SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs117044455 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569593 | AAAATTTATATGGAA[C/T]CACAAAAGTCCCAGA | 81550 |
rs117045266 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402516 | TAATATTAAGTGCAG[C/G]GTTTTTAAAATCTAG | 81550 |
rs117088110 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503893 | ATGAAACCTTATAGA[C/T]GATTCCATCTAATCT | 81550 |
rs117124504 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433876 | TCACCGATTTTACCT[A/G]CTTTCAAAGAAATGG | 81550 |
rs117159278 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476129 | AAGGCTAGTCTCAAG[A/G]AGGGTATTTCCTAGG | 81550 |
rs117169092 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485317 | TTTGAAGCCTGATAC[A/G]GGGGGTGGGTATGTT | 81550 |
rs117201090 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435855 | TCCATACTGTTTTCC[A/G]TAGTGGTTGTAGCAA | 81550 |
rs117219525 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422781 | AGAGAGAAAGTAGTC[A/G]AATATTATTCCTTTG | 81550 |
rs117226553 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440747 | TCTGATTGTTTTTCT[A/G]TGTAGCTTTATAATA | 81550 |
rs117234071 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425304 | TGCAAATTGAAACCA[C/T]TATGATGTATCACCT | 81550 |
rs117269692 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457542 | AGAGGAAGATGAGTG[A/G]GGCTGAGGCCAATAT | 81550 |
rs117343053 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413327 | ATATTCAGTTAGATA[C/T]ATATCTGCTTGAGAA | 81550 |
rs117356226 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559933 | AAAATGGAAACTGAG[A/G]TGATGGATATGTTAA | 81550 |
rs117356397 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498431 | ACGGTAGAAGCAAAA[C/T]GGCAATCAGAATATT | 81550 |
rs117360775 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487087 | TTGCATCTGTACTAA[A/C]TGTGTACAAACTTTT | 81550 |
rs117364885 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520128 | AAATATGTTTATTTT[A/G]AGCTTAGTCTTCAAT | 81550 |
rs117385472 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402335 | TACAACCTCTGCAGT[A/G]GCAGTAATGTAATTA | 81550 |
rs117416634 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482296 | CTCTGTTTGCATCAT[A/G]GCTACAAGCAGAAAG | 81550 |
rs117453619 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516774 | CCTCCACTCACCATG[C/T]ATCATTTCCACCTTC | 81550 |
rs117456345 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510999 | TTTCCCAAATTTGCT[C/T]ATATCTAGATGACAG | 81550 |
rs117503994 | snp | A/G | 0.021333 | 0.101051 | intron-variant | TDRD3 | GRCh38.p7 | 13:60570350 | AAATGCAAATCAAAT[A/G]CAATGAGATATCACC | 81550 |
rs117514241 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472497 | AACAAACAAACAAAA[A/C]CCCCCAGAAAATAGC | 81550 |
rs117533732 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553604 | TCTGCATGGCTCGAG[A/T]GGTCTCTGGAAACTT | 81550 |
rs117539220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470959 | GCTTATTGGCCATGC[A/G]TAGATCTTCTTTGGA | 81550 |
rs117578823 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549611 | GTGCACGTGGACAAA[C/T]GTGAGAGATATCAGT | 81550 |
rs117594782 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534050 | ACATAGTGGCTCATG[C/T]TTGTAATCCCAACAC | 81550 |
rs117599804 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488344 | AAGGCCTGAGTGTCA[C/T]TTCCTGAGGAAAGAA | 81550 |
rs117614694 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430608 | ACTTTTAAATTTATG[A/T]GGAGTCATGGTTTAC | 81550 |
rs117639634 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482765 | TCGTTACTCTTAATT[A/G]TCTTTATAAAATATA | 81550 |
rs117655118 | snp | A/T | 0.0486741 | 0.148216 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514332 | TTCAGTTTTAAAGGG[A/T]AAACACATGATAAAA | 81550 |
rs117685946 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405382 | ACATACTGCATCTAT[A/G]AAGAATACTAGAGAG | 81550 |
rs117707956 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561238 | ATGAGACATTTAATT[C/T]ATAGGAGTCAAGTAT | 81550 |
rs117723100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436341 | GCCTATGCCAATGTC[C/T]GAAGAGTTTTCCAAT | 81550 |
rs117764906 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | TDRD3 | GRCh38.p7 | 13:60562183 | CTGGGTTTGGTGGTG[A/C]GTGCCTGTAATTCCA | 81550 |
rs117829810 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500435 | TCATGGGGAGTCCCT[A/G]TGATCAGTTGACAGA | 81550 |
rs117840478 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490315 | GACTTGAAGGAGGTA[C/T]GAGAATTAACTACTT | 81550 |
rs117860661 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517677 | TTTACCATTCCATTC[A/G]TTTTGAAGTGCAAAT | 81550 |
rs117868870 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486309 | TGGGGATAATTTCCC[A/C]TTATTAATAGCAACT | 81550 |
rs117893166 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532054 | CTGTTACAATTGTTA[A/G]TAAAGGTCTAATGTT | 81550 |
rs117893426 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467772 | AGTTAGAATTTCACT[A/G]TAATGGAGGAGTTCT | 81550 |
rs117901484 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436407 | TTTCATGATTTCAGG[A/T]CTTAGATTTAAATCT | 81550 |
rs117941795 | snp | A/T | 0.00191441 | 0.0308794 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509753 | CAGCTTTTCTCTTTA[A/T]TCCTTCCAGGTTGAT | 81550 |
rs117957208 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467820 | TAGTCTCATTAGCTA[A/G]TATTTTTCCCCATTT | 81550 |
rs117965096 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478277 | TTTTTGTTAATCTAG[C/T]TAGCAGTCTACCAAT | 81550 |
rs117968194 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552134 | CCAGCATTAACTTAA[A/G]ATTCCAAGTCGAAAG | 81550 |
rs118011248 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486082 | CTTCTTGCATATTCC[A/G]TAACTGGGAATGCCC | 81550 |
rs118021891 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547159 | CTATACTTTGAGGTT[C/G]CAATGAATTTCACAT | 81550 |
rs118085874 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477611 | TATTGAAGGCCTTTT[C/T]TGCATCTATTAAGAT | 81550 |
rs118129722 | snp | A/G | 0.000309103 | 0.012428 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60444729 | TCCCCAGTGACATCA[A/G]TAGTGGAAAGGTAGA | 81550 |
rs118134718 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480657 | CTCTTTACATAACCC[C/T]ATATTTCTTAGAGGT | 81550 |
rs118149748 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427870 | AGTAATTACTGGAAT[G/T]TGTAATGGGTATATT | 81550 |
rs118152906 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60573711 | TAAGTAGCTGTGGTG[A/G]ATATTATTATTTGAA | 81550 |
rs118161583 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557312 | AAGCCAGAGAGCTCC[C/T]TTCACCAGAGTTATT | 81550 |
rs137904879 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524514 | TCCATCTCAAAAAAA[A/T]AAATAAATAAATAAA | 81550 |
rs137911915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494029 | TCATAATACTGAACT[A/G]TGGACATAATTTTAA | 81550 |
rs137913222 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559382 | TGAGCCAACTGACAC[A/G]TTTTGGAACAGAAAT | 81550 |
rs137922342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567745 | TTTTTTTCTCTGAGA[C/T]GAAGTTTCACTCTTG | 81550 |
rs137953436 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405909 | TCGACTTGACAGATA[G/T]TTGGAAGGTAAATGG | 81550 |
rs137960341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412233 | CCACACTTGAAGTAG[A/G]TCATATTTGACATAT | 81550 |
rs137980243 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420952 | CCGTCTCAAAAAAAA[A/G]GAAAATCTGTTGACC | 81550 |
rs138020007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506698 | GGAGGCGGAGTTTGC[A/G]GTGAGCTGAGATTGC | 81550 |
rs138104177 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549015 | GGTAAATTGTCATTC[A/T]TCTGCTGGATGAACT | 81550 |
rs138105306 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474193 | TGTCCTCTCTCTCTC[C/T]CCGCCTTGGCTGCCA | 81550 |
rs138120427 | snp | A/C | 0.000153988 | 0.00877328 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528757 | GATCAGGAAAAGGTC[A/C]CTCCTTTGCAGAGGC | 81550 |
rs138146698 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467175 | CGGTCTGTGTTGTTT[A/C]CCGCCCTGTGTCCAT | 81550 |
rs138149269 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399845 | GAAAAGTTTACAATT[C/G]TGAAAATGTGATCTT | 81550 |
rs138174494 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514608 | TTGGGGCAGTCCAAG[G/T]GGAGGGAGCACTATG | 81550 |
rs138194235 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434216 | GGCTCATGCCTGCAA[C/T]CCTAGCACTTTGGGA | 81550 |
rs138212958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444976 | TTTGTTTCAGAATTT[A/G]TAACTATGGCATGCT | 81550 |
rs138214036 | in-del | -/ATG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404011 | AGGCAGAATTTAAAC[-/ATG]ATATACACTGTTATT | 81550 |
rs138221017 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394769 | CGTCTTCATGTTTAA[C/T]TTGCTCAAATATCAC | 81550 |
rs138221514 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518590 | TTAAGTCATTATAGT[A/G]TTTTGACTTTGTAAA | 81550 |
rs138268747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462359 | TGTCTACTGTCATCC[C/T]TTGTTGAATTTATTG | 81550 |
rs138269818 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531008 | AGAATAAGGAGGAGT[A/G]CAGAGTGAAACAGCT | 81550 |
rs138270377 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474119 | TTTAGATAGCAGTAG[C/T]AGAATTAGTGAAAGT | 81550 |
rs138283041 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547506 | GGTAAGTTACCTAAT[A/C]TCTCTGGGTCCCAGT | 81550 |
rs138335413 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428384 | TGAAGAGGTATGGGG[A/G]ATGTAGTCAAATTAT | 81550 |
rs138356602 | in-del | -/TGTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442372 | TAAATAGGGATTTTA[-/TGTG]TGTGTGTGTGTGTGT | 81550 |
rs138378209 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398864 | AATCTCTTCTTTCAG[-/T]TTTTTTTACCCACAA | 81550 |
rs138405688 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488634 | GGTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 81550 |
rs138413837 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564039 | GTCAATGATTATTGC[A/G]GTTTTGTATCTTTTC | 81550 |
rs138422399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458804 | TGGCTGGAGGATTGT[A/T]TTGGACAGCATAGGC | 81550 |
rs138427655 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559838 | AGTCACTCCAATTAA[C/T]AGTAGTGTATTGTAT | 81550 |
rs138515493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420454 | TTCAAGTTTGTGAAG[A/G]TACTTTCTTATGCTT | 81550 |
rs138516741 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411202 | ATTAAAAGACACTCT[C/G]ATATAATTAGATGTA | 81550 |
rs138521317 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542303 | AATAAAGTAGTAAAA[C/T]AAGTGGATCTGAAGG | 81550 |
rs138521573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498949 | GGTCCAGTGGGTACG[C/T]GGACTCATCCTGTGG | 81550 |
rs138525974 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493063 | AGCTGGGACTACAGG[C/T]GCCCGCCAACATGCC | 81550 |
rs138567574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423269 | CAAGAGATAGAGCAA[C/T]TGGCTTTCTGAAACA | 81550 |
rs138574093 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501230 | TTAGGGGGTGTTGGA[C/T]GATGACTCTTTTGGC | 81550 |
rs138606242 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406149 | CATTAGGAAATACCA[A/G]TCTTGCACTCAGAAG | 81550 |
rs138615685 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488075 | CTGCACAGTAAGCCA[A/G]TCACTGAGACAATGA | 81550 |
rs138618410 | in-del | -/AAAAAAAA | 0.285519 | 0.247464 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557207 | GCGAAACTCTGTCTC[-/AAAAAAAA]AAAAAAAAAAAAAGT | 81550 |
rs138622338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522345 | AAAATAGGAGTTGGT[A/G]GTAGTGGGAATGTAT | 81550 |
rs138622426 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455442 | GAATAATTTAGTCAA[A/C]AACCTCCCTTGAAAT | 81550 |
rs138630360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552903 | CTGGGATACAGGACA[C/G]CAAGTTCTGGGGCTG | 81550 |
rs138633350 | in-del | -/TTCT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541147 | CTTTTTGTTTTTCTA[-/TTCT]TTCTTTCTTTCTTTC | 81550 |
rs138655122 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519066 | GCATATGATAATATT[A/G]TTACTTTTTTTGGTA | 81550 |
rs138656233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435470 | ATATCACTCTATATG[C/T]ATTTGCACCCTCATG | 81550 |
rs138656649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400219 | TTTATCTAGATAACA[A/G]TTTTACTCACTCTGC | 81550 |
rs138671937 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60543557 | TGGAAACCATCTTAA[C/T]TATTTGTTTTTATCT | 81550 |
rs138701416 | in-del | -/A | 0.0174175 | 0.0916809 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537408 | TGTGCATATAGATGT[-/A]AAAAAAACCCTGAAG | 81550 |
rs138720421 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501877 | AGCAGACTCAGTGAT[A/G]GTAAAATTTTTATGC | 81550 |
rs138746884 | in-del | -/TA | 0.0146672 | 0.084371 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481636 | TTTACTAGTTGAATT[-/TA]TGTTTTCTTTTAAAT | 81550 |
rs138767867 | snp | C/G | 0.000214449 | 0.0103527 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528501 | CCAAGAAATGAAAAA[C/G]CGCCTCGTTTTCAAA | 81550 |
rs138808765 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440542 | AAAAATTAGCTGGGC[A/G]TGGTAGTGTGTGCCT | 81550 |
rs138809450 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473532 | GCATAATAAAACATA[C/T]AGAATAAGAATAGTT | 81550 |
rs138827440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440437 | CCTGTAATCCAAGCA[C/T]GTTGGGAGGCCAAGG | 81550 |
rs138830132 | in-del | -/GTGT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442383 | TTTATGTGTGTGTGT[-/GTGT]GTGTGTATTTATGTG | 81550 |
rs138842785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542979 | AGTAAAAGAGTGGAG[C/T]TGTTCTGTTTCCCTG | 81550 |
rs138843401 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510884 | CAACTATAATATGAA[C/T]GTATATCCTGAGTGT | 81550 |
rs138880873 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470573 | ACATGGGTAAAATAG[A/C]ATATCATTATAGTTG | 81550 |
rs138881319 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479952 | TTGCTTCTTTATCCA[A/G]CTTGCCATCGTATTC | 81550 |
rs138891963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498542 | CCTACATAATTTAGA[C/T]AAGCAGAAAGCTTCT | 81550 |
rs138893992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60570330 | AACATCATTAATCAT[C/T]AGAGAAATGCAAATC | 81550 |
rs138947185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484027 | TAGTTATATTGTTGA[C/T]GTTTGCGAGAGCTGT | 81550 |
rs138966485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523125 | TATATTAGGATCTTA[A/G]TAAATATTAAGGCAT | 81550 |
rs139039366 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568412 | AGGTATTTTTCTTAC[A/G]GCATGGAATAACTGG | 81550 |
rs139044560 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468930 | TTTGTAAAGTCAGCC[A/G]AAGGCCTAAGCAATA | 81550 |
rs139095543 | in-del | -/A | 0.0170251 | 0.090679 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427986 | CAGAAGTCTGAAATC[-/A]AAATGTCTTTGGAGC | 81550 |
rs139103194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540525 | ATTCCATATGCATAA[A/G]TGTTACCTTAAAATT | 81550 |
rs139113445 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480537 | GCATGTTGACCTGTC[C/T]AGTGAGATTTGGAAA | 81550 |
rs139144671 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428854 | GAGTCTGGAGTTTAA[A/G]CAGATAAGGGAGTAT | 81550 |
rs139150822 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447428 | ACTACTCCCTTACAA[C/T]ATTGAAGACATAAAT | 81550 |
rs139152838 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532367 | ACTCTAAATAGATTA[C/T]ACCACCCTTAACCAT | 81550 |
rs139183678 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571983 | CTGGACACTGTCATA[A/G]CTGTTAAGACAGCTT | 81550 |
rs139222173 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420133 | GTGTATAAGAAGTAT[G/T]ATTTTTTCTACTTGT | 81550 |
rs139259357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568554 | GTGTGCTTATAATTA[A/G]AGCAATTTTAAAGGT | 81550 |
rs139272347 | snp | A/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528965 | GAATCCAGTTCGAAG[A/T]AATAGTTTCATTGGT | 81550 |
rs139298209 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465018 | CTGATTTGATCATTA[C/T]ACATTGTATATATGT | 81550 |
rs139310467 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531197 | CCAGCAGATTTGGAA[A/C]TATTTCACATGGCCA | 81550 |
rs139365097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412784 | CTGTTAGTGGTCTTT[C/T]AAAATGGTTTACCTT | 81550 |
rs139395811 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523615 | AGAGTCTTGCTCTGT[A/C]ACCCAGGCTAGAATG | 81550 |
rs139444819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503323 | TTGAGAAGGAACAGA[A/G]CAAGACAAGAATTGT | 81550 |
rs139452268 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437072 | ACTGGCTTTTTTTAA[C/T]GAGATTATCATATCA | 81550 |
rs139458398 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512208 | GAGAGCTTGTGGAGA[G/T]AAACCCTTATAAAGC | 81550 |
rs139458605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425887 | ACATTTTCTTTTTAT[G/T]GTAGGAATATAGTAC | 81550 |
rs139462915 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504034 | ATTTATGAAAAGATC[A/G]TATACTTTTTTGAAT | 81550 |
rs139499753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485026 | TGAAAAAATTCTTGT[A/G]TAGCATCTTGCAGCC | 81550 |
rs139533371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441975 | GTGAATTACATTTTT[A/G]GTTAGGGAGTGGTCC | 81550 |
rs139537183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545480 | GATATTAGAAGTCAG[C/T]TTAATTTTAGTTCAG | 81550 |
rs139538845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551784 | TCAGGAAACTTACAA[C/T]ATGGTAAAAGGTGAA | 81550 |
rs139568692 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424535 | TACAAAAATTATCTG[C/G]GCATAGTGGGATGCT | 81550 |
rs139573185 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | TDRD3 | GRCh38.p7 | 13:60573396 | GTACTTTAACAAAGT[C/G]TAAAAAAAAAATTTA | 81550 |
rs139574259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499733 | CCAGTGGTGTGGGGC[A/G]TGTTGAGATATTCGT | 81550 |
rs139598080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433477 | TTTGCTCTCCCAGTG[C/T]GTACAAAGTGACCTA | 81550 |
rs139602135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553279 | TTAGAAATTTCTTCA[C/G]CCAGATACCCTAAAT | 81550 |
rs139682031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566069 | TCTTCTTTCAGTGAT[A/G]ATAGGCCCCTCAGGA | 81550 |
rs139682863 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TDRD3 | GRCh38.p7 | 13:60442532 | GGACCCAGTCATCGT[C/T]CTAGCAATCCTGATA | 81550 |
rs139693182 | snp | A/C | | | intron-variant, missense | TDRD3 | GRCh38.p7 | 13:60527446 | CCTTGGGGAAATATA[A/C]GAATAATTACAGCTG | 81550 |
rs139730942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416337 | TACAAAACAGTGATT[A/G]TTGAAAGATGGTGAT | 81550 |
rs139739868 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481682 | TTAATAGCTGTTTAA[C/T]GCCCTATTTATTAGT | 81550 |
rs139746857 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555004 | GATACATGTCATTCA[A/G]TTTTCCTTTATCTAA | 81550 |
rs139774059 | snp | A/C | 1.6799e-05 | 0.00289814 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485884 | CTGTCAAACCTACAA[A/C]TGATAATGATGAATT | 81550 |
rs139779281 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560546 | TTACATTATATTAAT[G/T]TGTAGATCTTAGTGA | 81550 |
rs139844225 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402257 | GAGACACACCTTTTT[C/T]CCAGGAGATTGCTGG | 81550 |
rs139869242 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414183 | GTTTTTTTTTAAGTC[C/T]AGATACATTTTTTTT | 81550 |
rs139879259 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497024 | TCAGCTCAATTAGGA[C/T]GAACCGGGGACTTAG | 81550 |
rs139908945 | in-del | -/AT | 0.0225045 | 0.103662 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427019 | TTTATGTATTTAAAC[-/AT]ATTTGTATATTAAAA | 81550 |
rs139943757 | snp | A/G | 0.000544218 | 0.0164867 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528611 | TTCAGTATCTGAAGT[A/G]TGGGCTGAAGACAGA | 81550 |
rs139958389 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465558 | ATTGCTTTATTGAGA[C/T]AGCATTGGTGTATAA | 81550 |
rs139959140 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488881 | CTACCATGCCTGGCC[A/G]GGTTTATTTTTTGTT | 81550 |
rs139960412 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533121 | GGAGAGATAGGAAGG[C/T]ATAACAAGAATTCTA | 81550 |
rs139993292 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539084 | CCTTAACATACAATA[C/G]ACATCATCTTGGCCA | 81550 |
rs140012693 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531622 | GAAATCCCACAAAGA[C/T]CATACCCTGGGTAGT | 81550 |
rs140016836 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408276 | TCTTCCCAGTCCCAG[A/G]TATGTCTTTATCAGC | 81550 |
rs140033641 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561471 | GAAAGTGAGGAAGAG[A/G]AAGCCAAAGGGGTAC | 81550 |
rs140039522 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551966 | CCAGGTCTCTCCCTC[A/G]ACATGTGGGGATTAC | 81550 |
rs140053317 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468109 | CCTTCAGCATAGTTG[A/T]GATGCTTTTATTTCA | 81550 |
rs140103902 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546505 | TTTAGAAATAAAAAA[C/T]ATATATCTCAAGGTG | 81550 |
rs140106937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569816 | CCAAGAACATACATT[A/G]GAGTGATGATAGTCT | 81550 |
rs140129317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398564 | GAGGGATATAATCAC[A/G]ACTGTGCTTTGAAGA | 81550 |
rs140154693 | in-del | -/AT | 0.0333695 | 0.124785 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559085 | TAGGTAAACAAACTC[-/AT]GTGTTTTGAATAGAA | 81550 |
rs140167492 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443076 | ATGAACTGTTAGTTA[C/T]ATTATTGATATGATG | 81550 |
rs140171103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564460 | TCTCAGAATCTTAGG[C/T]GAAGATGACATTGGA | 81550 |
rs140171845 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517103 | AGCAGATATAAAGAT[A/G]CATTAATGGTTGATG | 81550 |
rs140176779 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461824 | GGAGTGGGGTTAAAA[C/T]ATGAGTAGGTATTTT | 81550 |
rs140199580 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450309 | ATTAATTTTTAAATA[C/T]GAATATTCTCATTGC | 81550 |
rs140203803 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520005 | TCATTTATAACAGCA[C/G]TAGTCTTATGCTTTA | 81550 |
rs140210621 | snp | C/G | 1.65228e-05 | 0.00287422 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529057 | CAGGACCTGTCACAG[C/G]TGTACCCTGTGATGA | 81550 |
rs140236521 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498019 | AATAGTTTATTTGCT[C/T]GGTTAGCTGAAATGT | 81550 |
rs140281059 | in-del | -/TGA | 0.00993419 | 0.0697739 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457210 | TACTAACTTAAGGCT[-/TGA]TGATTCAAATTAAGA | 81550 |
rs140288108 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474377 | GTGGTAGTGGCCCCC[C/T]CCGGGCCCAGCTGTC | 81550 |
rs140313152 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411534 | TAAAAAAAATGCCCT[A/G]CCTTAATTAGGTTGA | 81550 |
rs140313332 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533698 | GTAATAGAGTATTCA[A/G]ATACCCTAGCTTGAA | 81550 |
rs140372024 | snp | A/C | 0.0123103 | 0.0775472 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421014 | CTATTTGACTGTCCT[A/C]ATGCCAATATCACAC | 81550 |
rs140376111 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524478 | CACCACTGTACTCCA[A/G]CCTGGGCCACAGAGT | 81550 |
rs140379632 | snp | A/G | 0.000148413 | 0.00861305 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528555 | GTTTTAGAAGGCAGT[A/G]GATTACCTAGAAATA | 81550 |
rs140389318 | in-del | -/AATTATATGCT | 0.0130921 | 0.0798413 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474613 | TTGTAAGACCCATAC[-/AATTATATGCT]TTCATGTACCCAGTT | 81550 |
rs140409472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405539 | ATCTGGAGAATGAGT[A/G]GTAACTGACTAAGTG | 81550 |
rs140420823 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547210 | AAAAAATCTCATGAC[A/G]TTGTTCACCACTTTT | 81550 |
rs140430933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472329 | TTTGGTAAAATACAC[A/T]TAACGTAAAATTTAC | 81550 |
rs140435253 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515091 | CTTACTTTCAAAGGA[A/T]TTCATCATTTACTTA | 81550 |
rs140453643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505716 | TTGAAAAACATAGCA[C/T]GAGAACTTTGTGAAG | 81550 |
rs140491719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60562166 | AAATATAAAAAAATT[A/G]TCTGGGTTTGGTGGT | 81550 |
rs140499945 | in-del | -/T | 0.194278 | 0.243711 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454140 | AGAATATTAGGTTTG[-/T]TTTGGTTACGGATTT | 81550 |
rs140514967 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443381 | TTGTAAAAAGCATAA[A/G]TCTAAAGCATTGTTA | 81550 |
rs140526741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552103 | TCCCAACAGTTCCCC[A/G]AAGTCTTAACTCGTT | 81550 |
rs140546093 | in-del | -/TTTAGA | 0.249886 | 0.25 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453487 | CTAGCAACACTTTCC[-/TTTAGA]TTTAATCAGTTGAAC | 81550 |
rs140556861 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472943 | TTAATGGAATTCAGT[A/G]TGGAAAGTTTTAATT | 81550 |
rs140560686 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500926 | CAGCCACACCTATTA[C/T]ATTCCAATGTGCCCA | 81550 |
rs140601300 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513320 | CCTAGGCCTCCTGGC[C/T]TGTGATGGGAGGGGT | 81550 |
rs140631568 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473783 | CTCCCTGGTCTAGCG[C/G]ACAAGGCCACTAGAG | 81550 |
rs140697725 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433881 | GATTTTACCTGCTTT[C/T]AAAGAAATGGATCAA | 81550 |
rs140703555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460188 | CAGGAGACCTTTTTG[A/C]AGTTTTCTCTTTTAA | 81550 |
rs140732555 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439365 | TGGTATTAACAGATA[C/G]TTAAGTCGAGATTAT | 81550 |
rs140758963 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419734 | CAGCAAACCACCATG[A/G]CACATGTATACCTAT | 81550 |
rs140769649 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498329 | CAAAATTTAACTGCA[A/G]TGGGAATAATTGGAT | 81550 |
rs140779004 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497164 | ACGGCGGGTCTGGGA[C/T]GGCGGTGAACAGCAG | 81550 |
rs140791617 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569031 | TGGAGTGCAGTGGCA[C/T]CATCTCAGCTCACTC | 81550 |
rs140818372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530120 | ATTACTTTTTAAAAT[G/T]TATGACAACTTGTAA | 81550 |
rs140843060 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457562 | GAGGCCAATATACAG[C/T]ATTTTCTTCGCAATC | 81550 |
rs140870765 | snp | A/C/G | 0.00219034 | 0.0330212 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567535 | AATAGGAGGAAGAAG[A/C/G]CACCTACGATCAAAC | 81550 |
rs140874111 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492892 | CTTTGTATTTTCTTC[C/T]GTTTCAAATAATTTT | 81550 |
rs140874948 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566951 | GAAGCTTTCTTTATA[C/T]GTAAATTGTATTCCT | 81550 |
rs140896701 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60570174 | TATCCATCTGACAAG[C/T]GCTTAATAACCAGAA | 81550 |
rs140911407 | snp | A/G | 0.000148516 | 0.00861603 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460474 | CACCAAGGATGCTGC[A/G]ATTACAGATGACTGA | 81550 |
rs140949744 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542378 | CTTCTATTGGGCATG[C/T]ATCTTGACACTCATG | 81550 |
rs140955457 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458709 | TGCTCTCCATATATA[G/T]AACACTTGAAATATG | 81550 |
rs140972634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407553 | CAACTGTTAAGAGAT[A/G]TAACTAGTGATAATG | 81550 |
rs140978375 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521370 | TTTGCCTGATTCTGT[C/T]GTAGCTAAGCACTGG | 81550 |
rs140988326 | snp | A/G | 0.00026407 | 0.0114876 | TDRD3 | 13 | allele_origin=G(germline)/A(somatic) | 13:60528469 | TGAGACATCCTCCTC[A/G]AAATGATACCAGGCA | 81550 |
rs141048261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433765 | TTACTAGTCCTCGTG[C/T]AGACATGGCTGCCCC | 81550 |
rs141087039 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410908 | ATTCATCAAAAGTCT[C/T]TATAAACATATTAAT | 81550 |
rs141125361 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519625 | AATAACTCATGGTTA[C/T]TAATGATTTAATGCC | 81550 |
rs141150836 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396715 | AACTCGATCTGCCCG[C/T]GGGGACTCAAAAAAG | 81550 |
rs141151164 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417291 | AAAGTGCTCGGATTA[C/T]AGGTGTGAGCCATTG | 81550 |
rs141196732 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563611 | TTAGAGGGAATAACA[A/G]CTCCTTCCAGGGATT | 81550 |
rs141203696 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426456 | ACTGTGAGATGATAG[A/G]TATGTTAATAAGCTT | 81550 |
rs141224859 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513105 | TCCCAATCCCCAATT[C/T]TTAACTTCTGTGCAC | 81550 |
rs141225172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445933 | GATTCTTGTCTGCTC[C/T]CTTCACTCTTTCAGA | 81550 |
rs141228321 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60439918 | GTAGTGATGATGTTT[A/G]TTGAATTTAATAATC | 81550 |
rs141233117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514325 | AAAGGCATTCAGTTT[C/T]AAAGGGAAAACACAT | 81550 |
rs141269594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474150 | ACTAAAAGTCTTTGA[A/G]ATGCATAGAAGAAAT | 81550 |
rs141288302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552455 | GTGGCTCTGCAGGGT[A/G]CAGCCCTTATGACTG | 81550 |
rs141321294 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434236 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATTGT | 81550 |
rs141334191 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491109 | ACAAGAGCAAAACTC[C/T]ATCTCAAAAAAAAAA | 81550 |
rs141334294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443844 | TTATTATGCTAATCT[C/T]ACTATCTCAACCATC | 81550 |
rs141415202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427853 | TAAATCAATACTTCT[C/T]AAGTAATTACTGGAA | 81550 |
rs141427579 | in-del | -/TTTTC/TTTTCTTTTC | 0.337182 | 0.278841 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567344 | TTTTCTTTTCTTTTC[-/TTTTC/TTTTCTTTTC]CCTTCCCCTTGCCTC | 81550 |
rs141430048 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557742 | ATCTCTCCTACCACT[C/G]CAAGTTTTAGTACTT | 81550 |
rs141452375 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567294 | CTTACCACTATAAAT[A/G]ATGTTTTTCTATTAC | 81550 |
rs141466132 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499467 | GAAATATACCTTTAC[C/T]GTCCTTCCTCAGGGG | 81550 |
rs141478571 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487231 | CCAGGTGCAGTGGCT[C/T]ATGCCTGTAACCCCA | 81550 |
rs141574581 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568482 | AAAAGAATATGTAAG[A/G]ACTTTGGCAACTTTG | 81550 |
rs141598502 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456472 | GGTGCAATGATACAT[C/G]TTTCTAAGCCACTAA | 81550 |
rs141601692 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406179 | GAGAAGACTGGGCTA[C/G]AGATAAATTTGGAGT | 81550 |
rs141606465 | snp | A/G | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484927 | TTCTTAAGACTTTGA[A/G]GTGTGTTTTATAGCT | 81550 |
rs141617380 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404732 | GCCTCAGCCTCCTGA[A/G]TAGCTGGGATTACAG | 81550 |
rs141714979 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552878 | TTAGCCATGGCTGGA[C/G]CTGGGGTGGCTGGGA | 81550 |
rs141736791 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435246 | TGGTTTTGTTATGTT[C/T]AGAAAACCTTTTATA | 81550 |
rs141762044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422943 | GTAAATCCACACATT[G/T]AAAGTATGTCAAGTG | 81550 |
rs141767298 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424566 | CCTGTAGTCCCAGCT[A/G]CTCCGAAGGCTGAGG | 81550 |
rs141769328 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503050 | TTAAAGGCTGTAAAT[A/C]GTTCAAAATAAGTTT | 81550 |
rs141769371 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548005 | ACTGCTCCATTAGTT[A/T]GTAAGGTTGACTGGG | 81550 |
rs141809328 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479679 | AATCTGGGTGCTCCA[A/G]TGTTGGGTATATACA | 81550 |
rs141837501 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566861 | CTTGAACTGGTAGAT[-/A]ATACCCACTCAGTAA | 81550 |
rs141838930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535507 | CCAAAAATTTGTATG[C/T]GTGAAATGGGTTTTT | 81550 |
rs141881530 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464376 | AAAAATAGAAATACC[A/G]TATGATACAGCAGTC | 81550 |
rs141892423 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531793 | CCAGTACTTATCTGC[A/C]GTGTCTAATATCCTT | 81550 |
rs141909803 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469621 | GTTCTTTTTGGCTTT[A/C]TAGTTTTTGATTTGG | 81550 |
rs141984369 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423979 | CAAATAAGCCAAAAT[C/G]CTGATGTTTTCTCTC | 81550 |
rs142004008 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526911 | ACAATCTCGTCTCAC[C/T]GCAACCTCCATCTCC | 81550 |
rs142016546 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470686 | CCTCCCAGGTTCAAG[C/T]GATCTCCTGTCTCAG | 81550 |
rs142027812 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469456 | CACACACACACACAC[A/G]GAGTTTAGTAGTAGT | 81550 |
rs142077526 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506871 | ATTAGCCTTAAATGT[A/G]AATGGGCTAAATGTC | 81550 |
rs142103465 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523244 | CTGCTTCTGGAGAAT[A/T]TTCTGCAAAAAAGTA | 81550 |
rs142141071 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457882 | GTCTGTGTTTGTTTC[A/C]CCTTCTCTTCTAAGG | 81550 |
rs142148393 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402637 | CTTTTGGAAAGGATT[C/T]GAATCATTAAAACAC | 81550 |
rs142166836 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526445 | CTCATTTGTGTCCTG[A/G]TTATGGTCACTGCTA | 81550 |
rs142172295 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483667 | GCCTTTTTTTTTCCT[A/G]TTTCTTATAAGAATC | 81550 |
rs142175955 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399987 | TCAGTATTTTAAAAT[A/G]TAACTTCAAAAGTAG | 81550 |
rs142176068 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524368 | AAAAATTAGCCGGGC[A/G]TGGTGGTCTGCACCT | 81550 |
rs142206040 | in-del | -/A | 0.224116 | 0.248656 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509311 | CTCAAGTACTAGTTT[-/A]AAAAAAAAAGCTCCT | 81550 |
rs142217780 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468583 | TATCTGTTGAACAAT[A/G]TGTAGATACTGTGCT | 81550 |
rs142249025 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486456 | TTATCTTTACATTAT[A/G]TGTCTATTTACACAC | 81550 |
rs142281253 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443323 | AAGGCGTACAACGTG[A/C]GGTACGGTTTATATT | 81550 |
rs142330578 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420892 | GAGCTTGCAGTGAGC[C/T]GAGATCACGTCACTG | 81550 |
rs142331195 | in-del | -/T | 0.217851 | 0.247924 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456610 | ATTGGTATTTTTTTT[-/T]ACTTTGGAGTTGCTC | 81550 |
rs142362278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405945 | ACTTTTTGACAGATT[A/G]GACATGAATGTGACA | 81550 |
rs142385020 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554413 | TTAATTAATAATCTC[C/T]AGTCTTACACATTGC | 81550 |
rs142394753 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452866 | CTTATTACTGTTATC[A/T]GTTCTTAAATTGTTG | 81550 |
rs142410886 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60437846 | CTAAAATTGGTCTCA[A/G]CCTATACTTATCTCT | 81550 |
rs142418820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512660 | CCCATGCAAGTCCGA[A/C]ATCCAGCATGTTAGT | 81550 |
rs142421131 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540989 | ACTTTAATTACAATT[C/G]ATAAAATAATTTAAG | 81550 |
rs142445454 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488114 | AGGAAAGAAGGCTTT[-/A]TTTGGGTGCTACAGC | 81550 |
rs142449214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522758 | TCTGGCAGTCCTAGC[A/G]TCCAAATGTATTTTT | 81550 |
rs142496017 | in-del | -/GG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462276 | TCTGATTTTATGGCT[-/GG]GTATATTTCTCTGAG | 81550 |
rs142502900 | in-del | -/G | 0.0221141 | 0.102801 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434692 | TCTCCATTAGAGAGT[-/G]GAAAAAAAAAAGTGT | 81550 |
rs142518639 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471906 | AACTTTTAATATAGT[A/G]TTGAATGGAAGTGAT | 81550 |
rs142519713 | in-del | -/T | 0.38555 | 0.210062 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420381 | GATCAATTTTATCAG[-/T]TTTTTTTTTCTTTTA | 81550 |
rs142523796 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544883 | TTAAATCTTGATAGT[A/G]TCAGAATTTTAAGTT | 81550 |
rs142547326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508205 | TGCCCAAAGTAATGT[A/G]TAGATTCAGTGCTAT | 81550 |
rs142587224 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468113 | CAGCATAGTTGAGAT[A/G]CTTTTATTTCAAATG | 81550 |
rs142587268 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511069 | TATAATCTTATATAA[A/C]TTATTTTGCTTGTGA | 81550 |
rs142600061 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491182 | AAATTGGCAGGTTAG[A/G]GTTGCTTGCCTTGAA | 81550 |
rs142666896 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424774 | TCAAGAACATTTAAC[C/T]CGATATGCATTGGCA | 81550 |
rs142679665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551104 | GATGGAAAGCCTTTC[C/T]TTTTGGTCTACTTAT | 81550 |
rs142692737 | in-del | -/TT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484119 | AGAGGGTTTTTTTTT[-/TT]GAGGGAAATTCAAAA | 81550 |
rs142696817 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60529832 | AGAAGGAAGGAAAGA[C/T]AGAAGATGAGGGCAA | 81550 |
rs142710872 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480307 | CTTTTCTTTAAGGAT[A/T]TTGAAAATAGGCCCC | 81550 |
rs142714803 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553026 | ATGCCCTAGAGACAT[C/T]TTCCCCATTGTCTTG | 81550 |
rs142755705 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452412 | ATTCTTATATATTCT[A/G]TTCTTCTTCTTATTC | 81550 |
rs142759983 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520650 | TGTCTGCCTCTGCCC[A/G]TTATAACTAAGCTCC | 81550 |
rs142796239 | in-del | -/T | 0.0248432 | 0.108648 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440033 | TGATCAGTCATAGAC[-/T]TTTTTTAACATTTAC | 81550 |
rs142820351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399020 | AACATGACCCCCCCT[C/G]CTTTGGAAAGATTAG | 81550 |
rs142838090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505938 | GACAGGAAGAATGGA[A/G]CCAAGTTGGAAAACA | 81550 |
rs142838792 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428505 | AGCAGAGGCATGCAA[A/G]ATTAATTTTATCGTG | 81550 |
rs142861115 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466974 | TCAAATGTGTGTGTG[-/T]TTTTTTTGTTTTTTT | 81550 |
rs142873078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565354 | GCCACCGCGCCCGGC[A/C]GTCAGTATCTTTTTT | 81550 |
rs142878043 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484519 | ATCTGTGTTTCCATA[A/G]TAAGGTTTATCGTGT | 81550 |
rs142892490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414473 | TTACAGGAAAAGTTA[C/G]CCAATCTCTGCCCTA | 81550 |
rs142912148 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564274 | CAAGGTGGTCGGGAT[A/G]CACCTTGGTTTTATA | 81550 |
rs142914256 | in-del | -/T | 0.244205 | 0.249933 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436140 | GCTGATTTGTTTGAG[-/T]TCCTTGTAGATTCTG | 81550 |
rs142915926 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488639 | AGTGCAGTGGCGCGA[A/T]CTTGGCTCACTGTAA | 81550 |
rs142933008 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475251 | CCTCCCACCCTTCTC[C/T]CTTAAGCAGTCCCCA | 81550 |
rs142944849 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440932 | TCTAACGTTAAAAAA[C/G]TTACTTAAATTTATA | 81550 |
rs142950105 | snp | A/G | 0.00039655 | 0.0140754 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529077 | CCCTGTGATGATAAA[A/G]TATTTTACAATAGTG | 81550 |
rs142954788 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, missense | TDRD3 | GRCh38.p7 | 13:60527452 | GGAAATATAAGAATA[A/G]TTACAGCTGCATGTT | 81550 |
rs142979700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448900 | AATACTTTCTTATCA[A/G]TTCAGCTACTCGAGG | 81550 |
rs143015163 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563372 | AGCATTTACATCTTA[C/G]GGGTAGAAGCAGAGG | 81550 |
rs143022203 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531250 | TGAAAAGCAGATGCA[G/T]GTGGTCTTCACTATC | 81550 |
rs143022503 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463157 | ATCCCAGCACTTTGG[A/G]AAGTCAAGGCGGGCG | 81550 |
rs143042273 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445220 | ACACACATATGTATT[C/T]GTGTTATGAATTTTT | 81550 |
rs143103343 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572625 | AAGCAGTTAAATAAA[C/T]GCTGACTCACTTGGA | 81550 |
rs143150885 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440541 | CAAAAATTAGCTGGG[C/T]GTGGTAGTGTGTGCC | 81550 |
rs143154333 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513612 | ACATGTTGTGGGAGG[C/T]ACTCGGTGAGAGGTA | 81550 |
rs143158395 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474050 | GATGCTGTACTTCAG[-/T]TGGTCACGCTCCTGA | 81550 |
rs143193996 | snp | A/C | 1.65373e-05 | 0.00287548 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529000 | CAAATGGAGAAGTAG[A/C]AATGCCACTGAAAGG | 81550 |
rs143199438 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465729 | AGGCCAGTGATATTA[A/G]CATTCTTACTGGTTT | 81550 |
rs143250930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473498 | CCAAGGCAAGAGACC[A/G]AGGGCACAAACTGTT | 81550 |
rs143259184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546748 | AAATTAGCAAAATCA[A/G]CCCTTCCTAAGTTTA | 81550 |
rs143298497 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413075 | CCTAAGTACCCAATA[A/T]ATATGAACTAATAGG | 81550 |
rs143300540 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466677 | CCTGTAATCCCAGCT[A/G]CTCGAAAGGCTGAGA | 81550 |
rs143330992 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420939 | ACAGACTGAGACTCC[A/G]TCTCAAAAAAAAAGA | 81550 |
rs143364469 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420281 | GTCTTAAAATACATA[G/T]GCTATGAATGTTTTT | 81550 |
rs143376487 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559439 | AGCTTTTGGAATCTA[A/T]TTAATCTTTAGAAAT | 81550 |
rs143388282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426857 | GGGAACGTCACAGAG[C/T]GTTCTTACACAAACC | 81550 |
rs143398047 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531037 | CTAGATGGCATAGGC[A/T]TTTAAGATTTTTGTG | 81550 |
rs143429722 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522683 | TAGCAATCCAATTTT[A/C]AATAGAAGTTTAGGT | 81550 |
rs143438543 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441729 | TTGGGAGGATAATCC[A/G]TGAACAAGTTTTCTT | 81550 |
rs143464662 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400427 | CACGGGGTACCTAAT[C/G]AGTTGTGTTTTTGTT | 81550 |
rs143481616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539097 | TACACATCATCTTGG[C/T]CAGTAATTCTGGAAG | 81550 |
rs143498762 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533804 | CCTGAATGGGATGAT[A/C]TGTACTGAAAGATTG | 81550 |
rs143523519 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553974 | CAGAATGAAAGAACC[A/G]TGCTCCTTTAAGATA | 81550 |
rs143529298 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409443 | AACACCAGCCTGTGA[A/G]AGCAGCTGGGAGGAA | 81550 |
rs143565580 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478825 | TTTTTTTTTTTTGAG[A/T]TGGAGTCTCACTGTG | 81550 |
rs143596337 | in-del | -/A | 0.191147 | 0.242974 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533640 | GGACGACTCTGTCTC[-/A]AAAAAAAAAGAGAGA | 81550 |
rs143629382 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517105 | CAGATATAAAGATAC[A/G]TTAATGGTTGATGGG | 81550 |
rs143674340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508689 | AAACCTAGGCAATAC[C/T]ATTCAGGACATAGGC | 81550 |
rs143715582 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518739 | TGCTTTCTTAGACTA[A/T]TAATGTATCCAGCAC | 81550 |
rs143751086 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481227 | ACATGGTTGGTGTGC[A/G]TTTTATCCTGTTTGG | 81550 |
rs143752990 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526502 | CAGTAAACAATGCCA[A/G]CAGAAACTAAAAGTG | 81550 |
rs143824554 | in-del | -/T | 0.21695 | 0.247806 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530448 | AAATATTTTAAATAA[-/T]TTTTTTTTTGAGACG | 81550 |
rs143827720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571087 | TTTTGGATTCCTGAC[A/C]TCAATAAAAAAAAAT | 81550 |
rs143838946 | in-del | -/GTAATTTTGTTCTA | 0.0271762 | 0.113356 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492307 | TTCCAGACTTTTCAG[-/GTAATTTTGTTCTA]GTATATTAACCAAAA | 81550 |
rs143848004 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499364 | CTCCTGGTACCTGGT[A/G]TGTAGTCATTGACTT | 81550 |
rs143861758 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571345 | ATATATTCTTGAGAT[A/G]AAAGATATTTGTTTC | 81550 |
rs143883870 | in-del | -/A | 0.24449 | 0.249939 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404237 | GATATTTGGCTAAGG[-/A]AAAAACAAGGCACAT | 81550 |
rs143900181 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520382 | AATTAATGTTGATTA[C/T]GGCTTTACTTAGAAG | 81550 |
rs143905316 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550609 | ATGAACATTTTGTGA[A/G]TGACAAGATTCTTAG | 81550 |
rs143915504 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554007 | AATATTGGTTGCAAA[A/G]TTATAAAGATTTCAG | 81550 |
rs143942179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398685 | CCAAAATGACATAGC[C/T]AGAAAGTGGTGGAGT | 81550 |
rs143952293 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437220 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCAATTAT | 81550 |
rs144000769 | in-del | -/GC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402690 | TAGAGGAAACCAATT[-/GC]TTTTTTTTTTTTTTT | 81550 |
rs144008118 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500036 | CTAGTTGGAGCCTTT[C/T]GCAGGCCGCCATAGG | 81550 |
rs144047424 | in-del | -/TGTGCACGTGTA | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549583 | TAAGACACGTGTGTG[-/TGTGCACGTGTA]TGTGCACGTGGACAA | 81550 |
