs572911651 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405756 | TTTATATTTGAGACA[A/G]GGTCTCACTCTGTCT | 55626 |
rs572920267 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546442 | AGGATCTTGCTTTGA[-/T]GATCATGATCGGAGT | 55626 |
rs572930751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512414 | TGTCCATCTGAATGA[C/T]AACAGCCTCTCTGGC | 55626 |
rs572960547 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553196 | GATCCACCCGCCTCA[C/G]CCTCCCAAAGTGCTG | 55626 |
rs572988720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401929 | GAGGGCTCTCTGGCC[A/C]GACCCTTATCATGCT | 55626 |
rs572992622 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514472 | GAGGAAGAGAGGAAA[C/G]CAATAAAATACATCT | 55626 |
rs573010188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592457 | TGCAGTGACCAAACT[A/G]CTAATCAAATACAAC | 55626 |
rs573013578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402660 | TGAGCCACTGGAGAA[A/G]CACTTACATGTCTAG | 55626 |
rs573024619 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536851 | GATGGCCACATTTCA[C/T]ACTAAGGCCGTCAAT | 55626 |
rs573027962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496096 | GATAGAAAACAGGCC[A/G]GGCACAGTGGCTCAC | 55626 |
rs573033607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551646 | GAGGCCAAGGTGGGC[A/G]GATCACCTGAGGTCA | 55626 |
rs573049397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497081 | GCACCACTGCATTCC[A/C]GCCTGGGTGACAGGG | 55626 |
rs573074891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487060 | CCTAGGAGTTAGAGA[C/G]TAGCCTGGGCAACAT | 55626 |
rs573107070 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502308 | ATGGCTGGCTGATTC[C/G]TAACTGCTTTAAGCA | 55626 |
rs573112498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567315 | GACCTCTGGAGATCC[A/G]CCCACCTCAGCCTCC | 55626 |
rs573134004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593119 | AAACCACATGGTTCC[C/T]TTACTTCTGAAGCCT | 55626 |
rs573137883 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595919 | AGAAAGAAAACTCTC[A/C]TTCTTGGAGAGGCTT | 55626 |
rs573148689 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410232 | AAGCAGGAGGAAGGG[A/T]TGGGCCTCCAGCCAG | 55626 |
rs573155978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519154 | TCAGCCTCCCGAGTA[C/G]CTGGGGCTACAGGCA | 55626 |
rs573180590 | snp | A/G | 0.00019862 | 0.00996345 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397798 | AATGCGGTGGCTGAC[A/G]ATGATGTTGTTGCCG | 55626 |
rs573187393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480422 | GTGAGAAACAAGAAA[C/T]GTCTTATGCCACTAA | 55626 |
rs573218822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520086 | AGAGGTTGCAGTGAC[C/T]CAAGATGGCGCCATT | 55626 |
rs573234743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575399 | AAGGTGGAGGTTGTG[A/G]TGAGCTGAGAGAGCA | 55626 |
rs573240657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464125 | GGTTTGGAAACAATA[C/T]ACAGAATTAGGCAAT | 55626 |
rs573243913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410663 | GCTAAAAAAATAGCA[A/G]CAACAGATACAGGCA | 55626 |
rs573277645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464829 | AGGCAGTCGGATCAC[A/G]AGGTCAAGAGTTTGA | 55626 |
rs573294673 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447845 | CATCTACTCCACTCT[C/T]TGTGTGTATTGCATC | 55626 |
rs573298035 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567697 | TTTTGCACTTCTGAT[A/G]ACAAGATGACCCCAC | 55626 |
rs573307721 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504749 | GAGATAAATCTCAAT[C/G]GTCTTGCTCCACAGC | 55626 |
rs573324062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560509 | AGTGTGATCAAAACC[A/G]GAAATAGAAAGCAAT | 55626 |
rs573329220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479105 | TGGGAGGCTGAGGCC[A/G]GGGAATCACTTGAGC | 55626 |
rs573338094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433166 | AGCATTTCATTGGGT[C/G]CTTTATGCATCTCCA | 55626 |
rs573339580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534953 | TGCTGGGATTACAGG[A/C]ATGAGCCACCACACC | 55626 |
rs573364764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46591086 | TATTTCCTGCAGAAA[C/T]ATAATAAAATATTCC | 55626 |
rs573388564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582877 | AGGTACGAATTGAGA[C/T]GCAGAATCACAATCA | 55626 |
rs573405657 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478658 | TTCTCTTTTTTTTTT[-/A]TTTTTTTTTTTTGGA | 55626 |
rs573428301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535835 | TGCTCTCGAGGAAGG[C/T]GCAGACCCTGAGTCA | 55626 |
rs573440385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528233 | GTTGGAGTGCAGTGG[C/T]ACGATCCCGGCTCGC | 55626 |
rs573443379 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471269 | CAACATGGCAAAACC[C/T]CACCTCTGCTAAAAA | 55626 |
rs573445806 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472660 | TTTGTGTTCACAACA[C/T]ACATTTGAATACTAG | 55626 |
rs573446043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580796 | GGGGTGTTGCTGTTG[C/T]TATTGTTGTTTTGGA | 55626 |
rs573452935 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589745 | CTGCCTCAGTCTCCC[-/A]AGTAACTGGGACTAC | 55626 |
rs573453665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559337 | AAGTAAAGACAAGGC[C/T]TTGCACCATTACCAA | 55626 |
rs573455805 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485185 | TCAGGTGATCCGCCC[A/G]CCTTGGCCTCCCAAC | 55626 |
rs573458454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543563 | AACTGGCCTCAGATT[C/T]AAAATAATCACATGG | 55626 |
rs573464649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431802 | CCATCCTCAAATATC[C/T]AGATAAGAAAATAGA | 55626 |
rs573467032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581523 | AAGGCAGGAGAATGA[C/T]GTGAGCCCGGAGGCA | 55626 |
rs573468988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479692 | ACAGAGCGAGATTCC[A/G]TCACACACACAACCC | 55626 |
rs573475155 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560276 | ACTCAAAATAAGACC[A/G]ACCTCTGTATAGGAT | 55626 |
rs573505033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432473 | CTGGAGAGGAAAGGA[C/T]CACACCAGGCCACCC | 55626 |
rs573518589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551596 | TTAAACGACACCAGG[C/T]GCGATGGCTCACGCC | 55626 |
rs573525629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479838 | GTTATCAGTTTTCTA[C/T]AACTGCCATAACAAC | 55626 |
rs573528405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471774 | CTGGGACTACAGGCA[C/T]GCGTCACCATGCCCA | 55626 |
rs573534883 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523828 | TAAGAAGATGGTTTG[A/C]ACCCACTGACAGTTC | 55626 |
rs573542327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425575 | GGCTGGGCGCGGTAG[A/C]TCACGCCTGTAATCC | 55626 |
rs573547855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536009 | GACTTCCTTGTACAA[C/T]TCTAAGTAATACCGT | 55626 |
rs573554173 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477856 | TGAGACGGGCAGATC[A/G]CTTGAGGTCAGGAGT | 55626 |
rs573557052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439961 | ATCCAAAAATTTGAT[A/G]GTACATTCTATCAGC | 55626 |
rs573557455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592248 | CAGGCTGAATTTTTT[A/T]TTTTCCAAGAATGAA | 55626 |
rs573592069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425788 | AGGTTGCAGTGAGCC[A/G]AGATCGTGCCACTGC | 55626 |
rs573616394 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514629 | GTTGTGTGACACAGT[G/T]TAATTGGCAGGATTT | 55626 |
rs573636436 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591420 | GATTAAGGGCCCTTC[A/G/T]TTTAAATCTTGCTGA | 55626 |
rs573653755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426183 | ACTGAGTAATGGGCT[A/G]TTACAGTGATAGTGG | 55626 |
rs573683782 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527354 | GCATGGTGGCATGCA[A/C]CTGTAATCCCAACTA | 55626 |
rs573690532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418677 | AACAGGATGACTCTT[A/C]ACTCATGCCTGAGAA | 55626 |
rs573703626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575680 | CGCCACCACGCCCAA[C/T]TAATTTTTGTATTTT | 55626 |
rs573743283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416906 | CTGGCTGACTCCCAG[C/T]GTCTCTAATGAATGG | 55626 |
rs573763715 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429667 | TTTGTATTTTTGTTA[C/T]TATGCTTTCACTTGG | 55626 |
rs573764020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456854 | TAAACACTGGGAGAT[A/G]GCAGAAATGAAGATA | 55626 |
rs573779400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409118 | TTTAGCTTTACCTTC[C/T]TTCCAACTGTATGCT | 55626 |
rs573798823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447778 | GATAGATAGATAGAT[A/G]GTGATGGCAAATACT | 55626 |
rs573816148 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409963 | CTGGGCCATGGAGCA[C/G]ACTTCATGGGGCGGC | 55626 |
rs573847093 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590657 | GTCACATTCTGAACC[C/T]GTCCAGTTTTTAAAG | 55626 |
rs573862100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487455 | CACACCAGGCAACAA[A/G]CAGAAGGATGCCTGA | 55626 |
rs573881779 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546331 | AGGCGTGAGCCACCG[C/T]GCCCAGCCCACAGTT | 55626 |
rs573882843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543817 | GTCAAGATTATGGCT[A/G]TAACCCTGAATATAC | 55626 |
rs573899736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534350 | ATACAGAAAAGTTAG[C/T]CAGGCGTGGTGGCAG | 55626 |
rs573967528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526414 | AATTCTGGGCCTACC[A/G]TTTTAAGAGAACTGG | 55626 |
rs573979165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495173 | GAATAATAAGCCAAA[A/G]GGCACTGGCTGGACA | 55626 |
rs573992163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495831 | TAGCTTTTCATTATC[A/G]TATATTTCACTTATC | 55626 |
rs573998374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519081 | CAGGCTGGAGTACAG[C/T]GGCGCGATCTTGGCT | 55626 |
rs574001855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416000 | CACAACAAACTGGGT[A/G]TAGATTATTTTTGCA | 55626 |
rs574027287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566587 | TGAAAGATTACAGAC[A/G]GGACCCGGGGGGTGA | 55626 |
rs574034642 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585171 | GCTCGTTAAGAGTCA[A/T]CACCACTCCCTAATC | 55626 |
rs574054795 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411172 | ACAGTGCAGGCTCTC[A/G]CCCCTGGGGCGGCCT | 55626 |
rs574067999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401177 | CAGCATGGTCTGGGG[C/T]GTGCTGTGGCTGGCC | 55626 |
rs574077742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523899 | TTGAGATAGAGTTTC[A/G]CTCTTGTTGCCCAGG | 55626 |
rs574089709 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463241 | TAAAATTCAGCCCAC[C/T]AGGGGCCAACTCAAA | 55626 |
rs574101371 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512337 | TGACAGCAAATTGGG[C/T]TTTTTGTTTAATCTA | 55626 |
rs574104151 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566622 | TGAGCTACCTAACCC[C/G]TGAAGGCATTCTCCC | 55626 |
rs574115678 | snp | A/G | | | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430448 | CCCATTCTTATTCTG[A/G]TTTTAGGTCTGAAAT | 55626 |
rs574117022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567160 | TACTGCAGCCTCCGC[C/T]TTCCGGATTCAAGCT | 55626 |
rs574118260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485373 | TGAACGGGGACACAT[C/T]TGCAGAGCTTCTTCA | 55626 |
rs574125393 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508904 | AACAAGTATACACAG[C/T]TCCAGATTTGTCCTA | 55626 |
rs574141617 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515836 | ATGCGCCACCACACC[C/T]GGCTAATTTTTGTAC | 55626 |
rs574153846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516588 | GGCACCTGCCACCAT[G/T]CCTGGCTAATTTCTT | 55626 |
rs574179980 | snp | G/T | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542681 | GCACAGACAGCAAAC[G/T]CACCGAAGAGGCACT | 55626 |
rs574180964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405382 | CTTCACCGCTTTTAC[C/G]AAGTGGCTGACACAT | 55626 |
rs574183730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430518 | AAGTTGTCCAAGAAC[C/T]ACAGTTTGAGAAGCA | 55626 |
rs574205072 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503108 | TTTTTGCTTTGTGTT[C/T]ACAACTTGGCTGTTT | 55626 |
rs574216036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406364 | CAGCTGAGACTCTAT[C/G]TTTAAATTAAAAAAA | 55626 |
rs574221261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424187 | GGAACAAATCCCTAG[A/G]TTGCACATATCCAAA | 55626 |
rs574230241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463869 | AAAAATTCCTGCTCT[A/G]GCCTGTGGAAGATCC | 55626 |
rs574231653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478597 | TTCATTTCTCTGAAT[A/G]ACCCAAATAATTACC | 55626 |
rs574275781 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530501 | GAACCTTGCTTCAGG[A/C]CAGATAGTACAAGAA | 55626 |
rs574318810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479031 | CAGTGAAACCCTGTC[A/T]CTACAAAAAATACCA | 55626 |
rs574335300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570223 | GCAGAGATCGCACCA[C/T]TGAACTCCAGCCTGG | 55626 |
rs574360013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523042 | CCAGAGGCAAGGAGG[C/T]CAATTTCCCAGCTCA | 55626 |
rs574387935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580637 | TCTAAAATATCTACT[C/G]AATCTTTCTACTTCT | 55626 |
rs574397203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563650 | TTTGAGACCAGCCTG[A/G]CCAATGTAGTGAAAC | 55626 |
rs574404263 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412801 | CTACCTTACATTATG[C/T]AAGAGGTAAATGGCC | 55626 |
rs574430068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507881 | GAAGCTTTCCACGGT[A/C]ACTGGACATGCAAAA | 55626 |
rs574430170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470370 | GAGACGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 55626 |
rs574437780 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569306 | CCTTATAAACTCATA[C/G]TTCATACAAACATGT | 55626 |
rs574442767 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467673 | CCTGCCTCAGCATCC[C/T]GAGTAGCACACCACC | 55626 |
rs574467712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508506 | ATTAAAGGGCATTTA[A/C]CTCAACTCACCAGGA | 55626 |
rs574490972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460042 | AAAAATCTGTGCTAT[A/G]TAACTGAAGATGAGC | 55626 |
rs574518304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450895 | AATGATGTGTCTACG[C/T]TGGTTCATCAGCTGC | 55626 |
rs574522816 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594943 | AGATAGTCCCAGTTT[A/G]TCGGGCGCAGCGGCT | 55626 |
rs574551259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539124 | GGAATATAGATTAAA[A/G]AAAGCCAGCCAAGCA | 55626 |
rs574555667 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513269 | CTACGCTCTTTTTTC[-/T]TTTTTTTTTTTTTGT | 55626 |
rs574565975 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494565 | GTCTTGGGGGGTTGT[C/T]TTACATTATTTATCA | 55626 |
rs574579735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530611 | TCCAAACTAGAGAGA[A/G]AGCAAGTGCAGGAGT | 55626 |
rs574586600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489463 | TTTCTTTTTTATATT[C/T]AAAAAGAAGAAGAAG | 55626 |
rs574591030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497996 | ACTTAAAATAATGAT[A/G]TACTTAGAAAACTAC | 55626 |
rs574600816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490308 | TGGGTTGATGACCAA[C/T]TGGAGGCTACCAGAA | 55626 |
rs574612730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531243 | AACAGCAAAGTTGAG[C/T]AATTGCAACAGAGAC | 55626 |
rs574628309 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460603 | GCTGGCATTACAGGC[C/G]TGAGCCACCGCGTCC | 55626 |
rs574647249 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420743 | TGAGGGTTAACCTCA[A/C]TGGGTGCATGAGGGG | 55626 |
rs574655466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421583 | ACATGCCTGAAACCA[A/G]TGGACACTTGAACAA | 55626 |
rs574656226 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576119 | TAGATTACACAGCTA[A/C]GAAAAGAGTCATTTA | 55626 |
rs574660463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464888 | CGTCTCTACTAAAAA[G/T]ACAAAAATTAGCCAG | 55626 |
rs574687826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475469 | GTTTGCTGTATTCTT[A/T]GATTGAGTCTATTTC | 55626 |
rs574690943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449492 | CAAGGTCTATAGGAG[C/G]AAAGCTACAAAACTG | 55626 |
rs574695925 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562481 | AGCAATATAAGAGAT[G/T]AATAGTCATACTCAG | 55626 |
rs574711263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465388 | CTTCATCTTTTGTCC[C/T]TACCATATTGGAATA | 55626 |
rs574723384 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411352 | CATGGGTGTTGGCTA[C/G]GACAGAGACCAGGCA | 55626 |
rs574757038 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545418 | AGTGAGACAAGACTG[C/T]GCCACTGCACTCCAC | 55626 |
rs574758112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428679 | GCTGACCACGTCCAC[A/G]ACCAAATCCGCCTCT | 55626 |
rs574759477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449484 | AATATGTACAAGGTC[A/T]ATAGGAGGAAAGCTA | 55626 |
rs574763037 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522623 | TAAGAGGCAGTGTAT[A/C]CTAATTCACTGATTT | 55626 |
rs574769962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577011 | AGCCCAGCCAACAAC[C/T]CTGAAATCACATACT | 55626 |
rs574770316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586103 | GCCACTGCACCCAGC[C/T]GAAAATAATAATGAT | 55626 |
rs574828783 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396946 | TCCCTGTTGGTTTCA[C/G]TGGGGTAAGACGACG | 55626 |
rs574830600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466584 | CAGTGGGAAGCAAAG[C/G]CTTATATAAATAATA | 55626 |
rs574834795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577678 | AAATTCAGCCAGGCG[C/T]GGTGGCTCATGCCTA | 55626 |
rs574838683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553477 | TTTGGCCAGGTGCAG[G/T]GGCTCACACCTGTAA | 55626 |
rs574880694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530530 | AAACAAATTCTTTAT[G/T]CATTTATGCCTGCTC | 55626 |
rs574896359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567806 | TGCAACCCCAAACCA[A/G]TCAGCAGCACCCATT | 55626 |
rs574903934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554152 | TAAAAAAGTTCAGAA[A/G]AAACATCTTGAGAGT | 55626 |
rs574908135 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441835 | TGGAAAATGGCAGCT[G/T]AGTTTAAATAGTCAG | 55626 |
rs574916035 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594097 | AGCAATCGTTCAAGG[A/G]ACCACAGCCGAGCGC | 55626 |
rs574923431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420655 | ATTGTGGCTGGGATC[A/G]CTTAATCTGTTTAGT | 55626 |
rs574927218 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403531 | CCCTGAATGCCCACT[A/G]CAAGCTAGGGAGGCA | 55626 |
rs574939353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457663 | CCCAGCACTTTGGAA[G/T]GCCAAGGCAGGCAGA | 55626 |
rs574962724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412637 | TCCCCAAAATGTTTT[C/T]GATTTATGGTTTGTT | 55626 |
rs574974420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489227 | CCCCGCTCTCCCCAC[C/T]CCACAACAGGCCCCG | 55626 |
rs574978403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419339 | GTCAGTGGAAGAATA[A/G]AAGACATGGGCTTTA | 55626 |
rs575014178 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546012 | CTACAAGCATTAAGC[A/G]TATATACACAGTTCC | 55626 |
rs575039840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562744 | AAAATATGAATTCAA[A/G]AGAAACTTAAATTTT | 55626 |
rs575053969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568273 | GACCAGCCTGGCCAA[C/T]GTGGTGAAACCCCGT | 55626 |
rs575064439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529663 | GACGAAAGGGGCTGC[A/T]GTCCTACTCAATTCC | 55626 |
rs575079013 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470405 | CAATCCTGGCTAACA[C/T]GGTGAAACCCTATCT | 55626 |
rs575099961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505981 | TCCCAGGGCTCCACA[A/G]CATTAGTGAGAGAAA | 55626 |
rs575114414 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465725 | AAGGAGGTAGAAAGG[A/G]AAAAGGTTCATCCAT | 55626 |
rs575116363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561578 | GAATTCAGGCTTTTC[C/G]TTCAGATAGTACCAG | 55626 |
rs575121987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428088 | TAGGGTGAGGGGGAG[C/G]CATATTGCTAGCGCT | 55626 |
rs575122087 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458220 | CAAACATTAACACCA[C/G]GAACACAGTGGAAAA | 55626 |
rs575144623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576874 | TTGCTCTGAAGATGA[C/T]AGGAAGTTAAAACCA | 55626 |
rs575164229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402795 | CACAAAGTAAGTGCT[C/T]AAAAAAGAATGAATG | 55626 |
rs575220445 | in-del | -/GA | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445014 | GCATTCTCAACATGG[-/GA]GAAATATCATCCCCA | 55626 |
rs575227435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403704 | GCAAAAAAGCTGACG[C/T]GTGCAAATACCCCTG | 55626 |
rs575251633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515123 | GTGTTATCCTCCAAG[C/T]GGTCGTTTAGTAAGC | 55626 |
rs575256997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515696 | TTTTTTATTTTTTGA[C/G]ACGCAGTCTCACTCT | 55626 |
rs575261709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504927 | AAAGATGGGCTCTGA[A/G]TAATGGCTCCCTTGG | 55626 |
rs575281672 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530125 | TAGATACAGTAGAGA[A/C]GGGGATCTGAAGGGG | 55626 |
rs575334575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497144 | AAAATAAAATAAAAT[A/T]AAAAAATAAAGGGAA | 55626 |
rs575343927 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557616 | TTCAAGATCAGCCTG[C/G]TCAACATAGTGAGAC | 55626 |
rs575345367 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459225 | CTATACAGATGTATA[A/G]ATATACGTATGTTTT | 55626 |
rs575347260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545894 | GGGACTACTTTAAAT[A/T]CATCCTCTGTAAAAA | 55626 |
rs575362308 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527789 | GACCACTATAAAAAG[-/A]AAAAAAAAAACAGGA | 55626 |
rs575364974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489379 | TCAATCTCCTGACCT[C/G]ATGATCCACCTGCCT | 55626 |
rs575385512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545329 | GAGCCGGGCATGGTG[A/G]TGGGTGCCTGCAATC | 55626 |
rs575386555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480301 | CAGATCATTATTTTA[C/T]CTACTAAACCATCTA | 55626 |
rs575401402 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440621 | ACTTTAAATAAATTA[C/T]GGAACAGAAAGCTAG | 55626 |
rs575422325 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490777 | TTGGAGCTACAGGAA[A/G]GCAGGGATCATAGTC | 55626 |
rs575422572 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482388 | TGTTACCAGTCCAAC[A/G]GAAACCGTAAAAGAC | 55626 |
rs575425424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506950 | GCAGGCGGATCACAA[A/G]GTCAAGAGATGGAGA | 55626 |
rs575429847 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490170 | TCAGCAGGGGGAGCT[C/T]CTCAGACTTTTGTAT | 55626 |
rs575430248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434031 | GAGGCAGGAGAATCG[C/T]TTGAACCCGGGAGGT | 55626 |
rs575437795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467573 | TTTTTTTTTGGGATG[A/G]AGTCTCACTCTGTTG | 55626 |
rs575467046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427498 | ATCGCCCTACAGCCC[A/G]TGGTTCGTTCTTAAC | 55626 |
rs575487851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482148 | CTGGCTCCCTATGAA[C/T]TTTAGGATTGTTTTT | 55626 |
rs575498327 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495941 | GGGGAAAGGGTGGAG[A/G]CCTCTAAGCCTCAAA | 55626 |
rs575501615 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503213 | GACATAAAGTGAGAG[A/G]TGTGCAACTCTTCCT | 55626 |
rs575506243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441716 | TTCTATTCTTTTCTG[A/C]CCTCCTCCACTGAAA | 55626 |
rs575532602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593330 | CACGTCCCAGACATC[A/G]GCCTCAGTTTACCCA | 55626 |
rs575547996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513245 | TCCTGTCTATCCATT[C/G]TGCTCTGCCTACGCT | 55626 |
rs575563839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556464 | CTGAATTGTGTATCT[A/G]TTGTGTGCAAAAGAT | 55626 |
rs575563870 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552309 | AGGAGGCTGAGGCTG[C/T]AGTGAGCCAAGATGG | 55626 |
rs575571164 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551367 | ACCCAGGCTGGAGTG[C/T]GATGGTGCAATCATG | 55626 |
rs575574190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458087 | GTTTCACAGCATAAA[C/T]TGCTCTGAAACTTGA | 55626 |
rs575577855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514069 | GGAACGCATATTGTT[C/T]CTCTCCAGCAGCATC | 55626 |
rs575581306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457618 | CTTATAAGATGGGCT[A/G]GGCCAGGCGCAGTGG | 55626 |
rs575589960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481478 | AAGTGATTCTCCTGC[C/T]TCAGCCTCCTGAGTA | 55626 |
rs575600296 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584238 | GGGACATGGATGAAA[C/T]TGGAAATCATCATTC | 55626 |
rs575609938 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515391 | GGCACGAGAATCACT[C/T]GAACCTGGGAGGCAG | 55626 |
rs575614214 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585167 | GCATGCTCGTTAAGA[C/G]TCATCACCACTCCCT | 55626 |
rs575633220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403636 | GCAGGGTAGGAAAGC[G/T]TGCTGTAGAGTCAAA | 55626 |
rs575663615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560907 | AACAGACCTAATGAC[G/T]TTGGCAACAATATAC | 55626 |
rs575668521 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402853 | GCTCCCCCAGGGCTC[A/G]GTGTGGACAGCTTCA | 55626 |
rs575694260 | snp | A/C | 0.00716266 | 0.059414 | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46594004 | GCGCCGCCGCCGCTC[A/C]GGAGACATCAAGCAA | 55626 |
rs575715112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575099 | ACAAACCTAATAAAT[C/G]CTTCATTAAAAGTAC | 55626 |
rs575722218 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501996 | ACAGCTCTTTTCTAA[C/G]CCATTTTGTAAAGAC | 55626 |
rs575725192 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528257 | GGCTCGCTGCAACCT[C/T]CACCTCCAGGTTCAA | 55626 |
rs575729029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492800 | CACGCCTGTAATCCC[A/G]GCACTTCGGGAGGCT | 55626 |
rs575730540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448585 | ATTAAACCCAAAGTA[A/G]GCAGAAGAAAAACAT | 55626 |
rs575735123 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493472 | GTAAGGAACTGAATA[A/T]CAAACCAGGACCCCA | 55626 |
rs575768768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449209 | TCAGAAACCACCCCC[C/G]ACCGCAAAACAAAGT | 55626 |
rs575786636 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477135 | CTGCTTAAATACTGA[A/G]ACCCACAACAGATAA | 55626 |
rs575786705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468615 | CATCCTAGCTAACAC[C/T]GTGAAACCCCGTCTC | 55626 |
rs575799883 | snp | C/T | | | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518286 | AATGCAAAAATTAGC[C/T]GGGCGTGGTGGTGGG | 55626 |
rs575800579 | in-del | -/A | 0.431473 | 0.171952 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595886 | GCTACTCGGGACTAC[-/A]AAAAAAAAAAAAAAG | 55626 |
rs575823167 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463398 | AAATATATAGATGCT[C/G]TGCTGTAGAAGGTAT | 55626 |
rs575848015 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469282 | CTCCTAATCTTCCCT[C/T]CCTCCAAAATGAAAT | 55626 |
rs575858296 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467694 | GCACACCACCATACC[C/T]GGCTAATTTTTGTAG | 55626 |
rs575860278 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426273 | AAGTAACACACACTT[A/G]GGAAGCAAACGTTGC | 55626 |
rs575875923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575585 | ACAATGGTATGATCT[C/T]GGCTCACTGCAACCT | 55626 |
rs575895639 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529196 | AGATTTTACATAGTC[C/G]ATTTACATAGTCCAA | 55626 |
rs575897955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410730 | ACTAAGATGGCAAAT[G/T]TGAGGCTGGAGTGAG | 55626 |
rs575898502 | snp | A/G | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594966 | CAGCGGCTCACGTCC[A/G]TAATTCCAGCACTTT | 55626 |
rs575929380 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479310 | AATGGCCCCAAATGA[C/T]TTAGGCCCTTCTGTA | 55626 |
rs575938816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426098 | AAAAGAAAGAAAACA[C/T]TGTGGAAATGAGTAA | 55626 |
rs575940761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417752 | GGAGCTAATCCTACC[A/G]GCCCCTGTGGGAAGA | 55626 |
rs575942253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464857 | TGAGACCATCCTGGC[C/T]AACAGGGTGAAACCC | 55626 |
rs575957469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528914 | CTACCTCTGTGTAGG[A/G]GAGGAAAAAAGCAGA | 55626 |
rs575970733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499478 | TAAGCAATATTACAC[A/G]TTTTTAAGCAATAAA | 55626 |
rs575976030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418476 | TACATATGTATACAC[A/G]TGCCACGTTGGTGTG | 55626 |
rs576006632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548922 | CTTGAACCCAGGACG[C/T]AGAAGTTGCAGAGAG | 55626 |
rs576026019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444467 | TTCCTCCTCCTCCTT[C/T]TGAGGTGCATTTCAT | 55626 |
rs576048332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567731 | AACCAGCGATTCCTC[C/T]GTAGCCCCTAGCCAG | 55626 |
rs576050923 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46596041 | CGCCCAGGCTGGAGT[A/G]CAGTGGAGCGATCTT | 55626 |
rs576062647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565851 | AATCTTTGCTCACTG[C/T]ACCCTCCACCTCCCA | 55626 |
rs576063241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436387 | TTAGAATACATTGAT[C/T]AGGCTATTGTGCCAA | 55626 |
rs576070039 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400176 | CAAGGCTCTGAGGCT[G/T]CGAGGGATGGCTCCA | 55626 |
rs576082845 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576871 | GACTTGCTCTGAAGA[C/T]GATAGGAAGTTAAAA | 55626 |
rs576119737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557843 | CCGGCATGGTGATGC[A/T]TGCCTGTACTAACAG | 55626 |
rs576130995 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587925 | GGGAATATTTCTGAC[A/C]TCAGAAAAAAACACG | 55626 |
rs576166956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446026 | CAAATCCCGGCTCCA[A/G]AGGCATCCTGTACTG | 55626 |
rs576183619 | in-del | -/A | 0.36955 | 0.219562 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466346 | AGCAAGACTCTGTCT[-/A]AAAAAAAAAAAAAGG | 55626 |
rs576194020 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467002 | GGCTCACTGAAACCT[G/T]CACCTCCCGGATCCA | 55626 |
rs576194218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460815 | TGGGAGGCCAGGCAC[A/G]GTGGCTCACATCTGT | 55626 |
rs576215733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450477 | GAGGGTCTCACTCCA[C/T]TGCCCAGGCTGGAGT | 55626 |
rs576218494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517444 | GTAAGCCACCGCGCC[C/T]GGCTAGAAAGCATTT | 55626 |
rs576236782 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517000 | TTCCTTGTTTTCTCT[A/G]CTTGCCTGGTTCATT | 55626 |
rs576243677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555326 | CTTGTGCAATCTGAT[C/T]ATCTTATGCCAGGAA | 55626 |
rs576253780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573675 | TTTCTTTTTTTTTTT[C/T]TTTATTATACTTTAA | 55626 |
rs576280039 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533152 | TGGGCTACAAAGCGA[C/G]ACTCTGTCTCAAAAG | 55626 |
rs576290530 | snp | A/G/T | 6.88295e-05 | 0.00586606 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46443588 | AGACTGTCCATCACC[A/G/T]ATCACTGCCCCTTAT | 55626 |
rs576348789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414290 | TGGCTCTTAGAGCCT[C/T]GCCTGAAAGATGTGG | 55626 |
rs576354765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525543 | ATCACTTGAGGTCAG[G/T]AGTTCGAGACCAGCC | 55626 |
rs576360191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539960 | CCTCAGCTTCCCAAG[C/T]AGATGGGACTACAGG | 55626 |
rs576364146 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595180 | GAGGTGGAGGCTGCG[A/G]TGAGCCATGATCACA | 55626 |
rs576375728 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476022 | GGTCACTCTTCCATA[C/T]AGGGGAGACACTAAT | 55626 |
rs576387470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406842 | AAGCTGAGATTGCAC[C/T]ACTGCACTCCAGCCT | 55626 |
rs576387525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415121 | TTGGGAATGGGTGTG[C/G]CAGGGAGCTGTATCA | 55626 |
rs576416090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428808 | CTCTTGTGAGTCTCG[C/T]AGGTCGCTCACCCTC | 55626 |
rs576424374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407453 | GAAACCTGCAAAAAA[A/G]GGCCTGAAGATGGCA | 55626 |
rs576431222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429136 | GGCAATCCGGTTCTT[C/T]TTAGGCATCAACATC | 55626 |
rs576433839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530196 | AGCACACATACAGAC[A/G]TCACTGTAGTCCCCA | 55626 |
rs576442715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565261 | AAAATTCCCTCTAAA[A/C]AAAAAACGAAAAGGA | 55626 |
rs576457871 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408146 | ACACTGGTAGGGGGA[C/T]GACAAGCTAGGCTGT | 55626 |
rs576461105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508704 | GGTGCTCTTTACACA[C/G]AGCTGTGCTCATTCA | 55626 |
rs576468467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422674 | AACAAGATGGTCGTA[C/T]TTTTTTTCCCCTACT | 55626 |
rs576470945 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426272 | AAGTAACACACACTT[-/A]AGGAAGCAAACGTTG | 55626 |
rs576492478 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493966 | CTTTTGAATGTGGCT[A/C]ACCATCATCCGTCAA | 55626 |
rs576516711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399025 | GTGATCCACCCTCCT[C/T]GGCCTCCCAAAGTGC | 55626 |
rs576530811 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456179 | ACTGAAAGATTACTA[-/G]GAACAGTATTCCAAA | 55626 |
rs576540239 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427441 | GAGCAAGAACAAAAG[C/T]GGAAAGGATCAAGAT | 55626 |
rs576545619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459975 | TCAGAATAATACCCT[C/G]AGATGCCTTTCACAT | 55626 |
rs576557794 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490013 | TACAGAATGGAAATG[C/G]TACCACCTACCTCAC | 55626 |
rs576600789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484139 | GCACAAGGGGCCCAA[A/G]GTAGGGGATATCTAA | 55626 |
rs576621240 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397067 | GCTGCCTCGCGGGCC[C/T]CTGTCCAGGATGATT | 55626 |
rs576645378 | snp | A/G | 3.31912e-05 | 0.00407363 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397828 | GAAGCCGCCCATGGA[A/G]GCCATGGTGGTGCTC | 55626 |
rs576656576 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501368 | GGTGTGTGCATGAGT[A/G]CACCCTGTGACGGAA | 55626 |
rs576712194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476250 | TCTCTGTTAGTTCCA[A/T]CCAGTGGCAGCTCAA | 55626 |
rs576737668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507758 | AAAATCCGCCTCTTA[C/G]GGAAATCCAAGTATT | 55626 |
rs576742884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516696 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 55626 |
rs576742997 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569742 | GGCCAACATGGCTAG[G/T]CATGTTGAGAAATGA | 55626 |
rs576789229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572961 | CCGGGTGTGGTGGTG[G/T]ACGCCTGTAATCCCA | 55626 |
rs576791819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490413 | CTTTATTTTTTAATA[A/T]TTTAAAAATTCTTTT | 55626 |
rs576803132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406667 | GGGCATATCACTTGA[A/G]GTCAGGAGTTCAAGA | 55626 |
rs576803833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450711 | GCCTCCCAAAGTGTT[C/G]GGATTATAGGCATGA | 55626 |
rs576810599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500176 | TGGGGCCAGCAGGCA[C/T]TGACAAGTGATCTCA | 55626 |
rs576814235 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422322 | GAAATAGAATCAATA[C/T]GCTAGAAAGAAGAAA | 55626 |
rs576864378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500382 | TTAGAAAACATCAAG[C/T]CCTCAGACAATCAAT | 55626 |
rs576900277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556939 | GTCAGGAGTTCAAGA[C/T]CAGCCTGACCAACAT | 55626 |
rs576934758 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565206 | AAGGTTGCAATGAGC[C/T]GAGATTATGCCATTG | 55626 |
rs576963803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483577 | AAAGGAAACGAGAAA[A/G]AAAAGCTGATGTGAG | 55626 |
rs576967961 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46596026 | GGACTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 55626 |
rs576988540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458324 | TTTCAGTCTTGAAGC[C/T]TGTTTAAAACCCCAC | 55626 |
rs576993454 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461370 | AATGCATGTCATATA[C/T]ATGCCTGTATAGATA | 55626 |
rs577008489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523989 | TTCTCCTGCCTCAGC[A/G]TCCCACGTAGCTGGG | 55626 |
rs577010136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532308 | GAGAACAAATGTACA[C/T]TAACACCTCAAGGTG | 55626 |
rs577018056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524750 | TATCTGCAGGGAATA[C/T]GATGCCCTCTGTCCA | 55626 |
rs577020878 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533298 | GCTTTAAGAGGATAT[A/C]CACTTTCTACAATTG | 55626 |
rs577025052 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459104 | CTACACCATGGAACA[A/C]CACGCAGCCACTACT | 55626 |
rs577032747 | snp | G/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413593 | CCTCCCAGATTCGAG[G/T]GATTTTCCTGCCTCA | 55626 |
rs577050686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452895 | CAAATATATATGTGT[A/G]TCTGTCTGTTTAAAA | 55626 |
rs577055183 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467850 | TTAGAAGAGATCTGG[A/G]AGAGAGTGGAGATAA | 55626 |
rs577064255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414284 | AGCACCTGGCTCTTA[C/G]AGCCTCGCCTGAAAG | 55626 |
rs577095781 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539871 | GAGTCTTGCTCCATC[A/C]CCCAGGCTGGAGTGC | 55626 |
rs577105848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428790 | TATCTCTGTCAGCTT[C/T]CCCTCTTGTGAGTCT | 55626 |
rs577113997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468570 | TTGGGAGGCTGAGGT[A/G]GGTGCATCACAAGGT | 55626 |
rs577136518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429036 | GAAGGTTGGGCACAT[G/T]CTTGTCTGCCAGCTC | 55626 |
rs577157272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450308 | ATGAAAGAAGTCAAA[A/G]GCTACATACTATAGG | 55626 |
rs577168335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555282 | TATGCCACAACCCAG[C/T]GGGAATTAGAAGTTA | 55626 |
rs577172027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422580 | AGACAGGAAAAGAAT[A/G]AGAGGGAGCCAGGAG | 55626 |
rs577195724 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447717 | CATCTTGTAGATAGA[C/T]AGATAGATAGATAGA | 55626 |
rs577218315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435795 | GGTGGCAAGATCTGA[A/G]GGTGGAGGAATGTCT | 55626 |
rs577243693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491260 | CTTTAAAACAACTAC[A/G]AGGAGGCGGATCGGG | 55626 |
rs577271663 | snp | A/G | 9.92835e-05 | 0.00704499 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397747 | TGAGGAGGTGTGGGC[A/G]GCACCAGGTTCAGTG | 55626 |
rs577274566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586183 | AGATCGAGGTGGGCA[C/G]ATCACTTGAAGCCAG | 55626 |
rs577277199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | AMBRA1 | GRCh38.p7 | 11:46591164 | ATTCATTAGGAGCCA[A/G]TGAGATAGTCCTTAT | 55626 |
rs577301963 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486860 | ACAGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC | 55626 |
rs577308512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546113 | CAATCTCAGCACACT[A/G]CAACCTCTGCCTCCT | 55626 |
rs577320783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547003 | TTGAACCTGGGAGAC[A/G]GAGGTTGCAGCGAGC | 55626 |
rs577339177 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489539 | GCTCAAGACACTGGA[C/T]CAGGCCGTAATGACC | 55626 |
rs577358351 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479807 | CCAAATGCCAGATAC[A/C]TGTGTGAAACTATCT | 55626 |
rs577363846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592059 | CAAGTGATTCTCCTG[A/C]CTCAGCCTCCCAAGT | 55626 |
rs577364741 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455759 | TTGAACGCACCAGTG[C/T]CATCCAGAGTTCAGC | 55626 |
rs577367614 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523858 | CCTTGTGAGATGTCA[C/T]AGTTTTATTCATTTA | 55626 |
rs577372034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566512 | CAATCCAAATGGTTA[C/T]ATTCTATATAATTCC | 55626 |
rs577377896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575256 | TGAGGTCAGGAGTTC[A/G]AGATCGGCCTGACCA | 55626 |
rs577384679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539195 | CAGTTATACTTTTCT[A/C]TTCGTTTTTATATAT | 55626 |
rs577401879 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584724 | GGCAGTCCTCCTGCC[C/T]CAGCCTCGCAAGCAG | 55626 |
rs577401952 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417844 | CTAAAAGACCCCAGT[A/T]GGTGAATACTGATTA | 55626 |
rs577404188 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412614 | TGTTAATTTTCACTG[G/T]TTTTTTTTCCCCAAA | 55626 |
rs577432398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453033 | CAACCACCATCATTA[C/T]TGTCTAATTTCAGGC | 55626 |
rs577470275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498136 | TGAATTGGAAGATAT[C/T]TGCCAGATGAAAAGT | 55626 |
rs577471189 | in-del | -/TTTCA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414194 | TGGATAACATTCTTC[-/TTTCA]TTTATCAGTGACACG | 55626 |
rs577476360 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522241 | GGTAGTTATTTTTAA[C/T]ACATTTGTAAGATGA | 55626 |
rs577499363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563363 | CCCAGAAGCTGGGAC[C/T]ACAGGTGTATATAAC | 55626 |
rs577543935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439119 | CTATAAAAAAAAATT[A/T]AAAAATCAGCCAGAT | 55626 |
rs577544758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515039 | GGAGCAGCTGACTAT[C/T]CTAGAATACCTAGAA | 55626 |
rs577550392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559211 | AGACTGAGGTGGGAG[A/C]ATTGCTTGAACTCGG | 55626 |
rs577554772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447048 | GAACCTCAGTTTCCT[C/T]ATCTGTAGAAAAGGG | 55626 |
rs577561435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403899 | GCAGAGCAGGCTTCC[C/T]ACATTAATAAATCTG | 55626 |
rs577599071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404560 | TTTCTGAAAGGGGTA[C/T]GGTGTGTGGAACAGC | 55626 |
rs577607936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423430 | GGAGTCTCGCTCTGT[C/T]ACCCAGGCTGGAGTG | 55626 |
rs577615682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507568 | TCCCATGGCTCTCCC[C/G]GCTGACCACTCAAAA | 55626 |
rs577618671 | snp | C/T | 1.72794e-05 | 0.00293928 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545825 | TACAAGCTACCAGCA[C/T]ACTGGGAAGTCAATT | 55626 |
rs577621186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432640 | AGCTTACACTGAACC[G/T]AATTGGGTGGATTAA | 55626 |
rs577637689 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397017 | GTGTCTGGGTTCCTG[C/G]TGGCTCTGCCCACCC | 55626 |
rs577641759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487328 | AGTTAACAATAATAA[A/C]AAGTAAATTGTTGTT | 55626 |
rs577657665 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528311 | TGAGTAGCTGGGTTA[C/T]AGGTGCCCACCACCG | 55626 |
rs577671556 | in-del | -/T | 0.16846 | 0.236329 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467550 | TACTCTATGTTACTC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs577705311 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469065 | GGAGAATCACTTGAA[C/G]CTGGGAGGCGGAGGT | 55626 |
rs577714215 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554213 | CTTTCAAAGAAATAC[A/C]CTTAAACCATTTATA | 55626 |
rs577720989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416840 | CCTGATCGGCAGTGA[C/G]GCAGAGCTTCACACT | 55626 |
rs577722401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543686 | AAGCAGTGAGGGGAA[A/G]CAAAATGTCAACCAG | 55626 |
rs577755520 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463103 | TCACTAACCTGATTA[C/T]GATCTCCTCTTCAGA | 55626 |
rs577757969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573701 | TTTAAGTTTTAGGGT[A/G]CATGTGCATATTGTG | 55626 |
rs577767664 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507262 | AGGCGGGCAGATCAC[A/G]AGGTCAGGAGATCAA | 55626 |
rs577807156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400362 | CCTGCCTCATTAGAG[C/T]TGGATTTCCAGGCCA | 55626 |
rs577825975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540856 | GGTAAAGACCATGTA[C/T]TATACTTCTTTTGTA | 55626 |
rs577864346 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440348 | ACATACAGCATGCTA[C/T]CATTTGGGTTAAATA | 55626 |
rs577870605 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545487 | TAGGAGGAGCTATGA[A/G]GATGACAACTTGCCC | 55626 |
rs577889794 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541651 | AGGCAGAGAAAGTCA[A/G]TGGTTCCATCTCCTC | 55626 |
rs577889876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533416 | ATCTCTTGTTTACTA[C/T]TAATTTTTCAAGCTC | 55626 |
rs577894909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550576 | TTTAATGGGGGGAGA[C/T]GCTGAAAATATTCAT | 55626 |
rs577919890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464199 | CACTAGATGTTTTCA[C/T]GCATTCAAAAATTTC | 55626 |
rs577970192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470316 | CAGGTTGGCCGGGCG[C/T]GGTGGCTCACGCCTA | 55626 |
rs577989942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526202 | CAAGAGCGAAACATC[A/G]GCTCAAAAATAAATA | 55626 |
rs577993652 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502992 | CATGAACCTGGGAGG[C/T]GGAGCATGCAGTGAG | 55626 |
rs577999029 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518301 | CGGGCGTGGTGGTGG[A/G]CTCCCGTAGTCCCAG | 55626 |
rs578004069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503694 | AAAAGAGGACCCAAA[C/T]ATAAGCAAATTAATT | 55626 |
rs578034983 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580381 | TTTGTGAATCAGCCT[A/G]AAGACTACTTACTTG | 55626 |
rs578035932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408408 | TAATGCCACCAGGTG[A/G]GCATCACCCAGACAT | 55626 |
rs578050804 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425710 | CCGGGGTGGTGGCAT[A/G]CACCTGTAATCCCAG | 55626 |
rs578067408 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471085 | TAGATGAGGAGGAAA[C/T]TGAGGCTCAGATCAA | 55626 |
rs578073125 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462696 | CCTAGTCAATGTTTA[C/G]TAAAATCCCCTTCAT | 55626 |
rs578111943 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580453 | CATGACTAAAACTGA[A/G]GTCTTCATTCCACTC | 55626 |
rs578133406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549476 | GTTACATTGAGGTTG[G/T]TGTTTTTTTTGTATA | 55626 |
rs578136404 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541666 | ATGGTTCCATCTCCT[C/T]ATGCCTCTCTAACCT | 55626 |
rs578154746 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510691 | TAATGGTTTAAAAAG[C/T]ATTCCTGCCACAATT | 55626 |
rs578179784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493288 | TCACCAACCAAAACA[C/T]AAACACGGCACCTTT | 55626 |
rs578200916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445271 | CGTTCTAGATAAATG[A/G]ATACCCACAAAACAA | 55626 |
rs578236417 | in-del | -/T | 0.0422008 | 0.138995 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538503 | TTAATAGTTTCTGGG[-/T]TTTTTTTTTAGACGG | 55626 |
rs578244467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485000 | TGGAGTGCAATGGCG[C/T]GATCTCAGCTCACTG | 55626 |
rs578259386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477488 | ATGCTACCAAGCTCA[C/G]CTAATTTCTGGAAAA | 55626 |
rs745305953 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408273 | GTGCTCTCTCTTTGG[-/AA]AAAGAGACAGGGTCC | 55626 |
rs745307360 | in-del | -/CAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520578 | TTCCCCAGTGCCCCA[-/CAG]CATTTTGTTTTTCTT | 55626 |
rs745317157 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523705 | CAGATGCGCTTTATT[C/T]AGAAAAATCAGAGAC | 55626 |
rs745318913 | snp | C/T | 1.66949e-05 | 0.00288915 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443472 | CCACTGATACCCCCA[C/T]TTGACATTGACTTAC | 55626 |
rs745321495 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534528 | ATAGCACCTGAAATC[C/T]AGCAGGTGCTTGGTA | 55626 |
rs745332838 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469728 | GGAGTGCAGTGGTAC[A/G]ATCATTGCTCACTGC | 55626 |
rs745343548 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485704 | GCATAAGTGGGGAAA[G/T]ATCAAGAGGAAATTT | 55626 |
rs745404629 | snp | A/G | 6.59652e-05 | 0.00574267 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542247 | CTCGCCAGAGGAGTA[A/G]TTAGGTGTGGTTCTT | 55626 |
rs745419117 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432310 | ACAGAAAGTAAAAAG[C/T]TTGCAGGTAGCTGGA | 55626 |
rs745435988 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396550 | TTTTCATACTAAAAA[C/T]AAAATGATCAGAGCC | 55626 |
rs745438861 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431661 | TGATTTAAACGATTA[A/T]TCCACAATTAGGCCG | 55626 |
rs745438897 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578414 | GTTGCTTGAACCTGG[A/G]AGGCAGAAGTTGCAG | 55626 |
rs745455691 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430221 | AGATGGGAGGTGAGG[C/T]GCAGACAGCCAAAAA | 55626 |
rs745474109 | snp | A/C | 1.65743e-05 | 0.00287869 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547874 | TCCGGCAGTTCTACT[A/C]TCTGGGAGACAAAAA | 55626 |
rs745498029 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532500 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 55626 |
rs745507690 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411760 | AGGCATGAACCACTG[C/T]GCCCAGCCCAAATCT | 55626 |
rs745511313 | snp | A/G | 2.19137e-05 | 0.00331004 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443630 | CAAAGACAGCACATT[A/G]TATTATTTATCCACG | 55626 |
rs745530538 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462410 | CTTTACTCTCCTCAC[A/G]TCTGTCTTCAATGCC | 55626 |
rs745555677 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446146 | GCTCTCTGCCAATGG[C/T]GCCAGGGTGCTGAGG | 55626 |
rs745559189 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552852 | TCAGTAGTGGCATTA[C/T]TGGTGATTTAATAAT | 55626 |
