SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs772390764 | snp | G/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16860889 | CTGATTACAATATAT[G/T]CAGGCCGGGAGTGGT | 5931 |
rs772408026 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RBBP7 | GRCh38.p7 | X:16861936 | CTGCAGATATCAAGA[C/T]TGATGACACGTACCT | 5931 |
rs772469039 | snp | C/G | 2.41199e-05 | 0.00347266 | intron-variant | RBBP7 | GRCh38.p7 | X:16852488 | ACGAGTCTGGTATAG[C/G]TTAACTGATGAATCC | 5931 |
rs772470192 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16848557 | CAAAGTACAAGTGTG[C/T]CAAAAATGAGTACTG | 5931 |
rs772508356 | in-del | -/CG | 0.00475684 | 0.0485365 | utr-variant-5-prime, intron-variant | RBBP7 | GRCh38.p7 | X:16869697 | CCCCGAGGCGGTCAA[-/CG]CGCGCGCGCGCGTAG | 5931 |
rs772565967 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16846369 | CTAAGGTAATCAATC[C/T]GTTATATGCCATGTA | 5931 |
rs772617352 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | TXLNG, RBBP7 | GRCh38.p7 | X:16844674 | AAAACTTTATTTCTG[C/T]AAAGCCAATCAAGAA | 5931 |
rs772809179 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16866216 | AACTATCTAATTAAA[A/G]CAAATTTCTTAGAGA | 5931 |
rs772952143 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | RBBP7 | GRCh38.p7 | X:16857474 | GTCCTGGGGGAATGT[C/T]ACCACAATAATCAGC | 5931 |
rs773039081 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16850910 | CTGAGACCAGCCTGG[C/T]CAATATGGCAAAGCT | 5931 |
rs773102423 | snp | C/T | 2.3002e-05 | 0.00339123 | intron-variant | RBBP7 | GRCh38.p7 | X:16852524 | TTTCATTTCCTGACA[C/T]ACAGACACCAGAAAA | 5931 |
rs773141898 | snp | C/T | 6.96945e-05 | 0.00590274 | intron-variant | RBBP7 | GRCh38.p7 | X:16862943 | CAATATTGGAATATA[C/T]GATATACCTACCACC | 5931 |
rs773165271 | snp | C/T | 4.14869e-05 | 0.00455431 | upstream-variant-2KB, intron-variant | RBBP7 | GRCh38.p7 | X:16870006 | GCCGCCCCCCGCGGC[C/T]CCGGCGCGCGCCGCC | 5931 |
rs773179425 | in-del | -/GGGGGGG | 0.0026624 | 0.0363884 | intron-variant | RBBP7 | GRCh38.p7 | X:16860293 | AAAAGGGGGGGGGGC[-/GGGGGGG]GGGGCTTCCAAGTAG | 5931 |
rs773248438 | snp | A/G | 2.34376e-05 | 0.00342319 | missense | RBBP7 | GRCh38.p7 | X:16845061 | GTCCCTCCAGTTCGG[A/G]TGTCGTGACATCTGA | 5931 |
rs773267492 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16868825 | TACATTCAAGCCCAG[A/G]AAATGTCAAATATAT | 5931 |
rs773268581 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | RBBP7 | GRCh38.p7 | X:16861081 | CTTGAGGCTGAGGTA[C/T]GAGAATCACTTGAAC | 5931 |
rs773284233 | in-del | -/TT | 0.00455968 | 0.0475295 | intron-variant | RBBP7 | GRCh38.p7 | X:16847725 | TGGCTAATTTATGTA[-/TT]TTTTTTTTTTTTTTT | 5931 |
rs773313848 | snp | A/C | 2.29337e-05 | 0.00338619 | intron-variant | RBBP7 | GRCh38.p7 | X:16849313 | TTTACTGTAAGAATA[A/C]AGAATATAACGCTTT | 5931 |
rs773336946 | snp | A/G | 2.39949e-05 | 0.00346365 | intron-variant | RBBP7 | GRCh38.p7 | X:16869054 | AAATTTAAACAAAAT[A/G]AAAGTTGCCAGAAAC | 5931 |
rs773418252 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16847488 | GTACACAGGTGAATA[C/T]ATTTTAAGATCACTG | 5931 |
rs773420455 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16863766 | AATTTTACCGAGGTA[C/T]CTTTGTTACCTTGTT | 5931 |
rs773473874 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16862662 | TGCTGGGATTATAGG[C/T]GTGAGCCATGGCACC | 5931 |
rs773508313 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16849139 | TCCATTTTGAAACCA[C/T]CTGCAAGAGCTAGAA | 5931 |
rs773536118 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16868122 | TTTGAGAGACACGGT[C/G]TCACTCTGTTGGCTA | 5931 |
rs773548465 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16847065 | ACCTGGGAGGTGGAG[A/G]TTGCAGTGAACTAAG | 5931 |