rs144068148 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459779 | GTGCATGCCACCATA[C/T]CCAGCTAATTTTTGT | 81550 |
rs144076612 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465289 | TGCTTATTTTTATTT[A/G]TCCTTGTACAATGAC | 81550 |
rs144139208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462581 | AACCAGGTGCTAATA[C/T]GGATGTGTTACCTTA | 81550 |
rs144149186 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461463 | GCCATTCTGAGCTCT[G/T]TTTTCTGAGGTGGAA | 81550 |
rs144150083 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506760 | AAACAAACAAACAAA[A/C]AAAAGAACATCGACA | 81550 |
rs144221652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555148 | GGAAAGAGAATAATT[A/C]TTTTTAAAAGAGAGC | 81550 |
rs144223642 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481711 | GTTCATCATCTTTGT[C/T]ATCTATGGCCCAGTT | 81550 |
rs144224914 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431690 | CTGAGCAACAAAGCA[A/G]GACTATCTTTACCAA | 81550 |
rs144225138 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523791 | CATGTTGGCCAGACT[A/G]GTTTTGAACTCCTGA | 81550 |
rs144284013 | snp | A/G/T | 0.000348598 | 0.0131983 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528961 | ATCAGAATCCAGTTC[A/G/T]AAGTAATAGTTTCAT | 81550 |
rs144292271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467823 | TCTCATTAGCTAATA[C/T]TTTTCCCCATTTATA | 81550 |
rs144295439 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537542 | CTTTTTAAAAATTTT[A/G]GTAAGAGGAAACTGT | 81550 |
rs144303389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472533 | TTGGCGAAGATGTGG[A/G]AAAATTGGAACTAAG | 81550 |
rs144311670 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545796 | ATGGAAAAAGGAGAC[A/C]TATCAAGGGGTTGAG | 81550 |
rs144320584 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60495404 | TGCAGAGCCAGCTAT[C/T]GTGAGAGACTGGAGT | 81550 |
rs144323191 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412542 | CTTGTTGGTTTAATC[A/T]TGCTGATAACTAGTA | 81550 |
rs144357988 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480782 | AGTGAGGAGGGCCCC[A/C]CAGGCAGGGGGTATT | 81550 |
rs144439295 | snp | A/G | 0.00226748 | 0.0335946 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529121 | ATCTGGGCCAATTAA[A/G]CCAGAAAAAATACTA | 81550 |
rs144444017 | in-del | -/TT | 0.0178098 | 0.0926698 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516399 | TTTCTCAGCATTGAC[-/TT]TTTGTTGTTATATCT | 81550 |
rs144451576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487060 | TATTTTGGTGGGGGC[A/G]GGGAAGGATGGTTGC | 81550 |
rs144467722 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512165 | GGAGGAACAAGTCAC[A/C/T]TATTATGTAGGTGGC | 81550 |
rs144501318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560915 | AGGTTTTGGATCTGA[G/T]TTTTCTTTTGTCTTC | 81550 |
rs144503302 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486014 | TAGATTATTTGTGAT[C/T]GTTATTGTCTTTTCA | 81550 |
rs144553916 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452596 | TTCATTTAGTGTAAT[-/A]TTTTTTAGGATAATC | 81550 |
rs144565593 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406110 | TGTGAGGTCCCTTTA[A/G]GTCATCTAAAATAAG | 81550 |
rs144567516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461559 | CACTCACGTTTGCAG[C/T]TCGGGCTCCTCTAAG | 81550 |
rs144576630 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403903 | GAGAAATATGTAACT[C/G]TATACAATAATATGT | 81550 |
rs144578928 | snp | A/C/G | 6.60266e-05 | 0.0057454 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460495 | AGATGACTGATGGTC[A/C/G]TATAAGTTGCACAGC | 81550 |
rs144612384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471796 | GGAGTTTTCTACATA[C/T]AAGATCACGTTATCT | 81550 |
rs144613938 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410972 | AAAGTTTGTATATGC[A/G]TATATTAAAAACATA | 81550 |
rs144638580 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407647 | TAACATTTCTTTGCC[C/G/T]GAGACAACCAGCTGT | 81550 |
rs144667896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458741 | CTAGTACGATTGAAC[A/G]ATTTTTAATTTCACT | 81550 |
rs144671325 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489899 | TTGATTTACATTTAT[C/T]TCAAATGAACTTTTC | 81550 |
rs144675154 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565106 | TGTCGCCCAGGCCGG[A/G]GTGCCGTGGCACTGT | 81550 |
rs144684564 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525897 | ATTTTATATTTTCCT[A/G]TTAATATAGTTCTCC | 81550 |
rs144717742 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457689 | TCTCACAGTTTTGTA[C/G]GCCAGAAGTTTAAAA | 81550 |
rs144738089 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502046 | TATAGCAGTTCCCGC[A/G]AGTGTTGTGTAGTAC | 81550 |
rs144749295 | in-del | -/GT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484531 | ATAATAAGGTTTATC[-/GT]GTGTGTGTGTGTGTC | 81550 |
rs144766896 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458983 | ATTAGCAGCTTATCT[A/G]TACTTGTTAACAGTT | 81550 |
rs144776344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560288 | AAGGATTAAATAAGA[C/T]AACATGCAAAATGCC | 81550 |
rs144800646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406258 | AAGGCTGCAGCTGTC[C/T]GGTATGGTGGACATT | 81550 |
rs144810108 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515704 | ATTGTAAAATAAACA[A/G]ACAAACACAAAAACA | 81550 |
rs144810999 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TDRD3 | GRCh38.p7 | 13:60442418 | GCATATGTATGTGTG[C/T]GTGGGTAGGTAGATG | 81550 |
rs144824396 | in-del | -/CT | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544824 | GTTCATGCAAAGGAA[-/CT]CTATAAATAATCAAT | 81550 |
rs144884403 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421688 | TATGTGAGCACAGAG[A/G/T]ATGTGGAAACTATCA | 81550 |
rs144919764 | snp | A/C | 9.90181e-05 | 0.00703557 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528483 | CGAAATGATACCAGG[A/C]AGCCAAGAAATGAAA | 81550 |
rs144949686 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513272 | CACATAGCATGGGGA[C/T]CCTGGGCCCAGCCCA | 81550 |
rs144957455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540593 | GATAGCTAAGCCTAA[C/T]GGAATATTATGAAAA | 81550 |
rs144984414 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437219 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAATTA | 81550 |
rs144989006 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497409 | CTGTTTTTGCCTAAT[C/T]AGCATTTTAGTGAGC | 81550 |
rs145050463 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434968 | GTTACTGTGTTACTG[A/G]AGTTCTTGAAGCACA | 81550 |
rs145101844 | in-del | -/AACA | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490132 | TGGAGGCTTAAAACT[-/AACA]AACAAACTTGGGACT | 81550 |
rs145102458 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568002 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGAG | 81550 |
rs145111242 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433478 | TTGCTCTCCCAGTGC[A/G]TACAAAGTGACCTAA | 81550 |
rs145116408 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532794 | ATTAGTTTCCTTGCC[C/T]GAAACTTTATTCCTT | 81550 |
rs145129657 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507712 | AGGGAAAGACTGGCA[C/G]AAGACAAGGATGCCC | 81550 |
rs145135494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60570193 | TAATAACCAGAATAT[A/G]TAAGCTCAAACAACT | 81550 |
rs145212885 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498111 | AGAGGAAGGGATACA[A/G]TGGCTTAGGGAGATT | 81550 |
rs145212994 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455813 | TTGCCCACGCCTGTA[A/C]TCCCAGCACTTTAGA | 81550 |
rs145216668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486125 | GGATCTTACATATTT[C/T]ATTCATGTGTTCTTT | 81550 |
rs145218366 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569926 | AAATCAAAATGGATT[A/G]AATACTTAAGTCTAA | 81550 |
rs145219634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403103 | TGTTAAACTGTGCAA[A/G]TGTTCAGGTTTCAAG | 81550 |
rs145226488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518003 | AGTAAGTTTGAAATG[G/T]TCTGGTTTATGTTGT | 81550 |
rs145255222 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478594 | ACAGGCATGAGCTAC[C/T]GTGCCCGGTCCACAG | 81550 |
rs145263146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569105 | TCCCTAGTAGCTGGG[A/G]CCACAGGTGCACACC | 81550 |
rs145263308 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521463 | TAAAGCAGCTTTTTC[C/T]TAAAAAAAAAAAATG | 81550 |
rs145282376 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458511 | GTTGCTCCAGATATC[A/G]AATATTGGTAAAGTT | 81550 |
rs145354735 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567334 | AAAGAGTTTTAACAG[C/T]ATCCCTGCCTTTTTC | 81550 |
rs145357270 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493919 | CTTTTATATGCAGTC[A/G]GTAAGAAATGACATA | 81550 |
rs145425772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548521 | TGGAGCATAATAACA[A/G]TTACTCATATCATGA | 81550 |
rs145428850 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408620 | TTTGCCCCTGCCCTA[A/G]AGATTTGTGGAACTT | 81550 |
rs145444654 | snp | C/G | 1.65116e-05 | 0.00287324 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509896 | GCAATAAACAGAAAC[C/G]TGTTATGGGTCCTCC | 81550 |
rs145447586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465791 | TATGAGGTTTTAAGA[G/T]GTGAACAATGCAAAG | 81550 |
rs145458233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566980 | CTCCCCTATTCCAAA[C/T]CATTATTTTTTTCTG | 81550 |
rs145477811 | in-del | -/A | 0.219049 | 0.248077 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471986 | CCTTCACTATTGAAT[-/A]ATGATGTTAGTGGTG | 81550 |
rs145496491 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552604 | CAGTGCCCCAGTGGG[A/G]ACTCTGTATGTGGGC | 81550 |
rs145525685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504838 | GGAAGCACAAGGGGT[C/T]GGGGAACTGTCTCCC | 81550 |
rs145528145 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546593 | ATATGTGAATTTCCT[A/G]TCTATTCTAATGACT | 81550 |
rs145557435 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461317 | TTTCCTAGGAAATCA[C/T]TGGGAATGATTTTCC | 81550 |
rs145561227 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529322 | AGTCTTTTTCTACTA[C/T]TGTACCTGTTTAAAA | 81550 |
rs145590871 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408669 | TTTAAGGTATCTAGC[A/G]GAAGAAATTTCTAAG | 81550 |
rs145592346 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551796 | CAATATGGTAAAAGG[C/T]GAAGGAGAAACAAGC | 81550 |
rs145622279 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428013 | GAGCTGTTCTCCCTG[A/C]AGAGGCTTTAGGGGA | 81550 |
rs145623356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476227 | TTGCGTATGATGACT[A/G]GAAGGGGTCCAGTTT | 81550 |
rs145656803 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434077 | ACTTCTGAACACGAC[A/G]TGAAGACAGTTAAGT | 81550 |
rs145700891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547331 | TCTGCTCTGCTTGGC[C/G]TTTGAGAGAAGGGGA | 81550 |
rs145735216 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451442 | CAGCTTGTTCCAGCT[C/T]GTGAAGTTCATTGTC | 81550 |
rs145744558 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556942 | GGGTGCAGTGGCTGA[C/T]GCCTGTAATCCCAAC | 81550 |
rs145809200 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518785 | TCCAGACTTTACTAA[A/G]AGCCAAACCCAAAGG | 81550 |
rs145844139 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552085 | TCAAAACCAATCATG[G/T]CTTCCCAACAGTTCC | 81550 |
rs145875955 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433854 | ATAGCCAGTGAGTAA[C/G]TTAGATTCACCGATT | 81550 |
rs145876931 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508422 | GTACCAAAACAAATA[C/T]ATAGACCAATGGAAC | 81550 |
rs145920266 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483676 | TTTCCTATTTCTTAT[A/G]AGAATCTACTCAAAT | 81550 |
rs145966190 | in-del | -/TAAC | 0.0170251 | 0.090679 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537307 | ATCTGCATAAATAAT[-/TAAC]TTAGTTGAGAGAAAT | 81550 |
rs145966834 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401989 | AGTGATTATTGCACT[C/G]TTGTATTCAAGGGCC | 81550 |
rs145986579 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404991 | AGCTCTCTTTTTGCC[C/T]GCTGCCATTCACATA | 81550 |
rs145994363 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468197 | TTTAATTTTCAACTT[C/T]CTAAATTCTTCCACA | 81550 |
rs145995071 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538399 | TTTTTTTTTTTTTTG[G/T]CTGTCTTAAGGTATT | 81550 |
rs146012809 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470828 | CTTCAGGTGATCTGC[C/T]GGTCTCAGCCTCTAA | 81550 |
rs146013642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420900 | AGTGAGCCGAGATCA[C/T]GTCACTGTGCTCCAA | 81550 |
rs146013847 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TDRD3 | GRCh38.p7 | 13:60543456 | CTCCAAGAGAGATAT[A/G]TAATGTATGTGTTTC | 81550 |
rs146044240 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60449170 | GAAATCGGATGTTTT[-/T]AAAAAGAAAAGGAAT | 81550 |
rs146058508 | in-del | -/GA | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558337 | AATGACATAAACTAT[-/GA]GAGAGTGAAATAGTT | 81550 |
rs146111836 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449584 | CTTTGTGATTGAATA[C/T]GAGCAACTTATGTGC | 81550 |
rs146118466 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519996 | ATGATTTGTTCATTT[A/C]TAACAGCACTAGTCT | 81550 |
rs146132339 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398494 | ACCTACACAAGATCT[A/G]TATGGTTCGTGAAAG | 81550 |
rs146132351 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456285 | AATAAATTAACACAA[C/T]CATTTAAATCTGATA | 81550 |
rs146138266 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561296 | GGCAAAGGGAGAAAG[C/G]CTCTGAACTCAGAGC | 81550 |
rs146158889 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521892 | ACAAGAGTGAAACTC[C/T]GTTTCAAAAAAAAAA | 81550 |
rs146184529 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479852 | TTCTGTTTGCCTGAA[A/G]GATGTTTCTCCATCC | 81550 |
rs146232791 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424581 | ACTCCGAAGGCTGAG[A/G]CAGGAGAATTGCTTG | 81550 |
rs146251139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428740 | CACAGAGAAGACAGT[C/G]GTTCTGTCCAGGTGT | 81550 |
rs146258897 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540189 | TTTGGGAAACTTTCA[G/T]AGATCACCATGTGAG | 81550 |
rs146277418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544165 | AATCAAAAAAAGTGT[C/T]GGGTTGGGCATGGTG | 81550 |
rs146290843 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559931 | AGAAAATGGAAACTG[A/T]GGTGATGGATATGTT | 81550 |
rs146335060 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424447 | CTTTGGGAGGCTGAG[A/G]TTGGCGGATCACTTG | 81550 |
rs146355776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402923 | TTTTGAAATATTTTC[G/T]ATTTCTTTAATGAAC | 81550 |
rs146359439 | snp | A/C | 0.00168621 | 0.0289873 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485864 | AACATTGCAAGTTAC[A/C]ATGCCTGTCAAACCT | 81550 |
rs146380404 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520430 | CCAAGATCTTTGTAT[C/G]TGTTGTTCTCTCCTC | 81550 |
rs146398535 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523311 | CTTATGTACAGATTT[A/T]AATGATTTGTGACAA | 81550 |
rs146416598 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500131 | TCTTTTTTTGAGAGA[C/T]GGCTCTTGGCCTGTT | 81550 |
rs146437454 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461520 | CTCCCACCTGCCTTT[C/T]TTGGTCTTCTTTGTC | 81550 |
rs146447241 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501359 | TGTTCTGTCTACAGC[A/G]CCATTTGGAGTTTGA | 81550 |
rs146449864 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535220 | ATATCAAGCCCATTC[A/C]AACAGAGGCATGGGT | 81550 |
rs146464953 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60570103 | CCTACATAGCAAAGG[A/G]AACAGTCAACAAAGT | 81550 |
rs146518978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465407 | TCTTGAACGGTAATA[C/G]ATGGTTACTACATTT | 81550 |
rs146535507 | in-del | -/TTTTGT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561859 | TACTATGGGCCCAGG[-/TTTTGT]TTTTTTGTTGTTGTT | 81550 |
rs146543485 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555698 | ATATGTGATAAATTG[C/T]TCTGATGAGTATCAT | 81550 |
rs146546703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399775 | GGACACACTATTGTT[A/G]AATCTGTTCTATAGG | 81550 |
rs146584881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552224 | TAGTTACTTTCAAGA[C/T]ATAATGGAGGTACAG | 81550 |
rs146637239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443060 | TAATGTAAATGTTTT[C/T]ATGAACTGTTAGTTA | 81550 |
rs146639278 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516907 | ACCACAAATTTGATC[A/G]CACTACCTGCTGGCT | 81550 |
rs146662589 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533367 | TATTATTGGCTGGGC[A/G]CAGTGGCTCATGTCT | 81550 |
rs146674297 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496614 | CATGAGAGGCAAGGA[-/G]GTTTAGTGACTCTAT | 81550 |
rs146676977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418889 | TATTCTTGTCTGTAT[C/T]GGTAGTTCATTTTTT | 81550 |
rs146703330 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530590 | GGACTACAGAAATGC[A/G]CTACCATGCCCAGCT | 81550 |
rs146756376 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420983 | GTATTTTGTGGGTCT[A/G]TATTGTTTTATTATT | 81550 |
rs146785006 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517473 | TTGATGGAAATCTAT[A/G]GTAGAGTGCCTGTTT | 81550 |
rs146825783 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513293 | GCCCAGCCCATGAAA[A/C]CATTTTTTCCTCCTA | 81550 |
rs146842278 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469526 | CACTTGACTTCCTGC[A/G]AGCCACATTAGTATT | 81550 |
rs146865373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476174 | TTTTATTGTTTTAGA[C/T]GTTACATTAAAGTCT | 81550 |
rs146881440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398771 | GTTATTGTTGTTACA[G/T]TTTTTTCGCAGAACA | 81550 |
rs146884338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481650 | TTATGTTTTCTTTTA[A/C]ATACTTACACATAGT | 81550 |
rs146905366 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505630 | AGGAAGCTAAGAAAC[G/T]TGAAAAAAGGTTAGA | 81550 |
rs146906603 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462661 | CCTCCTGCCCTGCCC[C/G]TTGCTAGTTTTTATT | 81550 |
rs146943332 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558101 | GCTGGGATTACTGGC[A/G]TGAGCCACTGCACCC | 81550 |
rs146975776 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443974 | AAAGAGGACACAGTC[A/G]TAAAATATTCTGCTT | 81550 |
rs146992052 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452993 | TTTTAGTTTGATTCA[C/T]TTATTTTTCTTCTAC | 81550 |
rs147012856 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60562329 | CTTCCCCCCACCCCC[A/G]GCAAAAAAAAAGAAA | 81550 |
rs147032881 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421194 | ATTAATAAAAAAAAA[-/A]GAGGTTTAATGGACT | 81550 |
rs147049121 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536216 | CAAAAAACCTAATAG[G/T]AGTAATAATGTTTTG | 81550 |
rs147076132 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423090 | AAGAATTATAGTAGC[A/G]TCAAGCTTTTCAAAA | 81550 |
rs147092923 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426515 | TGTATCCTGTAACAT[A/C]ATGTTGTAAACCTTG | 81550 |
rs147114257 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498948 | GGGTCCAGTGGGTAC[A/G]CGGACTCATCCTGTG | 81550 |
rs147116994 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541947 | GGTCAGGCTGGTCTC[A/G]AACTCCCGACCTCAG | 81550 |
rs147134247 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514963 | TTAGTATTTAAAATA[C/T]CTCATTCAGAAAACA | 81550 |
rs147152483 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474335 | CATAGCTAGGCATTC[A/G]GGGTCACTACCGGTC | 81550 |
rs147170733 | snp | G/T | 0.00795819 | 0.0626103 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512442 | CCTTCGCAACAGTCC[G/T]CCAAAGTCTTAACTC | 81550 |
rs147177932 | in-del | -/TCTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567363 | CTTTTCTTTTCTTTT[-/TCTTT]CTTTTCCCTTCCCCT | 81550 |
rs147240484 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457001 | GCACCCAGCCTTAAG[A/G]TGATTTTAGATTCAG | 81550 |
rs147240876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499418 | TGGTCCATAAGGTCC[A/G]CCCGAAGCAATTTGC | 81550 |
rs147241174 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571938 | GAGACTTTAGGGGAG[A/T]TAGAGCCCAAAACTC | 81550 |
rs147257336 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459940 | GAGCATTCTTTTGGA[C/T]TGCTGCCATAAATTT | 81550 |
rs147278005 | snp | A/C/T | 0.0775846 | 0.181698 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568896 | ACAAATTCAGTAAAG[A/C/T]TGCAGGATACAAAAT | 81550 |
rs147344122 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480374 | GTGCTGTTAGCTGAG[A/T]GGGATTCTTTTTGTA | 81550 |
rs147348426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553222 | TGTAGATCACTGAAC[A/G]CTTTCAGGATAAGCC | 81550 |
rs147379976 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475171 | CTGAGGCTTGGTGTA[G/T]CAAAGATCCCATCAC | 81550 |
rs147385048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551381 | AATGCTTGGCACACA[A/G]GTTGTTAATTAATGC | 81550 |
rs147429217 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441184 | CTTGCACTGAAATTA[G/T]TTAATTCTATTGCTT | 81550 |
rs147450829 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531602 | AGTGACTCAGGCTTT[C/G]CATTGAAATCCCACA | 81550 |
rs147470249 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496427 | ACAAAATATTAAGGA[C/T]GTATTTGTTTCGTTA | 81550 |
rs147470467 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572741 | ATAGACTACTACATA[A/G]GTACTGTAAACTTAT | 81550 |
rs147487026 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528051 | TTGCAGTTCTATTTC[A/G]TTAATGTTTTAGGAA | 81550 |
rs147499826 | snp | A/G | 0.000661015 | 0.0181678 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529021 | CACTGAAAGGAAGAC[A/G]AATAGGACCTATTAA | 81550 |
rs147530468 | snp | A/C | 1.90871e-05 | 0.0030892 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485799 | TACTTGTTTTACTAG[A/C]AGTGTGTATCTCATG | 81550 |
rs147534052 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420413 | AATGAGGGCTTTTTA[C/T]GTCCTGTTCAAGAAT | 81550 |
rs147594443 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469133 | AAGTAATGTTCCACA[A/G]CTGCATTGTTTAATT | 81550 |
rs147608540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453518 | TCAAAAGGTTTGGTA[C/T]GTAAAATGAATATCA | 81550 |
rs147612109 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521626 | ATGGGCCGGGTGCGG[G/T]GGCTCACGCCTGTAA | 81550 |
rs147612333 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569143 | CTAGCTGATTTTTGT[A/G]TTTTTTGTGGAGATG | 81550 |
rs147624913 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434720 | GTGCTTTTGCTGGCT[-/G]GTTTTAGTAAACAAG | 81550 |
rs147625654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457838 | TAACTTTAATTTCTG[C/T]CTTCATTTTCAAATG | 81550 |
rs147648638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566796 | AATATTATCATTAAC[C/T]ATACTCTTTATGCTA | 81550 |
rs147683173 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565663 | TCTGCAGCCAAATAT[C/G]GAGAAAAGTAGTATT | 81550 |
rs147698700 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452663 | TTGGTGATTAATATT[C/G]CATTGTATGGATATC | 81550 |
rs147717389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505389 | CAGACTGCGTCTCTG[G/T]ATTCTTCCTCTCTGG | 81550 |
rs147752797 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546620 | GACTATACTTACATT[A/G]ATGAAATAGTCATTG | 81550 |
rs147763200 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433282 | TCACTTTCTGGCCAA[G/T]TAAAACATTCCTCCT | 81550 |
rs147787584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546031 | TTCCAACTCAGGACT[A/G]GTGCTCAAATGAAGT | 81550 |
rs147819190 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487096 | TACTAAATGTGTACA[A/G]ACTTTTTTTTTGTCT | 81550 |
rs147867130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407898 | TGGGAGGGACCCAGC[A/G]GGAGGTAATTGAATC | 81550 |
rs147890711 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524245 | CTGAGCACGGGGCTC[A/G]TGGTAATCCCAGCAC | 81550 |
rs147924439 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469620 | AGTTCTTTTTGGCTT[C/T]ATAGTTTTTGATTTG | 81550 |
rs147941183 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422763 | ATTTAAATAAGAAAT[A/G]TCAGAGAGAAAGTAG | 81550 |
rs147941323 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472865 | CACGGACTGGGGGAG[A/G]AGAGAATGGGGGAGT | 81550 |
rs147976370 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400611 | GCGTGGTGGCAGGCC[C/T]CTGTAATCCCAGCTA | 81550 |
rs147978204 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484637 | ATAAGTCATTTTTGC[A/T]TCAAACCTATTTTGA | 81550 |
rs148013305 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419620 | GGAACATCACACACT[A/G]AGGCCTGTTGTGGGG | 81550 |
rs148017515 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522692 | AATTTTCAATAGAAG[C/T]TTAGGTTTTTCTGCG | 81550 |
rs148032750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552837 | CACCCTTTGAAGCCA[C/T]AGCCCAAGTTGCATC | 81550 |
rs148083965 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508893 | TACAAAAGGCAGGAA[A/G]ATTTAGCCCATTCAC | 81550 |
rs148127221 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434447 | CATTCCAGCCTGGTG[-/A]AAAGTGAGACCCTGT | 81550 |
rs148151528 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541169 | TTTCTTTCTTTCTTT[C/T]TTTCTTTCTTTTTTT | 81550 |
rs148156580 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470057 | ATTCCTTCCTCCTCT[A/C]AGTCTTGGGCAACCA | 81550 |
rs148159738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571102 | ATCAATAAAAAAAAA[C/T]TGGTGGGGGACAGTG | 81550 |
rs148176029 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526637 | TTTTTTTTTTTTAAA[G/T]ATCTCTCTTATGGCC | 81550 |
rs148192815 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445680 | ACAGTTTTCCAGGAG[A/T]TGTAGAGTTCTAGGA | 81550 |
rs148223724 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461650 | TGTTCCAGCCCTTTA[A/G]TCCAGTGCTGGAGGT | 81550 |
rs148229192 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563460 | CTGCTCTGATACTTA[C/G]GAGTAGGAAGTGTCA | 81550 |
rs148254329 | in-del | -/CC | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60437972 | CTTTTCTGTGTTTTT[-/CC]CCCATCCCACAGCCA | 81550 |
rs148282590 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557369 | TGAAACGCCATGGAT[A/G]AATTTTGTGCTAAAG | 81550 |
rs148307472 | in-del | -/T | 0.0271762 | 0.113356 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399923 | AAGCGCAGTTTTTTT[-/T]CCTTCTTAAGGTTTT | 81550 |
rs148366256 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505694 | GAACATAAATGACCC[A/G]ATGGAATTGAAAAAC | 81550 |
rs148386119 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60495465 | ATTCAGGAATCAGAG[A/G]TATTTTTTTTTTTTT | 81550 |
rs148422279 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475223 | CTATAGGTAGCCTTC[A/C]AACTTATTTCCTCCT | 81550 |
rs148473795 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544696 | CAAACTCTTATTAGT[A/G]CTTAACTGCTCTTGA | 81550 |
rs148494888 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529738 | CCTTTTGGCTAAGAT[C/T]GAGTGTAAAAATTAT | 81550 |
rs148546254 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565156 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 81550 |
rs148560231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516235 | GAAGTCAGAATTTAG[C/T]GCAGTAAGCCTTGGC | 81550 |
rs148614767 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550924 | ATTAATTCATTTAAG[C/T]ATAGGAGCTGCTTAT | 81550 |
rs148683923 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506772 | AAAAAAAAGAACATC[A/G]ACACTATGAAGAAAC | 81550 |
rs148702946 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497600 | AAAAACAGACACAAG[C/T]TCTTATCATGTGAGT | 81550 |
rs148714770 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403676 | AACAGGTTGGTGATG[A/G]ACAAAAGGAGGAAAG | 81550 |
rs148719842 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486134 | ATATTTTATTCATGT[A/G]TTCTTTTTCCAGATC | 81550 |
rs148750884 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499460 | AAGGCCAGAAATATA[C/G]CTTTACTGTCCTTCC | 81550 |
rs148772744 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554085 | AGTTTGTAACAGCCT[C/T]CATAAATCAGTGATT | 81550 |
rs148850765 | snp | C/T | 0.000115661 | 0.00760377 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509902 | AACAGAAACCTGTTA[C/T]GGGTCCTCCTCTGAG | 81550 |
rs148862162 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465864 | TAGAAGTACTATTTG[A/C]AGTACTTCTTGCTGT | 81550 |
rs148881083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518361 | CTGAGAGGGACACAC[A/T]GTCCTCACTGTGCCT | 81550 |
rs148910414 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461357 | GTTTGGTTATTTTAA[C/T]AAGAATCTTTTAGAG | 81550 |
rs148917045 | in-del | -/ATA | 0.29992 | 0.244965 | cds-indel, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528442 | AAAATGGAGTAAAAG[-/ATA]ATAATCATCTGAGAC | 81550 |
rs148946245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440464 | AAGGCAGGAGGATCA[C/T]GAGGTCAGGAGTTCG | 81550 |
rs148995203 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399006 | TTTTACTGCTTTCCA[A/G]CATGACCCCCCCTCC | 81550 |
rs149001206 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508446 | ATGGAACAGAACAGA[C/T]GCCTCATAAATAACA | 81550 |
rs149038467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487557 | TCATTTTATGTAAGC[G/T]ACTTGAGCATGTTTT | 81550 |
rs149038609 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563294 | TATTGCTGGAGCTGA[C/G]GTAAGTATCTAAGTA | 81550 |
rs149052652 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540825 | GTTTTCCTTTATTGA[A/G]TAATGAAAATATAGA | 81550 |
rs149068029 | in-del | -/TCTTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565040 | ACCAAACTATCAGTA[-/TCTTTT]TTTTTTTTTTTTTTT | 81550 |
rs149087838 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457860 | TTTCAAATGGTCTTT[A/G]TACTCTGTCTGTGTT | 81550 |
rs149114838 | in-del | -/TTC | 0.0737376 | 0.17729 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568972 | TTTTTTTCCCCCCTT[-/TTC]TTCTTCTTTTTTGAG | 81550 |
rs149155394 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394885 | GTCCTGTGCTTTGTA[G/T]GATATTTAGCAGCAT | 81550 |
rs149160716 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478729 | ATTTCTTTTCTTCTG[C/G]TAGCTTCAGGGTTAG | 81550 |
rs149209795 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473278 | GCATTAATCTATTCA[A/T]GAGGGAAAAATATTC | 81550 |
rs149214321 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546646 | CATTGAGAGAACATG[A/G]TTAAGATAGGAAAAA | 81550 |
rs149226395 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426829 | ATGTGTTCTCAAGCA[A/C]CTTTGTCACTGTGGG | 81550 |
rs149245611 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455805 | AGGTATGGTTGCCCA[C/T]GCCTGTAATCCCAGC | 81550 |
rs149268499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515264 | CCTACCCATTGTTTC[G/T]AATGGCTACTAAATA | 81550 |
rs149286463 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471534 | AGGATAGATTTTTCT[A/G]TTTCTGCAAAAAAAA | 81550 |
rs149313877 | in-del | -/AT | 0.244776 | 0.249945 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461004 | GACTGTGTCTCAAAA[-/AT]ATATATATATATAAA | 81550 |
rs149315410 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400315 | GAAATATAAAATTCT[A/G]CTCACAGGAGAAAGA | 81550 |
rs149338218 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501936 | GCTATCAGGATAATA[A/G]TTACACAAAATACTA | 81550 |
rs149360425 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564658 | ATTAGATGGCCTTCC[A/C]GAACTGTGCCAGCTA | 81550 |
rs149387515 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424404 | CAGTTCTGGCTGGGC[A/G]CAGTGGCTCACGCGT | 81550 |
rs149393189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571017 | AGTTAAAACTTCCAT[C/T]GACAAAATGCTTGCT | 81550 |
rs149411414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560131 | ATGGAAATATATACC[A/G]TATGATGCAATGAAA | 81550 |
rs149530891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474207 | CTCCGCCTTGGCTGC[C/T]AAACAGGGAAGGGCC | 81550 |
rs149531809 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445000 | GCATGCTTACATGAA[C/T]GGTGAGACTTAAAAC | 81550 |
rs149533604 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549420 | TCAGTATTGGAAAAT[C/G]CCCTATAAAGCTGGT | 81550 |
rs149547563 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429270 | ACAGGGAATCGTTAT[A/G]CTATTAGATTGTAAG | 81550 |
rs149552429 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536837 | GTAGCTCTTCTATTC[A/G]GAGGTGTTTGGTCCT | 81550 |
rs149553988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568667 | GCAAGCCTTTCCTCT[A/C]TGATCTGGAACAAGA | 81550 |
rs149564245 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420620 | AAAAAAATTTTCTTT[A/G]TTGGATTGACTTGGC | 81550 |
rs149598963 | snp | G/T | 0.00611483 | 0.0549547 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528907 | ATGAAGCTTTCAGTG[G/T]TATAAAAATTGAAAA | 81550 |
rs149602119 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531014 | AGGAGGAGTACAGAG[C/T]GAAACAGCTAGATGG | 81550 |
rs149658300 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504160 | CTTATCAAATCTGAG[A/T]TAATCACTCATCCCT | 81550 |
rs149669879 | snp | A/G | 0.00059311 | 0.0172106 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509819 | CAGTAAGGAAGCATC[A/G]AGGCAAGCTCTTATG | 81550 |
rs149706976 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499747 | CGTGTTGAGATATTC[A/G]TTCTAAGGTGAAGGA | 81550 |
rs149723654 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461196 | GTAGTTGTGTGTATA[A/G]TAGTGTGTTCATCAC | 81550 |
rs149776597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489041 | AATTCTTAGCTATGC[A/C]GAAGCTTTTTAGTTT | 81550 |
rs149797071 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527251 | TGGCCTCCAGTGGCT[-/G]GTTTGGAAATGTTTG | 81550 |
rs149812081 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433834 | CGTTTCATTATCTAT[A/G]CATTATAGCCAGTGA | 81550 |
rs149815903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508404 | CCAAACAGCATGATA[C/T]TGGTACCAAAACAAA | 81550 |
rs149846531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451136 | AAACCTGAATTATCT[C/T]CCTGTGGGGGAATTT | 81550 |
rs149865658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468949 | GCCTAAGCAATATTT[C/T]AAGCTTTTGGTATTT | 81550 |
rs149869026 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540542 | GTTACCTTAAAATTC[A/G]TTCGTATCTAACTCT | 81550 |
rs149882302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421033 | CCAATATCACACTGT[C/T]TGGATTAATGAAGCT | 81550 |
rs149901267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398247 | GGGGATGAAAAAGAT[C/T]TGCAACGGCTCTCTG | 81550 |
rs149912743 | snp | A/T | 6.64308e-05 | 0.0057629 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529140 | GAAAAAATACTAGAA[A/T]CATCTATTCCTATGG | 81550 |
rs149939798 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497194 | GTGGTGGATGGCAAG[C/T]GAAAGCTCAGCTTGA | 81550 |
rs149986978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456831 | CTCCCAAGTAGCTGC[A/G]GCTACAAGCACACAC | 81550 |
rs150024075 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473016 | TTCCTGTTTTACTCC[A/G]TTTTCTGCTGCTATA | 81550 |
rs150055757 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403068 | TGATACTGTAAACTG[C/T]GAAAAATGACTGGAT | 81550 |
rs150097950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566979 | CCTCCCCTATTCCAA[A/T]CCATTATTTTTTTCT | 81550 |
rs150164476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455316 | GTGCTATTTAAAGCT[C/T]ATCTTTCAGGCTTTT | 81550 |
rs150171534 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552895 | TGGGGTGGCTGGGAT[A/G]CAGGACACCAAGTTC | 81550 |
rs150181276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440265 | CTTATAATTACTATT[A/C]ATGTTTTAGTGTATA | 81550 |
rs150186549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470560 | AGTAGCCATTCTAAC[A/G]TGGGTAAAATAGAAT | 81550 |
rs150187546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542863 | GGTATCTTTTGATGT[A/G]TATGGGCTACCCTTA | 81550 |
rs150202628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423982 | ATAAGCCAAAATCCT[C/G]ATGTTTTCTCTCCCT | 81550 |
rs150237547 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535014 | CTAAAGAATATTACA[C/T]ATTGGAACACTTTAA | 81550 |
rs150253060 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498460 | TTCTGACTTGTGTAG[A/C]GCTCTGGCATTGGCT | 81550 |
rs150253803 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420109 | ATATCATTTACATCA[A/T]GTTAATCAGTGTATA | 81550 |
rs150308473 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524501 | CACAGAGTGAGGCTC[C/G]ATCTCAAAAAAAAAA | 81550 |
rs150320979 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411837 | TATTAAAGAATCTTA[C/T]TGCACATTAAAGTGA | 81550 |
rs150321132 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548622 | GGTTTCTTGCTGAAG[-/T]TAGCAGTGTCATCTT | 81550 |
rs150376201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405695 | ACCTAGGGACAGGTC[A/T]CATAGCTTGGACCTT | 81550 |
rs150392257 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394750 | TTGTGGATTTATGTG[C/T]CTGCGTCTTCATGTT | 81550 |
rs150410216 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467022 | ACATGTGTAGGATGT[A/G]CAGATTTGTTACATA | 81550 |
rs150430441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517973 | GCTAAAACAAAAACC[C/T]TGGTCTTTCACTACA | 81550 |
rs150466880 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530751 | TGAGCCACCACGCCC[A/G]GCCCAAAATAAATAT | 81550 |
rs150499727 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441902 | CCAGAATTTCAGATC[C/T]CTCCCAGAAAACAGA | 81550 |
rs150504982 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545017 | TTCTTCAGACACCAA[A/G]CCTGTACATGACAGT | 81550 |
rs150521499 | snp | A/G/T | 0.0166325 | 0.0896639 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503894 | TGAAACCTTATAGAC[A/G/T]ATTCCATCTAATCTT | 81550 |
rs150536406 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484971 | AGAATATAATAAAAG[C/T]TATAATTTCAATAAT | 81550 |
rs150539850 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559789 | GTTTCAGTTATGCCA[C/G]ATGAATGGGTTCTGA | 81550 |
rs150554915 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435469 | TATATCACTCTATAT[A/G]TATTTGCACCCTCAT | 81550 |
rs150573117 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499604 | GATTGGATCCAGTAA[C/G]CACGAAGTAGCAAAC | 81550 |
rs150629719 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532197 | AATGTCATGTAGCAT[C/T]TAAAAAACAGTACCT | 81550 |
rs150643536 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415465 | ATTAACATATTGGTA[A/G]TAAGCAAACATACTC | 81550 |
rs150669749 | snp | A/T | 1.65021e-05 | 0.00287241 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460467 | CAGGCTGCACCAAGG[A/T]TGCTGCGATTACAGA | 81550 |
rs150694036 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488861 | TGGGATTACACAGGC[A/G]TGAGCTACCATGCCT | 81550 |
rs150694547 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406416 | TATTGATCATACTTT[A/C]AAATATATTTTGTTA | 81550 |
rs150711017 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398020 | CAATGTCAACTCGTG[A/G]GGGTGCTCGGTAGAA | 81550 |
rs150715307 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507059 | GGGGTTGCAATCCTA[C/G]TGTCTGATGAAACAG | 81550 |
rs150720827 | snp | A/G | 8.26262e-05 | 0.006427 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529079 | CTGTGATGATAAAAT[A/G]TTTTACAATAGTGGG | 81550 |
rs150747155 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519645 | GATTTAATGCCAGTA[A/G]TATAATGGTAGCTTT | 81550 |
rs150747457 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447148 | TTTCAAATAGGGCGT[A/G]CTAAAAACCAATGTT | 81550 |
rs150762487 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474169 | CATAGAAGAAATAAT[A/G]GCGTAAGCTGTCCTC | 81550 |
rs150851749 | snp | A/G | 0.00101586 | 0.0225144 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460527 | GTAGAATTTAGTTAT[A/G]TGTCAAAAATAAGGT | 81550 |
rs150889832 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563719 | GCATTTCACCTTACT[A/G]TTTGTGGAACACAGA | 81550 |
rs150892393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568546 | TAAGCTCAGTGTGCT[A/T]ATAATTAAAGCAATT | 81550 |
rs150907911 | snp | C/G/T | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456756 | GCCAGAGTGTAGTGG[C/G/T]GCAATCGTGGTTCAC | 81550 |
rs150910682 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554603 | AAAGTTGATTGTCTT[A/G]ATACTTTTCAGGAAG | 81550 |
rs150914032 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489894 | TTCTTTTGATTTACA[-/T]TTATCTCAAATGAAC | 81550 |
rs150946575 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466470 | GTGAAGACTAAACCT[A/C]ATTTCTTTGTCATTG | 81550 |
rs150946576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534016 | ACAGATAAATTTTAA[A/G]ATTGTAGTTATTGGC | 81550 |
rs150999918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529975 | CATTTTTTTCCTTCT[A/G]CCCAACATGCTCTTC | 81550 |
rs151011045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409595 | TTTGACTGTCCCACT[A/G]GATTTCAGACTTGCC | 81550 |
rs151013765 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491457 | AGCTAATAATGAACC[C/T]TGTAACACTTCAATT | 81550 |
rs151029002 | snp | A/G | | | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528966 | AATCCAGTTCGAAGT[A/G]ATAGTTTCATTGGTG | 81550 |
rs151030675 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481932 | TCAAGATGTGTATTC[A/G]AGCTTTGAAAGGAGT | 81550 |
rs151032007 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399201 | TTGACCTTGGAATGC[C/T]CCTGCCAGTCAGAAT | 81550 |
rs151069203 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520951 | ATAATCCTGTGGAAA[C/G]AATCATTACTGATAT | 81550 |
rs151086385 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475652 | GCTGGACTAGTTTAC[A/G]TTCCCAGCAACTGTG | 81550 |
rs151087418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551811 | TGAAGGAGAAACAAG[C/T]ACCTTCTTCATGAGG | 81550 |
rs151102823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433620 | AGGAGCAAATAATTT[A/G]AATAAACTAATGTGT | 81550 |
rs151159568 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500794 | AGTGGTCAAAAACTG[G/T]GAAGATGTTTGTATC | 81550 |
rs151210686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569695 | CAAAGCCGTAGTAAA[A/C]AAAATAGCATAGTAC | 81550 |
rs151226985 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524454 | GGAGGTTGCACTGAG[C/T]CGAGACTGCACCACT | 81550 |
rs151244701 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443328 | GTACAACGTGAGGTA[C/T]GGTTTATATTTCTTT | 81550 |
rs151280361 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486503 | TTAACTGACAAATAA[G/T]TACACATATATATGA | 81550 |
rs151282418 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60562093 | AGGTGTGTGGATCAC[C/T]TGAGATCAGGAGTTC | 81550 |
rs151296090 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512736 | ACATCTAGGTTATAC[A/G]GATGAAAGAGGAGAG | 81550 |
rs151296188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438995 | GGGTATGGGTAGAGA[C/T]GAATTTTTTTCCTTC | 81550 |
rs180673492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494618 | TAAAGTGTTATTTCT[G/T]AAAATGATTCTTTTA | 81550 |
rs180676062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436590 | TTGGCTGTATTTGGC[G/T]TTATTTCGAGGTTCT | 81550 |
rs180680026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474354 | TCACTACCGGTCTCC[A/G]CGCCTTGGTGGTAGT | 81550 |
rs180683475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413117 | TTAGCATGTGAAAAT[G/T]CTGCCAAGGAATGGG | 81550 |
rs180696391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532355 | GAGGAACTGTGGACT[C/G]TAAATAGATTACACC | 81550 |
rs180698116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485541 | CTCTTGATCCAGTGT[A/G]TGTTTTAAATATGTG | 81550 |
rs180701316 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552841 | CTTTGAAGCCACAGC[C/G]CAAGTTGCATCTTGG | 81550 |
rs180710650 | snp | A/G | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464643 | AAAGAATGAAATCTT[A/G]TCATTTGCAACAACA | 81550 |
rs180710804 | snp | C/G/T | 0.00562661 | 0.052742 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510780 | TTTAAAGTTGATTCC[C/G/T]TTTTTTTTCTTTCTT | 81550 |
rs180715374 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503979 | AAAGGGCAGATTGGC[A/C]TCAGAAGAAAACCTT | 81550 |
rs180755056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422260 | CAAAATAGAACTACA[C/T]AGGTGGAGGATTCAT | 81550 |
rs180768864 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402759 | CTAGAGTGCAATGGC[A/G]CGATCTTGGTTCGTC | 81550 |
rs180898141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565123 | TGCCGTGGCACTGTC[C/T]GGGCTCACTGCAAGC | 81550 |
rs180913049 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514506 | TCTCCTAGATGTACT[A/G]TGTGGGGAGGGCACA | 81550 |
rs180919349 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490560 | AGCCTTTGGAATGTT[C/T]TGAGCACAGCAATAA | 81550 |
rs180939456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407543 | TTATAGAATTCAACT[A/G]TTAAGAGATATAACT | 81550 |
rs180941337 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447146 | TCTTTCAAATAGGGC[A/G]TACTAAAAACCAATG | 81550 |
rs180942754 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527098 | CTTCAGCCTTCCAAA[A/G]TGCTTGGATTACAGG | 81550 |
rs180944951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550570 | ATAGATTGCCTCTGG[A/G]TTCCTTTCTTCATTG | 81550 |
rs180950095 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506414 | ATGGAAAGGAGCAAC[C/T]GGTACTAACCACTGC | 81550 |
rs180960344 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60556486 | AAAACTTTGTATTTA[G/T]GTTGGGAAAATAATT | 81550 |
rs180965439 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537544 | TTTTAAAAATTTTGG[C/T]AAGAGGAAACTGTAA | 81550 |
rs180973183 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469081 | TTTCTTATGATACTA[A/T]TGTGCTGTGATTTGG | 81550 |
rs180974390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428690 | CGTCTTGAGACATAC[A/G]TCCTCGTGCATCCTG | 81550 |
rs180978207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498161 | GTCTCTTTAGACCTA[C/T]TCATTCCAGCTGGGA | 81550 |
rs180982824 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399306 | AATGTTATATTGTAG[C/G]ATTTGCTACTTTATA | 81550 |
rs180994298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478758 | AGTTTGTTCTTTTTA[C/T]TCTTGTTCTTCTAGG | 81550 |
rs181024283 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418825 | TATAAAAATGGAAAC[C/G]TTATTTCTTCTGACA | 81550 |