rs745564534 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536133 | AAAGGCCAAACAGGA[C/T]TTATATTGCATATGA | 55626 |
rs745565926 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446626 | CATCGCAGAACATTT[A/G]GCATCCCTGGCCTCT | 55626 |
rs745589365 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498846 | ACTATTAAAAAATTT[C/T]TGTTTCCCTATGCTG | 55626 |
rs745605731 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513798 | AATATAGGCTCAGTA[C/T]TGCTGGCTTTTCCTA | 55626 |
rs745605857 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497743 | TCGACAGGAAGAGGG[A/G]AAAAGGCCATCAGTT | 55626 |
rs745610881 | snp | A/C/T | 3.3016e-05 | 0.00406289 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417890 | CCAGTGATCCCTCAA[A/C/T]CCCCACACTTTAAGC | 55626 |
rs745612540 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552190 | CCTGGCCAACATGGC[A/G]AAACCCCATCTCTAC | 55626 |
rs745622230 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519437 | AAAAAATTATAACCT[A/G]AAGATACTCTTTTAA | 55626 |
rs745631818 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410074 | TGGTTCTACAGCAAG[A/T]CTCTGAGAGCAGAGC | 55626 |
rs745649308 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570397 | TATATCTTTTCAGCA[G/T]AAAATGACAAGTGGA | 55626 |
rs745673960 | snp | A/C/G | 3.30859e-05 | 0.00406719 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410354 | CAGTAGTACTCAACA[A/C/G]CAGAGTTTAAGGCCC | 55626 |
rs745676189 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550825 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55626 |
rs745693773 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512521 | GTCCCAAAGGACAAG[A/G]GCTTGGTCATAACCC | 55626 |
rs745698528 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529877 | CACACAAACATGTTG[C/T]CAGGAATGCTTCCAA | 55626 |
rs745699008 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508226 | GTCGGTTCCCTCTAC[C/T]GATGGACCCTGGTTG | 55626 |
rs745715696 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432875 | GGACGTTCACTCAGG[C/T]ACGTTAGTCTGGCTG | 55626 |
rs745732839 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422056 | GAACACCCACCCTGT[A/C]CCCCACTCTTCTCTC | 55626 |
rs745762980 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588243 | AAGCTGAGGAGGGGG[A/G]ATCACTTGAACCTGG | 55626 |
rs745769976 | in-del | -/TT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481422 | GATGGAGTTTTGCTC[-/TT]GTTGAGCTCAGCACA | 55626 |
rs745789014 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476489 | CCCATAGGACCTTCA[C/T]ATTCTTCCCAGGTAA | 55626 |
rs745800164 | snp | C/T | 1.80847e-05 | 0.00300699 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397455 | ACGTTTGTCTCTACC[C/T]GTTCCGTGGTTCTCC | 55626 |
rs745807804 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475243 | TTATGAATAAGAGAA[G/T]AATTCAAGTCCTTGG | 55626 |
rs745809441 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491544 | CAAATGATACAACTG[C/G]CAATAGAATCTGGAG | 55626 |
rs745822819 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437167 | CAGAGGAGAGTACAA[A/G]TAAGATTTTCCTTCT | 55626 |
rs745824197 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464287 | GAATGCAGGCTTATC[C/T]CTCTTGGCACAAAAT | 55626 |
rs745843701 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503432 | GCCCCAAAACAATTA[C/T]AATTGATCACAGGTC | 55626 |
rs745869712 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519307 | GGGATTACAGGCATG[C/T]GCCACCATGCCCGGC | 55626 |
rs745882997 | snp | A/G | 3.43589e-05 | 0.00414467 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397616 | GGCAGGGTTGGCTGG[A/G]TTGGCTCCCGCCCAG | 55626 |
rs745885295 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502606 | AGCAGGAACAAGTAC[G/T]GTCAAGGACAGGTGG | 55626 |
rs745886854 | snp | A/G | 1.66136e-05 | 0.00288211 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543273 | GCCAGAAGAGCGGGA[A/G]GACAGCATGTGCAGG | 55626 |
rs745896319 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573083 | TCTAGCCTGGGCAAC[-/AA]GAGCAAAACTCTGTC | 55626 |
rs745907567 | snp | C/G/T | 1.69911e-05 | 0.00291466 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542159 | GGCCCTCAGTCCGCT[C/G/T]GAGAGGTGGCAACTG | 55626 |
rs745910829 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414760 | AGGGCGGGATGACTG[C/T]GCTATCAGCCCCTGG | 55626 |
rs745949785 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575974 | TCATGTATAACCAGG[G/T]ACCAAAGCTATTTTT | 55626 |
rs745969409 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517922 | AGTATACCCATATTC[A/G]TATATATATAGAGAG | 55626 |
rs745984552 | snp | G/T | 1.66701e-05 | 0.002887 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433479 | TGGCACTCACCCTCA[G/T]GGAGGTCTCTCCACC | 55626 |
rs745989246 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465697 | TCTTTGCAGTGTAAG[C/G]GATCATCAGTGTAAG | 55626 |
rs745996648 | in-del | -/AACTCCAGCCTGCT | 1.65534e-05 | 0.00287688 | frameshift-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542116 | CTAGCAGAGCTGCTC[-/AACTCCAGCCTGCT]GGAGCTGGGCGTTTG | 55626 |
rs746016550 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412246 | TTTGTATACTTAAAA[C/T]CATCTCTAGATTACT | 55626 |
rs746054697 | in-del | -/TATGT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528753 | TTAAGAGGGTAAATC[-/TATGT]TATGTTTTCTATCAC | 55626 |
rs746080945 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481198 | CCAAACAGCTCTGTT[C/T]TGGAATGTAATCACC | 55626 |
rs746097324 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480171 | CCCAGATAAATCAGG[A/T]TAATCTTCCCACCTC | 55626 |
rs746117017 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408203 | GGGTGTACTTCTCTG[A/G]AATGGCAGCTTGCAG | 55626 |
rs746122704 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442483 | GCAGTGATGGTCAGG[C/T]CACCTTGTCAGTGTG | 55626 |
rs746133724 | snp | G/T | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545649 | ACCACAGCAAAGGGT[G/T]CCCGTCGACTCCAGT | 55626 |
rs746167930 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437926 | CAGCAGCACACAAAC[-/T]TTTAACACGTATCAA | 55626 |
rs746172240 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494860 | GGACTGTTAACAGTC[A/C]ATGCAATAGTAGTAA | 55626 |
rs746183848 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562763 | AACTTAAATTTTTCC[A/T]ATAAATTAATAGTAT | 55626 |
rs746206663 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532125 | CTATGTCTCAGAAAT[A/T]AATTAATTAATTAAT | 55626 |
rs746236968 | snp | A/G | 1.66147e-05 | 0.0028822 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542915 | TACTGAAGGCAGACG[A/G]CCGGTTCAGGAGGCC | 55626 |
rs746254058 | in-del | -/GA | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46451055 | TCATTCACATTCTAG[-/GA]GACAGTGGGAACAGC | 55626 |
rs746285032 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457347 | ACTTGGTGGTCAAAG[A/G]TGAGGTTAGATCGGA | 55626 |
rs746285075 | snp | A/G | 1.83353e-05 | 0.00302776 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408530 | TCACCAGGACCTGAG[A/G]CGGCTGTCCCTGGCT | 55626 |
rs746326768 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562472 | CAGGGTTATAGCAAT[A/G]TAAGAGATGAATAGT | 55626 |
rs746359757 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476611 | ACTGGGCATTTTAAA[C/T]AATTTACTCCAGCTT | 55626 |
rs746370719 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455459 | TGAAAGAGGAGATGC[A/G]TAACTAGGTAGCGTG | 55626 |
rs746421551 | snp | A/C | 1.65501e-05 | 0.00287659 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512695 | GGGCCGCCCCTCCCC[A/C]CACCTAGTGCCATTT | 55626 |
rs746429942 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512138 | TGGGATTACAGGCGT[C/G]AGCCACCATGCCCAG | 55626 |
rs746444104 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525194 | TAGTCTCAGCTACTT[G/T]GGAGGCTGAGGCAAG | 55626 |
rs746460100 | snp | A/G | 3.33239e-05 | 0.00408177 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46493663 | AGGCTGTCCACGTTC[A/G]TGAAAAATCCCAGCA | 55626 |
rs746462531 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508703 | GGGTGCTCTTTACAC[A/G]GAGCTGTGCTCATTC | 55626 |
rs746494278 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404122 | TGAGCCCAGGAGGTC[A/G]AGGCTGCAGTGAGCC | 55626 |
rs746515263 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561810 | ACATTTCTTAGCCAA[C/T]CAAAAGAAGGCATTA | 55626 |
rs746517188 | snp | A/C | 5.22071e-05 | 0.00510889 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547899 | CAAAAAAAAAAAAAA[A/C]GTTAAAATACATGAT | 55626 |
rs746520487 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564727 | CCTTGGACAAATTCT[A/G]TAATATCCATGCCTC | 55626 |
rs746538470 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525586 | TGAAACCCTGTCCCT[A/T]TTAAAAATACAAAAA | 55626 |
rs746546959 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581106 | GCCCCAGAGTAACGT[A/T]TTAAAATCATATATA | 55626 |
rs746576739 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432905 | GAGGCCAAAAGGCCA[C/T]GAACCACAGGATGCC | 55626 |
rs746580462 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446413 | CCAGAGGGGGTTAAT[A/G]GACTGAGCTAGAAAG | 55626 |
rs746599029 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580043 | TCAAAATACACAGAC[C/T]ATCTCCACTTCGTCC | 55626 |
rs746608358 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417787 | CCTTTAAGGAGTGGC[A/G]CTGAGAATGAGGCAG | 55626 |
rs746611350 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479590 | TAATCCCAGCTACTA[C/G]GGAGGCTGAGGCAGG | 55626 |
rs746617341 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432627 | TATCCCTCTAAGGAG[C/T]TTACACTGAACCGAA | 55626 |
rs746635538 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442762 | ACAGACATAGAATAT[A/C]TTAATTATTTTAAGG | 55626 |
rs746639585 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487747 | AAGTCAGTAAAGAAG[A/G]AACAGAGGAATAAAA | 55626 |
rs746646452 | snp | C/T | 0.000237715 | 0.0108996 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408630 | ATGTCACTGAGGTGG[C/T]AGGGTTCCGGGGCTG | 55626 |
rs746655465 | snp | C/T | 1.71749e-05 | 0.00293038 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542987 | AGGGCTCGGTCTGTA[C/T]AAAAGAAAAGGAAGG | 55626 |
rs746729579 | snp | A/G | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595060 | GAGACTCCAGTCTCT[A/G]TAAAAAAAAAATAAA | 55626 |
rs746743129 | in-del | -/TTTA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406043 | AGCTGAGATTCTGTC[-/TTTA]TTTATTTATTTATTG | 55626 |
rs746744995 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463750 | CATAGCACAGTACTC[A/G]GGGCCCTAAGAAATT | 55626 |
rs746745526 | snp | C/T | 1.65636e-05 | 0.00287776 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548268 | TCCCATTTCATCCAC[C/T]GGGTTTTATCTTCTA | 55626 |
rs746764464 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554946 | TATGTACATAAGACA[A/T]ATGCCGGTCAGGCAT | 55626 |
rs746769592 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396854 | ATCAGGCAAGCAGGC[A/G]CCCCCTTACCCCACA | 55626 |
rs746783053 | snp | A/G | | | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46395943 | GACACAGTCAAGGGA[A/G]ACCTGAGCAGCTAGC | 55626 |
rs746821491 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581256 | AGCAGGTATATCACC[C/T]GAGGTCAGAAGTTCA | 55626 |
rs746822734 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553234 | AAGCGTGAGCCACCA[C/T]GCCCGGCCACCATTC | 55626 |
rs746840916 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447160 | ACGCCCATAACCCCA[A/G]CACTTTGGGAGGCCA | 55626 |
rs746864991 | snp | C/T | 1.65132e-05 | 0.00287339 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410282 | CAAACATACCCAGGC[C/T]GCTCGCTGCTCCTGC | 55626 |
rs746869795 | snp | A/G | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418021 | TGTCTCCGCTGGTCG[A/G]CAGGCATGGGATAAA | 55626 |
rs746891595 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542361 | GTTGTTCTCACTGCT[A/G]TGTGGGGTGGGCTGG | 55626 |
rs746896908 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571027 | GGCAAGTGTTACCCT[C/T]AAGGAAGTACAAAGT | 55626 |
rs746901735 | in-del | -/AAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562003 | GAGGATACTATAGTA[-/AAG]AAGAACATTCTTGCC | 55626 |
rs746922314 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478804 | GGATTACAGGCATGC[A/C]CCACCATGCCCGAAG | 55626 |
rs746928870 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462591 | CACTGCTCTCCAGAC[A/C]CATCACTTTGTACAT | 55626 |
rs746939545 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515590 | GACAGTACTGAGTGA[A/G]ATGAGATGATTTATT | 55626 |
rs746957260 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461761 | AGCTATTGAGTGACA[C/T]ATGGTCACATAAACT | 55626 |
rs746978331 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411495 | TTTTTCTGAGATGGA[C/G]TCTCACTCTGATGCC | 55626 |
rs746979442 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514290 | ACTTCCCCTAACAGC[C/T]TGGGGAAGAGACATA | 55626 |
rs746994387 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497318 | GAATGAGATCAGCTG[A/G]CTCAAATACACGCAG | 55626 |
rs747010844 | snp | A/G | 6.61048e-05 | 0.00574874 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544059 | AAAATCACAGAAGAA[A/G]GAGACAAAGACACAC | 55626 |
rs747012025 | snp | C/T | 1.65633e-05 | 0.00287774 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397808 | CTGACGATGATGTTG[C/T]TGCCGAAGCCGCCCA | 55626 |
rs747018983 | in-del | -/AATT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473108 | AAGCAAAGCCTCCTC[-/AATT]AAGAGGTCAACTTGA | 55626 |
rs747021965 | in-del | -/CCCATGTA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570421 | AGTGGAGATAATTCT[-/CCCATGTA]CCCATGTATAAGCTT | 55626 |
rs747023226 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479386 | ACAGCTTGCTTTAGC[-/T]GATGGAATGGACAAA | 55626 |
rs747027675 | snp | C/T | 8.23771e-05 | 0.0064173 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542269 | GTGGTTCTTTCCCAG[C/T]GCAGGGTATCGTTGT | 55626 |
rs747040417 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399983 | AACATCTACCTTGCA[C/T]GGTGCTGGAGAGAGA | 55626 |
rs747066407 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587434 | CTAGATATTTATAAG[C/T]CCTAGTTATCCTTGA | 55626 |
rs747092468 | snp | C/T | 5.09057e-05 | 0.00504482 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545810 | CAGATATTCTCAGGT[C/T]ACAAGCTACCAGCAC | 55626 |
rs747117916 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541051 | CTTCGACAGAGGATG[C/T]AATGCAGCGCAATAT | 55626 |
rs747152677 | snp | A/G | 1.65512e-05 | 0.00287669 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397741 | CTGGGGTGAGGAGGT[A/G]TGGGCGGCACCAGGT | 55626 |
rs747160673 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435404 | CAAAACCAAGATAAA[G/T]GAAAATGCAAACCCA | 55626 |
rs747184062 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577472 | AGGAAGGGCAGAATA[A/G]GGACAAACTGCTTAA | 55626 |
rs747184148 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557529 | AAAAATAAAACCAGC[C/T]AGGCACAGTGGCTCA | 55626 |
rs747195378 | in-del | -/A | 6.5999e-05 | 0.00574414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417895 | GATCCCTCAACCCCC[-/A]CACTTTAAGCCACTT | 55626 |
rs747199812 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414924 | ATGCCCAAGGAGCTT[C/G]TTCCTCTGTCTTTGT | 55626 |
rs747206810 | snp | C/T | 3.2956e-05 | 0.00405918 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542790 | CAACCCAGGAGCTAT[C/T]TCTCGGTGATACCTA | 55626 |
rs747226018 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503696 | AAGAGGACCCAAATA[C/T]AAGCAAATTAATTAG | 55626 |
rs747227871 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468223 | GCGTGGTGGGACCAA[C/T]CACTAATACAAAAAA | 55626 |
rs747228939 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413635 | AGCTGGGATTACAGG[C/T]GTGTGCCACCATGCC | 55626 |
rs747277995 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518015 | GTAAAGGGTATATGG[A/G]AATCCTCTATACGTT | 55626 |
rs747321994 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519466 | AACTGGTTGTCAGAT[A/C]ACAGAGAAAAATCAA | 55626 |
rs747367578 | snp | G/T | 3.80481e-05 | 0.00436149 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543107 | ACAGGATCCCAAGGT[G/T]CTGGCAGCACTCAGC | 55626 |
rs747384091 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444315 | TTGCTTGTAACATCT[C/T]CAGGTTTAACTTTCT | 55626 |
rs747388256 | snp | G/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593243 | ACTGGTAAGTGGGGG[G/T]AAGGGAATTGGTAAA | 55626 |
rs747407306 | snp | C/T | 0.00015252 | 0.00873138 | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518330 | AGCTACTTGGGAAGC[C/T]GAGGCAGGAGAATGG | 55626 |
rs747454573 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495927 | AAGGATCCTAAGCGG[A/G]GGAAAGGGTGGAGGC | 55626 |
rs747459600 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507668 | CTGAATGGGGGGTAA[C/G]AGTAGGGAGACCAAA | 55626 |
rs747467517 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405580 | ATGATTAAAAAAATA[G/T]CCAGGCATGGTGGCA | 55626 |
rs747481234 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592344 | CAAGCTGGGAAGGAA[A/C]AGGGAACCACAAAGG | 55626 |
rs747502536 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456106 | AGTATCATTACCTTT[A/C]TTCCACCCACAAACA | 55626 |
rs747507005 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541480 | CAAAAGATAAGGATT[A/G]GGAAGTGAACTCAGT | 55626 |
rs747512656 | in-del | -/AAAACAAAAACA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436638 | CCCAAGCCCTTTGCC[-/AAAACAAAAACA]AAAACAAAAACAAAA | 55626 |
rs747515801 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570261 | GTGAGACCATGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs747528394 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480656 | AGTCCAGATCTAGAG[A/G]TTATTGCTGAAGTTT | 55626 |
rs747554696 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418664 | TGTTTGGTTTTCGAA[A/C]AGGATGACTCTTAAC | 55626 |
rs747561283 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547486 | TTTTGGCTTGTCCAC[A/G]CTGTCCCCAAATGAC | 55626 |
rs747564847 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457443 | AACGGTTGACAATCT[A/T]GAGGGTGTTCCACAA | 55626 |
rs747589012 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510367 | GATGTTCGTGCACTG[G/T]TCTTATATCTGCCCA | 55626 |
rs747601193 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496116 | CAGTGGCTCACACCT[C/G]TAATCCCAACACTCT | 55626 |
rs747612817 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547689 | TTCCCTTTCCGACAC[A/G]GGGCCAAAGTGCTGT | 55626 |
rs747619883 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494990 | TTACAGAGAAGCGGA[C/T]GAAAGACCAGAGAGG | 55626 |
rs747632572 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512307 | GCCTTTTGATATTCT[A/C]AATTCCCTCTCAAAT | 55626 |
rs747634841 | in-del | -/TC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417056 | TGTAAATTGAGCTTT[-/TC]TTTTTTTTTTTTTGA | 55626 |
rs747639393 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511012 | TTTTGTATTCAAAGT[A/G]TAAAAATACCAACAC | 55626 |
rs747650808 | snp | C/T | 3.30153e-05 | 0.00406283 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410310 | TGCTGTTGGAATGGA[C/T]AGTGAAGACCGTCTC | 55626 |
rs747657992 | snp | C/T | 3.51154e-05 | 0.00419005 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408669 | TGGCATTCATCAGCC[C/T]CATGTCTCTGTCTGT | 55626 |
rs747662537 | snp | A/G | 1.6549e-05 | 0.0028765 | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548406 | AGCCACTGTCACACC[A/G]GGCCCAGGAAATGAA | 55626 |
rs747664449 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566586 | TTGAAAGATTACAGA[C/T]GGGACCCGGGGGGTG | 55626 |
rs747666081 | in-del | -/CGTC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436599 | AATTAGCACTGGGAC[-/CGTC]TGCTACTTACTACTC | 55626 |
rs747671375 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407805 | ACTTAGAAAATGTGT[C/G]TGTTTGGAGGCTGCT | 55626 |
rs747675455 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593479 | AATTGAGGCATGACA[C/G]CCGGAGACTTCGGGG | 55626 |
rs747679596 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549105 | GGAAAAAAAAAAATC[A/T]GGCTCCTTTTCTCAT | 55626 |
rs747693763 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459851 | TTGACATATACATTT[A/G]CTTATTCCATGAAGC | 55626 |
rs747702592 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564836 | TTAGTATTTGTAATA[C/T]ATACACAGATCATCA | 55626 |
rs747722400 | in-del | -/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450436 | CAGGTGAGCACAAGA[-/T]TTTTTTTTTTTTTCT | 55626 |
rs747756125 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586672 | ATATACAGCACCTAG[A/T]GCTGTTCTAAATGCT | 55626 |
rs747765154 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471969 | TGCCTCGTTTCACAT[A/C]CACATTAATTTTTAC | 55626 |
rs747781696 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474625 | ACTCCAGACCTCAGG[A/T]GATCCACCCACCTCG | 55626 |
rs747802249 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473273 | GAAGAGACAACTGAC[C/T]TCATCAAAGGAAGCT | 55626 |
rs747805376 | snp | C/G | 0.000181247 | 0.00951792 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46541991 | CAGGCATATCCTGAT[C/G]TAAGGCCTCCTGTGA | 55626 |
rs747820262 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507304 | CTAACATGGTGAAAC[C/T]CCATCTCTACTAAAA | 55626 |
rs747866933 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419175 | AATCACCGTTAAATT[A/G]ATTGTTTCTCTTTTT | 55626 |
rs747877759 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540581 | TTCCTACCCAGGGCC[C/T]TTAGTAACTGCCTAA | 55626 |
rs747878040 | in-del | -/GGGG | 1.6755e-05 | 0.00289435 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545587 | CCAGACAATGCAGAT[-/GGGG]GGGGCAGCGCACTCA | 55626 |
rs747879797 | snp | A/C | 4.94621e-05 | 0.00497279 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542520 | TCTCAGGTCACACTG[A/C]AGCTCATGGCGAATG | 55626 |
rs747889675 | snp | A/G | 5.9079e-05 | 0.0054347 | intron-variant, stop-gained, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543146 | AACTGACCCGCTGTC[A/G]GAGCCTGATGTAAGC | 55626 |
rs747892155 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578355 | AGCCAGGCGTGGTCA[C/T]GTGCGCTTGTAATCC | 55626 |
rs747903825 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589141 | CAGATCTCCTGATTA[C/G]TTAATCTATTTTCTC | 55626 |
rs747964138 | snp | C/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542383 | GTGGGCTGGTGGGAA[C/G]GGCCTGGCCTCTCAG | 55626 |
rs747965972 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539447 | CTATAATACCAGCTA[C/T]CCGGGAGGCTGAGGT | 55626 |
rs747967899 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556676 | TGGTATCTTGATTTC[C/T]AGGAATAGTTACTTA | 55626 |
rs747977891 | snp | A/G/T | 1.75795e-05 | 0.0029647 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397594 | AATGGGGACAGGGGA[A/G/T]GAAGAGGGCAGGGTT | 55626 |
rs748006215 | snp | C/T | 1.66051e-05 | 0.00288137 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545599 | AGATGGGGCAGCGCA[C/T]TCACCGGACCCGTTC | 55626 |
rs748009899 | snp | A/G | 1.73528e-05 | 0.00294552 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397606 | GGAGGAAGAGGGCAG[A/G]GTTGGCTGGGTTGGC | 55626 |
rs748013733 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396925 | GAATCTGGGAGCCTG[A/G]CCCGATCCCTGTTGG | 55626 |
rs748044483 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464197 | AGCACTAGATGTTTT[A/C]ATGCATTCAAAAATT | 55626 |
rs748044968 | snp | C/T | 1.65277e-05 | 0.00287464 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548292 | TCTTCTACCAGCTCC[C/T]GCAGAAGCCGCTGAG | 55626 |
rs748070184 | snp | A/G | 1.82713e-05 | 0.00302247 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493715 | AAGAAACGCCTACAA[A/G]AAGGAATCACATGTG | 55626 |
rs748070920 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403786 | ATTTTTATAGAACAA[A/G]AAAATGAGAAGTAGC | 55626 |
rs748084337 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502477 | CTTATCCCTCTCTGA[C/T]GATTTTACTTGCCAA | 55626 |
rs748096865 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448698 | ACAATAAACATCTAG[A/G]TAGGCCAACTACGAA | 55626 |
rs748131478 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555057 | TCAGCCCAGGTAATA[A/G]AGTGAGACCCTGTCT | 55626 |
rs748144752 | in-del | -/TCA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561474 | GACAGATGTGATTAC[-/TCA]TCATCAGACAAATAA | 55626 |
rs748144828 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526356 | ACTGAATCTAGACTG[C/T]TCTATCACTAGCTTT | 55626 |
rs748162089 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521917 | AGATCAGCCTTATTT[C/T]ACTATTATCAAATAT | 55626 |
rs748165581 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517074 | CTATTTGATCCATTG[A/G]ACAGCAAGGGGGAAA | 55626 |
rs748179586 | snp | A/T | 1.64789e-05 | 0.0028704 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508258 | CTGAGGAAGAGGAGG[A/T]GGTGGAAGAACGGAG | 55626 |
rs748196531 | in-del | -/AAAAAT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454752 | GAGACTCCATCTCAA[-/AAAAAT]AAAAATAAAAATAAA | 55626 |
rs748199294 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589987 | AAAATGTTTGGATTT[A/G]ATATTAATAAGCACC | 55626 |
rs748203537 | in-del | -/AT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469605 | CTAGGCACAATTTAA[-/AT]ATGTTATCTTCAGAG | 55626 |
rs748220944 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476761 | TGTGGCTTTTATAAG[C/T]TCTCAGTTAGCTCCT | 55626 |
rs748234377 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551096 | GTGAGACTCCGCCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs748267527 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542810 | GGTGATACCTAGAAG[A/G]GTGGCTAGACAGAGG | 55626 |
rs748269605 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544240 | CAGAGTAAAGGAATA[C/T]GTATCACAAAAATAA | 55626 |
rs748313876 | snp | A/G | 1.64972e-05 | 0.00287199 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417897 | TCCCTCAACCCCCAC[A/G]CTTTAAGCCACTTAC | 55626 |
rs748334318 | snp | C/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451417 | CTCTACCTTTGCTTC[C/T]CTCAGAAACTCTTCT | 55626 |
rs748366515 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437292 | GTATTATATGATGAC[A/G]ATTCCAAGTCAATAG | 55626 |
rs748376043 | snp | C/G | 1.65932e-05 | 0.00288034 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508334 | CCGTGAGAGATACTG[C/G]ATCATCCTCTGGGCG | 55626 |
rs748382431 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432639 | GAGCTTACACTGAAC[A/C]GAATTGGGTGGATTA | 55626 |
rs748393659 | snp | C/T | 1.69749e-05 | 0.00291327 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434939 | GAAAGCCCCTCTGGC[C/T]GCTGGGGATGAAAGC | 55626 |
rs748400776 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452761 | CACAGTCAATGTATC[C/T]TATAGCCTGGTACCT | 55626 |
rs748406069 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503864 | CTGTGCCAGCAACAG[C/T]CTTTTATTTGTTTAA | 55626 |
rs748418548 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468302 | AAGCACCTTAGGAGG[C/T]GCCAAGGCAGGAGGA | 55626 |
rs748429009 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560460 | ATGATGCTGCCTAAT[C/G]TCTGAAACACGGGAA | 55626 |
rs748429104 | snp | A/C | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542695 | CTCACCGAAGAGGCA[A/C]TGGTTCTGGGCGGGG | 55626 |
rs748440137 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504849 | AACTCAGACACTAAA[C/T]ATGCTTGCTCCTGTC | 55626 |
rs748444337 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504798 | AAAAATGGTGGTACA[C/T]CATTTTCAAAGGTTT | 55626 |
rs748466919 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507009 | TCTCTACTAAAAATA[-/C]AAAAAAAAAAAAAAA | 55626 |
rs748471567 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577595 | TTCATTTTAAGATGG[C/T]TAAATTTACGTGAAG | 55626 |
rs748478514 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538572 | AATCTCGGCTCACTG[A/C]AACCTCCGCCTCCCC | 55626 |
rs748481613 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535545 | TAGGAAAGAACCTTC[A/G]CATTTAAATTGGATT | 55626 |
rs748483712 | snp | A/G | 1.66341e-05 | 0.00288388 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542127 | GCTCAACTCCAGCCT[A/G]CTGGAGCTGGGCGTT | 55626 |
rs748494327 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415860 | GAGACTCTGGGATGC[C/T]GGAGCAACATATGGG | 55626 |
rs748494345 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398849 | TGTGATCTTGGCTCA[C/G]TGCAACCTCCGCCTC | 55626 |
rs748522485 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429794 | ATGAAAGCCGAGAGG[C/G]AACACAGGCAGTTTA | 55626 |
rs748532469 | snp | A/G | 3.93221e-05 | 0.0044339 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434812 | TGCCAAGGCACCAGC[A/G]TCCCTCTGTCATTAG | 55626 |
rs748544035 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578239 | CACCTGTAATCCCAG[A/C]ACCTTAGGAAGCCGA | 55626 |
rs748625771 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428246 | CTTTTCAATGTGTCC[G/T]ACGAACTATTGATTT | 55626 |
rs748641848 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482957 | GAGGTTGCAGTGAGC[C/T]GAGACCATGCCATTG | 55626 |
rs748645123 | in-del | -/AT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570901 | TACTCCAAGAAAGGG[-/AT]AGAGAACTGGAAAAA | 55626 |
rs748645727 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542700 | CGAAGAGGCACTGGT[C/T]CTGGGCGGGGGCATG | 55626 |
rs748652627 | snp | C/G | 1.6577e-05 | 0.00287893 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397816 | GATGTTGTTGCCGAA[C/G]CCGCCCATGGAGGCC | 55626 |
rs748662700 | snp | A/G | 3.30524e-05 | 0.00406511 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547205 | CACACCATGGAGTAC[A/G]GCGGTGTCCAATCAG | 55626 |
rs748668868 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522165 | AGAAGTCAGCCAGTT[-/C]CCCCCTGGGAACATA | 55626 |
rs748671621 | in-del | -/TGTTTCAAAAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525295 | AACCGATTGAAACCC[-/TGTTTCAAAAA]TAAATAAATAAATAG | 55626 |
rs748676676 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573329 | GAATCGCTGGAACCC[G/T]GAGGGCAGAGGTTGC | 55626 |
rs748713822 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444835 | AGAAGCCAAGAAATA[C/T]GAGAAAAGTACTCTC | 55626 |
rs748724561 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414865 | GATGGAGGATTTTTG[-/A]AGGCCTTAGTCTACT | 55626 |
rs748725775 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534566 | GTTAATGGAATGAGT[C/G]AATGGATGGATGCAT | 55626 |
rs748729524 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481825 | TGGTTTTGGGTAAAA[C/T]ACTTCATCTCTTTTA | 55626 |
rs748734520 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507130 | TGCAGTGAGCCGAGA[C/T]TGTGCCACTGCACTG | 55626 |
rs748754233 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483375 | GATATCCATGCTTGC[C/T]CTTCAACCTGAGTGG | 55626 |
rs748784289 | snp | C/G | 1.81013e-05 | 0.00300838 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397400 | AGTCAGCTGTGAGGT[C/G]CGGTTTCTGCTTGGC | 55626 |
rs748809240 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586519 | ACTGTGGGGAAAGAG[G/T]GACAAATATGCTGTT | 55626 |
rs748813324 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550724 | AAAAACTGAGGATAA[C/T]CAAGTGTCCATCTAA | 55626 |
rs748821999 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535949 | TAGGAACATAGCACA[C/T]AGTGAAACATCAGAG | 55626 |
rs748837437 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417712 | CATGATCACTAAATC[A/T]GTCTCTGGATGAAAT | 55626 |
rs748837618 | snp | A/G | 1.67284e-05 | 0.00289205 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543265 | ACCTGGATGCCAGAA[A/G]AGCGGGAGGACAGCA | 55626 |
rs748841110 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445987 | TGTGGATCTGCAAAT[A/G]GGAACACAAATGATT | 55626 |
rs748857105 | snp | C/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594594 | AAAAAAGCACACGGA[C/T]TGCTTTTCTCTTTTA | 55626 |
rs748892519 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461131 | GCCTATAGTCCCAGC[C/T]ATTTAGGAGGCTGAG | 55626 |
rs748897222 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408039 | TGAGAGGAAGGGGCT[A/G]ATGATAGGCCAGGCT | 55626 |
rs748930981 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503910 | CACTATGTTGCCCAG[A/G]CTGGTCTCGAACTCC | 55626 |
rs748931007 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444913 | CAGCATTAATTTATT[G/T]ACAGTCTTGTCTTTG | 55626 |
rs748933460 | in-del | -/TTTTTTTTTTTTTTTTTTTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400474 | TAGTTCTTTCTATAG[-/TTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 55626 |
rs748948398 | snp | A/G | 0.00326263 | 0.0402576 | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451776 | CATCCTGGAGACACA[A/G]TTACTATCTTTCTGC | 55626 |
rs748957345 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460143 | TATAAGAGTGAAAAA[C/T]CTAGAAAGTTAAATG | 55626 |
rs748961195 | snp | C/T | 1.73333e-05 | 0.00294386 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434964 | GAAAGCTGCCAGGAG[C/T]TGGCCATCTGCAGAA | 55626 |
rs748986195 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535446 | ACAAAAGATGAGAGC[A/G]CACATTTTCTCAAAC | 55626 |
rs748995684 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507177 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs749003856 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414852 | CTTCCCCTGGAGAGA[G/T]GGAGGATTTTTGAAG | 55626 |
rs749004867 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588090 | GTAATCACAGAACTT[G/T]GACAGGCCAAGTTGG | 55626 |
rs749018516 | in-del | -/GG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488679 | AGCACATGGGTAACA[-/GG]CTCTCTAGAAGAGCC | 55626 |
rs749028985 | snp | C/G | 1.78733e-05 | 0.00298937 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408688 | GTCTCTGTCTGTCCT[C/G]CATGTGGCTCTGCTG | 55626 |
rs749042753 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511253 | TTCCCTTATATTTAG[A/G]GTGTATAATCCTCAA | 55626 |
rs749056463 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421833 | TAACCCAGAGACTGG[A/G]TGAGTTGTGAGTCCC | 55626 |
rs749058774 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406197 | TAGCTGGGATTACAG[C/G]TGCCCACCACCATGC | 55626 |
rs749121684 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586898 | TCTGTCCTGTTTTCA[G/T]TGGTCGCCTAGAATA | 55626 |
rs749140064 | snp | A/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542629 | TCTGTGGCTGAAGTG[A/T]ACACAGATGCCTGAG | 55626 |
rs749153601 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420716 | CAGAGCACACCCAGA[C/G]TTAAGGAGGGATGAG | 55626 |
rs749157028 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473809 | ACACCCACCACCACG[A/C]CCGGCTAACTTTTTG | 55626 |
rs749158929 | in-del | -/TGGAACTGCTG | 1.6494e-05 | 0.00287171 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543953 | CAGTTTAGCTGGAAT[-/TGGAACTGCTG]GACTAACTTACCTGT | 55626 |
rs749202976 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449770 | AACCCAACTTCAAGA[C/T]TTAATATAGGCCGGG | 55626 |
rs749214346 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489633 | TATATCAGGTCCACA[G/T]CTGCTAGGAGCAGAT | 55626 |
rs749214604 | snp | A/G | 6.2029e-05 | 0.00556872 | intron-variant, synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543162 | GAGCCTGATGTAAGC[A/G]GAAGTCCTGGGGCGC | 55626 |
rs749222350 | snp | C/T | 1.65108e-05 | 0.00287317 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410320 | ATGGACAGTGAAGAC[C/T]GTCTCGTTCAGCTGG | 55626 |
rs749239246 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522763 | ATATCCTGGTAGAAT[A/C]ATTTATTGCTGTGAT | 55626 |
rs749258179 | snp | A/G | 1.6788e-05 | 0.00289719 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512863 | TCAATTACCAACTCA[A/G]AGGTCATTCATAAGG | 55626 |
rs749275505 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540762 | CCAATCTCGGTACCA[C/T]ACAATGAAGCATTTG | 55626 |
rs749278327 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471688 | GCTGGAGTGCAGTAG[C/T]GTGATCTCGGCACAC | 55626 |
rs749281976 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590517 | TAAAAATAATCAATT[C/G]TTTTCTAACGATATA | 55626 |
rs749283131 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480035 | GATGCAGAACTGAGG[A/T]TCCCACTCGCTGCTA | 55626 |
rs749292563 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552862 | CATTATTGGTGATTT[A/G]ATAATTTTAATAGGC | 55626 |
rs749319109 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515206 | TGGCTGGGCGTGGTG[C/T]CTCACGCCTGTAATC | 55626 |
rs749321962 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572873 | CTGAAGTGGATCACC[G/T]GAGATCAGGAGTTCA | 55626 |
rs749326933 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515924 | TCTGATCCGCCCGCT[G/T]TGGCCTCCCAAAGTG | 55626 |
rs749334669 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412129 | CTTTAAAAAGCAGTA[C/T]AGTTGTCCCTTGGTA | 55626 |
rs749343021 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591589 | TAGCCGGGCGCGGTG[A/G]CTCATACCTGTAATC | 55626 |
rs749397857 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571871 | ATTTTTGTGTTTTTA[C/G]TAGAGACAGGGTTTC | 55626 |
rs749413225 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531378 | AGGCTCAAACAGAGT[A/G]ACCTTCTTGGGCAGG | 55626 |
rs749413965 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428548 | CTCTAGGATCTGCAG[C/T]GATTAGGCAATGAGG | 55626 |
rs749445607 | snp | A/T | 1.65712e-05 | 0.00287843 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544083 | GACACACATAGAGAG[A/T]TTATGTTAACTGAGA | 55626 |
rs749447494 | in-del | -/AG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553806 | AGTCCTACACAGCAC[-/AG]AGTTACCTAAGGAGT | 55626 |
rs749457304 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440754 | CTTAGAAATAGATGG[C/T]TGCTGCTGAAGTTTC | 55626 |
rs749489455 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494749 | GCACAAGAAAAAGAC[A/G]GTACCTTCTTTTACA | 55626 |
rs749496739 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439092 | CCTGGGCAACACAGC[A/G]AGATCTCATCTCTAT | 55626 |
rs749498730 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460613 | CAGGCGTGAGCCACC[A/G]CGTCCAGCATAAACA | 55626 |
rs749499976 | in-del | -/AT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441648 | CCATAGGGTAAGCTA[-/AT]AGTGTCTGAAGCACC | 55626 |
rs749500151 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479019 | GTCTGGGCAACACAG[C/T]GAAACCCTGTCTCTA | 55626 |
rs749505080 | snp | A/G | 1.72791e-05 | 0.00293926 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433450 | GAGCTGCCATACAGT[A/G]AAGGCACAAGCAATG | 55626 |
rs749521467 | snp | C/T | 1.80804e-05 | 0.00300664 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397526 | AGAAGGTGGTTGTTA[C/T]TGGTCAACTCGCAGT | 55626 |
rs749543130 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455180 | GCATAAGCCACTGCA[C/T]CCAGCATAGGTTTTC | 55626 |
rs749554946 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580895 | CTCCGCAGATCAGAT[A/G]ATCCTCCCACCTTAG | 55626 |
rs749558478 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530045 | TTATGCAAACAGAAC[C/T]CCATACACCTGGTGT | 55626 |
rs749592474 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402139 | TGCTTCACAACTCCC[C/T]GTAGCTGTGGCATCT | 55626 |
rs749593705 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506098 | AAAAACCGTATCTAC[A/G]GGAGAACATATTTCA | 55626 |
rs749600835 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544486 | AAACCAGAAAATTGG[C/T]CTGTATTCGACTGGA | 55626 |
rs749610196 | in-del | -/AAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532794 | AATAAAACAGGAAAT[-/AAG]AAATACTTTATATAT | 55626 |
rs749617840 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560818 | GCAACAAAAAAAGAG[C/T]AGCTTCTGATGGAAG | 55626 |
rs749627560 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570359 | GGAACTATCCTGTGG[A/G]CCCAGAGGGAGAAGT | 55626 |
rs749629802 | in-del | -/AG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448047 | CAACAGACAGCTTAT[-/AG]AGAGATGTCCTTGTG | 55626 |
rs749640125 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523218 | TGAACTGCTTCTCTT[A/C]GTGACATTTGATTTC | 55626 |
rs749640272 | snp | A/T | 1.692e-05 | 0.00290856 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443450 | CTCACCAGCAAATAT[A/T]ACCCTTCCACTGATA | 55626 |
rs749654901 | snp | G/T | 1.65307e-05 | 0.0028749 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547217 | TACGGCGGTGTCCAA[G/T]CAGGGAATGAACACA | 55626 |
rs749681645 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505134 | TTAGGAGGATTACTC[A/G]CCATATCTACCTTAC | 55626 |
rs749695507 | in-del | -/TAGATAGATAGATAGA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447713 | AGACCATCTTGTAGA[-/TAGATAGATAGATAGA]TAGATAGATAGATAG | 55626 |
rs749723487 | snp | G/T | 1.64814e-05 | 0.00287061 | synonymous-codon, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508271 | GGAGGTGGAAGAACG[G/T]AGACGGTTCTGTTGG | 55626 |
rs749725002 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449633 | TCAACACAATCCCAA[C/T]CAAAATCCTGAATTA | 55626 |
rs749732849 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431353 | GCTGCTGGCTAGCTG[C/T]CTTGAGACCCTTGGC | 55626 |
rs749744611 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415997 | GGCCACAACAAACTG[A/G]GTGTAGATTATTTTT | 55626 |
rs749746961 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578295 | AGTTCGAGACCAGCT[A/G]GGTCAACATGGAGAA | 55626 |
rs749771017 | snp | C/T | 3.31153e-05 | 0.00406898 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542900 | TGCTGCTCTGGACTG[C/T]ACTGAAGGCAGACGG | 55626 |
rs749777879 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485078 | GAATAGCTGGGATTA[C/T]AGGCACCTGCCACCA | 55626 |
rs749796240 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469636 | GTAAAATGAATCTAA[A/G]AATAAGACTTAGCAA | 55626 |
rs749800366 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446019 | AGACTCCCAAATCCC[A/G]GCTCCAGAGGCATCC | 55626 |
rs749803303 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537382 | AACACCTCTTTAAGA[A/G]ATCATTTACTCTCTC | 55626 |
rs749814786 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484607 | TGACAGTGTATACGC[A/C]TTCCCTTTCCACTGC | 55626 |
rs749818328 | snp | A/G | 1.65089e-05 | 0.00287301 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542840 | GCCCTCCCAAAGAGC[A/G]GCGGGTAGGACCCAG | 55626 |
rs749842908 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556482 | GTGTGCAAAAGATAT[A/C]CAAGGATATGGCAAA | 55626 |
rs749849167 | snp | A/T | 1.67607e-05 | 0.00289483 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545586 | TGCCAGACAATGCAG[A/T]TGGGGCAGCGCACTC | 55626 |
rs749851931 | snp | A/G | 4.16563e-05 | 0.00456359 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547851 | ATAAGAAGGTAGAGC[A/G]TGGACTATCCGGCAG | 55626 |
rs749895755 | snp | A/C | 7.01742e-05 | 0.00592302 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397596 | TGGGGACAGGGGAGG[A/C]AGAGGGCAGGGTTGG | 55626 |
rs749897846 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502149 | CAGTGGCATAATCTC[A/G]GCTCACTGCAATCTC | 55626 |
rs749900257 | in-del | -/GAT | 1.6552e-05 | 0.00287676 | cds-indel, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397798 | AATGCGGTGGCTGAC[-/GAT]GATGTTGTTGCCGAA | 55626 |
rs749949518 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465176 | AAAATTATTCAAACC[A/G]ATCCAATCCTAAACT | 55626 |
rs749983093 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554743 | AGGAGAAAATGCCAG[C/T]CAATTGTGTTTTTCA | 55626 |
rs750025985 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463459 | AGGGCCACTTGAATA[C/T]ATCTGACTTGGACTA | 55626 |
rs750044595 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516875 | ATCTATCACAAGAAA[C/T]CAGGGAGGGCCTAGG | 55626 |
rs750050027 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411544 | CATGATCTCAGCTCA[C/T]TGCAACCTCTGCCTC | 55626 |
rs750057053 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500711 | CTCTACGCTTTTGCT[C/T]AAGCTACTCCCTTTA | 55626 |
rs750060463 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569828 | TAGCCAGGTGTGTTG[G/T]TATGCACAGGTAATC | 55626 |
rs750078437 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487402 | AAGTTAGATGAAAAT[A/G]AAAGTAAATTTTATG | 55626 |
rs750120363 | snp | C/G | 1.65233e-05 | 0.00287426 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508311 | GAGCGCTGGCGAATA[C/G]TGTCTCTCCGTGAGA | 55626 |
rs750127793 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520569 | CACCCTCTCTTCCCC[A/G]GTGCCCCACAGCATT | 55626 |
rs750142660 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572650 | GAAAAATTGTCAGCA[G/T]TATCATCATCATCTT | 55626 |
rs750157351 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424727 | TACCTCTAATCCTAG[C/G]TACTTGGGAGGCTGA | 55626 |
rs750190625 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441432 | GGCGGGAGAATCGCA[C/T]GAACCTGGGGGTGCG | 55626 |
rs750208714 | in-del | -/TTA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429664 | AATTTTGTATTTTTG[-/TTA]TTATGCTTTCACTTG | 55626 |
rs750227503 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589913 | AGGTGTGAGCCACCG[C/T]GCCCGGTCTAAAAAT | 55626 |
rs750242790 | in-del | -/TG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425314 | CTTGATCCATTTGTG[-/TG]TGTGTGTGTGTGTGT | 55626 |
rs750273261 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409210 | AAAGAACTGGAACTC[-/T]TTTTTTTTTTTTGGT | 55626 |
rs750276479 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440329 | GCAGGAAGTACAGAC[A/G]AGTACATACAGCATG | 55626 |
rs750286946 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494260 | GGAAGAATCATCCAC[C/T]AGCCCAAAAAGGAAA | 55626 |
rs750294203 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505987 | GGCTCCACAGCATTA[G/T]TGAGAGAAAGTCACC | 55626 |
rs750299463 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471446 | AGCTGGGCATGGTGG[C/T]GGGCGCCTGCAGTCC | 55626 |
rs750310075 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438838 | TTTCAAAATTATTTA[C/T]GCATGAGGCCTTATT | 55626 |
rs750314722 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418013 | TACTGACATGTCTCC[A/G]CTGGTCGGCAGGCAT | 55626 |
rs750326657 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494014 | CTGGGCTATGGGCCC[A/C]CTAGGAAACAATGCC | 55626 |
rs750359323 | snp | A/G | 4.94768e-05 | 0.00497352 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46512779 | CTGCTCCATCATAAC[A/G]GGATAATGAAATGAG | 55626 |
rs750376915 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492858 | ATTGAGATCATCCTG[A/G]CTAACACGTTGAAAC | 55626 |
rs750382699 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452504 | ACTTTAACTTTTCTC[C/T]TATGGATTATCTGAG | 55626 |
rs750394092 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470277 | GAGACCCCATATCTA[C/T]AAAAAATTTTTTAAA | 55626 |
rs750435974 | snp | C/T | 1.65089e-05 | 0.00287301 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542097 | AGTCCTCTCCTCCTG[C/T]GGACTAGCAGAGCTG | 55626 |
rs750486919 | snp | A/G | 1.80955e-05 | 0.00300789 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397423 | TGCTTGGCGGTTCGA[A/G]GGGAGGCACCAGTGC | 55626 |
rs750492121 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534319 | CCAACATGGTGAAAC[C/T]CCGTCTTTACTAAAA | 55626 |
rs750521275 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549998 | TAATTTTTGTATTTT[C/T]AGTAAAGACCAGGTT | 55626 |
rs750529053 | snp | A/G | 0.000152051 | 0.00871793 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543202 | GGCTGAGGGGGAGGC[A/G]GTGGGGGTGAGGGGG | 55626 |
rs750533022 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427854 | TCTCTACTAAAAATA[C/T]AAAAATTAGCCGGGA | 55626 |
rs750545837 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482742 | CCAGCCAGGCGTAGT[A/G]GCTCACGCCTGTAAT | 55626 |
rs750573822 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407153 | AGGCTGAAGTGAGCC[A/G]AGATCATGCCACTGC | 55626 |
rs750579619 | in-del | -/TGT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531083 | GATGTGGTTTTGACA[-/TGT]TGTTGGCCAGGCTGG | 55626 |
rs750589623 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445434 | TGGCGTATCATAAGA[C/T]GAGGTAAATATATAC | 55626 |
rs750598239 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496719 | CTGGGGAAAATGTGG[G/T]CCCGTACAACGTAGG | 55626 |
rs750610003 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410916 | GACCATCCTGGCCAA[C/T]ATTGTGAAACCCTGT | 55626 |
rs750614267 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444127 | CTACTATACAGCTGA[C/T]TGGATAGAAACAGAC | 55626 |
rs750680087 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567475 | GAGTTCAAGCAGTCC[A/T]CTGGCTCAACCTTTC | 55626 |
rs750706197 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458989 | ATATACATCCAGGAA[C/T]AGGACAAAGCAACTA | 55626 |
rs750734087 | snp | C/T | | | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397821 | TGTTGCCGAAGCCGC[C/T]CATGGAGGCCATGGT | 55626 |
rs750752083 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510358 | ACAGAAGTCGATGTT[C/T]GTGCACTGTTCTTAT | 55626 |
rs750757009 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518561 | TGTCTTCTTTTGTAA[A/T]TAAGTGGCTACTTTG | 55626 |
rs750768079 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421403 | AGCCAGAAAATGCCG[C/T]ACAAAGATCAGCAGC | 55626 |
rs750775617 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528315 | TAGCTGGGTTACAGG[A/T]GCCCACCACCGCACT | 55626 |
rs750775672 | snp | C/G | 2.73317e-05 | 0.00369664 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494135 | TTACCTTGGGACAAA[C/G]CGTCCAAGCGAAGGT | 55626 |
rs750777654 | snp | C/T | 1.68681e-05 | 0.00290409 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408616 | CTGGGTGCCCTGAGA[C/T]GTCACTGAGGTGGCA | 55626 |
rs750780673 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405390 | CTTTTACCAAGTGGC[C/T]GACACATGGTAAAAG | 55626 |
rs750794292 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564393 | TCACTTTTTCCTCAC[A/G]ATGATACTATGAAGA | 55626 |
rs750842731 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580883 | TGCAGTCTCAACCTC[C/T]GCAGATCAGATGATC | 55626 |
rs750857589 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419774 | AGAGTGGTACAATTA[C/T]AATTATTTTTCTGAC | 55626 |
rs750857751 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431390 | GCCAGGGGCTGACTG[G/T]ATTACCACATCTCCT | 55626 |
rs750869328 | snp | A/G | 1.6612e-05 | 0.00288196 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46493633 | CCTGTTAACAGAAGA[A/G]TGAGTAGCCAAGCCA | 55626 |
rs750898877 | snp | C/G | 2.25706e-05 | 0.00335928 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543065 | AGAGGGAAGGAACTC[C/G]AGTGCCAGAGCAGCG | 55626 |
rs750911870 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487530 | TTGTAATACATATAG[A/G]TGTAATATTAATATA | 55626 |
rs750926138 | snp | A/C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449269 | CTGTTTGTTGCCAGA[A/C/T]GACATCACTGTCTAA | 55626 |