rs773551687 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | RBBP7 | GRCh38.p7 | X:16854627 | CAGAAACCACCACAG[A/C]CATCAGGAGATGGGA | 5931 |
rs773571226 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16855510 | AAAGGAACATGTGGT[A/G]CTCCTGCCATTCACA | 5931 |
rs773611849 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16856445 | TAAGGCAGGAGAATC[A/G]CTTGGACCTGAGAGG | 5931 |
rs773654366 | snp | C/G | 2.46743e-05 | 0.00351234 | intron-variant | RBBP7 | GRCh38.p7 | X:16853857 | TCTAAGAGAGAAGGA[C/G]AGAAAAAAAAAAGAA | 5931 |
rs773661387 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16864262 | CCGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 5931 |
rs773694994 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16858547 | CTGAACTTGAGGATG[A/G]TTATGGGACCCCCAA | 5931 |
rs773897908 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16868413 | GGATGATGAAAAGTA[C/T]CTACAGCATAGTACT | 5931 |
rs773942157 | in-del | -/G | 0.00105904 | 0.0229869 | intron-variant | RBBP7 | GRCh38.p7 | X:16858394 | GGCCCTGGATGGGAA[-/G]GACTCAGACGCCTGT | 5931 |
rs773945019 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TXLNG, RBBP7 | GRCh38.p7 | X:16844330 | AAAAAAATGATGCAG[A/G]TATCTTCTAGTTTGT | 5931 |
rs773958698 | snp | C/T | 6.13911e-05 | 0.00554002 | intron-variant | RBBP7 | GRCh38.p7 | X:16845987 | ATACTCTCCTGTTAA[C/T]CCTAACAAAGGTTTT | 5931 |
rs774028248 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16867247 | ACAGCCCAGACAACA[C/T]GGCCCCAGTTCATGA | 5931 |
rs774035559 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16854443 | GACATTCAAGTACCC[C/T]AAATTCACTTAGACA | 5931 |
rs774046847 | snp | C/T | 2.61945e-05 | 0.00361892 | intron-variant | RBBP7 | GRCh38.p7 | X:16853882 | AAAGAACAAGGGCTA[C/T]AAGAGACTGATTTTT | 5931 |
rs774117030 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | RBBP7 | GRCh38.p7 | X:16849398 | AGTAATCTTAAAACA[A/T]AAACACACTCACAAA | 5931 |
rs774223217 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TXLNG, RBBP7 | GRCh38.p7 | X:16844405 | GATACGAATTGTTAA[C/G]AGGCAGTCTCGTTTT | 5931 |
rs774267329 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16850474 | CCAAACCTTGCTGTA[C/T]GCTTCATACAACCTC | 5931 |
rs774307045 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16866649 | TGAAGGACAATAGCT[A/G]AGAAAGTCCAAGTAA | 5931 |
rs774309971 | snp | A/G | 2.30643e-05 | 0.00339583 | intron-variant | RBBP7 | GRCh38.p7 | X:16852673 | TCTATGCTTTACCTA[A/G]GAATTTTCAAATATC | 5931 |
rs774322565 | snp | A/G | 5.12873e-05 | 0.0050637 | intron-variant | RBBP7 | GRCh38.p7 | X:16852475 | CAATAGTGGACCCAC[A/G]AGTCTGGTATAGCTT | 5931 |
rs774415434 | in-del | -/AAT | 0.00317376 | 0.039709 | intron-variant | RBBP7 | GRCh38.p7 | X:16853388 | TTTTCTTTTTTTCTA[-/AAT]AATAAGTGATCCTCC | 5931 |
rs774474577 | in-del | -/AACTG | 1.64735e-05 | 0.00286993 | intron-variant | RBBP7 | GRCh38.p7 | X:16852491 | AGTCTGGTATAGCTT[-/AACTG]ATGAATCCCTGGATT | 5931 |
rs774535837 | in-del | -/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16864096 | AATAAGAAAATACAA[-/G]ATGCAATTTTACCAA | 5931 |
rs774540917 | in-del | -/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16853488 | TAAATTTTGTGTAGA[-/G]TCTCACACTCCTGGT | 5931 |
rs774575506 | in-del | -/AG | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16861831 | GGGAACATGCACCTC[-/AG]AATGTTCTTTCTGTC | 5931 |
rs774696412 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16859050 | AAGCCCATTTGCACT[A/G]GAAAATATTGGTAGC | 5931 |
rs774743511 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16857495 | AATAATCAGCAGTAT[C/T]ATCTTAGAAAACCTT | 5931 |
rs774753075 | snp | A/T | 0.000529661 | 0.016265 | missense, intron-variant | RBBP7 | GRCh38.p7 | X:16869640 | CCCGCCTCGGCAGCC[A/T]TAGGCCTGAGGACCC | 5931 |