rs181032605 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456457 | ACATGCTTACCTGGA[A/G]GTGCAATGATACATC | 81550 |
rs181155107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462588 | TGCTAATACGGATGT[C/G]TTACCTTACATGGGC | 81550 |
rs181159337 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60403013 | AGCCTTGCCGACTTT[C/G]TGTCTCAAAATATGT | 81550 |
rs181166405 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434596 | TTTAGCCTTTTAATG[C/T]CCTGCTTGTCAGTAA | 81550 |
rs181198815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533004 | CATGCTAAGATATAG[C/T]ATGATTCAGTGTTTG | 81550 |
rs181199481 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483663 | GAAGGCCTTTTTTTT[C/T]CCTATTTCTTATAAG | 81550 |
rs181199824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423047 | TAAAATCCTTAGGAC[C/T]GACATGAAACAAGTC | 81550 |
rs181206084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60495047 | TATTTCTGGCATGCT[C/G]TAGTGTTCTCAGATC | 81550 |
rs181221858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511673 | GATTTTGGTTGGAGC[A/G]GTGATGTTATCAGAG | 81550 |
rs181232810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571683 | TGTAATTTGCACATT[A/C]TTTGATTATCCTAAA | 81550 |
rs181244728 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553293 | AGCCAGATACCCTAA[A/G]TCATCATTCACTATC | 81550 |
rs181252570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411705 | TTGCTTTGATGTCCC[C/T]TCACCCCTTGCTACT | 81550 |
rs181268503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451719 | GCACTTGTATCAACT[A/G]TGTTACCTTCAGTAT | 81550 |
rs181328671 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538192 | GTGGATATGTATTTT[C/T]ACTTCCAGAACATAC | 81550 |
rs181336392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474777 | TTCTACACATTTACC[A/T]TTTCCGTCCCTCTCT | 81550 |
rs181342220 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556787 | ATGATCAAGATGATG[A/G]AGATTCTGGAAATAA | 81550 |
rs181373258 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456725 | ACACCTTTTTGTGTG[G/T]ATGTGTGTCACCTGG | 81550 |
rs181378039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430016 | TTTATTCTTAGAAAA[A/C]CTCTGTAGATCAGTA | 81550 |
rs181383026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515129 | ACAAAACAGTACTGA[C/G]CAAAATATAAGTGCT | 81550 |
rs181399472 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498709 | CGACAGTTTATGCAG[A/T]GAGTCTTTCTTCTAT | 81550 |
rs181402372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479267 | TTCACCCAGAAGTTA[C/T]TCAGGAGTAAGTTTT | 81550 |
rs181432664 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408074 | TGATTCTGAGGCCTC[C/T]CCACCCGTGTGGAAC | 81550 |
rs181459097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550986 | CTGTCTGTTGAGAGT[A/G]GAAAGTATTATGGAT | 81550 |
rs181569802 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416945 | TTTCTTAGTTTCCTT[A/G]TTGGTACTAACAAAG | 81550 |
rs181600781 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512337 | TGTGGGCATTCAAGA[C/T]GAGATTTGGGTGGGG | 81550 |
rs181601322 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565428 | CAAGTTATGAGTTAC[A/G]TGAAAGAAATCTCAT | 81550 |
rs181602289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559971 | TGTGATTATTTCACA[A/G]TGTATACATATATCA | 81550 |
rs181605481 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534171 | TTTAAAAATTAGCCA[A/G]GCATGGTTGTATGCA | 81550 |
rs181608732 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496253 | CTGCAGATGGTCTAT[G/T]GTGGGACCTTGTGAG | 81550 |
rs181617104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544113 | AATTCCTTTTTTTTT[A/T]AATTTTTTTCTGTCG | 81550 |
rs181644584 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397965 | AGTGTGAATCTGCCT[G/T]CCGCGGCACACACAC | 81550 |
rs181739511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553744 | ACTATCACGAGAACA[A/G]CATGGGGGAAACCGA | 81550 |
rs181789992 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484816 | AGTGTAAACATTCTA[A/G]TAACTTATATTTGAA | 81550 |
rs181811864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521065 | CAAGCTCAGTGTTCT[C/G]TAGTGCAAATCAGAG | 81550 |
rs181826580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557073 | TAGCCGGGCATGGTG[A/G]CACATGCCTGTAATC | 81550 |
rs181834850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539729 | CAAATTCAAATAATA[C/T]TAATAAGCTATAAAT | 81550 |
rs181859210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435602 | AAAAGACATTATTTC[A/C]ATTCGTTTTTGTGGC | 81550 |
rs181890398 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445567 | ATTTCCCAGAGGTCT[A/G]GCTAGAACACAAATT | 81550 |
rs181910253 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398984 | ATTTTCATTTACAAA[C/T]TCAGTATTTTACTGC | 81550 |
rs181912894 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506135 | GGAAGCCAGAGAGAA[A/G]GGTCAGGTTACCCTC | 81550 |
rs181913075 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489055 | CAGAAGCTTTTTAGT[G/T]TGATATAATCTCGTT | 81550 |
rs181916648 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468324 | TACATTATTCATCTT[A/G]TTTTTTCTCTCCTGA | 81550 |
rs181927146 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571968 | CCAAACTTCTAGTTC[C/T]TGGACACTGTCATAA | 81550 |
rs182002719 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499149 | TTGCATCCCTGGAGG[G/T]ATTGCAGAGATTAGT | 81550 |
rs182018435 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525643 | AAAATAATATTTTAA[C/G]TACCAAGTGTAATGA | 81550 |
rs182025747 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503065 | CGTTCAAAATAAGTT[A/T]CCTTGACTCTGAAAG | 81550 |
rs182033223 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564694 | TAGTGTCAGATTTTT[A/T]AAAAAATGTTTGTAA | 81550 |
rs182060161 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571104 | CAATAAAAAAAAATT[G/T]GTGGGGGACAGTGCC | 81550 |
rs182086582 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457305 | TTTCTACCTTGCTTT[C/T]GAACCAGTTAACAAG | 81550 |
rs182112226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463509 | AGTAAAAATAGAAAA[C/T]TGGGATTAAATCAAA | 81550 |
rs182122842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412698 | GGGCCATTATATTGG[C/G]CAACTGCTTGATTTT | 81550 |
rs182205181 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509110 | GTTTTGTTTTTCTCA[G/T]CTGGCTTTGGTTCAA | 81550 |
rs182228819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566549 | GGATTAATTTCCAAA[A/G]TAATGCAAATTATTG | 81550 |
rs182243724 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551982 | ACATGTGGGGATTAC[A/G]ATTTGAGATGAGATT | 81550 |
rs182288668 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549910 | AAACAAAATCCAAAT[A/T]GGAAACCAAGTAATC | 81550 |
rs182289869 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544887 | ATCTTGATAGTATCA[G/T]AATTTTAAGTTAGTA | 81550 |
rs182293307 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516030 | TTCATATTAGCAGCA[G/T]CATTTATTTGGGTCT | 81550 |
rs182307111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479728 | CTTCTTATTGAGTTG[A/C]ATTCTTTATTATTAT | 81550 |
rs182344917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431900 | TACTTTAAATAGTAC[A/G]TACCTTTATTTATCT | 81550 |
rs182351058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409154 | GGGGGCACAAAGTCA[A/G]GAATTCAGGTTTGAG | 81550 |
rs182374245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480322 | ATTGAAAATAGGCCC[C/T]ACTCTCTTTTGGCTT | 81550 |
rs182376771 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458801 | ATGTGGCTGGAGGAT[C/T]GTATTGGACAGCATA | 81550 |
rs182385193 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431130 | AACCCTGAGTGATCT[G/T]TATATCAAACACAAA | 81550 |
rs182388115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424660 | CCAGCCTGCGCAACA[A/G]AAGGCAACTCTGTCT | 81550 |
rs182552407 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560607 | TGTATTTGCTTCTAG[C/T]GTCATTTAAAAATTA | 81550 |
rs182561060 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560293 | TTAAATAAGATAACA[A/T]GCAAAATGCCAGGCA | 81550 |
rs182564329 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521618 | GAAAGTGTATGGGCC[A/G]GGTGCGGTGGCTCAC | 81550 |
rs182579677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557444 | ACTATAGCTTTAGTA[C/G]TCAGCCTGATAATTG | 81550 |
rs182585973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453887 | AAAAGACAACTTCTT[A/G]ATTCAACTCATTAGT | 81550 |
rs182589976 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493068 | GGACTACAGGCGCCC[G/T]CCAACATGCCCGGCT | 81550 |
rs182590249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516446 | ACATAATTCTAGTTG[A/G]CGTTTTTATTAATAT | 81550 |
rs182592419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426325 | TCCAAGGACAAAAAA[C/T]AGATCTGTAGGATGA | 81550 |
rs182596579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486067 | ACGCTTAACCTTATT[C/T]TTCTTGCATATTCCA | 81550 |
rs182596726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465218 | TCTTAGGTAAATGAT[C/G]TAATTCATTAGCAAT | 81550 |
rs182600089 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405496 | GGGAGTTCGTGTTTT[C/T]ATGGTGGTCAGAGAA | 81550 |
rs182616687 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545304 | TTTAGGAAGTAATTC[A/G]GGAAGCCCAATATAG | 81550 |
rs182622927 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504105 | AATTTTAGAATTTTT[A/T]AAATCTTTTTATAAT | 81550 |
rs182624408 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522720 | GCGTTAATAGAAAGA[A/G]ATTATTAATTTTAGG | 81550 |
rs182636801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453291 | AAACATTTTCCCAAT[A/G]ACTGACTAAGCCTCA | 81550 |
rs182650886 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449306 | TAAACATCTACTTGT[A/T]TTAGAAAAAATGGAT | 81550 |
rs182655214 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404333 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 81550 |
rs182668868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401093 | TAAATCTTTGCCTTG[C/T]AGTGAATCAACTAAT | 81550 |
rs182745079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400007 | TTCAAAAGTAGCTAC[C/T]TGGCGGACTTAAAAT | 81550 |
rs182780301 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558939 | CTTGCATTGGCTCTT[C/T]CATTTTTTTCCAAAG | 81550 |
rs182813798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500590 | AATCTTCCCAGTGGG[C/T]AGAACTTCAAGCAGT | 81550 |
rs182814042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481047 | TGAAGGGGTGGCAGC[A/G]AGGTCACAGGCAAAC | 81550 |
rs182819947 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460164 | AATTATTAAAACAAA[A/G]TTGTTCTTCAGGAGA | 81550 |
rs182827649 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541317 | GCATTACAGGCACCC[A/G]CCACTATCCAGGCTA | 81550 |
rs182840749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535717 | TTGACGTATATATGT[A/G]CAGATTAACTATAAA | 81550 |
rs182849662 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517255 | ACTGCTTGAACTTTG[A/T]AGACTGAAGAATAGG | 81550 |
rs182857424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60573063 | GAGGCTAAAATAGGC[C/T]TGGAGCATACAAGTC | 81550 |
rs182873875 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541092 | GATTAAAAATATTAA[A/G]TATTAGGTTAGCATA | 81550 |
rs182873888 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470648 | GAGTACAATGGCACG[A/G]TTTCGGCTTACTGCA | 81550 |
rs182919788 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496938 | GAATGGAACCTTGGG[C/T]CATGCAGTGTTATAG | 81550 |
rs182926626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499856 | CATTTGGATGTGTTA[C/T]TCTGGCGGATTTATC | 81550 |
rs182930396 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475099 | TTTCTTCCTATTTTT[A/G]TTTTAGGTTAAGGAG | 81550 |
rs182936553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452611 | ATTTTTTAGGATAAT[C/T]GATAACATAGCATAT | 81550 |
rs182944970 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424160 | CCGAGTAGCTGGGAC[A/T]ACAGGCGCCCGCCAC | 81550 |
rs182959069 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396287 | CAATACGGGACGCCG[C/T]AGAGGTGAAAGACCA | 81550 |
rs182981826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413856 | AATCTTATAAATATT[A/G]GTGTCTCAAATTAAA | 81550 |
rs182994865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403960 | TATACCTCCTGTACA[C/T]AAAGCACTGTGTTGC | 81550 |
rs183073749 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560845 | TTTCTGTGATACTGG[A/G]ATGAAAATATTATGT | 81550 |
rs183126098 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554886 | GATGTTTCAGATGTG[A/G]AATTACAGGTTACTA | 81550 |
rs183139981 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513030 | GGGCCCGCCCCTGCA[A/G]CAAACTTCTGCCTTG | 81550 |
rs183154515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470329 | TGAATAATGCTGTTA[C/T]GAACATGGGTACACA | 81550 |
rs183164749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447993 | TACAATGCACTGGAG[A/C]TTCTCCAAGACATAT | 81550 |
rs183169747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420103 | AGATAGATATCATTT[A/G]CATCAAGTTAATCAG | 81550 |
rs183177100 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508548 | TAATAAATTTTGCTG[A/G]GAAAACTGGCTAGCC | 81550 |
rs183178790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528240 | TAAGATAATGAGGTA[A/G]GAAGATGGAAGAAGA | 81550 |
rs183191586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492432 | TCTCCAAATATCCCA[A/G]TGAGGTAGGTTTTCT | 81550 |
rs183192029 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436891 | GATATTAGTTTCCTG[A/G]TCTTCTACGATGCAG | 81550 |
rs183199806 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507306 | ACAGAAAATTAACAA[A/G]GATATTCAGGACTTG | 81550 |
rs183206949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477350 | CTCCTGAGTAGCTGA[C/T]ACTACAGGTGCACAC | 81550 |
rs183211538 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400874 | AGAACCAAGAATAGA[A/G]CCCAGATGTCTAGAA | 81550 |
rs183229212 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419473 | GAATGAGTTCATGTC[C/T]TTTGCAGGGACATGG | 81550 |
rs183232179 | snp | A/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395506 | TCCAGTAAAAAACCC[A/T]TTCTTTAAGAGAATT | 81550 |
rs183248666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432763 | TTTTTTAAATTATCT[C/T]TTATGTTTTTTCCCT | 81550 |
rs183256911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469839 | CTATAAGTTTTAGTG[C/T]CCCCAAACTGTAGAT | 81550 |
rs183285618 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559255 | GAAGATGTAGAAAAG[A/G]TTAGTAACGTGCCTA | 81550 |
rs183420752 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant, missense | TDRD3 | GRCh38.p7 | 13:60527464 | ATAATTACAGCTGCA[G/T]GTTGATTATGATGTA | 81550 |
rs183424388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512536 | TGCCTAAGAGCCTGA[A/G]AAATCAAAAGCAAGT | 81550 |
rs183424527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466530 | CAGTGGCTCACGCAT[A/G]TAATCCTAGCACTTT | 81550 |
rs183434519 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523076 | GATTACATGAAATTA[C/G/T]GTAGGCAAAAGACCT | 81550 |
rs183437126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554481 | CCTTTCTCTTTGTCC[A/G]GAGGATCTATTTGCT | 81550 |
rs183442968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572339 | TACATAAGAGTTTGA[A/C]TTTGTTGTGTTTGAT | 81550 |
rs183444771 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534907 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACCCT | 81550 |
rs183449912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504904 | GGAATAGTGGACTTC[A/G]GCCCAGATACTATGC | 81550 |
rs183451145 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488185 | GGGCTAAAATTAGGG[G/T]TTTATATAGCAGAGA | 81550 |
rs183470013 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396684 | GGGCATTTTCACTGT[G/T]GTGTCCGACTGGGGC | 81550 |
rs183490695 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491007 | CTATAATCCCAGCTA[C/T]TCGGGAGCCTGAGGC | 81550 |
rs183494910 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409659 | CACCCATTTGGAACA[G/T]CTGTATTTACCCAAT | 81550 |
rs183498410 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447285 | ATACGGACCAGGAAC[A/G]GATTAGAGACATCCA | 81550 |
rs183521412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487506 | AAAAAAAAAAGTATG[C/T]AAGAGGATGTGCATA | 81550 |
rs183631873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462149 | TGAAGAGTAGGATTC[A/G]TACTTTTGTGTAGAA | 81550 |
rs183635459 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433994 | AATAGTGTTTGTTTT[A/G]TCACAGTTTTCTGCC | 81550 |
rs183655792 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482836 | AGTGCACATGGTGGT[G/T]GTTTTTTTTTTTTAA | 81550 |
rs183658461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501828 | TTATTTGCATAGCCA[A/G]GGTGTGACATGTTAC | 81550 |
rs183681381 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410863 | GGATTTTTTGCTTTG[A/G]TTTTATGTTTTTTCC | 81550 |
rs183690451 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546209 | AATGGAAAGACTTTT[A/G]GAGACTGACTTGTAT | 81550 |
rs183693340 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566212 | ATTAGGGCAAAGTCA[C/G/T]AAAGCTTTCCCAAGC | 81550 |
rs183702582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504479 | TAAAACATTTAGCAA[A/C]CCTAGTATCTGACTT | 81550 |
rs183703256 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541596 | GAATATATGGCATTG[A/G]TTAATTAAGAAGTAT | 81550 |
rs183728703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414693 | CTATTTGATAGGAAT[G/T]TGTCAGTACTTGCAG | 81550 |
rs183736724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532742 | AAACTAGTTCAGCTA[C/T]TTTTTTCGTCAACTG | 81550 |
rs183754851 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465501 | CAGTTGTGATTGATC[A/G]CTAAAAATGATTAAG | 81550 |
rs183771521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552974 | CTCCCAGGCCTTCGG[G/T]CCTGTGATGGAAGGG | 81550 |
rs183851358 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478920 | GCAATTCTCCTGCCT[C/T]AGTCTCCTAAGTAGC | 81550 |
rs183853499 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456607 | TTTTCATTTGAAATT[A/G]GTATTTTTTTTACTT | 81550 |
rs183853528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524734 | GAATGATTGGAAATC[C/T]AAGAATGACTTCTTA | 81550 |
rs183857763 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488608 | TGACAGAGTCTTGCT[C/T]TGTTGCCCAGGGTGG | 81550 |
rs183864442 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428746 | GAAGACAGTGGTTCT[C/G]TCCAGGTGTGTTGAC | 81550 |
rs183875088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563422 | CAAACTCAAACTTCC[C/T]GAGGTTAGAATTCTT | 81550 |
rs183909066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519233 | ATAATGTGTCATTTA[C/T]TGAGCATCTGCTATG | 81550 |
rs183918979 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551472 | ACCTCCTGAAAGTAA[G/T]GCTTGTTGCCCCTTA | 81550 |
rs184012934 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546900 | TGGGTTGGTTTTGGT[A/G]TAACGTCTTCAACAT | 81550 |
rs184074206 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476530 | TAGGATTGTATTGGT[G/T]ATATGGGCTCATTTT | 81550 |
rs184087257 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502991 | CCAGGCAGAGAGAAA[A/C]AAACATGCTCCAAAC | 81550 |
rs184089826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520744 | CGACACCACCAGCAG[C/T]TGATGCTCAGTAACT | 81550 |
rs184104354 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484016 | TTCCTTCACTGTAGT[C/T]ATATTGTTGACGTTT | 81550 |
rs184105056 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559765 | GAGATGTTGGTCAAA[A/G/T]GTTACGAAGTTTCAG | 81550 |
rs184115361 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542929 | GTGCTGTTTATTCTA[A/G]CATCGTGTATAATGG | 81550 |
rs184172080 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561903 | TTGTTGTTTGTAGTA[C/G]AACTACAAATATTAA | 81550 |
rs184217278 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496794 | TGCTAAGATTGCCCT[A/C/G]AGTAAGAGTCTTATT | 81550 |
rs184234258 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524309 | GTCAGGAGTTTGAGA[A/C]CAGCCTGGCCAATAT | 81550 |
rs184306953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449967 | CTTACCTAGGAGAAC[C/T]CTGGTTTTTAGTGAA | 81550 |
rs184316874 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420817 | GGCGTGATGGCGGGC[A/G]CCTGTAGTCCCAGCT | 81550 |
rs184322823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559577 | ATGGCTGAAGCCATC[C/G]GTTTAGTTAAAATTA | 81550 |
rs184331029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401283 | ACAACAAAAATAATA[C/T]GAATAAAAAATAAAA | 81550 |
rs184373899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519630 | CTCATGGTTATTAAT[A/G]ATTTAATGCCAGTAG | 81550 |
rs184437988 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542313 | TAAAATAAGTGGATC[C/T]GAAGGATATTTTTGT | 81550 |
rs184445612 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511042 | AAACAGGTTGTTGTG[C/T]TGGAAATTTATTATA | 81550 |
rs184537862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497328 | CCAGCTCGAATGCCT[G/T]GGTTTAGATCCCGAT | 81550 |
rs184542809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477704 | TGTTGAACCAACATT[A/G]CATCCCAGGGATAAA | 81550 |
rs184550615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417084 | TACAGTGGCATAATC[A/G]TAGCTCACTGCAGCC | 81550 |
rs184557857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455571 | GACTTTAAGTAGATA[A/G]AAGAACTATGGAAGA | 81550 |
rs184559711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398052 | TTTTCTTGAAAGGAT[G/T]GTGTTCTGATTTTAA | 81550 |
rs184561963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536405 | GCCTAAAAACTCCAA[A/G]TCATCAATATCTAAT | 81550 |
rs184568354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555755 | AAACTATAAGGGTGA[A/G]AATGGAAAATGTAGT | 81550 |
rs184568494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513602 | TTGAATTCCCACATG[C/T]TGTGGGAGGCACTCG | 81550 |
rs184611887 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427323 | TGGATTTTGTAGTGC[A/G]TATTAATAGTGTTAA | 81550 |
rs184631622 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537684 | AAAGCTGCAGGGAAA[C/T]GGTTAGAGAGGCCTT | 81550 |
rs184635794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498400 | AAGGCAAGGTTAAGC[A/G]TGGCTACTGTAATGG | 81550 |
rs184677175 | snp | C/T | 0.000413042 | 0.0143649 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467414 | TGAACTTTTGAAACA[C/T]TACACTCTTTTTTAT | 81550 |
rs184692292 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416198 | CTTTTCAATAATTAA[A/G]GTTTCTCTAAGTGTA | 81550 |
rs184703872 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556630 | GATTAGATATCAGAT[G/T]GCCTAATAGATTTAT | 81550 |
rs184764034 | snp | C/T | 0.000761274 | 0.0194951 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494428 | TTTATCTTTCTCTTA[C/T]GTAAAGACCAAGACA | 81550 |
rs184767618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514674 | TGTGCCTGGGAATGT[A/G]TGGTAGAGGTAGTGC | 81550 |
rs184778143 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474106 | CCTGGCTCCACCTTT[C/T]AGATAGCAGTAGCAG | 81550 |
rs184782538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450439 | GGAATTCTAATTTGC[C/T]TCTTACTGACTGAGT | 81550 |
rs184790264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552529 | ACGGTGCAAGCTATA[A/G]GTGGATCTGCCATTC | 81550 |
rs184799756 | snp | A/G | 1.66746e-05 | 0.00288739 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510630 | CTTTTGCATCTAAAG[A/G]TAGAGGAAAAGGCAG | 81550 |
rs184805827 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532134 | TGAAAAAATTAAATT[A/T]AAAAAAATCAAAGTA | 81550 |
rs184823507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439662 | TGATTTTAGATAATA[C/T]TAAGCCATTTATTTT | 81550 |
rs184835083 | snp | C/T | 0.381503 | 0.21262 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397540 | CTCTCCCCGGGCCCT[C/T]CGGGCCGGCTCCGCC | 81550 |
rs184845085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422228 | AAGGAAAAGGGAAAA[A/G]TTAAGGCCCTGTGAG | 81550 |
rs184845633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438585 | TAATCTTCTATTGCT[C/T]TTCTGTACTGTTCTA | 81550 |
rs184854096 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415724 | CAGATGCCTTGATGG[A/C]TCTTCCGGGAACTAC | 81550 |
rs184881201 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552215 | AAAGCAACTTAGTTA[C/T]TTTCAAGATATAATG | 81550 |
rs184958182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509422 | AGAAGTATCAAAAAA[A/T]TTCCATTTTTTACCA | 81550 |
rs184972985 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473371 | AATATAAGTTTTGGA[A/G]AGACAGTCAAATCAT | 81550 |
rs184995173 | snp | A/G | 0.00141645 | 0.0265748 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567628 | TTTACCAACCACCCC[A/G]GGCTCGGAACTAATA | 81550 |
rs185007768 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530692 | ACTCCTGACCTCAGG[G/T]GATCCACCCGCCTCG | 81550 |
rs185021838 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537314 | TAAATAATTAACTTA[A/G]TTGAGAGAAATATCT | 81550 |
rs185048780 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556190 | TTGCTAAAAGAACTT[A/C]ATTTTACACTAAGAC | 81550 |
rs185058886 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462619 | TTTGCATTTCTCTGC[A/G]GTGCTTGTTTCTACT | 81550 |
rs185067919 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493525 | AAATTAGCCGGGTGG[C/T]AGTGGCACATACCTG | 81550 |
rs185079957 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412014 | GAGAGACATCGTATC[C/G]TTGGTTTCTAAGAAC | 81550 |
rs185130180 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564093 | TAAATATTAGTATAA[A/T]AGCTCATATTGAGTA | 81550 |
rs185132232 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525490 | GGAATTCTTATTTTT[A/T]AAAAATAATTTTCTT | 81550 |
rs185212658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488736 | GCACCACCGTGTCTG[A/G]CTAATTCTTTTTTTG | 81550 |
rs185235739 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548832 | TTTTGATTATTTTTT[C/G]CCAACACTTAAAAAT | 81550 |
rs185247218 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417578 | AACTCCTGACTTCAG[A/G]TGATCCACCTGCCTC | 81550 |
rs185254057 | snp | A/T | 0.000399281 | 0.0141238 | splice-donor-variant, downstream-variant-500B | TDRD3 | GRCh38.p7 | 13:60573881 | CTATTATTGTTTTAC[A/T]GTGTGTTTTATTTGC | 81550 |
rs185256585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406020 | CTCAAATCAATTACA[A/G]TTCAGTTAGGGACTG | 81550 |
rs185272610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504012 | TGTGCTTTTATTTCA[A/G]TGCTCAATTTATGAA | 81550 |
rs185274420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485715 | AAAAGATACAAGATA[C/T]TTTTGAAGAAGTATT | 81550 |
rs185285234 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464781 | GATAGTAAAATGGCA[G/T]CCAGGAAGGATAGTG | 81550 |
rs185311017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521633 | GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 81550 |
rs185320388 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505674 | GGAATAACTAGTTTA[C/G]AGAAGAACATAAATG | 81550 |
rs185332822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467866 | TCATCTTTCCAGTCA[C/T]GTAGGTTATCTTGTA | 81550 |
rs185337533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436632 | CATTGGTATCATTGC[A/G]TATTTTTATACCAGT | 81550 |
rs185350069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413362 | TATGGCTGGTGTTTA[C/T]GAGCATGGGCTCTTG | 81550 |
rs185396025 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407950 | GCTATTCTTGTGATA[A/G]TGAATACGTCTCGTG | 81550 |
rs185422266 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501096 | TTATATTGCACATTT[G/T]CCATCATGGAAAGGG | 81550 |
rs185462937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410071 | CAAGGGTTTCTGCTT[C/T]TGCTTCGTCCTCATT | 81550 |
rs185497829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461550 | CATTTTATACACTCA[C/T]GTTTGCAGCTCGGGC | 81550 |
rs185511088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527106 | TTCCAAAGTGCTTGG[A/T]TTACAGGTGTGAGCC | 81550 |
rs185518738 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60550629 | AAGATTCTTAGTCTC[C/T]TTTTAGTATTACATT | 81550 |
rs185520504 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506633 | GTTGTGGTGCATGCC[C/T]ATAATCCCAGCTACT | 81550 |
rs185551340 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565257 | AGACGAGGTTTCACC[A/G/T]TGTTAGCCAGGATGG | 81550 |
rs185574017 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474783 | ACATTTACCATTTCC[G/T]TCCCTCTCTCTTTTC | 81550 |
rs185586107 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451960 | ACATCTTTATATGAT[A/G]TGATATTACCAGTGA | 81550 |
rs185594341 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423361 | TATACTGCTTTCATT[A/G]CTAGTAATGATAGAT | 81550 |
rs185614030 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481353 | TCCCTCTTTGTGTTT[G/T]TTTTTTTTTTGTATT | 81550 |
rs185628559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402247 | AGTTTTCTTAGAGAC[A/G]CACCTTTTTTCCAGG | 81550 |
rs185636626 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433309 | TCCTCCTTAAAAATA[C/T]AAGTAGTCCTCAAAG | 81550 |
rs185650072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403240 | AAACTTGCTACCTCA[G/T]CAGGTTGAAAATAAT | 81550 |
rs185673535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513894 | GCAGCAAGAAAATGA[A/G]CTAATATAGTAAATT | 81550 |
rs185738833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478484 | TAATTTTGGCATTTT[C/T]AGTAGAGATGGGGTT | 81550 |
rs185751830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428416 | TTTTCTAAGTTAATA[C/T]AGGGGCCAAGGGAAA | 81550 |
rs185752283 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564695 | AGTGTCAGATTTTTT[A/T]AAAAATGTTTGTAAA | 81550 |
rs185758622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546097 | CCTCTAAAAGCTTTG[A/G]GCACAAATACATTGA | 81550 |
rs185765819 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504144 | TTACCTCTAGGTTTA[A/T]CTTATCAAATCTGAG | 81550 |
rs185770156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522757 | TTCTGGCAGTCCTAG[C/T]GTCCAAATGTATTTT | 81550 |
rs185792062 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560796 | AGAAAAAAGATTAGA[A/G]CCACAATGGGATGTC | 81550 |
rs185805115 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497805 | AAGAAACAGCTTCCC[C/T]ATCCCCAGTAATGGC | 81550 |
rs185830735 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515269 | CCATTGTTTCGAATG[A/G]CTACTAAATACTTTA | 81550 |
rs185835116 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498723 | GTGAGTCTTTCTTCT[A/G]TCCTTCCCCAAGGAG | 81550 |
rs185836812 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447671 | ATGCAGAATTCTACT[A/G]CTTGAGGTAGGTTGG | 81550 |
rs185839091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479564 | GTGTTATGTTTCTGC[A/T]TTGATGATTTGTCTA | 81550 |
rs185841284 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419833 | GGATGAAAGCAGAAA[A/G]GAAGAAAAGGAATAA | 81550 |
rs185844765 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406555 | AGAACCAAGCTTTGA[A/G]TAAGAGGCTAGGTTC | 81550 |
rs185855477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538563 | TTATTTTAGCAAAGT[A/G]AATGAAACATTATGG | 81550 |
rs185865620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556841 | TTAATAGAATAAGGA[A/G]AAGTAGAATATTTAT | 81550 |
rs185873989 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456105 | ATTAATGGCTGGCAT[A/G]TATTTTCAGGTTAAG | 81550 |
rs185883130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400069 | AAACTATTAGATTTT[A/G]CTGATTTGAACTTGA | 81550 |
rs185901900 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456916 | GCCCAGGCTGGTCTC[A/C]AACTCCTGGGTTCAA | 81550 |
rs185940637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560552 | TATATTAATGTGTAG[A/G]TCTTAGTGATGTTAG | 81550 |
rs185966266 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402792 | AACCTCCACCTCCCA[G/T]GTTCTCCTGCCTCAG | 81550 |
rs185996311 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451524 | TGGCCATGGAAATTG[A/G]CACAAATTACAGATT | 81550 |
rs186059723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544902 | GAATTTTAAGTTAGT[A/G]TATGAACTGGGTTGT | 81550 |
rs186062732 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512351 | ATGAGATTTGGGTGG[A/G]GACACAGCCAAACCA | 81550 |
rs186081455 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475427 | AAAGGACATTATTTC[A/T]TTCTTATTTATGGCT | 81550 |
rs186087399 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422688 | CAAGATACCCAAGGG[A/G]AAATGGACTAGAATG | 81550 |
rs186093028 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572001 | GTTAAGACAGCTTGG[A/T]AATATGAGCAGATAT | 81550 |
rs186101357 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534461 | AATGTCTTTAATCCT[A/G]TAAATACTGGATCTA | 81550 |
rs186109577 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553791 | CCTCCCACCAGGTCC[C/T]TCCATTGACATGTGG | 81550 |
rs186116820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474422 | TTTGTGTTGTGTCTT[C/T]ATTTCTACATACTCT | 81550 |
rs186140553 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452893 | GTTGGTTTGTGCCTT[C/T]ACTCTTTGCTTCTTG | 81550 |
rs186181663 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541230 | TGGAGGGCAATGGCA[C/T]GATCTTGGCTCAGTG | 81550 |
rs186206502 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419008 | TGAATAAGGCTTGGA[G/T]CATTCATTTATAAGT | 81550 |
rs186235320 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469112 | GTTGCTGTACTATGC[A/C]ATATAAAGTAATGTT | 81550 |
rs186325733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412788 | TAGTGGTCTTTTAAA[A/G]TGGTTTACCTTATCG | 81550 |
rs186339799 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557726 | AGCATTTCTTATAAT[G/T]ATCTCTCCTACCACT | 81550 |
rs186388669 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490840 | AGAATGAATCTAGCC[A/G]GGCGCAGTGGCTCAC | 81550 |
rs186403310 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399485 | GACTAGGCATGAGGA[G/T]CTCCTAGGCTTTCAG | 81550 |
rs186408347 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553528 | AGAGATACTACCTGA[C/G]ACTGGGTAATTTATT | 81550 |
rs186411990 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447219 | ATTTCAAGAAGCAGA[A/G]GAGGCATGGTTGTGG | 81550 |
rs186488426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487093 | CTGTACTAAATGTGT[A/G]CAAACTTTTTTTTTG | 81550 |
rs186491433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511805 | CTCCTAAAAGCTGCC[C/T]TCAGATTATTGCCAC | 81550 |
rs186524451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490157 | CTTGGGACTTGTGCA[A/G]GGTTATCCAGTGATA | 81550 |
rs186549085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506148 | AAAGGTCAGGTTACC[C/T]TCAAAGGGAAACCCA | 81550 |
rs186550973 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525912 | ATTAATATAGTTCTC[C/T]AGTATAGTTCCATAG | 81550 |
rs186560065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399051 | TCTCATTTTTTAGGT[C/T]CCGAACACGTGTTGA | 81550 |
rs186571255 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554678 | GACTTCGTGCTTTCC[C/T]AACTTGTTCTTGCTG | 81550 |
rs186575175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504918 | CGGCCCAGATACTAT[A/G]CTTTTCTCACAGTCT | 81550 |
rs186578121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446184 | CATACTTCCAACACA[A/G]TATTAATAAACTAAT | 81550 |
rs186580082 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524466 | GAGCCGAGACTGCAC[C/G]ACTGTACTCCAGCCT | 81550 |
rs186580264 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572817 | GTATTTTTAAATGTT[A/G]AAATTTTTTTTGACA | 81550 |
rs186585534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418442 | TCCTCAAGTAAACCA[A/G]GCTTCACTGGGACTA | 81550 |
rs186587439 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488201 | TTTATATAGCAGAGA[A/C]GAAATCTATGTGCAG | 81550 |
rs186609133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571876 | TCTTGGGGAGCATGT[A/G]GAAAAATAGGCCCAA | 81550 |
rs186610188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547208 | AAAAAAAATCTCATG[A/G]CATTGTTCACCACTT | 81550 |
rs186633704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466568 | TGAGGCAGGTGGATC[A/G]CCTGAGGTCATGAGT | 81550 |
rs186642269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438936 | GATTTTTGATGGTTG[A/C]TTTTAGAATTGTTGA | 81550 |
rs186648987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415786 | GAGCCATGAAAAGAT[C/G]AGATTTGCCAAGTTT | 81550 |
rs186676281 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565679 | GAGAAAAGTAGTATT[C/G]CATTCTAATTCCTGA | 81550 |
rs186706728 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533238 | TGTAATATTAAATAT[A/G]CTAGTTAAAAACCAA | 81550 |
rs186714523 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60495171 | AGCTTAAACCATGGA[A/C/G]GTTTATTATTTCATA | 81550 |
rs186742920 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527575 | ATGGAGGAAGAAAGT[A/G]TAAATGACATGGTAC | 81550 |
rs186752759 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491755 | CAGTGTGTGGGTTGA[C/T]GTGGTCAAAATCTAT | 81550 |
rs186794692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566805 | ATTAACTATACTCTT[A/T]ATGCTATTTAATCTG | 81550 |
rs186800187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529320 | TGAGTCTTTTTCTAC[C/T]ATTGTACCTGTTTAA | 81550 |
rs186803679 | snp | A/G/T | 0.00279242 | 0.0372774 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408081 | GAGGCCTCCCCACCC[A/G/T]TGTGGAACTGTAAGC | 81550 |
rs186806338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552093 | AATCATGTCTTCCCA[A/G]CAGTTCCCCAAAGTC | 81550 |
rs186880280 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551226 | GTCCACATACCTTGG[A/G]AAAGATATAGAATAT | 81550 |
rs186926620 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469968 | ATTGTTGCACAGCTG[G/T]TACCACCATCCACTT | 81550 |
rs186964622 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507387 | CCTCTAATCAAGAGC[A/G]TATACATTTTTCTCA | 81550 |
rs186983759 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499865 | GTGTTACTCTGGCGG[A/T]TTTATCAAGTGACCC | 81550 |
rs186996153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480536 | TGCATGTTGACCTGT[C/T]TAGTGAGATTTGGAA | 81550 |
rs187002087 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459074 | TATCTTTTCCAATTA[C/T]GTTCTCTAGGCCTAA | 81550 |
rs187006475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430180 | ATAGTCTCTCCAGCT[A/G]CTCATGAAAATGCCT | 81550 |
rs187056783 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432131 | CTTTTTTCATTTTCC[A/G]CCATTTTTCATAGTA | 81550 |
rs187061812 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503863 | GTTTATTAATGTTAA[A/C]CCCAATTGGTTTAAA | 81550 |
rs187064675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409596 | TTGACTGTCCCACTA[A/G]ATTTCAGACTTGCCT | 81550 |
rs187081033 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424242 | TAGCCAGGATGGTCT[A/G]GATCTCCTGACCTCG | 81550 |
rs187086803 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463570 | ATGAACAAAGTGAGG[A/T]GACTACCTACAGAAT | 81550 |
rs187199277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560126 | AAGAAATGGAAATAT[A/G]TACCGTATGATGCAA | 81550 |
rs187205555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521131 | AATCTTTTTCTGTGA[A/T]CATTTGAACTCAATC | 81550 |
rs187233539 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497017 | CTAGTGTTCAGCTCA[A/G]TTAGGACGAACCGGG | 81550 |
rs187234177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557076 | CCGGGCATGGTGGCA[C/T]ATGCCTGTAATCCCA | 81550 |
rs187234629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404208 | ATATGTTTTCTTTAA[A/C]TATTGTGTCTTCTGA | 81550 |
rs187236814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477597 | GGAATGTTGAATTTT[A/G]TTGAAGGCCTTTTCT | 81550 |
rs187240655 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435895 | CTGCCAGCAGTGTAA[A/G]CCACATCATGACAAC | 81550 |
rs187241244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454087 | TCTAAATATTTTTCA[A/G]TTAACCTTATGATTA | 81550 |
rs187265285 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60485437 | TATGGAAATTAAGCT[C/T]TTAATTACAAAACCA | 81550 |
rs187301349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426856 | TGGGAACGTCACAGA[A/G]TGTTCTTACACAAAC | 81550 |
rs187305715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405830 | AAGTATCCTTGGACT[G/T]AAGAAAATGGAGCTG | 81550 |
rs187322126 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431221 | AATGTCAGAAACCTT[C/T]AAGCTAGTTTAGTAT | 81550 |
rs187348722 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549992 | TAATAATCTTGTTGT[C/G]GCATTGAATAGTATG | 81550 |
rs187351832 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516059 | CTGTTATAGACTCAA[A/G]TTGACATTACAAAGA | 81550 |
rs187356162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479793 | TGTTGGTTTAAAGTC[A/T]GTTTTAGTTGACAGA | 81550 |
rs187435810 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541373 | GGTTTCACCATGTTG[A/G]CCAGGCTGGTCTTGA | 81550 |
rs187450336 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500664 | GTGCGATTATATACT[A/G]ATTTATGGGCTGTAG | 81550 |
rs187451973 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517334 | GAAGGAAACTAGGCC[A/G/T]AGACAAGAGAGAATG | 81550 |
rs187467157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559045 | TTTTCAGCAAAATCT[A/G]TCAGTCTATTTAGTT | 81550 |
rs187499837 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540358 | TCTTTTAGTAAAGTT[G/T]GGTTGTGTTAGATGG | 81550 |
rs187504676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481226 | AACATGGTTGGTGTG[C/G]GTTTTATCCTGTTTG | 81550 |
rs187531236 | snp | A/T | 3.32978e-05 | 0.00408017 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535083 | ATACCAGTTGTCATA[A/T]TTAAAACTCCTTTTG | 81550 |
rs187541561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60562198 | CGTGCCTGTAATTCC[A/C]GCTACTCGGGAGGCT | 81550 |
rs187550579 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438011 | TCCTATAACATTTTT[A/G]TAGTTATTTTGGCCT | 81550 |
rs187578892 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457409 | GGACAGCCAAATGGA[C/T]GCATTAACTGAACCA | 81550 |
rs187610955 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499300 | GTGGTGACTCCAATT[A/G]CAGCTGCTGTACCAG | 81550 |
rs187614670 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396404 | GGACGCCCAATCGCG[C/T]GGTAGCGTCCGCCGT | 81550 |
rs187626126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414826 | TTGGTTTCAATTGAG[C/T]ATTCCTATCACACTT | 81550 |
rs187641987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536480 | TACTCTTCTGAGAGG[C/T]TCTCATATGATGGCT | 81550 |
rs187664802 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60513655 | GGGCAAGTCTTTCCC[A/G]AGATGTTCTTGTGAT | 81550 |
rs187716533 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497341 | CTGGGTTTAGATCCC[A/G]ATCATTGTCCCTCCC | 81550 |
rs187717613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477918 | ATTTCCTCCTTCTTG[A/G]TATTTATGGAACAGT | 81550 |
rs187798817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420719 | AGGCCGAGGCGGGTG[A/G]ATCATGAGGTCAGGA | 81550 |
rs187809156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508888 | AAGCCTACAAAAGGC[A/C]GGAAAATTTAGCCCA | 81550 |
rs187814679 | snp | C/T | 0.000792093 | 0.0198851 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528332 | AATGCAGAGTCTTCA[C/T]CTTAATTTGCATATG | 81550 |
rs187818697 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492732 | AATGAATCTAGTAAT[C/G]AATCCTTGGTAATTG | 81550 |
rs187820028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509138 | CAAGAAATTTCTTCG[C/T]AGGATATGTTTATAC | 81550 |
rs187828769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471345 | AAAAATTATTTGGCC[A/G]TATATGAACAAATTT | 81550 |
rs187831604 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425899 | TATTGTAGGAATATA[A/G]TACATTATACATATA | 81550 |
rs187834401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566270 | TAATAGTTCTTTTTT[C/T]TTTTTTAAGACTACT | 81550 |
rs187849505 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512668 | AGTCCGAAATCCAGC[A/T]TGTTAGTCAAATCTT | 81550 |
rs187850761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551644 | TGTTAAAATTTTCTT[C/T]TCTGTTTCAATGTGT | 81550 |
rs187861016 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396841 | CTGGGGACACCTCTG[A/G]GTTTTGCTGCCCGCA | 81550 |
rs187863158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476741 | GATTTCTTTGAGCAA[C/T]GTTTTGTAATTCTCA | 81550 |
rs187883981 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410564 | TGCAAGTTGATATTC[A/G]GGGGCCTCTACTCCT | 81550 |
rs187885973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470342 | TATGAACATGGGTAC[A/G]CAAATACCTCTTTGA | 81550 |
rs187890614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448155 | CTGTTTTCAGCATTT[G/T]GGAACTTGAGAGTGG | 81550 |
rs188064610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554959 | TTACACCAAAATGTA[A/G]TATATCTAGTAGTCC | 81550 |
rs188067976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449603 | CAACTTATGTGCCCT[A/G]CTGTTATTTTGAGGG | 81550 |
rs188090533 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401097 | TCTTTGCCTTGCAGT[G/T]AATCAACTAATTGTG | 81550 |
rs188104143 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516474 | TATTCTGAAAAAAGT[A/G]AGGTTGGATTGCATT | 81550 |
rs188106228 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493130 | TCACCGTGTTAGCCA[A/G]GATGGTCTCGATCTC | 81550 |
rs188114395 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395699 | TAAATAATTGGTAAC[A/C]GAAAATTCTAACCGC | 81550 |
rs188128733 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436900 | TTCCTGATCTTCTAC[A/G]ATGCAGAAGGGAACA | 81550 |
rs188137496 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406763 | ACTTGCTGATATTGG[A/C]GACTCAGAGCACCTT | 81550 |
rs188149684 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550553 | AGGATTTGTCTTAGT[A/G]AATAGATTGCCTCTG | 81550 |
rs188157286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506160 | ACCCTCAAAGGGAAA[C/T]CCATCAGACTAATGG | 81550 |
rs188160857 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526482 | CCGAAATCTTTACTC[C/G]TGGGCAGTAAACAAT | 81550 |
rs188178158 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564942 | TGTTATGGGTAACCA[C/G]ATTTGCTCTCAACAG | 81550 |
rs188224060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490255 | AGATTGCAATTTTAA[A/G]TATAATAGTCTGTTT | 81550 |
rs188230140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468803 | TAAAAAATACTTGTG[A/G]TATAAATGAATTACA | 81550 |
rs188236182 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447020 | AACAGAATATTTGAA[G/T]AAGTAATCTGCCTAT | 81550 |
rs188239525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568109 | CACTGTCCTAGAATG[C/T]GATATGTCTTTATCT | 81550 |