rs750938816 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488606 | ATATTGACCAAGTAG[A/G]TTTAACCGACATCTA | 55626 |
rs750942875 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526764 | AAAAATAACTGAATC[G/T]GTTTTAAGTCACTAA | 55626 |
rs750944024 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502778 | AGAATATTAAATTGT[A/G]GGCCAGATGTGGTGG | 55626 |
rs750963786 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541871 | CCAGATACAGCCACA[A/G]CATCTATAGGACTCA | 55626 |
rs750980890 | snp | C/T | 1.65239e-05 | 0.00287431 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410254 | TCCAGCCAGCTGCTC[C/T]CTGCCTACTTCCCAA | 55626 |
rs750992657 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584641 | GACAGGGTCTTGCCA[C/T]GATGATGCCCAGGAT | 55626 |
rs751005771 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435994 | CACATCATGGGCCCG[G/T]GCAGAACAGCACAAC | 55626 |
rs751006614 | in-del | -/CTC | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595676 | GCACTTTACAAAAAT[-/CTC]CTCTAAGTCTTTGAA | 55626 |
rs751026553 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489004 | GCCTCCCAGGTTAAC[A/G]CCATTCTCCTGCCTC | 55626 |
rs751031033 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586323 | CTGAGGCACAAGAAT[C/T]GCTTGAACCCAGGAG | 55626 |
rs751035832 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540112 | TCTTGGATGACAGGC[A/G]TGAGCCACCGTGCCC | 55626 |
rs751041000 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566600 | ACGGGACCCGGGGGG[-/T]GAGGATTGAGCTACC | 55626 |
rs751089347 | snp | A/C/T | 4.94689e-05 | 0.00497317 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545725 | CCGTAGGGTGGAAAG[A/C/T]CAGGGAGGCAATGGC | 55626 |
rs751089457 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558685 | TTTTCTGAAAATATG[C/G]AAATTAATAAATTTA | 55626 |
rs751093773 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398163 | TGGTGGGGAAACTGA[C/G]GCCTAGGATGGCCAG | 55626 |
rs751097210 | in-del | -/AATTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476230 | CCAAATCCCATGGCC[-/AATTT]AATTTCTCTGTTAGT | 55626 |
rs751100001 | snp | C/G | 4.94548e-05 | 0.00497242 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542502 | ATACTCCAGAAAGAA[C/G]CGTCTCAGGTCACAC | 55626 |
rs751141290 | snp | A/C | | | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397502 | TCCCCCCTGCTGCTG[A/C]CACCATCCAGAAGGT | 55626 |
rs751172833 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397076 | CGGGCCTCTGTCCAG[A/G]ATGATTGGCCCAGAT | 55626 |
rs751180119 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502459 | AAATGAAGTAGATAA[C/T]ACCTTATCCCTCTCT | 55626 |
rs751181983 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414549 | TCCCGCCAGCACCTC[C/T]CCCTATCACATTTGT | 55626 |
rs751192985 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449293 | TGTCTAATCCCAAAG[A/C]ATCAACAAAAAAACT | 55626 |
rs751194537 | in-del | -/GTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427960 | TTGCAGTGAGCCAAG[-/GTT]GTTGTGCCACTGCAC | 55626 |
rs751196724 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514067 | GAGGAACGCATATTG[C/T]TCCTCTCCAGCAGCA | 55626 |
rs751253756 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411737 | GCCTCCCAAAGTGCT[-/A]GGATTACAGGCATGA | 55626 |
rs751268102 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517037 | ACCACTGGTGTCCAA[C/G]TGAGGTATACGAGGG | 55626 |
rs751276758 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465425 | AAATCCTGGGCACAC[A/G]TTACTACAGTTATGT | 55626 |
rs751285695 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579066 | AAAAAAAAAAAAAAA[A/G]ATAAGGAATGAACTT | 55626 |
rs751287907 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518965 | GTCAAAGAAAGCTCT[A/G]GAAAAGAAAAAAAGT | 55626 |
rs751290778 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413254 | GGTCCACTGCCAACA[A/G]AACAGGGGCCGTACT | 55626 |
rs751340591 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575239 | GAGGCAGGTGTATCA[C/T]CTGAGGTCAGGAGTT | 55626 |
rs751346316 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502993 | ATGAACCTGGGAGGC[A/G]GAGCATGCAGTGAGC | 55626 |
rs751347762 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480905 | GGTTTGGGGCACAGC[C/G]TCTTAAAGAGGGATC | 55626 |
rs751357096 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572775 | TCATCCCCCCACTGT[A/G]CATTTGTGGTCACCA | 55626 |
rs751361282 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592870 | TTGACCATCCTCTAC[C/T]AGACTCTAACCTCTA | 55626 |
rs751422579 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416790 | AAGTGGCATTTAGTC[A/G]GCTGGAACCTTGCAG | 55626 |
rs751424718 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426165 | TTGATTCAATTAGGG[C/T]GTACTGAGTAATGGG | 55626 |
rs751439079 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413822 | CAATACCCAGTGTCA[A/C]TGACTGTCTGTGAGC | 55626 |
rs751444685 | snp | A/T | 1.66244e-05 | 0.00288304 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512826 | CTCCTAGCAGAGATT[A/T]AAAAAATGGCAATAA | 55626 |
rs751448159 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533746 | TCTTTTTAAAATATA[A/T]GATCATGCTACTCCA | 55626 |
rs751451288 | snp | C/T | | | intron-variant, utr-variant-5-prime | AMBRA1 | GRCh38.p7 | 11:46591201 | AAATTCTACGCAGAA[C/T]TTATCAATTCCCAGT | 55626 |
rs751454251 | in-del | -/AAAAT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487105 | TCTACGAAAAGTACA[-/AAAAT]TAGATGGACATGGTG | 55626 |
rs751458401 | snp | A/G/T | 6.97075e-05 | 0.00590335 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397602 | CAGGGGAGGAAGAGG[A/G/T]CAGGGTTGGCTGGGT | 55626 |
rs751504100 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448952 | GCAATCATTAATAAT[A/C]TCCTAAAACAGAAAG | 55626 |
rs751515064 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494462 | AATGTGGTCCCTTAG[C/T]GTCTCAAACTGAAGC | 55626 |
rs751533029 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440454 | TAACAGTGGTTACAT[C/G]TGAGGAGGAGTGGTA | 55626 |
rs751543380 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457049 | ACATTCACATTAGGG[C/G]GCCCAGCTTCTAAAG | 55626 |
rs751596730 | snp | A/G | 3.41023e-05 | 0.00412917 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435064 | AAAGAAAGAAAAGAG[A/G]ATAAGAAACTTTGGA | 55626 |
rs751603016 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428591 | CTTCTTCTTCTTCTT[-/T]CTTTTTTTTTTAAGG | 55626 |
rs751612508 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546653 | GGAATGGAAGACAGG[G/T]AATTAGACTTCCTAT | 55626 |
rs751615485 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522658 | CTGGAATTTATTGAA[C/T]TCCATAATGTTGAAT | 55626 |
rs751659924 | in-del | -/ATAGTAGTAACTGCC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494866 | TTAACAGTCCATGCA[-/ATAGTAGTAACTGCC]ATTTATTAAGTATCT | 55626 |
rs751667852 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417011 | CCCCTCCTACTCCCT[A/G]CTTCAAGACCAGATA | 55626 |
rs751678308 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469273 | ACTCTCCAGCTCCTA[A/G]TCTTCCCTTCCTCCA | 55626 |
rs751679893 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579413 | GGTGAGCCGAGATCA[C/T]GCCATTGCACTCCAG | 55626 |
rs751686632 | snp | C/T | 0.000153164 | 0.00874978 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542187 | CTGGCTGCCACTTGA[C/T]GGCACACTCTCAAAG | 55626 |
rs751686720 | snp | C/G | 1.67829e-05 | 0.00289675 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434923 | AGGATGCCTTCATCA[C/G]GAAAGCCCCTCTGGC | 55626 |
rs751706174 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521149 | ACTGGCGACAAGACT[C/G]TCAGACAAGGTTGCT | 55626 |
rs751754356 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536564 | TCTATAGTAGTCAGG[C/G]TAAGAAGACTGCTAC | 55626 |
rs751757505 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415632 | TTTTGGGCCCTAAGG[C/T]TTGAGGCATTTGCCA | 55626 |
rs751759674 | snp | C/T | | | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430686 | CTTAAAATAAATCAA[C/T]GCTCTGGAGGATGTT | 55626 |
rs751774122 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429581 | CCCTATTCCTAAGTA[A/G]CACAGCACTTACTGA | 55626 |
rs751775365 | in-del | -/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592082 | CCCAAGTAGCTGGGA[-/T]TTACAGGCATGCGCC | 55626 |
rs751804797 | snp | A/G | 0.000396466 | 0.0140739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547795 | TATCACAAATCTTAA[A/G]TTATAGATAAATACT | 55626 |
rs751812076 | snp | A/T | 1.73881e-05 | 0.00294852 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397929 | CTCCACTGGCACCAT[A/T]CTCTGAACCCTCACC | 55626 |
rs751817618 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399625 | CCACCTAGGCCTCCC[-/A]AAGTGTTGGGATTAC | 55626 |
rs751822134 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482898 | CCTGTAGTTCCAGCT[A/G]CTCAGGACGCTGAGG | 55626 |
rs751833192 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498280 | GAGTACACAAATATG[C/T]TGGTATTGCTCCTCC | 55626 |
rs751835444 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473884 | CTCGATCTCCTGACC[C/T]TGTGATCGGCCCGCC | 55626 |
rs751840450 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445543 | GTAAGATACCTGAAC[A/G]ACTTTATTAAAAGGA | 55626 |
rs751845986 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535418 | TTCACTCTCATGATG[C/T]TCAGACTCCAAAACA | 55626 |
rs751846114 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551770 | CAGTGGCTCATGCCT[A/G]TAATCTCAGCACTTT | 55626 |
rs751850076 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571689 | TCAATCAATCAATCT[-/T]TTTTTTTTTTTTTTT | 55626 |
rs751860258 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550151 | AAGATCAGGAGAGTT[G/T]ACTTGTTAGAATGCC | 55626 |
rs751864172 | in-del | -/TAATGTGGGGATA | 7.57533e-05 | 0.00615393 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508407 | AACACAAACTAGCAC[-/TAATGTGGGGATA]TAATGTGGGGAATAC | 55626 |
rs751889756 | snp | G/T | 2.57543e-05 | 0.00358838 | intron-variant, synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543216 | CGGTGGGGGTGAGGG[G/T]GTAGCAGAATCTTGC | 55626 |
rs751890255 | snp | A/G | 1.65277e-05 | 0.00287464 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547176 | AAGGCCTGAGATGGT[A/G]GGATGAAAAGTGACA | 55626 |
rs751907339 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409076 | CATGGGATAAAGAGT[A/G]AGCACTAGAAGAAGG | 55626 |
rs751914224 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497190 | AATTTTATGTTATGT[G/T]TATTTTACCAACATT | 55626 |
rs751917921 | snp | C/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594367 | CACTCTTTATCCCAA[C/T]TGAGCAAATTAGTTA | 55626 |
rs751955166 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422347 | AAGAAATTTCTTAGA[A/G]TTAGTGCAGTCTCAG | 55626 |
rs751962314 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421616 | AGAATCTGGCCCATT[C/T]TGAAAAGCACCCAGA | 55626 |
rs751981685 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567722 | CCCCACCCCAACCAG[C/T]GATTCCTCTGTAGCC | 55626 |
rs751992706 | in-del | -/TGAG | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396799 | TACACCCCCCACTCC[-/TGAG]TGAGGACCTGCCCAC | 55626 |
rs751999905 | in-del | -/A | 0.441806 | 0.223559 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547884 | TACTCTCTGGGAGAC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs752003088 | snp | G/T | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543343 | TGCAGGAGGGCACGC[G/T]GACGGTAGTGGGATA | 55626 |
rs752004951 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459231 | AGATGTATAAATATA[C/T]GTATGTTTTTTATTA | 55626 |
rs752010183 | snp | A/G | 3.30295e-05 | 0.0040637 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410283 | AAACATACCCAGGCC[A/G]CTCGCTGCTCCTGCT | 55626 |
rs752038548 | in-del | -/AAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498557 | ATAAGTGCTGAATAC[-/AAG]AAGATGTATTTCCAG | 55626 |
rs752055334 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475821 | GATTCGGAGAAAGGT[A/G]GAACAGGAAACTGTG | 55626 |
rs752093987 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494570 | GGGGGGTTGTCTTAC[A/T]TTATTTATCATTTTA | 55626 |
rs752128984 | snp | A/G | 1.80919e-05 | 0.00300759 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397434 | TCGAGGGGAGGCACC[A/G]GTGCAACGTTTGTCT | 55626 |
rs752159067 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587716 | TGTTTCAGTCTAAAT[C/T]TCAATATTTATCAAA | 55626 |
rs752159469 | snp | A/C | 0.000199664 | 0.0099896 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508167 | GAGAGGAGAGGGAAG[A/C]AAGCAAGCTGAGTAT | 55626 |
rs752178984 | in-del | -/TTATAT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459427 | CAGAGACACTGATAC[-/TTATAT]TTATAACAACTTAAT | 55626 |
rs752195649 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513543 | GGTATGACTACATAC[A/G]TGAGAACACTGGGCC | 55626 |
rs752213791 | snp | G/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594135 | CAGCTCAACTCCTAC[G/T]CAAGGTCCGGCTCCT | 55626 |
rs752215736 | in-del | -/TTTC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549812 | TTTGTGACACTAGCT[-/TTTC]TTTCTTTTTTGGGGG | 55626 |
rs752230741 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543692 | TGAGGGGAAGCAAAA[C/T]GTCAACCAGCCAGAG | 55626 |
rs752241275 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476015 | AGAAAATGGTCACTC[C/T]TCCATATAGGGGAGA | 55626 |
rs752251171 | snp | A/G | 2.64044e-05 | 0.00363339 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494162 | AGGTGCAGACATCCG[A/G]GCATTGCGTGGAGCT | 55626 |
rs752251418 | snp | A/C | 8.23811e-05 | 0.00641746 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542742 | AGAGCGGGAGTTCAG[A/C]CTGAGTACTGTCCGG | 55626 |
rs752260143 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588043 | AAGTCAGAAAAGAAA[C/T]AGAAGGAGGATGGGT | 55626 |
rs752282968 | snp | A/C | 1.65674e-05 | 0.00287809 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417867 | ACTGATTACCCCAGT[A/C]CTCGGCCCCAGTGAT | 55626 |
rs752297556 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459118 | ACCACGCAGCCACTA[C/T]TAAGAATAAAGCAGA | 55626 |
rs752317488 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438324 | CCTCCCAATTAGAAA[C/T]GATTTCCAAGTGAAA | 55626 |
rs752321403 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427589 | GAGTTTCTGACTCAG[C/T]AGATCTTAAGTGGGG | 55626 |
rs752332809 | snp | C/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452216 | GATCCATTTCATTTC[C/G]TTAATAATTAAGAGT | 55626 |
rs752337636 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436494 | AATAAAATAATGATA[A/T]CCAAATACTCACTGC | 55626 |
rs752343453 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511354 | ATCAATCCTTATGTT[C/T]CCTGATCCTTAAGTT | 55626 |
rs752375008 | snp | A/G | 1.65059e-05 | 0.00287275 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545741 | CAGGGAGGCAATGGC[A/G]TTGTTGCTATCTGTG | 55626 |
rs752379692 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491228 | TAAGAAAAAGAATGA[C/T]ATTTTAATGTTTTGT | 55626 |
rs752388083 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560048 | GATTGCAAAGGAAAC[G/T]ACAGTGATTATAAAA | 55626 |
rs752390256 | snp | A/G | | | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542011 | GCCTCCTGTGACACA[A/G]TTCCAGATCTGCTGG | 55626 |
rs752398141 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504121 | TAGCAAAGCCTTTGC[C/T]ACAGTATCCCTTTGC | 55626 |
rs752440289 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577156 | AATAAGCCAATGCAC[A/C]TGCATGTTCAAAGCA | 55626 |
rs752473051 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411336 | GTGCTTCCTTCCTAA[A/C]CATGGGTGTTGGCTA | 55626 |
rs752473960 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398340 | GCTGAGCTGGGGTAT[A/G]CCACCCTTTCTCTGC | 55626 |
rs752480895 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531810 | CCCCCAATGACGAAT[A/C]CATTCGATATCTAAA | 55626 |
rs752487414 | snp | C/T | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542075 | CCTGGTTAAAGGCCA[C/T]CCCCACAGTCCTCTC | 55626 |
rs752487598 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467652 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 55626 |
rs752488700 | snp | C/T | 1.66283e-05 | 0.00288338 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397696 | TGCCAGTTGCCCGGC[C/T]TCTGGGAGCAGTCCC | 55626 |
rs752501415 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520054 | TGAGGCAGGAGAATC[G/T]CTTGAACCCAGGAGG | 55626 |
rs752557139 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445935 | AACTACAAACAGGAA[A/G]ACAGTTAAGGAATAA | 55626 |
rs752612952 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484185 | GAAATGTAAAGAAAT[A/G]TAACAAAGAAAGCTG | 55626 |
rs752625331 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542616 | AAAACCCCTCCCTTC[C/T]GTGGCTGAAGTGTAC | 55626 |
rs752645922 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496360 | GCACTCCAGCCTGGG[C/T]GACAAGAGTAAAACT | 55626 |
rs752657814 | in-del | -/CATATCTA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583197 | TCAGAAATAATGCCG[-/CATATCTA]CAACTATCTGATCTT | 55626 |
rs752660817 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519098 | GCGCGATCTTGGCTA[A/G]CTGCAACTTCTGCTT | 55626 |
rs752671915 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465572 | CAACAGGCTAAGATA[C/T]ATCACAGAGGAAGCC | 55626 |
rs752674159 | snp | A/G | 3.36395e-05 | 0.00410105 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547113 | TAAGGAAATACTCAC[A/G]TGTAAATCCCAAATC | 55626 |
rs752676972 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566133 | CAATTAAAAAGAGTG[G/T]AATTGGTCAGGGCGC | 55626 |
rs752683177 | snp | C/T | 1.6546e-05 | 0.00287624 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397790 | CTGCGGTGAATGCGG[C/T]GGCTGACGATGATGT | 55626 |
rs752709006 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556155 | TTTGGAAACTCCATA[C/T]GGATGGAAATACACA | 55626 |
rs752729161 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575388 | CTTGAACCCGGAAGG[C/T]GGAGGTTGTGGTGAG | 55626 |
rs752748864 | snp | G/T | 2.15575e-05 | 0.00328303 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547822 | TACTGAGTACCTGTC[G/T]GGGCTGAAGGCCAAT | 55626 |
rs752749076 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561999 | CACTGAGGATACTAT[A/G]GTAAAGAAGAACATT | 55626 |
rs752750370 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533998 | GGTTTGTTTTCGCAC[A/T]TCTTTAAGGTCTCCT | 55626 |
rs752761814 | snp | A/T | 1.66502e-05 | 0.00288527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548220 | ACCAGCACAAATCCT[A/T]TGTGAAATATAGCCA | 55626 |
rs752763831 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563515 | CAGGCATGAGCCACA[C/T]GGCACCCTGATGAGA | 55626 |
rs752809834 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403011 | CAGGGATCCAGGCAC[A/G]GTGGCAGACAGGGGG | 55626 |
rs752810118 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432613 | AGGGACCTGAGGGAT[A/G]TCCCTCTAAGGAGCT | 55626 |
rs752828335 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401777 | GTCTCCTCCCCTTCC[A/G]TCTAGTCTCCACACT | 55626 |
rs752934046 | snp | A/C/G | 0.000102779 | 0.00716799 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408574 | CTCAGTCTGTGTTTC[A/C/G]GCATTCTGCAGCTGA | 55626 |
rs752944933 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471259 | CCAGCCTGGCCAACA[C/T]GGCAAAACCCCACCT | 55626 |
rs752958728 | in-del | -/AT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576549 | AATGATCCCAGAAAG[-/AT]ATAGTCTTTGGAGAA | 55626 |
rs752963747 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577605 | GATGGCTAAATTTAC[A/G]TGAAGTGAATTTCAG | 55626 |
rs752977541 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485237 | GCCCCTATGCCCGGC[C/T]TCAAGAAGCCCAAAC | 55626 |
rs752987230 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522912 | TATACTGCAAACACT[A/T]TATAATAGGAAGTAA | 55626 |
rs752999953 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468230 | GGGACCAATCACTAA[C/T]ACAAAAAAAAGTGGG | 55626 |
rs753002167 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505881 | ACAGCTTGAAGGCAT[A/G]AGCCCCACATTTCAC | 55626 |
rs753008803 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396963 | GGGGTAAGACGACGA[-/AG]AGAGGCTGAAGCTCT | 55626 |
rs753041876 | snp | C/G | | | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396202 | CTGGGGAAGCAGGAA[C/G]TGGTGGCGTACAGAG | 55626 |
rs753044709 | snp | A/T | 1.64933e-05 | 0.00287165 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543953 | CAGTTTAGCTGGAAT[A/T]GGAACTGCTGGACTA | 55626 |
rs753048389 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487768 | AGGAATAAAAACATC[-/A]GAAATACAAAAAACA | 55626 |
rs753049310 | snp | C/G | 7.23484e-05 | 0.00601407 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397442 | AGGCACCAGTGCAAC[C/G]TTTGTCTCTACCTGT | 55626 |
rs753061754 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494114 | CTGTTGCTAGCAACT[C/T]GGTTCTTACCTTGGG | 55626 |
rs753069469 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499976 | AATTTTTCTAAGATA[C/G]TTAACTCCAACAAAG | 55626 |
rs753071339 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484359 | GAGAGAAGTAAAAGA[A/G]TTCTGGCATTATACT | 55626 |
rs753072354 | snp | C/T | | | intron-variant, utr-variant-3-prime | AMBRA1 | GRCh38.p7 | 11:46430908 | GTGCAAAGAGGGAGA[C/T]GCTGTACTGTCCCAT | 55626 |
rs753084009 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445828 | TTTCTCAGTACATGA[C/T]GAACAAAATGCTAGT | 55626 |
rs753123371 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420214 | TCCTGTAGGACTCAA[A/C]TCCAAATGTAAGGAA | 55626 |
rs753129374 | snp | C/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542322 | AGCACGACAGCGATT[C/G]AGGTGGCCACGGGAC | 55626 |
rs753150003 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46417968 | AGGCCAAGCCAAGCC[C/G]TGGCTCAGGCAGCCA | 55626 |
rs753153424 | in-del | -/A | 1.84613e-05 | 0.00303814 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408717 | TGGTTCTAGGGAGAG[-/A]AAGGCAGACTAAAGT | 55626 |
rs753166618 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455453 | ATGCTTTGAAAGAGG[A/T]GATGCATAACTAGGT | 55626 |
rs753175171 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527755 | ACCACATTTATTTAT[C/T]GCCTCACACCTGTTA | 55626 |
rs753180735 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406775 | TAATCCCAGCTACTC[C/G]GGAGGCTGAGGCAGA | 55626 |
rs753184162 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550571 | ACTTTTTTAATGGGG[C/G]GAGATGCTGAAAATA | 55626 |
rs753208419 | in-del | -/C | 1.65007e-05 | 0.00287229 | frameshift-variant, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508198 | GTACTTACTCAAAGT[-/C]CTCAAATTCCAAGTC | 55626 |
rs753219457 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514824 | CATAAAATAACGGCA[C/T]GTCTTTGAGTCTTTT | 55626 |
rs753222142 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582111 | CAGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs753230724 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498632 | AGGATTAATTGCCTC[A/G]GAGAGAGGCTGTAAT | 55626 |
rs753260798 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440054 | GTATAGAGTGTGGTA[C/T]GGCAATAACTACACA | 55626 |
rs753307934 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46417993 | CAGCCAACGGGCAGA[G/T]TTGATACTGACATGT | 55626 |
rs753337856 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479414 | AAAAGCAAACATGAC[A/G]TAAGGAGAGATTCAA | 55626 |
rs753381714 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411415 | GGTCCCAGGAGGTCC[C/T]AGGAGGCTGTGCTGC | 55626 |
rs753385923 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552158 | CAGATCACTTGAGGT[C/T]AGGAATTCGGTATTA | 55626 |
rs753398189 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409706 | TTGAGACTATCACCA[A/G]ACACTCACATTTCTA | 55626 |
rs753435982 | snp | C/T | 1.80833e-05 | 0.00300688 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397491 | GGCCTGCAGCGTCCC[C/T]CCTGCTGCTGCCACC | 55626 |
rs753438290 | snp | C/T | 3.30333e-05 | 0.00406393 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508305 | CGCATGGAGCGCTGG[C/T]GAATACTGTCTCTCC | 55626 |
rs753468010 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530467 | GCACACGATTCCCAA[C/G]AAAGAAAGTGAGGCT | 55626 |
rs753479444 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439971 | TTGATAGTACATTCT[A/G]TCAGCAAGAGTTTAT | 55626 |
rs753482143 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538272 | ATATAAATAATGTAA[C/T]TACTGTATTAATATA | 55626 |
rs753489758 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422930 | TGAGGCTAGAAGAGC[G/T]GTGGAAAAAGGTGCA | 55626 |
rs753497631 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513407 | TCTAGCCCAATAACA[A/G]ACTCAACTGATCATA | 55626 |
rs753502805 | snp | C/G | 1.70688e-05 | 0.00292132 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418082 | AGAGGGAAAAAAAGA[C/G]AATGGGAGGAGAAAC | 55626 |
rs753519749 | snp | G/T | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542756 | GACTGAGTACTGTCC[G/T]GGTCCACTCAGATCC | 55626 |
rs753519815 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543730 | AGTGACAAGCTATCC[A/C]ACACTGTCTAGTGAT | 55626 |
rs753528200 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478154 | AATGCCAAGTAAAAG[C/T]TAAGTCCTATGCTTG | 55626 |
rs753537765 | in-del | -/CT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444846 | AATATGAGAAAAGTA[-/CT]CTCTGCACTCTTCCG | 55626 |
rs753544048 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438608 | GAGCCCCCTGGATTT[C/T]AGAATAAGGCCTGTA | 55626 |
rs753559474 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492787 | AGGCACAGTGGCTCA[C/T]GCCTGTAATCCCGGC | 55626 |
rs753583619 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416657 | AAAGGCAACACGGAC[A/T]CTTCCGATAACCAGA | 55626 |
rs753604365 | snp | C/T | 1.65184e-05 | 0.00287384 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543405 | GTCATCACCCTGCAA[C/T]GTGGACCAGCATGGG | 55626 |
rs753608246 | snp | C/T | 1.65644e-05 | 0.00287783 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547143 | CCTAACCTCCCCATC[C/T]AGGCAGCCAGAAGCA | 55626 |
rs753616888 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561101 | AAGAATATTGTTGGG[C/T]CAGGCGCAGTAGCTC | 55626 |
rs753619928 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401074 | CTACCCTGGGAGCCA[A/C]GGGCTGCCTGGGGAG | 55626 |
rs753632637 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452391 | CCTCACTATGTTGCC[C/T]GGCTTGCCTTGAACT | 55626 |
rs753632827 | snp | A/C | 1.71167e-05 | 0.00292542 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547303 | AAGAGAGTCCTAGAA[A/C]ATCAAAGAGTAGAAC | 55626 |
rs753646559 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491403 | TATCTCATATGATTA[C/G]TGCAAGACAGAAACG | 55626 |
rs753692820 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474271 | AAATATTAGAACCAC[C/T]GGAGGAAAATACTTT | 55626 |
rs753710719 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469174 | AGATGTAATAAAATA[C/T]TAGATTTAGTTAGTT | 55626 |
rs753714405 | snp | A/G/T | 3.31094e-05 | 0.00406864 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397801 | GCGGTGGCTGACGAT[A/G/T]ATGTTGTTGCCGAAG | 55626 |
rs753737892 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424515 | TCTACTTCTGTGCTA[A/C]AAGAAATACTGAGGC | 55626 |
rs753763355 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415459 | GAGTGAAAAGCGCTC[G/T]GGATAGTAAAGTGAG | 55626 |
rs753774348 | snp | A/C | 3.29707e-05 | 0.00406008 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508210 | AGTCCTCAAATTCCA[A/C]GTCGGTTCCCTCTAC | 55626 |
rs753796583 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484154 | GGTAGGGGATATCTA[A/C]TCCTAAAGAAAGTTT | 55626 |
rs753796642 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467885 | ACATGTTCATTCTTT[C/G]ATGTTTACCAGAAGT | 55626 |
rs753804395 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504487 | CCACACCTTTACCCT[C/G]CTTATGAACATCTTT | 55626 |
rs753805282 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557300 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs753813542 | snp | C/T | 1.6522e-05 | 0.00287414 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542864 | GACCCAGACTGAGGT[C/T]GCGGAGCGTGTTGCC | 55626 |
rs753826350 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426633 | TCTCTGACAAATCAC[A/G]CCAGAGACACCTCTT | 55626 |
rs753849879 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587681 | CTCTGTCAGCCCTTG[C/T]TTATTTCCTTCAGAA | 55626 |
rs753866537 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559097 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 55626 |
rs753871891 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577870 | CAGGAGAATCACTTG[A/C]ACCCAGGAGGAGGAG | 55626 |
rs753885370 | snp | C/G | 1.689e-05 | 0.00290598 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542963 | ACGAGGCCTGCTCCG[C/G]GGGATGGAAGGGCTC | 55626 |
rs753895958 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546941 | CCAGGCATGATGGCA[C/T]ATGCCTGTAATCCCA | 55626 |
rs753897411 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548470 | CTAAAATGAGGCCAT[A/G]CAGGTCCTTGTAAGT | 55626 |
rs753899128 | snp | A/G | 1.99543e-05 | 0.0031586 | intron-variant, synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543054 | CTGGTGTGGCAAGAG[A/G]GAAGGAACTCGAGTG | 55626 |
rs753926346 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467325 | AATAGTTACATCCCA[C/T]GTTTGGGTTAATGTA | 55626 |
rs753948821 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593072 | CTACACTAGTTAAAA[C/T]GATACAGACTTTGAA | 55626 |
rs753950470 | snp | C/T | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548328 | ATGGCCCGAGCACCC[C/T]GTTCTCGCCCCCAGA | 55626 |
rs753958863 | in-del | -/GTCCCAGGAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411391 | AAGACGAGGGACTGT[-/GTCCCAGGAG]GTCCCAGGAGGTCCC | 55626 |
rs753963704 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419576 | CAGGGCCTATGAAAA[A/C]GACAGGAAGCTGAAA | 55626 |
rs753983804 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565783 | AAAATTCAGATTTTT[G/T]TTTTCAGAAGGGGTC | 55626 |
rs754032101 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458584 | TCAACTTTTCCTTCA[C/T]ATAATATTTTTTAAG | 55626 |
rs754047159 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585047 | GCACTCCAGCCTGGG[C/T]GACTGTGCTCTCTGT | 55626 |
rs754047733 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403570 | AGTGCTGGAAGCCAA[C/T]GGTGAGCCCAGGAAA | 55626 |
rs754066286 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526078 | GGCAGGGTGGAATAT[A/G]CCTGTAATCCCAGCT | 55626 |
rs754110925 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413701 | TCGCCATGTTGGCCA[A/G]GCTGGTCTCGAACTC | 55626 |
rs754118986 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499558 | AATACATTGAGGCTC[A/G]ACAGGTACCATATAG | 55626 |
rs754124723 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507981 | GAGGTCTCTGTCCTC[A/G]CGCGCCAGTGAATCA | 55626 |
rs754166222 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525025 | CAGATGTGGGCTGGG[C/T]ATGATGTCTCATGCC | 55626 |
rs754166282 | snp | A/C | 1.76767e-05 | 0.00297289 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46443596 | CATCACCGATCACTG[A/C]CCCTTATGAGGAAGA | 55626 |
rs754177766 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433997 | GCGCATGCCTGTAAT[A/G]CTAGCTACTCGGGAG | 55626 |
rs754188719 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410053 | GGATGGGAGAGGGCC[-/A]GGGGGTGGTTCTACA | 55626 |
rs754189496 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542444 | CCTGTTGGGTCTGGG[A/G]AGCTTCCCCACTCAG | 55626 |
rs754196190 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580490 | TCTAATCCAAATCTG[C/T]TCCTCCTCCAATGTT | 55626 |
rs754204728 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418819 | TTAGCTAACTAACTT[A/C]ATTGCTTTTAAATTA | 55626 |
rs754214667 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579749 | ATGGATTCTTGTTCT[C/G]TCACCCAGGCTGGAG | 55626 |
rs754251902 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526547 | AAAAAAAATTAAAAT[A/T]AAAAAAAAAAAAAAA | 55626 |
rs754252108 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538565 | GTGGTGCAATCTCGG[C/G]TCACTGCAACCTCCG | 55626 |
rs754257749 | snp | A/T | 1.79851e-05 | 0.00299871 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397558 | GAGGGTTGGTCCCTC[A/T]GCGCTGGGAAGGGAA | 55626 |
rs754264595 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396468 | TTTCCCTCATTAGCT[A/G]TAGACTATCCCCTCT | 55626 |
rs754267537 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432740 | GATTGCACAAAGTAC[C/T]AAGGAAATTCACAGG | 55626 |
rs754268638 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553569 | GGCCAACATAGTGAA[A/G]CCCTGTCTCTACTAA | 55626 |
rs754270420 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486513 | CTAGATGCCCACCCC[A/G]GTTGACTAAGTGAGA | 55626 |
rs754283826 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398017 | AGGTGGGCAGCCACC[A/G]GTAGCAGCTGGGGGA | 55626 |
rs754284161 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447987 | CATCTACTCCAATCT[C/G]TGTGTGTATTTCATC | 55626 |
rs754284387 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397160 | GCCCATGTTACTAGG[A/C]GAAAGTGGGGTGCCT | 55626 |
rs754296546 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434395 | CACCCCACCCTCCCG[C/T]AAAACAAACAAACAA | 55626 |
rs754307378 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500074 | GCCTAGGATGGGAAA[A/G]GGGCCGGCTCAAGAT | 55626 |
rs754310820 | snp | C/T | 1.66363e-05 | 0.00288407 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548228 | AAATCCTATGTGAAA[C/T]ATAGCCATTTTCCTT | 55626 |
rs754337642 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521040 | TCACATCCTAATTAA[C/T]ATGTAATAGGAAACC | 55626 |
rs754351460 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431708 | AGCTGTTGGGACTGG[A/G]ATTCCAGGTGGTGAA | 55626 |
rs754356287 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501764 | CACATTTATTTCAAT[A/G]TTTAATATAAGAAGT | 55626 |
rs754360086 | snp | C/T | 2.03486e-05 | 0.00318965 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408496 | TCCCACCCCCTCCAG[C/T]GCCACATGGCTCCTA | 55626 |
rs754378533 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470667 | CTCAGAAGGCTAAAG[C/T]GAGAGGATTGCTTGA | 55626 |
rs754407686 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420192 | CATTAGGAACCTCCT[A/G]CACCCTTCCTGTAGG | 55626 |
rs754440743 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554670 | AGAGATTTTACTCTG[C/T]TCCCTGTAAAGAACA | 55626 |
rs754456553 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527227 | GCTCACTCCTGTAAT[A/C]CCTGCATTTTGGGAA | 55626 |
rs754474668 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436324 | CTCTATTTGTTCTCC[C/T]TTCCCTGTGTGTTGC | 55626 |
rs754496852 | snp | A/C | 0.000164818 | 0.00907644 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542605 | CCTGATGCCGGAAAA[A/C]CCCTCCCTTCTGTGG | 55626 |
rs754526639 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510444 | CTCAAGTCAATCAGA[C/T]TAGAAAAGAATATAC | 55626 |
rs754535073 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590543 | ATATACAAAACTAAT[A/C]TTTTTCAAGTGATAT | 55626 |
rs754542874 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540293 | CTTGGTTTCTTAGAG[C/T]AGTAACTGAAGACAG | 55626 |
rs754578069 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586331 | CAAGAATCGCTTGAA[C/T]CCAGGAGGCAGAGGC | 55626 |
rs754594941 | snp | A/G | 5.62161e-05 | 0.0053014 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543140 | TGGGGTAACTGACCC[A/G]CTGTCGGAGCCTGAT | 55626 |
rs754646776 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577208 | GGCAGAAACAGCCCA[A/T]ATGTTCTTCAATGGA | 55626 |
rs754681275 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538446 | TATATTTTTTGGCAC[C/T]AGAAAAGAAAAAAAT | 55626 |
rs754704605 | snp | G/T | 0.000828998 | 0.0203424 | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548389 | CCTTCATGGCGCTCA[G/T]TAGCCACTGTCACAC | 55626 |
rs754709228 | snp | A/G | 0.000107231 | 0.00732147 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397572 | CAGCGCTGGGAAGGG[A/G]AACAGGAATGGGGAC | 55626 |
rs754721536 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417779 | AAGAGGGCCCTTTAA[C/G]GAGTGGCGCTGAGAA | 55626 |
rs754722821 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455380 | CTACTTTCTATGAAT[C/T]TGACTACTTTAGTTA | 55626 |
rs754723478 | snp | C/T | 5.22411e-05 | 0.00511056 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494150 | GCGTCCAAGCGAAGG[C/T]GCAGACATCCGGGCA | 55626 |
rs754741954 | in-del | -/CA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437563 | TTCTGTTTACAATTT[-/CA]TTCTCACATTTGCTG | 55626 |
rs754744727 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556609 | ATATATATGGGCCCC[A/G]CAGTCAGAATGGTTG | 55626 |
rs754759876 | snp | A/C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465482 | TCTAAGTTTTTACCA[A/C/T]ATTTTCTCAGAGAGT | 55626 |
rs754783552 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478881 | GCTGAAGCTTTCCTC[A/G]GTATATGTAAGGACA | 55626 |
rs754784906 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502460 | AATGAAGTAGATAAT[A/G]CCTTATCCCTCTCTG | 55626 |
rs754805933 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413296 | ATGTGTTGCTCCACT[A/G]TGCCTCCCCATCCCA | 55626 |
rs754819622 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517047 | TCCAAGTGAGGTATA[C/T]GAGGGGTTGTGCTAT | 55626 |
rs754829869 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480915 | ACAGCCTCTTAAAGA[A/G]GGATCTCTAACCCTT | 55626 |
rs754832450 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575262 | CAGGAGTTCGAGATC[A/G]GCCTGACCAACATGG | 55626 |
rs754834217 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554961 | AATGCCGGTCAGGCA[A/T]GGTGGGAGGCCAAGG | 55626 |
rs754847927 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561199 | TAGCCTGGCCAACAC[A/G]GTGAAACCCTGTCTC | 55626 |
rs754849712 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463793 | CAGGGGAAATATAAC[G/T]GCAGCCAAAACAAAG | 55626 |
rs754871969 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442241 | TCTGCCACACAGGTT[C/G]GAGCAATTCTTGTGC | 55626 |
rs754883819 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564671 | AAAGAATTAGTAAAT[A/C]TGAATGAATCTGAGT | 55626 |
rs754888935 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592881 | CTACTAGACTCTAAC[C/T]TCTAACCACAAACAC | 55626 |
rs754893789 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426443 | AATGACAGGGGCTCA[A/G]TAAAGTTTTTTTGAG | 55626 |
rs754906404 | snp | C/T | | | intron-variant, utr-variant-5-prime | AMBRA1 | GRCh38.p7 | 11:46591248 | TTCTCTACATTCTTT[C/T]CTCTGATATACATTC | 55626 |
rs754916234 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424863 | ACAAATAGGCCAGGT[A/G]TAGTGGCTCATGCCT | 55626 |
rs754920235 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479946 | CATTGGGCTAGAAGA[A/C]AGGTGTTGGCTGGCC | 55626 |
rs754955845 | snp | C/T | 1.66757e-05 | 0.00288749 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545595 | ATGCAGATGGGGCAG[C/T]GCACTCACCGGACCC | 55626 |
rs754961378 | in-del | -/TAAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496369 | CCTGGGCGACAAGAG[-/TAAA]ACTCTGTCTCAAATA | 55626 |
rs754994855 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452521 | ATGGATTATCTGAGC[C/T]CTCTGTAAATAAATA | 55626 |
rs755027819 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551765 | AGGTGCAGTGGCTCA[G/T]GCCTGTAATCTCAGC | 55626 |
rs755049350 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432586 | AGCCATCTACATGCA[C/T]AGCACTAAATGAGGG | 55626 |
rs755051945 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522688 | TTCTTAGCTAATTTT[A/T]TTCAGAAGCACAGAT | 55626 |
rs755054005 | snp | A/G | 1.65578e-05 | 0.00287726 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435065 | AAGAAAGAAAAGAGG[A/G]TAAGAAACTTTGGAG | 55626 |
rs755063647 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518755 | AGTATTGTGCACTGG[-/A]AAAAAAAACATCAAA | 55626 |
rs755064472 | snp | C/T | 1.65671e-05 | 0.00287807 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397809 | TGACGATGATGTTGT[C/T]GCCGAAGCCGCCCAT | 55626 |
rs755083758 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561902 | AAATAAAGAACACTT[A/G]AAGATGGGGAAGGAT | 55626 |
rs755100740 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504713 | CCTGATGCTGACCAA[C/T]CTCCAAAGCCACCCT | 55626 |
rs755102839 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467744 | TCACCATGTCAGCTA[A/G]GCTGGTCTCAAACTC | 55626 |
rs755108395 | snp | G/T | 1.65252e-05 | 0.00287443 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547178 | GGCCTGAGATGGTGG[G/T]ATGAAAAGTGACACA | 55626 |
rs755114985 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548775 | AGGAGATTGGATTGC[C/T]TGAGGTCAGGAGTTT | 55626 |
rs755127290 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400011 | AGAAAAGGAGCTAAC[A/G]CACAGCCCAGGCACT | 55626 |
rs755140253 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521164 | CTCAGACAAGGTTGC[C/T]AGATGCCCAAAACCT | 55626 |
rs755141834 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537144 | TCCTAGAAGCATTGT[C/G]TTAGTTACCATTCTA | 55626 |
rs755151212 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417109 | TAGGTTGGCGTGCAA[C/T]GGCATGATGTCAGCT | 55626 |
rs755174127 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578162 | AAGGACAATGTCCAT[A/G]TAAGCATTTCCCAGG | 55626 |
rs755199899 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547798 | CACAAATCTTAAGTT[A/G]TAGATAAATACTGAG | 55626 |
rs755203711 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468249 | AAAAAAAGTGGGGAG[A/G]GGTGGCGGGCAGCAT | 55626 |
rs755238909 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415662 | AACCTGACCCAAGAA[A/G]TCAGGAGAAACAGCA | 55626 |
rs755252829 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445579 | CTTGATTTTTCTATG[C/T]CTCTTTGATAATGAA | 55626 |
rs755254795 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526696 | GGAAGATCAGCAGAA[G/T]AACTTTCCAACTGAG | 55626 |
rs755262492 | snp | A/C | 1.76586e-05 | 0.00297136 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397937 | GCACCATACTCTGAA[A/C]CCTCACCTGGCAGAT | 55626 |
rs755278006 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577536 | TGTTTTGAAACTAAA[C/G]AGGTTGCAGAACATT | 55626 |
rs755281658 | snp | A/G | 2.24333e-05 | 0.00334906 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543223 | GGTGAGGGGGTAGCA[A/G]AATCTTGCACTGTGC | 55626 |
rs755291749 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482936 | ATCATTTGAACCTGG[A/G]AGGCGGAGGTTGCAG | 55626 |
rs755297972 | in-del | -/AAAAA/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579045 | CCACAAGAAAGCAAT[-/AAAAA/T]AAAAAAAAAAAAAAA | 55626 |
rs755301496 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535432 | GCTCAGACTCCAAAA[C/G]AAAAGATGAGAGCAC | 55626 |
rs755304341 | snp | C/T | 4.9436e-05 | 0.00497148 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542794 | CCAGGAGCTATTTCT[C/T]GGTGATACCTAGAAG | 55626 |
rs755308351 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487889 | CTAGATAAAAAACAA[C/G]CTCCAATCATATGCT | 55626 |
rs755323618 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490166 | AATGTCAGCAGGGGG[A/C]GCTCCTCAGACTTTT | 55626 |
rs755331256 | snp | C/G | 1.80912e-05 | 0.00300754 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397435 | CGAGGGGAGGCACCA[C/G]TGCAACGTTTGTCTC | 55626 |
rs755350957 | snp | A/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594466 | AGAGAGAATTCAAGC[A/T]GAGGAACAAAATGAA | 55626 |
rs755351365 | snp | C/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451805 | GCTTGGCTGTTATAT[C/G]AACCTGCCCTGGGCT | 55626 |
rs755355316 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550321 | ATGTGCCTATATACC[C/T]CAAGGTGGAGTACAT | 55626 |
rs755388126 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498363 | CAACAGCCTGAAGCT[A/G]ACTTTGAGCCAGCAG | 55626 |
rs755419125 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497266 | TAATGGCTTTATAGT[A/G]TTTAGAGATTAGTGG | 55626 |
rs755428428 | snp | C/T | 1.69241e-05 | 0.00290891 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434934 | ATCAGGAAAGCCCCT[C/T]TGGCTGCTGGGGATG | 55626 |
rs755442064 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548971 | ACTCCAGTGCCTGGG[C/T]GACAGAGCAAGACTC | 55626 |
rs755464260 | snp | A/C | 1.702e-05 | 0.00291714 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542194 | CCACTTGATGGCACA[A/C]TCTCAAAGGAGCTGG | 55626 |
rs755473473 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407551 | CTTATGGTCATGGCC[C/G]CAGCGAGGGGCTTCC | 55626 |
rs755477549 | snp | C/T | 1.65693e-05 | 0.00287826 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542118 | AGCAGAGCTGCTCAA[C/T]TCCAGCCTGCTGGAG | 55626 |
rs755480907 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444732 | GTAGTTTTTTTCTTT[C/T]AGAGAGCGGCATTTA | 55626 |
rs755489551 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405672 | TCAGGACTGCAGTGA[G/T]CCATGATGGTGCCAC | 55626 |
rs755502566 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521140 | TTGCCCCTCACTGGC[A/G]ACAAGACTCTCAGAC | 55626 |
rs755528935 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566238 | GGTCTGCCCAACACG[C/G]TGAAACCCGTCTCTA | 55626 |
rs755533769 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475825 | CGGAGAAAGGTGGAA[A/C]AGGAAACTGTGGCAT | 55626 |
rs755560363 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461105 | AAAATTAGCCAAGCA[C/T]GATGGTACACGCCTA | 55626 |
rs755565617 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459306 | CTTTGGAGAATGGGG[A/T]TGGAAGAGTGGGAAG | 55626 |
rs755571553 | in-del | -/AAGA | 1.85118e-05 | 0.0030423 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397962 | GCAGATACAAAGCAG[-/AAGA]GAGAGCGAATTGGCT | 55626 |
rs755580265 | snp | A/G | 1.65078e-05 | 0.00287291 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410311 | GCTGTTGGAATGGAC[A/G]GTGAAGACCGTCTCG | 55626 |
rs755580645 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512373 | AATTTCCCTATAAAT[C/T]AAAAACATTTTGTTC | 55626 |
rs755585845 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512257 | TCCTTTGGGCAGTCT[C/G]CAAAAATGTCAATAC | 55626 |
rs755607205 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476164 | GGAAAAAGTGTCCAT[A/G]AAGTTGAGAGGGGAA | 55626 |
rs755617486 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407862 | GGCTGGAGGTAGGGG[A/G]TGAGGATAGCAACTG | 55626 |
rs755634750 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513345 | AAAATATAAATATAT[A/G]TAAGAGTACTCCATA | 55626 |
rs755651167 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503060 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs755668440 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497505 | TTCCAAGTGTTGAGA[A/T]CTCTGAAGGAGAAAT | 55626 |
rs755684473 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528706 | CTAGAGATCTATTGA[A/G]CAATAATGTGTACTG | 55626 |
rs755706490 | in-del | -/A | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451529 | GAAATGAAAAGTATG[-/A]TTCAACAGTTCAGTG | 55626 |
rs755721480 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422900 | GCTGGCTGGAGGAAG[C/T]GGACAACTGGAAACT | 55626 |
rs755727114 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455652 | AGGGCTCATGCCATC[C/T]GGCCTGGTGAGCCTC | 55626 |
rs755747284 | snp | C/T | 1.67382e-05 | 0.00289289 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542139 | CCTGCTGGAGCTGGG[C/T]GTTTGGCCCTCAGTC | 55626 |
rs755757132 | snp | C/T | 5.42599e-05 | 0.00520836 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397444 | GCACCAGTGCAACGT[C/T]TGTCTCTACCTGTTC | 55626 |
rs755760748 | in-del | -/ATT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532327 | CACCTCAAGGTGGCA[-/ATT]ATTAGAATAAAACAA | 55626 |
rs755769881 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491314 | TCCATTCTTCTACTT[C/G]TTAGCTGCATTACTC | 55626 |
rs755770573 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588054 | GAAATAGAAGGAGGA[C/T]GGGTGCTGTGGCTCA | 55626 |
rs755788743 | snp | A/G | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543386 | CTATGGGGATCTCTG[A/G]TTCGTCATCACCCTG | 55626 |
rs755825159 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473892 | CCTGACCTTGTGATC[G/T]GCCCGCCTCAGCTTC | 55626 |
rs755828841 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449429 | TACACCACCACTTAC[A/G]TTAGCATCAAAAAAA | 55626 |
rs755829629 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436521 | CTGCTATCACCATTA[A/G]GCCTTTCTACTGCTC | 55626 |
rs755866542 | snp | A/C/T | 0.000132475 | 0.00813767 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417870 | GATTACCCCAGTCCT[A/C/T]GGCCCCAGTGATCCC | 55626 |
rs755867139 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487477 | GATGCCTGAGAAAAG[A/G]TTGTATTAATCAATA | 55626 |
rs755870359 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510284 | TTTCATTATCTGTTT[A/G]GGCCCCTGTTCCCAT | 55626 |
rs755879397 | snp | G/T | 1.69e-05 | 0.00290684 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543258 | CTCTCCCACCTGGAT[G/T]CCAGAAGAGCGGGAG | 55626 |
rs755884183 | snp | C/G | 0.000148288 | 0.00860943 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542030 | CAGATCTGCTGGACT[C/G]GGTGTAAATTCTTTC | 55626 |
rs755920501 | snp | G/T | | | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434910 | GGAGTACACTGCCAG[G/T]ATGCCTTCATCAGGA | 55626 |
rs755923534 | snp | C/T | 1.65059e-05 | 0.00287275 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545742 | AGGGAGGCAATGGCA[C/T]TGTTGCTATCTGTGA | 55626 |
rs755949357 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398381 | GGTACCCTATGGGTG[C/T]GGCCCAAAGGGAAAC | 55626 |
rs755967502 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504179 | AGGCAGGAAGGGCAG[C/G]AATATGGGCTAGGGA | 55626 |
rs755970667 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449588 | TCAGTACTGTTACAA[C/T]GTCAATTCTTCTCAG | 55626 |
rs755972105 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540609 | TAAGAACCTACACAT[A/C]CCATACCCTTTCCTC | 55626 |
rs755985471 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503293 | TCAATATTGCTGTGT[A/T]TCAGGGAATAGGAAG | 55626 |
rs756008473 | snp | C/G/T | 8.23885e-05 | 0.00641781 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542755 | AGACTGAGTACTGTC[C/G/T]GGGTCCACTCAGATC | 55626 |
rs756037275 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414707 | GGGCAGAGTGCAGGT[C/G]GGGGAGCAGAGGAGG | 55626 |
rs756046899 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588637 | AAAGTACAAAAATTA[A/G]CCAGCCACATGCCTG | 55626 |
rs756050115 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467769 | AAACTCCTGACCTCA[C/T]GTGATCCTCCCAAAG | 55626 |
rs756057802 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413396 | GCTGGACTACAATGA[G/T]CTCATGGATTTGGTT | 55626 |