rs774783438 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RBBP7 | GRCh38.p7 | X:16865247 | AAACACAAAAACAAA[A/G]AACAAAAATTTAAAT | 5931 |
rs774810845 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RBBP7 | GRCh38.p7 | X:16847120 | GGTGACAGAACCAGA[C/T]CTTGACTTAAAAAAA | 5931 |
rs774845178 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant | RBBP7 | GRCh38.p7 | X:16868916 | ACACTATACACCAGA[A/C]ATCATCCCACAAATC | 5931 |
rs774897309 | snp | A/G | 4.58937e-05 | 0.00479007 | intron-variant | RBBP7 | GRCh38.p7 | X:16852147 | GATAATTTTGAAAAT[A/G]TATTTAAAGAATCAT | 5931 |
rs774903118 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16855579 | GGCATGTGGGTAGCC[C/T]CTGGTAAATGTCAGC | 5931 |
rs774966621 | snp | C/G | 0.000250721 | 0.0111936 | upstream-variant-2KB, intron-variant | RBBP7 | GRCh38.p7 | X:16870023 | CGGCGCGCGCCGCCC[C/G]GCAGGGCCTCTTACT | 5931 |
rs775097642 | snp | A/G | 2.34401e-05 | 0.00342337 | intron-variant | RBBP7 | GRCh38.p7 | X:16858648 | AAGAAAACTGCTCAA[A/G]TAATGACCTAACTCT | 5931 |
rs775115511 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | RBBP7 | GRCh38.p7 | X:16870327 | TCCCAGCCCGCCCAG[A/G]CAGCTGAGCGCAGGC | 5931 |
rs775132734 | snp | G/T | 2.37321e-05 | 0.00344463 | intron-variant | RBBP7 | GRCh38.p7 | X:16863118 | GTTTAAGAAAGAAAA[G/T]AAGTCACACTAATCC | 5931 |
rs775135658 | snp | C/T | | | upstream-variant-2KB | RBBP7 | GRCh38.p7 | X:16872173 | GCTTGGGAGATGATT[C/T]GTATCCCTTTAATAC | 5931 |
rs775139618 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16854608 | CAAGTCTTTCACTTC[A/G]TGGCAGAAACCACCA | 5931 |
rs775171835 | snp | C/T | 2.28009e-05 | 0.00337638 | missense | RBBP7 | GRCh38.p7 | X:16852061 | CTTAAATCCCACACA[C/T]TCAGGCGGCGGTCAG | 5931 |
rs775189576 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16851326 | CACTTCAAAGCAATA[-/T]TATTTAATACAAGCA | 5931 |
rs775354912 | in-del | -/TT | 0.0110892 | 0.0736317 | intron-variant | RBBP7 | GRCh38.p7 | X:16867842 | CGCTGCCACGCCCGG[-/TT]TTTTTTTTTTTTTGG | 5931 |
rs775445248 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | RBBP7 | GRCh38.p7 | X:16867490 | AATCTGTTGTGGCTG[G/T]AAACGTCAATGCTTC | 5931 |
rs775511782 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16859486 | CATGAAAAAGGCCTT[A/G]TAAAGTAACAAAGTC | 5931 |
rs775561961 | snp | A/C | 2.51099e-05 | 0.0035432 | intron-variant | RBBP7 | GRCh38.p7 | X:16845945 | ATGAATAAACTGTTA[A/C]AAGAACAAAAAAAGC | 5931 |
rs775758218 | snp | A/G | 7.11946e-05 | 0.00596592 | intron-variant | RBBP7 | GRCh38.p7 | X:16869065 | AAATAAAAGTTGCCA[A/G]AAACCCTTACTTAGT | 5931 |
rs775802793 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | TXLNG, RBBP7 | GRCh38.p7 | X:16844851 | AGCAACATTCTTCTC[C/T]TCCCTAATAGCTACA | 5931 |
rs775816249 | snp | A/G | 0.00158814 | 0.0281345 | utr-variant-5-prime, intron-variant | RBBP7 | GRCh38.p7 | X:16869770 | CCGCCCCGGGGCCGA[A/G]GGCGCCGGAGGGAGC | 5931 |
rs775826059 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16848570 | TGCCAAAAATGAGTA[A/C]TGGCATTAGAACTAA | 5931 |
rs775826958 | snp | C/T | 4.72138e-05 | 0.00485846 | synonymous-codon | RBBP7 | GRCh38.p7 | X:16853729 | AAACAATGACTCGTG[C/T]AGCAGGTGCCAGGCC | 5931 |
rs775916842 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RBBP7 | GRCh38.p7 | X:16861945 | TCAAGATTGATGACA[C/T]GTACCTTCTTTTATT | 5931 |
rs775932540 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | RBBP7 | GRCh38.p7 | X:16857248 | ACCTTTGTGAATATA[C/G]TAAAACCCACTGAAC | 5931 |
rs775933973 | snp | G/T | 0.00633741 | 0.0559334 | upstream-variant-2KB | RBBP7 | GRCh38.p7 | X:16870725 | TAGCGGCAGCGGTGG[G/T]GGGGGTGAGAGGGGG | 5931 |