rs188279994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60573217 | GTGGAGCAACTCAAT[G/T]CAGAGGCGTTCACAG | 81550 |
rs188312430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520491 | TTCTTCTCATTAGGG[C/T]TCACCTAAACCCCAT | 81550 |
rs188321896 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502830 | AAAGGGAAGCATATC[C/G]TTCCAGTCAAAGCCT | 81550 |
rs188322112 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482873 | CACCTATTTTACATA[C/T]TTTAATCATAATGGT | 81550 |
rs188327817 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531438 | CTACCCTAGAAATAA[C/T]AGTCACTGTATCTGA | 81550 |
rs188337649 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409684 | CCCAATACCTGTACC[C/T]TCATTGTCTCTAGGA | 81550 |
rs188343852 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542487 | GTGAATTTCTGAGCT[G/T]CTTTCATCTGCATCT | 81550 |
rs188357810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536083 | CTTCATCATTGAAGG[A/G]TACATTGTTTTCTCA | 81550 |
rs188366463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460871 | AGCCAGGCATGATGG[C/T]GGGTGCCGGTAATCC | 81550 |
rs188370443 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414382 | CTGTAGCTGCTTTTG[A/T]GCTACAGGAGCAAAG | 81550 |
rs188385394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462194 | TCCTATGACGAATTC[A/G]GTCACACCCCTTGCA | 81550 |
rs188393348 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434067 | ATGCCAAGTGACTTC[C/T]GAACACGACGTGAAG | 81550 |
rs188399615 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410971 | GAAAGTTTGTATATG[C/T]GTATATTAAAAACAT | 81550 |
rs188403548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571632 | GCTGTTCAGTAAGTG[A/T]TTATTAAATCAGTAT | 81550 |
rs188406659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465342 | ATTTGCTGATTGTCT[A/G]GAATTGGGAACGCTT | 81550 |
rs188540372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546296 | CATTTATGTTGTATT[A/C]TTTAGAAATTAGCAA | 81550 |
rs188549214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514795 | GGCATTAAAGGGTTT[A/T]TGGCATAAGAGCCAT | 81550 |
rs188553613 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563625 | AACTCCTTCCAGGGA[C/T]TGGCTGATGCCCCCA | 81550 |
rs188559259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498438 | AAGCAAAACGGCAAT[C/T]AGAATATTCTGACTT | 81550 |
rs188561187 | snp | A/G | 0.21875 | 0.248039 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525012 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC | 81550 |
rs188568900 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60509466 | TTAAGTAGTTTTCTC[C/T]TCACTGTCTATATTA | 81550 |
rs188569492 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547834 | GTGGATTATTATGAC[C/T]CCTTCTTAACCTTCC | 81550 |
rs188583401 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465511 | TGATCACTAAAAATG[A/G]TTAAGCTTGGGGCCC | 81550 |
rs188590245 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552291 | TCAGCCAAAACAAAG[A/G]GGCCACAGGCCCCAT | 81550 |
rs188595610 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408039 | GCCGCCATGTAAGAA[A/G]TGCCTTTCACGTCCC | 81550 |
rs188612652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433239 | AGTGGGTAAAAGAGA[A/T]TAAAACTTTAATGTT | 81550 |
rs188623804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479015 | TGTCACCATCTTGGC[C/T]GGGCTGGTCTTGAAC | 81550 |
rs188624761 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504690 | CCTGCAGCTCCTAGC[A/G]AGACTAAGGCAGAAG | 81550 |
rs188625908 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456700 | GATGTTTTAGATGAC[C/T]TTTTTTGAGACACCT | 81550 |
rs188635571 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429903 | AAATATTTTGTAGAA[G/T]AAACAAGGGCACCAT | 81550 |
rs188796221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559496 | AAAATTATATATTCG[C/T]TCCTGTACTTAACTA | 81550 |
rs188798296 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559777 | AAAGGTTACGAAGTT[G/T]CAGTTATGCCAGATG | 81550 |
rs188814251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542976 | TCTAGTAAAAGAGTG[C/G]AGTTGTTCTGTTTCC | 81550 |
rs188827428 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561216 | GAGGTGAGTTTTTAA[C/T]TATAAAATGAGACAT | 81550 |
rs188827851 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482043 | TTTAGTCTGCATGGT[C/G]TGATCTGGCTGGATT | 81550 |
rs188844439 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433500 | GTGACCTAAAAGATA[A/C]TTGGTTCTTTTCTTG | 81550 |
rs188855877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519315 | GTAAATGCAAAATAT[A/G]TATTATTTCCGTTTG | 81550 |
rs188861831 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487625 | AGAACCAATCCCTCA[C/T]GGATACCAAAGGATG | 81550 |
rs188869976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503051 | TAAAGGCTGTAAATC[A/G]TTCAAAATAAGTTTC | 81550 |
rs188875841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520930 | TTTTCAAATTGAATC[A/G]TTACCATAATCCTGT | 81550 |
rs188882614 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523249 | TCTGGAGAATATTCT[A/G]CAAAAAAGTATTAAT | 81550 |
rs188902258 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455604 | AAACTATTTCATTTT[A/C]TCTTAATTTTAATCT | 81550 |
rs188921686 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400884 | ATAGAGCCCAGATGT[C/G]TAGAATAAAGATTCA | 81550 |
rs188990725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473655 | TTGTTTTATAATTAT[A/C]ACCTAGGAAAAACCA | 81550 |
rs189029281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401743 | AGGTCTCCTTCTTAC[A/C]TCTTGAATTTCACTT | 81550 |
rs189037868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556865 | TATTTATTTTTAAAT[A/G]ATATCTTTCATATAG | 81550 |
rs189049328 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450289 | CTTGACCTCTTTTGA[A/G]CAGAATTAATTTTTA | 81550 |
rs189057560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421632 | CTATACGGATGACTT[C/T]ACACCTAAGCAAAAT | 81550 |
rs189079237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418545 | GTAGATAGAGACTCA[A/G]CAAATGTTTATTGAA | 81550 |
rs189109160 | snp | A/C/G | 0.00914312 | 0.0669923 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537321 | TTAACTTAGTTGAGA[A/C/G]AAATATCTCCTCGAA | 81550 |
rs189112270 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461816 | GGTAACCAGGAGTGG[A/G]GTTAAAATATGAGTA | 81550 |
rs189119391 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497941 | AATTTATTGATTCAG[G/T]CCTGCTAAGTAGGCC | 81550 |
rs189138547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542077 | AGAGCCACAACTGAA[C/T]GGGGCTGGAATTGTT | 81550 |
rs189144644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501189 | CTGTATCATTCCCCC[C/T]GCTGGAGTGGTAACT | 81550 |
rs189241467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468213 | CTAAATTCTTCCACA[C/T]AGATCTTGTTGTAGC | 81550 |
rs189272697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398931 | GCCTTTCTCCCCATT[A/T]CTCATTAGGTTGAGC | 81550 |
rs189286211 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553229 | CACTGAACGCTTTCA[G/T]GATAAGCCAGGTCAC | 81550 |
rs189301566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445118 | ATGTTTATTTAATGA[A/G]CTTATTATATACAAA | 81550 |
rs189306911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418076 | TTTAGATCTTTTGTC[A/G]CCTACAGGATGAAGT | 81550 |
rs189326498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556255 | TGGTTCAAGATTAAG[C/G]TACATTTCAACTACC | 81550 |
rs189334488 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474437 | TATTTCTACATACTC[A/T]CATCTCCACACACGA | 81550 |
rs189358947 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478575 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCATGAGC | 81550 |
rs189369388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511624 | GCACAGCTTCATTGG[A/G]GCCTCTGTTTAAAGT | 81550 |
rs189381249 | snp | A/C/G | 0.0130921 | 0.0798413 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428518 | AAAATTAATTTTATC[A/C/G]TGCATAGCACAAGGG | 81550 |
rs189398189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422857 | GTCCCTAAGGGGAAA[A/G]AACCAAAACAATTGA | 81550 |
rs189402572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514276 | AAGAAATTTCTAAGC[A/G]GCAAAGCATTCAAGA | 81550 |
rs189470688 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532295 | TGAATGATCTTCTAC[A/G]ATGGCTACTTTGATT | 81550 |
rs189478408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552648 | TTCCCCTCTGAATTG[C/T]CCTAGTAGAGGTTCT | 81550 |
rs189480694 | snp | A/G | 0.00031385 | 0.012523 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510658 | CAGGGGGCGAATAAG[A/G]TCTGAAGATGAAGAG | 81550 |
rs189525622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566430 | AAGATTTAAAGAATA[A/G]AACTCAGTCTTCTTA | 81550 |
rs189539866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551708 | GATACTACCTGAGAC[C/T]GCGTAATTTATTTTA | 81550 |
rs189540501 | snp | A/C | 1.6823e-05 | 0.00290021 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494599 | AAAGAACTAACCACA[A/C]ATTTAAAGTGTTATT | 81550 |
rs189554291 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474262 | TGACCTTACCTATCA[C/T]TGTAGATGGCTCACA | 81550 |
rs189557965 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450686 | GTGCCAAGAGATAGG[G/T]ATGTAGAGATCAAGA | 81550 |
rs189624158 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451631 | AGGAATATAAACAGG[A/T]ATGGAACTCTACTGC | 81550 |
rs189626971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556752 | CAGAATGGTAACTAC[A/G]AAAATGTATAAAGGA | 81550 |
rs189632982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532823 | TTTTAAATTTGTCCT[C/G]AGTATTGCCACCACT | 81550 |
rs189637538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440058 | ATTTACAATAGCTAC[A/G]TAATAGTAGTAAAAA | 81550 |
rs189650555 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494803 | AATGTCCTAATAATA[C/T]ATTTTGGAATGGATT | 81550 |
rs189652412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559665 | ACACTACATGATCTT[A/G]CTTATATGTGGAATC | 81550 |
rs189671248 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488609 | GACAGAGTCTTGCTC[C/T]GTTGCCCAGGGTGGA | 81550 |
rs189685526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402898 | GGAGCTTATTGGAGA[A/C]ATCCTTCTATTTTGA | 81550 |
rs189716106 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397864 | GCCCGCGGGCCCATA[A/G]GAAGTTGAGGGCAGA | 81550 |
rs189778518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431588 | CATATTGTTTTGCAT[C/T]ATCAGAAGTTGTTTA | 81550 |
rs189790457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408973 | GGAAAAAGTGGCTTC[A/G]TGGGCTGGGCCCAGG | 81550 |
rs189884780 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538175 | TTATTTCTCCTTTTC[A/G]TGTGGATATGTATTT | 81550 |
rs189895778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462971 | TAAATCCACATACTT[A/G]TAGCCAACTCACTTT | 81550 |
rs189899409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493623 | AGCTGAGATTGCACC[A/G]CTGCACTCCAGTCTA | 81550 |
rs189909110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412069 | GGATTCTGAGAACTG[C/T]GGCCTAGCTCAGTGA | 81550 |
rs189912527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416298 | AGATTTTTTTTTTAA[A/C]TAAGGAAGTTTTAAG | 81550 |
rs189922263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505482 | GTCCCTGGGACAGAG[C/T]AACTGGGGGAAGGGG | 81550 |
rs189941427 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467670 | TTTATTTGTGTATAA[C/T]TCTTTCTGCAAAAAA | 81550 |
rs189950372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544907 | TTAAGTTAGTATATG[A/T]ACTGGGTTGTTAGCT | 81550 |
rs189970750 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522627 | AAAAGCTATGTAGTC[G/T]TTCTTTTGCTATTTC | 81550 |
rs189986487 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560579 | TTAGAGGAAGGACAA[A/T]GATGAATAGTACTGT | 81550 |
rs189998758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436859 | CTTCTGAAAACTTGA[A/G]TATCTAATAATTAGT | 81550 |
rs190006935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413588 | TGCTGAATGCCCAGT[A/G]AATACTTAATGTTCT | 81550 |
rs190026915 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504092 | GATTAATTTTAAAAA[C/T]TTTAGAATTTTTTAA | 81550 |
rs190027565 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445970 | TTACTTTTAAAAGTT[G/T]TGCACAGTGGTCTCT | 81550 |
rs190031019 | snp | A/C | 0.000146657 | 0.00856194 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485776 | GAACTACTAAGTTGA[A/C]TTATTCTTACTTGTT | 81550 |
rs190035933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465104 | AAAATTTAGCCCCTA[A/G]TTCCTTTTGTGGGAA | 81550 |
rs190148117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505737 | CTTTGTGAAGCATAC[A/G]CAAGTATCAATAGCC | 81550 |
rs190152081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435446 | CCAGTAGAGTCCCCA[A/G]AGTCCATTATATCAC | 81550 |
rs190162845 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549432 | AATGCCCTATAAAGC[C/T]GGTTTTAGCTTCTGC | 81550 |
rs190180296 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484313 | AATTGATTCTCAACA[A/G]TCTTCTCCAGCCTGC | 81550 |
rs190189108 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428277 | AATTTAATTACTTCT[C/G]TAAAGACTGTCTCTA | 81550 |
rs190201228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541256 | CAGTGCAACCTCTGC[C/T]TCCTGGGTTCAAGCC | 81550 |
rs190209391 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516913 | AATTTGATCACACTA[A/C]CTGCTGGCTTAAAAT | 81550 |
rs190217364 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565276 | TAGCCAGGATGGTCT[C/T]GATCTCCAGACCTCG | 81550 |
rs190249591 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432168 | CCTCTGAATTACCTT[A/T]TGTAGAATTCTGATC | 81550 |
rs190255923 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409625 | CTGGGCCCTGTAACC[C/T]CTTTGTTTTGGCCAA | 81550 |
rs190273828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500197 | GGTCATCAAGTCACC[A/G]TGCAACCTGAACTGC | 81550 |
rs190276051 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480672 | CATATTTCTTAGAGG[G/T]TTTGTTCATTTTCTA | 81550 |
rs190280008 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550820 | AAAAATAAAACTTTA[C/G]ATTTGTGAAGTAATA | 81550 |
rs190292426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459689 | GCAATGGCTTGATCT[C/T]GGCTCACTGCAACTT | 81550 |
rs190355671 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512129 | TGGCTGGGGAAGCCT[A/C]ACAATCACGGTGGAA | 81550 |
rs190395484 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489015 | AGGTTGTCTCTTCAC[C/T]CTGTTGATTGAATTC | 81550 |
rs190403416 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403878 | TACAATAATAAGTAA[C/G]GCATATACAGAGAAA | 81550 |
rs190417849 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560155 | AATGAAAAGAACTTC[A/C]GGTGTACAGCCTAAA | 81550 |
rs190421871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564095 | AATATTAGTATAAAA[A/G]CTCATATTGAGTATT | 81550 |
rs190423449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525555 | AGTAATGGATATGAA[A/G]TATGTTCATTATTAA | 81550 |
rs190424416 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60521534 | GAAAGATGCCCATGA[C/G]ATACTGTTCATTTTA | 81550 |
rs190426128 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474952 | CATTGAAAGATTTTT[A/T]AAATTTTTCTTAAGT | 81550 |
rs190434483 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452444 | AGATATAATTTTTAA[A/T]ACACCATTTACAACA | 81550 |
rs190445498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423862 | GAACTAAATTTTCAG[C/T]GAAACTAAAAAAGAT | 81550 |
rs190445666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406082 | TCATGAGTTAAGTTG[C/G]TCATTACTTGAGTGT | 81550 |
rs190451661 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402405 | TTTATGCATATAATA[A/G]GAGGGTATTAGAAGT | 81550 |
rs190459290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560806 | TTAGAACCACAATGG[A/G]ATGTCCCACAGTCCT | 81550 |
rs190526108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546099 | TCTAAAAGCTTTGGG[C/T]ACAAATACATTGACA | 81550 |
rs190610557 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539604 | ATATTTTCATGTTAG[C/T]GTACTTTAAAATGAA | 81550 |
rs190619787 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60491884 | AATGTGTAAAATAGT[G/T]GTCTAGAAGATTAGG | 81550 |
rs190645467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499422 | CCATAAGGTCCACCC[A/G]AAGCAATTTGCCTTC | 81550 |
rs190648889 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503964 | ATAATGCTTTTTGCT[A/G]AAGGGCAGATTGGCA | 81550 |
rs190655659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458593 | ATTTGAATGGAAGTG[C/T]GGTGCCTAGGATGCA | 81550 |
rs190664863 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544576 | TTTCTACTTTGTGTC[A/C]ACATTTATATTGCTC | 81550 |
rs190673587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470127 | ATATGTGTGGAATCA[C/T]ACAGTATATATCTTT | 81550 |
rs190677613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540399 | ATTTCTTCCTCATCT[A/G]TCACCCAGCCTTTTA | 81550 |
rs190678352 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499027 | AGCTGGCAGAACCCT[C/G]ACACTGGCTCCCTGA | 81550 |
rs190682476 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515347 | AAAGGTTTACCTTAC[A/C/T]AGGACCTGATTGCAC | 81550 |
rs190686194 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447878 | GGGTGTCATCTTAGT[A/G]GAAACTGCCTCCATT | 81550 |
rs190690460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400079 | ATTTTGCTGATTTGA[A/G]CTTGAATGTTCCAGG | 81550 |
rs190691015 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422237 | GGAAAAATTAAGGCC[C/G]TGTGAGACAAAATAG | 81550 |
rs190694570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419938 | TTTAATGTTTTTCCT[A/G]TAAGTAAAAATATTT | 81550 |
rs190851957 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572013 | TGGAAATATGAGCAG[A/T]TATAAAATAGAGAAA | 81550 |
rs190860403 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534771 | TCTCTATAAAAAATA[C/G]CAAAAAATTAGCCAG | 81550 |
rs190866238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554395 | TTTATTTCTCTTTGA[A/G]CCTTAATTAATAATC | 81550 |
rs190885180 | snp | A/T | 0.00319098 | 0.0398384 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512802 | TTGCAGGATACAGCC[A/T]CCCTCCCAGCTGCTT | 81550 |
rs190893333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476771 | ATTGTAGAGATCTTT[C/T]GCCTCTTTGTTAAGC | 81550 |
rs190900416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480012 | ATTCAGGGTCAATAT[C/T]GATATGTTAGGGTTT | 81550 |
rs190907879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554716 | TTTAGCTACAGCTGA[A/G]TGGCAAAGGAGAAAT | 81550 |
rs190919319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557413 | AGTGACTGCTGGAGT[A/G]CCTCACATTTTTGAA | 81550 |
rs190926610 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512435 | AATCATGCCTTCGCA[A/G]CAGTCCGCCAAAGTC | 81550 |
rs190927994 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516397 | TTTTTCTCAGCATTG[A/G]CTTTTTGTTGTTATA | 81550 |
rs190932146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496439 | GGATGTATTTGTTTC[A/G]TTAGATTTGGGATTT | 81550 |
rs190933158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475496 | TATCCAGTTCTGTGT[C/T]GATGGACCTCTTCAC | 81550 |
rs190957729 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395352 | CTAATTCTATCATTT[G/T]TTCTACATTTACTAT | 81550 |
rs190966431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399060 | TTAGGTCCCGAACAC[A/G]TGTTGACTTTGTTTT | 81550 |
rs191093108 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572844 | GACAATCTGGTCCAG[C/G]ATCAATGTCAGGAAA | 81550 |
rs191112476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436383 | CTAAACCATGAAAAT[A/G]TTTAGAATTTTCATG | 81550 |
rs191121588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412999 | CAACTTGCTTTTTGC[C/T]GTTACGGCCTGCCTG | 81550 |
rs191137634 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496873 | GCTTCCAAGATGGCA[A/G]CAAGCTGCTTGTTCT | 81550 |
rs191137993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410818 | TTTTGGTTGTTGCTG[A/G]TAAATTTTTTGACTG | 81550 |
rs191139483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470519 | TTACATCCTCACCAA[C/T]GGTTGGTATTTTGTG | 81550 |
rs191141871 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557972 | GGACTATAGGCACAC[A/G]CCACCACGCCCAGCT | 81550 |
rs191159103 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508988 | AAGACTTTAAATGGA[C/T]TGTCTTATATATGCT | 81550 |
rs191162934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461840 | ATGAGTAGGTATTTT[A/C]AGGTGCAGGGAGGGA | 81550 |
rs191173672 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535582 | TAAATTATGTCCAGC[A/T]GCTGTCAAATTCAAA | 81550 |
rs191177121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433853 | TATAGCCAGTGAGTA[A/G]GTTAGATTCACCGAT | 81550 |
rs191184339 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490977 | ACAAAATTAGCTGGG[C/T]GTGGTGGCGCATGCC | 81550 |
rs191207052 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447273 | AGGCATTAAATGATA[C/T]GGACCAGGAACAGAT | 81550 |
rs191210272 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527244 | ATACCTTTTGGCCTC[C/T]AGTGGCTGTTTGGAA | 81550 |
rs191247139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399521 | TTCTACTAGGTCTTT[A/G]ATTGGGGACTTACTA | 81550 |
rs191330968 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60562238 | GAATAGCTTGAATCC[A/G]GGAGGTGGAGGTTGC | 81550 |
rs191351169 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60547455 | AAGACCTGGGTTCGA[A/G]TCCTGGCTCTGCCAC | 81550 |
rs191385220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466775 | ACTTGAGGAGCTTGG[A/G]TGACGGAGGCTCTGT | 81550 |
rs191389244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439599 | TAGCAGAAGCACTTT[A/G]TAGTAGAAAACAAAA | 81550 |
rs191410337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504988 | GCCACCAGGACCCTG[A/G]GTTTCCAGCACAAAA | 81550 |
rs191412466 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524637 | AAATACTTACTTTAT[A/G]TATGACTTTATGATT | 81550 |
rs191427606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469748 | GTGAAGAAGCACTAA[A/G]CATTCAGTAAACTAT | 81550 |
rs191428524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488246 | AGGAGGGGTAAGGAA[A/G]CAATTCTGATGAATG | 81550 |
rs191439485 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533507 | TTAGCCAGGTGTAGT[A/T]GCACGTGCCTGTAAT | 81550 |
rs191447869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465494 | GTTTTGTCAGTTGTG[A/G]TTGATCACTAAAAAT | 81550 |
rs191458149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571955 | AGAGCCCAAAACTCC[A/G]AACTTCTAGTTCCTG | 81550 |
rs191469648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507224 | GAGACCTACAAAGAG[A/G]TCTTAGACTCCCACA | 81550 |
rs191470713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504371 | TATGGAGCCTAGGAC[C/T]CAGACAGAAGTGCAG | 81550 |
rs191496487 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419416 | TAGCCTAAAGAAAAT[A/G]TGGAACATATACACC | 81550 |
rs191510268 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60414405 | GAGCAAAGAGTAGTT[A/G]TGACAGAAATCAAAT | 81550 |
rs191580504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559759 | AATGAGGAGATGTTG[A/G]TCAAAGGTTACGAAG | 81550 |
rs191590948 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542829 | TTTAAATTTCTTTTT[A/C]TTTTTACCTCTGGTG | 81550 |
rs191611762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405109 | TTTTGTAAATTGCCC[A/G]GTCTCAGGTATGTCT | 81550 |
rs191665777 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520723 | GAGTGACTAGGAGAG[C/T]GTTGACGACACCACC | 81550 |
rs191673706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502895 | TTGCAAAAGGAAAAT[A/G]GATTCTTATTGAACT | 81550 |
rs191686242 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487392 | GAGGCAAGAGAATCA[C/G]TTGAACTCGGAAGGC | 81550 |
rs191705128 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436959 | ATACCTGTTCTTGTT[C/T]AATGTACTTTGGAGC | 81550 |
rs191708931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507810 | ATAAAGAGTATTCAC[A/G]TAGGAAGAGAGGAAG | 81550 |
rs191714012 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522856 | GGTGATAAAATTGAA[A/G]GTAACATGTTGTTGG | 81550 |
rs191730052 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551347 | CAGTAAACATTTTGT[A/T]AGGTCATTGAATGTT | 81550 |
rs191731130 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553585 | GGTTTAATTGACTCA[C/T]GGTTCTGCATGGCTC | 81550 |
rs191748117 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396028 | GAAATGAGAAAAATC[C/T]GTATTAAGGAATTTT | 81550 |
rs191752033 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430708 | CAAAGGAATTATTTA[C/T]AAATTTTTACTTGCT | 81550 |
rs191783581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401263 | AAAATAAAAATAACA[A/G]TACAACAACAAAAAT | 81550 |
rs191784572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479638 | TGTCTAAGTCTTTTC[A/T]TAGGTAAAGAAGAAC | 81550 |
rs191913558 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563651 | CCCCAGCCGAGGCAG[A/G]TAGCTCTCACTTGAG | 81550 |
rs191957327 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536187 | AAAAGAGAAATAAAA[C/T]GGCAACAGAAAAACA | 81550 |
rs191968588 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513585 | CCCACCCAAATCTCA[C/T]CTTGAATTCCCACAT | 81550 |
rs191972060 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452934 | TCAGTTATCAGTTTC[A/G]TTAGTCTTTGTTACA | 81550 |
rs191980224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485477 | CTTATTGTGCATTAG[C/T]CAAGATTGTTTGAAA | 81550 |
rs191984718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404283 | TTCAACAAATAATTC[A/G]TTTTTGTTGTTGTTG | 81550 |
rs191991710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527613 | AACAGAATAAAAATC[A/T]CTATGTGAAATACAG | 81550 |
rs192008032 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566201 | GTCTTAGAAGTATTA[G/T]GGCAAAGTCACAAAG | 81550 |
rs192010430 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426872 | TGTTCTTACACAAAC[C/T]TTAATGGTATTGCCG | 81550 |
rs192021156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405896 | AGAGAGCAGCAGATC[A/G]ACTTGACAGATATTT | 81550 |
rs192032519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497279 | AAACAGAGCTCCCAT[A/G]AAATGGGAGGGGACC | 81550 |
rs192047857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477633 | TATTAAGATGATTAT[A/G]TAGTTTTTGTTGTTA | 81550 |
rs192055044 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455269 | AAGAGATGTTTTGAC[A/G]GAGAAAGTAGGTAAA | 81550 |
rs192059866 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408202 | TGCCTTTCACCTCCC[A/G]CCATGATTCTGAGGC | 81550 |
rs192144287 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542100 | GAATTGTTCAGGTGA[A/T]CTTATTTTTCCCTTT | 81550 |
rs192158170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501452 | ACTAATATAAATGGA[A/G]CATTCCTTTTGGGAT | 81550 |
rs192227098 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559226 | GGTCATTACTATAAT[A/C]TATATGAGAAAACGA | 81550 |
rs192227303 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509580 | ACTCAAGGCACAACC[A/C]CACATATCATACAGA | 81550 |
rs192269109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422147 | AAATGCATAGCTTCT[G/T]GGGGAGAAAGAAACA | 81550 |
rs192290762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402133 | TTCTTTTCACATTCC[A/G]TTACATAGAGGCTTC | 81550 |
rs192293416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541492 | TTTTATTTTTTTTTG[C/T]ATACGTGAATAATAC | 81550 |
rs192293671 | snp | A/G | 1.67736e-05 | 0.00289595 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494397 | CTATTTTTAAATGCT[A/G]TCTACATACCTCTCT | 81550 |
rs192296397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473780 | GGGCTCCCTGGTCTA[A/G]CGGACAAGGCCACTA | 81550 |
rs192300647 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518897 | AATATTATTAGGGGC[A/G]TTTCTAAATTCAGAT | 81550 |
rs192302464 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450352 | CATCTGTTTTTAGTA[A/T]GTAACAAATATTATC | 81550 |
rs192310832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424654 | TGTACCCCAGCCTGC[A/G]CAACAGAAGGCAACT | 81550 |
rs192313264 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464304 | CAAACACCACTGATC[A/G]GAATGTAAATTAGTG | 81550 |
rs192454915 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555913 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 81550 |
rs192460832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488112 | CCAGGAAAGAAGGCT[C/T]TATTTGGGTGCTACA | 81550 |
rs192493369 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415203 | CCTAATGAGATCCTG[C/T]TTTACAATATTCATT | 81550 |
rs192496166 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60397153 | CTGGGAGCCCCACAC[C/T]AGGCCGGCCCCTACG | 81550 |
rs192501977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537034 | ATATTCTTCCTACTT[A/G]TTTGTGAATATTTAT | 81550 |
rs192508137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426116 | GAAGGAGATCCTGCC[A/G]TTTCTCACCCATGAA | 81550 |
rs192516426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519410 | TCTAAATGGTTTTTG[A/G]CCCACAAGTCTAGTG | 81550 |
rs192517320 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513672 | GATGTTCTTGTGATA[A/G]TGTAAGTCTCATGAG | 81550 |
rs192535302 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465863 | TTAGAAGTACTATTT[A/G]CAGTACTTCTTGCTG | 81550 |
rs192538391 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396585 | ACGGATGGTCCCAGG[A/G]GGAGGGCAACAGGAA | 81550 |
rs192540255 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438125 | TTACTAATCTTGTTA[C/G]TGATTTCACACAATA | 81550 |
rs192566221 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559555 | ACATGATGTTTATAG[A/T]AGCTTCATGGCTGAA | 81550 |
rs192588970 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448284 | GCTCTCATTCTAAGA[C/T]GCATCAGAGGCCTTC | 81550 |
rs192607275 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482521 | TATGGTATTATTTGC[A/C]ATTCATGAACTTTTC | 81550 |
rs192654100 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401048 | AAAGATAAAGGGCTT[A/G]TTCTGAGGGGTGATC | 81550 |
rs192700548 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530423 | TGTGAGAAGCAACTC[A/C]AAAGAGGAAAAATAT | 81550 |
rs192775665 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416013 | TCAGTTAATAATGTT[C/T]ATTAGTGTTAATGTT | 81550 |
rs192802992 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453592 | GCAAATGTTTAACCG[A/T]GGTTCTTGACAAAGT | 81550 |
rs192810594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505542 | AACATTCCTGCCTGC[C/T]GGCTCTGAAGCAAGC | 81550 |
rs192813916 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467855 | TAACAATATCTTCAT[C/T]TTTCCAGTCATGTAG | 81550 |
rs192825234 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60573848 | AATTTTTCTTCTGCC[A/G]TCAATAAAACCATTG | 81550 |
rs192827931 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548772 | GGATGCAGTGATATG[G/T]GTACTCTTATACATT | 81550 |
rs192893866 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509409 | CCTTCTAGTATGGAG[A/G]AGTATCAAAAAATTT | 81550 |
rs192901129 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471894 | AGCCCTGGCTAAAAC[C/T]TTTAATATAGTGTTG | 81550 |
rs192901470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552197 | TTTGAGCCTGTAAAA[C/T]CAAAAGCAACTTAGT | 81550 |
rs192931582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420752 | TCAAGACCATCCTGG[C/G]TAACATGGTGAAACC | 81550 |
rs192932103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552395 | ACATCCAGGGCACGC[G/T]AATGCAAGGGGTAGG | 81550 |
rs192958314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481266 | GAACTTTTTTGATCT[A/G]TGAGTTTATTGTTTT | 81550 |
rs192963568 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433252 | GAATAAAACTTTAAT[A/G]TTTGCTTTTATGGCT | 81550 |
rs193015264 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555198 | CCTTTTGAAATCTCA[A/G]TGTAAGCAAAAATTC | 81550 |
rs193019431 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488615 | GTCTTGCTCTGTTGC[A/C]CAGGGTGGAGTGCAG | 81550 |
rs193031989 | snp | C/G | 0.218151 | 0.247963 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525013 | AATCACTTGAACCCG[C/G]GAGGTGGAGGTTGCA | 81550 |
rs193051999 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440778 | AGCTATAAACAATCA[A/C]ATGTATGTACTACAA | 81550 |
rs193078037 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523404 | CAATTATCTCACAAA[C/T]ATACATTTTGAAAAT | 81550 |
rs193079993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497788 | GAATTTTTTTTTGCT[A/G]GAAGAAACAGCTTCC | 81550 |
rs193084158 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456063 | TGACAGAGTGAGACT[A/G]TGTCTCAAAAAAAAA | 81550 |
rs193096994 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561690 | ATTCCTTACCCTCAT[G/T]ACTGGGTACCACAGT | 81550 |
rs193107206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406118 | CCCTTTAAGTCATCT[A/G]AAATAAGATGTTAGG | 81550 |
rs193171831 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531690 | AAAGCAACTCTCTAC[A/G]GGATCAGGGATATCT | 81550 |
rs193176984 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60569469 | GTTCATGGATTAGAA[A/G]AATCGATAGTGTTAA | 81550 |
rs193183957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461250 | TTTATAGGCTAATAA[A/G]TTTTCCTAGGAAATG | 81550 |
rs193189786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500978 | GAGGGAGGGAGGTTA[C/T]GCTTGGGCTCAGCAA | 81550 |
rs193199788 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409825 | CTTTGGTGGACTGTT[C/T]GGAAGGCATGATTGG | 81550 |
rs193243937 | snp | A/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478015 | CTAGGATTTTTTTGG[A/T]TAAGAGATTTTTTTT | 81550 |
rs193246463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504840 | AAGCACAAGGGGTCG[A/G]GGAACTGTCTCCCAT | 81550 |
rs193250655 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546805 | TTAATAAAAACTTAC[A/C]CTCTTTTATACAAGA | 81550 |
rs193260369 | snp | A/C | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428332 | CAGGCATTAGGACAT[A/C]AGCATATCTTTTTGT | 81550 |
rs199548177 | snp | A/G | 1.86726e-05 | 0.00305548 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529244 | TTAAAGATATTATAC[A/G]CTAATATTACGAAAT | 81550 |
rs199570394 | in-del | -/AAAG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553565 | AAATAAAAAAAAAAA[-/AAAG]AGGTTTAATTGACTC | 81550 |
rs199600596 | in-del | -/T | 0.0174175 | 0.0916809 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569571 | TATAAATAGAAAAAA[-/T]AATTCTAAAATTTAT | 81550 |
rs199642725 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554852 | TAATCAGTTCCCCCA[A/G]CCTCTGTTGAACATC | 81550 |
rs199653593 | in-del | -/GT | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469307 | TAGAGATTTTTTAAA[-/GT]GTGGTAAAAAGTTCT | 81550 |
rs199663484 | in-del | -/ACACATACACACAC | 0.0225045 | 0.103662 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464566 | TATATGTGTGTGTAT[-/ACACATACACACAC]ACACATACACACACA | 81550 |
rs199694530 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476570 | TGAATTTTAGAATAG[-/T]TTTTTTTTTCTAATT | 81550 |
rs199725656 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524518 | TCTCAAAAAAAAAAA[-/T]AAATAAATAAATAAA | 81550 |
rs199748576 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430779 | GGTGAATGCCTTCAT[A/G]GATTGGTTTATGTAT | 81550 |
rs199775571 | in-del | -/T | 0.303438 | 0.244222 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436109 | CTTTTGGATGGGTTG[-/T]TTTTTTTTTTTTCTT | 81550 |
rs199785197 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524313 | GGAGTTTGAGACCAG[C/T]CTGGCCAATATGGTG | 81550 |
rs199803964 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527000 | CCACCACACCCAGCT[-/A]ATTTTTGTATTTTTA | 81550 |
rs199833716 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469433 | CAACACACACACACA[C/T]ATACACACACACACA | 81550 |
rs199860029 | snp | A/G | 1.64993e-05 | 0.00287218 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509888 | TCTTACAAGCAATAA[A/G]CAGAAACCTGTTATG | 81550 |
rs199882415 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402721 | TTTTTTTTTGAGACG[C/G]AGTTTCACTCTTGTT | 81550 |
rs199889576 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60521897 | GTGAAACTCCGTTTC[-/A]AAAAAAAAAAGAAAG | 81550 |
rs199904389 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568956 | TGTCAACCGCAATTG[-/T]TTTTTTTCCCCCCTT | 81550 |
rs199924422 | snp | G/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395220 | AGTAAGTTATGGCTT[G/T]AAACTTTGAGACCAT | 81550 |
rs199926535 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431106 | TGCTTACTAAATGAG[-/T]TTTTTTTAAACCCTG | 81550 |
rs199945423 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471810 | ATAAGATCACGTTAT[A/C]TGTGAAGAGTTAATT | 81550 |
rs199987288 | snp | C/T | 4.94295e-05 | 0.00497115 | synonymous-codon, missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567605 | ATCCACTCGGCCAAC[C/T]CAACAGTTTTACCAA | 81550 |
rs199994890 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455384 | AGGCAGCTTTCTTGA[A/G]ACATTGCCCTGTTAA | 81550 |
rs200008616 | in-del | -/T | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457802 | TAGCAGTCCTTGGCC[-/T]TTTTTTGGCTTGTAG | 81550 |
rs200011400 | in-del | -/TG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466977 | AATGTGTGTGTGTTT[-/TG]TTTTGTTTTTTTGTT | 81550 |
rs200056651 | in-del | -/TTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477213 | TTATTATTATTATTA[-/TTG]TTATTATTATTATTA | 81550 |
rs200082561 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60480706 | TATAATTTACCTCAG[G/T]TTGGGGGTGTTTTCA | 81550 |
rs200126114 | snp | C/T | 8.25525e-05 | 0.00642413 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535114 | CCTCCTCAGTTTTAC[C/T]GGGCAGAAGTTGAAG | 81550 |
rs200129552 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506420 | AGGAGCAACCGGTAC[C/T]AACCACTGCAAAAAC | 81550 |
rs200139136 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564740 | TTATTTTTTTGAGTT[-/G]TAAATCTCTTACAGA | 81550 |
rs200150336 | snp | A/G | 0.000615811 | 0.0175364 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510764 | GTGGAAGGTAAGCTA[A/G]TTTAAAGTTGATTCC | 81550 |
rs200167488 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407923 | TGAATCATGGGGGTC[A/G]GTCTTTCCCATGCTA | 81550 |
rs200178365 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550235 | TGAACATCCCATTTG[-/A]AAAAATGTATTCTAG | 81550 |
rs200188849 | in-del | -/GTTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561858 | CTACTATGGGCCCAG[-/GTTTT]GTTTTTTGTTGTTGT | 81550 |
rs200197577 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492955 | ACGGAGTCTCGCTGT[A/G]TCTCCCAGGTTGGAG | 81550 |
rs200205483 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560084 | TTGACTGTAGAAAAA[A/G]GTTCCTGATAGAAAA | 81550 |
rs200226325 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474170 | ATAGAAGAAATAATG[A/G]CGTAAGCTGTCCTCT | 81550 |
rs200252699 | in-del | -/AC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474690 | GTTACGAAGGTCACA[-/AC]ACACGTTTTAATTTT | 81550 |
rs200261711 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453482 | TTTCTCTAGCAACAC[-/T]TTTCCTTTAATCAGT | 81550 |
rs200273986 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429807 | CCTTTATCATTAATT[G/T]TATTCTCTTTCTTTC | 81550 |
rs200274019 | snp | A/G | 0.000742164 | 0.0192492 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528644 | CAAATGTGATAGACC[A/G]TATTCTAGATATGAC | 81550 |
rs200306828 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60510539 | AAGAAATTAAAATCC[G/T]TATTTAAAATTATTG | 81550 |
rs200497841 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520836 | AGCTGCTCAGTGGTT[A/G]GGACTGGAATTTAAT | 81550 |
rs200529221 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427315 | GGTAATTTTGGATTT[G/T]GTAGTGCATATTAAT | 81550 |
rs200543051 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497229 | TAACAAACATGGACC[A/G]GAAGAGTGTGCAGTT | 81550 |
rs200580339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425722 | TTTTCTTTGATTTCT[A/G]CCATGCCACCACTGA | 81550 |
rs200615235 | in-del | -/AAG | 0.0425829 | 0.139564 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553566 | AATAAAAAAAAAAAA[-/AAG]AGGTTTAATTGACTC | 81550 |
rs200650371 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401497 | ACTGAGGGATGACTG[C/T]ATCTGAAAAAGTGGG | 81550 |
rs200659190 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427401 | TGTTATTAAAGGTAC[-/T]TTTTTTTTTGTGGGG | 81550 |
rs200672430 | in-del | -/TC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555851 | ACCAACCTATTTCTT[-/TC]TTTTTTTTTTTTTTT | 81550 |
rs200705692 | in-del | -/C | 0.0146672 | 0.084371 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404703 | TCCACCTCCCAGGTT[-/C]AAGAGATTCTTCTGC | 81550 |
rs200709122 | in-del | -/TTC | | | upstream-variant-2KB, intron-variant, cds-indel | TDRD3 | GRCh38.p7 | 13:60397260 | GACCAGAGGAGTTTT[-/TTC]TTTTCTTTTCTTTTT | 81550 |
rs200713646 | snp | C/T | 1.65836e-05 | 0.0028795 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528787 | CAAAAGAAAATCCAC[C/T]TCCTCAAGGATCTGT | 81550 |
rs200771315 | snp | C/T | 1.64985e-05 | 0.0028721 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494541 | AAAAGTCAACCAAAT[C/T]AGAGGGAAAACATGA | 81550 |
rs200821042 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471751 | TTAGTATTCTAACAG[-/T]TTTTTTTTTCTTTTT | 81550 |
rs200821664 | snp | C/T | 3.29717e-05 | 0.00406015 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483851 | CTTTTGGACAGGTAA[C/T]GACTTTTGTGTTGGC | 81550 |
rs200908264 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60519489 | TATCTAAGTAGCTAA[A/C]TTACTCAGATACATG | 81550 |
rs200910470 | snp | A/G | 0.000230684 | 0.0107373 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567562 | AAACTCTGGAGTTCC[A/G]TAGGGGAGGTGATGG | 81550 |
rs200925098 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561866 | GGGCCCAGGTTTTTT[-/G]TTGTTGTTGTTGTTG | 81550 |
rs200925237 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561923 | CAAATATTAAAGTGG[-/A]AATTTTTTTAAACAA | 81550 |
rs200956867 | in-del | -/TTCTTTCTTTCT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541147 | CTTTTTGTTTTTCTA[-/TTCTTTCTTTCT]TTCTTTCTTTCTTTC | 81550 |
rs200978606 | in-del | -/AAAA | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532134 | TGAAAAAATTAAATT[-/AAAA]AAAATCAAAGTACCA | 81550 |
rs200982410 | snp | G/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60437981 | TGTTTTTCCCATCCC[G/T]CAGCCACTTTGAGCT | 81550 |
rs200999475 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490946 | AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT | 81550 |
rs201004925 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505590 | AGTGCTTCTTAACTA[A/T]AGGAGCATGTTCTAA | 81550 |
rs201025317 | snp | G/T | 1.64966e-05 | 0.00287194 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467259 | CACACCACCTGGAAC[G/T]AAAGTTAAGCTCTCA | 81550 |
rs201037022 | snp | A/C/G/T | 0.000148484 | 0.00861527 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528643 | TCAAATGTGATAGAC[A/C/G/T]GTATTCTAGATATGA | 81550 |
rs201045709 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501672 | AAATCATTTTATGAC[-/T]TTCCCCAAACCATCC | 81550 |
rs201145600 | in-del | -/AT | 0.145642 | 0.227177 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490946 | ACATGGAGAAACCCC[-/AT]GTCTCTACTAAAAAT | 81550 |
rs201162925 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526633 | TTTTTTTTTTTTTTT[-/T]AAAGATCTCTCTTAT | 81550 |
rs201169975 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486015 | AGATTATTTGTGATC[A/G]TTATTGTCTTTTCAT | 81550 |
rs201174692 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538974 | CTTTTTAAAAGTTCA[A/T]AGTATCTGCTTCTTG | 81550 |
rs201181028 | in-del | -/TGTTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561865 | TGGGCCCAGGTTTTT[-/TGTTG]TTGTTGTTGTTGTTG | 81550 |
rs201181278 | in-del | -/ATATT | 0.0142736 | 0.0832652 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518944 | CTGTGAATTTTTGAA[-/ATATT]AGATGTTATATCTAA | 81550 |
rs201185518 | in-del | -/G | 0.0123036 | 0.0774623 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561401 | TCAGTGAGTAGCAAA[-/G]GTTGAAGTAGGTTGG | 81550 |
rs201194406 | in-del | -/T | 0.0240643 | 0.107019 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414168 | GTGAGACAATGTACG[-/T]TTTTTTTTTAAGTCC | 81550 |
rs201194980 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466978 | ATGTGTGTGTGTTTT[-/G]TTTGTTTTTTTGTTT | 81550 |
rs201230258 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517558 | GCAGAAAGCAGAAGA[A/G]ATGTGTAGCTATCTA | 81550 |
rs201257520 | in-del | -/G | 0.0162398 | 0.0886349 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501071 | AGCCAGCTACCTGTT[-/G]GCACGTTGATTATAT | 81550 |
rs201258344 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474171 | TAGAAGAAATAATGG[C/T]GTAAGCTGTCCTCTC | 81550 |
rs201260188 | in-del | -/TTTTCTTTTC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567345 | ACAGTATCCCTGCCT[-/TTTTCTTTTC]TTTTCTTTTCTTTTC | 81550 |
rs201326973 | snp | A/G | 9.89805e-05 | 0.00703423 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509884 | TACTTCTTACAAGCA[A/G]TAAACAGAAACCTGT | 81550 |
rs201333949 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469435 | ACACACACACACACA[C/T]ACACACACACACACA | 81550 |
rs201344712 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60558983 | TTTTTTTTTTTTTCT[A/C]TTGAAAGCAATTTGA | 81550 |
rs201348122 | in-del | -/AC | 0.021333 | 0.101051 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550681 | GTAAAATCACTTTGT[-/AC]AAAGTGCCAGTTAAG | 81550 |
rs201351916 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454806 | TTCTTTTTTTTTTTT[-/T]ATTTTTGTTTTCTTG | 81550 |
rs201360419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565420 | AAAGACATCAAGTTA[C/T]GAGTTACGTGAAAGA | 81550 |
rs201363078 | snp | A/G | 0.000717653 | 0.0189291 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535068 | TGCCCTTTATAGACA[A/G]TACCAGTTGTCATAT | 81550 |
rs201387227 | snp | A/C | 1.65737e-05 | 0.00287864 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528772 | CCTCCTTTGCAGAGG[A/C]AAAAGAAAATCCACT | 81550 |
rs201447793 | snp | A/G | 0.00199791 | 0.031543 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567685 | GTGGTTTTCATATAA[A/G]GAAAGATGAAATTCA | 81550 |
rs201460246 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446559 | TTATATGTCATATAA[G/T]AATATATATTATTCT | 81550 |
rs201488596 | in-del | -/CCCCCACCCCAGC | 0.00893865 | 0.0662528 | utr-variant-5-prime, intron-variant | TDRD3 | GRCh38.p7 | 13:60397322 | GAGGCCTCCCCATCA[-/CCCCCACCCCAGC]CCCCCACCACCCCCG | 81550 |