rs756067203 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465624 | CAGGTGGTTAGAGAG[C/T]GCAAAGAGAAAAAGT | 55626 |
rs756067623 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519207 | TTTTGTATTTTTAGT[A/G]GAGACGGGATTTCAC | 55626 |
rs756083285 | snp | A/G | 1.64806e-05 | 0.00287054 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542619 | ACCCCTCCCTTCTGT[A/G]GCTGAAGTGTACACA | 55626 |
rs756102364 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457117 | CAGGGTACAGCATTA[C/T]AGCTGAGTCAGTTGG | 55626 |
rs756107109 | in-del | -/GCCTA | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594623 | TATTTTCTTCCAAAG[-/GCCTA]GAGCCACAGGTGTGC | 55626 |
rs756139255 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494463 | ATGTGGTCCCTTAGC[A/G]TCTCAAACTGAAGCC | 55626 |
rs756143611 | in-del | -/G | 1.64779e-05 | 0.00287031 | frameshift-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542441 | GGGCCTGTTGGGTCT[-/G]GGGAGCTTCCCCACT | 55626 |
rs756194862 | snp | A/C | 4.25044e-05 | 0.00460981 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408488 | GGTCCCTCTCCCACC[A/C]CCTCCAGCGCCACAT | 55626 |
rs756196910 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507877 | ATGAGAAGCTTTCCA[C/T]GGTCACTGGACATGC | 55626 |
rs756216549 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563733 | TAATCCCAGCAACTC[A/G]GGAGGCCGAGACAGG | 55626 |
rs756228143 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531286 | AAATCCTAAAATAAT[G/T]TACTATCTTGACCTT | 55626 |
rs756228323 | in-del | -/CT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498862 | TGTTTCCCTATGCTG[-/CT]CTGTTTCTACTCAAT | 55626 |
rs756242288 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546725 | GTCCTAAGAATCTGG[C/T]TAGGCTCTTCCAGAA | 55626 |
rs756244749 | snp | C/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580402 | TACTTACTTGATATC[C/G/T]GCACTTGTATGTTTT | 55626 |
rs756282856 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524866 | GTACCTGAGCCGTGA[A/G]AATCACATGCACCCC | 55626 |
rs756284782 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506002 | GTGAGAGAAAGTCAC[C/T]CAGGCTTTTCAGCAG | 55626 |
rs756292052 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562037 | CCCAAAAGCTTATGT[A/G]ATTTTTATATAATTA | 55626 |
rs756309592 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403058 | CTCCTCTGTAGCAAA[A/G]GCATCTGTTTTTGTC | 55626 |
rs756321063 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553590 | CTCTACTAAAAATAC[-/A]AAAAATTAGCCAGGC | 55626 |
rs756331086 | snp | C/T | 1.68545e-05 | 0.00290292 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542961 | TGACGAGGCCTGCTC[C/T]GGGGGATGGAAGGGC | 55626 |
rs756352581 | snp | A/C | 1.66846e-05 | 0.00288826 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512843 | AAAAATGGCAATAAT[A/C]CCTGTCAATTACCAA | 55626 |
rs756357746 | in-del | -/ACT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495086 | GTCCTAGATCTTTCC[-/ACT]ACATTTCACTGCTTC | 55626 |
rs756381895 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579699 | GTATACTTCTTATGA[A/G]GAAACAGACATGTTT | 55626 |
rs756390593 | snp | A/C | | | intron-variant, utr-variant-3-prime | AMBRA1 | GRCh38.p7 | 11:46430920 | AGATGCTGTACTGTC[A/C]CATTAAACCCTTGCT | 55626 |
rs756445526 | snp | A/T | 1.69553e-05 | 0.00291159 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542204 | GCACACTCTCAAAGG[A/T]GCTGGGGACCTGCCA | 55626 |
rs756458810 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470713 | GCTTGCAGTGAGCCA[C/T]GTCTGCACCACCATA | 55626 |
rs756476500 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578255 | ACCTTAGGAAGCCGA[G/T]GCGGGTGGATCACCT | 55626 |
rs756539644 | in-del | -/AACT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589749 | CTCAGTCTCCCAAGT[-/AACT]GGGACTACAGGCGCC | 55626 |
rs756546995 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518657 | CTTTACAGAAGATGT[A/T]CGCCCATTTCTGCTC | 55626 |
rs756575728 | snp | C/T | 2.10919e-05 | 0.00324739 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547833 | TGTCTGGGCTGAAGG[C/T]CAATAAGAAGGTAGA | 55626 |
rs756586927 | snp | A/G | 1.79913e-05 | 0.00299922 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397946 | TCTGAACCCTCACCT[A/G]GCAGATACAAAGCAG | 55626 |
rs756587006 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431392 | CAGGGGCTGACTGGA[C/T]TACCACATCTCCTCA | 55626 |
rs756587160 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446615 | AGAGTCTTGTGCATC[A/G]CAGAACATTTAGCAT | 55626 |
rs756624898 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429932 | TCAGACAGAAAATAA[C/G]ATTCTGAGTCATAGA | 55626 |
rs756641514 | snp | A/G | 1.69364e-05 | 0.00290997 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443446 | CTGGCTCACCAGCAA[A/G]TATAACCCTTCCACT | 55626 |
rs756660575 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467215 | AGCCACTGCACTAGG[C/T]CTATAACTGATTTTT | 55626 |
rs756664122 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409487 | ACAGGCATGAGCCAC[C/T]GCGCCCATCCAGGAC | 55626 |
rs756675131 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428369 | GGCTTTCCCTTAAAG[A/G]CCACAATACTGTTCC | 55626 |
rs756682317 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449137 | AGGAACAAGGCAAGG[-/A]AAGCCCCTTCTTACC | 55626 |
rs756709203 | snp | A/C/T | 4.94216e-05 | 0.00497079 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542332 | CGATTCAGGTGGCCA[A/C/T]GGGACAGGTTGGAGT | 55626 |
rs756712285 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569635 | AATGCAAGGTCTGCC[C/T]GAGCATAGTGGCTCA | 55626 |
rs756719051 | snp | A/G | 4.95561e-05 | 0.00497751 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543406 | TCATCACCCTGCAAC[A/G]TGGACCAGCATGGGG | 55626 |
rs756725635 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498641 | TGCCTCGGAGAGAGG[C/T]TGTAATTTGAAGGAA | 55626 |
rs756741607 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566602 | GGGACCCGGGGGGTG[A/G]GGATTGAGCTACCTA | 55626 |
rs756757050 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568997 | TTTTTAGTAGAGACA[A/G]GGTTTTGCCATGTTG | 55626 |
rs756764393 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515231 | GTAATCCCAACACTT[C/T]GGGAGGCCAGATGGG | 55626 |
rs756766440 | snp | A/C | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418004 | CAGAGTTGATACTGA[A/C]ATGTCTCCGCTGGTC | 55626 |
rs756787545 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500126 | AGCCAAGACTAGAAC[A/C]CAGGACTATTCCGTA | 55626 |
rs756806293 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537420 | TCATCAGAGAGAGAC[C/T]AGACTACAAAAGTTC | 55626 |
rs756810309 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554675 | TTTTACTCTGTTCCC[C/T]GTAAAGAACAAAGGG | 55626 |
rs756831195 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462342 | CAGGAAATAATCTTG[C/T]AGTCAACACTAAGCG | 55626 |
rs756919174 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478296 | GAGTTGCTTCTGTTC[A/G]AGGAGCTCTGGATTA | 55626 |
rs756931019 | snp | C/T | 3.29489e-05 | 0.00405874 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542337 | CAGGTGGCCACGGGA[C/T]AGGTTGGAGTTGTTC | 55626 |
rs756934850 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412524 | TCAAATTTCTGGGCT[-/A]AAAAATCTGCCTACC | 55626 |
rs756967405 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568216 | TAATCCCAGCACTCT[C/G]GGTGGCCGAGGCAGG | 55626 |
rs757003909 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479606 | GGAGGCTGAGGCAGG[A/C]GAATCACTTGAACCC | 55626 |
rs757014404 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476446 | TAAAGAGTCCCAAGC[C/G]AACCCGTGGTGCTGG | 55626 |
rs757034985 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438680 | TATCCCCTGTGGTAT[C/T]GCCTGCCCCACACCA | 55626 |
rs757061999 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542757 | ACTGAGTACTGTCCG[A/G]GTCCACTCAGATCCT | 55626 |
rs757071742 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505914 | CTGCAAAAAGATAAC[A/G]CAGTCTCCCAGGCGT | 55626 |
rs757082757 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570661 | TTGATTGCTGTTAAT[-/A]TTTTTTTTTAAGCCA | 55626 |
rs757093273 | snp | A/G | 3.30311e-05 | 0.0040638 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508306 | GCATGGAGCGCTGGC[A/G]AATACTGTCTCTCCG | 55626 |
rs757097545 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454278 | AAGTGATCCTCCTAC[C/T]TTGGCCTCTCAAAGT | 55626 |
rs757098489 | snp | A/C | 1.69496e-05 | 0.0029111 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397906 | CTGGATCCTGCTGAG[A/C]GCATCTTCTCCACTG | 55626 |
rs757123177 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588135 | GTCAGGGGTTCAAGA[C/T]CAGCCTGGCCAACAT | 55626 |
rs757135483 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543734 | ACAAGCTATCCAACA[C/T]TGTCTAGTGATGATA | 55626 |
rs757138762 | snp | C/T | 1.6531e-05 | 0.00287493 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417875 | CCCCAGTCCTCGGCC[C/T]CAGTGATCCCTCAAC | 55626 |
rs757141036 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491427 | AGAAACGAAATATGT[C/G]TAAAGCACGTAAAAC | 55626 |
rs757154026 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560240 | TGCACACAGGCAGCA[A/G]CATTAGTTTTTTATA | 55626 |
rs757158298 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415463 | GAAAAGCGCTCTGGA[C/T]AGTAAAGTGAGGAAT | 55626 |
rs757168643 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559128 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 55626 |
rs757207469 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450858 | AGCATGAACCCTAAT[A/G]TAAACGCATACTTTG | 55626 |
rs757235775 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398499 | TTTTATATTGATTGA[C/T]TGATTGATGGAGTCT | 55626 |
rs757242381 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444028 | GATAGTAAGCAGCAC[C/T]CTTTCAGACAAAGTA | 55626 |
rs757252697 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534063 | TGATCCTATTTCAAA[C/T]TGCAGCATCCCCTAC | 55626 |
rs757252925 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469218 | TATATCTATATCTAA[C/T]GTATTTTCATTGAAT | 55626 |
rs757263311 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481170 | TGATAAGAGCAGCAC[G/T]GTGCAATTACACCCA | 55626 |
rs757268178 | snp | G/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451349 | AAATCATAATAATCA[G/T]CACAGTCACATGATA | 55626 |
rs757280449 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534165 | ATTGTCTTTCTCCCA[A/T]TAGAATGAGAGAATT | 55626 |
rs757302517 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504587 | GCAGTTTGATAAACA[A/C]AAGGACCCTGCAGTC | 55626 |
rs757317819 | snp | A/G | 6.25332e-05 | 0.00559131 | intron-variant, synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543057 | GTGTGGCAAGAGGGA[A/G]GGAACTCGAGTGCCA | 55626 |
rs757319739 | in-del | -/GG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584373 | TCTGGGGACTGTTGT[-/GG]GGGGTGGGGGGAGGG | 55626 |
rs757329099 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593146 | GCCTCTTGTGACAGG[A/G]TCTATATTCCTAACA | 55626 |
rs757336175 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491979 | GGAGGTGCTGTATGG[C/G]GTGGTGGAGGCAGAT | 55626 |
rs757343470 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548565 | TTCTAATTGCAAATA[A/C]AATTCTAGCTCAAAA | 55626 |
rs757348904 | snp | C/G | 1.68233e-05 | 0.00290023 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512865 | AATTACCAACTCAGA[C/G]GTCATTCATAAGGAA | 55626 |
rs757351273 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495683 | TGGGGAGCCCACAAA[C/T]TATACATGTACACAG | 55626 |
rs757353536 | snp | A/G | 1.65157e-05 | 0.0028736 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545611 | GCACTCACCGGACCC[A/G]TTCCATCTCACTAGC | 55626 |
rs757434013 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547042 | CACCACTGGGCAACA[A/G]AGCGAGACTCCGTCT | 55626 |
rs757439454 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403720 | GTGCAAATACCCCTG[C/T]GGAGGGCTCCTCCTG | 55626 |
rs757493878 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564059 | TGAGGCAGGAGAATC[A/G]CTTCAACCCAGGAGG | 55626 |
rs757520512 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419597 | GAAGCTGAAACTCTA[C/T]AAACTGGAGTTTATT | 55626 |
rs757523227 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407444 | GAGTCCACAGAAACC[C/T]GCAAAAAAGGGCCTG | 55626 |
rs757548343 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507985 | TCTCTGTCCTCGCGC[A/G]CCAGTGAATCAGCAA | 55626 |
rs757557018 | in-del | -/CA | 8.29098e-05 | 0.00643801 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512817 | CCAGCAGCCTCCTAG[-/CA]CAGAGATTAAAAAAA | 55626 |
rs757576728 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525042 | TGATGTCTCATGCCT[A/G]TAATCCCAGCACTTT | 55626 |
rs757599567 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418962 | GTAACCACAGTGCTC[G/T]CACAGCAATGGGGAA | 55626 |
rs757612832 | snp | C/T | 2.08906e-05 | 0.00323185 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547852 | TAAGAAGGTAGAGCG[C/T]GGACTATCCGGCAGT | 55626 |
rs757613190 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402322 | CTTAAGGATGCTTGG[A/G]AAACCGGTCTTGTAA | 55626 |
rs757623218 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457330 | CTAACAAATCCCACA[G/T]AACTTGGTGGTCAAA | 55626 |
rs757633890 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455392 | AATTTGACTACTTTA[A/G]TTAGCCTCATATAAG | 55626 |
rs757641863 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472538 | CAAGTGGACAGAGGT[C/T]AAATGACTCACTCAA | 55626 |
rs757657472 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580612 | TCCATTAAGTCTTGC[C/T]TGTCCTAATTCTAAA | 55626 |
rs757713476 | snp | A/G | 3.67836e-05 | 0.00428841 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443604 | ATCACTGCCCCTTAT[A/G]AGGAAGAAGTCAAAG | 55626 |
rs757718300 | snp | C/G | 1.68923e-05 | 0.00290618 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542965 | GAGGCCTGCTCCGGG[C/G]GATGGAAGGGCTCGG | 55626 |
rs757731766 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471212 | TTTGGGAGGCTCGGG[C/T]GGGCGGATCACTTGA | 55626 |
rs757733926 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535608 | CAAGTATACCTTCAT[-/A]GAGATTGCAGAAGAA | 55626 |
rs757743287 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523223 | TGCTTCTCTTAGTGA[C/T]ATTTGATTTCACTGA | 55626 |
rs757761674 | snp | C/T | 3.37633e-05 | 0.00410859 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408594 | TCTGCAGCTGAAGGG[C/T]CAGAGTCTGGGTGCC | 55626 |
rs757773390 | snp | A/T | 1.92177e-05 | 0.00309975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408507 | CCAGCGCCACATGGC[A/T]CCTACCTTCACCAGG | 55626 |
rs757783138 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541686 | CTCTCTAACCTAATC[C/T]ACACTCTCCTTTCAA | 55626 |
rs757800741 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459935 | GTTCAGGAGCCTCAG[A/G]TTCCCTCTTTTCACT | 55626 |
rs757801081 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538617 | CTCCTGCCTCAGCCT[C/T]CCACGTAGCTAGGAC | 55626 |
rs757810755 | snp | C/T | 4.98907e-05 | 0.00499428 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548230 | ATCCTATGTGAAATA[C/T]AGCCATTTTCCTTAC | 55626 |
rs757823540 | in-del | -/TA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551347 | AACAGGGTATCACTC[-/TA]TATCACCCAGGCTGG | 55626 |
rs757828679 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396505 | ACCACAATGTTTCTA[C/T]GATGAGTTACAAACA | 55626 |
rs757833047 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485437 | TTGATCCAAGCCCAG[A/G]CTTACACCCCACCTC | 55626 |
rs757836617 | snp | G/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542353 | AGGTTGGAGTTGTTC[G/T]CACTGCTGTGTGGGG | 55626 |
rs757839846 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487577 | AGAGGTAGAAGGGAA[C/T]GGAGCCACAGGGGAA | 55626 |
rs757851116 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513564 | ACACTGGGCCCAGAA[A/G]TTAAAGTGTATCACT | 55626 |
rs757873234 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485710 | GTGGGGAAAGATCAA[A/G]AGGAAATTTCCTGGG | 55626 |
rs757907400 | snp | A/G | 1.66821e-05 | 0.00288804 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46493615 | TTCCTTACCTGCCAG[A/G]ACCCTGTTAACAGAA | 55626 |
rs757916629 | snp | C/T | 3.35095e-05 | 0.00409312 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545587 | GCCAGACAATGCAGA[C/T]GGGGCAGCGCACTCA | 55626 |
rs757920137 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554796 | GAAACAAGTTTCCCA[A/G]TCTGTCCCTTAAAGT | 55626 |
rs757927749 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502163 | CGGCTCACTGCAATC[G/T]CCGCCTCCTAGGTTC | 55626 |
rs757950310 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540225 | GAGGTACTACTAAAG[C/T]AGAATGGACAAAAGC | 55626 |
rs757957266 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448512 | ATGTATAAGAAAAGA[C/T]GAAAGATCTAAAATC | 55626 |
rs757980288 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556497 | CCAAGGATATGGCAA[A/G]GTGCTAACTGGTTAA | 55626 |
rs758003607 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397413 | GTCCGGTTTCTGCTT[A/G]GCGGTTCGAGGGGAG | 55626 |
rs758032744 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516974 | AAACACAATACAACC[A/G]AACAAAATACTTCCT | 55626 |
rs758038511 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539094 | TTATCTGATATCTAG[A/G]TGCCGGGAGCAGACG | 55626 |
rs758056540 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396578 | GCCTTGATTTCTCCA[C/T]TAGAAACTACACGTA | 55626 |
rs758076191 | in-del | -/AG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499955 | CCGCCCCCGGCTGAC[-/AG]GGGAAATTTTTCTAA | 55626 |
rs758077019 | snp | C/G | 1.66131e-05 | 0.00288206 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46493646 | GAGTGAGTAGCCAAG[C/G]CAGGCTGTCCACGTT | 55626 |
rs758112902 | snp | A/G | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542483 | CCAGCTCCTGAAGCC[A/G]GTCATACTCCAGAAA | 55626 |
rs758129244 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511595 | CTGCTAACCTGCCAA[-/C]CCCACAACTGTAAAT | 55626 |
rs758156857 | in-del | -/TAGATAGATAGATAGA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447721 | TTGTAGATAGATAGA[-/TAGATAGATAGATAGA]TAGATAGATAGATAG | 55626 |
rs758167089 | snp | C/T | 1.64893e-05 | 0.0028713 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443636 | CAGCACATTATATTA[C/T]TTATCCACGTTTCCA | 55626 |
rs758176455 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424790 | ATTTACAGTGGGCTA[A/T]GATAGTGCCACTGTA | 55626 |
rs758206774 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515438 | AGATCGCACTACTGC[A/G]CTCCAGACTGGGTGA | 55626 |
rs758210123 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462419 | CCTCACGTCTGTCTT[C/T]AATGCCAGATTGTTT | 55626 |
rs758225363 | snp | C/T | 1.65504e-05 | 0.00287662 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508320 | CGAATACTGTCTCTC[C/T]GTGAGAGATACTGGA | 55626 |
rs758226886 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529892 | TCAGGAATGCTTCCA[A/C]GAAAGAGCAGAAATA | 55626 |
rs758231699 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494319 | GGAGAGGACCCCACA[A/T]AAATTAGTCATCTGG | 55626 |
rs758245069 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533603 | TCTTGACAGAACAAG[C/T]CACTCCTCCTTTTTG | 55626 |
rs758245145 | snp | A/G | 7.1e-05 | 0.00595777 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418096 | AGAATGGGAGGAGAA[A/G]CAATTTGTTACCAAG | 55626 |
rs758258085 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570433 | TTCTCCCATGTATAA[G/T]CTTCTCCAAAATTAC | 55626 |
rs758292133 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401599 | CTATGGGTGCTGCTG[C/T]AGCCAAGCCCCCAGA | 55626 |
rs758298779 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566188 | CTCTGGGAGGCTGAG[A/G]AGGGTGGATCACCTG | 55626 |
rs758300235 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478498 | ATCCTAGAAAATACC[A/C]AGAGAAAGAGAAAAG | 55626 |
rs758301631 | snp | C/T | 1.80837e-05 | 0.00300691 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397508 | CTGCTGCTGCCACCA[C/T]CCAGAAGGTGGTTGT | 55626 |
rs758315687 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589914 | GGTGTGAGCCACCGC[C/G]CCCGGTCTAAAAATT | 55626 |
rs758320738 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492909 | AAAAAATTAGCTGGG[C/T]GTGGTGGCGGGCACC | 55626 |
rs758367371 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545480 | AAAAAAATAGGAGGA[A/G]CTATGAGGATGACAA | 55626 |
rs758398372 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454268 | TCCTGGGCTCAAGTG[A/T]TCCTCCTACCTTGGC | 55626 |
rs758416694 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467912 | AAGTCTAGGGCCACA[A/T]ACTGGCAAGTATTTC | 55626 |
rs758419614 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535252 | ATAGTATCTTGAATA[C/T]CAAAGACAACAATTC | 55626 |
rs758428222 | snp | C/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418016 | TGACATGTCTCCGCT[C/G]GTCGGCAGGCATGGG | 55626 |
rs758431460 | in-del | -/GTC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488868 | TAATAGGTCAAAGAA[-/GTC]GTACTGAGAAGTGAC | 55626 |
rs758463257 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401776 | AGTCTCCTCCCCTTC[C/T]GTCTAGTCTCCACAC | 55626 |
rs758467294 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414761 | GGGCGGGATGACTGC[A/G]CTATCAGCCCCTGGG | 55626 |
rs758476281 | snp | G/T | 1.64933e-05 | 0.00287165 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46512781 | GCTCCATCATAACGG[G/T]ATAATGAAATGAGGG | 55626 |
rs758483193 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542658 | AGAGCCACCTTCCTG[C/T]TGTCTCAGCACAGAC | 55626 |
rs758487984 | snp | A/G | 1.65119e-05 | 0.00287327 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542098 | GTCCTCTCCTCCTGC[A/G]GACTAGCAGAGCTGC | 55626 |
rs758504676 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482777 | GCACTTTGGGGTGCC[A/G]AGGCAGGCAGATCAT | 55626 |
rs758506448 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556376 | GTGGGGAAAAACATC[A/T]TAAATTTAGAACAGT | 55626 |
rs758513329 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429148 | CTTCTTAGGCATCAA[C/T]ATCTGGCAGGTCTCC | 55626 |
rs758518196 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519377 | CAGAAAGTCTGGGTA[C/T]TAGTCCATATGGAAT | 55626 |
rs758524915 | in-del | -/AAAAT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568151 | AGACTCTGTCTTAAA[-/AAAAT]AAAATAAAATAAAAT | 55626 |
rs758588023 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589764 | AACTGGGACTACAGG[C/T]GCCCACCACCATTCC | 55626 |
rs758593888 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577350 | TACGCTAAGTCAAAG[A/C]AGCCAGACACAAAAG | 55626 |
rs758604781 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534368 | GGCGTGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 55626 |
rs758615335 | snp | A/T | 3.33957e-05 | 0.00408616 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434899 | TGGGGGGCCAGGGAG[A/T]ACACTGCCAGGATGC | 55626 |
rs758634299 | in-del | -/CAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488831 | AAATATGGGAAAATT[-/CAA]CAACACACTCCCAAA | 55626 |
rs758641793 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458994 | CATCCAGGAACAGGA[A/C]AAAGCAACTATATTT | 55626 |
rs758642525 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407279 | CTTCTCCAAATCCCT[C/T]TCGCTGTCAGGGGTT | 55626 |
rs758645857 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420216 | CTGTAGGACTCAACT[C/T]CAAATGTAAGGAACT | 55626 |
rs758647876 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578803 | GGAGAATGGTGTGAA[C/T]CCGGGAGGTGGAGCT | 55626 |
rs758673067 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481302 | TCTTCTACAGGGCCC[A/T]CTTTCTAGGGGAAAG | 55626 |
rs758673614 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427865 | AATACAAAAATTAGC[C/T]GGGAGTGGTGGCGAG | 55626 |
rs758677671 | snp | C/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594216 | GAGCCTGCACTTCTG[C/T]CATTTTCTGTGGGTC | 55626 |
rs758686875 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495879 | GTACAACTAATTATC[A/G]TAAGAGGAGTTAGAA | 55626 |
rs758696241 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593194 | AATTGGGATCACAGA[A/C/G]GATCAAACAATAACT | 55626 |
rs758698851 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497027 | TAAGACACAAGAATC[A/G]CTTGAACCAGGAGGC | 55626 |
rs758718486 | snp | C/T | 1.68476e-05 | 0.00290233 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545794 | GTGAATGAACCAATT[C/T]CAGATATTCTCAGGT | 55626 |
rs758735144 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471306 | AAATTCGTCTGGGCA[C/T]GGTGGCTCATACCTG | 55626 |
rs758746512 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564165 | AAAAAAAAAAAAAAA[-/C]GTAAGAGCAATCTTA | 55626 |
rs758751727 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459564 | AAAAATACAAAAAGT[-/A]GCTGGGCATGGTGGC | 55626 |
rs758761403 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444165 | AACAAATAAGGTAAT[A/G]TTCATTCATCTCTTC | 55626 |
rs758767455 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422007 | CCCTGAAGCTCCCCA[A/T]GGGATGTTCAGAACA | 55626 |
rs758770486 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585954 | GAGATTACAGGCATG[C/T]ACCACCACACCCAGC | 55626 |
rs758786146 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442615 | ATGTTGTGATTCCAA[C/T]AGAACAACTGGGATG | 55626 |
rs758788527 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512144 | TACAGGCGTGAGCCA[C/T]CATGCCCAGCCTCAA | 55626 |
rs758798163 | in-del | -/AAG | 3.31989e-05 | 0.00407411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410392 | CAGTTGGGAAGGGTA[-/AAG]AAGAAGGTGAAAGGC | 55626 |
rs758801383 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474171 | GATTTAGGAAGAAAA[A/T]AAAAAAAGAGTAGCA | 55626 |
rs758831081 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565976 | GACAGATTGCCCAGG[C/G]TGGTCTCAAAGCAAT | 55626 |
rs758837916 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534940 | TGGCTTCTCAGAGTG[-/C]TGGGATTACAGGCAT | 55626 |
rs758845209 | in-del | -/GAG | 3.29554e-05 | 0.00405914 | cds-indel, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508251 | TGGTTGTCTGAGGAA[-/GAG]GAGGAGGTGGAAGAA | 55626 |
rs758863111 | snp | A/G | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46541966 | AGTGAATCCTCCTCA[A/G]AGCTCTCCTCAGGCA | 55626 |
rs758894561 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491145 | TAGGAACCATTTAAA[C/T]AGAATAATTAAAACA | 55626 |
rs758902295 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505213 | CTGACTTTCCTTCTA[A/G]TTACCAAAGCTAAGG | 55626 |
rs758917379 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573441 | AAAACTCAGTCCATG[C/T]ATTTTTCCTGCTGTA | 55626 |
rs758923675 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526827 | GTGAACAAAGTAGTT[C/G]CTTATCTTTGTAAAA | 55626 |
rs758945941 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581437 | CACATGAAACCCCGT[C/G]TCTACTAAAAATACA | 55626 |
rs758949344 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434568 | GAGGTTTTAAATACA[C/T]AATGCCAAACTGTCT | 55626 |
rs758957000 | snp | C/T | 2.70764e-05 | 0.00367933 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543079 | CGAGTGCCAGAGCAG[C/T]GGCTGCAAAGGCACA | 55626 |
rs758979657 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490757 | TCATGGCTAACCACC[C/T]AGACTTGGAGCTACA | 55626 |
rs758983431 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462090 | TGGCAAATTTCTAGC[A/T]TTTACAAGAGATATC | 55626 |
rs759050793 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461802 | AAAGGCAGAGACTCT[-/A]AAAGCCATGGAATTC | 55626 |
rs759084833 | snp | A/G | 1.67725e-05 | 0.00289585 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508147 | CTTGGAAGCACTCCA[A/G]GCTTGAGAGGAGAGG | 55626 |
rs759100322 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416120 | AACAGGGAAAGAAAG[G/T]CCTGTAACTGAAGTG | 55626 |
rs759105029 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504033 | AGCTGAATGTAATTA[C/T]CCAGTGGCTAGTATA | 55626 |
rs759106309 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560010 | CACACAAAGAAGTCT[C/T]GCACCTACAGTTCTA | 55626 |
rs759120852 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415324 | ATGTCTCAACACAAT[A/C]TAAAGCTGCATTCTT | 55626 |
rs759147314 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558715 | AGGTAACCAAAGATA[C/T]CTCAAAATAAATTTA | 55626 |
rs759152857 | snp | C/T | 1.81207e-05 | 0.00300999 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434995 | ATGTCACAGCTGGCA[C/T]CATTGTAGATCTTGC | 55626 |
rs759163796 | snp | A/G | 1.65086e-05 | 0.00287298 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542844 | TCCCAAAGAGCGGCG[A/G]GTAGGACCCAGACTG | 55626 |
rs759174806 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467232 | TATAACTGATTTTTC[A/T]ATTTCCGCTATTATC | 55626 |
rs759191810 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409568 | AACAGACCCTTGCAG[C/G]TAGGGAGCACAGGCT | 55626 |
rs759192539 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482373 | CATGTCATTCCTTTA[C/T]GTTACCAGTCCAACG | 55626 |
rs759204499 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428507 | GAAAAGCAAACTACG[C/G]CTGGTGAGATTCAAG | 55626 |
rs759251326 | snp | A/C | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542731 | GATTCCGCCTCAGAG[A/C]GGGAGTTCAGACTGA | 55626 |
rs759251932 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458391 | CCTGCCTACACACTA[C/T]TAGCTGTTTTTCATA | 55626 |
rs759267788 | snp | C/T | 1.80987e-05 | 0.00300816 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397411 | AGGTCCGGTTTCTGC[C/T]TGGCGGTTCGAGGGG | 55626 |
rs759290134 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483756 | AATACAAAAATTAGC[G/T]GGGCGTGGTGGTGTA | 55626 |
rs759301736 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483635 | GCAGGCATGGTGGCT[C/T]ATGCCTGTAATCGCA | 55626 |
rs759316503 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593644 | CAGCAACTCTCCCTC[C/T]TTTCGGCTTCTCCCT | 55626 |
rs759334193 | in-del | -/TTGA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474230 | TGATATTTTTCCTGG[-/TTGA]TTAATTTCATTATTA | 55626 |
rs759341402 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516116 | GGTTCTTTTGGAACA[C/T]GCATCCCCTGTGCCT | 55626 |
rs759353117 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567015 | AGTGAGCCCTGTCTC[A/G]AGAAAATAAATAAAA | 55626 |
rs759355834 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496309 | ATCCCTTGAACCCAG[A/G]AGATGGAGGTTGCAG | 55626 |
rs759363758 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427730 | AAAATGGTAACAGGC[C/T]GGGAGCGCTGGCTCA | 55626 |
rs759380950 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565381 | CATGCTTGGGCATTT[A/T]TCCAGAAAAATGATA | 55626 |
rs759403126 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578990 | GAATGAATAAAGAGG[-/T]TTAACCAAGCACCTC | 55626 |
rs759405154 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534891 | GTTGCCCAGGCTGGT[C/T]GCAAATTCCTGAGCT | 55626 |
rs759407130 | snp | A/G | 1.64947e-05 | 0.00287177 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541933 | GCAGAAGATAGGAAA[A/G]CGACTGCTTACCTCC | 55626 |
rs759417764 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549560 | TCATTATGCAACTCC[C/T]AGGAAGAAGGATGTT | 55626 |
rs759421797 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533887 | ACTCCATCCCTTGCT[A/G]TGCTCCAGCTGCACT | 55626 |
rs759459299 | snp | A/G | 0.000103688 | 0.00719953 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547085 | ATTAGAACACCAAAA[A/G]AAAAGGGTATCTTAA | 55626 |
rs759475608 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470393 | GGAGATCGAGACCAA[G/T]CCTGGCTAACACGGT | 55626 |
rs759499940 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443729 | GGCTGAAGAAAGCTA[A/G]TGAGTCCCATCTGGC | 55626 |
rs759507676 | snp | G/T | | | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548350 | GCCCCCAGAGTATCC[G/T]GACAGCATTCTTTTC | 55626 |
rs759508811 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513463 | CTTTTTTTGATGCCA[-/G]GTAATAGGTAATACT | 55626 |
rs759517388 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511320 | CTCATCATCTATGGT[A/G]CCTGCCTGTTTTAAA | 55626 |
rs759539111 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542301 | GAAGGTCAGGAGATT[A/G]TGGCAAGCACGACAG | 55626 |
rs759558414 | in-del | -/AG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427523 | CTTAACTTAGCGCGC[-/AG]AGTCATCAGGAAGGC | 55626 |
rs759567256 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495466 | AGGGATATTGGAAGC[A/T]GATCCATTGAAAGTA | 55626 |
rs759574792 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404994 | AGGCCTCACTCCCAG[C/G]CCAGTCCCAGTAACT | 55626 |
rs759580621 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589713 | CAAGCTCCGCCTACC[A/G]GGTTCACGCCATTCT | 55626 |
rs759611371 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524670 | CTGTGTCAAGCACAG[A/T]AGCCAGTACAGTCTA | 55626 |
rs759613495 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538387 | CAGGGACTTCATTTT[C/T]ATAATACACATTTTT | 55626 |
rs759619434 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396940 | GCCCGATCCCTGTTG[A/G]TTTCAGTGGGGTAAG | 55626 |
rs759627083 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554189 | TCTTAACAGTGCAAT[A/T]TAAAGGCACTTTCAA | 55626 |
rs759640929 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580339 | ATCTATATACTAATA[C/T]CATCCAGATTTCTCT | 55626 |
rs759656029 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459769 | ACACACACACACACA[C/T]ACACACCCTGGAATA | 55626 |
rs759715949 | snp | C/T | 0.000253073 | 0.011246 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397530 | GGTGGTTGTTATTGG[C/T]CAACTCGCAGTGGAG | 55626 |
rs759733230 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432414 | AAAAGTGGCTCAGTG[C/T]AGTTGGACAGAGGAT | 55626 |
rs759735739 | snp | C/T | 2.27622e-05 | 0.00337351 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408468 | TGGCACTCACTCGGT[C/T]TTAGGGTCCCTCTCC | 55626 |
rs759742299 | snp | A/G | | | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396159 | ACTCACCCTGGCACT[A/G]GAAGGTGGCCCCAGT | 55626 |
rs759760858 | snp | A/T | 1.66671e-05 | 0.00288674 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548203 | GGTCTCATTCTACCA[A/T]CACCAGCACAAATCC | 55626 |
rs759809484 | snp | A/G | 3.3173e-05 | 0.00407252 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46443543 | CCACTGGAGCCGGTA[A/G]GTAGTATTGGCAATG | 55626 |
rs759813892 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446542 | TGGAACAAGCTAGAC[C/T]CAGAGTTTCTCAACC | 55626 |
rs759816371 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416415 | CACAAAACATTCTTG[-/C]AGCTCCAAGAGCAGC | 55626 |
rs759832291 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411230 | AGTCAGCTATTTAAC[A/C]TAGAGGCCTAGGTCA | 55626 |
rs759842152 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479205 | CCTATCTCAAAAGAA[A/G]GAAAAGAAAAAAAAA | 55626 |
rs759842389 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406659 | GCTGAGGTGGGCATA[C/T]CACTTGAGGTCAGGA | 55626 |
rs759866379 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409093 | GCACTAGAAGAAGGT[C/G]CTTTCTCTCTTTAGC | 55626 |
rs759882270 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499880 | GGCTAGTCTTGAACT[C/G]CTGACCTTGTGATCC | 55626 |
rs759883448 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46417960 | AGTACCATAGGCCAA[A/G]CCAAGCCCTGGCTCA | 55626 |
rs759891936 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462018 | AATGTTTACTAAAAT[C/T]CCCTTCATCCTTCAT | 55626 |
rs759899558 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560011 | ACACAAAGAAGTCTC[A/G]CACCTACAGTTCTAA | 55626 |
rs759912205 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551830 | GTCAGGAGTTCGAGA[A/C]CAGCCTGGTCAACAT | 55626 |
rs759932665 | in-del | -/TTG | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452336 | TTATTTTAAGGTTTT[-/TTG]TTGTTGTTGTTGTTG | 55626 |
rs759933770 | snp | C/T | 1.65699e-05 | 0.00287831 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418052 | GGACGTTGAAAACTC[C/T]CTAGGTAGAGGAAAA | 55626 |
rs759951057 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524479 | CTAACCAAGAAAACT[C/G]TGAGTAACTAAAATA | 55626 |
rs759953306 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530242 | AGAGCTGACAGAAGC[A/G]ATTACATCTTTTCAT | 55626 |
rs759954319 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422712 | AATAAAACTCAGACG[A/G]GTAGTTCAAGCAGCA | 55626 |
rs759969746 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514620 | TATTTTACAGTTGTG[G/T]GACACAGTTTAATTG | 55626 |
rs759988473 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513023 | TGGACATGACCACTG[C/T]ATTCTGCTGAATACT | 55626 |
rs760001622 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477683 | ATACCATTTTGAATG[C/T]ACATGCCTAGGATAA | 55626 |
rs760007843 | in-del | -/AAGTA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589745 | CTGCCTCAGTCTCCC[-/AAGTA]ACTGGGACTACAGGC | 55626 |
rs760055723 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589287 | TTGATCACATTAACT[C/T]GGGGGAGCCTGAAAA | 55626 |
rs760072932 | in-del | -/A | 0.000102084 | 0.00714365 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494208 | TCACCATTGTCCCTG[-/A]AAAAAATAAAAACAC | 55626 |
rs760085848 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439521 | CATACTTTGATTATT[G/T]GGGACTAAATTTCCT | 55626 |
rs760091642 | snp | A/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591492 | TCACATGAGAATACT[A/T]AAATAGTGGGAGAAT | 55626 |
rs760093445 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492305 | AAACATACTATTTAG[G/T]AAAGGCCAGATCCCA | 55626 |
rs760093664 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553583 | AACCCTGTCTCTACT[A/G]AAAATACAAAAATTA | 55626 |
rs760110980 | snp | C/G | 1.80817e-05 | 0.00300675 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397484 | CCCCTAGGGCCTGCA[C/G]CGTCCCCCCTGCTGC | 55626 |
rs760111208 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439311 | AAAACATAAAACCTC[A/T]AAGATTAAACTCACG | 55626 |
rs760124943 | snp | C/T | 3.29815e-05 | 0.00406075 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543346 | AGGAGGGCACGCTGA[C/T]GGTAGTGGGATAATT | 55626 |
rs760131276 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438245 | TCAGGGGGCAGCTCC[A/G]GAGGGAGAAAAAACA | 55626 |
rs760139011 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472850 | CCTGTCACCTGCTCA[C/G]CAGGCAAACTCCACA | 55626 |
rs760177880 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477948 | AGAGCTAATTTTTGT[A/G]TTTTAAAAGAACTCT | 55626 |
rs760192977 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493159 | CGTCTCCCTCTTTTC[C/T]TTCCTCAGAAGATTC | 55626 |
rs760195639 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545261 | GGCCAGGAGTTCAAG[A/T]CCATCCTGGACAACA | 55626 |
rs760238878 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402495 | GCCTCCCGAGTAGCT[A/G]GGATTACATGTGTGC | 55626 |
rs760246563 | snp | C/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452291 | TTTTAGATGGTCTAC[C/T]AGTGTCTTATGTACA | 55626 |
rs760247256 | snp | A/G | 8.27959e-05 | 0.00643359 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542847 | CAAAGAGCGGCGGGT[A/G]GGACCCAGACTGAGG | 55626 |
rs760254566 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400891 | GGCTGCCCTTCCCCA[C/T]TTCCTCCTGGGACAC | 55626 |
rs760257484 | in-del | -/A | 0.000590232 | 0.0171688 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547882 | TCTACTCTCTGGGAG[-/A]ACAAAAAAAAAAAAA | 55626 |
rs760258796 | in-del | -/AAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545306 | CTTTATTAAAAATAC[-/AAA]AAAATGAGCCGGGCA | 55626 |
rs760265843 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492518 | CCTCTAAATGTGGCT[C/T]GATTTTTATACCTTT | 55626 |
rs760294915 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506517 | AGCTTTGTTGCAAGA[A/T]GACTTGTGAGGAACT | 55626 |
rs760301062 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589583 | CATTTTCTCTTATTC[C/T]TTTAAGAGTGAGATA | 55626 |
rs760301262 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439958 | AATATCCAAAAATTT[A/G]ATAGTACATTCTATC | 55626 |
rs760302067 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46417985 | GGCTCAGGCAGCCAA[C/T]GGGCAGAGTTGATAC | 55626 |
rs760302235 | snp | A/C | 1.6543e-05 | 0.00287597 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512699 | CGCCCCTCCCCCCAC[A/C]TAGTGCCATTTCTCA | 55626 |
rs760311996 | snp | A/G | 3.32795e-05 | 0.00407905 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542924 | CAGACGGCCGGTTCA[A/G]GAGGCCCTGGTCCTG | 55626 |
rs760337498 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561524 | AGGTTAAGAAATTCA[A/T]CTAGATTCACAGATG | 55626 |
rs760345140 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416326 | GAAACTGAGAGACCC[A/C]AGGAGATAATGAAAA | 55626 |
rs760345279 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438086 | AATAATCCTTAGTCT[A/G]GGAGATGCATCTCCA | 55626 |
rs760360123 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46453932 | CAGACTTCAATGGTT[A/G]CGTGTCTTATTTGTA | 55626 |
rs760366844 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560097 | CTCTAATTAACCACC[C/T]GACAAATTGAAAACA | 55626 |
rs760389022 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526857 | ACTTTCAAGCTAGGC[A/G]CAACAGCAACATTAG | 55626 |
rs760389679 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536258 | AGGGATATATACAGA[A/C]ATGATCACTGCCTTC | 55626 |
rs760391709 | snp | A/G | 3.39524e-05 | 0.00412008 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542160 | GCCCTCAGTCCGCTC[A/G]AGAGGTGGCAACTGG | 55626 |
rs760391826 | snp | C/G | 1.65121e-05 | 0.00287329 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508301 | GTAGCGCATGGAGCG[C/G]TGGCGAATACTGTCT | 55626 |
rs760428560 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430335 | CCACAATGGCAAGTA[C/G]ACCTGAGACTGACTC | 55626 |
rs760456763 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577798 | TCTACTAAAAGTACA[A/T]AATGTGCCGGGCATC | 55626 |
rs760466138 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427388 | GTATAAAAGAAAGCA[A/C]GCAATCTAATGTTTA | 55626 |
rs760477500 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551509 | TGGTGCAAACCACTG[A/C]ACTAGGTGCTGAAAT | 55626 |
rs760482434 | in-del | -/TCAAGTTTATAACAAGAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559690 | ATATAGGAGTATCAG[-/TCAAGTTTATAACAAGAA]TCAGTGATTTAATAA | 55626 |
rs760490717 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557136 | GCGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs760492963 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579149 | AAGAAAGGCTAAACA[C/T]AGCAAATTTTAAAAG | 55626 |
rs760519604 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592483 | ACAACAAAACTGGGC[A/G]GGCGCGGTGGATGCC | 55626 |
rs760527350 | snp | A/G | 1.67548e-05 | 0.00289432 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434890 | CCCAGGTTATGGGGG[A/G]CCAGGGAGTACACTG | 55626 |
rs760528734 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423985 | CCAGGCTGGTCTCGA[A/T]CTCCTAATCTCAGGT | 55626 |
rs760532290 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522308 | ACACATTACACTATA[A/G]TTGTAAGACTTGAAT | 55626 |
rs760613537 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535133 | ACGTCATAATTTGCC[G/T]GTATCACAAATGAAA | 55626 |
rs760623358 | snp | C/T | 1.6953e-05 | 0.0029114 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547286 | TCACATGGGTGGAGG[C/T]TAAGAGAGTCCTAGA | 55626 |
rs760656063 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428565 | ATTAGGCAATGAGGA[C/T]CTTTTCCACTTCTTC | 55626 |
rs760663984 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498051 | TGCTGATACAAGGTC[A/G]ACATCAAGCCAAGGC | 55626 |
rs760669840 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540015 | TTTTGTATTTTTAGT[A/G]GAGATGGGGATTTAC | 55626 |
rs760674182 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579196 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55626 |
rs760675863 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525976 | TTTGGGAGGTCAAGG[C/T]GGACAGATCACCTGA | 55626 |
rs760677728 | snp | C/T | 3.66441e-05 | 0.00428027 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493571 | TCTGGCTCCTTGGCC[C/T]TTCACATTTTCAAAA | 55626 |
rs760683763 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533281 | CAGATCTCTGAGCAG[C/T]GGCTTTAAGAGGATA | 55626 |
rs760701585 | snp | C/T | 1.81046e-05 | 0.00300865 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408537 | GACCTGAGGCGGCTG[C/T]CCCTGGCTCCGGCAC | 55626 |
rs760742152 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580423 | TGTATGTTTTCACAG[A/G]CATCTCACAATTAGC | 55626 |
rs760754455 | snp | A/G | 8.28727e-05 | 0.00643657 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397813 | GATGATGTTGTTGCC[A/G]AAGCCGCCCATGGAG | 55626 |
rs760789579 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536313 | AACAAATAATTTTCT[C/G]TCATGGGTGCAATAT | 55626 |
rs760797750 | in-del | -/AAAAAAAAAAAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527478 | AAGTGAGACTGTCTC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 55626 |
rs760840929 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571670 | GACAGAATGAGTCCG[C/T]GTCTCAATCAATCAA | 55626 |
rs760842701 | snp | C/T | 1.64917e-05 | 0.00287151 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542550 | GCTGCCCGAGTTGTT[C/T]TGGCTGGAGCCATTC | 55626 |
rs760874159 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582260 | AATGTGTCAAGTTCT[C/G]TCCCATCCTGAGAAT | 55626 |
rs760883158 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415439 | AGAATTTTAAAGGGG[-/T]TTTTGAGTGAAAAGC | 55626 |
rs760897483 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553557 | CGAGACCAGCCTGGC[C/T]AACATAGTGAAACCC | 55626 |
rs760898909 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449125 | TCCCCCTAAGACCAG[A/G]AACAAGGCAAGGAAG | 55626 |
rs760900510 | snp | C/G | 7.38989e-05 | 0.00607816 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543042 | GGGGACACTGTCCTG[C/G]TGTGGCAAGAGGGAA | 55626 |
rs760922916 | snp | C/G | 1.86834e-05 | 0.00305636 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408726 | GGAGAGAAAGGCAGA[C/G]TAAAGTCAGATGGGG | 55626 |
rs760954567 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589602 | AAGAGTGAGATAAAT[C/T]GGAAGTGTGAGAGAA | 55626 |
rs761018492 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411365 | TAGGACAGAGACCAG[C/G]CAGGGCCTGGAAGAC | 55626 |
rs761032235 | snp | A/G | 3.60894e-05 | 0.00424775 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397546 | CAACTCGCAGTGGAG[A/G]GTTGGTCCCTCAGCG | 55626 |
rs761032442 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501381 | GTGCACCCTGTGACG[C/G]AATGGCATCCTGTCC | 55626 |
rs761033506 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486414 | GATCTGCTATATAGT[A/G]ATTAAGCAATTTGTT | 55626 |
rs761039216 | snp | G/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542433 | CATTTCCTGGGCCTG[G/T]TGGGTCTGGGGAGCT | 55626 |
rs761045683 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568184 | ATCCAGCTGGATGCC[A/G]CAGTGGCACACACCT | 55626 |
rs761065060 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396960 | AGTGGGGTAAGACGA[C/T]GAAGAGAGGCTGAAG | 55626 |
rs761071769 | snp | A/C | 6.73843e-05 | 0.0058041 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397642 | CCCAGGGGTACCAGG[A/C]TGGTCCCAGGAAGCT | 55626 |
rs761073472 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538525 | TTTAGACGGAGTCTT[C/G]CTCTGTCGCCCAGGC | 55626 |
rs761094463 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555871 | GCAAGAAGCTGTTAA[A/T]ATGGAGTCCAATCTC | 55626 |
rs761103859 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551311 | GTTAGTTTGTGGGGA[C/T]TTTATTTTTATTTTT | 55626 |
rs761132642 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516724 | AGGCGTGACCCACTG[A/C]GCCCGGCCAAAAGAT | 55626 |
rs761133575 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543972 | ACTGCTGGACTAACT[C/T]ACCTGTTGATTAGAG | 55626 |
rs761155701 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479323 | GATTTAGGCCCTTCT[A/G]TATCCATGGCCTTAG | 55626 |
rs761159227 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554622 | AAGGATAAGGGACTT[C/G]TCTCCTGATATGCTC | 55626 |
rs761174676 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524592 | CTTGGGCAAGTTCAT[C/T]ATCCTCTGCTTCCAC | 55626 |
rs761194863 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425864 | AAAAAAGAAAACAGC[A/G]GGCTGGGCGTGGTGT | 55626 |
rs761221749 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532256 | TGTGATTGTCAGAGA[C/T]AGAACAGGGCTATGT | 55626 |
rs761231114 | snp | G/T | 1.77278e-05 | 0.00297718 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543026 | CTCTGGCAGAAGCAG[G/T]GGGGACACTGTCCTG | 55626 |
rs761245404 | in-del | -/GGCAGGGTT | 1.74662e-05 | 0.00295513 | cds-indel, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397600 | ACAGGGGAGGAAGAG[-/GGCAGGGTT]GGCAGGGTTGGCTGG | 55626 |
rs761286047 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505182 | AAAAAAATATAAATC[A/G]TGACTGCACATGCCT | 55626 |
rs761292587 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592435 | AGCCTTTTTTAGCTT[C/T]TGTATGTGCAGTGAC | 55626 |
rs761297675 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516819 | ATGCGATGGCAGTTC[C/T]GCACATTCTGCTGTG | 55626 |
rs761305146 | snp | C/T | 1.69083e-05 | 0.00290755 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545571 | ATCACGTCAGTCCTG[C/T]GCCAGACAATGCAGA | 55626 |
rs761306034 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587506 | CATATTACATGTAGC[A/T]ATCAATCTTAAATGA | 55626 |
rs761335335 | snp | C/T | 1.68159e-05 | 0.0028996 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545583 | CTGTGCCAGACAATG[C/T]AGATGGGGCAGCGCA | 55626 |
rs761370550 | in-del | -/AAAAT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487260 | GAGACCCCATCTCTA[-/AAAAT]AAAATAAAAATAAAA | 55626 |
rs761371924 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397334 | ACCCTGACCCTCTTC[C/T]TCCTCCTGTTCCCTG | 55626 |
rs761378244 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439998 | TTATGAAATCAGGCA[C/G]TCTCATGAACTCCAA | 55626 |
rs761393921 | snp | C/G | 1.64893e-05 | 0.0028713 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46512739 | TACCTCGCTGGGTCT[C/G]GGTAAATTGGGTGCT | 55626 |
rs761404834 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402633 | CCTCCCAAAGTGCTG[C/G]GATTACAGGCATGAG | 55626 |
rs761418350 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553368 | TCCAAATACAGACAG[-/A]AAAAAAACATTAACA | 55626 |
rs761420028 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520397 | AAATAGTTTTGACTT[C/T]GGGGATCCATTGTTC | 55626 |