rs775946326 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16861031 | ATACAAAAATTAGCC[A/G]GGCATGGTGGTGGAC | 5931 |
rs776073741 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | RBBP7 | GRCh38.p7 | X:16857815 | GCAACTGCACACGAA[C/T]GAGATCTGGTCTTTA | 5931 |
rs776110763 | snp | A/C | 2.28496e-05 | 0.00337998 | intron-variant | RBBP7 | GRCh38.p7 | X:16852700 | TATCTGATTAAGGCA[A/C]AAGAGAACTGGGTTT | 5931 |
rs776182946 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16864488 | CTCAAGATCACACCA[C/T]TGCACTCCAGCCTGG | 5931 |
rs776205907 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16856485 | CAGTGAGCTGAGATC[A/G]TGCCACTATACTCCA | 5931 |
rs776238901 | snp | A/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16869384 | GGAGAAAATACTAAC[A/T]ATCAGGAAGCCTATT | 5931 |
rs776274897 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16857285 | CTTAAAAAATACTTT[A/G]TATTAATCAGGTCCC | 5931 |
rs776371820 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16865311 | AGAAAGAAGGCACCA[C/T]AGAGCAATGCTGGTA | 5931 |
rs776421928 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16851397 | AAGATGACATCTTAC[A/G]GAGGAGTATGTAACT | 5931 |
rs776463149 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16864409 | CTGTAATCCCAGCTA[C/T]TCAGGAGGCGGAGGC | 5931 |
rs776490782 | in-del | -/A | | | intron-variant | RBBP7 | GRCh38.p7 | X:16853860 | AAGAGAGAAGGAGAG[-/A]AAAAAAAAAGAACAA | 5931 |
rs776492998 | snp | G/T | 2.29387e-05 | 0.00338656 | synonymous-codon | RBBP7 | GRCh38.p7 | X:16858695 | TTTAGCAGGGTGTTT[G/T]GTATAGTCAAAAACC | 5931 |
rs776506937 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | RBBP7 | GRCh38.p7 | X:16860248 | CTGATTCCTTTAGCT[A/G]AAACAACCTGAAGAG | 5931 |
rs776558877 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16861176 | GAGACCCTGCCTCAT[A/G]ACAAACAAAAACAAA | 5931 |
rs776563103 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16867974 | ACAGGCGTGAGCCAC[C/T]GCACCCAGCCAAAAT | 5931 |
rs776575941 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16850782 | CAAAATCCAAAACTT[C/T]AAGCACCACGTGACA | 5931 |
rs776602733 | snp | A/T | 2.34028e-05 | 0.00342065 | intron-variant | RBBP7 | GRCh38.p7 | X:16862915 | TTTGAAAGAGACATT[A/T]TCCCTTTGACACCAA | 5931 |
rs776697406 | snp | A/G | 2.30896e-05 | 0.00339769 | missense | RBBP7 | GRCh38.p7 | X:16869092 | TAGTCACTTCAGGAA[A/G]CCACTGAACGGTAAG | 5931 |
rs776860294 | in-del | -/T | 0.0152018 | 0.0858476 | intron-variant | RBBP7 | GRCh38.p7 | X:16853892 | GCTATAAGAGACTGA[-/T]TTTTTTTTTTTTTCC | 5931 |
rs776886198 | snp | A/T | 0.000186306 | 0.00964979 | splice-donor-variant, intron-variant | RBBP7 | GRCh38.p7 | X:16869492 | GTTACAGCTGTTCGC[A/T]CCTGTTCTAAGATGA | 5931 |
rs776937962 | snp | A/T | | | | | GRCh38.p7 | X:16872437 | AGTTTTGCATTTTTG[A/T]TGTTGTTAAATTGAA | 5931 |
rs776967276 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16854519 | CAAATGCACATCCTA[A/G]AAGTTTACACTGGGA | 5931 |
rs777044865 | snp | A/C | | | upstream-variant-2KB | RBBP7 | GRCh38.p7 | X:16871064 | CCGAAGCCGATTTAC[A/C]CTGTTACATTTTAAT | 5931 |
rs777070401 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16849382 | CAGTATCAGCCCAGA[A/T]AGTAATCTTAAAACA | 5931 |
rs777075854 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16847194 | AGTGAATATACTGGC[C/T]GGGTGTGGTGGCTCA | 5931 |
rs777081130 | snp | C/T | 2.27946e-05 | 0.00337591 | synonymous-codon | RBBP7 | GRCh38.p7 | X:16852824 | GACTTCGGCAGTGTG[C/T]GCATCCACCAAGTGA | 5931 |
rs777169033 | snp | C/T | 2.2843e-05 | 0.0033795 | intron-variant | RBBP7 | GRCh38.p7 | X:16852708 | TAAGGCACAAGAGAA[C/T]TGGGTTTTATAAACA | 5931 |