rs201512505 | snp | C/T | 3.29707e-05 | 0.00406008 | stop-gained, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494501 | AATGCTGCTGGTAAC[C/T]GAAATAGGGAAGTTT | 81550 |
rs201523246 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404404 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 81550 |
rs201540199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508129 | AGAGAGGATACAAAC[A/G]AATGGAAAAATATTC | 81550 |
rs201553731 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557822 | TTTTTTTTTCCTGAT[A/T]TTTTTTTTTTTTTTT | 81550 |
rs201569785 | in-del | -/T | 0.0217236 | 0.101931 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487099 | TAAATGTGTACAAAC[-/T]TTTTTTTTGTCTTGT | 81550 |
rs201573908 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60573398 | ACTTTAACAAAGTCT[-/A]AAAAAAAAATTTATT | 81550 |
rs201579691 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430526 | TAATGTATGAAAATA[C/T]AGAATTAGAGGAAGG | 81550 |
rs201585030 | snp | A/G | 8.24368e-05 | 0.00641963 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494523 | GGGAAGTTTTACAGA[A/G]AGAAAAGTCAACCAA | 81550 |
rs201726739 | snp | A/T | 1.64944e-05 | 0.00287175 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528509 | TGAAAAACCGCCTCG[A/T]TTTCAAAGAGACTCC | 81550 |
rs201736531 | in-del | -/TC/TTTCTTTCTTTC | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541179 | CTTTCTTTCTTTCTT[-/TC/TTTCTTTCTTTC]TTTTTGAGACGGAGC | 81550 |
rs201739194 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411587 | CCTGGAGAACATAGG[-/T]TTTTTTTTGGTTTTT | 81550 |
rs201745470 | snp | A/G | 0.000461513 | 0.0151837 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60483802 | CACAATAGAAGCAAT[A/G]TTGGAACTGAAGGTG | 81550 |
rs201752910 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486537 | ACATGTGATATTTTG[A/T]TACGTGTATACAATA | 81550 |
rs201762964 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553554 | TTATTTTTTTTAAAT[-/A]AAAAAAAAAAAAAGA | 81550 |
rs201773244 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490767 | GATTCTGGAATTTTG[A/G]AGGAGCCATTAGGGT | 81550 |
rs201787340 | in-del | -/G | 0.228842 | 0.249103 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561869 | CCCAGGTTTTTTGTT[-/G]TTGTTGTTGTTGTTG | 81550 |
rs201790388 | in-del | -/T | 0.0162398 | 0.0886349 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427154 | GACTGTATTGAAAAC[-/T]TTTTTTTTCTTAAGA | 81550 |
rs201820811 | snp | A/G | 1.69063e-05 | 0.00290738 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535283 | TATTTTGAAGAAAAT[A/G]TATAGCTCTAAAGAA | 81550 |
rs201827844 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544459 | AAAAAAAAAAAAAAA[A/G]GAAAGAAAGAAAAAA | 81550 |
rs201852530 | snp | A/G | 0.00148739 | 0.0272302 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484697 | TTTTTACTGAGTTTG[A/G]AAGAAGAAATAGCCA | 81550 |
rs201961402 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477014 | GAGAGATAGTTTGAC[-/T]TTTTTTTTTATTTGG | 81550 |
rs201968142 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482856 | TTTTTTTTTAACTTT[A/C]TCACCTATTTTACAT | 81550 |
rs202044586 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466792 | GACGGAGGCTCTGTC[-/T]TTTAAAAAAAAAAAA | 81550 |
rs202085018 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499228 | TCCCCATTCAACTCT[A/C]CCATTTGGCCTGTGC | 81550 |
rs202105603 | in-del | -/CAGCAG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516746 | CAGCAACAGCAGCAG[-/CAGCAG]ATGCAACAGCATCCT | 81550 |
rs202127102 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519326 | ATATATATTATTTCC[A/G/T]TTTGACAGATAAGGA | 81550 |
rs202146264 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478802 | TGTTAATTTGAGGAC[-/T]TTTTTTTTTTTTTTT | 81550 |
rs202162907 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422599 | ACAGGGACAAATGGG[A/G]GAAAATGTTGATGGA | 81550 |
rs202193060 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474159 | CTTTGAAATGCATAG[A/T]AGAAATAATGGCGTA | 81550 |
rs202198281 | in-del | -/A | 0.0356815 | 0.128715 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560587 | AGGACAATGATGAAT[-/A]GTACTGTATTTGCTT | 81550 |
rs202240390 | snp | A/T | 1.65127e-05 | 0.00287334 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460451 | GGATAATGAAGAATC[A/T]CAGGCTGCACCAAGG | 81550 |
rs202244614 | snp | A/G | 3.30759e-05 | 0.00406655 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528722 | TGCTTTTAAAAAAAG[A/G]GATAACTCTATGCAA | 81550 |
rs202247036 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405782 | TTTTAATCATGATGT[A/G]AGGGTTATGGTGGGA | 81550 |
rs207473844 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567252 | TTGGAAATAGTTTCC[C/T]TTTCTAGAATAAAAT | 81550 |
rs267603855 | snp | C/T | 0.000138405 | 0.00831766 | TDRD3 | 13 | allele_origin=T(somatic)/C(germline) | 13:60460382 | TCTGTTTTGACAGCT[C/T]GAAGGTCCATGTGTT | 81550 |
rs367605358 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490611 | GAAAGAGTAATTGTG[C/G]CTGCTGTGTTCAGAC | 81550 |
rs367627008 | snp | A/G | 1.65282e-05 | 0.00287469 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460441 | CTGCACCAAAGGATA[A/G]TGAAGAATCTCAGGC | 81550 |
rs367694402 | snp | A/G | 0.000275962 | 0.0117433 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467431 | ACACTCTTTTTTATT[A/G]CATTAAAGAGCTCTT | 81550 |
rs367702272 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418500 | TTTTCATCTTTGAAT[C/T]CTTGGGACTAGTACA | 81550 |
rs367708613 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60449759 | TCTAGTAAATATACA[A/T]CTATATTTATAATTT | 81550 |
rs367714356 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439252 | TTGAGAAGATAATGT[A/C/G]AGAAAGTCCAGAGAG | 81550 |
rs367724611 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484250 | TGCTACTTTGAAGCA[G/T]CCCCCCTTCTGACCA | 81550 |
rs367735492 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470955 | GTGTGCTTATTGGCC[A/G]TGCGTAGATCTTCTT | 81550 |
rs367756553 | in-del | -/C | | | downstream-variant-500B | TDRD3 | GRCh38.p7 | 13:60574357 | CATGAAAGACTGATT[-/C]TTTTTTTTTTTTTTT | 81550 |
rs367769491 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60521717 | CCTGACCAACATGGA[C/G]AAACCCCGTCTCTAC | 81550 |
rs367812790 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508706 | TTCAGGACATAGGCA[G/T]GGGCAATATATTTCT | 81550 |
rs367813066 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572606 | GGTCAAGGCTCAATG[C/T]GTAAAGCAGTTAAAT | 81550 |
rs367815069 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538383 | CTAGATTTCACCTGT[A/T]TTTTTTTTTTTTTTG | 81550 |
rs367823414 | snp | A/G | 1.67315e-05 | 0.00289231 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494401 | TTTTAAATGCTGTCT[A/G]CATACCTCTCTTTTA | 81550 |
rs367856637 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514870 | AGGAAAATAGGGTAA[A/G]ATGGGATTGAGATTG | 81550 |
rs367884307 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405598 | AGGGCACTAGGGAGC[A/G]TGGTGAATACAAACA | 81550 |
rs367924603 | snp | A/G | 1.6563e-05 | 0.00287771 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494569 | TGAAGGTGTCTATAG[A/G]GAACTGGTAAGGCTA | 81550 |
rs367953449 | in-del | -/TA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468674 | AACTTACTTTATGAT[-/TA]GACAGATGATGGATC | 81550 |
rs367979228 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436978 | GTACTTTGGAGCTCA[C/T]CAATTGAATTTGTCT | 81550 |
rs368007026 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404800 | AGTTGATATGGTTTG[A/G]TTCTGCGTCCTCACC | 81550 |
rs368007429 | in-del | -/TTCTTTCT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541147 | CTTTTTGTTTTTCTA[-/TTCTTTCT]TTCTTTCTTTCTTTC | 81550 |
rs368012569 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465364 | GGAACGCTTCTTCAC[G/T]ATTGTAATTGTATTC | 81550 |
rs368020343 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436086 | TGTCTATTTCCATCC[C/T]TTGCCCACTTTTGGA | 81550 |
rs368021146 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450552 | TGGAGGTAAATTAAA[G/T]AACTTATGTAAAGAT | 81550 |
rs368032575 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416888 | TCCTTTCTCATCATT[C/T]GTTGTCTTTTTATGA | 81550 |
rs368040761 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549099 | ATAAGTGATTAAAAG[A/C]AATTTATAGCTTGAA | 81550 |
rs368126576 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425274 | GGTGCTCAAGATCAC[A/G]AATGATCAGGGACAT | 81550 |
rs368136613 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432188 | GAATTCTGATCCTTC[C/T]GTTTATTATGCTTAA | 81550 |
rs368194753 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507935 | CAAACTCTCAGGATA[C/T]AAAGCCAATGTGCAA | 81550 |
rs368217969 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460600 | GTGCTATTCAATTGG[A/T]ATAACTTAAGAATTT | 81550 |
rs368251421 | in-del | -/AA | 0.225398 | 0.248787 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471542 | TTTTTCTATTTCTGC[-/AA]AAAAAAAAAATCATT | 81550 |
rs368254462 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451002 | CACTATATTTAATGT[A/T]TTCTATTACACAAAA | 81550 |
rs368279999 | snp | A/G | 9.90132e-05 | 0.00703539 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567521 | CACTACTCTTTGCAA[A/G]TAGGAGGAAGAAGGC | 81550 |
rs368325280 | snp | A/G | 8.23974e-05 | 0.00641809 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509822 | TAAGGAAGCATCGAG[A/G]CAAGCTCTTATGGAT | 81550 |
rs368352089 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455747 | GTATACAGATTGAGA[A/C]ATTTCTTTCTCAAGA | 81550 |
rs368355203 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477456 | CTAGCCTCAAGCAAT[C/T]CTCCTTGTTTGGCCT | 81550 |
rs368376514 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501437 | AGATGTTGCTGAAAC[A/G]CTAATATAAATGGAA | 81550 |
rs368462643 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467394 | AGTAAGTGTAAACTA[C/T]GGCTTGAACTTTTGA | 81550 |
rs368516744 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423877 | CGAAACTAAAAAAGA[C/T]CAAGGTAAGTCAAAA | 81550 |
rs368517023 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442069 | CTGCCTCAGATCTGC[C/T]ATGTAACTTTTAGGC | 81550 |
rs368521217 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565475 | AAAACCATTTACTTG[C/G]ATCTGGTTAGTTCAG | 81550 |
rs368628295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555954 | CTCCCAGGTTCACGC[C/T]ATTCTCCTGCCTCAG | 81550 |
rs368640420 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501951 | ATTACACAAAATACT[A/G]TAGCAATGGAAACTC | 81550 |
rs368656905 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525166 | TATATTAAGGGAATT[C/T]TTTTTTTTTTTTTTT | 81550 |
rs368673500 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517500 | GTTTGGAAACCAGGG[A/G]TAAATGGTTGCTATG | 81550 |
rs368681462 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500589 | TAATCTTCCCAGTGG[-/G]CAGAACTTCAAGCAG | 81550 |
rs368683541 | snp | A/C | 6.62241e-05 | 0.00575392 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528986 | TTTCATTGGTGTTCC[A/C]AATGGAGAAGTAGAA | 81550 |
rs368724185 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456844 | GCGGCTACAAGCACA[C/T]ACCACCACGCTTGGC | 81550 |
rs368725310 | in-del | -/TTTG | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424016 | CATGCAGTGGTTTTT[-/TTTG]TTTGTTTGTTTTTGT | 81550 |
rs368757392 | in-del | -/AG | 0.001629 | 0.0284929 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472825 | AGTAGCAAAAATTAT[-/AG]AGAGAGAGTACAATG | 81550 |
rs368762550 | snp | A/G | 1.69392e-05 | 0.00291021 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509970 | TTTGCTTTTCAGAGT[A/G]ATATATGTTATTGAC | 81550 |
rs368820496 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566970 | AATTGTATTCCTCCC[C/T]TATTCCAAACCATTA | 81550 |
rs368832480 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433888 | CCTGCTTTCAAAGAA[A/G]TGGATCAAAAGAAAA | 81550 |
rs368842611 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60569652 | AGAAAGCTGGAGGCA[G/T]CAGACTACCTAATTT | 81550 |
rs368861276 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493113 | TTAGTAGAAACGGGG[C/T]TTCACCGTGTTAGCC | 81550 |
rs368908025 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402851 | GCGCCACCACGCCTG[A/G]CTAGCCAATTGCTTT | 81550 |
rs368922668 | in-del | -/ACA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60435909 | AACCACATCATGACA[-/ACA]TCTATGGTTTTTTTT | 81550 |
rs368972998 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427032 | ACATATTTGTATATT[-/A]AAAAATATGTAAACA | 81550 |
rs368978903 | snp | C/G | 0.000231718 | 0.0107613 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485774 | TGGAACTACTAAGTT[C/G]ACTTATTCTTACTTG | 81550 |
rs369007441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412928 | TACATATCTAAGATG[C/T]GTACTTTAAAAGTTG | 81550 |
rs369059219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420713 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCATGAGG | 81550 |
rs369071171 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487882 | CACTAATTTACATTC[A/C]CACCAACAGTACATA | 81550 |
rs369079194 | in-del | -/AGTTTACCTCTCTC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526245 | TATACAAGGGACCTT[-/AGTTTACCTCTCTC]TGTTAAGCCTCATAA | 81550 |
rs369118060 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405601 | GCACTAGGGAGCATG[A/G]TGAATACAAACATCT | 81550 |
rs369153678 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497815 | TTCCCCATCCCCAGT[A/G]ATGGCTTGAGTTTTC | 81550 |
rs369171180 | snp | C/T | 1.67142e-05 | 0.00289081 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509947 | AAGCAGTGTGCCAGA[C/T]AGTATTGTTTGCTTT | 81550 |
rs369220736 | in-del | -/GT | 0.0869089 | 0.189476 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484530 | ATAATAAGGTTTATC[-/GT]GTGTGTGTGTGTGTC | 81550 |
rs369229674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462069 | AGAAGATATGTTTGT[C/T]GAAAATGTTGATTTC | 81550 |
rs369241451 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60550507 | CTTGCATGAATTTTA[C/T]AAAAATGATGACTGT | 81550 |
rs369325728 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422999 | TAACTCCAAGACATA[-/T]CCCAGTTAAAAATTA | 81550 |
rs369387872 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458896 | TATAATAACCATAAC[A/G]TGCCTGTGATTTAAT | 81550 |
rs369435331 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396505 | GCGAAGGGCATCGGC[A/G]GGGAAGCGGCTGTGG | 81550 |
rs369439757 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419683 | AAATACCTAATGCAT[A/G]TGGGGCTTAAAACCT | 81550 |
rs369441320 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486935 | AGAATGGCAGGATTT[C/T]TTTCTTTTATATAAC | 81550 |
rs369459882 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553430 | ACCCAGTTCCAAAGT[C/T]GCTTCCACATTTTCA | 81550 |
rs369497405 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60483087 | AAATTGCTTTTGCCA[C/G]AAGATTTTCTTTCCG | 81550 |
rs369510089 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419220 | ACCAATATTCTATTT[C/T]CAGTCCTTTTGATTT | 81550 |
rs369564590 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444328 | ACATACTATGTATAT[A/G]TATTCAAAAGCTGTC | 81550 |
rs369630835 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466963 | TGGGAAAGAGCTTCA[A/T]ATGTGTGTGTGTTTT | 81550 |
rs369670025 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439295 | ACTCAGTTTAAAACA[A/G]TGTTTATTTTAGTTT | 81550 |
rs369673639 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482044 | TTAGTCTGCATGGTC[G/T]GATCTGGCTGGATTG | 81550 |
rs369673809 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533926 | AGCAACATTCAGACC[C/T]ACAATTTGGGTCCTG | 81550 |
rs369714615 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478666 | GTTCCATTGATCTTT[A/T]ATTTGGATTTTGGCA | 81550 |
rs369772252 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426108 | TTTAAAAAGAAGGAG[A/T]TCCTGCCGTTTCTCA | 81550 |
rs369777224 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445040 | TTGGCACTCATTACA[A/G]TGACCTTTTCTTACC | 81550 |
rs369787048 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467708 | GCATCTATGTGAATA[C/T]ATGTATACCTGTCTT | 81550 |
rs369794773 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493007 | CACTGCAAGCTCCGC[C/T]TCCCAGGTTCATGCC | 81550 |
rs369856917 | snp | C/T | 0.000214711 | 0.010359 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483770 | TGACTGGATTTTTTC[C/T]GCAGAGCTTATCAAA | 81550 |
rs369865030 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445663 | AAGAATTTGCATTTC[A/G]AACAGTTTTCCAGGA | 81550 |
rs369867791 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60547638 | CCTTCTTCTCCCCTA[C/T]TCTGTAGTCTATTGT | 81550 |
rs369875898 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568271 | CTTCTGAATTACTGT[A/T]GCCAGCCAATGTAGC | 81550 |
rs369880940 | in-del | -/AAAA | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563247 | AAAAAAAAAAAAAAA[-/AAAA]GGCAAGGCGATTCAT | 81550 |
rs369916303 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557971 | GGGACTATAGGCACA[C/T]GCCACCACGCCCAGC | 81550 |
rs369924519 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60547674 | AATATCCCTTTTTAA[-/A]GCAAGCCAGAATGAC | 81550 |
rs369994319 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416404 | TATGGTCAACTACTA[A/G]TTCCATTCTTAGTGC | 81550 |
rs370007313 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459227 | CATTTCTCTTTGCTG[A/G]AAATATAAATTAATA | 81550 |
rs370013061 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483751 | ATGTATAACTGCTCT[A/T]TTGTGACTGGATTTT | 81550 |
rs370016780 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482751 | GTTGTGCTTGACTGT[C/T]GTTACTCTTAATTAT | 81550 |
rs370032965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534888 | AGCCAAGATCTTGCT[A/G]TTGCACTCCAGCCTG | 81550 |
rs370041167 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506083 | GACACATAATCATCA[A/G]ATTCACCAAGGTTGA | 81550 |
rs370059236 | in-del | -/AACTC | 0.0456336 | 0.143994 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463654 | ATAAGGAGCTCAAAT[-/AACTC]AATAGCAAAAAACAA | 81550 |
rs370081446 | multinucleotide-polymorphism | AC/GG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525012 | GAATCACTTGAACCC[AC/GG]GAGGTGGAGGTTGCA | 81550 |
rs370131000 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534212 | CAGCTACTTGGGAGG[C/T]TGCAGCAAGAGGACA | 81550 |
rs370134719 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430041 | TCAGTATTTTCAGTA[C/T]GGTCTTTTTCGGCAA | 81550 |
rs370142703 | snp | A/G | 1.66866e-05 | 0.00288842 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529154 | ATCATCTATTCCTAT[A/G]GAGTATGCAAAAATG | 81550 |
rs370190509 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483744 | ATTTTTTATGTATAA[C/G]TGCTCTTTTGTGACT | 81550 |
rs370270180 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471088 | TAACATAATATGTTT[C/T]GCAAATATTTTTCCC | 81550 |
rs370277694 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407979 | TGAGATCTGATGGGT[C/T]TTTCAGGGGTTTCCG | 81550 |
rs370381972 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396465 | CTCAGGGACCCACCC[A/T]GCGCCCCAGCCCTCT | 81550 |
rs370448567 | in-del | -/T | 0.07844 | 0.181844 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510803 | TCTTTCTTTTCTTTC[-/T]TTTTTTTTTTTTTTA | 81550 |
rs370456678 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506350 | ATGCTGAGAGATTTT[-/T]ATCACCACCAGGCCT | 81550 |
rs370461202 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500536 | GCTACAGCCTACAGC[C/G]CCTTTCTAAGACATT | 81550 |
rs370465930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540600 | AAGCCTAACGGAATA[C/T]TATGAAAAACTTGAG | 81550 |
rs370500241 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455219 | CACCTGGCTTATATT[A/T]ATTTATTAAAGTCAA | 81550 |
rs370500822 | in-del | -/TAG | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564252 | AGGTCCTAAGAAAAA[-/TAG]TGTGCCCAAGGTGGT | 81550 |
rs370503351 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476985 | TCTAGATATAGAATG[A/G]TATCATCAGCAAAGA | 81550 |
rs370526156 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60513021 | CTCTTTGAAGGGCCC[A/G]CCCCTGCAGCAAACT | 81550 |
rs370553361 | snp | G/T | 3.31928e-05 | 0.00407373 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528796 | ATCCACTTCCTCAAG[G/T]ATCTGTAGATTATAA | 81550 |
rs370564882 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454806 | TTTCTTTTTTTTTTT[A/T]ATTTTTGTTTTCTTG | 81550 |
rs370595011 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60437144 | TTTTTTTTTTTTTTT[G/T]AGGCAGAGTTTTGCT | 81550 |
rs370615037 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450463 | ACTGAGTGACCACTG[G/T]TAAAGTACTTTATCC | 81550 |
rs370639458 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541044 | AGTGGACATTAGTTC[C/T]ACTTCATGGTTAAAC | 81550 |
rs370643866 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506726 | TGCACTACGGCACTC[C/T]AGCCTGGGTGACAGA | 81550 |
rs370647748 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477803 | GATCTTCTCATCTAC[A/G]TGCATCAGGAATACT | 81550 |
rs370660671 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453696 | ACAAGACCCTGCAGG[A/C]TACTGGAATGCTCCC | 81550 |
rs370688718 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398457 | TGGAGATGACACAGG[G/T]AAGCGCTTATTGTTT | 81550 |
rs370704102 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60519434 | TCTAGTGCCTCGTAT[A/G]TAAATACCTGTTTAT | 81550 |
rs370731432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414650 | GACTAGTATGAATAG[A/G]GCTGCCTCATAAATT | 81550 |
rs370765886 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459028 | ACTTGGAATTTTTTT[-/T]CGTAAGTGAAAATTA | 81550 |
rs370801454 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423003 | TCCAAGACATATCCC[A/C]GTTAAAAATTATCAG | 81550 |
rs370847689 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470015 | TTCCCAAACTTAAAC[A/T]CTGTACCCATTAAAC | 81550 |
rs370853932 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60513181 | CACCATCTGCAGTCA[C/T]GGCCCCAGCTCTACA | 81550 |
rs370854961 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492917 | AATTTTCTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 81550 |
rs370865311 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60536211 | AAAAACAAAAAACCT[A/G]ATAGTAGTAATAATG | 81550 |
rs370872166 | snp | C/G | | | downstream-variant-500B | TDRD3 | GRCh38.p7 | 13:60574199 | ATAAAAGGTGCAGTG[C/G]ATCTTTAAGGATGCA | 81550 |
rs370880656 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551071 | ACTAATTTCATTATG[C/T]ATTTAAAATGCGAGT | 81550 |
rs370885734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483524 | TCCTTAGGGGAATGG[C/T]CTGATAAATATTTCT | 81550 |
rs370951945 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520493 | CTTCTCATTAGGGCT[C/T]ACCTAAACCCCATTT | 81550 |
rs371005899 | snp | A/G | 1.68125e-05 | 0.00289931 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485928 | ACGGCTGCTATTGCT[A/G]AAGTTGCAAAGAGCA | 81550 |
rs371052315 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458698 | GTCTAACTCTGTGCT[C/T]TCCATATATAGAACA | 81550 |
rs371087093 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60403244 | TTGCTACCTCAGCAG[A/G]TTGAAAATAATTTTC | 81550 |
rs371112160 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493575 | GGCTGAGACAGGATA[A/T]TCACTTGAGCCTGGG | 81550 |
rs371263310 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546773 | AGTTTAAGGGAAAAG[C/T]TATTTTTAAAAACAA | 81550 |
rs371284476 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459821 | AGACGGGGATTCACC[A/G]TGTTGGCCTGGCTGG | 81550 |
rs371288395 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542006 | TGCTGGGATTACAGT[C/T]GTGAGCCACCGCACC | 81550 |
rs371307313 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448311 | CTTCAGAAAGGCGTC[A/G/T]TCCTGAAGCTTTGAA | 81550 |
rs371318514 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60494061 | GATTCAAGATAACCT[G/T]GCCTGGTAGCTGGAT | 81550 |
rs371325365 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476601 | CTGTGAAGAATAACA[A/T]TGATAGTTTGATAGG | 81550 |
rs371334871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571745 | CCCCCAACCCTCCAC[A/G]CACATATACTTCCTC | 81550 |
rs371349241 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417021 | AGTCTCTCTCTCTCT[C/T]TTTTTTTTTTTTTGA | 81550 |
rs371373181 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon, missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567542 | GGAAGAAGGCACCTA[C/T]GATCAAACTCTGGAG | 81550 |
rs371455023 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567627 | TTTTACCAACCACCC[C/T]GGGCTCGGAACTAAT | 81550 |
rs371457948 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60403995 | CTATGATGTACAAGA[C/T]AGGCAGAATTTAAAC | 81550 |
rs371484157 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418701 | TAAATGTTATATAGA[A/G]TGTTTTCATCACCCA | 81550 |
rs371491228 | snp | A/G | 5.25785e-05 | 0.00512704 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510605 | TTGCATATACAGTAC[A/G]TATTTCTTGCTTTTG | 81550 |
rs371491333 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523012 | GGCACATTATTTTTT[C/T]ACTTGCAAAATAAAG | 81550 |
rs371497272 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465433 | CATTTACCACCACAG[C/T]TCTCTACTTAAGGGT | 81550 |
rs371511311 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478877 | GGTGCAATCTTGGCT[C/T]ACTGCAACCTCTGCT | 81550 |
rs371523478 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523092 | GTAGGCAAAAGACCT[C/T]TAACATAGAGTCAGG | 81550 |
rs371557343 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494355 | TAATTACTTCAGTTG[C/T]TTTTAGTCATAGCTT | 81550 |
rs371559720 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60509055 | GAAATCAGGAAAACA[A/G]TGTATAAACATGTTA | 81550 |
rs371563778 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407341 | TGGTATCATTCATCA[-/T]TTTGCTTTTGTGTCC | 81550 |
rs371577950 | snp | C/T | 0.000109351 | 0.00739349 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485970 | AATCAAATCATTACA[C/T]GTTTTATTTCTTATC | 81550 |
rs371599544 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461729 | TAATTAAGTAGGCAC[A/G]TAGGCATACAAATAT | 81550 |
rs371671543 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428686 | CATACGTCTTGAGAC[A/G]TACGTCCTCGTGCAT | 81550 |
rs371672503 | snp | C/G | 0.00993419 | 0.0697739 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394668 | GGCAGAGCGAGACTC[C/G]CGTCTCAAAAAAAAA | 81550 |
rs371692753 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508683 | AGAAGAAAACCTAGG[C/T]AATACCATTCAGGAC | 81550 |
rs371801109 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533546 | CTCGGGAGCCTGAGG[C/T]AGGAGAATCATTGGA | 81550 |
rs371838894 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470465 | CTGGTGGAAATGAGT[A/G]TAAAGTAAATATAAA | 81550 |
rs371867156 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555610 | GTAAATGATACCAAC[A/G]TACTTGAGAATTTTT | 81550 |
rs371870244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530534 | TAACCTCCACCTCCC[A/G]GGTTCAAGCAATTCT | 81550 |
rs371878651 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410350 | AGTTGTCATAGAGTT[C/T]AAGTCCACTGGGGTT | 81550 |
rs371920911 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542244 | TTTTACCATTCTTTC[A/G]CAAATATATGTAGAA | 81550 |
rs371976962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549371 | TCTGTGTCATCATAG[C/T]GACTATATTATTGCC | 81550 |
rs371988916 | snp | A/G | 0.000449779 | 0.0149896 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494584 | AGAACTGGTAAGGCT[A/G]AAGAACTAACCACAA | 81550 |
rs372010456 | in-del | -/AAA/AAAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525086 | GCAAAATTTTCTCTC[-/AAA/AAAA]AAAAAAAAAAAAAAA | 81550 |
rs372020497 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471819 | CGTTATCTGTGAAGA[C/G]TTAATTTTATTTCTT | 81550 |
rs372025992 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496070 | GAGCACAATCTAGTC[A/C]CCTGCCAGTATGGCT | 81550 |
rs372068313 | in-del | -/CAAGTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399898 | GTAGACCAATCTGTT[-/CAAGTTT]ACATTATTTTTAAGC | 81550 |
rs372071249 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404864 | ATGTTGTGGGAAGGA[C/T]CTGGTGGGAGATGAT | 81550 |
rs372095307 | in-del | -/TATTA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518945 | TGTGAATTTTTGAAA[-/TATTA]GATGTTATATCTAAT | 81550 |
rs372096520 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60439961 | GTTATTAATATCTGT[G/T]ATACAGAATCCAATG | 81550 |
rs372105652 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60556934 | CAGAGGCCGGGTGCA[G/T]TGGCTGACGCCTGTA | 81550 |
rs372117827 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566404 | GTAAAATTGCAGTAA[G/T]TGGATCTATAAAGAT | 81550 |
rs372164036 | in-del | -/A | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439110 | AATAAGACAATGCGT[-/A]AAAAAAACTGAAAAG | 81550 |
rs372169299 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542149 | GTCCTAAAACTTGTT[C/T]TCCTGGAAGTGCAAA | 81550 |
rs372182659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531085 | ATTTAGAAACAGCAT[C/T]TCTGTCACATCTTTA | 81550 |
rs372218547 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467302 | ATAAAAAATGGATTC[C/T]TGCTCTTGAATGACT | 81550 |
rs372275896 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549697 | AGAAAGTAAGAAAAC[A/C/G]TAGAAAATAATTTTG | 81550 |
rs372300193 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508358 | GCATCATGCTACGTG[A/G]CTTCAAACTATACTA | 81550 |
rs372330303 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458191 | TCATAGTCAACCAGA[C/T]GTAGGAGATCACCAA | 81550 |
rs372409148 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477718 | TGCATCCCAGGGATA[A/G]AGACCAGTTGATTAT | 81550 |
rs372452294 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464463 | CACTCCCATTTTTAT[C/T]GTAGCACTATTCACA | 81550 |
rs372458700 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487970 | TATAGCAGTTTTAAC[G/T]GGGTTGAAATGAGAT | 81550 |
rs372499760 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564331 | TCAAATACATTTAAG[A/T]AATACATTGGTTTGG | 81550 |
rs372505295 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60540412 | CTATCACCCAGCCTT[C/T]TACCATTTTTGTGGG | 81550 |
rs372509798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512490 | AAAGTCCACAGTCCA[A/G]AGTCTCATCTGAGAC | 81550 |
rs372514948 | in-del | -/AA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425139 | AAAATAAGAAATAAC[-/AA]AGAGAAGTCATCTTT | 81550 |
rs372560276 | snp | A/G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462582 | ACCAGGTGCTAATAC[A/G/T]GATGTGTTACCTTAC | 81550 |
rs372602208 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551711 | ACTACCTGAGACTGC[A/G]TAATTTATTTTAAGA | 81550 |
rs372650491 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60491587 | TGTTAAACTTATCAA[-/A]GGCAATTGAAAAGTT | 81550 |
rs372665242 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482335 | ACCTGTTTTTTTTTC[-/C]TCTTTCTCTCAGGGA | 81550 |
rs372685872 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402427 | ATTAGAAGTTTTGCT[A/C]CCTCACCATTCCAGT | 81550 |
rs372694052 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445145 | CAAATATAAGATTAT[G/T]AAAGTATTAGGAGCA | 81550 |
rs372807308 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418066 | TTGTCTAATCTTTAG[A/G]TCTTTTGTCACCTAC | 81550 |
rs372807465 | snp | C/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438919 | TGGGGTTTTTACAAG[C/T]GGATTTTTGATGGTT | 81550 |
rs372819624 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461249 | TTTTATAGGCTAATA[A/C]ATTTTCCTAGGAAAT | 81550 |
rs372854036 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405047 | TCTGCCATGATTGTG[A/T]GGCCTCCCCAGCCAT | 81550 |
rs372864342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537232 | CGTTTTATGAATTTG[C/T]GTAGGTTACTATAAC | 81550 |
rs372866010 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451037 | CCTTTGTAGTGGAAA[C/G]TAAAGAATAAAAAAT | 81550 |
rs372889757 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467993 | TAGTGTAGGTCTTTA[G/T]TATCTCTTGCCTGGA | 81550 |
rs372916852 | snp | A/G | 3.29913e-05 | 0.00406135 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509881 | ACGTACTTCTTACAA[A/G]CAATAAACAGAAACC | 81550 |
rs372934742 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533084 | AACACAAAAGTGTGG[C/G]GCTAAGAAATAAAGG | 81550 |
rs372961829 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60569728 | ACATAAAAACAAACA[C/G]ACCAATGGAACAGAA | 81550 |
rs372970688 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519393 | AATAACATAAGGTTA[A/T]TTCTAAATGGTTTTT | 81550 |
rs372995888 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453549 | GCTCTTATTGGAATA[G/T]CACTTGGGAAGTGCA | 81550 |
rs373020366 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445777 | AAAGTAAATAATATC[A/G]AAGCAGTGTCTGTAC | 81550 |
rs373062918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430051 | CAGTACGGTCTTTTT[C/T]GGCAAGGGTAAACTG | 81550 |
rs373073401 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412260 | ATATTTGAATTTTTC[A/T]TTCAGTGATATTGTT | 81550 |
rs373075507 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60558926 | AAGAACCTTTCTTCT[-/T]GCATTGGCTCTTTCA | 81550 |
rs373095878 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474661 | TATGCTGGTTTTGTT[A/G]TATACTTTACATTCG | 81550 |
rs373116566 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60539216 | TTATGTATCTAGTAC[A/G]TCTCTTAGTTGTCGG | 81550 |
rs373164382 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497340 | CCTGGGTTTAGATCC[C/T]GATCATTGTCCCTCC | 81550 |
rs373219831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414306 | CAAATCTGGCCTGCT[A/G]CCAGTTTTTGTAAAT | 81550 |
rs373229702 | snp | A/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396099 | CCAATTTCCTCCCCA[A/T]TCCCAAGAGCGCCTC | 81550 |
rs373232795 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557033 | AACGTGGAGAAACCC[C/T]GTCTCTACTAAAAAT | 81550 |
rs373289716 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534273 | AGCTATGATCACACC[A/G]CTGCATTCCAGCCTG | 81550 |
rs373320501 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436243 | GATTTCTTTTGTTGT[G/T]CAGAAGCTTTTAGTT | 81550 |
rs373327978 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458875 | AAAATAAACAGAATT[A/T]TGAGCTATAATAACC | 81550 |
rs373365946 | snp | A/G/T | 3.31007e-05 | 0.0040681 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483754 | TATAACTGCTCTTTT[A/G/T]TGACTGGATTTTTTC | 81550 |
rs373381614 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493435 | GGGAGGGCAAGGTGG[A/T]TAGATCATCTCAGGT | 81550 |
rs373392470 | snp | A/T | 1.65247e-05 | 0.00287438 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529069 | CAGCTGTACCCTGTG[A/T]TGATAAAATATTTTA | 81550 |
rs373411452 | in-del | -/GA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557819 | GATTTTTTTTTTCCT[-/GA]TTTTTTTTTTTTTTT | 81550 |
rs373450881 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544577 | TTCTACTTTGTGTCA[A/G]CATTTATATTGCTCT | 81550 |
rs373455433 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475618 | TCTTTGAGGAATCTC[C/T]GAACTGTTTTCCACA | 81550 |
rs373467024 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512053 | ATGCTGCTGATGAAG[A/C]TATACCTGAGACTAG | 81550 |
rs373500085 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400262 | TCTCTTCAGAGGTTC[A/C]TTCTCCTTTAGGATG | 81550 |
rs373526248 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563740 | GGAACACAGAACCTG[A/T]CTTCTATTTAAGTGT | 81550 |
rs373531557 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396124 | CGCCTCTGCCCAGTT[C/T]CGCAGTCTCTGCTCC | 81550 |
rs373557286 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453440 | TACTGAATTAGTACC[A/T]GTTTTTCTTTTTCAC | 81550 |
rs373576051 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498205 | ATACCCTTGAGCAAC[A/G]CCTTGCAAAATAGAT | 81550 |
rs373639125 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425076 | AAAAGTTAACAAAAT[A/G]GACAAACCATTAGCT | 81550 |
rs373649104 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60485364 | TAAGTGCAGAGACAT[C/G]TTTTTATATGTTAAT | 81550 |
rs373650828 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466591 | TCATGAGTTGGAGAC[A/C]ACCCTGGCCAACATA | 81550 |
rs373658767 | in-del | -/CA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486475 | CTATTTACACACACA[-/CA]AATCCTCCTTTTTAA | 81550 |
rs373693675 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494360 | ACTTCAGTTGTTTTT[A/T]GTCATAGCTTAGTTT | 81550 |
rs373699721 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398073 | CTGATTTTAAGAGGC[C/T]TTTCGTGTCAAGATT | 81550 |
rs373711248 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534927 | AGCAAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA | 81550 |
rs373723896 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553664 | TAGCACCTTCTTCAC[A/G]AGGTTGCAGTAGAGA | 81550 |
rs373725812 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451310 | TGTCAGTAATAGTTG[A/C]AGTTGCAGCAAGATT | 81550 |
rs373762330 | in-del | -/CTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568980 | CCCCCTTTTCTTCTT[-/CTT]TTTTGAGACAGAGTC | 81550 |
rs373770386 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60491115 | GCAAAACTCCATCTC[A/C]AAAAAAAAAAAAAAA | 81550 |
rs373771350 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434503 | GCACTTACTAAACTG[C/T]GGTGACTTAAAAATT | 81550 |
rs373772882 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60456850 | ACAAGCACACACCAC[C/G]ACGCTTGGCTAATTT | 81550 |
rs373847912 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477991 | AATTTGGCTGTGAAT[A/G]TATCTGGTCTAGGAT | 81550 |
rs373856705 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523573 | TTGCAATACATTTTT[-/C]TTTTTTTTTTTTTTT | 81550 |
rs373874007 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412271 | TTTCATTCAGTGATA[A/T]TGTTCAGCTTACGGT | 81550 |
rs373874672 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398509 | ATATGGTTCGTGAAA[A/G]ATGTGGATTTGATTT | 81550 |
rs373875972 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477183 | TGATGTTGGCTATAC[A/G]TTTGTTATAGATGGT | 81550 |
rs373885643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441567 | TTATCATCTTTTAAT[A/G]AAATTTAGGCATTTG | 81550 |
rs373887286 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409980 | CCCAGGGGGAGGTAA[C/T]TGAATCATGGGGGCC | 81550 |
rs373891926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401233 | ACAGATCTAAAATAT[G/T]TGGAAAAATAAAAAA | 81550 |
rs373924113 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554726 | GCTGAATGGCAAAGG[A/G]GAAATAGCTTCATCC | 81550 |
rs373928338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529418 | GGGACAATCTGTCCC[A/G]TAAGATTTGGTTAAG | 81550 |
rs373937433 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501303 | AGGGCTCCTCCTAGG[A/T]TCAATCTAAAGGTCC | 81550 |
rs373987771 | snp | A/G | 3.32342e-05 | 0.00407627 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528956 | TGATTATCAGAATCC[A/G]GTTCGAAGTAATAGT | 81550 |
rs374020985 | snp | C/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438540 | TTCTGACTTTTATCG[C/T]CTTGGTCTTGCTCAT | 81550 |
rs374021676 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494461 | TGGAGGAGGTGGTGG[C/T]GGTGCTAGAAGTAAT | 81550 |
rs374065371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521846 | AGGTTGCGGTGAGCC[A/G]AGATCGCACCATTGC | 81550 |
rs374080975 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60556572 | ATGGCAAGCACAATA[C/T]GAGTGACCAGTAATT | 81550 |
rs374086102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468706 | TGAGCACAATCCAAG[A/T]CCATTTTTTTCTGTT | 81550 |
rs374098746 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561982 | ATAATACATGACTCC[C/T]ATGGGCACCAAGGTT | 81550 |
rs374112617 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471283 | AGTTTTCCCAGCACT[A/C]CTTTTTGAAAATAGT | 81550 |
rs374126390 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60397088 | CCTGAACCGTCCTGA[C/T]TCCAGCCACCAGCCG | 81550 |
rs374126672 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60573738 | TGAAGAAAGAAAAAA[C/T]AGATTTTAGGGTGGA | 81550 |
rs374127090 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520648 | GTTGTCTGCCTCTGC[C/G]CATTATAACTAAGCT | 81550 |
rs374192559 | snp | C/T | 1.65803e-05 | 0.00287922 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567498 | GAGCCATTTTGAACA[C/T]GTAAAATCACTACTC | 81550 |
rs374198014 | snp | C/T | 3.36905e-05 | 0.00410416 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460416 | CAAATTCAAAAAATT[C/T]GCAATGTTGCTGCAC | 81550 |
rs374199464 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442375 | ATAGGGATTTTATGT[A/G]TGTGTGTGTGTGTGT | 81550 |
rs374225640 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460231 | GAAAAAACTTGATAA[G/T]ATATAATTTCAGTTT | 81550 |
rs374228745 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492045 | GGCAACACCAGTTAC[C/T]TTATGGGTAATATTT | 81550 |
rs374248989 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430640 | AAGATGAATAACAAC[A/G]TAGTTAGGTTACCAT | 81550 |
rs374268882 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514772 | ATTCTGTCCGAATGT[A/G]ATACAAAGGCATTAA | 81550 |
rs374280654 | in-del | -/GAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457214 | AACTTAAGGCTTGAT[-/GAT]TCAAATTAAGAAGTG | 81550 |
rs374297541 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527717 | TTTCTGACACTTTTT[C/T]GGTATTTCCACTTTT | 81550 |
rs374368679 | in-del | -/CTT | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459529 | CAATTACAACTCATA[-/CTT]CTTCAACTTTTTAGT | 81550 |
rs374369946 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509740 | GTGGGCTATCAGCCA[C/G]CTTTTCTCTTTATTC | 81550 |
rs374399233 | in-del | -/A | 0.276267 | 0.248616 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521465 | AAGCAGCTTTTTCTT[-/A]AAAAAAAAAAATGTA | 81550 |
rs374435602 | in-del | -/GATCT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474848 | TTAGTTCAGGTTAGC[-/GATCT]TGATGATGAAGTGTT | 81550 |
rs374439293 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487018 | AACTCTTCCTAACTA[A/T]GGATTCAACCAACAG | 81550 |
rs374468759 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404399 | CACTGCAAGCTCCGC[C/T]TCCCGGGTTCACGCC | 81550 |
rs374471751 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537395 | TTAAAAAATATTTGT[A/G]TGCATATAGATGTAA | 81550 |
rs374564866 | snp | A/G/T | 3.33919e-05 | 0.00408596 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528892 | CACAAACAATAAATA[A/G/T]TGAAGCTTTCAGTGG | 81550 |
rs374603590 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422584 | AGAAGTGGACAATAA[A/G]CAGGGACAAATGGGG | 81550 |
rs374604358 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526014 | ATCAAATTCTGCCAC[A/G]TCTGCCAAGCCTGGC | 81550 |
rs374621109 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455193 | GCTGGGATTACAGGT[C/G]TGTGCCACCACACCT | 81550 |
rs374678843 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565298 | CAGACCTCGTGATCC[G/T]CCCGCCTCGGCCTCC | 81550 |
rs374752776 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469639 | GTTTTTGATTTGGTA[A/G]CCACAGCAATGTAGG | 81550 |
rs374773827 | snp | C/G/T | 0.000150042 | 0.00866027 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535078 | AGACAATACCAGTTG[C/G/T]CATATTTAAAACTCC | 81550 |
rs374780699 | in-del | -/CTCAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463656 | AAGGAGCTCAAATAA[-/CTCAA]TAGCAAAAAACAAAA | 81550 |
rs374788930 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544337 | TAGTCCCAGCTACTG[A/C]GGAGTCTGAGATGGG | 81550 |
rs374806907 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490451 | AGAGGGACAAGTAGT[A/G]GAAGATAAAGTCAAG | 81550 |
rs374844931 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425385 | TGGCAGGGGTGTGGA[C/G]AAACACCCTAGTACA | 81550 |
rs374845881 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565124 | GCCGTGGCACTGTCT[C/G]GGCTCACTGCAAGCT | 81550 |
rs374868525 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548152 | TATAGTAGAGGGAAG[A/G]CATAAGAATTTGGTG | 81550 |
rs374870787 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571759 | CACACATATACTTCC[C/T]CATTGTGGTGAGAGA | 81550 |
rs374884666 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541997 | CTCCCAAAGTGCTGG[A/G]ATTACAGTCGTGAGC | 81550 |
rs374928095 | snp | G/T | 1.64914e-05 | 0.00287149 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467340 | CACAGTTCTTGGTGG[G/T]GAAGTGGAACACCTT | 81550 |
rs374961236 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503459 | TATAATTAGACATTC[A/G]ACTTTTAGAAATTCC | 81550 |
rs374968405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60495712 | TCAGATGATCCACCC[A/G]CTTCTTCGGCCTCCC | 81550 |
rs374970680 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450583 | CCTGCTATATTTTCT[C/G]GTATGTATCTAGGAA | 81550 |
rs375041339 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541862 | CCTCCTGAGTAGCTA[C/G]GATTACAGGCATGGG | 81550 |
rs375051406 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572937 | AGGATTATAGTACCC[C/G]ACGCTCTGTATTTTC | 81550 |
rs375090318 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60569275 | TGCACCCAGCCTCAA[C/T]AGCAAACAATCTGAA | 81550 |
rs375100259 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60437701 | ACAGTTTCCTTTCTA[A/G]AAAACAAAATATTCT | 81550 |
rs375111812 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60483544 | TAAATATTTCTGAAA[G/T]CTTTATGTGAATATG | 81550 |
rs375113730 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443730 | ATAATTTATGTGGTT[A/G]AATGCACTTTAAGTC | 81550 |
rs375119999 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398455 | GCTGGAGATGACACA[G/T]GGAAGCGCTTATTGT | 81550 |
rs375133444 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429638 | CTGAATGATTTAAAC[A/C]AAATAAATAATAAAG | 81550 |
rs375137662 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450724 | TGTCTTATTGGAGCA[C/G]ATAGCCTAATGAGAG | 81550 |
rs375144105 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60521775 | GGCAGCACATGCCTG[G/T]AATCCCAGCCACTCA | 81550 |
rs375165262 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544033 | CCAGCAGTGAGGTAT[A/T]TTCATCATTTCTTTG | 81550 |
rs375178352 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549462 | CTGGTAACATTAATA[C/T]AATCCTAAAAATATT | 81550 |
rs375180493 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421528 | TAACATCAGTTTGTC[C/T]ATTTGCTGAAGAAAA | 81550 |
rs375192780 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471824 | TCTGTGAAGAGTTAA[A/T]TTTATTTCTTCCTTC | 81550 |
rs375212296 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60536712 | TAAGAGATTAATTTT[A/C]TTCTTCTCTCCCTAA | 81550 |