rs761423550 | snp | C/T | 0.000115692 | 0.00760477 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433530 | AGACCTGGGCCACCA[C/T]GTGCTCTGTGGAGGG | 55626 |
rs761458493 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456503 | AGCAGCATAAGAATG[A/G]GCAAAGAGAGGGGTG | 55626 |
rs761472892 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469630 | TTCAGAGTAAAATGA[A/G]TCTAAGAATAAGACT | 55626 |
rs761475477 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546379 | AAAACTCAAGCTCGG[C/T]GCACAACATGGTGCA | 55626 |
rs761479201 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545375 | GCTGAGGCACGAGAA[G/T]CGCTTGAACCTAGGA | 55626 |
rs761492318 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433923 | GAGTTTGAGACCAGC[C/T]TGACCAACATGGAGA | 55626 |
rs761512291 | snp | A/G | 1.71846e-05 | 0.00293122 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418087 | GAAAAAAAGAGAATG[A/G]GAGGAGAAACAATTT | 55626 |
rs761514982 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441371 | ATACAAAAATTAGCT[C/G]GGTGTGGTGGCGTGC | 55626 |
rs761541909 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524278 | AATGTGGCAATGTCT[A/G]CTGACATTTTTGGTT | 55626 |
rs761543942 | snp | A/G | 3.31055e-05 | 0.00406837 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46443505 | TTACTGATTTCAGGG[A/G]GGTCAAACTTAGTGA | 55626 |
rs761544937 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471906 | GCCAGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 55626 |
rs761547071 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454169 | AGTGTATGAGGAAAG[C/G]AAAAGAAATAGCTAT | 55626 |
rs761549062 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419342 | AGTGGAAGAATAAAA[C/G]ACATGGGCTTTAGAG | 55626 |
rs761568190 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561649 | GTTCAGTGTTTTCCA[A/G]TCTTATAGTCAGCCC | 55626 |
rs761588250 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509127 | GGCACTGGGCAATAT[C/G]GAAGGTGAGAGTTGT | 55626 |
rs761596203 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575488 | AGGTAGCTTATAAAC[A/C]ACAGAAATTTGTTTT | 55626 |
rs761596685 | in-del | -/GAA | 1.64727e-05 | 0.00286986 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443607 | ACTGCCCCTTATGAG[-/GAA]GAAGTCAAAGACAGC | 55626 |
rs761608512 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456716 | CAGCAGGAGGGAAAC[A/G]ACCTTTATTGCTGCA | 55626 |
rs761633378 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563075 | TGTGCTGAAACTACC[A/G]TGCCTGGCCTGCTTC | 55626 |
rs761636598 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506597 | GCCCCAGACCTGACC[C/T]GGCTATGTCAAGATG | 55626 |
rs761689520 | snp | C/T | 1.75668e-05 | 0.00296363 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547333 | CTGAATTCAGAAGCA[C/T]GTGGAAGGGTAACCA | 55626 |
rs761699385 | snp | A/G | 3.30486e-05 | 0.00406487 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542867 | CCAGACTGAGGTTGC[A/G]GAGCGTGTTGCCGGC | 55626 |
rs761705156 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489066 | CGCAACCGCCCGGTT[A/C]ATTTTTTTTTTTATT | 55626 |
rs761706459 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470192 | TCATGCCTATAACCC[A/G]AGCACTTTGGAGGCC | 55626 |
rs761708624 | in-del | -/GCAATAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541351 | GAGAATCTCAACTGA[-/GCAATAG]GCTGCCCAAAAACAA | 55626 |
rs761717558 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442315 | CTCAGCTAATTTTTG[-/T]TATTTTTAGTAGAGA | 55626 |
rs761746129 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530828 | TGAAAATTATATGAA[A/T]ATCAAATTTATCTCC | 55626 |
rs761776311 | in-del | -/TTCT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428590 | TTCTTCTTCTTCTTC[-/TTCT]TTTTTTTTTAAGGTT | 55626 |
rs761801153 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564140 | CAAGAGCAAAACTCC[A/G]TCTCAAAAAAAAAAA | 55626 |
rs761803856 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573101 | GCAAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 55626 |
rs761816709 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496529 | GCAAGATCCAAAGAT[A/T]CACCTCCTTCTGGAC | 55626 |
rs761822003 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511681 | TGCCTTTTTAGATCA[C/T]GAACAGAATCCGTAA | 55626 |
rs761831837 | snp | G/T | 3.84527e-05 | 0.00438462 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408747 | TCAGATGGGGCTTGG[G/T]ACAGCACCCCTCACA | 55626 |
rs761842679 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432103 | AAGTGTCAGGTTCCG[C/T]ATGAAGTTCTTGGAC | 55626 |
rs761844382 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570359 | GAACTATCCTGTGGG[-/C]CCCAGAGGGAGAAGT | 55626 |
rs761852354 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406946 | AGCACTTTGGGAGTC[C/T]GAGGTAGGCGGATCA | 55626 |
rs761857886 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522565 | TGCCACATGCACACA[C/T]GCCCCCTACATGCAA | 55626 |
rs761866199 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485041 | CTCCCGGGTTCAAGC[G/T]ATTCTCCTGCCTTGG | 55626 |
rs761886990 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512849 | GGCAATAATCCCTGT[C/G]AATTACCAACTCAGA | 55626 |
rs761894991 | snp | C/T | 8.27465e-05 | 0.00643167 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410360 | TACTCAACACCAGAG[C/T]TTAAGGCCCTAAAAA | 55626 |
rs761906985 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567653 | GGCGTGAGCCACCGT[G/T]CCCAGCCTTTTAAGA | 55626 |
rs761919668 | in-del | -/AAAAAAAAAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518430 | GCAAGACTCCGTCTC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 55626 |
rs761922636 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448010 | ATTTCATCTACAGTT[A/C]CACTACTACTTACAT | 55626 |
rs761934275 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482819 | TTTGAAACCAGCCTG[A/G]CCAACACAGTGAAAC | 55626 |
rs761943341 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567339 | AGCCTCCCAAAGTGC[C/T]GGGATTACAGGCATG | 55626 |
rs761945038 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460407 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCCC | 55626 |
rs761959831 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565863 | CTGCACCCTCCACCT[C/T]CCAGGCTCAAGTGAT | 55626 |
rs761978177 | snp | C/T | 1.65015e-05 | 0.00287237 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543310 | TGGAGGAGAGGCGTC[C/T]GGCGAACTGGCTGTG | 55626 |
rs762021243 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421313 | GAGTCCTTAAACAGT[A/G]CCGAAAGGGCAGTTC | 55626 |
rs762050275 | snp | C/T | 4.94792e-05 | 0.00497365 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542079 | GTTAAAGGCCACCCC[C/T]ACAGTCCTCTCCTCC | 55626 |
rs762065127 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587340 | AGCCAAGATTGCACC[A/G]CTGCACTCCAGCCTG | 55626 |
rs762095291 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466539 | GTTACTGCTCAAAGT[A/G]GATTCAGGGGTCAAG | 55626 |
rs762106497 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475432 | TGAGGGGGTAGACTG[C/G]ACCTTAATTCCACAT | 55626 |
rs762184558 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488513 | ACAATTCAATAATAA[C/T]AGAGATTTCAATACC | 55626 |
rs762194184 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473960 | CGGACAGGATCCTTT[A/G]AGGATTCTTAAAGAA | 55626 |
rs762197243 | snp | C/T | 3.35149e-05 | 0.00409345 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397661 | TCCCAGGAAGCTGTC[C/T]GGGGGCTTAGGCCTC | 55626 |
rs762198928 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450139 | TTTATTTATTCATAA[C/T]TGTCAAAACTTGGAA | 55626 |
rs762242348 | snp | A/G | 9.89234e-05 | 0.0070322 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548329 | TGGCCCGAGCACCCC[A/G]TTCTCGCCCCCAGAG | 55626 |
rs762266328 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582868 | AGTCTGAAAAGGTAC[A/G]AATTGAGATGCAGAA | 55626 |
rs762281481 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409202 | TGGAAGGAAAGAACT[-/G]GGAACTCTTTTTTTT | 55626 |
rs762286361 | snp | C/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542447 | GTTGGGTCTGGGGAG[C/G]TTCCCCACTCAGGCT | 55626 |
rs762289661 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502440 | CAAAGGGAACTCTAT[C/T]TCAAAATGAAGTAGA | 55626 |
rs762310192 | snp | A/G | 1.73918e-05 | 0.00294883 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434860 | TTACCAAATCGCTTG[A/G]TGTAGAGCATTTCGC | 55626 |
rs762324502 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550075 | CCACCCGCCTCAGCC[C/T]CCCAAAGTGCTGGGA | 55626 |
rs762337153 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558282 | ATCACCGGGCGCAGT[C/T]GCTCACACCTGTAAT | 55626 |
rs762344782 | snp | A/G | | | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518291 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCTCCC | 55626 |
rs762346705 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498598 | AGAAACACAGCAGCA[A/G]CTCTTTTGCTAAATG | 55626 |
rs762361342 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519753 | GCATTTGGTATTCAA[C/G]CTTTGCAGCCAAATT | 55626 |
rs762374019 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556418 | TCCCGAAGGCAAACA[C/T]ACCTAGAAGCAGAAA | 55626 |
rs762390386 | snp | C/T | 2.81092e-05 | 0.00374884 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494131 | GTTCTTACCTTGGGA[C/T]AAAGCGTCCAAGCGA | 55626 |
rs762402757 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397246 | CGGGCTCCAGATCCT[A/G]GAAGGTTCTAGTTCC | 55626 |
rs762416639 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428349 | ATTGACCCTTAGGTA[C/T]TGGAGGCTTTCCCTT | 55626 |
rs762419165 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413187 | TTTCCATCCAGGCAG[A/C]AGCATGGAGCATCAT | 55626 |
rs762435423 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412651 | TTGATTTATGGTTTG[C/T]TGACTCCATGAATGT | 55626 |
rs762460695 | snp | A/G | 1.66626e-05 | 0.00288635 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397686 | GGCCTCGCTCTGCCA[A/G]TTGCCCGGCCTCTGG | 55626 |
rs762461625 | snp | C/T | 3.29766e-05 | 0.00406045 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542585 | CATCTGACTCAGTTG[C/T]CAACCCTGATGCCGG | 55626 |
rs762480486 | snp | C/T | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542566 | TGGCTGGAGCCATTC[C/T]CTCCATCTGACTCAG | 55626 |
rs762480885 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516544 | CGAGCCATTCTCCTG[C/G]CTCAGCCTCCCAAGT | 55626 |
rs762502501 | snp | A/G | 1.65422e-05 | 0.0028759 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397766 | CCAGGTTCAGTGCCC[A/G]TCTGAGAGCTGCGGT | 55626 |
rs762502825 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467060 | ATAGCTGGGACTAAG[C/G]TGCACGCCACCACAC | 55626 |
rs762503147 | in-del | -/TTTG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563247 | ACCTCATCTCTTTTT[-/TTTG]TTTGTTTTTGTCAAC | 55626 |
rs762505897 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576876 | GCTCTGAAGATGATA[C/G]GAAGTTAAAACCATG | 55626 |
rs762528722 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593591 | GGGGGTGCCCTAGAC[C/T]CAACATCTCCTCCCT | 55626 |
rs762532121 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547649 | TCTCATGATTTTTCA[C/G]GTTAGCACTGCTCAT | 55626 |
rs762540889 | snp | A/C | 3.47252e-05 | 0.0041667 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547076 | AAAAAAAAAATTAGA[A/C]CACCAAAAGAAAAGG | 55626 |
rs762552379 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518682 | CTGCTCTAAAACATT[G/T]GCTTACATAGAATTC | 55626 |
rs762554577 | snp | C/T | 1.66054e-05 | 0.00288139 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433594 | CATTACATATCTGCC[C/T]ATTGGGGACAGGCTC | 55626 |
rs762563628 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462357 | CAGTCAACACTAAGC[G/T]CCGGGCCCTTGTCCC | 55626 |
rs762566166 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589626 | AGAGAAATTGCCAAC[-/T]TTTTTTTTTTTGAGA | 55626 |
rs762580043 | snp | C/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542017 | TGTGACACAGTTCCA[C/G]ATCTGCTGGACTGGG | 55626 |
rs762611372 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443230 | CCAAGAGCTAAACCT[C/T]GTGACCCTTTTAGGA | 55626 |
rs762619276 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592530 | TGAGAGGCCGACGTG[A/G]ACGAATCACTTGAGG | 55626 |
rs762629963 | snp | C/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545715 | AGGAGCTGAGCCGTA[C/G]GGTGGAAAGCCAGGG | 55626 |
rs762641846 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501360 | TGAGTGTGGGTGTGT[G/T]CATGAGTGCACCCTG | 55626 |
rs762661839 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465189 | CCGATCCAATCCTAA[A/G]CTTACTTAGCCTCAC | 55626 |
rs762693015 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458066 | GAGAGCATGGTGAAT[A/G]GGTCTGTTTCACAGC | 55626 |
rs762699231 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441487 | GCGACTGCACCCCAG[C/G]CTGGTGACAGAGCAA | 55626 |
rs762713834 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533474 | CTTCTTGTTTGGAGG[C/T]TGGGGAAGAGTGGAG | 55626 |
rs762720296 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496270 | ATCTTGTAATCTCAG[C/T]TGTTCAGAGGCTGAG | 55626 |
rs762751812 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480863 | GCCATCCAACTATCT[A/C]TCCTTTACGTATAGA | 55626 |
rs762756235 | snp | C/T | 1.76721e-05 | 0.00297249 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408553 | CCCTGGCTCCGGCAC[C/T]TCCCTCTCAGTCTGT | 55626 |
rs762764884 | in-del | -/G | 1.68069e-05 | 0.00289882 | frameshift-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434884 | TTTCGCCCAGGTTAT[-/G]GGGGGGCCAGGGAGT | 55626 |
rs762785453 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572209 | GGGAGGCTAAGGCAG[A/G]AGAATCGCTTAAACC | 55626 |
rs762841668 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520203 | TATGGGTTTCCACTA[C/T]CAATATTTAATTTCA | 55626 |
rs762843150 | in-del | -/TGTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567068 | ATATTAAGTAGTGTT[-/TGTT]TGTTTGTTTGTTTGT | 55626 |
rs762852514 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456912 | CCTCCCCTCCTCTTC[C/T]GCCCCCACTCAGCAC | 55626 |
rs762852821 | snp | A/C/T | 3.35229e-05 | 0.00409396 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542949 | GTCCTGCTGCGTTGA[A/C/T]GAGGCCTGCTCCGGG | 55626 |
rs762854837 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546547 | TGTACTATGTCACAA[C/T]GGGCTGAAGGAAGCA | 55626 |
rs762855047 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565363 | CACATGAATCAGCAA[C/T]TGCATGCTTGGGCAT | 55626 |
rs762865518 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486840 | GAACCCAGGAGATGG[A/C]GGTTACAGTGAGCCA | 55626 |
rs762915822 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419430 | AACTTAGAACAAACA[C/T]ATACATTCAAATAAT | 55626 |
rs762930754 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525880 | TCACGCCATTGCACT[C/G]CAGCCTGGGTGACAG | 55626 |
rs762942353 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563374 | GGACTACAGGTGTAT[A/G]TAACTACGCCCCAGT | 55626 |
rs762967968 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433197 | GATTAAAAGTTTCAC[A/G]TAGAAGTAAGGAAGT | 55626 |
rs762975319 | snp | A/C | 5.42805e-05 | 0.00520935 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397430 | CGGTTCGAGGGGAGG[A/C]ACCAGTGCAACGTTT | 55626 |
rs762997202 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418989 | GGAATTGGAGGTGAT[-/A]GGGGGGCGGGAGGGG | 55626 |
rs763000447 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560869 | CTTAACCCCAGAAAC[A/G]GAAACTGAAACCAGC | 55626 |
rs763010785 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471939 | CCAGGAATAACTTTC[A/T]ACTTCAGGATTTGTT | 55626 |
rs763048096 | snp | C/T | 1.82824e-05 | 0.00302338 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543038 | CAGGGGGGACACTGT[C/T]CTGGTGTGGCAAGAG | 55626 |
rs763058376 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477662 | CGTCTTTATTGTACA[C/T]AGGCTATACCATTTT | 55626 |
rs763072636 | snp | A/G | 1.80817e-05 | 0.00300675 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397475 | CGTGGTTCTCCCCTA[A/G]GGCCTGCAGCGTCCC | 55626 |
rs763079832 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410702 | TGAGTATTCTTCAGA[C/T]ACAGAGAAAGGAACT | 55626 |
rs763082604 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536516 | ACTCAGCTAGATCAA[C/T]GGCACAGAAAAACTA | 55626 |
rs763088925 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446363 | CCCAACCATTTAGTA[C/G]GCCTCTGGCCACTAA | 55626 |
rs763119185 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550109 | CAGGTGTGAGCTACT[A/G]CACCCAGCCGACACT | 55626 |
rs763130499 | in-del | -/TCAGCTAATTTCTGG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477485 | CACATGCTACCAAGC[-/TCAGCTAATTTCTGG]AAAAAAAAAAAAAAA | 55626 |
rs763144529 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46417933 | TCGGCAGATCACCAG[A/G]TCTCCTTTGTTAGTA | 55626 |
rs763151116 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477232 | GACACTAGCTCAATC[A/T]CATCACCACAACCTC | 55626 |
rs763189644 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498331 | CAGGGAAACACCAGA[A/G]AAACCCTCATCAATT | 55626 |
rs763208062 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588890 | CTCTACTATACCTAC[C/T]GTGTGATCTTGGTTA | 55626 |
rs763210929 | snp | C/T | 4.88091e-05 | 0.00493985 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435043 | TTCACGGAAGCTGCA[C/T]CAGACAAAGAAAGAA | 55626 |
rs763224382 | snp | A/G | 1.65132e-05 | 0.00287339 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543926 | TGGAATACTAGTTAA[A/G]AAAAGAACTCACAGT | 55626 |
rs763230511 | snp | A/C/T | 5.11107e-05 | 0.00505501 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542179 | GGTGGCAACTGGCTG[A/C/T]CACTTGATGGCACAC | 55626 |
rs763242762 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492134 | GGCACGGACCACAGC[A/T]TCTGTTTTACAACTA | 55626 |
rs763274375 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510237 | GAATCAGAGTACAAG[A/C]GCTAGTTCCTAAAAG | 55626 |
rs763359961 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435918 | CCTCTGAGTCCCACC[A/G]TGTGATTCCCTGCCA | 55626 |
rs763376025 | snp | C/T | 8.23825e-05 | 0.00641751 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542714 | TTCTGGGCGGGGGCA[C/T]GGATTCCGCCTCAGA | 55626 |
rs763377664 | snp | A/G | 0.000598587 | 0.0172897 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543176 | CGGAAGTCCTGGGGC[A/G]CTCCGTGGAGGGCTG | 55626 |
rs763394995 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529287 | TCATCCAGCAAATAA[C/G]CTTGGAACCTCCATT | 55626 |
rs763398998 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415223 | TTTGAGACTGGAGAC[C/G]ACTCATCTGTAGACC | 55626 |
rs763411935 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528325 | ACAGGTGCCCACCAC[C/T]GCACTCGGCTAAGTT | 55626 |
rs763412301 | snp | A/C | 2.71374e-05 | 0.00368347 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494136 | TACCTTGGGACAAAG[A/C]GTCCAAGCGAAGGTG | 55626 |
rs763418927 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437757 | GCCACAGGAAAGTAA[C/T]GTACTAATGACAAAG | 55626 |
rs763485268 | in-del | -/ATTG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509882 | GGAAATCAGAAAAAA[-/ATTG]ATTAAGAACAGAAAC | 55626 |
rs763495876 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399135 | GCTGGAGTGCAATGA[C/T]GCGATCTCAGCTCAC | 55626 |
rs763497191 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503977 | GTGCTGAGATTACAG[A/G]TGTGAGCTGCCACAC | 55626 |
rs763506625 | snp | C/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451681 | TTTAACTTGAGACTT[C/T]CTAATTCAGAATGGC | 55626 |
rs763511767 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488721 | CCATAAAACAAGTTC[C/T]AATAAAATTAAAATG | 55626 |
rs763519414 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478096 | GCCCAATCTATGCAA[G/T]TCACATTTGGTCCCC | 55626 |
rs763522123 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528304 | AGCCTCCTGAGTAGC[C/T]GGGTTACAGGTGCCC | 55626 |
rs763522288 | snp | A/C | 1.66181e-05 | 0.00288249 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410395 | TTGGGAAGGGTAAAG[A/C]AGAAGGTGAAAGGCA | 55626 |
rs763541860 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439959 | ATATCCAAAAATTTG[A/G]TAGTACATTCTATCA | 55626 |
rs763545801 | snp | A/C | | | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430521 | TTGTCCAAGAACCAC[A/C]GTTTGAGAAGCACTG | 55626 |
rs763564551 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517075 | TATTTGATCCATTGG[A/T]CAGCAAGGGGGAAAT | 55626 |
rs763567052 | snp | C/T | 1.65116e-05 | 0.00287324 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508302 | TAGCGCATGGAGCGC[C/T]GGCGAATACTGTCTC | 55626 |
rs763570501 | snp | C/T | 0.000198432 | 0.00995876 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542858 | GGGTAGGACCCAGAC[C/T]GAGGTTGCGGAGCGT | 55626 |
rs763575582 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444629 | AGAGTTTACCAGCCT[C/T]GGAAAAATGGACAAT | 55626 |
rs763618953 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590702 | GAACCCAATCTAACA[C/T]TGACAGAACACCACA | 55626 |
rs763620266 | in-del | -/AA | 0.114624 | 0.210175 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547885 | TACTCTCTGGGAGAC[-/AA]AAAAAAAAAAAAAGT | 55626 |
rs763630989 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589677 | CAGGCTGGAGTGCAG[C/T]GGTGCTAACTCGGCT | 55626 |
rs763635967 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530457 | CTCCTCATTTGCACA[C/T]GATTCCCAAGAAAGA | 55626 |
rs763638197 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424507 | CTGAGGAATCTACTT[C/G]TGTGCTAAAAGAAAT | 55626 |
rs763651547 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479389 | GCTTGCTTTAGCTGA[C/T]GGAATGGACAAAAGC | 55626 |
rs763658953 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569829 | AGCCAGGTGTGTTGG[C/T]ATGCACAGGTAATCC | 55626 |
rs763675092 | in-del | -/AG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564946 | GTGCACCAAGAATGT[-/AG]AGTGTGAGTACTCTA | 55626 |
rs763712424 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465318 | GTGTGGCATGGCACA[C/T]GCTCATCTCTTGGGA | 55626 |
rs763741733 | snp | A/C | 1.8085e-05 | 0.00300702 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397488 | TAGGGCCTGCAGCGT[A/C]CCCCCTGCTGCTGCC | 55626 |
rs763742004 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543728 | TGAGTGACAAGCTAT[C/T]CAACACTGTCTAGTG | 55626 |
rs763758561 | snp | C/T | 3.30671e-05 | 0.00406602 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512705 | TCCCCCCACCTAGTG[C/T]CATTTCTCACTTTGG | 55626 |
rs763760751 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46417986 | GCTCAGGCAGCCAAC[A/G]GGCAGAGTTGATACT | 55626 |
rs763802088 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547731 | TTCAGAGAGACTTTA[A/G]GGACTGACTTGGAAG | 55626 |
rs763833504 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572248 | GGAGGTTGCAGGGAG[C/T]AGAGATCGTGCAACT | 55626 |
rs763849615 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582493 | GGACTATAATCTCCA[C/T]ACAGGCATGGACATC | 55626 |
rs763853697 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545028 | GATACTCATAAGACT[A/G]AGGTGGGAGGATTGC | 55626 |
rs763862868 | in-del | -/CT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416731 | CACTCTGGGAAAAGA[-/CT]CTGCACCAAGTGGAG | 55626 |
rs763870403 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419316 | AACTTAATCAGAGAT[-/A]GGGGCAGGTCAGTGG | 55626 |
rs763888240 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438489 | GCCAGATGAGGCCAC[A/G]GGAGCAATTAGCAGT | 55626 |
rs763891470 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469135 | GTGACAACAGGGAAA[C/T]TCCACCTCAAAAAAA | 55626 |
rs763892292 | in-del | -/TATTTTATTATTTATATATAAATATG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418306 | TAAATATATAATATA[-/TATTTTATTATTTATATATAAATATG]TATTTTATTATTTAT | 55626 |
rs763900320 | snp | C/T | 1.66721e-05 | 0.00288717 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547128 | GTGTAAATCCCAAAT[C/T]CTAACCTCCCCATCT | 55626 |
rs763903350 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415455 | TTTTGAGTGAAAAGC[A/G]CTCTGGATAGTAAAG | 55626 |
rs763904240 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560104 | TAACCACCTGACAAA[C/T]TGAAAACAAATAATT | 55626 |
rs763907989 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450894 | TAATGATGTGTCTAC[A/G]TTGGTTCATCAGCTG | 55626 |
rs763945218 | snp | A/G | 0.000152451 | 0.00872938 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46435033 | CACCAGCACATTCAC[A/G]GAAGCTGCATCAGAC | 55626 |
rs763951471 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505358 | AGTTTACTGTAGAGG[A/G]AGGTGGGCAGGGAAG | 55626 |
rs763963093 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448799 | CCAAAAGGACAATAA[A/G]GGAATACTATGAACA | 55626 |
rs763966082 | snp | C/T | 1.65553e-05 | 0.00287705 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397800 | TGCGGTGGCTGACGA[C/T]GATGTTGTTGCCGAA | 55626 |
rs763970721 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535201 | ATGCCGAACTTCTAA[C/T]TAAGAAGAACTCAGA | 55626 |
rs763979307 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484036 | AGTCTCTTTACTCAC[C/T]CTGTAAAGACAGTCT | 55626 |
rs763997295 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577303 | AAGTACTGATAAATA[C/T]TCCAATGGAGATAAA | 55626 |
rs764012801 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443607 | ACTGCCCCTTATGAG[A/G]AAGAAGTCAAAGACA | 55626 |
rs764023832 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467549 | TACTCTATGTTACTC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs764024898 | in-del | -/TGT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529872 | TTGCTCACACAAACA[-/TGT]TGTCAGGAATGCTTC | 55626 |
rs764033868 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565735 | ATAAAAATGTTAACA[A/G]CAGTTTTATTCATAG | 55626 |
rs764036930 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486885 | CACTCCAGCCTGGGT[A/G]ACAGAACAAGACTCC | 55626 |
rs764045939 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522309 | CACATTACACTATAG[A/T]TGTAAGACTTGAATG | 55626 |
rs764066093 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520256 | AAAATTTTAATACAC[A/C]AGCACACATTCAATT | 55626 |
rs764072638 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563741 | GCAACTCGGGAGGCC[A/G]AGACAGGAGAATTCA | 55626 |
rs764079041 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458545 | TCCTTCTTCTTGAGA[A/T]GGTGAACTCCTTGAG | 55626 |
rs764096778 | snp | C/T | 0.000151782 | 0.00871023 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542148 | GCTGGGCGTTTGGCC[C/T]TCAGTCCGCTCGAGA | 55626 |
rs764126747 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495582 | AAGGAGGGGCAAGGA[G/T]AAAGAGATAAGACTA | 55626 |
rs764137075 | snp | A/G | 1.64931e-05 | 0.00287163 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548321 | AGCTCCCATGGCCCG[A/G]GCACCCCGTTCTCGC | 55626 |
rs764149197 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528559 | ACTGCAAGATTCCAT[C/T]AATAAGAGGTACCTA | 55626 |
rs764175605 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556444 | AGAAAAACTCCAACT[A/C]TTCCCTGAATTGTGT | 55626 |
rs764177732 | in-del | -/AAAG | | | intron-variant, utr-variant-5-prime | AMBRA1 | GRCh38.p7 | 11:46591332 | ATCTAGATTCTCCAT[-/AAAG]ATAGTCTGGTGGCTC | 55626 |
rs764187065 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546743 | GGCTCTTCCAGAATT[A/C]AAAAACCAATGGTAA | 55626 |
rs764214913 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509891 | AAAAAAATTGATTAA[A/G]AACAGAAACAGGAAT | 55626 |
rs764217625 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405041 | CCAGTGTCAGTTCTC[C/T]ACATGCACCAGACAT | 55626 |
rs764221807 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407155 | GCTGAAGTGAGCCGA[A/G]ATCATGCCACTGCAC | 55626 |
rs764223244 | snp | A/C | 1.66349e-05 | 0.00288395 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548227 | CAAATCCTATGTGAA[A/C]TATAGCCATTTTCCT | 55626 |
rs764224419 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589912 | CAGGTGTGAGCCACC[A/G]CGCCCGGTCTAAAAA | 55626 |
rs764232463 | snp | A/G | 1.70606e-05 | 0.00292062 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408577 | AGTCTGTGTTTCGGC[A/G]TTCTGCAGCTGAAGG | 55626 |
rs764244549 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578009 | GGTGGTTTGTACCTG[-/T]AATCCAGCTACTTGG | 55626 |
rs764245855 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444756 | GCATTTATTGCACTG[C/T]TACTCCTGGTGTCCC | 55626 |
rs764250777 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457248 | GCTAAGGACAGCATG[A/G]TGTCAGTCCACTGCA | 55626 |
rs764253044 | snp | G/T | 1.88802e-05 | 0.00307242 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543047 | CACTGTCCTGGTGTG[G/T]CAAGAGGGAAGGAAC | 55626 |
rs764255347 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525019 | AAAATACAGATGTGG[A/G]CTGGGCATGATGTCT | 55626 |
rs764268173 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582286 | AGAATTTCATACATG[C/T]TATTCCCTTCCCTTT | 55626 |
rs764273792 | snp | A/G | 1.89052e-05 | 0.00307445 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408735 | GGCAGACTAAAGTCA[A/G]ATGGGGCTTGGGACA | 55626 |
rs764277390 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560899 | CTGCCTCAAACAGAC[C/T]TAATGACTTTGGCAA | 55626 |
rs764277608 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418788 | GGCTCTAATAATGCG[A/C]TCTCCTTAGAGCCTT | 55626 |
rs764286819 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473921 | TCCCAAAGTGCTGGG[A/G]TTACAGGCGTGAGCC | 55626 |
rs764299310 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440669 | TCATTTTCAATAAGG[A/G]AAAATGTGGATTGTG | 55626 |
rs764301069 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477873 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGTC | 55626 |
rs764324195 | snp | C/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591992 | CTCTTGTTGCCTAGG[C/G]TGGAGTGCAACGGCG | 55626 |
rs764339167 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397059 | AGGGCAAAGCTGCCT[C/T]GCGGGCCTCTGTCCA | 55626 |
rs764342544 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419570 | GATCATCAGGGCCTA[C/T]GAAAACGACAGGAAG | 55626 |
rs764346684 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563735 | ATCCCAGCAACTCGG[G/T]AGGCCGAGACAGGAG | 55626 |
rs764361329 | snp | G/T | 3.60822e-05 | 0.00424733 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397547 | AACTCGCAGTGGAGG[G/T]TTGGTCCCTCAGCGC | 55626 |
rs764374675 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472399 | GGGTGCTAGGACATA[G/T]ATTTAATTTTCTTCC | 55626 |
rs764416484 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538532 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTTGAGTG | 55626 |
rs764433270 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501399 | TGGCATCCTGTCCAG[A/G]GCAGGTTCTCCCTGT | 55626 |
rs764444865 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441970 | AAAAAAAAAAAAAAC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs764462156 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447943 | CAAATACTAAGTGTC[G/T]AATAAATGGCCTTTA | 55626 |
rs764462288 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498520 | AGAAAAAAAACACCC[A/T]TCAAACAATCAAGTA | 55626 |
rs764485151 | in-del | -/GA | 1.73782e-05 | 0.00294767 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508373 | AGCAGGAGATAATCT[-/GA]GAGAGACAGAGATGG | 55626 |
rs764519575 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494368 | GCACATTAATAAAAC[A/G]TATTTCTGGAGAACC | 55626 |
rs764532380 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486487 | TCCTAAAAGTTAGCA[A/G]GCCTGAGGCTCTAGA | 55626 |
rs764534014 | snp | A/G | 1.68698e-05 | 0.00290424 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545575 | CGTCAGTCCTGTGCC[A/G]GACAATGCAGATGGG | 55626 |
rs764549693 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410249 | GGGCCTCCAGCCAGC[C/T]GCTCCCTGCCTACTT | 55626 |
rs764604006 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500039 | GTTATCTAATCTCAT[C/T]TTACACATCAGACAC | 55626 |
rs764607562 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556128 | TAGAAGCCTAAAACT[G/T]CCCCAGTACTCTTTG | 55626 |
rs764608295 | snp | C/T | 5.12825e-05 | 0.00506346 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493597 | CAAAAGCCAAAGAAA[C/T]ATTTCCTTACCTGCC | 55626 |
rs764616710 | snp | C/T | | | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396378 | AATCCCCACCCCTCC[C/T]CCATCCTCCTTGGAA | 55626 |
rs764617873 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485362 | CACTCAAAAGATGAA[C/T]GGGGACACATTTGCA | 55626 |
rs764618047 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579982 | CCTCCCAAAGTGCTG[C/G]GATTACAGGCGTGAG | 55626 |
rs764620287 | snp | C/G | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543975 | GCTGGACTAACTTAC[C/G]TGTTGATTAGAGGGG | 55626 |
rs764647870 | snp | A/G | 1.72139e-05 | 0.00293371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418088 | AAAAAAAGAGAATGG[A/G]AGGAGAAACAATTTG | 55626 |
rs764649563 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448291 | ACTAAACTAGAAATC[C/T]GTAATAAAAAGATAA | 55626 |
rs764669049 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412410 | CTACCTCAGCCTCCC[G/T]AGTAGCTGGTACTAC | 55626 |
rs764684911 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515184 | AGTGACCAAAAAACA[A/T]CCTTCTTGGCTGGGC | 55626 |
rs764688248 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425953 | AGATCAAGACCATTC[G/T]GGCTAACACGGTGAA | 55626 |
rs764694278 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544294 | GAGTTGCCATCCCAG[A/G]AAACAGCTACCTTAA | 55626 |
rs764701018 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518655 | CCCTTTACAGAAGAT[A/G]TTCGCCCATTTCTGC | 55626 |
rs764713896 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572495 | TCCATGAGTAAATAA[G/T]CATAGCAGTTTAAAA | 55626 |
rs764730391 | snp | A/T | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542438 | CCTGGGCCTGTTGGG[A/T]CTGGGGAGCTTCCCC | 55626 |
rs764738891 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532412 | AATTTACTACTGATA[A/T]GCTTAAGAGCTTATG | 55626 |
rs764747408 | in-del | -/TGTTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579709 | ATGAGGAAACAGACA[-/TGTTT]TGTTTTGTTTTGTTT | 55626 |
rs764785641 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412725 | CTAAACAGCCATTTT[C/T]GTGGGGTTTGGGGAT | 55626 |
rs764792683 | snp | C/G | | | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547278 | ATTATGGTTCACATG[C/G]GTGGAGGCTAAGAGA | 55626 |
rs764793140 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516825 | TGGCAGTTCTGCACA[C/T]TCTGCTGTGACCACC | 55626 |
rs764793811 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554727 | CACAGGGCTGCTGAT[G/T]AGGAGAAAATGCCAG | 55626 |
rs764821864 | snp | C/T | 1.6722e-05 | 0.00289149 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397673 | GTCCGGGGGCTTAGG[C/T]CTCGCTCTGCCAGTT | 55626 |
rs764824921 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546426 | AGTTACTAGGACAAA[G/T]AGGATCTTGCTTTGA | 55626 |
rs764842330 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592446 | GCTTTTGTATGTGCA[A/G]TGACCAAACTACTAA | 55626 |
rs764842787 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480856 | TTTCACTGCCATCCA[A/G]CTATCTCTCCTTTAC | 55626 |
rs764912965 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448555 | ACCTACCATAAGAAA[A/G]AAGAAAAAGAGCAAA | 55626 |
rs764928631 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458757 | TTGAGTCACCATGAC[C/T]AGAACCTCACATTTT | 55626 |
rs764956335 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577502 | ACTGGTAAGGGGTTT[C/T]ACTTTGCAGAGATGG | 55626 |
rs764971937 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530572 | AGAATCCCACAAGAG[C/T]CAATACTTACTTAGA | 55626 |
rs764989472 | snp | G/T | 1.65542e-05 | 0.00287695 | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433563 | GCAGCAGGATCCTTC[G/T]TGAGGCCAAGCCCAC | 55626 |
rs765010889 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456511 | AAGAATGGGCAAAGA[A/G]AGGGGTGAAGGTAGG | 55626 |
rs765025578 | snp | C/T | 1.6492e-05 | 0.00287154 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46512778 | CCTGCTCCATCATAA[C/T]GGGATAATGAAATGA | 55626 |
rs765029943 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505654 | GAAATGTAAATTCAG[A/G]TCATGCTAAAGCCAG | 55626 |
rs765079240 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440019 | TGAACTCCAAGTGGA[A/G]TAATAATTTGGCACG | 55626 |
rs765088387 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484944 | CCACTGTGCCCAGGC[-/T]TTTTTTTTTTAAGAC | 55626 |
rs765106494 | snp | A/G | 1.65433e-05 | 0.002876 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547924 | CATGATTTGTAGACC[A/G]TGGTTCACCGTATCT | 55626 |
rs765108678 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531240 | TACAACAGCAAAGTT[C/G]AGTAATTGCAACAGA | 55626 |
rs765119288 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470264 | TGAGCAACATAGGGA[A/G]ACCCCATATCTACAA | 55626 |
rs765126398 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545419 | GTGAGACAAGACTGC[A/G]CCACTGCACTCCACC | 55626 |
rs765142366 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438136 | GGCAAAAAACATATT[-/G]GGAAAAAAATGATGG | 55626 |
rs765150858 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506849 | AAGCAGCAGATGAGA[A/G]AATGCAAAACCCAGC | 55626 |
rs765169984 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563097 | GCCTGCTTCCTATTC[G/T]TAAATAATTATACAT | 55626 |
rs765191919 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418232 | ATTTTATTATTTATA[C/T]ATAAATATATATAAT | 55626 |
rs765194546 | snp | A/C | 2.99639e-05 | 0.00387054 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547783 | AGAAAGCACTGTTAT[A/C]ACAAATCTTAAGTTA | 55626 |
rs765194662 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492832 | AGGCAGGCAGATCAC[A/G]AAGTGAGGAGATTGA | 55626 |
rs765200776 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515142 | CGTTTAGTAAGCTGA[-/G]GCCCTTTGGCAAGCA | 55626 |
rs765239086 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520142 | GAAACTCCGCCTCGA[-/A]AAAAAAAAAAAAAAA | 55626 |
rs765257675 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561703 | AATAGGGAAAGAAAA[A/C]ATTTCCCTCGAGGCT | 55626 |
rs765282451 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579350 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGA | 55626 |
rs765282685 | snp | A/G | 1.65124e-05 | 0.00287331 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543199 | GAGGGCTGAGGGGGA[A/G]GCGGTGGGGGTGAGG | 55626 |
rs765282713 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482737 | AAAAACCAGCCAGGC[A/G]TAGTGGCTCACGCCT | 55626 |
rs765339767 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445341 | CAGTCATGCTCTCCC[C/T]GAGACCTGAGAATGA | 55626 |
rs765368549 | snp | C/T | 0.00019917 | 0.00997724 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543064 | AAGAGGGAAGGAACT[C/T]GAGTGCCAGAGCAGC | 55626 |
rs765368607 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496641 | TGCCAGTGCCCAAAG[G/T]TAACACAGAGCTTGG | 55626 |
rs765394689 | snp | A/G | 1.65952e-05 | 0.00288051 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410385 | TAAAAATCAGTTGGG[A/G]AGGGTAAAGAAGAAG | 55626 |
rs765409442 | snp | C/G | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542091 | CCCCACAGTCCTCTC[C/G]TCCTGCGGACTAGCA | 55626 |
rs765409662 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510268 | CCTCAACTGGAGGAA[C/T]TTTCATTATCTGTTT | 55626 |
rs765429181 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444037 | CAGCACTCTTTCAGA[C/T]AAAGTATCTCCTCCT | 55626 |
rs765429238 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460414 | GCAAGCTCCGCCTCC[C/T]GGGTTCCCACCATTC | 55626 |
rs765439848 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405250 | ACAGGCTGGGCAAAG[C/T]CCCTCCTCCTCTATG | 55626 |
rs765442843 | snp | G/T | 1.70255e-05 | 0.00291761 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542173 | TCGAGAGGTGGCAAC[G/T]GGCTGCCACTTGATG | 55626 |
rs765443017 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511824 | TTGAAATAACTTCTG[C/T]TTTGTTTTTTATCTC | 55626 |
rs765454521 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587527 | TCTTAAATGAAGACT[A/G]AAGACTTAGATGGCA | 55626 |
rs765460827 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565937 | GCCATCACATCGGCT[A/G]ATTTTTTTTGTATTT | 55626 |
rs765483914 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418805 | CTCCTTAGAGCCTTT[A/T]AGCTAACTAACTTCA | 55626 |
rs765490880 | snp | A/G | 1.64917e-05 | 0.00287151 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542571 | GGAGCCATTCCCTCC[A/G]TCTGACTCAGTTGCC | 55626 |
rs765493274 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505487 | CTATTAAAAACAAGA[G/T]TCTAGTCTACATCAG | 55626 |
rs765496337 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548706 | TGTAGCTAAAGAAAG[C/G]ATCAGGCCAAGCACA | 55626 |
rs765505923 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421316 | TCCTTAAACAGTGCC[A/G]AAAGGGCAGTTCTCA | 55626 |
rs765527816 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488515 | AATTCAATAATAATA[A/G]AGATTTCAATACCCA | 55626 |
rs765537340 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475462 | TGTATTAGTTTGCTG[C/T]ATTCTTTGATTGAGT | 55626 |
rs765543004 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584619 | ATTTTTTTTTTAATT[A/T]TTCTGAGACAGGGTC | 55626 |
rs765567606 | in-del | -/CCA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575763 | CTCGTGATCTGCCTG[-/CCA]CGGCATCCCAAAGTG | 55626 |
rs765577059 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528278 | CCAGGTTCAAGCGAT[C/T]CTCCTGCCTCAGCCT | 55626 |
rs765580297 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409852 | TGATGAAAGGATCAG[C/T]ACCAGATTTCTACTA | 55626 |
rs765582719 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545684 | GAAGTGGATCTCATT[A/G]GCAGTGGCAATCAGC | 55626 |
rs765597686 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458699 | ATTCATGGCCTCAAG[A/T]GATCCTCCCACTTCA | 55626 |
rs765634058 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494062 | AGACCAGAAAGTAGG[C/T]TTAAAACTAAATCCT | 55626 |
rs765666115 | snp | G/T | 1.66504e-05 | 0.0028853 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46493620 | TACCTGCCAGGACCC[G/T]GTTAACAGAAGAGTG | 55626 |
rs765683087 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527426 | TGGAGGTTACAGTGA[A/G]CCGAGATCATGCCAC | 55626 |
rs765686194 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502876 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 55626 |
rs765709475 | snp | G/T | 1.6531e-05 | 0.00287493 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410233 | AGCAGGAGGAAGGGA[G/T]GGGCCTCCAGCCAGC | 55626 |
rs765722504 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439807 | AGAAAAATTGGTAAA[A/G]CACATGGACAGGTCA | 55626 |
rs765749168 | snp | G/T | 1.64879e-05 | 0.00287118 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548335 | GAGCACCCCGTTCTC[G/T]CCCCCAGAGTATCCG | 55626 |
rs765758231 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542448 | TTGGGTCTGGGGAGC[C/T]TCCCCACTCAGGCTC | 55626 |
rs765797976 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420608 | CCATTTAACTTTTAA[C/T]ACTAAAAGGACAATG | 55626 |
rs765813738 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449210 | CAGAAACCACCCCCC[A/G]CCGCAAAACAAAGTA | 55626 |
rs765823612 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540038 | GGATTTACCATGTTG[C/G]CCAGGCTGGTCTCGA | 55626 |
rs765849424 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545717 | GAGCTGAGCCGTAGG[A/G]TGGAAAGCCAGGGAG | 55626 |
rs765859973 | in-del | -/ATCAAACAAT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540154 | GTATCTCTAATTATC[-/ATCAAACAAT]AGAGTTTATTTAAAC | 55626 |
rs765868168 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494134 | CTTACCTTGGGACAA[A/G]GCGTCCAAGCGAAGG | 55626 |
rs765895666 | snp | A/G | 1.72537e-05 | 0.0029371 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434864 | CAAATCGCTTGGTGT[A/G]GAGCATTTCGCCCAG | 55626 |
rs765904073 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482090 | GTTTTGTTTTGTTGT[G/T]GTTGTTTTTGCTTAG | 55626 |
rs765937742 | snp | A/G | 1.67307e-05 | 0.00289224 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545590 | AGACAATGCAGATGG[A/G]GCAGCGCACTCACCG | 55626 |
rs765959994 | in-del | -/GT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458045 | CAGGAGCAAAAATAA[-/GT]GAGAGAGAGCATGGT | 55626 |
rs765963271 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558491 | GAGGTGGAGGTTGCA[A/G]TGAGCTGAGATCCCA | 55626 |
rs765986421 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450366 | GGAAAAGTTATAGAG[A/C]CAGAAAAATGATGGG | 55626 |
rs765996962 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467157 | CCTGATCTCAAGGGA[A/T]CTGCCCACCTCAGCC | 55626 |
rs766004029 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578883 | GAGAGACTCAGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs766009588 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576964 | TAGAACTCAGTTCTT[C/T]ATACAGGAAAGAGAT | 55626 |
rs766022920 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447241 | TGAGACTCTTATCGC[-/A]AAAAAAAAAAAGGCC | 55626 |
rs766031735 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575201 | GATGGCTCACACCTG[A/T]AATCCCGGCACTTTG | 55626 |
rs766035809 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593610 | CATCTCCTCCCTAAA[A/G]AACCACACCGGGAAG | 55626 |
rs766036168 | in-del | -/A | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595883 | CAGCTACTCGGGACT[-/A]ACAAAAAAAAAAAAA | 55626 |
rs766053672 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478747 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC | 55626 |
rs766074323 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516996 | ATACTTCCTTGTTTT[C/G]TCTACTTGCCTGGTT | 55626 |
rs766099322 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426151 | ATCTCATTACTACCT[G/T]GATTCAATTAGGGCG | 55626 |
rs766125834 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592714 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 55626 |
rs766234359 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532715 | GCTGGGATTACAGGC[A/G]TGAGCCACAGTGCCC | 55626 |
rs766236680 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543854 | AAGCTAGCTTTAAAT[C/T]TTGACTGGAAAGATA | 55626 |
rs766245855 | snp | G/T | 7.34605e-05 | 0.00606011 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543040 | GGGGGGACACTGTCC[G/T]GGTGTGGCAAGAGGG | 55626 |
rs766246006 | snp | G/T | 1.66018e-05 | 0.00288108 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512822 | CAGCCTCCTAGCAGA[G/T]ATTAAAAAAATGGCA | 55626 |
rs766252820 | snp | C/T | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548312 | AAGCCGCTGAGCTCC[C/T]ATGGCCCGAGCACCC | 55626 |
rs766254314 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480865 | CATCCAACTATCTCT[A/C]CTTTACGTATAGAGA | 55626 |
rs766263976 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456979 | TCTTAACCAACTCTT[C/T]TGTTAAAACTTTCCT | 55626 |
rs766315565 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548036 | AGAGATAAACCTAAA[C/T]TACCTTCAGGAAAAC | 55626 |
rs766328786 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525898 | GCCTGGGTGACAGAG[C/T]GAGACTCTGTCTCAA | 55626 |
rs766348143 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593134 | TTTACTTCTGAAGCC[C/T]CTTGTGACAGGATCT | 55626 |
rs766366264 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505302 | CCTCCTCACAGAGCA[C/G]GTGGACACTCAGAGG | 55626 |
rs766405378 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546567 | TGAAGGAAGCAAAAG[C/T]AGATGTTCATCTTAG | 55626 |
rs766416528 | snp | A/G | | | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396130 | GAATAGCCTTCTGTC[A/G]TTCCTTCCTACATAC | 55626 |
rs766423864 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563381 | AGGTGTATATAACTA[C/T]GCCCCAGTAATTTTC | 55626 |
rs766433502 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499604 | CAGGAAGGCCCCTTA[A/C]TTTTCTGAGACTTTT | 55626 |
rs766434950 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469260 | TGTTTTATGCTGAAC[C/T]CTCCAGCTCCTAATC | 55626 |
rs766479537 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467238 | TGATTTTTCAATTTC[C/T]GCTATTATCTACTGA | 55626 |
rs766490337 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419449 | CATTCAAATAATTTG[A/G]GAGATTAAAAGAGAT | 55626 |
rs766504525 | snp | C/G | | | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430633 | TATGGGATTGTGTCA[C/G]AGATCATCTCTTGGG | 55626 |
rs766519529 | snp | G/T | 1.65485e-05 | 0.00287645 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46443519 | GAGGTCAAACTTAGT[G/T]AAGTCCCACCACTGG | 55626 |
rs766521795 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470588 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs766547813 | in-del | -/AAAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496074 | GACTCTCATCTCTTT[-/AAAG]AAAGATAGAAAACAG | 55626 |
rs766554974 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413590 | CAGCCTCCCAGATTC[A/G]AGTGATTTTCCTGCC | 55626 |
rs766574123 | snp | A/C | 1.8082e-05 | 0.00300677 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397478 | GGTTCTCCCCTAGGG[A/C]CTGCAGCGTCCCCCC | 55626 |
rs766574658 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535409 | TTAACAAGGTTCACT[C/T]TCATGATGCTCAGAC | 55626 |
rs766577723 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498234 | AGCCAACACCCTTTC[C/G]AAGGGTAATGACTTA | 55626 |
rs766577766 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432044 | ATTTTTATTTATTTA[-/T]TTTTTTTTGAGATTC | 55626 |
rs766588992 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550138 | CTAGCTTTTCTAAAA[G/T]ATCAGGAGAGTTGAC | 55626 |
rs766592349 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446389 | ACTAAGATGAAGGCA[C/G]GAAATGTGCCAGAGG | 55626 |
rs766597425 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422310 | CATCTATGAAGGGAA[A/G]TAGAATCAATATGCT | 55626 |
rs766609568 | snp | A/C | 3.08333e-05 | 0.00392628 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435058 | TCAGACAAAGAAAGA[A/C]AAGAGGATAAGAAAC | 55626 |
rs766624950 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568901 | AACCTCCGCCTCCCA[A/G]GTTCAATCGATTCTC | 55626 |
rs766637409 | in-del | -/CA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513151 | GAGTGAAAAATTAGG[-/CA]CACACAGAGATTATC | 55626 |
rs766638360 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460566 | CTGACCTCGTGATCC[A/G]CCCACCTCAGCCTCC | 55626 |
rs766648602 | snp | C/T | 1.67998e-05 | 0.00289821 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508143 | CCAACTTGGAAGCAC[C/T]CCAAGCTTGAGAGGA | 55626 |