rs777174301 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | RBBP7 | GRCh38.p7 | X:16870806 | AAAATGGTTCCTGTT[C/T]TCGAGAGATTACTGT | 5931 |
rs777322217 | in-del | -/TAAGTGAAAGAA | | | intron-variant | RBBP7 | GRCh38.p7 | X:16857017 | TTGAAAACATTATGC[-/TAAGTGAAAGAA]GCCAAACAGAAAAGG | 5931 |
rs777344549 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TXLNG, RBBP7 | GRCh38.p7 | X:16844192 | AGTACATTTCTTGGT[C/T]TTGAGACCAGTATTT | 5931 |
rs777350642 | snp | A/G | 0.000184963 | 0.00961494 | intron-variant | RBBP7 | GRCh38.p7 | X:16849352 | AAATTCTTGTAGCAC[A/G]AACATCTGCTAAACC | 5931 |
rs777393096 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16845671 | ACCATATGGGACTAA[A/G]GATTGTATTGTTGAA | 5931 |
rs777447035 | snp | A/G | 5.18329e-05 | 0.00509056 | intron-variant | RBBP7 | GRCh38.p7 | X:16845953 | ACTGTTACAAGAACA[A/G]AAAAAGCTTTGATTT | 5931 |
rs777513631 | snp | C/T | | | upstream-variant-2KB | RBBP7 | GRCh38.p7 | X:16871942 | GCGTTCCGATAAAAC[C/T]ACAGACACTAAAATC | 5931 |
rs777518808 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16867114 | AACAGGAAGGGGTGG[C/G]AGAATCAGCATCAGT | 5931 |
rs777558981 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | RBBP7 | GRCh38.p7 | X:16853961 | GATCTCGGCTCACTG[C/T]AGCCTCCGCCTCCAG | 5931 |
rs777620194 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16868887 | CAACAGCTTCTTTCT[C/T]CCCTTTTACCACCAC | 5931 |
rs777625673 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16854249 | AACAAAACTATTCAA[C/T]TATATAAGTTTGAGG | 5931 |
rs777632567 | snp | C/T | 0.000183453 | 0.00957563 | missense | RBBP7 | GRCh38.p7 | X:16845886 | ATGACCCAAGGCTCA[C/T]TGGGGTTCCAGCTAA | 5931 |
rs777655034 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RBBP7 | GRCh38.p7 | X:16862454 | ACTTTTACCAAAGTG[A/G]AATACTGTAATTACA | 5931 |
rs777660548 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16848943 | CCAACTGAATAGCAA[C/T]TATACTCACTCCCCA | 5931 |
rs777847565 | in-del | -/AAAC | | | intron-variant | RBBP7 | GRCh38.p7 | X:16849399 | GTAATCTTAAAACAT[-/AAAC]ACACTCACAAAAACA | 5931 |
rs777851713 | snp | C/G | 2.4154e-05 | 0.00347511 | intron-variant | RBBP7 | GRCh38.p7 | X:16869251 | AGCCCACACGATTAA[C/G]TGGCTGAGATAGATC | 5931 |
rs777925751 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, utr-variant-5-prime | RBBP7 | GRCh38.p7 | X:16870352 | GCAGGCGCATCCGCC[C/T]TGGGAAAAGTGAGAG | 5931 |
rs777936777 | snp | A/G | 2.82298e-05 | 0.00375688 | intron-variant | RBBP7 | GRCh38.p7 | X:16852465 | ACATTTTTTTCAATA[A/G]TGGACCCACGAGTCT | 5931 |
rs777938962 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16856893 | AAAATAGCCCCAAAG[G/T]AGAAAGAACTCAAAT | 5931 |
rs777939217 | snp | C/G | 2.29655e-05 | 0.00338855 | synonymous-codon | RBBP7 | GRCh38.p7 | X:16857642 | CAAATTTGAATTCCA[C/G]GAGAGACCATAGCCT | 5931 |
rs778027047 | in-del | -/TCA | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16856203 | TACAAGAAAAGATGC[-/TCA]TCATCATTAGTCATC | 5931 |
rs778081770 | snp | A/C | | | intron-variant | RBBP7 | GRCh38.p7 | X:16865600 | TTTCCTAAACTAATC[A/C]ATATGACACTATTTT | 5931 |
rs778310713 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16850322 | GATTATAGACATGAG[C/T]CGCCATGCCTGGCCC | 5931 |
rs778336887 | snp | A/C | 2.29611e-05 | 0.00338822 | intron-variant | RBBP7 | GRCh38.p7 | X:16858852 | AAGCCACCAAATTCT[A/C]ATGTGAGGAGAAAGA | 5931 |
rs778338277 | snp | C/T | 9.98153e-05 | 0.00706383 | intron-variant | RBBP7 | GRCh38.p7 | X:16852390 | ATCCCAGAAGCTTTT[C/T]AATTCTTCAACAAGG | 5931 |
rs778414912 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16851950 | TAGGTTTCTTGAAGG[C/G]GGGATTACCAAATTG | 5931 |
rs778429909 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16861965 | CTTCTTTTATTACTG[A/G]GTCCTCAGTTTGTAT | 5931 |