rs375258311 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572713 | TCAGAAACCTTAAAA[A/C]CAATAGCTAAGCATA | 81550 |
rs375308133 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523870 | GCGTGAGCCATAGCA[C/G]TGGTCCTGTAGTACA | 81550 |
rs375343342 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474086 | TTCATGTTCCACCCT[C/G]TACACCTGGCTCCAC | 81550 |
rs375354041 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490050 | AATTAAAGCATCTTA[G/T]TTTTTTTTTTTTTTT | 81550 |
rs375387292 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525011 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 81550 |
rs375413717 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523005 | TAGTTGAGGCACATT[A/G]TTTTTTCACTTGCAA | 81550 |
rs375432503 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508478 | CACACATCTGCAACC[A/G]TATGATCTTTGACAA | 81550 |
rs375440701 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469669 | GAAACAGGGAAAGTG[A/C]AGTTACTTGAGCAGC | 81550 |
rs375470823 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467429 | TTACACTCTTTTTTA[C/T]TGCATTAAAGAGCTC | 81550 |
rs375498063 | in-del | -/G | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395154 | CTTTGATCTCTTAAG[-/G]CAGTGATTTTTTTTT | 81550 |
rs375504191 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492788 | AGTTAAATGTAAATA[C/T]TGTAGTTTATCAGCT | 81550 |
rs375562678 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444655 | TCTTTTCTATAATTC[C/T]ATTTTAATAATAATA | 81550 |
rs375593230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462845 | ACAAAGCTGGAGGTA[C/T]CACGTTACTTGATTT | 81550 |
rs375646271 | snp | G/T | 1.65652e-05 | 0.0028779 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528759 | TCAGGAAAAGGTCCC[G/T]CCTTTGCAGAGGCAA | 81550 |
rs375687598 | snp | C/G | 0.000437904 | 0.0147905 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483908 | TTTTTCATTAGCATT[C/G]AAGCTGTGTTTCATT | 81550 |
rs375698911 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482578 | GATTTATAGCTGTTT[A/G]AATAGTCTTTGTTTA | 81550 |
rs375705695 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405134 | ATGTCTTTATCAGCA[C/G]CATGAAAAAGGACTA | 81550 |
rs375729485 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404412 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 81550 |
rs375737260 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532098 | TAAAAAATTAATACT[C/G]TCCATCAGTAATAGC | 81550 |
rs375739106 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497133 | CACCCTGCTGGATCC[A/G]GAAGGGTGGAAGTCA | 81550 |
rs375743774 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471677 | TGTTCTAAATTGTTA[A/G]TGTAGAGAAACACAA | 81550 |
rs375764414 | in-del | -/C | 0.000930129 | 0.0215453 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510802 | TTCTTTCTTTTCTTT[-/C]TTTTTTTTTTTTTTT | 81550 |
rs375802388 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471026 | AGGTCAGCTGTTGTT[G/T]TTGTTATTGTATGAG | 81550 |
rs375846270 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517210 | TTATTCAAGTTTCAG[A/G]TCACTTTGGATAGTT | 81550 |
rs375852710 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509907 | AAACCTGTTATGGGT[A/C]CTCCTCTGAGAGGTA | 81550 |
rs375859506 | in-del | -/GG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464344 | GGAAAACGGTATGGC[-/GG]GGTTCCTAAGGAAAC | 81550 |
rs375888733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494158 | CATAATGCTTGTAGT[A/G]TTTTCTTCTCTATAG | 81550 |
rs375893508 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461353 | CTTTGTTTGGTTATT[C/T]TAATAAGAATCTTTT | 81550 |
rs375901159 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506966 | AGGAGACCCATCTCA[C/T]GTGCAAAGACACACA | 81550 |
rs375960332 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483101 | AGAAGATTTTCTTTC[C/T]GTTTTCATAATACAT | 81550 |
rs375978575 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537233 | GTTTTATGAATTTGC[A/G]TAGGTTACTATAACA | 81550 |
rs375985929 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466862 | TCTATTCATATGATA[C/T]AGTCAGCCTCCTGAA | 81550 |
rs375989562 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433362 | TATATGTCCAGTTTG[A/T]AAAATATTTATGTCA | 81550 |
rs375992433 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434601 | CCTTTTAATGCCCTG[C/T]TTGTCAGTAAAATGT | 81550 |
rs376009821 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60521568 | CTGAATTGCAGCCCA[C/T]GAGATGTAGCATGAG | 81550 |
rs376038543 | snp | C/G | 0.000152862 | 0.00874116 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529177 | CAAAAATGTGGAAAC[C/G]TGGAGATGAATGTTT | 81550 |
rs376073695 | snp | A/C | 0.000153988 | 0.00877328 | missense, synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567600 | AGACGATCCACTCGG[A/C]CAACCCAACAGTTTT | 81550 |
rs376154565 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423266 | CATCAAGAGATAGAG[C/T]AACTGGCTTTCTGAA | 81550 |
rs376155964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504601 | ACTAAAAAGCATTAC[A/G]GCTTTTATCTTTCCT | 81550 |
rs376161278 | snp | A/C | 8.26262e-05 | 0.006427 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567679 | TGTGAAGTGGTTTTC[A/C]TATAAAGAAAGATGA | 81550 |
rs376169111 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447591 | AGAGATCTTCAAGGG[A/G]ATTCAATAAATAAGG | 81550 |
rs376230602 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497767 | ACTGAGTTTGTAAAC[C/G/T]CTGATGAATTTTTTT | 81550 |
rs376286079 | in-del | -/TCTCCTGACCTCGTGATCCACCCACC | 0.191461 | 0.24305 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424244 | CCAGGATGGTCTGGA[-/TCTCCTGACCTCGTGATCCACCCACC]TCTCCTGACCTCGTG | 81550 |
rs376293405 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402719 | TTTTTTTTTTTGAGA[C/T]GGAGTTTCACTCTTG | 81550 |
rs376295311 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512577 | CTAGATACAATGGGG[A/G]TACAGGCATTAGGTA | 81550 |
rs376314249 | snp | A/C/T | 0.00279242 | 0.0372774 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488880 | GCTACCATGCCTGGC[A/C/T]GGGTTTATTTTTTGT | 81550 |
rs376317616 | in-del | -/GTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401691 | TTGTTTTGTTTGTTT[-/GTTT]TGAGGGCAGAGATGG | 81550 |
rs376351663 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441266 | TAGGAAAGAGATTTT[A/G]TGACAATTTGCTGGG | 81550 |
rs376357205 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463818 | ACAGTTAGAATGCCT[A/T]TTATCAAAAAGACAG | 81550 |
rs376405138 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551031 | AGTAAGAACTATAGC[A/G]TATAAATTATATCTA | 81550 |
rs376412425 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60485087 | ACTGTGTATTTATTG[G/T]TGTCAATATGATATG | 81550 |
rs376433687 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544798 | AGCTCACTTGAGAGA[C/T]TTCAAAGTGAGTTCA | 81550 |
rs376483037 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493485 | TGGCCAACATGGTGA[A/G]ACCCCATCTCTACTA | 81550 |
rs376485918 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459716 | ACTTCCATTTCCCGG[A/T]TTCAAGTGATTCTTC | 81550 |
rs376486311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539205 | ACAAATATTCATTAT[A/G]TATCTAGTACATCTC | 81550 |
rs376498993 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499272 | ATCTTGGAGAATTAC[-/A]GTGGATTATCAAGTG | 81550 |
rs376523692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433919 | TTGGCCCTCTTCTTT[C/T]CTTACTGATGGTAAA | 81550 |
rs376548736 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557130 | AGAATCGCTTGAACC[C/T]AGGAGGCGGAGCTTG | 81550 |
rs376567702 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530188 | CACTACCATGATATT[-/A]AAGTTCCTTGAAGGC | 81550 |
rs376585722 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441490 | GATGCCATATGATAG[C/G]AAAAAAAACCATTTT | 81550 |
rs376612880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456830 | CCTCCCAAGTAGCTG[C/T]GGCTACAAGCACACA | 81550 |
rs376613990 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445610 | ACAACCTCTACTCCC[A/G]TCTGAGTTTCTGATT | 81550 |
rs376622586 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567903 | GATTTTTTTTTTTTT[-/G]TTTTTGTATTTTTAG | 81550 |
rs376628146 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465568 | TGAGATAGCATTGGT[A/G]TATAAAAATTGTATA | 81550 |
rs376629524 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502876 | TTTTTCTAATTGTGT[C/T]CTGTTGCAAAAGGAA | 81550 |
rs376676902 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564269 | GTGCCCAAGGTGGTC[G/T]GGATGCACCTTGGTT | 81550 |
rs376721079 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436082 | GAAATGTCTATTTCC[A/G]TCCTTTGCCCACTTT | 81550 |
rs376785858 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563232 | GACTCCATATCAATT[A/T]AAAAAAAAAAAAAAA | 81550 |
rs376795717 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501634 | ACCAAAGATTCTTTT[G/T]AGGACAAGTGTTTAC | 81550 |
rs376816251 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60519248 | TTGAGCATCTGCTAT[A/G]TGCCAGGACTATGCT | 81550 |
rs376827466 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410412 | TCTTGTTATCTTGCA[A/G]TTATGAGCACCAAAA | 81550 |
rs376852261 | snp | G/T | 0.000330633 | 0.0128533 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483894 | ATTAGGAAAAAGTGT[G/T]TTTCATTAGCATTCA | 81550 |
rs376874985 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510642 | AAGGTAGAGGAAAAG[G/T]CAGGGGGCGAATAAG | 81550 |
rs376918446 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60540116 | TAAGTTTGCAGTTAT[A/G]ATTTTTCATACTTAC | 81550 |
rs376938781 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454473 | TATGATTTCATTTTT[C/G]TTGATCTTTCTCTGT | 81550 |
rs376947376 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499901 | GCTGCCAGTTTTGAG[C/T]GGGGTCCAGAACAGG | 81550 |
rs376951025 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562672 | ATTTCAAGGACTATT[A/G]CAGAGTACACTGAAT | 81550 |
rs376960148 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60509256 | GGGTATAGCTGTCAA[A/C]GCATCATAGATAGTA | 81550 |
rs377026221 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445755 | AATGCAACAAATCTC[C/T]ATAGGAAAAGTAAAT | 81550 |
rs377028581 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60403870 | AATATCTTTACAATA[A/G]TAAGTAAGGCATATA | 81550 |
rs377030623 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534650 | AGAATTGTTGGCTGG[G/T]CGCAGTGGCTCACAC | 81550 |
rs377032952 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60480641 | GAGTTGTATGTTTGG[C/T]CTCTTTACATAACCC | 81550 |
rs377129576 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60513593 | AATCTCATCTTGAAT[G/T]CCCACATGTTGTGGG | 81550 |
rs377145032 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520166 | GTGTTGTATCTATAA[A/C]GATTTTAATGAGAAC | 81550 |
rs377160463 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468099 | AGGTTTTCTTCCTTC[A/G]GCATAGTTGAGATGC | 81550 |
rs377183539 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517671 | TTCCTTTTTACCATT[C/T]CATTCGTTTTGAAGT | 81550 |
rs377188303 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488635 | GTGGAGTGCAGTGGC[A/G]CGATCTTGGCTCACT | 81550 |
rs377196812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418464 | CTGGGACTAAACTTA[C/T]TTGAGGTCAGTACCA | 81550 |
rs377219880 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421407 | TGCCTTCTTGATTCA[A/G]TTACTTCCCACTGGG | 81550 |
rs377275599 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557861 | ACAGAGTCTCGCTCT[A/G]TCACCAGGCTGGAGT | 81550 |
rs377294670 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492912 | CAAATAATTTTCTTT[C/T]TTTTCTTTTTTTTTT | 81550 |
rs377332574 | snp | A/G | 3.46326e-05 | 0.00416114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460573 | TTGTGTATTTGTTAC[A/G]GAATGTTGAAGGTGC | 81550 |
rs377364991 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60540742 | AATTCTAATATCTGA[A/T]AATAACATATTATAA | 81550 |
rs377389359 | snp | A/G | 1.66058e-05 | 0.00288143 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528434 | TACTGAGCAAAATGG[A/G]GTAAAAGATAATAAT | 81550 |
rs377405814 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60556689 | AACTAATAGCATTGT[A/G]TTCCAAGTAAGCCAT | 81550 |
rs377462860 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60437015 | GCTTTTGTCTGTGTG[A/T]GCTGAAGTATCTAGC | 81550 |
rs377478523 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431399 | ATCTAGGTTTAACTT[C/T]TCAGAATTTAAACAC | 81550 |
rs377484286 | snp | C/G | 0.000144168 | 0.00848899 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485820 | GTATCTCATGTCCAA[C/G]TGGATAGCAGAGAAC | 81550 |
rs377487156 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476155 | CTAGGGTTTCTTCTA[A/G]GGTTTTTATTGTTTT | 81550 |
rs377604133 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405455 | AGCCTTTTCATGGTG[G/T]TCAGAGAATAGCAGA | 81550 |
rs377612963 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570944 | ATATCAAATAACAAC[A/G]CACACAGTTCCTAAT | 81550 |
rs377614683 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60545660 | CGAATGTATTTTTTT[A/C]TCAAGGTGATCAGAT | 81550 |
rs377615775 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520760 | TGATGCTCAGTAACT[A/C]TGATGAGTAACAGTG | 81550 |
rs377643014 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406576 | GGCTAGGTTCAAGTA[A/C]TGAGAAATTTTAGCA | 81550 |
rs377647446 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498398 | CAAAGGCAAGGTTAA[A/G]CGTGGCTACTGTAAT | 81550 |
rs377661422 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430675 | ACTATACTATGTAAT[A/G]TATCAATTATGGGAT | 81550 |
rs377665437 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474438 | ATTTCTACATACTCT[C/T]ATCTCCACACACGAG | 81550 |
rs377665605 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525463 | ACAGGGGTGAACCAC[C/T]GCACCTGGCCAGGAA | 81550 |
rs377727440 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549739 | GTTTAATCTCATGAG[C/G]CTTAACCTATTGACT | 81550 |
rs377743527 | snp | A/G | 3.62417e-05 | 0.00425671 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485969 | AAATCAAATCATTAC[A/G]CGTTTTATTTCTTAT | 81550 |
rs377754852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468799 | GTTATAAAAAATACT[C/T]GTGGTATAAATGAAT | 81550 |
rs377756897 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493918 | GCTTTTATATGCAGT[C/T]GGTAAGAAATGACAT | 81550 |
rs386379408 | in-del | -/TTCT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429846 | AAATTGTATTCTCTT[-/TTCT]TCTCATTAGAATCCA | 81550 |
rs386379409 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527837 | TGTAACATAAACTCT[-/T]TTTTTATAGTAGGAT | 81550 |
rs386379410 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527842 | CATAAACTCTTTTTT[-/T]ATAGTAGGATATCTG | 81550 |
rs386771429 | multinucleotide-polymorphism | CA/TG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419619 | GGGAACATCACACAC[CA/TG]AGGCCTGTTGTGGGG | 81550 |
rs386771430 | in-del | AAT/GAGGA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457528 | TAGGCTAGATCTCAA[AAT/GAGGA]AGATGAGTGAGGCTG | 81550 |
rs386771431 | multinucleotide-polymorphism | AA/GC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465863 | TTAGAAGTACTATTT[AA/GC]AGTACTTCTTGCTGT | 81550 |
rs386771432 | in-del | A/CTAAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492604 | ACCTTGCCTCCTAGT[A/CTAAT]AAATTTTGTATCACA | 81550 |
rs386771433 | multinucleotide-polymorphism | CA/TG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554413 | TTAATTAATAATCTC[CA/TG]GTCTTACACATTGCT | 81550 |
rs397687560 | in-del | -/GTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427361 | gatttttgttctgtt[-/GTT]ttacactgatgaata | 81550 |
rs397693851 | in-del | -/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572828 | GTTGAAATTTTTTTT[-/T]GACAATCTGGTCCAG | 81550 |
rs397698069 | in-del | -/TT | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538397 | ATTTTTTTTTTTTTT[-/TT]GGCTGTCTTAAGGTA | 81550 |
rs397705580 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517196 | TTGCTTTTTTTTTTT[-/T]ATTCAAGTTTCAGGT | 81550 |
rs397742402 | in-del | -/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474895 | GAATGTTTTTTTTTT[-/T]CTTTACTTTTTAAGG | 81550 |
rs397811778 | in-del | -/TG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559930 | AGAAAATGGAAACTG[-/TG]AGGTGATGGATATGT | 81550 |
rs397978072 | in-del | -/GT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442392 | TGTGTGTGTGTGTGT[-/GT]ATTTATGTGTGCATA | 81550 |
rs398023016 | in-del | -/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402714 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTTTCAC | 81550 |
rs398023017 | in-del | -/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470609 | TTTTTTTTTTTTTTT[-/T]GATATGGAGTGTTGC | 81550 |
rs398023019 | in-del | -/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520835 | CAGCTGCTCAGTGGT[-/T]AGGACTGGAATTTAA | 81550 |
rs398023020 | in-del | -/A | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524517 | ATCTCAAAAAAAAAA[-/A]TAAATAAATAAATAA | 81550 |
rs398037657 | in-del | -/T | 0.5 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523574 | TGCAATACATTTTTC[-/T]TTTTTTTTTTTTTTT | 81550 |
rs398117393 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60403148 | ATTTTTTTTTTTTTT[-/T]CTGGTGACTAACCTA | 81550 |
rs398117394 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60456618 | ATTGGTATTTTTTTT[-/T]ACTTTGGAGTTGCTC | 81550 |
rs398117395 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478031 | AAGAGATTTTTTTTT[-/T]ATTAATTATTCAATT | 81550 |
rs398117396 | in-del | -/TT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484127 | AGAGGGTTTTTTTTT[-/TT]GAGGGAAATTCAAAA | 81550 |
rs398117397 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534572 | TGCAATTTTTTTTTT[-/T]AGTCAGATATTTCTG | 81550 |
rs527247056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531487 | AGGTGAGGATGGAAA[A/C]GTGTTTTCTGTATTG | 81550 |
rs527262446 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478769 | TTTATTCTTGTTCTT[C/T]TAGGTGCAACATTAG | 81550 |
rs527274156 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429092 | TGAGAATTACTAATT[C/G]ATATTTATCAGCTGA | 81550 |
rs527291735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421420 | CAATTACTTCCCACT[C/G]GGTCCCTCCTGTGAC | 81550 |
rs527339693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523472 | CATACTAAACTCATA[C/T]AGCATTCTTTGATTA | 81550 |
rs527379132 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494311 | AAGTTAATATTTTAT[G/T]TTTTCATGTAAAACA | 81550 |
rs527387668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478007 | TATCTGGTCTAGGAT[C/T]TTTTTGGTTAAGAGA | 81550 |
rs527397330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486655 | ATTTTGAAATATACA[A/G]TAAATTATTGTTAAT | 81550 |
rs527398329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530822 | GAGTGTGTGGCTAAA[A/G]GGAATGGTGTAAGTA | 81550 |
rs527414565 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436530 | TTTATTGAAAAGGGT[G/T]TCCTTTCCCCAATTT | 81550 |
rs527415452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428421 | TAAGTTAATATAGGG[A/G]CCAAGGGAAAATTTT | 81550 |
rs527446602 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538815 | TGGTCAGGCAAACTT[C/T]TTGTGTTGTTGCTTC | 81550 |
rs527454013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404471 | GCCCGCCACTACGCC[C/T]GGCTAATTTTTTGTA | 81550 |
rs527469424 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435063 | ATGTTTATAAAAATG[A/G]AAAGATTAATTTGTA | 81550 |
rs527527928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405107 | TCTTTTGTAAATTGC[C/T]CGGTCTCAGGTATGT | 81550 |
rs527529111 | snp | C/G/T | 3.47085e-05 | 0.00416573 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509662 | ACATTTTTACATAAG[C/G/T]ATGGGATGTAATTTT | 81550 |
rs527533275 | snp | A/G | 0.00119737 | 0.0244387 | synonymous-codon, intron-variant | TDRD3 | GRCh38.p7 | 13:60397385 | CCAGGTGGCCGGCGC[A/G]GCGTTGTCCCAGGCG | 81550 |
rs527561197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515925 | TTTCTAAGATAAATC[G/T]AGAAAGTGTTTCAGG | 81550 |
rs527573589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471082 | TCCTACTAACATAAT[A/G]TGTTTTGCAAATATT | 81550 |
rs527593316 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432704 | GCAGTAGGTCAGTTA[C/T]TTCCATATTTGCTAA | 81550 |
rs527628822 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471895 | GCCCTGGCTAAAACT[G/T]TTAATATAGTGTTGA | 81550 |
rs527631946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463327 | AGAACACACCATTGC[A/G]CTCCAGTCGGTGTGA | 81550 |
rs527653800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514249 | AGAGAGATGATTTAG[A/G]GTATCTGGCAGAAGA | 81550 |
rs527658803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552804 | CACCACGTGGAAGCC[A/G]CTAAGGCTTGGGTCT | 81550 |
rs527666650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569952 | TCTAAGACTTGAAAC[G/T]ATGACACTCGTAGAT | 81550 |
rs527671876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561891 | TTGTTGTTGTTGTTG[C/T]TGTTTGTAGTAGAAC | 81550 |
rs527690563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514766 | GTTTTAATTCTGTCC[A/G]AATGTGATACAAAGG | 81550 |
rs527735258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402827 | CCAAGTAGGTAGGAT[C/T]ACAGGCATGCGCCAC | 81550 |
rs527761035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410417 | TTATCTTGCAATTAT[C/G]AGCACCAAAAAGGAC | 81550 |
rs527772315 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407599 | AAGGTATATGTTTGT[A/T]TTTAGTTAGAAGAAA | 81550 |
rs527828642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469354 | ATATAATTTTCCCAC[A/C]ACCCAGTCCCATAGC | 81550 |
rs527830049 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569388 | AAGATCTCTACAATG[A/T]AAACTGTAAAACATT | 81550 |
rs527841151 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503150 | CTGAGTTTAGTCCAT[C/T]TAGTTAACTTCTGTT | 81550 |
rs527899406 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436043 | TCTTATGTCTGTTGG[C/T]TGTTTTTATATATCT | 81550 |
rs527906760 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400209 | TGACTCTGAATTTAT[A/C]TAGATAACAATTTTA | 81550 |
rs527911772 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525994 | TTCCTTTTAGAAGAA[A/T]TGAAATCAAATTCTG | 81550 |
rs527916458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548321 | GCTAAGGAAGAAAGA[C/G]AACTTGCCTTCTGGA | 81550 |
rs527916615 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539625 | TTAAAATGAAGAGCT[A/G]TCAATCTCAAGTTTT | 81550 |
rs527917016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493459 | CTCAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 81550 |
rs527934105 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525212 | GAGATCTCTGTCTGT[C/T]GCCCAGGCTGGAGTT | 81550 |
rs527938190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508401 | AACCCAAACAGCATG[A/C]TATTGGTACCAAAAC | 81550 |
rs527945114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500869 | TTAGTAATCAAGTGG[A/C]TAGGATGACCCATTC | 81550 |
rs527950334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403397 | TGGCATTTTGACTTA[C/T]CATGTTTCAGTTAAG | 81550 |
rs527959416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553860 | AGTCAAACTATATCA[C/T]AATGTTACTAATATA | 81550 |
rs527993364 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499827 | TATTTGGATTTTGGA[A/G]GCAACACATTACTCA | 81550 |
rs527997321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501376 | CATTTGGAGTTTGAT[G/T]GCTGTCAGCCATTCC | 81550 |
rs528010050 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455070 | AGGCGCCTGCCACCA[C/T]GCCCGGCTAATTTTG | 81550 |
rs528014341 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396483 | GCCCCAGCCCTCTAC[A/G]GCGCGGGCGAAGGGC | 81550 |
rs528018979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444495 | CTGTTCATCTTACTG[A/G]TATACTTTAAACAAC | 81550 |
rs528029750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453002 | GATTCATTTATTTTT[C/T]TTCTACCTGATTTGA | 81550 |
rs528049295 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60414699 | GATAGGAATGTGTCA[A/G]TACTTGCAGTGGGGG | 81550 |
rs528077531 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567317 | TCTATTACCAAGGAT[A/C]AAAAGAGTTTTAACA | 81550 |
rs528096221 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433777 | GTGCAGACATGGCTG[C/T]CCCCTTTAGCTCAGT | 81550 |
rs528102200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545609 | TCTTATCTTGAAAAG[A/C]CTTAATAAGGCTGAA | 81550 |
rs528133011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401218 | TGGATTCAACCAGTC[A/G]CAGATCTAAAATATT | 81550 |
rs528176519 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459684 | GCAGTGCAATGGCTT[G/T]ATCTCGGCTCACTGC | 81550 |
rs528191129 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440095 | ATTCATTAAAATGAA[G/T]TGCCATTTAATTTAC | 81550 |
rs528246488 | snp | A/C/T | 0.000399281 | 0.0141238 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528783 | GAGGCAAAAGAAAAT[A/C/T]CACTTCCTCAAGGAT | 81550 |
rs528261346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476216 | TGAGTTAATGTTTGC[A/G]TATGATGACTGGAAG | 81550 |
rs528276636 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423915 | AGAAAAATAATAACT[A/G]TAAAAGCAGAAATTG | 81550 |
rs528277331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427296 | TTTCGTTCTTTGTAT[A/G]TTGGGTAATTTTGGA | 81550 |
rs528317916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529450 | TCGGTTTGGTTTTAG[A/C]TTACATGCCAGAAAA | 81550 |
rs528335704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521350 | TATTTACTGAGTGCC[A/G]CCTATTTGCCTGATT | 81550 |
rs528387930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418609 | GCAGCACAATTAATG[C/T]ACATTAAAATGCACA | 81550 |
rs528394799 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491513 | GTGGAACCAGCCAAG[G/T]TGTGACCAGTAACAG | 81550 |
rs528401816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434068 | TGCCAAGTGACTTCT[C/G]AACACGACGTGAAGA | 81550 |
rs528407429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484064 | AAAGATTGAAGCAAT[G/T]AAGAGCCATATCTGA | 81550 |
rs528489231 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424336 | AGTGGTTTTTAAAAA[A/C]CAACTTTATTGAGTT | 81550 |
rs528496442 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481095 | TGTCAGCAAAAGTGC[A/T]CTGGTGGGGCAGTGG | 81550 |
rs528498824 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446847 | TTCATTGGAATGCTT[C/T]TATTAACCAGCATTT | 81550 |
rs528500199 | in-del | -/T | 0.139564 | 0.224285 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437122 | TTTGATAAATTAAAC[-/T]TTTTTTTTTTTTTTT | 81550 |
rs528528853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526692 | TCTTAGAAAAATCTT[A/C]ATTCTTTGTCACAGT | 81550 |
rs528533721 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504903 | AGGAATAGTGGACTT[C/T]GGCCCAGATACTATG | 81550 |
rs528562581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488731 | GGTGTGCACCACCGT[A/G]TCTGGCTAATTCTTT | 81550 |
rs528597037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534123 | TGAGACCAGCTTGGG[C/T]AACCTAGCAATACCC | 81550 |
rs528601891 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507223 | AGAGACCTACAAAGA[G/T]ATCTTAGACTCCCAC | 81550 |
rs528609109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60543825 | ATTTTATTGCATACA[A/C]ATATTTTATTTTACA | 81550 |
rs528611535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440668 | CCTGGGCAACAGAGT[A/G]AGACTCTGTCTCAAA | 81550 |
rs528628158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432071 | AATGTGGTAATATTA[A/G]TAGAAGAGGTACTTA | 81550 |
rs528655285 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559770 | GTTGGTCAAAGGTTA[C/T]GAAGTTTCAGTTATG | 81550 |
rs528659669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417732 | GAAATACTCTGCACA[A/G]TTCGAACTAGGTATC | 81550 |
rs528660290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567817 | TAACTTCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 81550 |
rs528664481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512907 | GGTCTGGAGGATGGT[G/T]GCCCTCTTCTTATAG | 81550 |
rs528665188 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458837 | GATATTTGTCAATGC[A/C]TAGGCTAAAAATATG | 81550 |
rs528706996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564130 | ATTTAGTTTTATAAA[A/T]CCTATCTGATAACAT | 81550 |
rs528725019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408972 | AGGAAAAAGTGGCTT[C/T]GTGGGCTGGGCCCAG | 81550 |
rs528756164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450365 | TATGTAACAAATATT[A/G]TCATACTTTTAGAAT | 81550 |
rs528821133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567043 | GATTTCATCAGATGG[A/G]GACAGACAGCTGATG | 81550 |
rs528839147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467077 | CTGCACCTATCAACC[C/T]ATCACCTAGCTATTA | 81550 |
rs528844085 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TDRD3 | GRCh38.p7 | 13:60574046 | AAAACAGCCTGAAGC[C/T]AAATAGCAGTTCTTA | 81550 |
rs528859313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517399 | TTCCTCAAGAATCAT[C/G]TATGTATTGACTATT | 81550 |
rs528859699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565306 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 81550 |
rs528863203 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415409 | CTATTTCATCAGAAT[A/C]TTTACGCTTCAGCCA | 81550 |
rs528907309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572039 | AGAAATTATACACAG[G/T]TCTTTAGTCCAACCA | 81550 |
rs528929611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510838 | ATTTCTTTTTAAAAG[A/G]CCAAACTTTATTTAG | 81550 |
rs528948198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472112 | AGATGCTTCCTCTGC[A/G]TCAATTGAGATGATC | 81550 |
rs528956996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423298 | CAGAAACTTCAGGAG[C/T]TTGCAGGGACACATA | 81550 |
rs528965714 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395213 | TGTAATAAGTAAGTT[A/G]TGGCTTGAAACTTTG | 81550 |
rs528971169 | in-del | -/GTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477215 | ATTATTATTATTATT[-/GTT]ATTATTATTATTATT | 81550 |
rs528974723 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516702 | CAAATTAGATAATGT[A/G]TATGAAGTGCTAAGC | 81550 |
rs528974964 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524823 | ACAATTTTCGGCCAG[A/G]CGCAGTGGCTCACAC | 81550 |
rs528975742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480400 | TTGTAAGGCCCCTTT[C/T]CTCTAGCTGCCTGTA | 81550 |
rs528994153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60573023 | GGAACTCCACTAGTC[C/T]CTGCCTAAGCACGCT | 81550 |
rs529040673 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508062 | AATACAACTTACAAG[G/T]GATGTGAAGGACCTC | 81550 |
rs529088327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497304 | GGGACCCAAAGGGGG[C/T]TGTCATTGCCAGCTC | 81550 |
rs529117059 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504672 | GAATAGGAACAGCTC[C/T]GGCCTGCAGCTCCTA | 81550 |
rs529127528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542749 | AGTCTTACTTTTATC[G/T]TCTTATGAGTCATCT | 81550 |
rs529127566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551981 | GACATGTGGGGATTA[C/T]GATTTGAGATGAGAT | 81550 |
rs529130357 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465982 | TCCTTTGCCAGAGGG[A/T]TAAGAGGGTAAACAT | 81550 |
rs529148187 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511576 | AACAATGCAACTTTA[G/T]TACCTTATAGTTTCT | 81550 |
rs529150408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565863 | ATAAATAACTTCTTT[C/T]CTGAATACTTTTATG | 81550 |
rs529161358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399012 | TGCTTTCCAACATGA[C/T]CCCCCCTCCTTTGGA | 81550 |
rs529161420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406786 | AGCACCTTTTAAAAC[A/G]CTCTTTATAAATTTA | 81550 |
rs529166406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498744 | CCCCAAGGAGACCTC[C/T]GGCCTTTTACCAGGG | 81550 |
rs529190208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558989 | TTTTTTTCTGTTGAA[A/G]GCAATTTGAAGAATA | 81550 |
rs529191772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457920 | TCATTGGCTTTAGGG[A/C]CCACTGTAATTCACA | 81550 |
rs529218972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449198 | AATTGAAAAAAGTTT[C/T]AACTTTTGATTTAAT | 81550 |
rs529238091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548690 | AAATGCAAATTGAAA[C/T]AGTAAAATACACTTT | 81550 |
rs529239302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456666 | AAGATTTAGAAATTA[A/G]TTCTTGTCTATTTTT | 81550 |
rs529242338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556593 | ACCAGTAATTGAGCA[C/T]CTACTAAAAATATTA | 81550 |
rs529280043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549448 | GGTTTTAGCTTCTGC[G/T]GGTAACATTAATATA | 81550 |
rs529291106 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462016 | CTTTTTTCTTCTTTC[A/T]TCTGGTGTCTGCCTC | 81550 |
rs529310075 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60556100 | ATCTGCCTGCCTCGG[A/C]CTCCCAAAGTGCTGG | 81550 |
rs529310289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447523 | GGTATTTTTATCTTG[A/G]AAGTCTAAGAATATG | 81550 |
rs529327027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502996 | CAGAGAGAAACAAAC[A/G]TGCTCCAAACTTTGT | 81550 |
rs529330898 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516184 | TTTGTATCAGCATAA[A/G]CTGTCTGAGGATTTT | 81550 |
rs529332407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509332 | AAAAGCTCCTGGGGG[G/T]TATCATTTTGTTAGC | 81550 |
rs529334542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563603 | TCTACCCATTAGAGG[G/T]AATAACAACTCCTTC | 81550 |
rs529354682 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60573306 | TTTCGGTAATCCTCC[A/G]TTACAAACAGTTCGG | 81550 |
rs529368272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455275 | TGTTTTGACAGAGAA[A/G]GTAGGTAAAAAAGAG | 81550 |
rs529375582 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398797 | GAACAGCATGGGCGT[A/G]AAAGATTGTAGAGTT | 81550 |
rs529385302 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463171 | GGAAGTCAAGGCGGG[A/C]GGATCACCTGAGATC | 81550 |
rs529387873 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60397289 | TTTTTTTTTTTTAAG[C/G]GGGGGGGTCTCAAGT | 81550 |
rs529399370 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461239 | TCTTGCAGAGTTTTA[C/T]AGGCTAATAAATTTT | 81550 |
rs529399720 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427093 | TAATCTTAGAGGACC[A/G]CAGTCATATATGTAT | 81550 |
rs529444114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430208 | CCTTCCAATTTTTGT[A/G]ATACCTTACATTTAT | 81550 |
rs529451702 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407816 | TAGCACTTCAGTGAT[-/A]ATGGTGTGGCTGTGT | 81550 |
rs529457887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430855 | TTTGTTGTTTATTAC[C/T]TATCTCACGATCATT | 81550 |
rs529476086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422375 | ATATTGTAAAACAGC[C/T]CAATGTCACAAAAAT | 81550 |
rs529492441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479865 | AAAGATGTTTCTCCA[A/T]CCCTTTACCTTGAGC | 81550 |
rs529530117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533034 | GTTTAATTTACCTGA[A/G]CTGGCATAATTTGGC | 81550 |
rs529539355 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488077 | GCACAGTAAGCCAAT[C/G]ACTGAGACAATGAGT | 81550 |
rs529551709 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524052 | ATATCTTAGTATATT[G/T]ATTAGAGTGATGGCA | 81550 |
rs529564594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60495270 | TTTGTGGGTATTTCC[A/T]TGATTTCTTGGCTTT | 81550 |
rs529568889 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546295 | CCATTTATGTTGTAT[G/T]CTTTAGAAATTAGCA | 81550 |
rs529588615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486824 | TGAGACAACTTTTTT[A/G]TCTCTCACATATGAG | 81550 |
rs529610825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539572 | GGGTTTGGGTTCTTT[C/T]TTTATGATAATTATA | 81550 |
rs529611037 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432926 | TGGTAGCAGATAATC[A/G]GGTGTAGGTTAGAAC | 81550 |
rs529627737 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467833 | TAATATTTTTCCCCA[G/T]TTATATTAACAATAT | 81550 |
rs529629390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487408 | TTGAACTCGGAAGGC[A/G]GAGGTTGCAGTGAGC | 81550 |
rs529680920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450525 | AAATAATCCTAGGGT[A/G]CTTTATATTTCTGGA | 81550 |
rs529681651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530746 | AGGTGTGAGCCACCA[C/T]GCCCGGCCCAAAATA | 81550 |
rs529704430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419827 | ATAGATGGATGAAAG[C/T]AGAAAGGAAGAAAAG | 81550 |
rs529778406 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476003 | TTTTCTGTGTACCCT[C/G]TTTATAGTTTCCTTT | 81550 |
rs529804053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523353 | ATTCTTAATTATTCT[C/T]GCATTTCAAATCATG | 81550 |
rs529810638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538461 | ACTTTCTAGTTAACA[C/T]ACATGAGATGCACAG | 81550 |
rs529822545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412133 | CTGTAAAACCTTGTG[G/T]TAGTGTGAGATTGCT | 81550 |
rs529828217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571031 | TCGACAAAATGCTTG[C/T]TTTGGATTGTACTGT | 81550 |
rs529831649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547556 | GAGAATTAAATGATC[C/T]ATGTAAATGTGCTCT | 81550 |
rs529849346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435288 | TTTCTTATTTCAATA[A/G]TTTTTTTGGGTACAG | 81550 |
rs529862313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514902 | AAACAGACAATAGTT[A/G]TATGTGTTGTGGGGA | 81550 |
rs529883557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421104 | TTTTCTTTCAGGTTA[A/G]TTTGGGAATTCTTGA | 81550 |
rs529884968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403549 | AATTTGAGAAACACT[C/T]GTGAAGTCATAGCAC | 81550 |
rs529884982 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412909 | AAATATGATTATAGA[A/T]CTCTACATATCTAAG | 81550 |
rs529913694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522710 | AGGTTTTTCTGCGTT[A/C]ATAGAAAGAGATTAT | 81550 |
rs529948839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508530 | GGGAAAGGATTTCCT[A/G]TTTAATAAATTTTGC | 81550 |
rs530022718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470214 | GCATGTGTCAGAATT[C/T]CCTTCCTTTTTAAGG | 81550 |
rs530071787 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543946 | GAAGACTCCCATTAT[C/T]GTTTTTGTAATATAG | 81550 |
rs530092726 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555912 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 81550 |
rs530099764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409322 | AGAGTCCCTACTGGG[A/G]CACTGCCTAGTAGAG | 81550 |
rs530104037 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426449 | AAAAGTAACTGTGAG[A/T]TGATAGATATGTTAA | 81550 |
rs530127255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475329 | TAGCTCCCACTTATA[A/G]GTGAGAACATATGGT | 81550 |
rs530131547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483990 | AGGAATTTAATAATT[C/T]TGAGGTTTTTTTCCT | 81550 |
rs530157066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513533 | TAACTTCATGATTTA[A/G]GAGACACTATAGAAG | 81550 |
rs530159254 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410242 | AATGGTCTAGTATAT[C/T]CAGTTAGAAAGGAGT | 81550 |
rs530186475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454210 | TGATAGCTGTATTTT[A/G]AAATTTGTAGAGTCT | 81550 |
rs530208155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507413 | TCTCAGCACTATGTC[A/G]TACTTTAAAATTGAC | 81550 |
rs530208703 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500044 | AGCCTTTCGCAGGCC[A/G]CCATAGGTGAATCAC | 81550 |
rs530267409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500661 | AATGTGCGATTATAT[A/G]CTGATTTATGGGCTG | 81550 |
rs530276615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443077 | TGAACTGTTAGTTAC[A/G]TTATTGATATGATGG | 81550 |
rs530284641 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442775 | TGGTGGTGTTTTTCC[A/G]TTTTATAGAGGAGTA | 81550 |
rs530297232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569192 | CAGGTTGGTCTCAAA[C/G]TCCTGAGCTCAAGCA | 81550 |
rs530314858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513948 | CAGAAAAGATAACCC[A/G]AAAATGTGGAAGTGA | 81550 |
rs530341683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444117 | CATAGTTATTTGTTT[A/G]CCACCTTCTATTTCT | 81550 |
rs530372527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402144 | TTCCATTACATAGAG[A/G]CTTCTTCTCAAACAC | 81550 |
rs530384509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561166 | TTTTCTCATATGTTA[A/G]TGAAACCCGAGGGTT | 81550 |
rs530396563 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460824 | AGCCTGACCAATGTG[C/G]TGAAACCCTGTCTCT | 81550 |
rs530418025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560163 | GAACTTCAGGTGTAC[A/G]GCCTAAAGGTCTCAC | 81550 |
rs530421106 | snp | G/T | 0.00121359 | 0.0246033 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561863 | TATGGGCCCAGGTTT[G/T]TTGTTGTTGTTGTTG | 81550 |
rs530422880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553407 | AACTGTTGTATCCTC[C/T]GCCTGTTACCCAGTT | 81550 |
rs530442740 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395078 | TAAGTGATGTGTATG[C/T]CTAGTTGCATTACAT | 81550 |
rs530448518 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451911 | GTTTTGATTGAAATT[C/G]CATTGAATCTGCGCA | 81550 |
rs530449449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440939 | TTAAAAAAGTTACTT[A/C]AATTTATATTTATAG | 81550 |
rs530453183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552533 | TGCAAGCTATAGGTG[A/G]ATCTGCCATTCTGGG | 81550 |
rs530464106 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453236 | AACTTACTGAAGGGT[A/G]ACATACATAAAATGG | 81550 |
rs530479538 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407971 | ACGTCTCGTGAGATC[G/T]GATGGGTTTTTCAGG | 81550 |
rs530487046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451063 | AAAATAAAGCTTGAC[A/G]GATCTTGACTGGTAA | 81550 |
rs530496406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505033 | GGCAGACACTAACCT[A/G]GCTGCAGGAGTTATT | 81550 |
rs530499660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458221 | AAATAGTCCTATTCC[C/T]GCCCTGTGTTTGCAT | 81550 |
rs530501147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427901 | TATTTCCTGTGGCTG[C/T]GGTAGCAAATTACCA | 81550 |
rs530526280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559735 | TTGCCAGGAGCAGAG[A/G]GTGAGGGAAATGAGG | 81550 |
rs530562223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448642 | AATTGTGACTGGAAG[A/G]AAGTGTGGTAGGGAA | 81550 |
rs530562326 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505581 | TCTCAGCACAGTGCT[C/T]CTTAACTAAAGGAGC | 81550 |
rs530597175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467015 | TCAGGGTACATGTGT[A/G]GGATGTGCAGATTTG | 81550 |
rs530601970 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445757 | TGCAACAAATCTCTA[C/T]AGGAAAAGTAAATAA | 81550 |
rs530616915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433740 | AATCAAATCTGACGC[A/G]GTAACTGCTTTACTA | 81550 |
rs530646771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400469 | ATCTTCTGGCTGGGC[A/G]CAGTGGTGGCTCATG | 81550 |
rs530652231 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537273 | GGATCATGCACATTA[C/T]GATCAGCCTTTCTTC | 81550 |
rs530666443 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417253 | CTCCTGGCCTCAAAG[C/G]GCTTCTCCTGCCTCA | 81550 |
rs530669152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489690 | AGCTCTCAGTAAACA[C/T]GACTATTGCTATTCT | 81550 |
rs530720460 | in-del | -/TTT | 0.0222719 | 0.10315 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452816 | GATCACTGTTCTTAG[-/TTT]TTTTTTTTTTTAATT | 81550 |
rs530725260 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418142 | TTGTGGCATCCATTT[C/T]TGCTCCTACCTCTCC | 81550 |
rs530733030 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461624 | TTTCTCTTGAGCAGG[A/C]ATTTATCAGGTGTTC | 81550 |
rs530749379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433004 | ATTAAGAACACCATG[C/T]ACCAGTCACTGTCCA | 81550 |
rs530749679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441756 | TCTTCTCTTCTTTCT[A/G]TGGGGTAGACACTGA | 81550 |
rs530780778 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420532 | AAATTATGTTGGTTT[A/G]TGGAGTGGGAAAGAA | 81550 |
rs530786067 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60531952 | TAATATTCAACAAAT[A/C]ATAACTGAGTAGCTA | 81550 |
rs530814006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423602 | CTCTGATTACAGTGG[A/G]CTAAAACTAGGATTT | 81550 |
rs530847719 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490682 | AATTATTGAAGTAAT[C/G]TAGGATTTAAAAAAA | 81550 |
rs530880521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550698 | AAGTGCCAGTTAAGA[A/G]CTAGTTTCGCATTTT | 81550 |
rs530901673 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454757 | CGTACATGGATGACA[C/T]TGGGAATGTTTCTGA | 81550 |
rs530912457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450917 | TGCCCCATATCGGGC[A/G]TATTTAAAATCTTAG | 81550 |
rs530918691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542015 | TACAGTCGTGAGCCA[C/G]CGCACCTGGCCTCCT | 81550 |
rs530927018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488282 | TGTGGCATCTCATTG[C/T]CTGGATGTGGTGATC | 81550 |
rs530930318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542626 | TTGATGGTGATGGAC[C/T]AAAAGTGGACTTATG | 81550 |
rs530930855 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424743 | CAGAGATTTGTAATC[A/C]TCACTACTATCTAAT | 81550 |
rs530936585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431988 | AGTCCTGGTTTAATT[A/G]TTGGAATACAGATTG | 81550 |
rs530964402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488636 | TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 81550 |
rs530972247 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526606 | ATTAGGCAGATATTC[C/T]TGGGGGAAAGTTTTT | 81550 |
rs530973947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518419 | GTGAGCATAATAAAG[C/T]GAATGTTCTTTTATG | 81550 |
rs531043829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551553 | CATTCCAAATTACCT[C/T]TCTAGGAAGTAAACC | 81550 |
rs531052811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438959 | ATTGTTGAGTTTATC[A/T]AAGAGTTTCAAAATG | 81550 |
rs531057820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539834 | TTGTGATACATATAA[C/T]CATGAGTTTAAAATG | 81550 |
rs531066117 | snp | A/C | | | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528586 | GAGGTTCTGAAAGAC[A/C]AAGTACTTCTTCAGT | 81550 |
rs531091645 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466394 | TTTTATTCTATTTAT[C/T]ATGTCTTTATCACAG | 81550 |