rs766656973 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475810 | GTAAGGTCTCAGATT[C/T]GGAGAAAGGTGGAAC | 55626 |
rs766661766 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461972 | TCATACTGCCCCCCA[C/T]TATCTAGACTCCTTC | 55626 |
rs766687665 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438020 | AACAAATTCCCAGGT[G/T]TCTCTGATGTTGCCG | 55626 |
rs766713815 | snp | A/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401046 | ACCTACGGCCTTGGT[A/G/T]CCCACAGAGATTCTA | 55626 |
rs766730255 | in-del | -/CT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575134 | GGTATCAGTAACTCC[-/CT]CTTAGTCCTTTTGGG | 55626 |
rs766762490 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421461 | GCTTAGCACACTCTA[C/G]TGCGGTGTGGGAAGG | 55626 |
rs766764696 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434224 | CTATTTTGAAACCCA[C/T]CTTTTTCATTTAATA | 55626 |
rs766767464 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587708 | AGAATACTTGTTTCA[A/G]TCTAAATTTCAATAT | 55626 |
rs766803928 | snp | A/G | 0.00018657 | 0.0096566 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543214 | GGCGGTGGGGGTGAG[A/G]GGGTAGCAGAATCTT | 55626 |
rs766814821 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553562 | CCAGCCTGGCCAACA[C/T]AGTGAAACCCTGTCT | 55626 |
rs766818043 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431663 | ATTTAAACGATTATT[C/G]CACAATTAGGCCGGA | 55626 |
rs766819746 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490673 | AGGTCTGCCAAATTT[A/C]CAAGCTTCATCCCTG | 55626 |
rs766827123 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566623 | GAGCTACCTAACCCC[-/T]GAAGGCATTCTCCCT | 55626 |
rs766887174 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587628 | ACTGAAGACTCTAAT[C/T]CCTGTAAATACCCAG | 55626 |
rs766905018 | snp | A/G | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451446 | CTCTTCTGTTGCTTG[A/G]AAAGAATTAGGAATC | 55626 |
rs766912210 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512230 | CCATTTACTCCTTCT[C/T]CGGTCGTCTCTTCCT | 55626 |
rs766932712 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528453 | TGGGATTACAGGCGT[A/G]AGCCACCGCGCCCAG | 55626 |
rs766937318 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541732 | CTTGAGCTTAGCCGA[A/G]ATAGAGCTAGCGCAG | 55626 |
rs766958239 | in-del | -/AAC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487375 | AATAACAATTTTATT[-/AAC]AAGTTAATAAAGTTA | 55626 |
rs766988577 | in-del | -/GAG | 1.65723e-05 | 0.00287852 | cds-indel, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397733 | GTGGAGGGCTGGGGT[-/GAG]GAGGTGTGGGCGGCA | 55626 |
rs766993260 | snp | A/C | 3.44246e-05 | 0.00414863 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547089 | GAACACCAAAAGAAA[A/C]GGGTATCTTAAGGAA | 55626 |
rs767001495 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491108 | CCTCAGCAAGCACCA[C/G]TGGATCATAAAAACC | 55626 |
rs767029672 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492448 | TCACATGGCCCAGAT[C/T]CTCCAAAACAGAATG | 55626 |
rs767039388 | snp | A/G | 1.6623e-05 | 0.00288292 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410400 | AAGGGTAAAGAAGAA[A/G]GTGAAAGGCATTAGA | 55626 |
rs767052330 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399522 | CAGGCTCCCACCACA[C/T]CTGGCTAATTTTTTG | 55626 |
rs767065916 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438284 | GACAGCAGGAAGCCA[C/T]GTTCCAGACTCTGCA | 55626 |
rs767067087 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543637 | GCAGCTGACAAACCA[A/G]TTGTCTTACAAAAGA | 55626 |
rs767068601 | in-del | -/G | 1.84137e-05 | 0.00303422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493567 | TTTATCTGGCTCCTT[-/G]GCCCTTCACATTTTC | 55626 |
rs767096576 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587981 | AAAAAATTTAGGTAG[A/C]GAAGTGAAGATTATT | 55626 |
rs767102032 | snp | C/T | 6.59642e-05 | 0.00574262 | synonymous-codon, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508283 | ACGGAGACGGTTCTG[C/T]TGGTAGCGCATGGAG | 55626 |
rs767119982 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469061 | GGCAGGAGAATCACT[C/T]GAACCTGGGAGGCGG | 55626 |
rs767129001 | snp | A/G | 5.03157e-05 | 0.00501551 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397873 | CACGGCTGTCATGCC[A/G]CCCTCCGCCATCAGC | 55626 |
rs767153767 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523591 | ATCAGAAGATGTAAA[C/T]TGCCTTCTTTTTATT | 55626 |
rs767155024 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560018 | GAAGTCTCGCACCTA[C/T]AGTTCTAAGAGAAAG | 55626 |
rs767155527 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436340 | TTCCCTGTGTGTTGC[C/T]AATGAGATGACAGTG | 55626 |
rs767171530 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558745 | ATTTTATCACACTGG[G/T]GATCCTTTCTTAGGA | 55626 |
rs767190003 | snp | G/T | 1.65261e-05 | 0.0028745 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542845 | CCCAAAGAGCGGCGG[G/T]TAGGACCCAGACTGA | 55626 |
rs767208717 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520544 | TACCTGACTCCTCCA[A/G]CCAGAAGTTCACCCT | 55626 |
rs767219422 | snp | A/G | 1.67683e-05 | 0.00289549 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508148 | TTGGAAGCACTCCAA[A/G]CTTGAGAGGAGAGGG | 55626 |
rs767227712 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503232 | GCAACTCTTCCTTTT[A/T]CTTGAACATACAGAG | 55626 |
rs767241078 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414649 | TGGTTATCAGTGGGG[A/G]TGCTGGCTGGCTGGC | 55626 |
rs767241176 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428530 | GATTCAAGTTCCTAG[C/T]GCCTCTAGGATCTGC | 55626 |
rs767279865 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531762 | TCTATCCTCATTCCC[-/A]TATTGCCAAAGAGAA | 55626 |
rs767302747 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519945 | GGGAGTTCAAGACCT[A/G]CCTGACCAACATGGA | 55626 |
rs767303405 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577147 | ATAACTGAAAATAAG[A/C]CAATGCACATGCATG | 55626 |
rs767305893 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480922 | CTTAAAGAGGGATCT[C/T]TAACCCTTCACTAGC | 55626 |
rs767315638 | snp | C/T | 3.29641e-05 | 0.00405968 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542053 | ATTCTTTCCCAGTGG[C/T]CTGTCTCCTGGTTAA | 55626 |
rs767327013 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427731 | AAATGGTAACAGGCC[A/G]GGAGCGCTGGCTCAT | 55626 |
rs767346385 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482477 | TAACTATATCAATAT[A/G]GTAGATTCTGGAGAC | 55626 |
rs767357015 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406576 | CATACATATATACAT[A/G]CTACAAACACACATA | 55626 |
rs767375021 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445129 | CCCCTCCAAAGCATC[A/G]GAGTATATAAATAGA | 55626 |
rs767392254 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496343 | GCTGAAATTGCGCCT[C/T]TGCACTCCAGCCTGG | 55626 |
rs767397190 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505939 | AGGCGTGCATGGAAA[C/G]AGGGCTAGGCAATCC | 55626 |
rs767412313 | snp | A/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592916 | GTTATAAGATTTCCA[A/T]AGAGGCTGGGGAGAA | 55626 |
rs767412983 | snp | C/T | 0.000100257 | 0.00707945 | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433612 | TGGGGACAGGCTCAC[C/T]GAAATGGCATTGGGA | 55626 |
rs767445465 | snp | C/G | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545730 | GGGTGGAAAGCCAGG[C/G]AGGCAATGGCATTGT | 55626 |
rs767452711 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537849 | TAAGGCCAATGAACA[A/G]AACTTTCTCCTTTCA | 55626 |
rs767458928 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593819 | CTCCCAGGCTCCTCC[C/T]GGGCCTACCTGCAAG | 55626 |
rs767462067 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534973 | GCCACCACACCCAGC[C/T]CTCAGTACCCTATTC | 55626 |
rs767481056 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549711 | TCTAATCAAAACTCA[A/G]GCAACGACTTTGGAC | 55626 |
rs767496674 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496806 | TTTATCCCTTCATTT[-/A]AAAAAAAAAAAAAAA | 55626 |
rs767500993 | snp | A/G | 1.65446e-05 | 0.00287612 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397786 | AGAGCTGCGGTGAAT[A/G]CGGTGGCTGACGATG | 55626 |
rs767552318 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533910 | GCTGCACTGGCTGAC[A/G]GTGCCAAGCATCTCA | 55626 |
rs767580184 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498664 | TGAAGGAATGAAAAA[C/T]GCACCTACAGACTGC | 55626 |
rs767580350 | in-del | -/TG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425310 | TTTGCTTGATCCATT[-/TG]TGTGTGTGTGTGTGT | 55626 |
rs767589027 | snp | C/T | 1.69006e-05 | 0.00290689 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434877 | GTAGAGCATTTCGCC[C/T]AGGTTATGGGGGGCC | 55626 |
rs767603649 | in-del | -/G | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594077 | CATCAAAGGAGGAAC[-/G]CCCAAGCAATCGTTC | 55626 |
rs767624224 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454322 | GCGTGAGCCATCATG[A/C]CTGGCAAACTGTGAA | 55626 |
rs767634929 | snp | C/T | 1.66676e-05 | 0.00288679 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548206 | CTCATTCTACCATCA[C/T]CAGCACAAATCCTAT | 55626 |
rs767643136 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561046 | TCCTGGGAGCACCAC[A/G]TTGCCCCCAATTCTT | 55626 |
rs767645986 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418729 | GGATTCTCTTAGTTT[C/T]GGGGAGAGCTAGGTC | 55626 |
rs767650550 | in-del | -/CCCTCTCTGGCTACTGAAACTCTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413452 | ATAGAGTTGAAGACA[-/CCCTCTCTGGCTACTGAAACTCTT]AGCTTTCTTTCTTTC | 55626 |
rs767665001 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432512 | TCACTTTGTATATAA[A/T]GGGTGCTATCTCTAG | 55626 |
rs767682480 | snp | C/T | 3.51679e-05 | 0.00419318 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408556 | TGGCTCCGGCACCTC[C/T]CTCTCAGTCTGTGTT | 55626 |
rs767684020 | snp | C/T | | | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430892 | CCACCTATACTTACC[C/T]GTGCAAAGAGGGAGA | 55626 |
rs767686233 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445273 | TTCTAGATAAATGAA[A/T]ACCCACAAAACAAGA | 55626 |
rs767709433 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486248 | TACCAGATGGGTACA[C/T]GGCAGAAAGATAAAG | 55626 |
rs767724709 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411280 | GTTACCTCCATAAAG[A/G]GCAAACATCCCCAAG | 55626 |
rs767736559 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564403 | CTCACAATGATACTA[C/T]GAAGATGGGTACTGT | 55626 |
rs767740370 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410523 | AGAGCTGCTGCCTCA[A/T]CAGGATGCTCAGTGC | 55626 |
rs767747456 | snp | A/G | 3.29788e-05 | 0.00406058 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543351 | GGCACGCTGACGGTA[A/G]TGGGATAATTCTGTT | 55626 |
rs767755952 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537196 | TTATCTAACAGACCT[C/G]CAATTTCTTACAATA | 55626 |
rs767771993 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446543 | GGAACAAGCTAGACT[C/G]AGAGTTTCTCAACCT | 55626 |
rs767772554 | snp | G/T | 3.68725e-05 | 0.00429359 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493562 | GAAGCTTTATCTGGC[G/T]CCTTGGCCCTTCACA | 55626 |
rs767773744 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46417961 | GTACCATAGGCCAAG[C/G]CAAGCCCTGGCTCAG | 55626 |
rs767785779 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554301 | AAAAACCGACCTTCC[A/G]ACCTCCTGTTACTCA | 55626 |
rs767796869 | snp | A/C | | | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396194 | AGCAGGCCCTGGGGA[A/C]GCAGGAAGTGGTGGC | 55626 |
rs767819159 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551982 | GTAGTGAGCCAAGAT[C/T]GCACCACTGCACTCC | 55626 |
rs767826618 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447582 | GCCAGGTGTGGTGGC[A/G]TGTACCTGTAGTCCC | 55626 |
rs767858087 | snp | A/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530335 | GATGAGGGATAATTT[A/G/T]GATCAGCCTAGTAGG | 55626 |
rs767877255 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462076 | CTGAGAAAGGCCTGT[G/T]GCAAATTTCTAGCTT | 55626 |
rs767880578 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424407 | CAAAGACAGTCAGAG[A/G]ACAAGCTTTTTATTT | 55626 |
rs767897576 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466598 | GGCTTATATAAATAA[C/T]AATAGAGATCAGGTT | 55626 |
rs767936094 | snp | A/G/T | 3.39451e-05 | 0.00411966 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542203 | GGCACACTCTCAAAG[A/G/T]AGCTGGGGACCTGCC | 55626 |
rs767944999 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572216 | TAAGGCAGGAGAATC[A/G]CTTAAACCCGGGAGG | 55626 |
rs767946157 | snp | C/T | 0.000126572 | 0.00795424 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397485 | CCCTAGGGCCTGCAG[C/T]GTCCCCCCTGCTGCT | 55626 |
rs767968334 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587430 | CATGCTAGATATTTA[G/T]AAGTCCTAGTTATCC | 55626 |
rs767969336 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477717 | CCAGGGTTTATCAAC[A/G]GCAGAGCCCCCAGCC | 55626 |
rs767976047 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551234 | GCTGGGGACTGGAGG[G/T]ACTAGATAAATGGAA | 55626 |
rs767984775 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457655 | CCTATAATCCCAGCA[A/C]TTTGGAAGGCCAAGG | 55626 |
rs767993965 | snp | C/T | 7.2351e-05 | 0.00601417 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397441 | GAGGCACCAGTGCAA[C/T]GTTTGTCTCTACCTG | 55626 |
rs767998639 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513046 | TGAATACTGCTCTTC[A/G]ATGAGAAATGAACAA | 55626 |
rs768009155 | snp | C/T | 4.9423e-05 | 0.00497082 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542311 | AGATTGTGGCAAGCA[C/T]GACAGCGATTCAGGT | 55626 |
rs768017118 | snp | A/G | 1.80742e-05 | 0.00300612 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397533 | GGTTGTTATTGGTCA[A/G]CTCGCAGTGGAGGGT | 55626 |
rs768029199 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548077 | TAAAGGAAAAAGATA[C/T]TTCTAGCACATTAGT | 55626 |
rs768080576 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568038 | CTGTAATTCCAGATA[C/T]TTGGCAGGCTGAGGC | 55626 |
rs768087178 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564789 | ACTGGAGGTTAACTA[C/T]TATTTGCCTCCTAGT | 55626 |
rs768103000 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529565 | TTGAGCTAATGCAAT[A/G]GTCAAGTACACAAAA | 55626 |
rs768127427 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422714 | TAAAACTCAGACGAG[C/T]AGTTCAAGCAGCAAA | 55626 |
rs768146233 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441283 | CTTTGGGAGGCCGAG[C/G]TGGGTGGATCACCTG | 55626 |
rs768151651 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589384 | TTAAGACACTGAAAG[A/C]TCTCTCTGAGTTTAT | 55626 |
rs768162115 | snp | C/T | | | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433617 | ACAGGCTCACCGAAA[C/T]GGCATTGGGACCTGA | 55626 |
rs768184871 | snp | A/G | 4.99347e-05 | 0.00499648 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542927 | ACGGCCGGTTCAGGA[A/G]GCCCTGGTCCTGCTG | 55626 |
rs768192103 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546352 | GCCCACAGTTCCATG[A/C]AAAGCCTGAGAAAAA | 55626 |
rs768215596 | in-del | -/TATGAAAATATGTACATTA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469539 | TATATATGAAAACTG[-/TATGAAAATATGTACATTA]TATGAAAATATGTAC | 55626 |
rs768244209 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456245 | ACCCCAAACACAAAC[A/T]TCTAGCATTCGCTCC | 55626 |
rs768258869 | snp | C/T | 3.41583e-05 | 0.00413255 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408638 | GAGGTGGCAGGGTTC[C/T]GGGGCTGAAGCCCAA | 55626 |
rs768264918 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417868 | CTGATTACCCCAGTC[C/T]TCGGCCCCAGTGATC | 55626 |
rs768272054 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495037 | ATAACTAGTAAGTGG[A/T]TAAGGCAGGATTCAA | 55626 |
rs768272763 | snp | A/C | 2.69096e-05 | 0.00366798 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547903 | AAAAAAAAAAAAGTT[A/C]AAATACATGATTTGT | 55626 |
rs768277800 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402507 | GCTGGGATTACATGT[A/G]TGCACCACCACACTT | 55626 |
rs768283518 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579180 | TACATAAAAAGGGCC[A/G]GGCATGGTGGCTCAC | 55626 |
rs768288508 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508958 | ACCTCTTTTTCTCTC[C/T]CTTAAGAATTAGTCA | 55626 |
rs768333703 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550126 | ACCCAGCCGACACTA[C/G]CTTTTCTAAAAGATC | 55626 |
rs768334358 | snp | A/G | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542270 | TGGTTCTTTCCCAGC[A/G]CAGGGTATCGTTGTT | 55626 |
rs768344438 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562951 | GATTACAGGCACATG[C/G]CACCACACCTAATTT | 55626 |
rs768347648 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573643 | AGGGTTTCTCTTTTT[-/A]AAGAAGCAGAATCCT | 55626 |
rs768347859 | in-del | -/ATAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486912 | TCCATCTCAACATAA[-/ATAA]ATAAATAAATAAATA | 55626 |
rs768351394 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504173 | AAAAAGAGGCAGGAA[A/G]GGCAGGAATATGGGC | 55626 |
rs768365295 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488737 | AATAAAATTAAAATG[A/T]ATAAAATCACACAAA | 55626 |
rs768376452 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506548 | AGCCATTCAGTTAAG[A/G]AAGAAAGCTGAGGGG | 55626 |
rs768378676 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586676 | ACAGCACCTAGTGCT[A/G]TTCTAAATGCTTTAT | 55626 |
rs768384290 | in-del | -/AACC | 1.69222e-05 | 0.00290875 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443449 | CTCACCAGCAAATAT[-/AACC]AACCCTTCCACTGAT | 55626 |
rs768416443 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522896 | AGGTCCTTCACCCTG[G/T]TATACTGCAAACACT | 55626 |
rs768435300 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470105 | GTATTATCTTCCTTA[C/G]AGCTAAAGAAAACAT | 55626 |
rs768437405 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485940 | CGAATGCTCCAGTGA[C/T]TGGTGGACACCAAAT | 55626 |
rs768465365 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411795 | TTTTAATTTTTTTTT[C/T]ATTTTTTATTGTTTG | 55626 |
rs768475083 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492486 | AAAACTTTTAATAAA[A/G]ATGCTTATTAAAGAT | 55626 |
rs768498249 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541298 | AATTATTCTTCTTCT[-/C]CACCCCAAGGTGAAA | 55626 |
rs768517716 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553604 | ACAAAAATTAGCCAG[A/G]CGTGGTAGCTCATGC | 55626 |
rs768526483 | snp | A/G | 3.31779e-05 | 0.00407282 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46443489 | TGACATTGACTTACC[A/G]TTACTGATTTCAGGG | 55626 |
rs768567584 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421064 | TACAGGGATTAACAG[A/G]CAAATATTATCTATT | 55626 |
rs768578944 | in-del | -/A | 1.64936e-05 | 0.00287168 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543956 | TTTAGCTGGAATTGG[-/A]ACTGCTGGACTAACT | 55626 |
rs768595897 | snp | C/T | 5.14218e-05 | 0.00507033 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443641 | CATTATATTATTTAT[C/T]CACGTTTCCACTGCA | 55626 |
rs768604947 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447205 | CTTGAGCCCAGGAAT[C/T]TGTAACCAGCCTGGA | 55626 |
rs768609312 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571109 | CACATTTGCCTCCTT[A/T]CAATGGTTCTGGCTT | 55626 |
rs768627603 | snp | C/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542371 | CTGCTGTGTGGGGTG[C/G]GCTGGTGGGAAGGGC | 55626 |
rs768655538 | in-del | -/AGTC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441845 | CAGCTTAGTTTAAAT[-/AGTC]AGAGTACTGTCACTT | 55626 |
rs768666021 | snp | C/T | 1.9572e-05 | 0.00312819 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397982 | AGAGCGAATTGGCTG[C/T]TGGCCTGGGCCTCTG | 55626 |
rs768667043 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551587 | TTTAAAATATTAAAC[A/G]ACACCAGGCGCGATG | 55626 |
rs768700636 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546197 | CATGGCACCATGCTC[A/C]GCTAATTTTATATAA | 55626 |
rs768704634 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541168 | AAATCAAGATAGATG[C/T]GCACATAGCCATACA | 55626 |
rs768721087 | snp | A/G | 4.94328e-05 | 0.00497131 | synonymous-codon, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508232 | TCCCTCTACTGATGG[A/G]CCCTGGTTGTCTGAG | 55626 |
rs768749560 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398523 | GGAGTCTCACTCTTT[A/C]ACCCAGGCTGGAGTG | 55626 |
rs768754614 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46451188 | TATTCTGATGACAGA[A/C]AAAACAAGGAGGAAA | 55626 |
rs768814141 | in-del | -/TT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517471 | ATTTTATTAATAAGG[-/TT]TTTTTTTTTTTTTTT | 55626 |
rs768831488 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482392 | ACCAGTCCAACGGAA[A/G]CCGTAAAAGACTGTT | 55626 |
rs768834226 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435648 | AACAAAGCCCAGCTG[C/T]GGCTGGATGGCCAGG | 55626 |
rs768839624 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414894 | CTGCCAAGTGGGTTT[C/T]AGTACCACCAAGAGA | 55626 |
rs768845209 | snp | A/T | 6.59598e-05 | 0.00574243 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542546 | GAATGCTGCCCGAGT[A/T]GTTTTGGCTGGAGCC | 55626 |
rs768853969 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475298 | GGTGTGTCTCCATGA[A/C]ATTTGCTAACGTTCA | 55626 |
rs768861542 | snp | C/T | 3.31972e-05 | 0.004074 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512684 | GGCAACCCCAAGGGC[C/T]GCCCCTCCCCCCACC | 55626 |
rs768870639 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490048 | TTGTTGCAAAGATGA[A/G]AAGAGATAACGTGGG | 55626 |
rs768927133 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464885 | CCCCGTCTCTACTAA[A/C]AATACAAAAATTAGC | 55626 |
rs768927315 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570759 | AACACATGACAACAG[-/A]AAAAAATTCAAGACA | 55626 |
rs768936681 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426735 | TGTGCCACATCTCAG[A/G]AGTCAACTTTAAGAT | 55626 |
rs768938202 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559256 | AGTGAGCCGAGATCA[C/T]GCCACTGTACTCCGC | 55626 |
rs768971927 | snp | C/G | 3.2022e-05 | 0.00400125 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494201 | GGATCTGTCACCATT[C/G]TCCCTGAAAAAAATA | 55626 |
rs768975240 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535549 | AAAGAACCTTCGCAT[A/T]TAAATTGGATTATCC | 55626 |
rs768975513 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519521 | TGGACTTTCTCCAAC[C/T]ACTGGAAACAATCAA | 55626 |
rs768995710 | snp | G/T | 1.65367e-05 | 0.00287543 | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433516 | CTGTTGCAGCCTGAA[G/T]ACCTGGGCCACCATG | 55626 |
rs768998411 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466054 | AGCTTTTTGATGGCT[C/G]AGTGAGAACTGAATA | 55626 |
rs769004853 | snp | C/T | 1.65507e-05 | 0.00287664 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397742 | TGGGGTGAGGAGGTG[C/T]GGGCGGCACCAGGTT | 55626 |
rs769007575 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414946 | TGTCTTTGTGCTTGG[A/G]GAGACTGCTGAGGCA | 55626 |
rs769034025 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558121 | ACAACTGATGTTACA[C/G]AGGGGAGAAGGACCA | 55626 |
rs769045225 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502825 | CAGCACTTTGGGAGG[C/T]CGAAGTGGGCAGATC | 55626 |
rs769054106 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592421 | TGATTTCTACACACA[A/G]CCTTTTTTAGCTTTT | 55626 |
rs769065392 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534446 | GTTACAGTGAGCCCA[A/G]ATCGCACCATTGCAC | 55626 |
rs769082619 | in-del | -/A | 0.258924 | 0.249841 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547885 | TACTCTCTGGGAGAC[-/A]AAAAAAAAAAAAAAG | 55626 |
rs769084699 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480660 | CAGATCTAGAGATTA[C/T]TGCTGAAGTTTAACC | 55626 |
rs769088382 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481457 | CAAACTCTGCCTCCC[A/G]GGTTCAAGTGATTCT | 55626 |
rs769089882 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504288 | AAAGCATACACACCA[-/C]CTCTTTTGTAGGCCT | 55626 |
rs769120191 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572593 | CCTATCTTTGATATG[A/G]CAGAAGCTCTTAGGC | 55626 |
rs769131945 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444861 | CTCTCTGCACTCTTC[C/T]GGTTGCTGCTGGCCA | 55626 |
rs769162297 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534582 | AATGGATGGATGCAT[G/T]GATCAATCACAGTTT | 55626 |
rs769169720 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547497 | CCACACTGTCCCCAA[A/G]TGACACATGCCACAT | 55626 |
rs769172527 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586095 | AGGCATTAGCCACTG[C/T]ACCCAGCCGAAAATA | 55626 |
rs769173349 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532276 | CAGGGCTATGTTTTT[A/C]TCATACAAGGGTGTC | 55626 |
rs769190157 | snp | G/T | 3.74763e-05 | 0.0043286 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433670 | TTTCCTAGGCTTCTG[G/T]CCATTCCAAGGAAAC | 55626 |
rs769195745 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576281 | ATATACTCATGAAAA[C/T]GCCAGAGACATTGGT | 55626 |
rs769198463 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593439 | GGTCCCTTCAAAGGC[C/T]GGACTCAGTAGGGGT | 55626 |
rs769228239 | snp | A/G | 1.64942e-05 | 0.00287173 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542553 | GCCCGAGTTGTTTTG[A/G]CTGGAGCCATTCCCT | 55626 |
rs769230335 | snp | A/C | 1.69968e-05 | 0.00291515 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545811 | AGATATTCTCAGGTT[A/C]CAAGCTACCAGCACA | 55626 |
rs769253896 | snp | A/C | 1.67722e-05 | 0.00289583 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397656 | GCTGGTCCCAGGAAG[A/C]TGTCCGGGGGCTTAG | 55626 |
rs769254101 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549147 | CTTACAAGGAGAAAA[A/C]TTCATCAGAAATTAA | 55626 |
rs769256719 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427375 | TGGATACCCAACGGT[A/G]TAAAAGAAAGCAAGC | 55626 |
rs769294588 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427420 | TTTCAGAGATAGTAA[A/G]AGACAGAGCAAGAAC | 55626 |
rs769320987 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460004 | ATGTTTAAGAAGTAA[C/G]AGTGTTATAGCTTTA | 55626 |
rs769330318 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495942 | GGGAAAGGGTGGAGG[C/T]CTCTAAGCCTCAAAA | 55626 |
rs769336200 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404386 | CTGGGCTCAAAGAGA[C/G]CCCTGATCCCTGGGC | 55626 |
rs769341562 | snp | G/T | 0.000180848 | 0.00950744 | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518408 | GTACTCCAGCCTAGG[G/T]GACAGAGCAAGACTC | 55626 |
rs769349117 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485268 | TCTTAAACATTTCAC[C/T]ATACTGTCTCTCAGA | 55626 |
rs769350998 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447601 | ACCTGTAGTCCCAGC[C/T]ACCCAGGAGACTGAG | 55626 |
rs769378610 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500818 | TCAAATCCATGAAGC[C/T]TTCTCACCTCTCCCC | 55626 |
rs769381027 | snp | G/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542003 | GATGTAAGGCCTCCT[G/T]TGACACAGTTCCAGA | 55626 |
rs769409197 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533325 | ATTGTACATTTCTGT[A/C]ATGTTTGATTTTTTA | 55626 |
rs769414188 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481867 | CTCATCTGTAAAAAT[A/G]ACAGTGTATCATAGC | 55626 |
rs769420361 | snp | A/G | 5.85086e-05 | 0.00540841 | intron-variant, synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543147 | ACTGACCCGCTGTCG[A/G]AGCCTGATGTAAGCG | 55626 |
rs769430727 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496177 | TCAGGAGTTCGAGAC[C/T]AGCCTGGCCAACGTG | 55626 |
rs769435734 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511124 | GTCGTTAAGTATCCT[G/T]GTAGAACACTGCCAG | 55626 |
rs769466533 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414553 | GCCAGCACCTCCCCC[-/T]ATCACATTTGTAGGG | 55626 |
rs769482390 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457745 | GTCTCTACTAAAAAT[A/G]CAAAAAATGAACCAG | 55626 |
rs769489448 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488031 | TAATATAAGAAAAAA[C/T]TGACTTTAAGACAAA | 55626 |
rs769497530 | snp | C/T | | | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396264 | CCTGACCAGCTCTGG[C/T]GAAGGGGTCAGAGGG | 55626 |
rs769512553 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566594 | TTACAGACGGGACCC[A/G]GGGGGTGAGGATTGA | 55626 |
rs769547130 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486230 | ATCTGCCTGGCTACT[C/G]GGTACCAGATGGGTA | 55626 |
rs769550565 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522653 | TCCCCCTGGAATTTA[C/T]TGAATTCCATAATGT | 55626 |
rs769553273 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549885 | GTGCAACAGCGCAAT[C/T]TCGGCTCACTGCAAC | 55626 |
rs769560850 | snp | C/T | 2.74217e-05 | 0.00370271 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443648 | TTATTTATCCACGTT[C/T]CCACTGCAAAACATA | 55626 |
rs769562980 | snp | C/T | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542530 | CACTGAAGCTCATGG[C/T]GAATGCTGCCCGAGT | 55626 |
rs769569186 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473672 | TTTGTTTGTTTTTGA[C/G]ACGGAGTCTCGCACT | 55626 |
rs769575608 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502578 | AGTCCTAGAAATTCC[C/T]GGCTCAGAAGAGAGC | 55626 |
rs769589664 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471916 | CAGGCGTGAGCCACC[A/G]TGCCTGGCCAGGAAT | 55626 |
rs769592447 | in-del | -/TT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571688 | CTCAATCAATCAATC[-/TT]TTTTTTTTTTTTTTT | 55626 |
rs769600737 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564922 | CAGAAATCACGGTAA[A/G]TAAGTTATGTGCACC | 55626 |
rs769613540 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527571 | GTTTAATGTCCATAA[C/T]ATATGGGGAACTCCT | 55626 |
rs769650747 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539457 | AGCTACCCGGGAGGC[A/T]GAGGTAGGAGAATCA | 55626 |
rs769657410 | snp | C/T | 3.57731e-05 | 0.0042291 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408547 | GGCTGTCCCTGGCTC[C/T]GGCACCTCCCTCTCA | 55626 |
rs769715526 | snp | G/T | | | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408560 | TCCGGCACCTCCCTC[G/T]CAGTCTGTGTTTCGG | 55626 |
rs769719007 | snp | C/G | 0.000158975 | 0.00891417 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408675 | TCATCAGCCCCATGT[C/G]TCTGTCTGTCCTCCA | 55626 |
rs769744335 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555101 | AAACAAACAAAAAGA[C/T]AAATGCCAAGATTCC | 55626 |
rs769758770 | snp | A/T | 1.91775e-05 | 0.00309651 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493727 | CAAGAAGGAATCACA[A/T]GTGAAAAGCTGACTA | 55626 |
rs769763048 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581516 | GGAGGCTAAGGCAGG[A/T]GAATGACGTGAGCCC | 55626 |
rs769783049 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396928 | TCTGGGAGCCTGGCC[C/T]GATCCCTGTTGGTTT | 55626 |
rs769794078 | snp | A/G | 1.77244e-05 | 0.00297689 | intron-variant, synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543027 | TCTGGCAGAAGCAGG[A/G]GGGACACTGTCCTGG | 55626 |
rs769826645 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433111 | TATTACTTTTTACAG[C/G]TTGTTCCCTCACACA | 55626 |
rs769827829 | in-del | -/CTGA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529681 | CCTACTCAATTCCTG[-/CTGA]CTGTTAGGTGGGAAT | 55626 |
rs769853154 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580277 | CTCCTCCTACTCTAT[A/G]CTTGTTCTCTAGGAG | 55626 |
rs769865475 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491952 | CAGAGATCTGCCGGC[A/G]GTAGAGAAGCAGGAG | 55626 |
rs769879877 | snp | C/G | 3.30535e-05 | 0.00406518 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548293 | CTTCTACCAGCTCCT[C/G]CAGAAGCCGCTGAGC | 55626 |
rs769898659 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514352 | TTCCTGCCCAGGACA[A/G]CCAACTATCAAGTAA | 55626 |
rs769907385 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588645 | AAAATTAGCCAGCCA[C/T]ATGCCTGTAGTCCCA | 55626 |
rs769948403 | snp | A/G | 1.65553e-05 | 0.00287705 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543445 | AGAGCAAGGCAGTTA[A/G]GTAGAACCTCCAAGT | 55626 |
rs769949602 | in-del | -/TTG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533255 | TAACACACACACAAA[-/TTG]TTGTTAATAGCAGAT | 55626 |
rs769965761 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512235 | TACTCCTTCTTCGGT[C/T]GTCTCTTCCTTTGGG | 55626 |
rs769968276 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590034 | AAAACAAAAGTTTTA[C/T]AAGTTTCCTAACACA | 55626 |
rs769976829 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439033 | CCCAGTACTACGGGA[A/G]GCCAAGGCAGGGTAA | 55626 |
rs769980147 | snp | A/G | 1.648e-05 | 0.0028705 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508263 | GAAGAGGAGGAGGTG[A/G]AAGAACGGAGACGGT | 55626 |
rs769994673 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539462 | CCCGGGAGGCTGAGG[G/T]AGGAGAATCACTTGA | 55626 |
rs769996801 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537342 | TCTTCAGGGCCCAGG[-/A]GTTCAAACCCCACTT | 55626 |
rs770004003 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446699 | CAACCAAAAATGTCT[C/T]CAGACACTGCCGAAT | 55626 |
rs770019488 | snp | C/T | 0.000108483 | 0.0073641 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397471 | GTTCCGTGGTTCTCC[C/T]CTAGGGCCTGCAGCG | 55626 |
rs770038320 | snp | A/G | 3.30017e-05 | 0.00406199 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543311 | GGAGGAGAGGCGTCC[A/G]GCGAACTGGCTGTGA | 55626 |
rs770053483 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529811 | TGAGGACTATTTTGC[A/G]ATATCTTGGTTAATG | 55626 |
rs770061042 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437644 | TAAGTGTCACTGCTT[C/T]CATTCACTTGTGCAG | 55626 |
rs770067099 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456421 | GCTTAGGTGGGTCCC[C/T]AGGTGAAGCCAGGAA | 55626 |
rs770073143 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529222 | TCCAAAAGAAGGTTG[C/T]TCTCATACTGCATAA | 55626 |
rs770078196 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450199 | GAATGGATAAACTGT[A/G]GCACATCCATACAAT | 55626 |
rs770083302 | in-del | -/CA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428276 | TGTCTGGGTAACACT[-/CA]CTCAACTCTTGGCTA | 55626 |
rs770091202 | snp | A/G | 3.29717e-05 | 0.00406015 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418027 | CGCTGGTCGGCAGGC[A/G]TGGGATAAAGGACGT | 55626 |
rs770129286 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542827 | TGGCTAGACAGAGGC[C/T]CTCCCAAAGAGCGGC | 55626 |
rs770151053 | snp | A/C | 1.65444e-05 | 0.00287609 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397749 | AGGAGGTGTGGGCGG[A/C]ACCAGGTTCAGTGCC | 55626 |
rs770154182 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415863 | ACTCTGGGATGCTGG[A/G]GCAACATATGGGGAG | 55626 |
rs770154516 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400074 | GTCTGCAGCAGTGGA[C/G]CTCTATTGCTGTGGG | 55626 |
rs770160427 | snp | A/T | 5.27644e-05 | 0.00513609 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547071 | CTCAAAAAAAAAAAA[A/T]TAGAACACCAAAAGA | 55626 |
rs770170975 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438546 | TACCGATTTGGAAAA[-/C]CCAAGGGGGGTTAAA | 55626 |
rs770184796 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490513 | TCTCTTGTGGGAGGA[A/G]GTAGAACGGATCTTG | 55626 |
rs770196052 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562797 | AAATATAATGCAACA[C/T]TGGTTCTTTTTTTTT | 55626 |
rs770202849 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576626 | TCAGGAAGTTCTTTC[A/T]AACATGTAATCTACA | 55626 |
rs770214356 | in-del | -/TAACT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589748 | CCTCAGTCTCCCAAG[-/TAACT]GGGACTACAGGCGCC | 55626 |
rs770215466 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468495 | TAGCACAAGCATCAC[C/T]CTTAAAGAAAAGGAA | 55626 |
rs770221211 | snp | A/G | 3.30551e-05 | 0.00406528 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547208 | ACCATGGAGTACGGC[A/G]GTGTCCAATCAGGGA | 55626 |
rs770231705 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559490 | ATAACCTCAAAAATG[G/T]CAGTAAAATTTTTTT | 55626 |
rs770270944 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559408 | ATCACGAGAGGGCCA[A/G]GCAAGAGAGTAAGCA | 55626 |
rs770274339 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428248 | TTTCAATGTGTCCTA[C/G]GAACTATTGATTTGT | 55626 |
rs770292360 | snp | A/G | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594502 | TACGTAAAAGCTCCA[A/G]TTTAGTCCCCACAAA | 55626 |
rs770317960 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577602 | TAAGATGGCTAAATT[G/T]ACGTGAAGTGAATTT | 55626 |
rs770341521 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484609 | ACAGTGTATACGCAT[C/T]CCCTTTCCACTGCAT | 55626 |
rs770347233 | snp | C/T | 1.65806e-05 | 0.00287924 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397818 | TGTTGTTGCCGAAGC[C/T]GCCCATGGAGGCCAT | 55626 |
rs770354305 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542706 | GGCACTGGTTCTGGG[C/T]GGGGGCATGGATTCC | 55626 |
rs770357121 | snp | A/G | 4.37685e-05 | 0.00467785 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494227 | AAATAAAAACACTAC[A/G]CATAAGAGAGTCACT | 55626 |
rs770374153 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430200 | AAAGCAGCAACAGCC[C/T]AGAAAAGATGGGAGG | 55626 |
rs770404081 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415160 | TAGGCAGCTGCCTAT[C/G]AGACACACAAGAACC | 55626 |
rs770437654 | snp | A/G | 1.66621e-05 | 0.00288631 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397851 | TGGTGCTCTGCTCCC[A/G]CTGCACCACGGCTGT | 55626 |
rs770447704 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409201 | TTTGGAAGGAAAGAA[C/T]TGGAACTCTTTTTTT | 55626 |
rs770463476 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483163 | GGCCTATGATAAACC[C/T]AGGGACTCCCCTCAA | 55626 |
rs770467866 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500382 | TTAGAAAACATCAAG[-/C]CCTCAGACAATCAAT | 55626 |
rs770476260 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577709 | TAATGCCAGCACTTT[C/G]GGAGGCCGAGGCGGG | 55626 |
rs770483580 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477223 | GAATAGAAGGACACT[A/G]GCTCAATCTCATCAC | 55626 |
rs770485265 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483552 | TAAACGAGGCTGCTT[A/G]GAGATAGGAAAAGGA | 55626 |
rs770512698 | snp | G/T | 4.96003e-05 | 0.00497973 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547226 | GTCCAATCAGGGAAT[G/T]AACACACTTGCCAGT | 55626 |
rs770525898 | snp | C/G | 1.79287e-05 | 0.002994 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434991 | AGAAATGTCACAGCT[C/G]GCATCATTGTAGATC | 55626 |
rs770537126 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497332 | GGCTCAAATACACGC[A/G]GTCTCAGACTGAAGG | 55626 |
rs770537293 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428501 | CCGAGAGAAAAGCAA[A/G]CTACGCCTGGTGAGA | 55626 |
rs770537493 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446016 | TTAAGACTCCCAAAT[A/C]CCGGCTCCAGAGGCA | 55626 |
rs770544800 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519867 | AAATTATGAGGATCC[C/T]GGTGGCTCACGCCTG | 55626 |
rs770549333 | snp | A/C | 1.68179e-05 | 0.00289977 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542146 | GAGCTGGGCGTTTGG[A/C]CCTCAGTCCGCTCGA | 55626 |
rs770561183 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534860 | TGAGCTTTTTGTAGA[A/G]ATAGGGTTTCACCAT | 55626 |
rs770568717 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460165 | AGTTAAATGTTCATC[A/T]ATCGGGAACAGACAA | 55626 |
rs770575308 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497560 | AGGAAAATGTGAAAC[A/T]TAATAAACACAATAT | 55626 |
rs770598710 | snp | A/C | 1.72815e-05 | 0.00293946 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547081 | AAAAATTAGAACACC[A/C]AAAGAAAAGGGTATC | 55626 |
rs770609382 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496304 | GGAGAATCCCTTGAA[C/T]CCAGGAGATGGAGGT | 55626 |
rs770623569 | snp | A/G | 3.02211e-05 | 0.00388711 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494192 | TCGGTGCCTGGATCT[A/G]TCACCATTGTCCCTG | 55626 |
rs770639548 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443336 | TGGTTAATGGACCTG[A/G]AAAGAAAGTTACAGA | 55626 |
rs770651299 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550746 | TCCATCTAAAGGGTA[A/C]TGGATGACTAATCTA | 55626 |
rs770656720 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475064 | GTGAATTGAATATAT[C/G]TTAAACTGAAAAACA | 55626 |
rs770671778 | snp | C/G | 5.05932e-05 | 0.00502932 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443457 | GCAAATATAACCCTT[C/G]CACTGATACCCCCAT | 55626 |
rs770680983 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566836 | CAGTTTAAATGATAA[C/T]AGCCCTTCTTAAAAC | 55626 |
rs770718723 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408234 | GAGGGAGTCTCCCTT[C/T]AGCCCTTTCAATCCA | 55626 |
rs770789026 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528015 | GCACACCCATGTTCA[C/T]TGCAGCATTTTTCAA | 55626 |
rs770806536 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421957 | GACACCCTAAAAACA[C/T]CTCAAGTAAAGGTTT | 55626 |
rs770806742 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406205 | ATTACAGGTGCCCAC[C/G]ACCATGCCCGGCTAA | 55626 |
rs770808155 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585598 | TTGAACCAAGGAGGC[A/G]GAGGTTGCAGTGAGC | 55626 |
rs770813259 | snp | C/T | 1.81023e-05 | 0.00300846 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397401 | GTCAGCTGTGAGGTC[C/T]GGTTTCTGCTTGGCG | 55626 |
rs770834624 | snp | C/T | 3.33873e-05 | 0.00408565 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543268 | TGGATGCCAGAAGAG[C/T]GGGAGGACAGCATGT | 55626 |
rs770852598 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447426 | TGTAGTCTCAGTTAC[G/T]TGGGATGCTGAGGCA | 55626 |
rs770857057 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418700 | CCTGAGAACTTGGGG[C/T]AGCAGGAGAGATGGG | 55626 |
rs770857768 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464228 | TCCATGTATTTAAAA[G/T]GTCATCAGGACGCCC | 55626 |
rs770883194 | snp | G/T | 0.000445614 | 0.0149201 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543931 | TACTAGTTAAGAAAA[G/T]AACTCACAGTTTAGC | 55626 |
rs770920081 | in-del | -/C | 1.64999e-05 | 0.00287222 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417896 | ATCCCTCAACCCCCA[-/C]ACTTTAAGCCACTTA | 55626 |
rs770923048 | snp | A/C | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542020 | GACACAGTTCCAGAT[A/C]TGCTGGACTGGGTGT | 55626 |
rs770934645 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462854 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTTGCTTC | 55626 |
rs770956427 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412159 | ATCTTTGGGGAATTG[A/G]TTCCAAGACCCCCTG | 55626 |
rs770967673 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435207 | AACAAAACACAGGAG[G/T]CAAGAAAAGTATGTC | 55626 |
rs770978471 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565450 | AGTGGCTCACACCTA[C/T]AATCCCAGCACTTTG | 55626 |
rs771013163 | snp | C/G | 6.1529e-05 | 0.00554623 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543163 | AGCCTGATGTAAGCG[C/G]AAGTCCTGGGGCGCT | 55626 |
rs771018825 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501110 | ATATTCCATGCTGTT[C/T]CATGTTTCTATGACC | 55626 |
rs771033840 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489701 | AGACAGCTAATACCC[C/T]ACATTACCCAGGCCC | 55626 |
rs771034890 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425432 | TGAATTGATTTTCCA[A/T]TTCTTGAAAAAAAGG | 55626 |
rs771054124 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500037 | AGGTTATCTAATCTC[A/G]TTTTACACATCAGAC | 55626 |
rs771065302 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590090 | CAGTATAAAAATGTA[G/T]GGCCGAGCGAGGTGG | 55626 |
rs771074894 | snp | A/G | 3.29511e-05 | 0.00405887 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542384 | TGGGCTGGTGGGAAG[A/G]GCCTGGCCTCTCAGA | 55626 |
rs771081799 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545963 | ATCAGATAAATACTA[A/T]ACAATCAGTTCAGTT | 55626 |
rs771119800 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410857 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 55626 |
rs771122706 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440901 | AAGTCTTATAATATC[A/T]TACAGACAAGATAGA | 55626 |
rs771179552 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476430 | GTGGTGGGGAGATAC[A/G]TAAAGAGTCCCAAGC | 55626 |
rs771184887 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536632 | CCTACAATCAGCCCC[A/G]CAGACACCCATTTAT | 55626 |
rs771187709 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559785 | CGCTGGCTTGTTATA[C/T]AATCTTGGACAAATC | 55626 |
rs771201630 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488676 | TCAAGCACATGGGTA[-/T]ACACTCTCTAGAAGA | 55626 |
rs771215569 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531695 | GCCTGGGTGACAGAG[C/T]GAGACTCCATCTTAA | 55626 |
rs771215708 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514477 | AGAGAGGAAAGCAAT[A/G]AAATACATCTCTCTG | 55626 |
rs771237920 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572047 | GTAGCTCACGCCTAT[A/C]ATCCCAGGACTTTGC | 55626 |
rs771249814 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423935 | CGCCTGGTTAATTTT[A/G]TATTTTTAGTAGAGA | 55626 |
rs771266131 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439216 | GAGTTTGAGGTTATA[A/G]TGAGATATGATCACG | 55626 |
rs771285567 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492175 | CTCCTCAGATGAGGC[C/T]GTCAGGAGATTGTGG | 55626 |
rs771290269 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505136 | AGGAGGATTACTCGC[C/T]ATATCTACCTTACAT | 55626 |
rs771300172 | snp | A/G | 4.97822e-05 | 0.00498885 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512685 | GCAACCCCAAGGGCC[A/G]CCCCTCCCCCCACCT | 55626 |
rs771313492 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528123 | TGGAATATTATTCAG[-/C]CTTTGAAAAGAAGGA | 55626 |
rs771321343 | snp | C/G | 1.65083e-05 | 0.00287296 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542841 | CCCTCCCAAAGAGCG[C/G]CGGGTAGGACCCAGA | 55626 |
rs771327564 | snp | A/G | 1.83105e-05 | 0.00302571 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397956 | CACCTGGCAGATACA[A/G]AGCAGAAGAGAGAGC | 55626 |
rs771340316 | snp | A/G/T | 3.616e-05 | 0.00425193 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397528 | AAGGTGGTTGTTATT[A/G/T]GTCAACTCGCAGTGG | 55626 |
rs771345419 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416040 | ACTAGAAATTTGGCT[G/T]GGACAAAAGTTAGTG | 55626 |
rs771354267 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462089 | GTGGCAAATTTCTAG[-/C]TTTTACAAGAGATAT | 55626 |
rs771364414 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402201 | GGACTCAGCTGTATT[C/G]TCTTTTCAGCCAAGT | 55626 |
rs771368584 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544558 | ACAGACAATATGTTT[A/T]GATCTTGAGGACTAA | 55626 |
rs771371723 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559756 | GGTAAGAAGCTTTAA[C/T]AACTGATTTTTATCG | 55626 |
rs771448751 | snp | C/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453175 | TAATGAAATCATATG[C/G]TAGGTGGCCTTCTGT | 55626 |
rs771461747 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506336 | TTTCTTTCACATTTA[C/T]ATCTTTCTCAGACAA | 55626 |
rs771524951 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442662 | CTAGAAGCAAGGAAA[A/C]TGAAACAGTCATGTT | 55626 |
rs771579046 | snp | C/G | 1.67242e-05 | 0.00289168 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547268 | TAATATAGATATTAT[C/G]GTTCACATGGGTGGA | 55626 |
rs771618282 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469655 | AAGACTTAGCAACAT[A/G]TATTTCTTTCTTTTT | 55626 |
rs771632265 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558951 | GAGTTTTAAAAAGTG[C/T]GGTGGTTATGAGTTC | 55626 |
rs771643408 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534349 | AATACAGAAAAGTTA[C/G]CCAGGCGTGGTGGCA | 55626 |
rs771654209 | snp | A/C | 0.000283086 | 0.0118938 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547885 | TACTCTCTGGGAGAC[A/C]AAAAAAAAAAAAAAG | 55626 |
rs771657339 | snp | C/T | 6.64772e-05 | 0.00576491 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542917 | CTGAAGGCAGACGGC[C/T]GGTTCAGGAGGCCCT | 55626 |
rs771689468 | snp | A/C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590837 | AGAATTGCTTCAATC[A/C/T]GGGAAGTGGAGGTTG | 55626 |
rs771691088 | in-del | -/TAGA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447709 | AGCCAGACCATCTTG[-/TAGA]TAGATAGATAGATAG | 55626 |
rs771700911 | in-del | -/AAAAACAAAAAAAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445066 | AGGGGCAAAAAAAAG[-/AAAAACAAAAAAAA]AAAAACAAAAAAAAA | 55626 |
rs771727518 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410094 | GAGAGCAGAGCTTTT[C/G]TTCTCTTTCTTAGCC | 55626 |
rs771732046 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431701 | GAAGAGCAGCTGTTG[A/G]GACTGGGATTCCAGG | 55626 |
rs771750385 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578679 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 55626 |
rs771754021 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483852 | GCAGGAGTGTGCCAC[C/T]GCACTCCAGCCTGGG | 55626 |
rs771766234 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456818 | ACTGGCAGCTTTCCT[C/T]ATCTGTCGATCACAG | 55626 |
rs771773854 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472560 | CTCACTCAAATTGTA[C/T]AGAGAATTACTGAAG | 55626 |
rs771777936 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430222 | GATGGGAGGTGAGGC[A/G]CAGACAGCCAAAAAA | 55626 |
rs771781644 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553422 | ACTGGAGTACTAAGA[C/T]GTAAAAGTCAGAAAG | 55626 |
rs771784011 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522066 | AGAGCACAACATAAT[C/T]GCAGACAGCAAAAGG | 55626 |
rs771797503 | in-del | -/A | 5.28416e-05 | 0.00513984 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547803 | TCTTAAGTTATAGAT[-/A]AAATACTGAGTACCT | 55626 |
rs771824013 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447093 | CAACTTACAGGATTG[C/T]TGGAAGAACTTACTA | 55626 |
rs771841519 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499077 | CATTCATAGGGAATA[A/G]CTAATAGCATAGGTC | 55626 |
rs771857689 | snp | A/G | 5.42923e-05 | 0.00520991 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397416 | CGGTTTCTGCTTGGC[A/G]GTTCGAGGGGAGGCA | 55626 |
rs771860065 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514160 | CCTGCAGGATAAGGA[C/T]AGCAGCTACCAATCT | 55626 |
rs771861719 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497797 | TGGACCAAAGGCACA[A/G]TTCCAAATAACTAAA | 55626 |