rs778603763 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16848184 | GCTATAGTTTCTTTT[A/G]GAGGGGATGAATAAT | 5931 |
rs778640032 | in-del | -/AG | | | intron-variant | RBBP7 | GRCh38.p7 | X:16848599 | AAAATCGTAAATGAC[-/AG]AGTGATGAGTGACTA | 5931 |
rs778692504 | in-del | -/T/TT | 0.0454913 | 0.143919 | intron-variant | RBBP7 | GRCh38.p7 | X:16867841 | CGCTGCCACGCCCGG[-/T/TT]TTTTTTTTTTTTTTT | 5931 |
rs778696154 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | RBBP7 | GRCh38.p7 | X:16854230 | TTAAAATAATTTCAT[G/T]ACAAACAAAACTATT | 5931 |
rs778716781 | in-del | -/A | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:16846740 | ATCACACTTTCTGAC[-/A]AAGTCTGATTTGACT | 5931 |
rs778720917 | snp | A/G | 0.000317712 | 0.0125998 | | | GRCh38.p7 | X:16869672 | AGCAACCCCCGGACA[A/G]GGGCCGCGACCCCGA | 5931 |
rs778739751 | snp | A/G | | | | | GRCh38.p7 | X:16856117 | CTTGACAATAAAAAG[A/G]CAAAATTAAAATATG | 5931 |
rs778777827 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16857030 | GCTAAGTGAAAGAAG[C/T]CAAACAGAAAAGGCC | 5931 |
rs778788367 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | RBBP7 | GRCh38.p7 | X:16855029 | GTGATCATGAAAGGG[C/T]TTCATCTGTTTTTAT | 5931 |
rs778792603 | snp | A/G | | | upstream-variant-2KB | RBBP7 | GRCh38.p7 | X:16872069 | GGGTTAGATTTAGTC[A/G]GAGGACTGTAGTTTG | 5931 |
rs778882123 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16865828 | TCCATCAGCAAGGAA[C/T]TGGTATCATACATTA | 5931 |
rs778906895 | snp | A/G | 2.29145e-05 | 0.00338478 | intron-variant | RBBP7 | GRCh38.p7 | X:16852010 | TTGCCAGATAGGCAC[A/G]TTTATGCAGTATCTT | 5931 |
rs778933046 | in-del | -/T | 2.42869e-05 | 0.00348466 | intron-variant | RBBP7 | GRCh38.p7 | X:16869261 | ATTAAGTGGCTGAGA[-/T]AGATCAAAGTCAGAA | 5931 |
rs778947359 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16857492 | CACAATAATCAGCAG[C/T]ATTATCTTAGAAAAC | 5931 |
rs778991028 | snp | A/G | 2.3079e-05 | 0.0033969 | intron-variant | RBBP7 | GRCh38.p7 | X:16852654 | ATAACAAGTGAAAAT[A/G]ATTTCTATGCTTTAC | 5931 |
rs779048676 | in-del | -/AA | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16862537 | CAGATTTTTCTCATT[-/AA]AAAAAAAAAAATTTT | 5931 |
rs779066022 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16868741 | ATGTGTGAACTTTTC[C/T]GTAAATATTCTATTT | 5931 |
rs779098134 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16849121 | GCAATAACCTTCAGG[C/G]CCTCCATTTTGAAAC | 5931 |
rs779152260 | snp | A/C | | | intron-variant | RBBP7 | GRCh38.p7 | X:16853303 | TCGACCTCCAACTGG[A/C]ATCACTCTGGATCTC | 5931 |
rs779172942 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16866912 | ATCCCACAACCCAAT[A/C]CCACAACAGCTTTGT | 5931 |
rs779186592 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16848549 | CTCATGGACAAAGTA[A/C]AAGTGTGCCAAAAAT | 5931 |
rs779228349 | in-del | -/G | 0.0214859 | 0.101397 | upstream-variant-2KB | RBBP7 | GRCh38.p7 | X:16870463 | CGGAGGCGGGCTTCT[-/G]GGGGGTGGGCGGAGC | 5931 |
rs779253750 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16852363 | TCAATAAATTTATTC[A/G]ACCCCATAACCATCC | 5931 |
rs779272327 | snp | C/T | 4.68851e-05 | 0.00484152 | intron-variant | RBBP7 | GRCh38.p7 | X:16858874 | GGAGAAAGAAACACA[C/T]ACACACACACTCAGG | 5931 |
rs779278449 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16857220 | ATTCTAGAATTAGTG[A/G]CAATAGTTGTGCACC | 5931 |
rs779337974 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16860818 | ATTATGCAGAGACTG[C/T]TAAACTGCAAGCCCG | 5931 |
rs779375279 | snp | A/T | 2.43888e-05 | 0.00349196 | intron-variant | RBBP7 | GRCh38.p7 | X:16858885 | CACACACACACACAC[A/T]CAGGATTAAAATTCA | 5931 |