rs531133861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525851 | AATCAGAAATTCTTT[A/G]AGTAGATTGGATCTG | 81550 |
rs531136153 | in-del | -/TAACTC | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422472 | AACAACCGTGAACTA[-/TAACTC]TAAGTTCATACTCCA | 81550 |
rs531149865 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426147 | TGGACCTATAGGATG[-/T]TATGCTAAGTGAAAA | 81550 |
rs531171862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471944 | ACATCCTTCTCTTGT[C/T]CTTGATCTTAGAGGA | 81550 |
rs531181181 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568500 | TTTGGCAACTTTGTG[C/T]TGTATAAGACAGAAC | 81550 |
rs531183279 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519265 | GCCAGGACTATGCTA[G/T]GTGCTTTGCATACTA | 81550 |
rs531225595 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481316 | GATTTGGCCATTATT[C/T]CTTCATATGTATTTT | 81550 |
rs531231170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473960 | AGAGAAGACTCTGCT[C/T]CACCACCTCTTGTGA | 81550 |
rs531242773 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487896 | CCCACCAACAGTACA[C/T]AAGAGTTCTTCTTTC | 81550 |
rs531267739 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542065 | GCATCATCGGTGAGA[A/G]CCACAACTGAACGGG | 81550 |
rs531293557 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523957 | TACCCATTTCTACTT[C/G]TGCTTTTTTTTTTCC | 81550 |
rs531296264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478947 | TAGCTGGAACTACAG[A/G]CACACACCACCATGC | 81550 |
rs531308112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471241 | TTAGTAAAGGGTCCA[A/G]ATTCATACTTTTGCA | 81550 |
rs531308121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479743 | AATTCTTTATTATTA[C/T]GTATGTCATTTCTTT | 81550 |
rs531312740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413109 | ACAGGAAGTTAGCAT[C/G]TGAAAATGCTGCCAA | 81550 |
rs531321123 | in-del | -/ATAAC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452613 | TTTTTAGGATAATCG[-/ATAAC]ATAGCATATGTTGAT | 81550 |
rs531329763 | in-del | -/TATTAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60545684 | ATCAGATAATATAAA[-/TATTAT]TATTAGGAAATCATG | 81550 |
rs531334976 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60573272 | GAAAGACGTGGTTCA[-/T]TTGGCAGACTGCATC | 81550 |
rs531350049 | in-del | -/CTC | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407459 | TATGAAAAATGTGAT[-/CTC]CTCAGAAATGCAGGA | 81550 |
rs531425797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487342 | TTAGCTGGGTATGCT[A/G]GTGCATGCCTGTAAT | 81550 |
rs531457472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523579 | TACATTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 81550 |
rs531460541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405135 | TGTCTTTATCAGCAG[C/T]ATGAAAAAGGACTAT | 81550 |
rs531482818 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464486 | TATTCACAATACCCA[C/T]GATATGGAATCAACC | 81550 |
rs531492582 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497377 | GCTCTCAGGTGATAG[A/G]TGATTGGCTATTTCT | 81550 |
rs531496058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457196 | CTGAATTGTGGAACT[A/G]CTAACTTAAGGCTTG | 81550 |
rs531496664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448078 | TCATCTCCTGAAAGC[A/C]CAAAGTAAATGATCA | 81550 |
rs531498926 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429745 | AGGCTTACCAGTAAG[C/G]AAGCATATACACTTT | 81550 |
rs531505359 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458427 | CAACACCCAGGGGAC[A/G]TAGAACTCCCAAAAT | 81550 |
rs531512413 | snp | G/T | 1.65496e-05 | 0.00287655 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510762 | ATGTGGAAGGTAAGC[G/T]AATTTAAAGTTGATT | 81550 |
rs531517165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557581 | TACATTGGGCCCTGC[C/T]TGCTTTAAGGCTTAA | 81550 |
rs531549067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448991 | CTAAGTTCTAAGAAT[A/G]ACAGGTTGTATATAC | 81550 |
rs531560138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455207 | TGTGTGCCACCACAC[C/T]TGGCTTATATTTATT | 81550 |
rs531561015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398982 | ATATTTTCATTTACA[A/T]ACTCAGTATTTTACT | 81550 |
rs531581970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563491 | TTTGCCTAGCCTAGG[A/G]TTTCTCAACTTCAAC | 81550 |
rs531610198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445328 | TCATCAGGAGAAATG[C/G]AGTACATCTGGTTAC | 81550 |
rs531620688 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60539468 | GATAAAATTAATGTG[A/G]AAGAAGAAAGCATAA | 81550 |
rs531632629 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490004 | TTTTTGTTGTCACAA[C/T]TGATATTATATTTTC | 81550 |
rs531638626 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60509555 | AGTGTTACTTGTGAG[C/G]TCAGAGAATACTCAA | 81550 |
rs531646660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411914 | CATTGTCTTCATGGT[C/T]ATAGCAGAGTAGCTG | 81550 |
rs531669784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60570015 | TCTGGGCAAAAACTT[C/T]TTGAGTAAGACCTCA | 81550 |
rs531680993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465076 | TATGTATAATTATGA[C/G]AACACAAAAATAAAA | 81550 |
rs531682196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565260 | CGAGGTTTCACCTTG[C/T]TAGCCAGGATGGTCT | 81550 |
rs531725864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403468 | GATATAGAAGTAGCC[A/G]AAGAACAGTATTGCC | 81550 |
rs531782585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509179 | GTTCTTGAATTCTAT[C/T]CAGGTCTAGATTTTT | 81550 |
rs531802679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436631 | CCATTGGTATCATTG[C/T]GTATTTTTATACCAG | 81550 |
rs531816721 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401248 | TTGGAAAAATAAAAA[A/T]AAATAAAAATAACAA | 81550 |
rs531871321 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552515 | GCTTTTCCAAGCACA[C/T]GGTGCAAGCTATAGG | 81550 |
rs531910343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446740 | AAACCAGAGTACATA[G/T]TCAAGGAATATATTT | 81550 |
rs531919656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548584 | GTTTTTTTAAGCCTT[A/G]AACCATTCACTTATG | 81550 |
rs531962704 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483619 | AAGTTAAGAATAATA[C/T]ATTTTTTTGTGGTTT | 81550 |
rs531968584 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541181 | TTTCTTTCTTTCTTT[C/T]TTTGAGACGGAGCCT | 81550 |
rs531976118 | snp | C/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439454 | GCTTTTCTCAGAAAG[C/T]GTATGAATAATCCTA | 81550 |
rs531988515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493700 | AAATATTGTTTAACC[A/G]AATGTTTCATACTGT | 81550 |
rs531998009 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501991 | TATTCCAGTTAGAAG[A/G]TGGTAACGTGTATAA | 81550 |
rs532003519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547743 | GAAAATATTATTTCT[A/G]TCCTCTGTCTGATAA | 81550 |
rs532004413 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520729 | CTAGGAGAGCGTTGA[C/T]GACACCACCAGCAGT | 81550 |
rs532010930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538276 | GTACACATTTATATG[A/G]CCAAAATTGTGTTTC | 81550 |
rs532012067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546591 | GAATATGTGAATTTC[C/T]TATCTATTCTAATGA | 81550 |
rs532016379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435203 | TTTCTTGAAAATTAT[A/G]GAGTAAACCTATAAG | 81550 |
rs532020373 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60397126 | GTGGATCAGGTCCCG[A/G]AGCTCCGCAGCCTGG | 81550 |
rs532021674 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500167 | GTTTTGGTGGAAACC[A/G]AACATTTGACTATGG | 81550 |
rs532057529 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436111 | TTTGGATGGGTTGTT[G/T]TTTTTTTTTTCTTGC | 81550 |
rs532065115 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394956 | TCCTCAGATTGTGAC[A/T]ACCTAGACATTGCTA | 81550 |
rs532119133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553772 | CGACCCCATGATCCA[A/G]TCACCTCCCACCAGG | 81550 |
rs532123984 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434181 | TTAAAAAGTTTTGAG[C/T]ACTTAAGGCTGGGTG | 81550 |
rs532127450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500601 | TGGGCAGAACTTCAA[C/G]CAGTGCACCTAGTTG | 81550 |
rs532131892 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530606 | CTACCATGCCCAGCT[A/T]ATTTTTTGTATTTTT | 81550 |
rs532136810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443895 | ATAATTGGATCTTTT[C/T]TATGAGTACTGACAG | 81550 |
rs532147423 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497675 | CTACTTTTAAAGTGA[A/G]GGCATTGGTTGGAAA | 81550 |
rs532156425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419738 | AAACCACCATGGCAC[A/G]TGTATACCTATGTAA | 81550 |
rs532173659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484219 | AGAAAAATAAAGCCA[C/T]ACAGAGTGATCAAAG | 81550 |
rs532204207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553325 | GCATTTTGGTCAACA[C/T]CATTCAACAAGTCTC | 81550 |
rs532212533 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411043 | TGCCTGTGTTTACAT[A/T]GTTGTTAGTGCAAAG | 81550 |
rs532216825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420589 | AGATATTCAGGTATT[C/T]CAGTGACATTTGTAA | 81550 |
rs532251680 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491636 | GAATTAATATAGAAT[C/G/T]GAGGAAGTTGTTTAT | 81550 |
rs532293149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522043 | ATCAAGAGTAATTTT[C/T]TTACTTTTTAAATAT | 81550 |
rs532311849 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60413795 | AATCTTTATATCTTA[C/T]GGATTTTTAATCTCA | 81550 |
rs532319352 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477761 | TTTTGATGTGCTGCT[A/G]GATTAGTTTGCTAGT | 81550 |
rs532452699 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527937 | GGCTAGAACATGACT[A/G]ATAATAATAGCTATA | 81550 |
rs532468154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482580 | TTTATAGCTGTTTGA[A/C]TAGTCTTTGTTTAAT | 81550 |
rs532471305 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420602 | TTCAGTGACATTTGT[-/A]AAAAAAAAATTTTCT | 81550 |
rs532477793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483379 | TAACTAATAAATTTG[C/G]TGTCTAAAAAATTTA | 81550 |
rs532483802 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502026 | ACTGCAAATAGTAGA[C/G]TGAGTATAGCAGTTC | 81550 |
rs532496320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527718 | TTCTGACACTTTTTC[A/G]GTATTTCCACTTTTG | 81550 |
rs532526275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417221 | GCTCTTGCTATGTTG[C/T]CCAGGCTGGTCTGAA | 81550 |
rs532537185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513457 | CTCAGAAAATGGGAT[G/T]TTCTTTTCTATCACA | 81550 |
rs532558483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460696 | TGCATTTCTGCTTCA[C/T]CTGTATAAAAATAGT | 81550 |
rs532590561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417967 | CAGGCCTTTATTCTT[A/G]AGAGTAGCCTCCTGA | 81550 |
rs532611582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506469 | CATTGACACTGGCCG[A/T]GTGCAGTGGCTCATG | 81550 |
rs532618534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425079 | AGTTAACAAAATAGA[C/G]AAACCATTAGCTAAC | 81550 |
rs532622669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402046 | TAGCTACTACAAAGA[C/T]GTGGAACAACTTCAG | 81550 |
rs532677169 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521024 | GGTGCATTACTGCAA[A/C]ACTAGAAAAGCAGTT | 81550 |
rs532703183 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449523 | AAAAGTGTTGCTTTT[A/G]GCTGGTAGTCCCACA | 81550 |
rs532726411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458000 | GTTCCCAAACGAGGT[C/T]ATATTTATAGGTTCT | 81550 |
rs532742095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468638 | TTATCCTCCTAGTAG[C/T]CTTTATAAGGGCTGT | 81550 |
rs532775394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453113 | AGAAACTATGCAATA[C/T]AAAAGTTTAACGATG | 81550 |
rs532776861 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432386 | ATTTTTACCTTACTA[A/G]TCTTGTTATTCATTA | 81550 |
rs532780485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450391 | AGAATATGCACTACA[A/G]AGACAGGCTTTGGCA | 81550 |
rs532793166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409031 | CTTGGTGCCCTGTGT[C/T]CCAGCCACTCCAGCC | 81550 |
rs532836382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416128 | TGATTTTAGATTTAA[C/T]ATGGTACAATATCAA | 81550 |
rs532871772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465353 | GTCTGGAATTGGGAA[A/C]GCTTCTTCACTATTG | 81550 |
rs532886848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459790 | CATACCCAGCTAATT[G/T]TTGTATTTTTAGTAG | 81550 |
rs532897158 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477300 | GTTCAATACAACCTT[G/T]AACTCCTGGGTTCAA | 81550 |
rs532903307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560366 | TTGTAAACTCATGTG[G/T]TTTCAAATGGAAGAG | 81550 |
rs532909270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565911 | TGCTTTGCTAAATTA[C/T]AGATATAATATCTGA | 81550 |
rs532927778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407074 | CTAAATAAATTAAGC[C/G]AGTATTTTATAATGA | 81550 |
rs532964056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512368 | ACACAGCCAAACCAT[A/G]TCGTTCCACCCCCAG | 81550 |
rs532986166 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565213 | GGCGCCCGCCACCGC[A/G]CCCGGCTAATTTTTT | 81550 |
rs533000567 | in-del | -/G | 0.0162398 | 0.0886349 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500587 | GGTAATCTTCCCAGT[-/G]GGCAGAACTTCAAGC | 81550 |
rs533002302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504519 | AGACCACATATTTGC[A/G]TTTTGATGACACTTG | 81550 |
rs533018151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456002 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 81550 |
rs533021100 | in-del | -/AGGG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419647 | GGGGGCGGGGGGCAA[-/AGGG]AGGGAGAACATTAGG | 81550 |
rs533029078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473874 | TGGCCTAGCGGTAGC[A/G]TCAGTACCTGGGGAA | 81550 |
rs533036392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497362 | TGTCCCTCCCCCTGT[G/T]CTCTCAGGTGATAGA | 81550 |
rs533052547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551701 | ACATAAAGATACTAC[C/T]TGAGACTGCGTAATT | 81550 |
rs533094421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466290 | CTTTGTAACAAAAAA[A/G]CAGTATTTTTTCTGT | 81550 |
rs533104801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60439992 | AAAAAGGAAAAAATG[A/G]AATTAACATCCCTTT | 81550 |
rs533140701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440910 | AAAACATAAATAAAT[A/G]TATAAATCTAACGTT | 81550 |
rs533157859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432857 | CAAGAATTCATTTAT[C/T]AAACTCCCATTTTGG | 81550 |
rs533160526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544003 | ACCTTATAACCTACA[G/T]GAAGTTTATATGTCC | 81550 |
rs533186834 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489600 | TAATAATGGTACCTA[A/C]TTCATATGTGAGAAT | 81550 |
rs533187772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541946 | TGGTCAGGCTGGTCT[C/T]GAACTCCCGACCTCA | 81550 |
rs533198350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544843 | ATAAATAATCAATAG[A/G]TGTATACTATAAGTA | 81550 |
rs533214802 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508013 | AATCATGAGTGAACT[G/T]CCATTCACAATTGCT | 81550 |
rs533228893 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530996 | TTGCCTGATGATAGA[A/G]TAAGGAGGAGTACAG | 81550 |
rs533240329 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556744 | AGGTTATGCAGAATG[G/T]TAACTACGAAAATGT | 81550 |
rs533269444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552031 | CAAACCATATCTTTC[C/G]ACCCTGGCTTCTCCC | 81550 |
rs533281035 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510936 | CTGAAAACATAATGG[C/G]AGCTTATTTTGCCCC | 81550 |
rs533295750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447987 | GCTCAGTACAATGCA[C/G]TGGAGCTTCTCCAAG | 81550 |
rs533322329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524908 | TTGAGACCAGTCTGG[C/T]CAACCCCGTCTCTAC | 81550 |
rs533328924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423471 | TGAATGCTATACCTC[A/G]ATAAGAGAAAATACT | 81550 |
rs533357922 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422378 | TTGTAAAACAGCCCA[A/G]TGTCACAAAAATGAA | 81550 |
rs533368463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438846 | GCAATGGTGATGGTA[C/T]CATTAGCCATTTGGT | 81550 |
rs533395072 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496726 | ATGAAAGAAAATGAT[C/G]AACTCAGGCATCCTA | 81550 |
rs533400178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415473 | ATTGGTAATAAGCAA[A/G]CATACTCATTTAACA | 81550 |
rs533404265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517499 | TGTTTGGAAACCAGG[G/T]ATAAATGGTTGCTAT | 81550 |
rs533465719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533188 | GCTAACATTCAGACC[G/T]GGAAAGGAAACACCG | 81550 |
rs533467907 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457618 | TAGTAGTTATCTGAG[A/G]CTGCTGTAACAAATT | 81550 |
rs533488660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503868 | TTAATGTTAACCCCA[A/G]TTGGTTTAAATGAAA | 81550 |
rs533494965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400792 | GCATAGCTTAACTCT[C/T]TCTCTGTGCATATGA | 81550 |
rs533531636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411286 | AGAGTGCAGTGTAGT[A/G]GTATATACTTTTACA | 81550 |
rs533547218 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572752 | ATAGGTACTGTAAAC[-/T]TTATTTTCAAAGTCC | 81550 |
rs533613545 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60545983 | TTTATTCATCTTATG[C/T]GTGTCATGTGGCTTT | 81550 |
rs533628823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568992 | CTTCTTTTTTGAGAC[A/G]GAGTCTGGCTCTGTC | 81550 |
rs533643408 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430945 | AAATACTTTTTGTAA[C/G]TATTCTACAGCAAAA | 81550 |
rs533650937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477257 | TCTTGCTCTGTCACA[C/T]AGGCTGAAGCACAAT | 81550 |
rs533656836 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458794 | TAGCTACATGTGGCT[A/G]GAGGATTGTATTGGA | 81550 |
rs533701383 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518059 | CCTGCATTCTGACAG[A/C]ATGATAGCTTTTGTC | 81550 |
rs533702980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446011 | CTTTGAATGTAGCTA[A/G]CAAGAAGAAAAATAA | 81550 |
rs533730587 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501685 | GACTTCCCCAAACCA[A/T]CCACAAAATGCTTAA | 81550 |
rs533792281 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412269 | TTTTTCATTCAGTGA[C/T]ATTGTTCAGCTTACG | 81550 |
rs533806346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563105 | TGATGGCTGGTACCT[A/G]TAATCCCAGTTGCTC | 81550 |
rs533854614 | in-del | -/CTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401735 | ATAAACAAAGGTCTC[-/CTT]CTTACCTCTTGAATT | 81550 |
rs533863166 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570170 | AAACTATCCATCTGA[C/G]AAGCGCTTAATAACC | 81550 |
rs533900547 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446597 | TTAATAATTGTCTTC[A/G]CCAGTATTAATGAAG | 81550 |
rs533909443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569777 | AGCTCTATATTTACA[A/G]CCAACTCATTCTTGA | 81550 |
rs533919460 | in-del | -/G | 0.00716266 | 0.059414 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395153 | GCTTTGATCTCTTAA[-/G]GCAGTGATTTTTTTT | 81550 |
rs533924812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506718 | GCTGAGATTGCACTA[C/T]GGCACTCCAGCCTGG | 81550 |
rs533926741 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553431 | CCCAGTTCCAAAGTC[A/G]CTTCCACATTTTCAG | 81550 |
rs533974547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467030 | AGGATGTGCAGATTT[A/G]TTACATAGGTGATAT | 81550 |
rs533984403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500166 | GGTTTTGGTGGAAAC[C/T]GAACATTTGACTATG | 81550 |
rs533991673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568798 | ATTGGAAAGGAAGAG[C/T]CAAATTATTCTTGTT | 81550 |
rs534003718 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60550707 | TTAAGAGCTAGTTTC[A/G]CATTTTGTGTTAGGT | 81550 |
rs534004887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541796 | GCAATGGCACAATCT[C/T]GGCTCACCACAACCT | 81550 |
rs534013682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460137 | CTCATTACCTTCTGA[A/T]AATGAATTCAGAATT | 81550 |
rs534024102 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545508 | CAGTATGATTCAAAC[-/TG]TAAAATTTAGGGACA | 81550 |
rs534037369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502217 | GGATAATTGTCCAGA[A/G]CTAGGATATTGATCC | 81550 |
rs534067091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403731 | TGTACCATAGCACTG[C/G]AACTCCAATAGGATT | 81550 |
rs534070793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460928 | GAATAGCTTGAACCT[A/G]GTAGGCGGAGGTTGC | 81550 |
rs534072622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452654 | TCCTGTTTATTGGTG[A/G]TTAATATTCCATTGT | 81550 |
rs534099379 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540490 | TGACACAGAAGGACA[C/G]AGCATTTATTCATAA | 81550 |
rs534128205 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455332 | ATCTTTCAGGCTTTT[A/T]AAGCAGCTATAGGCA | 81550 |
rs534151645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60442480 | TAAAAGTTTTCCTGT[A/G]TTATTATTTTTTGTT | 81550 |
rs534162476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530049 | ACCTCCTAGAAGAAA[C/T]CTTCTTTGACCTGCC | 81550 |
rs534166105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492074 | TTAGGTTGTGATGGT[C/T]CTAGATATTTATATG | 81550 |
rs534226482 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495122 | AATGACTTTGGTTGA[-/T]TTTTTGTCTTTAGGG | 81550 |
rs534232747 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395240 | TTTGAGACCATGTGA[A/G]GATCCTGTACTCCTA | 81550 |
rs534259901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401601 | TAGCATTTCCATTTT[G/T]TTCTGAAAGAACATG | 81550 |
rs534278087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433205 | ATTTGAATGGGCATT[C/T]ATTATTTCAATGGGT | 81550 |
rs534297453 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485147 | TGGAACACATTTCTT[C/T]GAGATCTTCCCATTT | 81550 |
rs534352031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536391 | TTTAATTGCTCTTTG[C/T]CTAAAAACTCCAAAT | 81550 |
rs534396606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419335 | AATGTGACTATTAGC[C/T]CTTCATAAAGTATCT | 81550 |
rs534396707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427808 | AGCTAAGGGATGGAT[A/G]GCCTTTCAAAATAAT | 81550 |
rs534400169 | snp | A/G | 1.66263e-05 | 0.00288321 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529142 | AAAAATACTAGAATC[A/G]TCTATTCCTATGGAG | 81550 |
rs534401402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451175 | AAGAGTTTTGGTGGT[A/G]GAGAAGAAGAAAATG | 81550 |
rs534414720 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60408326 | ATAGTAAATTAGTAC[C/T]AGTAGAGTGGGGCAT | 81550 |
rs534438175 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405550 | GAGTGGTAACTGACT[A/C]AGTGAGGGGAGCACA | 81550 |
rs534487559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468061 | CTTTCTCCATCTTCT[A/G]ATTTATTTTATGTAC | 81550 |
rs534497953 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500463 | AGAGGAAGAGAAGAC[C/T]GGGGCCTGGTTCACA | 81550 |
rs534506757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546769 | CCTAAGTTTAAGGGA[A/G]AAGTTATTTTTAAAA | 81550 |
rs534515262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418367 | GTAGGTACCCTTCTT[C/G]TGAGGTCCTTTAACA | 81550 |
rs534531999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567992 | TCCACCTGCCTTGGC[A/C]TCCCAAAGTGCTGGG | 81550 |
rs534549120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473850 | AGGTGCCGATTACCT[A/G]GTGGACCTTGGCCTA | 81550 |
rs534580225 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526333 | TAAAGTGCTAGTGTG[A/G]GCTATGTAATACATA | 81550 |
rs534603845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535331 | ATATGCAAGTGGAAT[C/T]ATATTTTGAATTTAC | 81550 |
rs534620134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475447 | TATTTATGGCTGTGT[A/G]GTATTCTATCATGTA | 81550 |
rs534628887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528075 | TTAGGAAATGATTTA[C/T]CAGAATAGCATATGT | 81550 |
rs534635260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567441 | TTAAGAGAGATATTA[C/T]TAAAATAGGGACCAT | 81550 |
rs534635819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482811 | TCAGGAACTCTGGAA[C/T]ATGCTTGAAAGTGCA | 81550 |
rs534643361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527158 | TTGAGTCTTGATCTT[A/T]AATCAGTGACCTGTT | 81550 |
rs534654941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517809 | CCAGAGCCACTTAGT[A/G]TCTAGTCAACAAAAA | 81550 |
rs534680513 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474090 | TGTTCCACCCTGTAC[A/T]CCTGGCTCCACCTTT | 81550 |
rs534716149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511055 | TGTTGGAAATTTATT[A/T]TAATCTTATATAACT | 81550 |
rs534719053 | in-del | -/TT | 0.477345 | 0.103991 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567891 | ACCATGCCCAGCTGA[-/TT]TTTTTTTTTTTTTTT | 81550 |
rs534731502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489870 | TTTTAAAATGATTAT[A/G]GAAAGATGTTCTTTT | 81550 |
rs534732422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565494 | TGGTTAGTTCAGTTC[A/G]TGAATTCTTTAAACA | 81550 |
rs534737369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518533 | TTTAAAAAAAAACTG[A/G]TGAGTGAAAAACACC | 81550 |
rs534751305 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441534 | CCTATACCAGACAAA[C/T]CATCTATTTTTCCAA | 81550 |
rs534765532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512735 | CACATCTAGGTTATA[C/T]GGATGAAAGAGGAGA | 81550 |
rs534765582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520538 | TCCCTCTACATTGCT[C/G]TACTCCCCACTCCTC | 81550 |
rs534803615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472678 | GGCTATAAACCCAAA[A/T]GAATGGAAAACAGGT | 81550 |
rs534808014 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525376 | ACAGGGTTTCACCAT[G/T]TTGGCCAGGCTGGTC | 81550 |
rs534811543 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444180 | TAAAGGTTACTATAA[C/T]TTCTTTGGTATTCCA | 81550 |
rs534857819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513258 | AAGTCCCTAGGCTGC[A/G]CATAGCATGGGGACC | 81550 |
rs534861497 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502221 | AATTGTCCAGAACTA[A/G]GATATTGATCCAGAT | 81550 |
rs534913514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474676 | ATATACTTTACATTC[A/G]TTACGAAGGTCACAA | 81550 |
rs534934180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519728 | TCCCCCAGCTCTACC[C/T]TGTGCTAGTTGTGTG | 81550 |
rs534952227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417519 | GCTAATTTTTGTATG[G/T]TTAGTAGAGATGGAG | 81550 |
rs534954892 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505123 | AAGGGGGCTGAAGCC[A/G]GGGCGCCAAGTAGTC | 81550 |
rs534955729 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559985 | AGTGTATACATATAT[A/C]AAAACATTAAGTTGT | 81550 |
rs534957654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512005 | CTCCTGTCCCCTTAC[A/G]TTTGCTTTTGACTCC | 81550 |
rs534959546 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399244 | GCCTCTGCAGAAGCT[G/T]AGGTAGAGTCCCACC | 81550 |
rs534959825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407473 | TCTCCTCAGAAATGC[A/G]GGAAATAGCCTGTTA | 81550 |
rs534969315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558236 | TTTTAGCATTAAAAG[A/C]ATTCTGGCATTATGA | 81550 |
rs534979496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504195 | AAAATTTACATTTTC[A/C]TGCTTTCTGATAATC | 81550 |
rs535089738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502684 | TAAACCAGGAGCTCC[C/T]GGTCCTGTTAGAAAG | 81550 |
rs535128144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494725 | GGATTACAATTAAAT[A/C]ATTAAAAATTTGGAT | 81550 |
rs535128661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473475 | GTGGGCGGCAAGCCA[C/T]CCAGGTGCCAAGGCA | 81550 |
rs535136431 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60535454 | TATAATGTTTTGTTG[C/T]ATTATGCTTTGGAAA | 81550 |
rs535151283 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423767 | ACAGTGACACTTTAT[A/G]TCATAATTTATGTGG | 81550 |
rs535160345 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506211 | CTACAAGCCAGAAGA[A/G]TGGTGGCCACTATTC | 81550 |
rs535170652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463697 | TCCAATTAAAAATTG[A/G]TAAAAGACCTGAATA | 81550 |
rs535173386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509467 | TAAGTAGTTTTCTCC[C/T]CACTGTCTATATTAT | 81550 |
rs535204835 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456386 | GGAATGATGCCTGGA[C/T]TAATGGCCTGAGAGA | 81550 |
rs535279226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497624 | TGTGAGTGGCTGACA[C/T]GAAATGAAAGGTGCA | 81550 |
rs535283168 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532628 | ATTAGTATACATATT[G/T]CTTAAAAAATTTCCT | 81550 |
rs535287701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566222 | AGTCACAAAGCTTTC[A/C]CAAGCTTCAGTATTC | 81550 |
rs535301163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488342 | GAAAGGCCTGAGTGT[C/G]ATTTCCTGAGGAAAG | 81550 |
rs535311717 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423042 | GATAATAAAATCCTT[A/C]GGACCGACATGAAAC | 81550 |
rs535323096 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417964 | CTTCAGGCCTTTATT[C/T]TTGAGAGTAGCCTCC | 81550 |
rs535378678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559344 | TGCCAGTGCTGTGAT[A/G]TAGTATCTCTTAAGG | 81550 |
rs535383598 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458446 | AACTCCCAAAATTCC[A/G]TGAAGATGCCTAGTG | 81550 |
rs535383978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487728 | GTGACTAGTGCTGCA[A/G]TAAATATGGGAGATA | 81550 |
rs535416319 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427997 | AATCAAAATGTCTTT[G/T]GAGCTGTTCTCCCTG | 81550 |
rs535416656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436214 | TCTGTGGGTTGTCTG[C/T]TTACTCTGCTGATGA | 81550 |
rs535416907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510000 | CAGAGGCTGTTATTT[C/T]TGTGAGGGCTGTAAT | 81550 |
rs535419575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549016 | GTAAATTGTCATTCA[A/T]CTGCTGGATGAACTA | 81550 |
rs535427086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397755 | CCTGCAGCGCCGTCC[G/T]CGCGGCTTCTCCGGG | 81550 |
rs535439009 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536601 | TTGAGTCCTGGTTTG[C/G]TATTTATTATGTTCC | 81550 |
rs535474569 | in-del | -/TTG | 0.0264148 | 0.111847 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561863 | ATGGGCCCAGGTTTT[-/TTG]TTGTTGTTGTTGTTG | 81550 |
rs535476050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428672 | ATGGGCTTGGAGAAC[A/G]TACGTCTTGAGACAT | 81550 |
rs535480563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503421 | TTACAATAACTTGAC[A/C]ACCTTAATTATGATT | 81550 |
rs535494432 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60408299 | TTATCAGCAGCATGA[A/G]AAAGAACTAATATAG | 81550 |
rs535508542 | in-del | -/AC | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542444 | GCATCCTTGTTGAAT[-/AC]ACACACACACACCTG | 81550 |
rs535513094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404680 | CATGATCTTGGCTCA[C/T]TGTAACCTCCACCTC | 81550 |
rs535520660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547022 | TAGAACTTAATAAAA[C/T]GTCTAGATTGAAAAA | 81550 |
rs535520695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554747 | AGCTTCATCCTTGAA[C/T]GAGAAGAATATAACA | 81550 |
rs535532054 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60456952 | CCACCCACCTCCATC[C/T]TCCAAAGTGCTGAGA | 81550 |
rs535554890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547869 | CTCACCTTTCTTCTT[C/T]AATATTCCCAGAATT | 81550 |
rs535560828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444875 | AGGTGAACAGGTCAC[A/G]AAGTCATTGTTATGG | 81550 |
rs535582834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556135 | ACAGGCGTGAGCCAC[C/T]GCACCCGGCCCAACC | 81550 |
rs535604461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439006 | GAGACGAATTTTTTT[C/T]CTTCAGATTCAGTAA | 81550 |
rs535663709 | in-del | -/TTC | 0.00209302 | 0.0322821 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485780 | TACTAAGTTGACTTA[-/TTC]TTACTTGTTTTACTA | 81550 |
rs535671354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533353 | CTCTTAAGAGATACT[A/G]TTATTGGCTGGGCGC | 81550 |
rs535680027 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425250 | AAATGTCTAAGAGGT[G/T]TATGAAAAGGTGCTC | 81550 |
rs535683495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571429 | CCAGCCATTTGACTT[C/T]CAGCAAATATAAGCA | 81550 |
rs535711997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550007 | GGCATTGAATAGTAT[A/G]CCTGCATCATGAACA | 81550 |
rs535722575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448278 | TTTACAGCTCTCATT[C/G]TAAGACGCATCAGAG | 81550 |
rs535753400 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421263 | AATCTTGGCAGAAGA[C/T]GAAGGAGGAGCAAAG | 81550 |
rs535763908 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553358 | GGAAGTTCCAAACTT[G/T]CCCACATCTTCCTGT | 81550 |
rs535767538 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455266 | ACTAAGAGATGTTTT[A/G]ACAGAGAAAGTAGGT | 81550 |
rs535792611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438155 | ACTTTTCACATAAGC[A/G]GGGCATAATATTTAT | 81550 |
rs535831825 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60540744 | TTCTAATATCTGATA[A/G]TAACATATTATAATC | 81550 |
rs535853245 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410585 | CTCTACTCCTAGGAA[C/T]TGGCCACGATCTTTT | 81550 |
rs535856782 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466982 | GTGTGTGTTTTTTTG[-/T]TTTTTTTGTTTTAAG | 81550 |
rs535870231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419261 | TCTGGTGTGAAATGG[C/T]ATCTCATTGTGGTTT | 81550 |
rs535884916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522081 | CATTTTTAATATAGA[A/G]AAAAATTAAAGGATG | 81550 |
rs535911823 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493127 | GTTTCACCGTGTTAG[C/T]CAAGATGGTCTCGAT | 81550 |
rs535913639 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501578 | CATCTAAGACATGCT[G/T]AAACTTTCCTACTTG | 81550 |
rs535939853 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396251 | GATGGGGACGCTGCC[C/T]CTTAGAAGCCTTTTT | 81550 |
rs535967600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485692 | TTGTGTAGGCTTTTA[A/G]CTATTGTAAAAGATA | 81550 |
rs535982135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476411 | CCGTGAGTCTGTTTT[C/T]GTACCCAGTACTCAT | 81550 |
rs536005429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523685 | AGGTTCAAGCAATTC[A/G]CCTACCTCAGCCTCC | 81550 |
rs536022710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403028 | CTGTCTCAAAATATG[C/T]TACATATTGCTTTAC | 81550 |
rs536028031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454575 | TTCTGCCTTGAGCTA[A/G]TGGGGGTGCTACTTG | 81550 |
rs536046040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507680 | AATCTCTGGGACACA[C/T]TTAAAGCAATTTGTA | 81550 |
rs536047204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421787 | TGTCCCACTTGTGGG[A/G]CTTTGGTGATCCAAG | 81550 |
rs536054075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413349 | GCTTGAGAAGCTGTA[C/T]GGCTGGTGTTTACGA | 81550 |
rs536091524 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60521842 | GTGGAGGTTGCGGTG[A/G]GCCGAGATCGCACCA | 81550 |
rs536096493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516142 | TTCTAATACAGTTGC[A/G]TAATCAAACCTTTCT | 81550 |
rs536108665 | snp | A/G | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569687 | TTATACTACAAAGCC[A/G]TAGTAAACAAAATAG | 81550 |
rs536160833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531717 | ATCTGCTTATATTCT[C/T]TCTGCCAGTAGAAAA | 81550 |
rs536163001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479110 | CCACACCCAGCCAAT[C/T]TGAGAACCTTCTAAC | 81550 |
rs536172351 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522944 | GTTTTAGCTTCAGTT[A/G]GATTTCAGTTTAATT | 81550 |
rs536183011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60570590 | AGGAAATCAGGGTAT[C/T]TTATTTCTTTTTAAT | 81550 |
rs536183509 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565787 | ATTTGTCTTAAAATA[C/G]CTACTTTTCACATTT | 81550 |
rs536192900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60562074 | CCAGCACTTTGAGAG[G/T]CCAAGGTGTGTGGAT | 81550 |
rs536206655 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433023 | AGTCACTGTCCAGAT[A/G]TCTTCTTATTTTTTT | 81550 |
rs536259013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569018 | CTGTCACTCAGGCTG[G/T]AGTGCAGTGGCACCA | 81550 |
rs536283959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513682 | TGATAGTGTAAGTCT[C/T]ATGAGATCTGATGGC | 81550 |
rs536284280 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468906 | GTGACACCCTCAAAT[A/C]TTGCCTGTTTTGTAA | 81550 |
rs536307052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475694 | TCCTTTCTTGGCAAC[C/T]TTGCCAGCATTGGTT | 81550 |
rs536440551 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545803 | AAGGAGACATATCAA[A/G]GGGTTGAGAGTATTG | 81550 |
rs536444689 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433031 | CCAGATATCTTCTTA[-/T]TTTTTTTTGACATAG | 81550 |
rs536456540 | in-del | -/CAGA | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446728 | GTAACTATCTTAAAC[-/CAGA]CAGAGTACATATTCA | 81550 |
rs536462758 | in-del | -/AG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465309 | TGTACAATGACTGTC[-/AG]AGTTATGAAAATCTG | 81550 |
rs536497781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561524 | CCCACTTTAACCTAG[A/G]CCCATATATTTTATA | 81550 |
rs536543491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461256 | GGCTAATAAATTTTC[C/G]TAGGAAATGATTGAA | 81550 |
rs536544420 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400428 | ACGGGGTACCTAATC[A/G]GTTGTGTTTTTGTTT | 81550 |
rs536553703 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461772 | ATAAACTGAGAGGTC[G/T]AAGAGTCTCAAAAAT | 81550 |
rs536605146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431870 | AGATTAACACTACAT[G/T]CTGGTACTTAGAAGT | 81550 |
rs536615986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491537 | GTAACAGGATAAAAA[C/G]AGACAATGCAGAAAA | 81550 |
rs536620223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488603 | ATTTTTGACAGAGTC[C/T]TGCTCTGTTGCCCAG | 81550 |
rs536620913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451457 | CGTGAAGTTCATTGT[C/T]GGCATCTTTTTCCAA | 81550 |
rs536625487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560503 | CACTGAATTTTCACA[A/G]GTGCTTAACCTGCCA | 81550 |
rs536703777 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567308 | TGATGTTTTTCTATT[A/T]CCAAGGATCAAAAGA | 81550 |
rs536774590 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466779 | GAGGAGCTTGGGTGA[C/T]GGAGGCTCTGTCTTT | 81550 |
rs536782984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559928 | GAAAGAAAATGGAAA[C/G]TGAGGTGATGGATAT | 81550 |
rs536796365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518816 | ACCTGATTTTTCAGA[A/G]CTAGTCTCTGTAAAA | 81550 |
rs536799261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450468 | GTGACCACTGGTAAA[A/G]TACTTTATCCTCTGT | 81550 |
rs536803099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433850 | CATTATAGCCAGTGA[A/G]TAAGTTAGATTCACC | 81550 |
rs536850117 | in-del | -/TAACTGAAGA | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530842 | TGGTGTAAGTAAAGG[-/TAACTGAAGA]TTTCAAGGAATTGAA | 81550 |
rs536852727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425161 | AGTCATCTTTGAAAC[A/G]GAATACATTAAAAAT | 81550 |
rs536874511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426115 | AGAAGGAGATCCTGC[C/T]GTTTCTCACCCATGA | 81550 |
rs536898139 | in-del | -/CAGCAG | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516737 | GCTTGGCATCAGCAA[-/CAGCAG]CAGCAGCAGATGCAA | 81550 |
rs536914286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552850 | CACAGCCCAAGTTGC[A/G]TCTTGGCCCCTTTTA | 81550 |
rs536936343 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60437406 | GCTGGGGTTAGAGGC[G/T]TGAGCCACTGTGCCC | 81550 |
rs536958244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545151 | GAGAAGTAGAAGGTA[C/T]GTTTTCTTCCCTTCA | 81550 |
rs536959481 | snp | C/G/T | 0.000197923 | 0.00994609 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535134 | AGAAGTTGAAGCCCT[C/G/T]CATTCTTCGGGTATG | 81550 |
rs536966109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474174 | AAGAAATAATGGCGT[A/G]AGCTGTCCTCTCTCT | 81550 |
rs537022550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497525 | ATTCTTAGTCGGCCT[A/G]GGAAATCCAGCTAGT | 81550 |
rs537028906 | in-del | -/AA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526772 | ATTTTAAAAGTATTT[-/AA]AAAGCCTTTTGGCTT | 81550 |
rs537050871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414748 | GTTATCAGGTGTTTT[A/G]AAATGGTCTACTAAT | 81550 |
rs537055776 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561953 | AGGATAATTGGTAAA[A/G]TTCAGTATTGATAAT | 81550 |
rs537066524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572342 | ATAAGAGTTTGAATT[C/T]GTTGTGTTTGATGCT | 81550 |
rs537072236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432519 | TGTCTCTGACTAGGT[A/T]TAGTATAGTAAGAGT | 81550 |
rs537088416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488903 | TTTTTTGTTTTGTTT[A/G]GTTTTGTTTTGCTTT | 81550 |
rs537092330 | in-del | -/ATT | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529700 | TATAATAATTTTAAA[-/ATT]ATTAAACCATTGCTT | 81550 |
rs537151173 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418600 | TTTTAAATTGCAGCA[C/G]AATTAATGTACATTA | 81550 |
rs537163528 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532573 | AGATACCATAATCTT[A/C]TTAATTGCATTGTAA | 81550 |
rs537227768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398485 | TTTTGCAGAACCTAC[A/T]CAAGATCTATATGGT | 81550 |
rs537228512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557990 | ACCACGCCCAGCTAA[C/T]TTTTGTATTTTAAGC | 81550 |
rs537232880 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60535601 | GTCAAATTCAAATCT[C/G]TGTTGGATGTGCAAT | 81550 |
rs537238436 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416619 | TTTGCATTAGTCTTA[A/C]TTATAGCTACTGTTT | 81550 |
rs537252382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417353 | TTAAACTAATTTCAT[A/T]TTTTTTTTTTTTTTT | 81550 |
rs537252446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407696 | ATGTTCTGTTTCAAG[G/T]TAATATTAGTAGAAA | 81550 |
rs537296531 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508656 | TGTAAGACCTAAAAC[C/T]ATAAAAATCCTAGAA | 81550 |
rs537302958 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502602 | CTTTTAAAGCTGAGC[C/T]CAGCCATGGGTTTGT | 81550 |
rs537312840 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533536 | ATCCCAGCTACTCGG[A/G]AGCCTGAGGCAGGAG | 81550 |
rs537314764 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415604 | CTTAAAGAATATGAG[A/G]ATTTTGAAGAGTACA | 81550 |
rs537347503 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456896 | AGATGGGGTCTCCCT[A/G]TGTTGCCCAGGCTGG | 81550 |
rs537358820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526322 | GATAATGTATATAAA[A/G]TGCTAGTGTGGGCTA | 81550 |
rs537369895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510214 | GTGACTGGTTCTATT[A/C]TTTCTAGAACTCTGC | 81550 |
rs537371801 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407958 | TGTGATAGTGAATAC[A/G]TCTCGTGAGATCTGA | 81550 |
rs537387795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424491 | AGACCAGCCTGGCCA[A/G]CATGGCAAAACCCCT | 81550 |
rs537430663 | in-del | -/AAGGGATC | 0.00478085 | 0.0486577 | intron-variant, frameshift-variant | TDRD3 | GRCh38.p7 | 13:60547294 | AAAGGATTTGGTGAA[-/AAGGGATC]AAGGGATCTCTGAGG | 81550 |
rs537450305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509445 | TTTTACCATGAAAAA[A/T]TTTCATTAAGTAGTT | 81550 |
rs537450444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501776 | GTACTTACTATACAA[C/G]ATCCTTTCTTATATA | 81550 |
rs537451161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422941 | ATGTAAATCCACACA[C/T]TGAAAGTATGTCAAG | 81550 |
rs537468284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472571 | AACTCCTGGTGGGAA[C/T]ATAAAATGGCATAGT | 81550 |
rs537497981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60570269 | TGAATAGGCATTTCT[C/T]AATAGAAGACATACA | 81550 |
rs537499188 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479522 | AGGTCCAATTGATTG[A/G]GTGTTGAGTTTCAGT | 81550 |
rs537502655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487617 | GGAGTCCTAGAACCA[A/G]TCCCTCACGGATACC | 81550 |
rs537506107 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482752 | TTGTGCTTGACTGTC[A/G]TTACTCTTAATTATC | 81550 |
rs537536108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470428 | ATTGTATTTTTAATT[C/T]TTTGAAGAATTGCCA | 81550 |
rs537546954 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462713 | AAGTGAGATTAAAGG[A/T]ACCTTTGGGTGCCAA | 81550 |
rs537550067 | in-del | -/TAAGTCCTTT | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566767 | GTATTTTGTTGCTTC[-/TAAGTCCTTT]TAAGTCCTTTTCAAA | 81550 |
rs537560452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479978 | TATTCCTTTTAAGTG[C/T]GTCATTTAACCAGTT | 81550 |
rs537619886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494628 | TTTCTTAAAATGATT[A/C]TTTTATTCTTTCTTA | 81550 |
rs537636434 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567792 | GCAGTGGCGTGATCT[C/T]GGCTCACTGTAACTT | 81550 |
rs537641661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504121 | AAATCTTTTTATAAT[G/T]TGCTTAATTACCTCT | 81550 |
rs537667214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429548 | GCATTAGAAATTCTG[C/T]TCCAGGCAGAAACAG | 81550 |
rs537676652 | snp | C/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531819 | TCCTTTAAAAAGTTA[C/T]GAGCCATAGTTAAAA | 81550 |
rs537693234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399059 | TTTAGGTCCCGAACA[C/T]GTGTTGACTTTGTTT | 81550 |
rs537708804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60573424 | TTATTTTCAAAAAAA[A/T]TTTGCTTTTTTCTTT | 81550 |
rs537712205 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502372 | ACTGGAATTTAATGA[C/T]AAATGTATAAGCTTT | 81550 |
rs537719657 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463743 | AAGACATACACATGG[C/T]CAACAGGCATATGAA | 81550 |
rs537721364 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564268 | TGTGCCCAAGGTGGT[C/T]GGGATGCACCTTGGT | 81550 |