rs771874165 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552369 | GTGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 55626 |
rs771893093 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568277 | AGCCTGGCCAACGTG[A/G]TGAAACCCCGTCTCT | 55626 |
rs771898183 | snp | C/T | 1.90623e-05 | 0.0030872 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397971 | AAGCAGAAGAGAGAG[C/T]GAATTGGCTGCTGGC | 55626 |
rs771923046 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544664 | TACCACCCAAACTTC[-/T]TTCAGGTTTTCCCAA | 55626 |
rs771949660 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512666 | CGGAGCTTCCAACAG[A/T]GTGGCAACCCCAAGG | 55626 |
rs771966929 | snp | A/G | 1.68778e-05 | 0.00290493 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408617 | TGGGTGCCCTGAGAT[A/G]TCACTGAGGTGGCAG | 55626 |
rs771979354 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542252 | CAGAGGAGTAGTTAG[A/G]TGTGGTTCTTTCCCA | 55626 |
rs771998994 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588420 | CATGGAAGTTAACAA[C/T]TGAAGAGTACTTTAT | 55626 |
rs772027851 | snp | C/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450104 | CAAACACCTACACAT[C/G]GATATTTATAGCAGC | 55626 |
rs772038426 | snp | A/G | 3.29544e-05 | 0.00405908 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542404 | GGCCTCTCAGATTCA[A/G]TGTTATTGTTGAGCA | 55626 |
rs772046544 | snp | A/G | 1.70263e-05 | 0.00291768 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397626 | GCTGGGTTGGCTCCC[A/G]CCCAGGGGTACCAGG | 55626 |
rs772054193 | snp | C/G/T | 0.000126567 | 0.00795423 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397460 | TGTCTCTACCTGTTC[C/G/T]GTGGTTCTCCCCTAG | 55626 |
rs772071789 | snp | C/T | 1.83189e-05 | 0.0030264 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46435001 | CAGCTGGCATCATTG[C/T]AGATCTTGCAGTTCT | 55626 |
rs772072983 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449031 | AAATTGTACCAGTTC[C/T]CTAACGTCTCTTCCA | 55626 |
rs772073270 | snp | G/T | 1.65337e-05 | 0.00287517 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543426 | CCAGCATGGGGCAGG[G/T]GGTAGAGCAAGGCAG | 55626 |
rs772079072 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485805 | AGGCCCAGTATTTTT[C/T]CCTAGAAAAGCCTGA | 55626 |
rs772116578 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422100 | ATGCCGTGCAGCTAC[A/G]CCACCAAATTCTATT | 55626 |
rs772130643 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449798 | GGGCGCAGTGGCTCA[C/G]GCCTGTAATCCCAGC | 55626 |
rs772160762 | snp | C/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398299 | TGTCTGCCTGCTCCC[C/G/T]GTTGTGGAAACTCAG | 55626 |
rs772168898 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413566 | TGTGATCTCGGCTCA[C/T]TGCAACCTCAGCCTC | 55626 |
rs772171222 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555443 | TGTCTGCTTCATAGG[A/G]TTGTTATGAGACTCC | 55626 |
rs772172842 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465730 | GGTAGAAAGGAAAAA[C/G]GTTCATCCATCCCCA | 55626 |
rs772186287 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476570 | TGTCCCTGTGGCCTC[C/T]CCACCTAGAACATGG | 55626 |
rs772187352 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427081 | TGATTAGGACTATAT[G/T]ATAAGTTCAATTCAA | 55626 |
rs772192489 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529217 | CATAGTCCAAAAGAA[C/G]GTTGCTCTCATACTG | 55626 |
rs772225704 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519148 | CTTGCCTCAGCCTCC[C/T]GAGTAGCTGGGGCTA | 55626 |
rs772227750 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396957 | TTCAGTGGGGTAAGA[C/T]GACGAAGAGAGGCTG | 55626 |
rs772247866 | snp | A/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545653 | CAGCAAAGGGTTCCC[A/G]TCGACTCCAGTCCCA | 55626 |
rs772273682 | snp | A/G | 3.75213e-05 | 0.0043312 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494101 | ACGAAGGCTCCCTCT[A/G]TTGCTAGCAACTCGG | 55626 |
rs772282470 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502616 | AGTACTGTCAAGGAC[A/T]GGTGGCTAGAATTCT | 55626 |
rs772329485 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567849 | GTGTGCCAAACTATA[C/G]TTGAAAAACCTAGCT | 55626 |
rs772332165 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464532 | GGTGGTTCAAGAAAC[C/T]CCTGAAATAGCAAAT | 55626 |
rs772341177 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412290 | TGTAAATTATGCAAA[C/T]AGTTATTATACTGTA | 55626 |
rs772353111 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538651 | AGGCATGCACCACCA[C/T]GCCTGGCTAATTTTT | 55626 |
rs772363663 | snp | A/G | 9.89479e-05 | 0.00703307 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542542 | TGGCGAATGCTGCCC[A/G]AGTTGTTTTGGCTGG | 55626 |
rs772370209 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501305 | TCCCAAAGATGTGCA[C/T]ATTGGATGAACTGGC | 55626 |
rs772401062 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470064 | CAAGATACTTTATAC[A/T]TTAATCAGTTATATA | 55626 |
rs772412363 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575993 | AAAGCTATTTTTATA[A/G]GAAAGAGATTGCCGG | 55626 |
rs772421911 | snp | A/G | 6.62504e-05 | 0.00575507 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433497 | AGGTCTCTCCACCAT[A/G]GGCCTGTTGCAGCCT | 55626 |
rs772428841 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572963 | GGGTGTGGTGGTGGA[C/T]GCCTGTAATCCCAGC | 55626 |
rs772461914 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516297 | TTCATAGTTACAATA[A/C]GAGTACTATCTGGAG | 55626 |
rs772502000 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494862 | ACTGTTAACAGTCCA[C/T]GCAATAGTAGTAACT | 55626 |
rs772516039 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592136 | TTTTAGGTTTCTCCA[C/T]GTTAGTCAGGCTGGT | 55626 |
rs772546229 | snp | C/T | 1.65756e-05 | 0.00287881 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433581 | AGGCCAAGCCCACCA[C/T]TACATATCTGCCCAT | 55626 |
rs772555398 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532216 | ATAAGACACAGAAGA[C/G]TAAGTGGATGAAGGC | 55626 |
rs772556155 | in-del | -/TCTG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414929 | CAAGGAGCTTGTTCC[-/TCTG]TCTTTGTGCTTGGAG | 55626 |
rs772573608 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536250 | GGTAGACAAGGGATA[C/T]ATACAGACATGATCA | 55626 |
rs772592193 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508355 | CCTCTGGGCGTAGTA[C/T]GCAGCAGGAGATAAT | 55626 |
rs772601094 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562655 | GTGTTATGTTTGCGG[A/G]TGGGGGAGCAGATTA | 55626 |
rs772621177 | snp | A/T | 0.000187319 | 0.00967596 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518250 | GCCTGGCTAACATGG[A/T]GAAACTCCATCTCTA | 55626 |
rs772636344 | snp | A/G | 1.65236e-05 | 0.00287429 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541895 | GGACTCAAGGAAATG[A/G]TACAAGGAGAAAAGC | 55626 |
rs772648934 | snp | A/G | 5.08919e-05 | 0.00504414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545561 | AATGTTCTCTATCAC[A/G]TCAGTCCTGTGCCAG | 55626 |
rs772675416 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590270 | ACTTGAACCCAGGAG[A/G]CAGAGGCTGCAGTGA | 55626 |
rs772675450 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441008 | ACAGTAATGTACTAC[A/G]AGGTTTGGTGCAATG | 55626 |
rs772701478 | in-del | -/CT | 2.25655e-05 | 0.0033589 | frameshift-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547872 | TATCCGGCAGTTCTA[-/CT]CTCTGGGAGACAAAA | 55626 |
rs772704734 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452565 | TTACAAAAAATAATT[A/C]TCAGAGCAAGGGAAC | 55626 |
rs772717062 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576769 | AAGCCCATTTCAAAT[A/G]GCTTCATGTAAATGC | 55626 |
rs772717400 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444864 | TCTGCACTCTTCCGG[C/T]TGCTGCTGGCCACTG | 55626 |
rs772730379 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496240 | ATACAAAAAATTAGC[C/T]AGGCATGGTGTTGCA | 55626 |
rs772741125 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415348 | CATTCTTTACCTGAG[A/G]TCTTAAAGAGTTACA | 55626 |
rs772742147 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593561 | GTTCCTGGAAAGCCA[C/T]TTTCGCCACACACTG | 55626 |
rs772750519 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511135 | TCCTTGTAGAACACT[C/G]CCAGGTTAAAAGTTC | 55626 |
rs772797568 | snp | A/G | | | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547836 | CTGGGCTGAAGGCCA[A/G]TAAGAAGGTAGAGCG | 55626 |
rs772805213 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443130 | ATTTCTCTGCTCTGA[A/G]GAGTTTGTGGACTAG | 55626 |
rs772815516 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438034 | TGTCTCTGATGTTGC[C/T]GGACTGGGACTACAC | 55626 |
rs772827490 | in-del | -/AT | 1.8927e-05 | 0.00307622 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493726 | ACAAGAAGGAATCAC[-/AT]GTGAAAAGCTGACTA | 55626 |
rs772856782 | in-del | -/CAGCAGCAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427317 | TTTAATGAACTTGAT[-/CAGCAGCAG]CAGCAGCAGCAGCCA | 55626 |
rs772885859 | snp | A/G | 5.91488e-05 | 0.00543792 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543149 | TGACCCGCTGTCGGA[A/G]CCTGATGTAAGCGGA | 55626 |
rs772887807 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575456 | AGCAAAACTCTGTCT[-/A]AAAAAAAAAAAAAAC | 55626 |
rs772904295 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592477 | TCAAATACAACAAAA[C/T]TGGGCGGGCGCGGTG | 55626 |
rs772916345 | snp | A/G | 3.29674e-05 | 0.00405988 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545712 | AGCAGGAGCTGAGCC[A/G]TAGGGTGGAAAGCCA | 55626 |
rs772919421 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489505 | GAAATTAGGATAACT[A/G]GGCACAAAGCCATCT | 55626 |
rs772920064 | snp | C/T | 1.82613e-05 | 0.00302164 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434843 | GTTGGGCTTCCTATC[C/T]CTTACCAAATCGCTT | 55626 |
rs772923950 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461115 | AAGCACGATGGTACA[C/T]GCCTATAGTCCCAGC | 55626 |
rs772928316 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495373 | ACTGGGAACTTCACA[A/G]GCCAGAAACAAAAGT | 55626 |
rs772946716 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553470 | CACCAAGTTTGGCCA[C/G]GTGCAGTGGCTCACA | 55626 |
rs772966193 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549158 | AAAACTTCATCAGAA[A/G]TTAAAATTCTACTAA | 55626 |
rs772967520 | snp | A/G | 1.92106e-05 | 0.00309919 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493728 | AAGAAGGAATCACAT[A/G]TGAAAAGCTGACTAA | 55626 |
rs773000357 | in-del | -/AG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442522 | CAGAAGCAGTCAAGC[-/AG]AGAGGCTGGACCATC | 55626 |
rs773016274 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509326 | TATAATTTGACGCTA[C/T]GGACTGAAAACATGA | 55626 |
rs773033996 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524638 | TCTTATTTCACATGG[C/T]TATTATGATTAAGAA | 55626 |
rs773034716 | snp | A/G | 5.35365e-05 | 0.00517353 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408548 | GCTGTCCCTGGCTCC[A/G]GCACCTCCCTCTCAG | 55626 |
rs773042201 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486220 | CACTCATGTTATCTG[C/T]CTGGCTACTGGGTAC | 55626 |
rs773045641 | snp | A/G | | | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542889 | GTTGCCGGCAGTGCT[A/G]CTCTGGACTGTACTG | 55626 |
rs773047333 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456633 | AATTGCTGAGACTCC[C/T]GCAGCTTTTATTGTT | 55626 |
rs773055209 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404531 | CTGACCCACACCTCC[C/T]CTGCCCTGACTGGTT | 55626 |
rs773072415 | snp | C/T | 6.60284e-05 | 0.00574542 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548301 | AGCTCCTGCAGAAGC[C/T]GCTGAGCTCCCATGG | 55626 |
rs773092773 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548035 | GAGAGATAAACCTAA[-/A]TTACCTTCAGGAAAA | 55626 |
rs773104794 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579019 | TCAGCTAATTAGCTA[C/T]AGCAACAATGACCAC | 55626 |
rs773132382 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462762 | TTCACCCCCCTCCTT[C/T]TTTTTTTGAGACAGG | 55626 |
rs773152206 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419346 | GAAGAATAAAAGACA[C/T]GGGCTTTAGAGTTAA | 55626 |
rs773157267 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457060 | AGGGGGCCCAGCTTC[G/T]AAAGGGTGAAAAGCT | 55626 |
rs773160077 | snp | A/G | 3.55461e-05 | 0.00421566 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408683 | CCCATGTCTCTGTCT[A/G]TCCTCCATGTGGCTC | 55626 |
rs773160168 | snp | C/T | 1.66751e-05 | 0.00288744 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548200 | TAAGGTCTCATTCTA[C/T]CATCACCAGCACAAA | 55626 |
rs773164563 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581622 | AAAAATAAATAAATA[A/C]ATACATAAATAAATA | 55626 |
rs773205078 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551597 | TAAACGACACCAGGC[A/G]CGATGGCTCACGCCT | 55626 |
rs773206939 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571535 | CAAAAATTAGCCAGC[C/T]ATGGTGGCACATACC | 55626 |
rs773208175 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514358 | CCCAGGACAACCAAC[C/T]ATCAAGTAATGTTTT | 55626 |
rs773212919 | snp | A/G | 1.64988e-05 | 0.00287213 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543314 | GGAGAGGCGTCCGGC[A/G]AACTGGCTGTGATTG | 55626 |
rs773240343 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433188 | GCATCTCCAGATTAA[A/G]AGTTTCACGTAGAAG | 55626 |
rs773246070 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418534 | TAGGTATATCTTCTA[A/C]TGCTATCCCTCCCCA | 55626 |
rs773265162 | snp | A/G | 1.78083e-05 | 0.00298393 | intron-variant, synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543030 | GGCAGAAGCAGGGGG[A/G]ACACTGTCCTGGTGT | 55626 |
rs773295019 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408889 | GTCCATTCTCCCCCA[A/G]GGTTAGTCTATACCC | 55626 |
rs773298853 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568592 | AGCCTGACCAACAGA[A/G]ACACCCCATCTCTAC | 55626 |
rs773305075 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467798 | AGTGCTGGGATTATA[-/G]GTGTGAGCCACTGCA | 55626 |
rs773314579 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483121 | ATGCTGGGCTCCTTC[C/T]TCATGGCACAAAGCT | 55626 |
rs773324615 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580311 | TCATCCATTTCCCTT[A/G]GTTGTAAATACCATC | 55626 |
rs773327088 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475754 | ACTTTGCTCTGGATA[C/T]GAGAATCCCGTAATT | 55626 |
rs773330938 | snp | C/T | 3.61624e-05 | 0.00425205 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397473 | TCCGTGGTTCTCCCC[C/T]AGGGCCTGCAGCGTC | 55626 |
rs773384601 | snp | A/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450375 | ATAGAGACAGAAAAA[A/T]GATGGGTAGTTGGTA | 55626 |
rs773384949 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498192 | TAGGAACAGTGAAGG[A/G]TGCTAAATACCGGGC | 55626 |
rs773402062 | snp | C/T | 1.64844e-05 | 0.00287087 | splice-donor-variant | AMBRA1 | GRCh38.p7 | 11:46417912 | ACTTTAAGCCACTTA[C/T]TCTGGTCGGCAGATC | 55626 |
rs773409684 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520141 | TGAAACTCCGCCTCG[-/A]AAAAAAAAAAAAAAA | 55626 |
rs773411756 | snp | A/G | 5.11043e-05 | 0.00505465 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542178 | AGGTGGCAACTGGCT[A/G]CCACTTGATGGCACA | 55626 |
rs773415420 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476902 | TGGATCAGCCAGGAG[A/T]TCGAAACCAGCCTGG | 55626 |
rs773431100 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437669 | GTGCAGCTTCCTCTC[A/G]TAAGGCTGAAATTTT | 55626 |
rs773439528 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587575 | TACGCAATTATGATT[A/C]GTGATTCCAACTTTT | 55626 |
rs773442446 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492078 | GAAAAAAGCTTTAAC[G/T]TGCCTTCGGTTAAGC | 55626 |
rs773449550 | in-del | -/TC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410096 | GAGCAGAGCTTTTGT[-/TC]TCTTTCTTAGCCACA | 55626 |
rs773483632 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461867 | ATGAAGCATGCAAAC[A/G]CATGCCCAGGCCCAA | 55626 |
rs773483925 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571112 | ATTTGCCTCCTTACA[A/G]TGGTTCTGGCTTCAA | 55626 |
rs773491987 | snp | A/G | 1.65968e-05 | 0.00288065 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410387 | AAAATCAGTTGGGAA[A/G]GGTAAAGAAGAAGGT | 55626 |
rs773519052 | snp | C/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451641 | AAGGAAATGATTAAA[C/T]TACATTTCAGTCCTG | 55626 |
rs773541559 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505137 | GGAGGATTACTCGCC[A/G]TATCTACCTTACATG | 55626 |
rs773546892 | snp | A/G | 8.29373e-05 | 0.00643908 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397819 | GTTGTTGCCGAAGCC[A/G]CCCATGGAGGCCATG | 55626 |
rs773548640 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434082 | ATCACGCCATTACAT[C/T]CCAGCCTGGCCAACA | 55626 |
rs773559598 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530044 | GTTATGCAAACAGAA[C/T]CCCATACACCTGGTG | 55626 |
rs773602128 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505072 | GAAGTGCTGAGAAGG[C/T]GAGGATACCAAACAA | 55626 |
rs773625928 | in-del | -/TGGGTAGTTATTTTTAATACA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522203 | CTGCTAACTGTCTGG[-/TGGGTAGTTATTTTTAATACA]TGGGTAGTTATTTTT | 55626 |
rs773634879 | snp | C/T | 9.92736e-05 | 0.00704464 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397765 | ACCAGGTTCAGTGCC[C/T]GTCTGAGAGCTGCGG | 55626 |
rs773644914 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510893 | CTAACAAAGAGCTGG[-/A]AAATCATCAAACAAC | 55626 |
rs773692694 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504021 | CAGTTTTCAAGAAGC[C/T]GAATGTAATTATCCA | 55626 |
rs773693636 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435887 | TATAGGCCTTGTTTC[A/G]GTTTTCATTTGAATC | 55626 |
rs773695384 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507558 | TAGCGCATCCTCCCA[A/T]GGCTCTCCCCGCTGA | 55626 |
rs773707115 | snp | A/G | 1.65436e-05 | 0.00287602 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397777 | GCCCGTCTGAGAGCT[A/G]CGGTGAATGCGGTGG | 55626 |
rs773710070 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519698 | CCCAAATTAACAGCT[C/T]CCTTCTGCCTAGGAA | 55626 |
rs773713655 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450201 | ATGGATAAACTGTGG[C/T]ACATCCATACAATGG | 55626 |
rs773746262 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415244 | TCTGTAGACCGCTCA[A/G]AAGACATGAATGCGC | 55626 |
rs773779272 | snp | C/T | 1.65097e-05 | 0.00287308 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542839 | GGCCCTCCCAAAGAG[C/T]GGCGGGTAGGACCCA | 55626 |
rs773780616 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433813 | GAGTGTAGTGTTTGA[C/T]ATATAGAAAGCACAT | 55626 |
rs773792114 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578394 | TGGGAGGCTGAGGCA[A/G]CAGAGTTGCTTGAAC | 55626 |
rs773805481 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483570 | GATAGGAAAAGGAAA[C/T]GAGAAAGAAAAGCTG | 55626 |
rs773813114 | in-del | -/TATC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418204 | TTTCTTTTTTTTCTA[-/TATC]TATCTATCTATTTTA | 55626 |
rs773832386 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558272 | CTAACCTAATATCAC[C/T]GGGCGCAGTCGCTCA | 55626 |
rs773833289 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541550 | ATCTCTACCATGCAG[G/T]GTTCTCTTTTACTTA | 55626 |
rs773867986 | snp | C/T | 4.46e-05 | 0.00472208 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494228 | AATAAAAACACTACA[C/T]ATAAGAGAGTCACTA | 55626 |
rs773884620 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466908 | CTAATGTTTCTTTTT[C/T]TCTTTTCTTTTTTCT | 55626 |
rs773895482 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497686 | TTGAATACCGGAATG[A/G]GTAAGGTGGCAAAGG | 55626 |
rs773903252 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590469 | CCTCATCTCTTCAGG[-/A]AAAAAAAAAAAATTA | 55626 |
rs773903991 | in-del | -/GACC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436596 | TCTAATTAGCACTGG[-/GACC]GTCTGCTACTTACTA | 55626 |
rs773915826 | snp | C/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594993 | CTTTAGGAGACGAGG[C/T]TGGTGGATTGCTTTG | 55626 |
rs773925990 | snp | C/T | | | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396085 | TACATCACTTCAGGC[C/T]TGTAGTCCTGGGTGG | 55626 |
rs773956471 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575275 | TCGGCCTGACCAACA[C/T]GGTGTAATCCCATCT | 55626 |
rs773972249 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469727 | TGGAGTGCAGTGGTA[C/T]GATCATTGCTCACTG | 55626 |
rs773978024 | snp | A/G | 1.65343e-05 | 0.00287521 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547228 | CCAATCAGGGAATGA[A/G]CACACTTGCCAGTCT | 55626 |
rs773989600 | snp | A/G | | | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430564 | GAAGAACTGCTTAGA[A/G]TAAGTGCATCAAGGC | 55626 |
rs774000002 | in-del | -/A | 1.67188e-05 | 0.00289121 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443471 | TCCACTGATACCCCC[-/A]TTTGACATTGACTTA | 55626 |
rs774005987 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504314 | GGCCTTAGCAACTAC[C/G]GGCCATAGCACTTAA | 55626 |
rs774047489 | snp | A/C | 1.68238e-05 | 0.00290028 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542147 | AGCTGGGCGTTTGGC[A/C]CTCAGTCCGCTCGAG | 55626 |
rs774054584 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492586 | GAGGTGGGAGGGAGG[C/T]AGGGAAAGACTGTGA | 55626 |
rs774062481 | snp | C/T | 1.66571e-05 | 0.00288587 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397852 | GGTGCTCTGCTCCCG[C/T]TGCACCACGGCTGTC | 55626 |
rs774062809 | snp | A/G | 5.54237e-05 | 0.00526391 | intron-variant, stop-gained, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543041 | GGGGGACACTGTCCT[A/G]GTGTGGCAAGAGGGA | 55626 |
rs774068069 | snp | C/G | 1.72279e-05 | 0.0029349 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434865 | AAATCGCTTGGTGTA[C/G]AGCATTTCGCCCAGG | 55626 |
rs774072323 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482333 | AAACTTCACTCTAAT[A/G]AGCAGGAGTGACTGC | 55626 |
rs774101813 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458279 | GCTGCTAAAAGGACG[C/T]ACCTGGAACACAGCC | 55626 |
rs774112609 | snp | C/T | 1.65282e-05 | 0.00287469 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410342 | TTCAGCTGGTCCCAG[C/T]AGTACTCAACACCAG | 55626 |
rs774118336 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456664 | TGGTGGAAGCACAAG[C/T]GAGTGGAATTGGACC | 55626 |
rs774119304 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550466 | TTTACAATTAGCAAT[A/C]TGTGGCAATTATTTG | 55626 |
rs774120906 | snp | C/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588974 | TGGGGAAATTAACAT[C/G/T]TACTCTAAAGGACTC | 55626 |
rs774171534 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512488 | GTTCCTCCTCTAGCA[C/T]CACACTTGCGGAAAT | 55626 |
rs774185025 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593619 | CCTAAAGAACCACAC[A/C]GGGAAGCCCCAGCAA | 55626 |
rs774191684 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420936 | CTGTGCTGCGTTTTT[C/T]AAATGGGGGTCTGAA | 55626 |
rs774194297 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443714 | GAAAAACTAGACTAT[C/G]GCTGAAGAAAGCTAA | 55626 |
rs774195724 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582110 | CAGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs774195909 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565585 | GGTGGCATGTACCTG[C/T]GGTCCCAGTTACTTA | 55626 |
rs774209094 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534862 | AGCTTTTTGTAGAGA[C/T]AGGGTTTCACCATGT | 55626 |
rs774219126 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408262 | CCAGGCTTTCTGTGC[C/T]CTCTCTTTGGAAAAA | 55626 |
rs774219843 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566925 | GAACTCTGCTAAAAT[C/G]TAAGAATATGAACCC | 55626 |
rs774230418 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555274 | CTAGAGAGTATGCCA[C/G]AACCCAGTGGGAATT | 55626 |
rs774241658 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496308 | AATCCCTTGAACCCA[A/G]GAGATGGAGGTTGCA | 55626 |
rs774257435 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511255 | CCCTTATATTTAGGG[A/T]GTATAATCCTCAAAC | 55626 |
rs774260397 | in-del | -/CTGGGCTCAAAGAGAGCCCTGATCC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404371 | TCTGCATGGGGAAAT[-/CTGGGCTCAAAGAGAGCCCTGATCC]CTGGGCTCCCCTGAA | 55626 |
rs774264137 | in-del | -/CAAAGAC | 3.30677e-05 | 0.00406605 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544063 | CACAGAAGAAAGAGA[-/CAAAGAC]CAAAGACACACATAG | 55626 |
rs774269168 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448870 | TAACTTTCCTTGAAA[A/G]ACACAGTATATTACA | 55626 |
rs774272385 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460174 | TTCATCAATCGGGAA[C/T]AGACAACAAGACATA | 55626 |
rs774273907 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509701 | TTGAAGAATGGTCTG[C/T]ATACACTAATACATA | 55626 |
rs774287976 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528154 | AATTATGATACATAC[A/T]TACAACTTTTTCTTT | 55626 |
rs774290472 | snp | A/G | 3.62017e-05 | 0.00425436 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397402 | TCAGCTGTGAGGTCC[A/G]GTTTCTGCTTGGCGG | 55626 |
rs774290887 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475116 | TTAAAGTATTTTAGG[C/T]TCTTCTGCAAAGTAG | 55626 |
rs774310326 | in-del | -/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452354 | TTGTTGTTGTTGTTG[-/T]TTGTTTGTTTTTTAG | 55626 |
rs774337877 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572255 | GCAGGGAGCAGAGAT[C/T]GTGCAACTGCACTCC | 55626 |
rs774347827 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522970 | AAGCGAGTTAGTACG[C/T]GAAGCCTCAAGAGAA | 55626 |
rs774371826 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538352 | GAGCATAAATATAAA[A/C]TTGTTTACAGTGAGA | 55626 |
rs774374127 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542300 | TGAAGGTCAGGAGAT[C/T]GTGGCAAGCACGACA | 55626 |
rs774386636 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587405 | TAAAAAATTAAACTC[A/T]TTAGTCAAGCATGCT | 55626 |
rs774412707 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396929 | CTGGGAGCCTGGCCC[A/G]ATCCCTGTTGGTTTC | 55626 |
rs774435398 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412243 | CCTTTTGTATACTTA[A/C]AATCATCTCTAGATT | 55626 |
rs774436853 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512709 | CCCACCTAGTGCCAT[G/T]TCTCACTTTGGCCTT | 55626 |
rs774440639 | snp | G/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542029 | CCAGATCTGCTGGAC[G/T]GGGTGTAAATTCTTT | 55626 |
rs774449186 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542387 | GCTGGTGGGAAGGGC[C/T]TGGCCTCTCAGATTC | 55626 |
rs774463643 | snp | C/T | | | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396157 | ATACTCACCCTGGCA[C/T]TGGAAGGTGGCCCCA | 55626 |
rs774465826 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461995 | ACTCCTTCCTCCCTG[A/C]CCTAGTCAATGTTTA | 55626 |
rs774525389 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482432 | TGCTGTTGGGAGTCA[C/G]CAAATATTACAAAAA | 55626 |
rs774527865 | snp | A/G/T | 9.89094e-05 | 0.00703178 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508276 | TGGAAGAACGGAGAC[A/G/T]GTTCTGTTGGTAGCG | 55626 |
rs774535662 | snp | A/C | 1.65102e-05 | 0.00287312 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543934 | TAGTTAAGAAAAGAA[A/C]TCACAGTTTAGCTGG | 55626 |
rs774543774 | snp | C/T | 1.65184e-05 | 0.00287384 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418042 | ATGGGATAAAGGACG[C/T]TGAAAACTCTCTAGG | 55626 |
rs774553145 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432258 | GGTACAATGATAGCA[C/G]AAGGAACGAGTGATC | 55626 |
rs774556915 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447962 | AAATGGCCTTTAAAG[C/T]TATATCTGTCATCTA | 55626 |
rs774561931 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447439 | ACTTGGGATGCTGAG[G/T]CATGAGAATTGCTTG | 55626 |
rs774567886 | snp | A/G | 1.6577e-05 | 0.00287893 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46443539 | CCCACCACTGGAGCC[A/G]GTAGGTAGTATTGGC | 55626 |
rs774572110 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462898 | AGCTGGGATTACAGG[C/T]GTGCACCACCATGTC | 55626 |
rs774581014 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439220 | TTGAGGTTATAGTGA[A/G]ATATGATCACGCCAC | 55626 |
rs774582665 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515848 | ACCCGGCTAATTTTT[-/G]TACTTTTAGTAGAGA | 55626 |
rs774611560 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589149 | CTGATTACTTAATCT[A/G]TTTTCTCCTTACATT | 55626 |
rs774631588 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568804 | ACCCTCAACCCTACC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs774642351 | snp | A/G | 1.651e-05 | 0.0028731 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397957 | ACCTGGCAGATACAA[A/G]GCAGAAGAGAGAGCG | 55626 |
rs774644644 | snp | C/T | 5.42451e-05 | 0.00520765 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397482 | CTCCCCTAGGGCCTG[C/T]AGCGTCCCCCCTGCT | 55626 |
rs774674353 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425500 | ACCTCTCATCATGTC[G/T]CAGTGCTGGAACTAG | 55626 |
rs774699693 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544584 | ACTAAATAAATGTCA[A/G]TTATGTGCTTACATC | 55626 |
rs774700384 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506403 | AGCACAAATGCTAGT[-/A]GTGTGTTTAATGACA | 55626 |
rs774700965 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572105 | CAAGAGATCGAGACC[A/G]TCCTGGCCAACATGA | 55626 |
rs774716279 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514601 | TGTGTCTGAGGTTGG[A/G]GTGTATTTTACAGTT | 55626 |
rs774721893 | snp | A/G | 6.58903e-05 | 0.00573941 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46417959 | TAGTACCATAGGCCA[A/G]GCCAAGCCCTGGCTC | 55626 |
rs774737126 | snp | A/G | 1.65089e-05 | 0.00287301 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542843 | CTCCCAAAGAGCGGC[A/G]GGTAGGACCCAGACT | 55626 |
rs774743448 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477648 | CCTCTTTGAGGACAC[A/G]TCTTTATTGTACATA | 55626 |
rs774763821 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502058 | AAGAGAGGTTTTTGT[C/T]TCTCTCCAGGTCATT | 55626 |
rs774784238 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420191 | GCATTAGGAACCTCC[-/T]ACACCCTTCCTGTAG | 55626 |
rs774786623 | in-del | -/AGG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408282 | TTTGGAAAAAGAGAC[-/AGG]AGGGTCCTCACATTT | 55626 |
rs774800012 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590091 | AGTATAAAAATGTAT[A/G]GCCGAGCGAGGTGGC | 55626 |
rs774844291 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535789 | GGGTACCAAAAAGAT[-/A]AAAAAAAGGGAAGGC | 55626 |
rs774873649 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415056 | ACAGCCACCTGTTTC[A/G]GAGGGAGGGCTGCAA | 55626 |
rs774876634 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438028 | CCCAGGTGTCTCTGA[C/T]GTTGCCGGACTGGGA | 55626 |
rs774885684 | snp | C/T | 1.67256e-05 | 0.0028918 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547270 | ATATAGATATTATGG[C/T]TCACATGGGTGGAGG | 55626 |
rs774903349 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529401 | CATGTCAGCCTACAG[C/T]AAGCAGGGGGAGCCC | 55626 |
rs774904022 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464658 | AGCAACTGTACCTCC[C/G]AGGGTTAGTTACTTC | 55626 |
rs774915255 | snp | G/T | 0.00732527 | 0.0600747 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542846 | CCAAAGAGCGGCGGG[G/T]AGGACCCAGACTGAG | 55626 |
rs774919136 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545059 | TTGGGCCCATGAGGT[A/C]AAGGCTGCAGTAACT | 55626 |
rs774923936 | snp | C/T | 1.65575e-05 | 0.00287724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512693 | AAGGGCCGCCCCTCC[C/T]CCCACCTAGTGCCAT | 55626 |
rs774928319 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46453921 | TTTTCTAAATACAGA[C/T]TTCAATGGTTACGTG | 55626 |
rs774934161 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505195 | TCGTGACTGCACATG[C/T]CTCTGACTTTCCTTC | 55626 |
rs774948963 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469978 | CCACTGTGCCCAGCC[C/T]ATTTCATTTTAAAAA | 55626 |
rs774961723 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413068 | CATGTACTTCCTGAC[C/T]CGGAACCTTCCTTCC | 55626 |
rs774968837 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400355 | CTCTCTGCCTGCCTC[A/C]TTAGAGTTGGATTTC | 55626 |
rs774978894 | snp | C/T | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543340 | GATTGCAGGAGGGCA[C/T]GCTGACGGTAGTGGG | 55626 |
rs774997179 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417782 | AGGGCCCTTTAAGGA[C/G]TGGCGCTGAGAATGA | 55626 |
rs774999134 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400686 | CAGAGACGGTTTCGC[C/T]GTGTTGCCCAGGCTG | 55626 |
rs774999525 | snp | A/C | 1.6507e-05 | 0.00287284 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547895 | GAGACAAAAAAAAAA[A/C]AAAAGTTAAAATACA | 55626 |
rs775042308 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455635 | TAACTCAAACAGAGG[A/T]TAGGGCTCATGCCAT | 55626 |
rs775102523 | in-del | -/GTCCCAGGAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411400 | ACTGTGTCCCAGGAG[-/GTCCCAGGAG]GTCCCAGGAGGTCCC | 55626 |
rs775108633 | snp | A/G | 3.81898e-05 | 0.0043696 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397972 | AGCAGAAGAGAGAGC[A/G]AATTGGCTGCTGGCC | 55626 |
rs775111273 | snp | A/G | 3.32497e-05 | 0.00407722 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542918 | TGAAGGCAGACGGCC[A/G]GTTCAGGAGGCCCTG | 55626 |
rs775113372 | snp | A/G | 1.65051e-05 | 0.00287267 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508297 | GTTGGTAGCGCATGG[A/G]GCGCTGGCGAATACT | 55626 |
rs775139225 | in-del | -/TTA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483942 | GTTAGTTAGCATGGG[-/TTA]TTAACTTCCAGCATT | 55626 |
rs775151358 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428543 | AGTGCCTCTAGGATC[C/T]GCAGCGATTAGGCAA | 55626 |
rs775158601 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484897 | TGATCCACCTGCCTC[A/G]GCCTCTGAAAGTGCT | 55626 |
rs775160426 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416244 | AGACAATCAGCATCA[C/T]GTGCTTTGGGGAAAA | 55626 |
rs775182199 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506386 | TTCCTTTTGCTTCTA[A/C]GAGCACAAATGCTAG | 55626 |
rs775214784 | snp | C/T | 5.42942e-05 | 0.00521001 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397420 | TTCTGCTTGGCGGTT[C/T]GAGGGGAGGCACCAG | 55626 |
rs775218510 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522666 | TATTGAATTCCATAA[G/T]GTTGAATTCTTAGCT | 55626 |
rs775253113 | in-del | -/AGA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475239 | TTAATTATGAATAAG[-/AGA]AGAATTCAAGTCCTT | 55626 |
rs775275015 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581888 | GAGAGGCCAAGGTGG[A/G]GAAGGAGCTCTTGAG | 55626 |
rs775276795 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523934 | AGTGCAATGGCATGA[C/T]CTAGGCTCACCGCAA | 55626 |
rs775303283 | snp | A/G | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542254 | GAGGAGTAGTTAGGT[A/G]TGGTTCTTTCCCAGC | 55626 |
rs775332239 | in-del | -/TAGATAGATAGA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447717 | CATCTTGTAGATAGA[-/TAGATAGATAGA]TAGATAGATAGATAG | 55626 |
rs775332474 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486243 | CTGGGTACCAGATGG[A/G]TACACGGCAGAAAGA | 55626 |
rs775339548 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430301 | TAATTAGCAAAGAAT[C/T]AAAGCACCATGCACA | 55626 |
rs775359634 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446184 | AAGCCTGGCACCAAG[A/G]AGAGTCATTTTTTTT | 55626 |
rs775360274 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549767 | TCCTAGAATGGCCTC[C/T]ATGTTTTGTTTTGTT | 55626 |
rs775371735 | in-del | -/A | 0.000140088 | 0.00836805 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433645 | GAGGGCCAACAAAAC[-/A]AGAGAAATATTTCCT | 55626 |
rs775387132 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536223 | TCTACTGTGTGGCCA[C/G]GTAGTATTCTAGGTA | 55626 |
rs775402187 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498034 | TCTGCCACTCACTTC[C/T]GTGCTGATACAAGGT | 55626 |
rs775404882 | snp | A/C | 3.30175e-05 | 0.00406296 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543306 | ATTGTGGAGGAGAGG[A/C]GTCCGGCGAACTGGC | 55626 |
rs775419341 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582208 | TCCCCTACTGTTCAC[C/T]GTATTCCAACCATAT | 55626 |
rs775454873 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527478 | AAGTGAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs775477635 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568349 | TGTAATTCCAGCTAC[C/T]CAGAAGGCTGAGGGA | 55626 |
rs775501614 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432932 | TGCCCAGAAGGCTTT[C/T]ATGGCAATATAAGAG | 55626 |
rs775510622 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525932 | AGAAATAGGCTAGGT[A/G]CGGTGGCTCACACCT | 55626 |
rs775520263 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461662 | AAAAGATTATGCCCA[C/T]AGAAACATGTCCTGA | 55626 |
rs775530288 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396828 | CCCACTGTCCCTTGA[C/T]CCCATCCTGTATCAG | 55626 |
rs775531384 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549910 | TGCAACCTCTGCCTC[C/T]TGGGTTCATGCAATT | 55626 |
rs775546785 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534993 | GTACCCTATTCTAAA[G/T]CCTGAGTTTACCTTC | 55626 |
rs775549478 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46449857 | TGAGGTCAGGAGTTT[A/C]AGACCAGCCTGACCA | 55626 |
rs775568948 | snp | C/T | 3.29891e-05 | 0.00406122 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548319 | TGAGCTCCCATGGCC[C/T]GAGCACCCCGTTCTC | 55626 |
rs775583513 | snp | C/T | 5.59425e-05 | 0.00528849 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46435005 | TGGCATCATTGTAGA[C/T]CTTGCAGTTCTGCAC | 55626 |
rs775591239 | snp | C/T | 3.70487e-05 | 0.00430383 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494102 | CGAAGGCTCCCTCTG[C/T]TGCTAGCAACTCGGT | 55626 |
rs775639955 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433755 | CCTGGTGTTATCTCA[A/T]AGGACTGTAGTGAGG | 55626 |
rs775669050 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516668 | TTGATCTCCTGACCT[C/G]ATGATCCGCCCACCT | 55626 |
rs775690762 | snp | A/G | 4.94319e-05 | 0.00497127 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542417 | CAATGTTATTGTTGA[A/G]CATTTCCTGGGCCTG | 55626 |
rs775698062 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419471 | AAAAGAGATGATGTA[C/T]AAAATGCCTGCCATG | 55626 |
rs775703311 | snp | A/G | 1.69634e-05 | 0.00291229 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397631 | GTTGGCTCCCGCCCA[A/G]GGGTACCAGGCTGGT | 55626 |
rs775709711 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412322 | TGCATCTCACTCTGT[G/T]GCCCAGTCTGAAGTG | 55626 |
rs775716281 | in-del | -/TT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428363 | ATTGGAGGCTTTCCC[-/TT]AAAGACCACAATACT | 55626 |
rs775761468 | snp | G/T | 1.64789e-05 | 0.0028704 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545656 | CAAAGGGTTCCCGTC[G/T]ACTCCAGTCCCAGAA | 55626 |
rs775762605 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539727 | TTATAAAATGGAAAA[C/T]TGAATACCTGACTTG | 55626 |
rs775763512 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488190 | GCCAGATGCAGTGGC[G/T]CACGCCTGTAACTCC | 55626 |
rs775777602 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512411 | GGCTGTCCATCTGAA[A/T]GACAACAGCCTCTCT | 55626 |
rs775779359 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480427 | AAACAAGAAATGTCT[C/T]ATGCCACTAAATTTG | 55626 |
rs775781631 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473751 | CGCCTCGCGGGTTCA[C/T]ACCATTCTCCTGCCT | 55626 |
rs775796043 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575512 | TGTTTTTTTCTTTCC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs775817413 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578319 | TGGAGAAACCCTGTC[C/T]CCACTAAAAATACAA | 55626 |
rs775820079 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444472 | CCTCCTCCTTCTGAG[A/G]TGCATTTCATACACA | 55626 |
rs775827700 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413615 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 55626 |
rs775832301 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532246 | CCAGTATGTATGTGA[C/T]TGTCAGAGATAGAAC | 55626 |
rs775835129 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509962 | TGCAAAGAGGTCCTC[A/G]GTAAGTCTACCAACC | 55626 |
rs775849254 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486410 | TGAAGATCTGCTATA[C/T]AGTGATTAAGCAATT | 55626 |
rs775850099 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555566 | CAAACAATAGGGCCA[A/C]CTGAAACCCCAGAGA | 55626 |
rs775895160 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412480 | TTGTTTTGTAGAGAC[A/G]GGGTTTCACCATGTT | 55626 |
rs775941302 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573162 | GTAATCCTAGCACTT[C/T]GGGAGACTGAGGTGG | 55626 |
rs775965143 | snp | A/G | 1.64972e-05 | 0.00287199 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46512730 | CTTTGGCCTTACCTC[A/G]CTGGGTCTGGGTAAA | 55626 |
rs776006885 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425834 | ACAAGAGCGAAACTC[C/T]GTCTCAAAAACAAAA | 55626 |
rs776028703 | snp | A/C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404384 | ATCTGGGCTCAAAGA[A/C/G]AGCCCTGATCCCTGG | 55626 |
rs776073585 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441331 | CCAGCCTGGCCAATA[C/T]GGCAAAACCCCGTCT | 55626 |
rs776089429 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494025 | GCCCACTAGGAAACA[A/G]TGCCAGATGTGGACA | 55626 |
rs776096615 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424448 | CCGCTGCTTTCCAAA[A/G]GCCACCCCTGGCCAT | 55626 |
rs776098541 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441121 | CTGAGAAAGAAGGAC[G/T]AAAACAAAGTTCAAA | 55626 |
rs776100533 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481323 | TAGGGGAAAGGATCT[A/G]CGACAAGGATATAAG | 55626 |
rs776122631 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546377 | GAAAAACTCAAGCTC[A/G]GTGCACAACATGGTG | 55626 |
rs776126578 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529464 | GTGGTGCGGGTACTG[C/T]AATGACCAGTGACTC | 55626 |
rs776137482 | snp | A/G | 1.691e-05 | 0.0029077 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545570 | TATCACGTCAGTCCT[A/G]TGCCAGACAATGCAG | 55626 |
rs776143713 | in-del | -/AAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547885 | TACTCTCTGGGAGAC[-/AAA]AAAAAAAAAAAAGTT | 55626 |
rs776154052 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513883 | AATTTTAGCTACAAC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs776163102 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547515 | ACACATGCCACATTC[A/G]GAAAATATTTTTTCC | 55626 |
rs776186709 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419157 | TTGTTTCTAGCTTAT[A/G]TAAATCACCGTTAAA | 55626 |
rs776187555 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592427 | CTACACACAGCCTTT[C/T]TTAGCTTTTGTATGT | 55626 |
rs776209213 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563070 | CCCAATGTGCTGAAA[C/T]TACCGTGCCTGGCCT | 55626 |
rs776218048 | in-del | -/CT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407195 | GGTGACAGAGTGAGA[-/CT]CTGTCTCAAAAATAA | 55626 |
rs776262529 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425905 | TAATCCCAGCACTTT[G/T]GGAGGCTGCGGTGGG | 55626 |
rs776283264 | in-del | -/AAAC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515477 | ACTGCATCTCAAAAC[-/AAAC]AAACAAACAAACAAA | 55626 |
rs776293062 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474144 | ACTTTTACTGGTTCA[-/G]GGTGCTGCCCTGATT | 55626 |
rs776298396 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562685 | AAAGGGATAAATCAA[C/T]AGTTTAGGATCACTT | 55626 |
rs776334199 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495165 | CATCAAAAGAATAAT[A/C]AGCCAAAGGGCACTG | 55626 |
rs776334268 | snp | C/T | 1.65312e-05 | 0.00287495 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548288 | TTTATCTTCTACCAG[C/T]TCCTGCAGAAGCCGC | 55626 |
rs776351508 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497429 | TTATTTAACATCTTG[G/T]CTAAGAATGGAGAAA | 55626 |
rs776361008 | snp | A/G | 0.00331674 | 0.0405878 | synonymous-codon, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518363 | TGAACCTGGGAGGCG[A/G]AGCTTGCAGTGAGCC | 55626 |
rs776422991 | snp | A/G/T | 8.09061e-05 | 0.00635976 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494092 | TAGGCTCTAACGAAG[A/G/T]CTCCCTCTGTTGCTA | 55626 |
rs776437884 | snp | A/G | 1.65531e-05 | 0.00287686 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46443504 | ATTACTGATTTCAGG[A/G]AGGTCAAACTTAGTG | 55626 |
rs776439438 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506572 | TGAGGGGGAGATGAG[A/T]ACTCTTAAGGCCCCA | 55626 |
rs776448711 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542274 | TCTTTCCCAGCGCAG[A/G]GTATCGTTGTTGAAG | 55626 |
rs776456127 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454000 | AATAAACTCCTAAAG[G/T]CTCCAAAGAAGGATA | 55626 |
rs776456858 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485941 | GAATGCTCCAGTGAC[C/T]GGTGGACACCAAATA | 55626 |
rs776457619 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499506 | AAATCAAAGTCCTCA[A/G]TAAGAGCTAGAATTC | 55626 |
rs776518169 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567225 | TACAGGTGCACACCA[A/C]AACACCCAGTTAATT | 55626 |
rs776572453 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432066 | TTGAGATTCTCTTTC[A/G]TTCATTCATTCACTT | 55626 |
rs776576372 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544095 | GAGATTATGTTAACT[C/G]AGAAGAGGAAACTTG | 55626 |
rs776603733 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553802 | TCCTAGTCCTACACA[A/G]CACAGAGTTACCTAA | 55626 |
rs776623655 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429040 | GTTGGGCACATTCTT[A/G]TCTGCCAGCTCCGGG | 55626 |
rs776645233 | snp | C/G | 3.98145e-05 | 0.00446157 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397990 | TTGGCTGCTGGCCTG[C/G]GCCTCTGAGGCAGGT | 55626 |
rs776672436 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464239 | AAAATGTCATCAGGA[C/T]GCCCTGTGAGCAGAC | 55626 |
rs776697756 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437263 | CTCAAATCCAGGCCA[C/T]TGTGCTTGCATTTGT | 55626 |
rs776708726 | snp | C/T | 2.82841e-05 | 0.00376049 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547909 | AAAAAAGTTAAAATA[C/T]ATGATTTGTAGACCA | 55626 |
rs776720064 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587500 | CAGACACATATTACA[C/T]GTAGCAATCAATCTT | 55626 |
rs776724460 | snp | C/G | 3.30956e-05 | 0.00406776 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410357 | TAGTACTCAACACCA[C/G]AGTTTAAGGCCCTAA | 55626 |
rs776725665 | snp | C/G | 1.91064e-05 | 0.00309077 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408741 | CTAAAGTCAGATGGG[C/G]CTTGGGACAGCACCC | 55626 |
rs776850715 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490294 | GATGGGGAAAGGCCT[C/G]GGTTGATGACCAATT | 55626 |
rs776853392 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488678 | CAAGCACATGGGTAA[C/T]ACTCTCTAGAAGAGC | 55626 |
rs776881278 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528242 | CAGTGGCACGATCCC[A/G]GCTCGCTGCAACCTC | 55626 |
rs776891245 | snp | C/T | 2.90727e-05 | 0.00381255 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494126 | ACTCGGTTCTTACCT[C/T]GGGACAAAGCGTCCA | 55626 |
rs776895859 | in-del | -/GTTA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478007 | TGTGAAGAAGCACAG[-/GTTA]GTTTACTGGTGAATG | 55626 |
rs776930166 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473946 | TGAGCCACCGCACCC[A/G]GACAGGATCCTTTAA | 55626 |
rs776936961 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503791 | TCTCATTGAGATGTT[C/T]TTTCCAGGCAGAAAT | 55626 |
rs776947747 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481627 | CTCGGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 55626 |
rs776949386 | snp | G/T | 1.67638e-05 | 0.0028951 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397657 | CTGGTCCCAGGAAGC[G/T]GTCCGGGGGCTTAGG | 55626 |
rs776957454 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405888 | AGATGCGTGCCACCA[A/T]GCTCGGCTAATTTTT | 55626 |
rs776957807 | snp | A/C | 3.29843e-05 | 0.00406092 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434808 | ACCATGCCAAGGCAC[A/C]AGCGTCCCTCTGTCA | 55626 |
rs776964718 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537253 | CAATGACCTACATGA[A/G]CAACAGAGGTTTTGA | 55626 |
rs776997833 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559966 | ACTCAAGATAGAACA[A/G]TAACCAGAGTATGTG | 55626 |
rs777041784 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593463 | TAGGGGTCCCCAGTG[C/T]AATTGAGGCATGACA | 55626 |
rs777045799 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449174 | TTTCAACATCATATT[A/G]GAAGTCCTAGCTAAT | 55626 |
rs777047702 | snp | A/G | 1.65288e-05 | 0.00287474 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433529 | AAGACCTGGGCCACC[A/G]TGTGCTCTGTGGAGG | 55626 |
rs777048790 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541290 | CTTCCATGAATTATT[A/C]TTCTTCTCCACCCCA | 55626 |
rs777072928 | snp | A/C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558126 | TGATGTTACACAGGG[A/C/G]AGAAGGACCATCCAG | 55626 |
rs777085970 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575432 | ATTGCACTCTAGCCT[-/G]GGCAACAAGAGCAAA | 55626 |
rs777086970 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409659 | ACTGCCTTGGAATAG[C/G]TGGAGCTGGCAGCAG | 55626 |
rs777116994 | snp | C/G | | | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518236 | GGAGTTCGAGACCAG[C/G]CTGGCTAACATGGTG | 55626 |
rs777135444 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516728 | GTGACCCACTGCGCC[C/T]GGCCAAAAGATCTTT | 55626 |
rs777145856 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589705 | GCTAACTGCAAGCTC[C/T]GCCTACCGGGTTCAC | 55626 |
rs777159124 | snp | C/G | 1.68587e-05 | 0.00290329 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545578 | CAGTCCTGTGCCAGA[C/G]AATGCAGATGGGGCA | 55626 |
rs777161005 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556291 | CACCACAAGCCAGCA[C/T]CCACACCTGACTCCA | 55626 |
rs777208903 | snp | A/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594584 | GGCAGGGGGAAAAAA[A/T]GCACACGGATTGCTT | 55626 |
rs777227173 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480759 | ACATGAAAAAAATAT[A/G]TACATACTGCAAGTC | 55626 |