rs779380972 | snp | C/T | 2.40854e-05 | 0.00347017 | downstream-variant-500B, utr-variant-3-prime | TXLNG, RBBP7 | GRCh38.p7 | X:16845003 | ATTCATGTAGCATTA[C/T]ATTCAACAGAAACAT | 5931 |
rs779448922 | in-del | -/AGTT | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16866153 | TTTAGGTAGACAATA[-/AGTT]AGTCTCAATATATTT | 5931 |
rs779457169 | snp | A/C | 0.000529661 | 0.016265 | downstream-variant-500B, utr-variant-3-prime | TXLNG, RBBP7 | GRCh38.p7 | X:16844681 | TATTTCTGCAAAGCC[A/C]ATCAAGAAGTGTTGG | 5931 |
rs779570304 | snp | G/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16848500 | GGACATTCAATATAC[G/T]CCATAGGTTCACAGA | 5931 |
rs779754100 | snp | A/G | 2.33236e-05 | 0.00341486 | missense | RBBP7 | GRCh38.p7 | X:16863099 | AATCTTTTCCTTCAG[A/G]TCTGTTTAAGAAAGA | 5931 |
rs779834633 | snp | C/T | 0.000145993 | 0.00854256 | upstream-variant-2KB, utr-variant-5-prime | RBBP7 | GRCh38.p7 | X:16870088 | CCCTCGCCGCCGCCT[C/T]GGACTCCTCTCGTTA | 5931 |
rs779846507 | snp | C/T | 2.29276e-05 | 0.00338575 | missense | RBBP7 | GRCh38.p7 | X:16852592 | CGAAGGTATGGAGTT[C/T]TAATTTTAAGTTACG | 5931 |
rs779975886 | snp | A/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16858408 | AGGACTCAGACGCCT[A/G]TAGCTAACCCCTCTG | 5931 |
rs780027189 | snp | C/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16857211 | AATGAAAACATTCTA[C/G]AATTAGTGGCAATAG | 5931 |
rs780111521 | in-del | -/CT | 0.0026455 | 0.0362733 | intron-variant | RBBP7 | GRCh38.p7 | X:16856069 | TGAAAATCATAGGGA[-/CT]TATACCTAGAATACA | 5931 |
rs780113264 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RBBP7 | GRCh38.p7 | X:16862794 | TCAATTCTGCAATTA[C/T]GACTAAAATCCTTGT | 5931 |
rs780113546 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | RBBP7 | GRCh38.p7 | X:16846915 | AGGCGGATGGCTCGA[G/T]CTCAGGAGTTCAAGA | 5931 |
rs780128268 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16868770 | TTTTCAGTAAAGTTT[C/T]AAAGAAACGCATTAG | 5931 |
rs780149251 | snp | G/T | | | missense | RBBP7 | GRCh38.p7 | X:16853804 | ATCCACAATTTTGCC[G/T]TCTTTTGGTCCTGCG | 5931 |
rs780190045 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RBBP7 | GRCh38.p7 | X:16864033 | AGGATTCAATTTTTT[C/T]TTTTTTTCTAAAAAG | 5931 |
rs780201213 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | RBBP7 | GRCh38.p7 | X:16855123 | GGCACAATTTTGGCG[A/C]ACTACAACCTCCGCC | 5931 |
rs780214462 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16850122 | ACAATCTCAAACCTG[C/T]GGGATTGCTAGACAA | 5931 |
rs780358523 | snp | C/T | 2.36451e-05 | 0.00343831 | synonymous-codon | RBBP7 | GRCh38.p7 | X:16845927 | CTTAGCAGTGTGTCC[C/T]CCATGAATAAACTGT | 5931 |
rs780450117 | snp | A/G | 0.000427031 | 0.0146059 | utr-variant-3-prime | RBBP7 | GRCh38.p7 | X:16845024 | ACAGAAACATTTCTC[A/G]TACTTTGGGTTTAAG | 5931 |
rs780455163 | in-del | -/A | 0.000129026 | 0.00803095 | intron-variant | RBBP7 | GRCh38.p7 | X:16845131 | AATAAATTCACAGGT[-/A]AAAAACTCCCTATGG | 5931 |
rs780542959 | in-del | -/GGATTAAAATT | 2.38681e-05 | 0.00345448 | intron-variant | RBBP7 | GRCh38.p7 | X:16858888 | ACACACACACACTCA[-/GGATTAAAATT]CACAAATCACTTAGT | 5931 |
rs780550040 | snp | A/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16863491 | CCACCTAAAGAAATC[A/T]TCTTCCCACCTAAAA | 5931 |
rs780597271 | snp | C/G | | | intron-variant | RBBP7 | GRCh38.p7 | X:16846606 | AGAGAGCAGTTGTTC[C/G]CCGCAAGAGACAACC | 5931 |
rs780598436 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B, utr-variant-3-prime | TXLNG, RBBP7 | GRCh38.p7 | X:16844796 | TCAAAGGCAATACCC[C/T]GCTACTTGTATTTAA | 5931 |
rs780688151 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16867674 | AGATTATTATTATAA[C/T]AATTATTTTTATTTT | 5931 |
rs780693235 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16845592 | ACAACAATGAAAATC[A/G]GTGCAGATGCAGAGA | 5931 |