rs777238636 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427382 | CCAACGGTATAAAAG[A/C]AAGCAAGCAATCTAA | 55626 |
rs777239184 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575001 | TTGTTGCCAATTCAA[C/G]AAAGCTCAATAAATA | 55626 |
rs777240208 | in-del | -/TT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500278 | AGAGTAAAAAAGGAC[-/TT]AGCATTTTTTTTTTA | 55626 |
rs777242623 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412441 | AGGCGTGCCTCACCA[C/T]GCCTGGCTAATTTTT | 55626 |
rs777248016 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445960 | GAATAATACCAGATG[C/G]TTTTTGAGTACTGTG | 55626 |
rs777269214 | snp | A/G | 1.64923e-05 | 0.00287156 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542559 | GTTGTTTTGGCTGGA[A/G]CCATTCCCTCCATCT | 55626 |
rs777285866 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508546 | TGCAGAATATACTTA[C/T]CAGACTATCACCAGT | 55626 |
rs777305479 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511643 | AAAGCCTCCTAATGT[C/G]CTCTAGTATTGCTTA | 55626 |
rs777317255 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442753 | GGAAATGCCACAGAC[A/T]TAGAATATCTTAATT | 55626 |
rs777319823 | snp | C/G/T | 3.61731e-05 | 0.0042527 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397445 | CACCAGTGCAACGTT[C/G/T]GTCTCTACCTGTTCC | 55626 |
rs777323952 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590892 | CACTCAAGCCTGGGC[A/G]GCAGAGTGAGACTCC | 55626 |
rs777325482 | snp | A/C | 1.64857e-05 | 0.00287099 | missense, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508209 | AAGTCCTCAAATTCC[A/C]AGTCGGTTCCCTCTA | 55626 |
rs777325811 | snp | A/G | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410312 | CTGTTGGAATGGACA[A/G]TGAAGACCGTCTCGT | 55626 |
rs777352637 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460055 | ATATAACTGAAGATG[A/T]GCCAGAACAATTTCA | 55626 |
rs777365128 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586891 | ATATTTTTCTGTCCT[C/G]TTTTCAGTGGTCGCC | 55626 |
rs777368634 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475816 | TCTCAGATTCGGAGA[A/C]AGGTGGAACAGGAAA | 55626 |
rs777371785 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407963 | GCTAATTGGTTTTTA[A/G]AAGTGTGAGGCTGGC | 55626 |
rs777380244 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550686 | AGAGTAGTTACTACT[C/T]CTGTCTTATTGCTTA | 55626 |
rs777385178 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542623 | CTCCCTTCTGTGGCT[A/G]AAGTGTACACAGATG | 55626 |
rs777396764 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474767 | GATTAGTACTCATTC[C/T]GGATTTTCCCTATGG | 55626 |
rs777398266 | in-del | -/GC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405506 | GGAGGCTTGCTTGAA[-/GC]TAGGAGTTCAAGACC | 55626 |
rs777407570 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561655 | TGTTTTCCAATCTTA[C/T]AGTCAGCCCAGGTCA | 55626 |
rs777440190 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450651 | TTTCACCATGTTGCC[C/T]AGCCTTGTCTCCAAC | 55626 |
rs777446544 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513600 | GCACATAACTATTAA[A/G]AGATAGTAACAGGAC | 55626 |
rs777485171 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489554 | CCAGGCCGTAATGAC[C/T]TGTGGCTAGGAGCAA | 55626 |
rs777491524 | in-del | -/AT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459738 | AAAAAAAAAATACAC[-/AT]ACACACACACACACA | 55626 |
rs777495266 | snp | C/T | 3.33428e-05 | 0.00408293 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545775 | CAGCTTTCACTGCCA[C/T]CCTGTGAATGAACCA | 55626 |
rs777498593 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527626 | ACAAATAACCATACT[A/G]AACAATGGGCCAAAG | 55626 |
rs777518872 | in-del | -/AAAAAAAAAAAAAAAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454584 | CACTAAAAATACAAA[-/AAAAAAAAAAAAAAAA]AAATTCTCCGGGCGA | 55626 |
rs777542062 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559054 | TCCTGTAATCCAGCA[A/C]TTTGGGAGGCTGAGT | 55626 |
rs777548816 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588088 | ATGTAATCACAGAAC[G/T]TTGACAGGCCAAGTT | 55626 |
rs777571634 | snp | C/T | 1.65051e-05 | 0.00287267 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543389 | TGGGGATCTCTGGTT[C/T]GTCATCACCCTGCAA | 55626 |
rs777577003 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566371 | TGCAGTGAGCCGAGA[C/T]TGAGCCACGGCACTC | 55626 |
rs777595723 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491359 | CTCTGGGATTCAGTT[G/T]CCTCCACTGTTAATT | 55626 |
rs777605085 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580947 | CAGGTGTGAGCCACC[A/G]CACCCAGCTAATTTT | 55626 |
rs777614522 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463478 | TGACTTGGACTATTC[A/G]ACTGTCAGCTCCTTA | 55626 |
rs777616901 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421822 | ATCAGTCTTTCTAAC[A/C]CAGAGACTGGGTGAG | 55626 |
rs777625145 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566634 | CCCCTGAAGGCATTC[C/T]CCCTGGATCTTCTGG | 55626 |
rs777641997 | in-del | -/GGA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561155 | GAGGCCAAGGCAGGT[-/GGA]GGATCACCTGAGGTC | 55626 |
rs777689689 | snp | A/G | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542531 | ACTGAAGCTCATGGC[A/G]AATGCTGCCCGAGTT | 55626 |
rs777702689 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436620 | CTACTTACTACTCAG[A/G]GTCCCAAGCCCTTTG | 55626 |
rs777703904 | in-del | -/AAG | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452800 | TCCCTGATGACAAAT[-/AAG]AAGACTTCTTCCATG | 55626 |
rs777706554 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420518 | TTTATTCTTTCTCAT[A/G]GAGGTTTTCACCTTC | 55626 |
rs777721218 | snp | A/G | 1.81177e-05 | 0.00300974 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434994 | AATGTCACAGCTGGC[A/G]TCATTGTAGATCTTG | 55626 |
rs777722646 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449593 | ACTGTTACAATGTCA[A/G]TTCTTCTCAGCTGGA | 55626 |
rs777732182 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440682 | GGGAAAATGTGGATT[G/T]TGGTTAATTTCCAGC | 55626 |
rs777759077 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488165 | ATTAATCAAAAATTG[A/T]CAAAATTGGGCCAGA | 55626 |
rs777781431 | snp | A/G | 0.000115734 | 0.00760616 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542880 | GCGGAGCGTGTTGCC[A/G]GCAGTGCTGCTCTGG | 55626 |
rs777786484 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503340 | AGAGATGGGGGAATC[G/T]CCAGTGAGTGGAGCA | 55626 |
rs777799465 | in-del | -/CTGAATC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471053 | TGCTGAAAGAATTTA[-/CTGAATC]CTGAATCCCTATCTA | 55626 |
rs777810983 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497187 | ATAAATTTTATGTTA[C/T]GTGTATTTTACCAAC | 55626 |
rs777823831 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424891 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 55626 |
rs777826813 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556847 | ATTAGTATGAAAATG[A/G]TAATAAGGGCTGGTT | 55626 |
rs777843359 | snp | G/T | | | intron-variant, utr-variant-5-prime | AMBRA1 | GRCh38.p7 | 11:46591312 | ATTCTTAGCTTAACT[G/T]CCCAATCTAGATTCT | 55626 |
rs777873932 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479992 | CTCCTTGTCCATTTC[A/G]GTTGCTGGCAGAATT | 55626 |
rs777874801 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525682 | TTTGAATCCGGGAGG[C/T]GGAAGTTGCAGTGAC | 55626 |
rs777885957 | snp | A/G | 1.68644e-05 | 0.00290378 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542962 | GACGAGGCCTGCTCC[A/G]GGGGATGGAAGGGCT | 55626 |
rs777889668 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479036 | AAACCCTGTCTCTAC[-/AA]AAAATACCAAAATTA | 55626 |
rs777900122 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493207 | CCACATGCTGGCAGT[A/G]CCAAAGGAGTGGAGA | 55626 |
rs777924321 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522107 | GAAACAGAATGTATA[A/C]ATAGTGTGCAATCAT | 55626 |
rs777954204 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531354 | GCAGGGAACACACAC[A/T]GAATTCAGAGGCTCA | 55626 |
rs777974579 | snp | C/T | 7.66754e-05 | 0.00619127 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508411 | ACAAACTAGCACTAA[C/T]GTGGGGAATACTATG | 55626 |
rs778001826 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398392 | GGTGTGGCCCAAAGG[C/G]AAACAGTCTGCTCTG | 55626 |
rs778021583 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459630 | GCAGGAGAATTGCTC[A/G]GACCTGGGAGGTGGA | 55626 |
rs778054395 | snp | C/G | 1.70755e-05 | 0.00292189 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434946 | CCTCTGGCTGCTGGG[C/G]ATGAAAGCTGCCAGG | 55626 |
rs778068398 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541210 | GTGGGCGATCAACTA[C/T]ACCTACTCTGTTTCT | 55626 |
rs778072154 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579707 | CTTATGAGGAAACAG[A/T]CATGTTTTGTTTTGT | 55626 |
rs778079734 | snp | A/G | 1.73249e-05 | 0.00294315 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433448 | GGGAGCTGCCATACA[A/G]TGAAGGCACAAGCAA | 55626 |
rs778083797 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435593 | TCTGGAACAGCTCCT[C/T]GCTAATACTAATCTC | 55626 |
rs778085288 | snp | C/T | 8.38947e-05 | 0.00647613 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512861 | TGTCAATTACCAACT[C/T]AGAGGTCATTCATAA | 55626 |
rs778088609 | in-del | -/CT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398806 | TGAGACAGAGTCTTG[-/CT]CTGTCACCCAAGCTG | 55626 |
rs778103169 | in-del | -/TGTG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425311 | TTTGCTTGATCCATT[-/TGTG]TGTGTGTGTGTGTGT | 55626 |
rs778108268 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403297 | TCTGGGAGTACTGGT[C/T]TTCCAGCCCCTCCCT | 55626 |
rs778132565 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417203 | ACTACAGGCACGTGC[C/T]ACTATGCCCGGCTAA | 55626 |
rs778134969 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545919 | TAAAAAGATGTAGAA[A/G]ATCAGCGATCTGGTA | 55626 |
rs778142044 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521516 | ACTCTGCAACTCCCC[A/G]ATCTCTGCCTTGGCG | 55626 |
rs778157077 | snp | A/G | 1.65299e-05 | 0.00287483 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547216 | GTACGGCGGTGTCCA[A/G]TCAGGGAATGAACAC | 55626 |
rs778159170 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560607 | AACGGAAGTTTTATC[G/T]GCAAATTATTCTGGA | 55626 |
rs778160309 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535844 | GGAAGGCGCAGACCC[C/T]GAGTCATCAGTGTAA | 55626 |
rs778161630 | in-del | -/C | 1.65059e-05 | 0.00287275 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417890 | CCAGTGATCCCTCAA[-/C]CCCCACACTTTAAGC | 55626 |
rs778165109 | snp | C/T | 1.69222e-05 | 0.00290875 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443449 | GCTCACCAGCAAATA[C/T]AACCCTTCCACTGAT | 55626 |
rs778198180 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401994 | AGGTACCCGGCAGCC[C/T]TGCTCCCTGCCTGCA | 55626 |
rs778218416 | snp | C/T | | | intron-variant, utr-variant-3-prime | AMBRA1 | GRCh38.p7 | 11:46430981 | CCTTAAACGGTGATA[C/T]AGCACAGCTATCCAA | 55626 |
rs778225205 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583650 | AACTCAAACAAATTT[-/A]CCAAAAAAAAAAAAA | 55626 |
rs778238333 | snp | C/G | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46544019 | TGAGTAAGTAGTGTC[C/G]AAGTGGATCAAATCT | 55626 |
rs778256601 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485682 | ACAGAAAGGGCACAC[A/G]GGTAAAGCATAAGTG | 55626 |
rs778257539 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470754 | GGTGACAAGGTGAGA[C/G]TGTCTCAAAAAAATA | 55626 |
rs778306230 | in-del | -/CAAGAC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535587 | ATTTTTGAACTAAAT[-/CAAGAC]CAAGTATACCTTCAT | 55626 |
rs778337364 | snp | C/T | 1.66355e-05 | 0.002884 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542228 | CCTGCCAAGAGGAAC[C/T]AGCCTCGCCAGAGGA | 55626 |
rs778342932 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537332 | AAGGGTGCCCTCTTC[A/G]GGGCCCAGGAGTTCA | 55626 |
rs778363833 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484550 | CTCAATCCAGACATA[C/T]GGACATTAAGATTTC | 55626 |
rs778387097 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474467 | AATCTCGGCTCACTG[C/T]AACCTCCACCTCCCA | 55626 |
rs778389173 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431597 | CCTGGCTTATGAAAG[A/C]AGCTAGAGAGGTCTG | 55626 |
rs778442382 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538465 | AAGAAAAAAATACTT[-/A]AAACAAAAAATTATG | 55626 |
rs778451710 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46483327 | CAGTCACCTATTTGC[A/G]GGAGTTTCTTTCCCC | 55626 |
rs778496454 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446908 | TTTTCCATATCTGCC[A/G]ATGGGATCTTACGGC | 55626 |
rs778497069 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507295 | CCACCCTGGCTAACA[A/T]GGTGAAACCCCATCT | 55626 |
rs778507815 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568241 | GGCAGGAAGATCTCC[G/T]GAGGTCAAGAGTGCA | 55626 |
rs778549986 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396526 | GTTACAAACAGAAAG[A/G]AAATCACATTTTCAT | 55626 |
rs778551078 | snp | A/G | 4.94499e-05 | 0.00497217 | synonymous-codon, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508214 | CTCAAATTCCAAGTC[A/G]GTTCCCTCTACTGAT | 55626 |
rs778558752 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513590 | TCACTCTGTGGCACA[A/T]AACTATTAAGAGATA | 55626 |
rs778568501 | in-del | -/TCC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495643 | AATGGAATCAGGAGT[-/TCC]TCCTGACCAGCAGAC | 55626 |
rs778571191 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422971 | CAAGGGGGCTTTGAG[A/G]AAGAAAGGAACTGTG | 55626 |
rs778575385 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549973 | ACAGGCACCTGCCAC[C/T]ACACCCAGCTAATTT | 55626 |
rs778587739 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438796 | AATCATAGTGAATCT[A/C]ATGTGCCACTTTTTT | 55626 |
rs778644871 | snp | C/G | 3.29554e-05 | 0.00405914 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542765 | CTGTCCGGGTCCACT[C/G]AGATCCTGTCAACCC | 55626 |
rs778653285 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442262 | ATTCTTGTGCCTCAG[C/T]CACCCGAGTAGCTGG | 55626 |
rs778680920 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507478 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs778680953 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552502 | CCATCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 55626 |
rs778699166 | in-del | -/ATCTCTAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419401 | CCACTACAAAACAAT[-/ATCTCTAG]ATCTCTAGATCTCAA | 55626 |
rs778700671 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589889 | CGCCTCCCAAAGTGC[A/T]GGGATTACAGGTGTG | 55626 |
rs778715414 | snp | C/T | 3.36638e-05 | 0.00410253 | | | GRCh38.p7 | 11:46443460 | AATATAACCCTTCCA[C/T]TGATACCCCCATTTG | 55626 |
rs778728249 | snp | A/C | | | | | GRCh38.p7 | 11:46529839 | ATGTAACAATAGGCC[A/C]ACCCATGAAAGCAAA | 55626 |
rs778751841 | snp | C/T | | | | | GRCh38.p7 | 11:46495244 | TGAACCTTTGAGAGC[C/T]TGATTTGGGATATTT | 55626 |
rs778752987 | snp | C/T | 3.61716e-05 | 0.00425259 | | | GRCh38.p7 | 11:46397450 | GTGCAACGTTTGTCT[C/T]TACCTGTTCCGTGGT | 55626 |
rs778760722 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410023 | CACCCCAAGTGTGCC[C/G]AGGCACCATGGCCAG | 55626 |
rs778765210 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418008 | GTTGATACTGACATG[C/T]CTCCGCTGGTCGGCA | 55626 |
rs778766666 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550772 | ATCTATGGCAAGGAA[G/T]ATTCTCTGGCTACTG | 55626 |
rs778770555 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534340 | TTTACTAAAAATACA[-/G]AAAAGTTAGCCAGGC | 55626 |
rs778774869 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508471 | ATCTCCCTGCTGAGG[G/T]GAACTCTGGAGACAT | 55626 |
rs778788484 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422011 | GAAGCTCCCCATGGG[A/T]TGTTCAGAACAAAGC | 55626 |
rs778794674 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445661 | TTTCATTCTGATCCA[G/T]GCTCAGTTCCACTGA | 55626 |
rs778837759 | snp | A/G | 3.1453e-05 | 0.00396554 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494198 | CCTGGATCTGTCACC[A/G]TTGTCCCTGAAAAAA | 55626 |
rs778841023 | snp | A/G | 1.70153e-05 | 0.00291674 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433460 | ACAGTGAAGGCACAA[A/G]CAATGGCACTCACCC | 55626 |
rs778861324 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452393 | TCACTATGTTGCCCG[A/G]CTTGCCTTGAACTCC | 55626 |
rs778880290 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427074 | GCACAGATGATTAGG[A/G]CTATATTATAAGTTC | 55626 |
rs778882012 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572948 | TAAAAAAAATTAGCC[A/G]GGTGTGGTGGTGGAC | 55626 |
rs778884108 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432624 | GGATATCCCTCTAAG[G/T]AGCTTACACTGAACC | 55626 |
rs778922064 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476474 | TGGTACTGCTTCTAT[C/T]CCATAGGACCTTCAC | 55626 |
rs778931063 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464508 | CCTTGGGTCTACAGA[C/T]AGGCTTCAGGTGGTT | 55626 |
rs778936331 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491463 | CTAGTATATAGCAAG[C/T]GCTCAATAAATGTTA | 55626 |
rs778939377 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467846 | TAATTTAGAAGAGAT[C/T]TGGGAGAGAGTGGAG | 55626 |
rs778941994 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504597 | AAACACAAGGACCCT[A/G]CAGTCTCAATCCTTG | 55626 |
rs778942264 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526342 | TGGTCCCCTCCCACA[A/C]TGAATCTAGACTGCT | 55626 |
rs778944255 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561342 | GCCGAGATCATGCCA[C/T]TGCACTCCAGCCTAG | 55626 |
rs778947930 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437161 | GGTGTGCAGAGGAGA[A/G]TACAAGTAAGATTTT | 55626 |
rs778956962 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398221 | AGCAGGTTGGCCTCA[A/G]TGAGTTCTCTCAGCA | 55626 |
rs778970357 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399973 | AAAAATCCCTAACAT[C/T]TACCTTGCACGGTGC | 55626 |
rs778986594 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575924 | ATTAAGAATCCATTG[C/T]CGTGGTCTATTATTA | 55626 |
rs778998798 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532980 | AAAACATGGCCAACA[C/T]GGTGAAACCCTGTCT | 55626 |
rs779010064 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560256 | CATTAGTTTTTTATA[C/T]ATAAACTCAAAATAA | 55626 |
rs779021120 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547066 | TCCGTCTCAAAAAAA[A/G]AAAATTAGAACACCA | 55626 |
rs779031029 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551825 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGTC | 55626 |
rs779031937 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465691 | CCTGGCTCTTTGCAG[G/T]GTAAGGGATCATCAG | 55626 |
rs779047068 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480090 | CTTTGATCATTGCAG[C/T]ACCTTGACTGACCCT | 55626 |
rs779112531 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585062 | CGACTGTGCTCTCTG[C/T]GCTCTCTGAAACATG | 55626 |
rs779155209 | snp | A/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593161 | ATCTATATTCCTAAC[A/T]GTCTATATTCCTAGG | 55626 |
rs779159723 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467506 | CTTTTTACAATGAAT[-/A]ATATACTTTTGTCTA | 55626 |
rs779198762 | snp | A/G | 3.32309e-05 | 0.00407607 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542914 | GTACTGAAGGCAGAC[A/G]GCCGGTTCAGGAGGC | 55626 |
rs779208772 | snp | A/T | 1.65026e-05 | 0.00287246 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545617 | ACCGGACCCGTTCCA[A/T]CTCACTAGCTGTCTT | 55626 |
rs779209113 | snp | C/T | 3.32425e-05 | 0.00407678 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548234 | TATGTGAAATATAGC[C/T]ATTTTCCTTACCTTG | 55626 |
rs779213805 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573243 | AACTCTGTCTCTACT[C/G]AAAATACAAAAATTA | 55626 |
rs779242172 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520583 | CAGTGCCCCACAGCA[-/T]TTTGTTTTTCTTTTC | 55626 |
rs779275869 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403850 | GGCCAAGGGGAGTGG[C/G]GAGGGGCAGGGCACA | 55626 |
rs779278382 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418977 | TCACAGCAATGGGGA[A/T]TTGGAGGTGATAGGG | 55626 |
rs779281379 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506172 | TTCACTGCTGATATA[C/T]GCATCCACCTCACCC | 55626 |
rs779289074 | snp | A/G | 2.08997e-05 | 0.00323256 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547862 | GAGCGTGGACTATCC[A/G]GCAGTTCTACTCTCT | 55626 |
rs779293666 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523434 | AATTTCCACTCTCCT[C/T]CCCCGTTCCCAAAAA | 55626 |
rs779296190 | snp | C/G | 1.72985e-05 | 0.00294091 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397610 | GAAGAGGGCAGGGTT[C/G]GCTGGGTTGGCTCCC | 55626 |
rs779311819 | snp | C/G | 1.68493e-05 | 0.00290248 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408610 | CAGAGTCTGGGTGCC[C/G]TGAGATGTCACTGAG | 55626 |
rs779316542 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442332 | ATTTTTAGTAGAGAC[A/G]AGGTTTCATCATGTT | 55626 |
rs779360720 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580984 | CTTTTTGTAGAGATG[G/T]GATCTTACCATGTCA | 55626 |
rs779368474 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580689 | ATCCAAACCATCATC[A/G]CCTTTTGCCTGGACC | 55626 |
rs779384162 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508014 | AAAGCAACTGCCAGA[A/G]GTGGGAGTGCTCTGG | 55626 |
rs779385843 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417815 | CAGGCTCTAGATGGA[C/T]TGACATTTCCCTTCT | 55626 |
rs779409186 | snp | C/G | 1.68957e-05 | 0.00290647 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542966 | AGGCCTGCTCCGGGG[C/G]ATGGAAGGGCTCGGT | 55626 |
rs779410228 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457337 | ATCCCACAGAACTTG[C/G]TGGTCAAAGGTGAGG | 55626 |
rs779441570 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417499 | GGGTTTCAACAATAC[C/G]TATTTCCAATTCTTT | 55626 |
rs779462010 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579838 | CTGCCTCAGCCTCCT[A/G]AGGAGCTGGGATTAC | 55626 |
rs779463018 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525188 | TGCCTATAGTCTCAG[C/T]TACTTGGGAGGCTGA | 55626 |
rs779478148 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540232 | TACTAAAGCAGAATG[A/G]ACAAAAGCTAACCAG | 55626 |
rs779478985 | snp | C/T | 2.19233e-05 | 0.00331077 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443629 | TCAAAGACAGCACAT[C/T]ATATTATTTATCCAC | 55626 |
rs779535080 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432028 | ATAAAGAGGATGCTT[C/T]ATTTTTATTTATTTA | 55626 |
rs779539650 | snp | C/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419141 | CATTCAGGCACACAA[C/G/T]TTGTTTCTAGCTTAT | 55626 |
rs779540334 | in-del | -/CC | 2.16504e-05 | 0.0032901 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408486 | AGGGTCCCTCTCCCA[-/CC]CCCTCCAGCGCCACA | 55626 |
rs779561872 | snp | C/T | 1.65652e-05 | 0.0028779 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548267 | CTCCCATTTCATCCA[C/T]CGGGTTTTATCTTCT | 55626 |
rs779568975 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538670 | TGGCTAATTTTTTTT[G/T]TATTTTTAATAGAGA | 55626 |
rs779584306 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537975 | CAGGGACACCTTTTC[C/T]TCCCAGTCATCCTAA | 55626 |
rs779585944 | in-del | -/TTTAT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523878 | TTATTCATTTATTTA[-/TTTAT]TTTGAGATAGAGTTT | 55626 |
rs779595873 | snp | G/T | 4.83723e-05 | 0.0049177 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443638 | GCACATTATATTATT[G/T]ATCCACGTTTCCACT | 55626 |
rs779600245 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469157 | TCAAAAAAAGAAAAA[G/T]AAGATGTAATAAAAT | 55626 |
rs779624346 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417603 | AATCTTTGATATCTA[C/T]GCTTTTGACTGCAGG | 55626 |
rs779627741 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485760 | CAGAAAAACTTACAC[A/G]TATAAAAGGAACAGA | 55626 |
rs779627859 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502242 | AGAAGTTTTTGTCTC[A/G]TTCCACATTAAGAAC | 55626 |
rs779629601 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535233 | GTTAGAAAGCGTTTA[C/T]TGTATAGTATCTTGA | 55626 |
rs779630623 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432880 | TTCACTCAGGCACGT[C/T]AGTCTGGCTGAGGCC | 55626 |
rs779651808 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503767 | ATCTTAAGGCTAAAA[G/T]ACTAGAATTCTCATT | 55626 |
rs779670657 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552985 | GAGTCTCGCTCCGTC[A/G]CCCAGGCTGCAGTGC | 55626 |
rs779682243 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471598 | TTTTGGCATTTCCCC[C/T]AAAAGGGTTAAGAAA | 55626 |
rs779682643 | snp | A/G | 3.29641e-05 | 0.00405968 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46418020 | ATGTCTCCGCTGGTC[A/G]GCAGGCATGGGATAA | 55626 |
rs779684425 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542356 | TTGGAGTTGTTCTCA[C/T]TGCTGTGTGGGGTGG | 55626 |
rs779689599 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570345 | TAAGTCTCCTCCATG[G/T]AACTATCCTGTGGGC | 55626 |
rs779716895 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397418 | GTTTCTGCTTGGCGG[C/T]TCGAGGGGAGGCACC | 55626 |
rs779751806 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539117 | AGCAGACGGAATATA[A/G]ATTAAAGAAAGCCAG | 55626 |
rs779757583 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525473 | GTCAAGTCTGGGCGC[A/G]GTGGCTCATGCCTGT | 55626 |
rs779766095 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554864 | TGTGATACCGTCACA[C/G]AGTCCCCAAAATCAA | 55626 |
rs779781364 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572745 | CTTACAACAACTCTT[A/G]AAAGGTAGGTGTTAT | 55626 |
rs779788974 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471620 | GTTAAGAAATAACTT[A/T]CTTTCTGTTTTGTTT | 55626 |
rs779789375 | snp | A/G | 1.65397e-05 | 0.00287569 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543433 | GGGGCAGGGGGTAGA[A/G]CAAGGCAGTTAGGTA | 55626 |
rs779792273 | snp | G/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451530 | AAATGAAAAGTATGA[G/T]TCAACAGTTCAGTGA | 55626 |
rs779794287 | snp | C/T | 1.68997e-05 | 0.00290682 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408622 | GCCCTGAGATGTCAC[C/T]GAGGTGGCAGGGTTC | 55626 |
rs779838036 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552405 | AAAAAAAAAAAAAAA[-/G]GGCCAGGCACGGTAG | 55626 |
rs779863954 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396789 | CTGGCCAGCCTACAC[C/G]CCCCACTCCTGAGTG | 55626 |
rs779887419 | snp | A/G | 3.6169e-05 | 0.00425243 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397513 | GCTGCCACCATCCAG[A/G]AGGTGGTTGTTATTG | 55626 |
rs779934442 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398503 | ATATTGATTGATTGA[C/T]TGATGGAGTCTCACT | 55626 |
rs779940790 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570887 | GATGCAGCAAGCCCT[A/C]CTCCAAGAAAGGGAT | 55626 |
rs779949010 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46591112 | ATTCCTAAGATTGCT[C/T]CATGACACTCACAGC | 55626 |
rs779961691 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441312 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 55626 |
rs779975161 | snp | C/G | 3.31378e-05 | 0.00407036 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397729 | AGAGGTGGAGGGCTG[C/G]GGTGAGGAGGTGTGG | 55626 |
rs779983940 | snp | A/C | 1.65247e-05 | 0.00287438 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544058 | TAAAATCACAGAAGA[A/C]AGAGACAAAGACACA | 55626 |
rs779986008 | in-del | -/A | 1.73567e-05 | 0.00294586 | intron-variant, frameshift-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543005 | AGAAAAGGAAGGGGT[-/A]AGTAGCTCTGGCAGA | 55626 |
rs779998908 | in-del | -/CT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401816 | ACCATCCTAATTCAG[-/CT]CTCTGCTGACTTGAG | 55626 |
rs780001942 | in-del | -/AG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540208 | CAGAATAGCACATGA[-/AG]AGAGGTACTACTAAA | 55626 |
rs780010490 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440409 | TTGTATATACATATA[A/G]TATTTCTGAAAAGAT | 55626 |
rs780010704 | in-del | -/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594870 | TACCTTACCTGCTCC[-/T]TAGGGAGGTTTACAC | 55626 |
rs780022242 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414900 | AGTGGGTTTTAGTAC[C/G]ACCAAGAGATGCCCA | 55626 |
rs780044108 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529905 | CAAGAAAGAGCAGAA[A/G]TAAGATGTACTGAAT | 55626 |
rs780051547 | snp | C/G | 1.65611e-05 | 0.00287755 | synonymous-codon, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508325 | ACTGTCTCTCCGTGA[C/G]AGATACTGGATCATC | 55626 |
rs780059961 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479815 | CAGATACATGTGTGA[A/G]ACTATCTGTTATCAG | 55626 |
rs780061196 | snp | A/G | | | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46545719 | GCTGAGCCGTAGGGT[A/G]GAAAGCCAGGGAGGC | 55626 |
rs780061800 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462540 | GCCCTCCTCGATCTG[A/G]ACCTGTCTGTCATCT | 55626 |
rs780062309 | snp | C/T | 1.78694e-05 | 0.00298905 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433424 | CCCTCATTACCCTTC[C/T]AAGCCTAGGGGAGCT | 55626 |
rs780071031 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499414 | ATATGTATTTTACTT[A/G]CCCAGTAATTCTAAT | 55626 |
rs780077451 | snp | C/G | 1.67027e-05 | 0.00288982 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434905 | GCCAGGGAGTACACT[C/G]CCAGGATGCCTTCAT | 55626 |
rs780100073 | in-del | -/AAAAAAAAAAAAAAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411101 | CAAGACTCTGTCTCA[-/AAAAAAAAAAAAAAG]AAAAAAAAAAAAAAG | 55626 |
rs780112177 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467977 | GCAGGAAACTGCTAC[A/G]AAAGCATAATGGCCT | 55626 |
rs780118705 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415491 | AATTCTAGTTCTGTC[A/T]TCTGTTAGGAGGCCT | 55626 |
rs780121154 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580830 | AGAGCCTTGCTCTGT[C/T]ACCCGGCCTGGAGTG | 55626 |
rs780124251 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425793 | GCAGTGAGCCGAGAT[C/T]GTGCCACTGCACTCC | 55626 |
rs780131961 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439107 | AGATCTCATCTCTAT[-/A]AAAAAAAAATTTAAA | 55626 |
rs780144278 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545510 | ACTTGCCCTGAGCAG[G/T]GATAACAACCTGACT | 55626 |
rs780166952 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588693 | GGCAGGAGAATCGCT[C/T]GAACCCAGGAGGCGG | 55626 |
rs780167353 | snp | G/T | 6.60731e-05 | 0.00574736 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542102 | TCTCCTCCTGCGGAC[G/T]AGCAGAGCTGCTCAA | 55626 |
rs780201624 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465756 | CCCCAAAATAGTGAT[A/G]CTCATGATAAATTAG | 55626 |
rs780255076 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497040 | TCGCTTGAACCAGGA[A/G]GCGGAGGTTGCAGTG | 55626 |
rs780257970 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534427 | TTGAACCCGGGAGGC[A/G]GAGGTTACAGTGAGC | 55626 |
rs780359173 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494958 | TTCTGGCTAGGCCAC[A/G]AAGTATTATTACTAT | 55626 |
rs780385926 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457384 | ACTCCTAAATACAAC[A/G]CTCAGTCCAACTTCA | 55626 |
rs780399106 | snp | A/C | 3.77629e-05 | 0.00434512 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46397969 | CAAAGCAGAAGAGAG[A/C]GCGAATTGGCTGCTG | 55626 |
rs780404056 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577470 | GGAGGAAGGGCAGAA[C/T]AAGGACAAACTGCTT | 55626 |
rs780418999 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533070 | CGGGAGGCTGAGGCA[C/T]GAGAATCGCTTGAGC | 55626 |
rs780440554 | snp | A/G | 1.65272e-05 | 0.0028746 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547173 | AATAAGGCCTGAGAT[A/G]GTGGGATGAAAAGTG | 55626 |
rs780450436 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567413 | GCTCTGTCTCCCAGG[A/T]GGGAGTGCAGTGGCG | 55626 |
rs780470471 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459152 | AGATACACGGACAGA[C/T]AGAAATCCTGGATAT | 55626 |
rs780485738 | snp | A/C | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594326 | TTGTGTAACTATAGT[A/C]CCCCAACTGTTCTAT | 55626 |
rs780488044 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564518 | GTTGCCAAATGAGCA[A/G]TATTGTATAGTGCTC | 55626 |
rs780529523 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495925 | AAAAGGATCCTAAGC[A/G]GGGGAAAGGGTGGAG | 55626 |
rs780532598 | in-del | -/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46451287 | CTCATTCCAGAGTCA[-/G]GGTCTTCAACTTGTA | 55626 |
rs780533083 | snp | C/T | 5.23245e-05 | 0.00511464 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46494156 | AAGCGAAGGTGCAGA[C/T]ATCCGGGCATTGCGT | 55626 |
rs780544369 | snp | A/C/G/T | 8.2397e-05 | 0.00641819 | synonymous-codon, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46541971 | ATCCTCCTCAGAGCT[A/C/G/T]TCCTCAGGCATATCC | 55626 |
rs780553090 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444217 | AATAAAAATTTATGA[C/G]CCTCACTTTGTAGCA | 55626 |
rs780557375 | in-del | -/AT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487540 | ATAGATGTAATATTA[-/AT]ATATATATATAACAG | 55626 |
rs780559267 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427195 | GTTATATAAATTCTG[A/G]TCAGTGCTGACAGCA | 55626 |
rs780576380 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566096 | AAACTACAGTACATC[C/T]AAACCATGAAATACT | 55626 |
rs780591185 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403965 | AGTACTTTGGGAGGC[C/G]AAGGTGGGAGGATCA | 55626 |
rs780643169 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510360 | AGAAGTCGATGTTCG[C/T]GCACTGTTCTTATAT | 55626 |
rs780675321 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46504154 | AGAAAGCAAAGCAGC[-/T]TATAAAAAGAGGCAG | 55626 |
rs780687088 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405744 | TTCATTTATTTATTT[A/G]TATTTGAGACAGGGT | 55626 |
rs780689601 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520141 | TGAAACTCCGCCTCG[-/AA]AAAAAAAAAAAAAAA | 55626 |
rs780718992 | snp | C/T | 5.81751e-05 | 0.00539297 | intron-variant, missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543145 | TAACTGACCCGCTGT[C/T]GGAGCCTGATGTAAG | 55626 |
rs780719792 | snp | C/T | 1.71525e-05 | 0.00292847 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408643 | GGCAGGGTTCCGGGG[C/T]TGAAGCCCAATGGCA | 55626 |
rs780727462 | snp | C/G | 0.000181577 | 0.00952656 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46410297 | CGCTCGCTGCTCCTG[C/G]TGTTGGAATGGACAG | 55626 |
rs780730789 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508603 | GGCAGCTTAACCAGA[C/T]ATCTTCTGAGGAAAA | 55626 |
rs780746651 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474515 | TGCCTCAGCCTCCCG[A/C]GTAGCTGGGACTACA | 55626 |
rs780797050 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539387 | ACATGGAGAAAATCC[A/G]TCTCTACTAAAAATA | 55626 |
rs780819953 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457712 | TCAAGACCAGCCTAA[C/T]CAACATAGTAAAACC | 55626 |
rs780825777 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532350 | AATAAAACAAAAGTT[C/T]TTCTCAAAAACTTGA | 55626 |
rs780829877 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484466 | GGGATTTAATAATCT[C/T]TGAGATCATTTTAGG | 55626 |
rs780837593 | snp | A/G | | | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397582 | AAGGGAAACAGGAAT[A/G]GGGACAGGGGAGGAA | 55626 |
rs780850925 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487971 | AAGGATGGAAAATGA[C/T]ATCTCATGTAATCAA | 55626 |
rs780872929 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564811 | CCTCCTAGTGGGCTA[C/T]GAATATTAATTAGTA | 55626 |
rs780881095 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527306 | GTAACACAGCAAGAC[C/T]CCATCTCTACTAAAA | 55626 |
rs780912434 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542379 | TGGGGTGGGCTGGTG[A/G]GAAGGGCCTGGCCTC | 55626 |
rs780914135 | snp | A/G | 4.99139e-05 | 0.00499544 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545596 | TGCAGATGGGGCAGC[A/G]CACTCACCGGACCCG | 55626 |
rs780938094 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579045 | ACCACAAGAAAGCAA[-/T]AAAAAAAAAAAAAAA | 55626 |
rs780954351 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503236 | CTCTTCCTTTTTCTT[A/G]AACATACAGAGGTCA | 55626 |
rs780960295 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585913 | GGGGTTCAAGCTATT[C/T]TCCTGCCTCAGCCTC | 55626 |
rs781007443 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534219 | TGGTGCCAGCCAGGT[A/G]CGGTGGCTCAGGCCT | 55626 |
rs781016036 | in-del | -/AACT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419599 | AGCTGAAACTCTATA[-/AACT]GGAGTTTATTTCCCT | 55626 |
rs781024457 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549645 | TATCATTCGAATTTT[-/C]CCCATTGTCCAAAAA | 55626 |
rs781061826 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581329 | AATGAAAAAATTAGG[C/T]CAGGCGCAGTGGCTC | 55626 |
rs781075781 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575318 | CAAAATTATCCCAGC[A/G]TGGTGGCACGTGCCT | 55626 |
rs781075974 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555032 | AGCCATGATTGCACC[A/G]CTGCACTCTTCAGCC | 55626 |
rs781081344 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396882 | ACAGTAGTCCCCCAT[C/T]AGTAAATGCCGAAGT | 55626 |
rs781097803 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588550 | GGAGGCCAAGGCAGG[C/T]GGATCACCTGAAGTC | 55626 |
rs781108348 | snp | A/G | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542504 | ACTCCAGAAAGAAGC[A/G]TCTCAGGTCACACTG | 55626 |
rs781125232 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449464 | CTTAGGTATAAATCT[A/G]ACAAAATATGTACAA | 55626 |
rs781125404 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432978 | AAGACAGGGTCCTAG[A/G]CAGGACCTTTTCTCC | 55626 |
rs781131523 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471322 | GGTGGCTCATACCTG[G/T]AATCCCAGCACTTTG | 55626 |
rs781134560 | in-del | -/AACC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480672 | TTATTGCTGAAGTTT[-/AACC]AAAGTCAGCCTTATT | 55626 |
rs781141877 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448680 | ACTTTGAAAGATCAA[C/T]AAACAATAAACATCT | 55626 |
rs781153547 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426596 | TAGTGTTATTTTTAA[C/T]TTTTATCTTGCCCCC | 55626 |
rs781155596 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412014 | AGAGCCACAGCCAAA[C/T]AAAAGTGCTCTTCTT | 55626 |
rs781170169 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460311 | ATACGACCCCATTTA[G/T]ATAAACACAACTCTT | 55626 |
rs781173410 | snp | C/T | 1.65236e-05 | 0.00287429 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547197 | AAAAGTGACACACCA[C/T]GGAGTACGGCGGTGT | 55626 |
rs781181966 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501072 | ACAGTCTAGCCACAC[C/T]TATCAACAAAGCAAT | 55626 |
rs781244073 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460087 | CTCTGTGTAAACATC[A/T]TAGAGAAGACACCAC | 55626 |
rs781244856 | in-del | -/AAAAAAAAAAAA | 0.000851426 | 0.0206152 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518430 | GCAAGACTCCGTCTC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAGA | 55626 |
rs781265017 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517071 | GTGCTATTTGATCCA[C/T]TGGACAGCAAGGGGG | 55626 |
rs781305322 | snp | A/C | 1.66432e-05 | 0.00288467 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397695 | CTGCCAGTTGCCCGG[A/C]CTCTGGGAGCAGTCC | 55626 |
rs781330571 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522784 | TTGCTGTGATACTAG[C/T]AAGCCTGTGAAGGTC | 55626 |
rs781350986 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492079 | AAAAAAGCTTTAACG[G/T]GCCTTCGGTTAAGCC | 55626 |
rs781374826 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542796 | AGGAGCTATTTCTCG[A/G]TGATACCTAGAAGGG | 55626 |
rs781392902 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476620 | TTTAAACAATTTACT[A/C]CAGCTTTGCACTGAT | 55626 |
rs781398799 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479918 | CTATAGGCCTGAAGT[C/T]AAACAAAGGACTCAT | 55626 |
rs781399773 | in-del | -/A | 0.000169276 | 0.00919834 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418072 | TAGAGGAAAAGAGGG[-/A]AAAAAAAGAGAATGG | 55626 |
rs781417044 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428121 | AGAGGGAGAAGGGGT[A/G]TAAAGGGATAGACCA | 55626 |
rs781454511 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417122 | AATGGCATGATGTCA[A/G]CTCACTGCAACCTCT | 55626 |
rs781487586 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525907 | ACAGAGCGAGACTCT[A/G]TCTCAAAAAAGAAAT | 55626 |
rs781515125 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444830 | TTCATAGAAGCCAAG[A/C]AATATGAGAAAAGTA | 55626 |
rs781530276 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560390 | GGGGGAGAAGTGAAG[C/T]ACCAGCTTTCCTGCT | 55626 |
rs781549154 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577580 | AATGCCACTGAATTG[C/T]TCATTTTAAGATGGC | 55626 |
rs781562495 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564219 | AAAAATCCCAGTATT[-/A]AAAAAAAAAAAAAGA | 55626 |
rs781567109 | snp | A/G | 6.59087e-05 | 0.00574021 | synonymous-codon, intron-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46508247 | ACCCTGGTTGTCTGA[A/G]GAAGAGGAGGAGGTG | 55626 |
rs781584073 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519584 | AATGCTGGCTCCCAG[A/C]AGGTAAGGTGCCACT | 55626 |
rs781588086 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468255 | AGTGGGGAGGGGTGG[C/T]GGGCAGCATGGTGGC | 55626 |
rs781597965 | snp | A/C | 1.66037e-05 | 0.00288125 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542124 | GCTGCTCAACTCCAG[A/C]CTGCTGGAGCTGGGC | 55626 |
rs781607072 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407759 | TGGCTTTTCCTCCCA[C/T]GGTCTCTTCTGGGCA | 55626 |
rs781616027 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415733 | CAACTTGGTCTGTGA[C/G]AGGACACTGTTCAAT | 55626 |
rs781617801 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407993 | CACAGAGAGTCAGGG[C/G]CGAGTGTGGCAGAGC | 55626 |
rs781619713 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559385 | ATTTCATTACGCACA[C/T]GTCATTGATCACGAG | 55626 |
rs781619834 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429697 | GTTACAACCAAAGTT[A/G]TTATACTGTGCAAGT | 55626 |
rs781632313 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445683 | TTCCACTGAGTTTCC[G/T]AATTGTTTCCTGGGC | 55626 |
rs781632789 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460852 | AACACTTTGAGAGGC[C/G]AGGGTGGGAAGATCA | 55626 |
rs781664368 | in-del | -/AAAACA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436649 | GCCAAAACAAAAACA[-/AAAACA]AAAACAAAAACAAAA | 55626 |
rs781685241 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536072 | TGACTCTCTGTAAGA[-/C]CAAATGATGGGATAT | 55626 |
rs781687172 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415006 | ATTGAGAGCACAAAA[A/T]GGGGTGCAGCTGCCT | 55626 |
rs781697688 | in-del | -/TAAAT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552063 | AATTAATCAAAAAAA[-/TAAAT]TAAATTAAATATTAA | 55626 |
rs781703844 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428212 | GGAAGAAGAGGAGAG[A/G]GAGAGAGATGGATAC | 55626 |
rs781708500 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516418 | AACCTCAAAGAAAGA[C/T]CTTTCTTTTTTTTTT | 55626 |
rs781717755 | snp | C/T | 1.702e-05 | 0.00291714 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545812 | GATATTCTCAGGTTA[C/T]AAGCTACCAGCACAC | 55626 |
rs781719776 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550450 | AAGGAATATCTCCCC[A/C]TTTACAATTAGCAAT | 55626 |
rs781720249 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514588 | TTTCACCTTTGAATG[C/T]GTCTGAGGTTGGGGT | 55626 |
rs781735497 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497399 | TAAGGGGAGGTGCTC[A/G]TGCTGGTCCTCAGTT | 55626 |
rs781747948 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545426 | AAGACTGCGCCACTG[C/T]ACTCCACCCTGGGTG | 55626 |
rs781766346 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541690 | CTAACCTAATCTACA[C/T]TCTCCTTTCAAGGCT | 55626 |
rs781773242 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496065 | GCAACAAGAGACTCT[C/T]ATCTCTTTAAAGAAA | 55626 |
rs796076700 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400634 | TAGTAGGGAGTACAG[A/G]CAAGCACCACTCCTG | 55626 |
rs796081705 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574403 | GTTTTGATTTGCATT[C/T]CTCTGATGGCCAGTG | 55626 |
rs796147344 | in-del | AA/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588785 | ATCTCAAAAAAAAAA[AA/G]AAAAAAGTATTATGA | 55626 |
rs796208359 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565257 | AGAAAAATTCCCTCT[-/A]AAAAAAAAAACGAAA | 55626 |
rs796231298 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582427 | GTTTGGCACACACTG[A/C]AATTATATGTTTATT | 55626 |
rs796240891 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459109 | CCATGGAACACCACG[C/T]AGCCACTACTAAGAA | 55626 |
rs796251828 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422698 | CCCTACTGCATGCCA[A/G]TAAAACTCAGACGAG | 55626 |
rs796266977 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545162 | AAAAAAAAAAAAGCC[-/G]GGGGGGGGGGGGTGG | 55626 |
rs796278499 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490952 | TGCTTACTGCTAAAA[A/G]GTCAATTGCTCTTTC | 55626 |
rs796311751 | snp | C/T | | | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46395991 | CAGATAGGACCAAGC[C/T]CCTCCACCTGCCTAG | 55626 |
rs796318052 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489985 | TAACTTTCTGAGCCT[C/T]AGTTTTCTTCCCTAC | 55626 |
rs796326490 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471637 | TTCTGTTTTGTTTTG[-/T]TTTTTTTTTTAGATG | 55626 |
rs796328087 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582131 | AAAAAAAAAAAAAAA[A/T]TCGAAAGCCTTGACA | 55626 |
rs796342059 | multinucleotide-polymorphism | ATG/GTC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572919 | CCTGGTGAAACTCCG[ATG/GTC]CTACTAAAAATAAAA | 55626 |
rs796342715 | in-del | C/GGG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545164 | AAAAAAAAAGCCGGG[C/GGG]GGGGGGGTGGTGGTG | 55626 |
rs796372813 | in-del | -/AG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418079 | AAAAGAGGGAAAAAA[-/AG]AGAATGGGAGGAGAA | 55626 |
rs796425705 | in-del | -/AAAAAAAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568779 | TCCATCTCAAAAAAA[-/AAAAAAAG]AAAAAAGGAACCCTC | 55626 |
rs796432810 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559249 | AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGT | 55626 |
rs796490668 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441421 | CGGGAGGCTGAGGCG[G/T]GAGAATCGCATGAAC | 55626 |
rs796520906 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453204 | GTGTCTGGCTTCTTT[C/T]ACTCAGCATAACATT | 55626 |
rs796548346 | snp | C/G | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453539 | GAAAATATACTGTGT[C/G]GAAAACCAGCAATCA | 55626 |
rs796572726 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563034 | AACTCCTGACCTCAG[A/G]TGATCTGCCTGCCTT | 55626 |
rs796580767 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520720 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 55626 |
rs796595446 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46581112 | GAGTAACGTTTTAAA[A/G]TCATATATAAGGTCA | 55626 |
rs796613051 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555538 | CTCTGAGGTTCACTA[C/T]GGTTTCCCTCACCAA | 55626 |
rs796632931 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466056 | CTTTTTGATGGCTGA[A/G]TGAGAACTGAATATT | 55626 |
rs796644779 | snp | C/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594322 | CTTGTTGTGTAACTA[C/T]AGTCCCCCAACTGTT | 55626 |
rs796665828 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574422 | TGATGGCCAGTGATG[A/G]TGAGCATTTTTTCAT | 55626 |
rs796691002 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577452 | TGATGGTTATCAGGG[A/G]CTGGAGGAAGGGCAG | 55626 |
rs796707099 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492642 | AAAAATGGAATTCTG[C/G]TTTACTTCCTTCTCT | 55626 |
rs796708218 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462155 | TCTGTCAGAGCTGCA[C/T]GCATCTCCCAGAAAA | 55626 |
rs796712688 | in-del | -/CT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537391 | TTAAGAAATCATTTA[-/CT]CTCTCTGTTTTGTCA | 55626 |
rs796720620 | in-del | -/TG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425311 | TTTGCTTGATCCATT[-/TG]TGTGTGTGTGTGTGT | 55626 |
rs796744117 | in-del | -/TGT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442601 | ATGAGAGGTTTAAAA[-/TGT]TGTGATTCCAATAGA | 55626 |
rs796749049 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567803 | GATTGCAACCCCAAA[A/C]CAATCAGCAGCACCC | 55626 |
rs796762059 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547601 | TATTGAGAAACTTTC[A/C]AAGTTTTGATCCTCT | 55626 |
rs796768148 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551311 | GTTAGTTTGTGGGGA[-/C]TTTATTTTTATTTTT | 55626 |
rs796784265 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426070 | ACTCCATCTCAAAAT[-/A]AAAAAAAAAAAAAAA | 55626 |
rs796804696 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553610 | ATTAGCCAGGCGTGG[C/T]AGCTCATGCCTGTAG | 55626 |
rs796813067 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569590 | AGAGTCTGTGTACTA[C/T]AGAAATAGCATTCCA | 55626 |
rs796816741 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528376 | GAGTTTCACCATGTT[A/G]GCCAGGCTGGTCTCG | 55626 |
rs796832283 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513268 | CCTACGCTCTTTTTT[C/T]TTTTTTTTTTTTTTG | 55626 |
rs796862862 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425315 | CTTGATCCATTTGTG[C/T]GTGTGTGTGTGTGTG | 55626 |
rs796869640 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403887 | CAATTACCACAAGCA[A/G]AGCAGGCTTCCCACA | 55626 |
rs796893271 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417057 | TAAATTGAGCTTTTC[-/T]TTTTTTTTTTTTTGA | 55626 |
rs796952613 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545168 | AAAAAAGCCGGGGGG[C/G]GGGGGGTGGTGGTGG | 55626 |
rs796967252 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479534 | AAACCCTGTCTCTAC[C/T]AAAAATACAAAAATT | 55626 |
rs796968025 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445922 | GGGAAGGGATAAGAA[C/T]TACAAACAGGAAAAC | 55626 |
rs796989233 | multinucleotide-polymorphism | AG/GA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573331 | TCGCTGGAACCCGGA[AG/GA]GCAGAGGTTGCAGTG | 55626 |
rs797001359 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574385 | AGATGGTATCTCATT[A/G]TGGTTTTGATTTGCA | 55626 |