rs780799690 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16853101 | AAATTAGATTCCTAT[C/T]TTAATTACCAACTAT | 5931 |
rs780804469 | snp | A/T | 2.39575e-05 | 0.00346095 | intron-variant | RBBP7 | GRCh38.p7 | X:16869236 | CTGAAATTTGGAGAA[A/T]GCCCACACGATTAAG | 5931 |
rs780865840 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16866271 | CCAAATCAACACCTG[C/T]AATCCCAGCACTCTG | 5931 |
rs780875922 | snp | C/T | 2.4406e-05 | 0.0034932 | intron-variant | RBBP7 | GRCh38.p7 | X:16863150 | ACAAGAAATCTCCAA[C/T]TGCTAACAAATTCAG | 5931 |
rs780881741 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16861589 | CCAGGCTCAAGCGTT[C/T]CTCCTGCCTTGGCCT | 5931 |
rs780887542 | snp | A/C/G/T | 5.204e-05 | 0.00510071 | intron-variant | RBBP7 | GRCh38.p7 | X:16852474 | TCAATAGTGGACCCA[A/C/G/T]GAGTCTGGTATAGCT | 5931 |
rs780889296 | snp | A/G | 2.53113e-05 | 0.00355739 | intron-variant | RBBP7 | GRCh38.p7 | X:16845946 | TGAATAAACTGTTAC[A/G]AGAACAAAAAAAGCT | 5931 |
rs780895806 | snp | A/G | 2.28071e-05 | 0.00337684 | intron-variant | RBBP7 | GRCh38.p7 | X:16852744 | TAATGCAAAAACTTC[A/G]AAACCTTATCCGCAG | 5931 |
rs780933291 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16858607 | AGTATGCTACTTTGA[C/T]CTTAAAAACATTACC | 5931 |
rs780946169 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16869421 | ATTGAGATCAATACC[C/T]CCTGCGTACACCATG | 5931 |
rs781046494 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, utr-variant-5-prime | RBBP7 | GRCh38.p7 | X:16870176 | ACTGTCGAAAGCCCG[A/G]GCCCCGTCTTGCTGC | 5931 |
rs781250962 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16855347 | GTGAGCCACTGTGCC[C/T]AGCCACATGAAGGAC | 5931 |
rs781276838 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16855786 | TGGATCACTTGAGCC[C/T]GGGAGTTCAAGACCA | 5931 |
rs781337363 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RBBP7 | GRCh38.p7 | X:16864123 | CCAAAATTTGGCTTA[C/T]GGTAAAAAAGTGTGT | 5931 |
rs781365012 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RBBP7 | GRCh38.p7 | X:16856116 | ACTTGACAATAAAAA[A/G]ACAAAATTAAAATAT | 5931 |
rs781380123 | snp | A/C | | | intron-variant | RBBP7 | GRCh38.p7 | X:16848780 | AAGCTTTCAAAGGGC[A/C]AAGGAGATGCGTGAT | 5931 |
rs781385619 | snp | A/G | 2.30049e-05 | 0.00339145 | intron-variant | RBBP7 | GRCh38.p7 | X:16857581 | AACAAATTACAAAGA[A/G]TACGTTTCTCACATG | 5931 |
rs781386019 | snp | A/G | 0.000369959 | 0.0135957 | utr-variant-5-prime, intron-variant | RBBP7 | GRCh38.p7 | X:16869680 | CCGGACAAGGGCCGC[A/G]ACCCCGAGGCGGTCA | 5931 |
rs781589309 | in-del | -/AA | | | intron-variant | RBBP7 | GRCh38.p7 | X:16860273 | GAAGAGCTCTCCTTT[-/AA]AAAAAAAAGGGGGGG | 5931 |
rs781703977 | snp | C/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16863642 | CTTAAAACACAACCT[C/T]CCTGGGGCCTCAGTT | 5931 |
rs781734845 | in-del | -/AGAA | 2.31629e-05 | 0.00340307 | intron-variant | RBBP7 | GRCh38.p7 | X:16858861 | AATTCTAATGTGAGG[-/AGAA]AGAAACACACACACA | 5931 |
rs781755027 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RBBP7 | GRCh38.p7 | X:16859858 | AGTTCCAGGCAGCTC[C/T]TTCTATGTGGAATGC | 5931 |
rs781764392 | snp | C/G | 2.35671e-05 | 0.00343264 | missense | RBBP7 | GRCh38.p7 | X:16853791 | AGATGGCTTTAGCAT[C/G]CACAATTTTGCCTTC | 5931 |
rs781779438 | in-del | -/T | 0 | 0 | intron-variant | RBBP7 | GRCh38.p7 | X:16859293 | ACAGTATGAACACCC[-/T]TTTGAGTCTGAAGTC | 5931 |
rs796109985 | in-del | -/T | | | intron-variant | RBBP7 | GRCh38.p7 | X:16853905 | TGATTTTTTTTTTTT[-/T]CCCTCGAGACAGTGT | 5931 |
rs796902015 | in-del | -/AATTA | | | intron-variant | RBBP7 | GRCh38.p7 | X:16866963 | CACATTAAATAATTT[-/AATTA]AAGCATTTTGTTACA | 5931 |