rs537754884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548957 | AGGATTATCATGGTA[A/G]TGAAAAACCAGAAGC | 81550 |
rs537802388 | in-del | -/AAAT | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484208 | TAGAGGGGGAGAGAA[-/AAAT]AAAGCCACACAGAGT | 81550 |
rs537809147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516044 | ATCATTTATTTGGGT[C/G]TGTTATAGACTCAAA | 81550 |
rs537811121 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463475 | TTTTGGATAAGACCT[C/G]AAAAACATAGGCAAC | 81550 |
rs537822020 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563808 | AATTTATGATGAACT[G/T]TTATAACACGGCTCA | 81550 |
rs537836414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546905 | TGGTTTTGGTGTAAC[A/G]TCTTCAACATGTCGC | 81550 |
rs537895181 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453425 | GAGTAATTGTTTTTC[C/T]ACTGAATTAGTACCA | 81550 |
rs537906266 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395401 | AAAAGATTTTGTCCT[C/T]CTTCATTTTTGGTGG | 81550 |
rs537970473 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60485267 | TTAGGCAGTGATGCC[-/T]TTTTTTTTACTTTAT | 81550 |
rs537982410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563256 | AAAAAAAGGCAAGGC[A/G]ATTCATTAAGTAAAA | 81550 |
rs537988705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571326 | GCTCTTGTTACATAA[C/T]GGAATATATTCTTGA | 81550 |
rs537998724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443389 | AGCATAAGTCTAAAG[C/T]ATTGTTACACATGAG | 81550 |
rs537998778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454382 | TCCTTAGGGGCTTAA[A/C]ATTTTTTTTAATAAT | 81550 |
rs538000187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437104 | TAGTATCAGCATTAA[C/T]TGTTTGATAAATTAA | 81550 |
rs538001460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553993 | TCCTTTAAGATAACA[A/G]TATTGGTTGCAAAGT | 81550 |
rs538004235 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399017 | TCCAACATGACCCCC[A/C]CTCCTTTGGAAAGAT | 81550 |
rs538035915 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549828 | TTGAATGAGAAAAAA[A/T]TTTTTTAGTGCTCAT | 81550 |
rs538060675 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546384 | AGATGGGAAATTAAA[A/G/T]TATGTAATTCATTTA | 81550 |
rs538073037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541452 | GATTATGGGTGTGAG[C/T]CACCTTGCCCAGTCC | 81550 |
rs538074503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478158 | TTTTCTAGTCTGTGT[A/G]CATAGAGATGTTCAT | 81550 |
rs538083292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60495704 | TCCTGACCTCAGATG[A/G]TCCACCCGCTTCTTC | 81550 |
rs538089733 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433977 | AACAATGAGTTTAAA[A/G]CAATAGTGTTTGTTT | 81550 |
rs538092767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522823 | ATTTCTACATCTCAC[C/T]AGAAATGAACAGATA | 81550 |
rs538097667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397517 | GGAGGCTGTCGTCCG[C/T]CCCCGGCCTCTCCCC | 81550 |
rs538104395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556036 | TATTTTTAGTAGAGA[C/T]GGGCTTTCACCAAGT | 81550 |
rs538111247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485510 | TAAAATTATTTATTA[A/C]CCTAAAATGAAGGCT | 81550 |
rs538116993 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466475 | GACTAAACCTCATTT[-/C]TTTGTCATTGAGATA | 81550 |
rs538118189 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560667 | TTGTTTAGATTGTGC[-/T]TTTACTAAGAAGAGC | 81550 |
rs538124743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446262 | GAGTCTTGCTCTGTT[G/T]CCCAGGCTGGAGTGC | 81550 |
rs538138560 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513562 | AGTTGATATGGTTTG[A/G]CTGTGTCCCCACCCA | 81550 |
rs538160497 | in-del | -/TA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406819 | TATCTGAAAGTCTTT[-/TA]AAAAATTCCCCACAA | 81550 |
rs538218870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492351 | TAGTAAATACCATCT[A/G]TTATTGAGTGTTTGC | 81550 |
rs538246947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528280 | AGTAGTTTGATAATT[C/T]TGTATTAATAGAATA | 81550 |
rs538281360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517455 | AAACAGCATTACTAC[A/G]TATTGATGGAAATCT | 81550 |
rs538283662 | snp | A/G | 9.96777e-05 | 0.00705896 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528823 | ATAATAATCAAAAAC[A/G]TGGAAAAAGAGAAAG | 81550 |
rs538301226 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543693 | TAATAGAGATTAAAT[A/G]TATAAACAGCAATTT | 81550 |
rs538305993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500229 | TATCATGAACTGGGT[A/G]CTTTCTGACCTATCT | 81550 |
rs538307906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507578 | CTGAACAACCTTCTC[C/T]TGAATGACTACTGGG | 81550 |
rs538312416 | in-del | -/CTT | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446526 | GCCACTGTGCCTGGC[-/CTT]CTCACAGAATTATTC | 81550 |
rs538319784 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446935 | ACTTACTAACATTAT[A/G]TAAGTTATAGTTCTT | 81550 |
rs538337384 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469003 | TTTCTTAGTTGGGAA[A/G/T]TGCCTGTGTTTGGGA | 81550 |
rs538338632 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441291 | GCTGGGGTTTTTTTT[A/T]ATTTATATTCTTAGG | 81550 |
rs538373727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425318 | ACTATGATGTATCAC[C/T]TCACACCTATAAGGA | 81550 |
rs538380446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433830 | GCTCCGTTTCATTAT[C/G]TATACATTATAGCCA | 81550 |
rs538399992 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459104 | AATTTATAATAACAA[A/T]ATTACTCCTTTTTTA | 81550 |
rs538403081 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552971 | TCCCTCCCAGGCCTT[C/T]GGGCCTGTGATGGAA | 81550 |
rs538419497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461033 | AAATAAAAATAAATT[A/T]AAAAATAGTTAAGTA | 81550 |
rs538422650 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524374 | TAGCCGGGCGTGGTG[G/T]TCTGCACCTGTAATT | 81550 |
rs538427022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410520 | TCAGAATGGCAAGTA[A/C]TGGCAACCCTTTGTG | 81550 |
rs538433473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522414 | CCTGATGTGTCATCA[A/G]TTAAGTTTATTTGCT | 81550 |
rs538438664 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531000 | CTGATGATAGAATAA[A/G]GAGGAGTACAGAGTG | 81550 |
rs538446542 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411393 | TTATCTTGAAAGTTC[A/G]ACAGAGCCTTGACAT | 81550 |
rs538455434 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565436 | GAGTTACGTGAAAGA[A/T]ATCTCATGGTTGGTC | 81550 |
rs538511340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538860 | AAACCTGGGAAAACA[C/T]TGTTGGGTCCTCATT | 81550 |
rs538521688 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554242 | TTTTCCTCCTCACTT[C/T]AGAGCAGCTTTTAAA | 81550 |
rs538547961 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486053 | AACTAATTCAACAAA[C/T]GCTTAACCTTATTCT | 81550 |
rs538549075 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540031 | TGCCAATTAGTATTT[A/C]GTAAACAATACAAGC | 81550 |
rs538558690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468869 | GCAAAACTGATTACT[C/T]CTCGAGCTGAAATGT | 81550 |
rs538563203 | snp | A/C | | | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494550 | CCAAATCAGAGGGAA[A/C]ACATGAAGGTGTCTA | 81550 |
rs538579237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521483 | AAAAAAAAATGTAAT[A/C]CAGAAATGAATGAGA | 81550 |
rs538591331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568929 | ACATACAAAAATGCT[A/G]CTATTTCTATATGTC | 81550 |
rs538629096 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552115 | CCCAAAGTCTTAACT[C/T]GTTCCAGCATTAACT | 81550 |
rs538662146 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520653 | CTGCCTCTGCCCATT[A/G]TAACTAAGCTCCACA | 81550 |
rs538672392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474608 | GCGTATTGTAAGACC[A/C]ATACAATTATATGCT | 81550 |
rs538806400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401774 | TCCCCTTTGGGGTTA[C/T]CTCCATTTGATTATT | 81550 |
rs538866834 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525906 | TTTCCTATTAATATA[C/G]TTCTCCAGTATAGTT | 81550 |
rs538905299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499198 | AAAGACACAGGGGTG[A/G]TGATTCCCACCACAT | 81550 |
rs538925509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476382 | TTCTAGGTTCTTTAT[C/T]CTGTTCCATTGGTCC | 81550 |
rs538926053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460197 | TTTTTGAAGTTTTCT[C/T]TTTTAATACCAAAAC | 81550 |
rs538946538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513280 | ATGGGGACCCTGGGC[C/T]CAGCCCATGAAACCA | 81550 |
rs538949355 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458882 | ACAGAATTATGAGCT[A/G]TAATAACCATAACAT | 81550 |
rs539004667 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534312 | AGTGAGAACTTGTCT[C/G]TAGAAATAAATATAA | 81550 |
rs539009109 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458544 | ATTTTTTTGACTACT[A/G]AACATTAAATAAAAG | 81550 |
rs539041313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496144 | AGGCTCCCAGCCTAC[A/G]TCTTTATCCTGTGCT | 81550 |
rs539055674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567144 | ACATTTAGAAGCCCA[A/G]ATATTCAAGAAAATT | 81550 |
rs539104860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565362 | GCCCGGCCGTCAGTA[G/T]CTTTTTTACTTTTTT | 81550 |
rs539118697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557043 | AACCCCGTCTCTACT[A/G]AAAATACAAAAAATT | 81550 |
rs539128994 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530108 | ATCAGTGCCTTAATT[A/G]CTTTTTAAAATTTAT | 81550 |
rs539129130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503557 | TCGGAAATCCAATGT[C/G]ACTAAACATGCCAAA | 81550 |
rs539145201 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518599 | TATAGTATTTTGACT[G/T]TGTAAATACATGTAA | 81550 |
rs539147319 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60437923 | TAGAAGGTGCTTCAC[A/G]CTTACTCACTTCCAT | 81550 |
rs539173928 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441282 | TGACAATTTGCTGGG[G/T]TTTTTTTTTATTTAT | 81550 |
rs539178079 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405325 | TCTTAGTATAGTCAG[A/C]TATAGTCTTATAGAA | 81550 |
rs539193974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457511 | CCCTCATGTTCCCTA[C/G]CTAGGCTAGATCTCA | 81550 |
rs539203608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550149 | TGTTTCAAAGTTTAT[A/G]CCACTGCATGTTATA | 81550 |
rs539206489 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544439 | AAGCAAGACCATATC[G/T]CTTTAAAAAAAAAAA | 81550 |
rs539248253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437483 | TAGGAGTCATTTTTG[C/T]TTTTAACTTTGCATC | 81550 |
rs539250287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60442040 | ACCTTGTAAGCTGGC[C/T]TTTCTAAAGATAGCT | 81550 |
rs539264235 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490125 | GAATTTATGGAGGCT[G/T]AAAACTAACAAACAA | 81550 |
rs539301355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488365 | GAGGAAAGAACTCAG[A/G]TAAAGATAAATCAAA | 81550 |
rs539314957 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455802 | GCCAGGTATGGTTGC[C/T]CACGCCTGTAATCCC | 81550 |
rs539318631 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443329 | TACAACGTGAGGTAC[A/G]GTTTATATTTCTTTT | 81550 |
rs539340460 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411530 | TGCTTAAAAAAAATG[C/T]CCTGCCTTAATTAGG | 81550 |
rs539364406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480810 | ATTATAGCCAGCATG[A/G]TGGGGAGTGCTGCAA | 81550 |
rs539365795 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474371 | CCTTGGTGGTAGTGG[-/C]CCCCCCCCGGGCCCA | 81550 |
rs539374311 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447611 | AATAAATAAGGTAAG[A/G]CAAATTGGTAAATCA | 81550 |
rs539379399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451395 | ATCTCTGGTACAAGA[A/C]ATAGTGTTAGATGCT | 81550 |
rs539400185 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504085 | TTTGCAAGATTAATT[G/T]TAAAAATTTTAGAAT | 81550 |
rs539404092 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490412 | CAGAGAAACAGCGGA[G/T]TGGCCAGTGGAAGCA | 81550 |
rs539416829 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503019 | AACTTTGTTCACAGA[A/G]TACCTTATTCAATTA | 81550 |
rs539419964 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396090 | CCGTAACTGCCAATT[G/T]CCTCCCCAATCCCAA | 81550 |
rs539440398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429404 | TTTTAAATGTAAATT[A/G]TAAAATGGCTAATTT | 81550 |
rs539455882 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537390 | CTATTTTAAAAAATA[A/T]TTGTGTGCATATAGA | 81550 |
rs539464862 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507342 | AGCTCTGGACCAAGC[A/G]GACCTAATAGACATC | 81550 |
rs539479566 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505743 | GAAGCATACACAAGT[A/G]TCAATAGCCGAATTG | 81550 |
rs539489819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398349 | GTACGTACAGAGGAA[C/T]AGATGAGTGCACTGT | 81550 |
rs539516007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540199 | TTTCAGAGATCACCA[C/T]GTGAGCAGTGCTCAT | 81550 |
rs539521684 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548830 | CCTTTTGATTATTTT[G/T]TCCCAACACTTAAAA | 81550 |
rs539532466 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544414 | GTACTACACTCCAGC[C/T]TGGTCAACAAAGCAA | 81550 |
rs539553614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540908 | TGAAATAACATGACA[C/T]GATATTACCTAACAC | 81550 |
rs539595943 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568748 | AAGTACTAGCTAGAG[C/T]AATTAAACAAGAGAA | 81550 |
rs539621840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404752 | TGGGATTACAGGTGC[C/T]CACCACCACACCCAG | 81550 |
rs539649862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415874 | AAGACAATTTACGGA[A/G]AAACATTCTTTAGAG | 81550 |
rs539652111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526019 | ATTCTGCCACATCTG[C/G]CAAGCCTGGCTGAAC | 81550 |
rs539666914 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564718 | TTTGTAAACTATGAA[A/T]TTAAAATTATTTTTT | 81550 |
rs539719638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542124 | TCCCTTTGATACTTA[C/T]GGTTCAGTAGTCCTA | 81550 |
rs539738835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571570 | ACAGTCATAGGTTTT[C/T]TTTTTATGTTTTGAG | 81550 |
rs539755954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533371 | ATTGGCTGGGCGCAG[C/T]GGCTCATGTCTGTAA | 81550 |
rs539756077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542881 | TGGGCTACCCTTACT[A/T]CTGATCTTAATTTAT | 81550 |
rs539756534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463982 | CCATCCTTGCAGTGA[A/G]TGAGTTCTTTATTAC | 81550 |
rs539758240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481884 | AATTAGCTTTGGTCA[A/G]CAGTTAATTTACTTT | 81550 |
rs539776940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572226 | CGAGGGAAGCAGAGT[C/T]CACAGCAAGTGGCTC | 81550 |
rs539839918 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565228 | GCCCGGCTAATTTTT[C/T]GTATTTTTAGTAGAG | 81550 |
rs539853014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500588 | GTAATCTTCCCAGTG[A/G]GCAGAACTTCAAGCA | 81550 |
rs539864125 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570134 | TAAGAGACCACCCAC[A/C]GAATGGGAGAAGATA | 81550 |
rs539873356 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476416 | AGTCTGTTTTTGTAC[A/C]CAGTACTCATTGTTA | 81550 |
rs539877167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479266 | GTTCACCCAGAAGTT[A/G]TTCAGGAGTAAGTTT | 81550 |
rs539880406 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395628 | AACCAGTGAGAAATT[C/G]TGATGATTGGTACAA | 81550 |
rs539881454 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396771 | CCGGGCGGACCAAAA[A/G]GCGAGGTGAAGGGAA | 81550 |
rs539919940 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420805 | AAAAATTAGCCGGGC[G/T]TGATGGCGGGCGCCT | 81550 |
rs539951957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436994 | CAATTGAATTTGTCT[A/C]GTTCTGCTTTTGTCT | 81550 |
rs539959066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513778 | CTTGCTCCTCCTTGC[C/T]TTCTGCCATGATTGT | 81550 |
rs540025417 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539116 | TAATTCTGGAAGGTG[A/G]TAGGCAAATTGTTAT | 81550 |
rs540085944 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60513942 | GTGCTGCAGAAAAGA[A/T]AACCCGAAAATGTGG | 81550 |
rs540093395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546557 | TATTGAAAATATTTA[A/G]AGTGGTCATGAAAAG | 81550 |
rs540121397 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422107 | ATTTCAAAGAATAGG[C/T]ACGATTTAAAGGGTT | 81550 |
rs540136098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479951 | CTTGCTTCTTTATCC[A/G]ACTTGCCATCGTATT | 81550 |
rs540186089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538255 | TATTAATGTTGTGGT[C/T]TTTGAGTACACATTT | 81550 |
rs540191228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60442826 | TTAGTGACAGTGTCC[C/T]AGATCATATGATTCT | 81550 |
rs540198880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435078 | AAAAGATTAATTTGT[A/T]AATCCCAAATTATTG | 81550 |
rs540276232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483275 | TAGTATAAGGAAGGT[C/T]AAGGAAATTTTAGTA | 81550 |
rs540287477 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410686 | TGATTTGACTTCTTT[C/T]CTCAGTTTTGCTTCT | 81550 |
rs540311850 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497265 | ATTTAATAGAGTGAA[A/C]ACAGAGCTCCCATAA | 81550 |
rs540322258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469088 | TGATACTAATGTGCT[A/G]TGATTTGGGTTGCTG | 81550 |
rs540325854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569072 | CTTCTGGGCTCAAGA[C/T]GTCCTGCCATCTCAG | 81550 |
rs540337650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498806 | AACGTTTTGGGGACT[A/G]CTGGAAACTGGCTCA | 81550 |
rs540349081 | snp | A/G | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395087 | TGTATGTCTAGTTGC[A/G]TTACATCAGTAAGCA | 81550 |
rs540350214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451686 | ACTTTACAAGATAAT[A/G]CCAAATTATCTTGCA | 81550 |
rs540353018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506274 | TTCATATCTAGATTT[C/T]CATACCAGCCAAACT | 81550 |
rs540354529 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518520 | CTAGAATTGTGATTT[-/A]AAAAAAAAACTGGTG | 81550 |
rs540358526 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60435295 | TTTCAATAGTTTTTT[G/T]GGGTACAGGTGGTTT | 81550 |
rs540375189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435636 | GTAGTATTCTATGGT[A/G]TATATATGCCACATT | 81550 |
rs540405384 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512848 | GAGTGTCTGTGGCTT[C/T]TCCAGGTAAATGGTG | 81550 |
rs540407828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484991 | ATTTCAATAATATTA[C/T]TTGGTTATAAAGTTC | 81550 |
rs540409362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529652 | TTCAGCTTACTTTTT[A/T]AAAAAGTTAACATAT | 81550 |
rs540413502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441514 | CCATTTTGATTAGGG[C/T]GAAGCCTATACCAGA | 81550 |
rs540444721 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488874 | GCGTGAGCTACCATG[C/T]CTGGCCGGGTTTATT | 81550 |
rs540458499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513415 | CTCCTTGTTACTTAC[A/G]CATATTTTTGCAGCT | 81550 |
rs540459534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418695 | CCATTCTAAATGTTA[C/T]ATAGAATGTTTTCAT | 81550 |
rs540472114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410017 | TCCTGTGCTAGTCTC[A/G]TGATAGTGAATAAGT | 81550 |
rs540479315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554341 | TGAAGAATGTAGCTT[A/G]TCAACACTGTTAGAA | 81550 |
rs540491921 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541411 | ACCTCAGGTGATCCG[C/T]CTGCTTTGGCCTCCG | 81550 |
rs540500847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492446 | AATGAGGTAGGTTTT[C/T]TAATCCCAGTTTTAA | 81550 |
rs540527306 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430785 | TGCCTTCATGGATTG[C/G]TTTATGTATGGGGAA | 81550 |
rs540572204 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444535 | GACACTGTTACTTGA[A/T]AGATTGATAATACAT | 81550 |
rs540588796 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433535 | GAAAGGAAGTTGGCT[A/C]TGAATGTTATACTAT | 81550 |
rs540591230 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TDRD3 | GRCh38.p7 | 13:60574156 | TCCAAATGTAATTCA[A/G]TTTTAAAAAACAGGT | 81550 |
rs540592192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475787 | TTACATTTCTCTAAT[A/G]ATTAGTGATAATGAG | 81550 |
rs540605075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536052 | ATATTCTAGAAAATT[A/G]TATCATCCAGAGTAA | 81550 |
rs540612827 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460634 | AAAGTAGGAATGGAC[C/T]CTTAATTGTGTGTTA | 81550 |
rs540649318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433866 | TAAGTTAGATTCACC[C/G]ATTTTACCTGCTTTC | 81550 |
rs540652971 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522881 | GTTGGTTACATTCTG[-/T]TTTTTTTTCCTCTGG | 81550 |
rs540660139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466165 | CATTTGATCTTTGAC[G/T]TGATGGTGAACAAAA | 81550 |
rs540673235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416796 | TGGAATTCACTGTTA[A/G]GACATAGTGTCTTAA | 81550 |
rs540692152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552392 | CTTACATCCAGGGCA[C/T]GCTAATGCAAGGGGT | 81550 |
rs540694018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60543935 | TTGTTATTTATGAAG[A/C]CTCCCATTATCGTTT | 81550 |
rs540698417 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60489012 | TGTAGGTTGTCTCTT[C/T]ACTCTGTTGATTGAA | 81550 |
rs540707722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474222 | CAAACAGGGAAGGGC[A/C]CCTCTGGTGGACACG | 81550 |
rs540756517 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424135 | CACGCCATTCTCCTG[C/T]CTTAGCCTCCCGAGT | 81550 |
rs540799418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459201 | AGTGTAAATATTTGT[A/C]TATCATTTCACATTT | 81550 |
rs540833069 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484223 | AAATAAAGCCACACA[G/T]AGTGATCAAAGTGCT | 81550 |
rs540838537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568411 | TAGGTATTTTTCTTA[C/T]GGCATGGAATAACTG | 81550 |
rs540853561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521784 | TGCCTGTAATCCCAG[C/T]CACTCAGGAGGCTGA | 81550 |
rs540858504 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438494 | GTACCTCATTTTGTT[A/G]ACATTCTTGGTTTGA | 81550 |
rs540874630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505465 | ATAGATAAAACTCCC[A/G]TGTCCCTGGGACAGA | 81550 |
rs540880489 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508423 | TACCAAAACAAATAT[A/G]TAGACCAATGGAACA | 81550 |
rs540890950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560125 | CAAGAAATGGAAATA[C/T]ATACCGTATGATGCA | 81550 |
rs540898238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537081 | TATTAACCTATTTTC[C/T]TTCTCTGCAGTCAAC | 81550 |
rs540924063 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457964 | TAGATCCTTACCTTA[A/C]TTACATCTGAAAAGA | 81550 |
rs540925968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466861 | GTCTATTCATATGAT[A/G]TAGTCAGCCTCCTGA | 81550 |
rs540933584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407786 | TCTTTTTGATATTTC[A/G]GAATTGCTTACAGCT | 81550 |
rs540944579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435392 | TGTACACTGTACCCA[A/G]TATGTAGTCTTTTAT | 81550 |
rs540947573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417822 | AAGTTCTTCTTCTCT[C/T]TACACTCTTGTTTTA | 81550 |
rs540957482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426201 | ATTATGTGATCTTAC[G/T]TATATGTGCAATATT | 81550 |
rs540992292 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416492 | ATATTTATTAAGCAA[C/G]ACTTTTTTCTCCAAA | 81550 |
rs541020885 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518309 | TGGCTGTTGAGCCCC[C/T]CTCAAGCTGTGCATC | 81550 |
rs541023304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407049 | ATGTAAGTATTGATG[A/G]AAAAACTTGCTAAAT | 81550 |
rs541026401 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555828 | TTTACATAGGGTAGG[-/A]AAAAAAAACCAACCT | 81550 |
rs541026428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397918 | CCGGAGCCGCCTCTT[C/G]TTACCCCTTATTTCA | 81550 |
rs541034423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557887 | GGAGTGCAGTGTGCA[A/G]TCTCGGCTCACTGCA | 81550 |
rs541059606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518952 | TTTTTGAAAGATGTT[A/G]TATCTAATATAATTG | 81550 |
rs541060657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503022 | TTTGTTCACAGAATA[A/C]CTTATTCAATTATTA | 81550 |
rs541075656 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411655 | ACAGTTCTGCTTTGT[G/T]CTGTCATTTAAGGAC | 81550 |
rs541127645 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525616 | TGTACATCATCATCA[A/G]TTCAGTAACTGAAAA | 81550 |
rs541158713 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409857 | TTTGAAATGTGAGGG[C/T]ATGAGATTTGGAGGG | 81550 |
rs541164849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564354 | TGGTTTGGTCAAGGC[G/T]GGACAACTTGAAGCG | 81550 |
rs541181489 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430879 | GATCATTTTAAAATC[A/G/T]TCATGCTGTATTTTG | 81550 |
rs541186624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450906 | TAGTGGGTAGATGCC[C/T]CATATCGGGCGTATT | 81550 |
rs541198195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509649 | TTGTATTAGAATGAC[A/G]TTTTTACATAAGTAT | 81550 |
rs541204062 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556604 | AGCACCTACTAAAAA[C/T]ATTAAAGCAAGATTA | 81550 |
rs541216174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504886 | TGAGGTATTGTGCCA[C/T]GAGGAATAGTGGACT | 81550 |
rs541222157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439425 | CATCCCTTAAGTATA[C/T]TGACATTTAAATAGC | 81550 |
rs541228737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498082 | GAAATGCCTGATCTC[C/T]CTTGGCTTAATGTAG | 81550 |
rs541239354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400955 | TAATTTAAATTATTG[A/T]TCAAAAGTGACACAT | 81550 |
rs541242204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423381 | TAATGATAGATTTAA[A/G]TGGACAAAATATAAG | 81550 |
rs541257367 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546635 | AATGAAATAGTCATT[G/T]AGAGAACATGATTAA | 81550 |
rs541277225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498988 | CCAGTGCCAGAATGC[A/G]TAATTGGAATAGACA | 81550 |
rs541289749 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550548 | CTGGTAGGATTTGTC[A/T]TAGTAAATAGATTGC | 81550 |
rs541294582 | in-del | -/T/TT/TTT | 0.211516 | 0.24702 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484118 | TAGGATGGGAGAGGG[-/T/TT/TTT]TTTTTTTTTGAGGGA | 81550 |
rs541295771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399691 | TCACTGACAAACCAT[A/T]TTTCTTAGTATTCAA | 81550 |
rs541311594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480453 | CCTTGGAGAATCTGA[C/T]GACTATGTGTCTTGG | 81550 |
rs541333762 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527075 | CCTGGCCTCAAGCAA[C/T]ACACCTGCTTCAGCC | 81550 |
rs541356702 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512348 | AAGATGAGATTTGGG[C/T]GGGGACACAGCCAAA | 81550 |
rs541408325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494283 | GTAGATATTTTTGCT[A/G]TTCAAAAGGAGTAAG | 81550 |
rs541411146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510520 | ACTATACAAAAAATA[C/T]GAAAAGAAATTAAAA | 81550 |
rs541436051 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60545904 | TTCTCTCTTTTTTCT[A/C]TTTATCTAAGCTCCT | 81550 |
rs541439889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557363 | TTTGTGTGAAACGCC[A/G]TGGATGAATTTTGTG | 81550 |
rs541468013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486635 | TTCAAAACTCTCATC[C/T]AGCTATTTTGAAATA | 81550 |
rs541532922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464328 | ATTAGTGCAACCACC[A/G]TGGAAAACGGTATGG | 81550 |
rs541533416 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411982 | GCAGAGAGCCATAGA[A/G]TCAGTTCCCTGAGGA | 81550 |
rs541536585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572558 | AGGAAGCCTTTGTAA[A/G]ACAGATCAGCAGGAA | 81550 |
rs541545225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456693 | TTTTGTGGATGTTTT[A/G]GATGACTTTTTTTGA | 81550 |
rs541547016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464944 | TTAAAAGAGTAGATT[C/G]ATAATGTTCTCGCAA | 81550 |
rs541617072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523832 | TCCACCCACCTTGGC[A/C]TCCCAAAGTGCTGGG | 81550 |
rs541620121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412922 | GATCTCTACATATCT[A/G]AGATGCGTACTTTAA | 81550 |
rs541653785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516448 | ATAATTCTAGTTGAC[A/G]TTTTTATTAATATTC | 81550 |
rs541656558 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503181 | TTGCTTGATACTTGT[A/G]AACATTTCAGTTCTT | 81550 |
rs541683495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487205 | GAGATGATTTAAATA[C/T]ACAAGAATGGCCAGG | 81550 |
rs541690296 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448636 | TGTAAAAATTGTGAC[C/T]GGAAGGAAGTGTGGT | 81550 |
rs541717311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496649 | ATACCTTTGACCATA[G/T]GTGGAGAACCAAGGA | 81550 |
rs541726460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523365 | TCTTGCATTTCAAAT[C/T]ATGGTGATGTAAAAC | 81550 |
rs541751329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438706 | GTAAGGTTTACTTTG[A/G]TAAGTATCTTAGAAT | 81550 |
rs541787133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421186 | ATACCCGAGACTGGG[C/T]AATTAATAAAAAAAA | 81550 |
rs541801108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436462 | GTATAAGGTGAGAGA[C/T]GGGGATCCATTTTCA | 81550 |
rs541852999 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469285 | ATAATTGTATTTTTT[A/T]AATCAGTAGAGATTT | 81550 |
rs541862493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429059 | TTGTATTTAAGATGC[A/G]TTTTAAAGAAATGGA | 81550 |
rs541890416 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455744 | TAGGTATACAGATTG[A/G]GAAATTTCTTTCTCA | 81550 |
rs541902297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434970 | TACTGTGTTACTGAA[A/G]TTCTTGAAGCACATT | 81550 |
rs541907332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547559 | AATTAAATGATCTAT[G/T]TAAATGTGCTCTATA | 81550 |
rs541907423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555176 | AGCTAATTACTAATA[C/T]GTTGAACCTTTTGAA | 81550 |
rs541908700 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538349 | ACTTTTGTTGTCATC[C/T]CTGATTTATTTGTTC | 81550 |
rs541919632 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396873 | CGTGACCTTTTTAGC[A/G]CGGTCCTGGACGCGT | 81550 |
rs541920032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484909 | AGACTTATGATCTAA[C/T]TATTCTTAAGACTTT | 81550 |
rs541930525 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507556 | GAATGGCACAAATAG[A/G]TGGAAACTGAACAAC | 81550 |
rs541951659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446504 | AGTATTGGGATTACA[G/T]GTGTGAGCCACTGTG | 81550 |
rs541962672 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445347 | ACATCTGGTTACCTT[A/C]CTTTGTAAATAATTA | 81550 |
rs541966276 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422168 | GAAAGAAACAAAAAG[A/G]AGGGAAGGCGTTTCC | 81550 |
rs541977469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476758 | TTTTGTAATTCTCAT[G/T]GTAGAGATCTTTCGC | 81550 |
rs541993182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548234 | CAGAAATTAAGTCCT[A/G]GCCCACCCTCAGCCA | 81550 |
rs542028251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455034 | TTCTCCTGCCTCAGC[C/T]TCCCAAGTAGCTGGG | 81550 |
rs542029540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413975 | ATATTCAGTCTCTTA[A/G]TATGGACATGAACTT | 81550 |
rs542044421 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563305 | CTGAGGTAAGTATCT[A/C]AGTATTTTCAGCAAA | 81550 |
rs542047135 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426092 | GGGATATAATTGAGC[C/T]TTTAAAAAGAAGGAG | 81550 |
rs542056394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571760 | ACACATATACTTCCT[C/G]ATTGTGGTGAGAGAA | 81550 |
rs542067256 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396325 | GGAGCAAACTTTTAG[C/G]GAGCGCCTCTTGGGC | 81550 |
rs542071707 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454202 | GGACTGAATGATAGC[C/T]GTATTTTGAAATTTG | 81550 |
rs542100921 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419179 | CAACCAACAGTGTAT[A/G]AGAGATCTGGTTTCT | 81550 |
rs542111396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531983 | CTGCTATGTGCCAGG[G/T]GATTGGGGCATATCA | 81550 |
rs542184305 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495077 | CTAAGGATGTTTGCA[A/G]AAATTCATTTTCCTC | 81550 |
rs542199295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530391 | AAGGGAGTTACAGAG[C/T]GAAGGGTCTGGGAGG | 81550 |
rs542214342 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541814 | CTCACCACAACCTCC[A/G]CCTCCTGGGTTCAAG | 81550 |
rs542217592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569281 | CAGCCTCAACAGCAA[A/G]CAATCTGAAAAGGAA | 81550 |
rs542223995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401894 | CAGCTTATTAAGGTC[C/T]TTGTCAAAATGTAGA | 81550 |
rs542228338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560730 | TGATTTCATGATATC[C/G]TGTAGAATCATAAAC | 81550 |
rs542237831 | snp | C/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521871 | CATTGCACTCCAGCC[C/T]GGGCAACAAGAGTGA | 81550 |
rs542238812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513965 | AAATGTGGAAGTGAC[C/T]TGGGAACTGGGTAAC | 81550 |
rs542253745 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571245 | TTATGAAAGACTATG[A/C]AGTAGAATGAAATAT | 81550 |
rs542257092 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60483517 | TGTTTTCTCCTTAGG[A/G]GAATGGCCTGATAAA | 81550 |
rs542272487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522469 | TATTGGGTGCTTATT[A/G]AAGCCAGATACTGTC | 81550 |
rs542288387 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460315 | GAAACACTATAAATG[A/C]AAACACAGCCCTGAA | 81550 |
rs542346332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529407 | ATGGATGCCTAGGGA[C/T]AATCTGTCCCGTAAG | 81550 |
rs542346982 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568475 | CAGAATCAAAAGAAT[A/G]TGTAAGGACTTTGGC | 81550 |
rs542350690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560235 | AGCCTTAGTTTTTTC[A/G]TCTATAAAATGGTGA | 81550 |
rs542350734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408762 | AGAGCACAAAAGTTT[A/G]GAAAATTTGCAGCAT | 81550 |
rs542361945 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399758 | AGTAGATGCTAAAAC[A/G]TGGACACACTATTGT | 81550 |
rs542381700 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421488 | TTGGGTGGGGACACA[A/G]CCAAACCATATCACA | 81550 |
rs542382596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568221 | CTTCTCATGTAGTAG[C/T]AGTCTGCCTAGAGTG | 81550 |
rs542383469 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433940 | TGATGGTAAAGGGTG[A/G]TAATGGAGATCTACT | 81550 |
rs542383518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443583 | CATGTGGATATTTCA[A/G]ATAGGAGGATGTTTT | 81550 |
rs542389757 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546430 | CTAGAGACTAGAAAG[A/T]CTAAATTTTGTTATA | 81550 |
rs542399995 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518896 | GAATATTATTAGGGG[C/T]GTTTCTAAATTCAGA | 81550 |
rs542418437 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469950 | GGCATTAAGAACATT[C/T]GCATTGTTGCACAGC | 81550 |
rs542418750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509008 | TTATATATGCTCAAA[C/G]GTCTGAGAGAAACCA | 81550 |
rs542442049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403341 | AATATGACTATATCA[A/G]CTTTTTTGGCTTATG | 81550 |
rs542458077 | snp | A/C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418153 | ATTTTTGCTCCTACC[A/C/T]CTCCAGCAGTTTATG | 81550 |
rs542464689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554490 | TTGTCCGGAGGATCT[A/G]TTTGCTCTACTTTTT | 81550 |
rs542465282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553146 | CTGCAAATTTTCCAA[A/G]TCTTTATGCTCTGCT | 81550 |
rs542485744 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515245 | TTTTATTGCCAAAAT[A/G]AGACCTACCCATTGT | 81550 |
rs542504941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492835 | TAATATGTTATCCAT[C/T]AGTGCTCATCCAACA | 81550 |
rs542519181 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525715 | TTGTTAAATAATAAG[A/C]TGTTCAGGAATTTTT | 81550 |
rs542520256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60442719 | TAAACTTTGAGCGTG[G/T]AGTCTTTTTTTAGCC | 81550 |
rs542548414 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411835 | CTTATTAAAGAATCT[G/T]ATTGCACATTAAAGT | 81550 |
rs542553322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553601 | GGTTCTGCATGGCTC[A/G]AGAGGTCTCTGGAAA | 81550 |
rs542556309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514723 | ATTGGTAGGCTAGAG[C/T]CAGATCACAAGGATT | 81550 |
rs542574564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402772 | GCGCGATCTTGGTTC[A/G]TCGCAACCTCCACCT | 81550 |
rs542578258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451924 | TTGCATTGAATCTGC[A/G]CATTAGCTTAAAAAC | 81550 |
rs542596669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497858 | ACAGAAATCTGAAGA[A/G]CAGACATGGGAATGT | 81550 |
rs542640622 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437062 | TGGATAGCTACTGGC[-/T]TTTTTTTAATGAGAT | 81550 |
rs542683486 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60495467 | CAGGAATCAGAGGTA[-/T]TTTTTTTTTTTTTGA | 81550 |
rs542699197 | snp | A/C | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60397096 | GTCCTGACTCCAGCC[A/C]CCAGCCGGTGTTTGG | 81550 |
rs542716147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464619 | ACTGGAATATTATTC[C/T]GCCATAAAAAAGAAT | 81550 |
rs542724318 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400125 | GTGATAATGTTTAAA[G/T]AATGCACTAAATGGT | 81550 |
rs542739248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467811 | TTGACTTCCTAGTCT[C/T]ATTAGCTAATATTTT | 81550 |
rs542746871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458599 | ATGGAAGTGCGGTGC[C/T]TAGGATGCATGAGTC | 81550 |
rs542763190 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450740 | ATAGCCTAATGAGAG[A/C/G]TTGAGAAACCAGCCG | 81550 |
rs542810381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425362 | AAAAGATACAAGATA[A/G]CAAATGTTGGCAGGG | 81550 |
rs542829299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491470 | CCCTGTAACACTTCA[A/G]TTTGAACTTAGAGCC | 81550 |
rs542856694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484000 | TAATTTTGAGGTTTT[G/T]TTCCTTCACTGTAGT | 81550 |
rs542877527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417676 | TACTGATGATTCCTA[A/C]ATCTTTCTGGGCCTG | 81550 |
rs542887881 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60573071 | AATAGGCCTGGAGCA[C/T]ACAAGTCTTCTCTCG | 81550 |
rs542983596 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60543809 | TGTCATTAGTAATAC[G/T]ATTTTATTGCATACA | 81550 |
rs543037190 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499309 | CCAATTGCAGCTGCT[G/T]TACCAGATGTGGTTT | 81550 |
rs543045610 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431385 | CTTAACAAAAAGCTA[C/T]CTAGGTTTAACTTTT | 81550 |
rs543056867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489284 | AATTTTAGGTCATAA[A/G]TTAGTTGCTACATAG | 81550 |
rs543072213 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434610 | GCCCTGCTTGTCAGT[A/G]AAATGTATTCAGATG | 81550 |
rs543079771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517363 | TGTGTATATATTAGG[C/T]TAGATGTTATTGTGA | 81550 |
rs543096841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551581 | ACCCAAACTGCTTCT[C/T]TGCACTACCCTTTTC | 81550 |
rs543096938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559470 | GGGTTTCAGAGAGGT[A/C]CACATTTTTAAAAAT | 81550 |
rs543098675 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470836 | GATCTGCCGGTCTCA[C/G]CCTCTAAAAGTGCTG | 81550 |
rs543099331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438538 | TTTTCTGACTTTTAT[C/T]GCCTTGGTCTTGCTC | 81550 |
rs543112428 | in-del | -/CAAA | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60570611 | TCTTTTTAATTGCTT[-/CAAA]CAAAGTTTTAAATTG | 81550 |
rs543157289 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431655 | AAAATTTTTTTTTGC[A/G]TATTAATCCTTTCAC | 81550 |
rs543168838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417044 | TTTTTTGAGTCCAGG[C/T]CTTATTCTGCTGCCC | 81550 |
rs543240652 | in-del | -/ATTA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412640 | CTTATACTTTTAGTT[-/ATTA]ATTAGTATTTGTTTT | 81550 |
rs543253247 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554791 | ATCATACATTTATTA[A/T]GTTCTTCCTTTGTGT | 81550 |
rs543264843 | in-del | -/AATT | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439036 | ATCTCTTTACTCTTG[-/AATT]AATTGTCTCTGACAG | 81550 |
rs543266224 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566510 | AAAGAAGATTCAAAG[A/T]TAAAGTAAGGAAGAG | 81550 |
rs543268111 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60550509 | TGCATGAATTTTATA[A/G]AAATGATGACTGTAT | 81550 |
rs543277770 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475060 | ATCTTTTCTTTATCT[A/T]CTTTTAAGTCTTTTC | 81550 |
rs543325792 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410364 | TCAAGTCCACTGGGG[A/T]TTTACCTGAGGACTC | 81550 |
rs543325950 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441840 | TCTCCAGGGAAGCCC[G/T]CTGAAGACTAATACC | 81550 |
rs543350847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424745 | GAGATTTGTAATCAT[C/T]ACTACTATCTAATTC | 81550 |
rs543364996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474346 | ATTCGGGGTCACTAC[C/T]GGTCTCCGCGCCTTG | 81550 |
rs543384237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480386 | GAGTGGGATTCTTTT[C/T]GTAAGGCCCCTTTTC | 81550 |
rs543387635 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433356 | GTTCTTTATATGTCC[A/G]GTTTGTAAAATATTT | 81550 |
rs543401578 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527734 | GTATTTCCACTTTTG[A/C]CACTTTTCTGTATTT | 81550 |
rs543409414 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413460 | TTTCTTAACTGCTCA[A/T]GTCTCAGTTTGCTTA | 81550 |
rs543413676 | in-del | -/AT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530763 | CCCGGCCCAAAATAA[-/AT]ATTTTATAGGTTGCA | 81550 |
rs543419991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404965 | TTTAAAAATGGGAGG[C/T]GCCCTGCACAAGCTC | 81550 |
rs543442625 | in-del | -/AAC | 0.00319871 | 0.0398638 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420181 | TAATGTTTTTTACCT[-/AAC]AACAACAACAACAAC | 81550 |
rs543481935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455961 | TGTAATCCCAGCTAC[G/T]AGGGAGGCTGAGGAA | 81550 |
rs543504522 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561035 | TGCTCTGGAGGGATG[A/G]GAGACTATAATTCTT | 81550 |
rs543516082 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524709 | AAGAATGATTGGATG[A/T]TGAATCCAAGAATGA | 81550 |
rs543534610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554109 | AGTGATTTTCGTTTT[A/G]GCTCTGGCATAAAGT | 81550 |
rs543537929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563555 | GTGTGGGCTGTCCTG[G/T]GCATTGTAGGATATT | 81550 |
rs543541527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571018 | GTTAAAACTTCCATC[A/G]ACAAAATGCTTGCTT | 81550 |
rs543544042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532825 | TTAAATTTGTCCTCA[A/G]TATTGCCACCACTGT | 81550 |
rs543553190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430742 | CTGTTACAATTTTTT[A/T]AATACCAAATAAGCA | 81550 |
rs543566124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515675 | TGCCAGTATTCTTAG[A/G]TGAGCTGGGGTATAT | 81550 |
rs543580122 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60558166 | ATAGGTGTCCGTGGC[A/G]TACTGTATCTGTCTG | 81550 |
rs543581480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448520 | CAGAACCTTGATGCA[A/G]AAGTTTCAGAAAAAT | 81550 |
rs543602089 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511426 | TCATAAAAATTGAAG[C/T]ATGTTTGCTAGATTA | 81550 |
rs543635070 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541185 | TTTCTTTCTTTTTTT[C/G]AGACGGAGCCTTGCT | 81550 |
rs543654126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558821 | TCCCCAAAACAAAAA[A/C]AATGGTAACAATAAA | 81550 |
rs543660418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556403 | TTAATTTCAGAATAT[A/G]CCAACAATAATACTG | 81550 |
rs543674577 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563130 | TGCTCAGGAGGCTGA[-/G]GGGGGGAGAATCACT | 81550 |
rs543707038 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445912 | CTCATAGAATAGTAG[C/T]ACAGAGATTCTTGTC | 81550 |
rs543714832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447485 | CATATGGCAAGCTTC[A/G]AGAATTATGAGCAAT | 81550 |
rs543772711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415925 | TTTTTCTTAAGGAAA[A/G]GTGAAGAAAGGGAGA | 81550 |
rs543793385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501235 | GGGTGTTGGACGATG[A/C]CTCTTTTGGCTACTT | 81550 |
rs543828527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464303 | TCAAACACCACTGAT[C/T]GGAATGTAAATTAGT | 81550 |
rs543868304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493247 | AATGTTATTGTATTA[C/T]ATATAATTTATATGT | 81550 |
rs543876899 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563466 | TGATACTTAGGAGTA[A/G]GAAGTGTCATTTGCC | 81550 |
rs543929572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500623 | ACCTAGTTGTGCACT[G/T]TGCATTTAAGGAGAA | 81550 |
rs543929688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507978 | TTCCTATACACTGGT[C/G]ATATACAAACAGAGA | 81550 |
rs543964520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420601 | ATTTCAGTGACATTT[A/G]TAAAAAAAAATTTTC | 81550 |
rs543976945 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473709 | AGGGACATGGTGAGA[A/G]GTGACCAGAAGACAA | 81550 |
rs543977615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550302 | AAAGTATACAGAACA[G/T]AATTATTTGTATTCA | 81550 |
rs543992646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531359 | ATTTAGATATTTCTC[C/T]TTCATGGTGGAGGCA | 81550 |
rs544032036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496516 | TCTACTTCTAATAGT[A/G]TGGAGAACACTGATA | 81550 |
rs544064224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397903 | CAGCCCGCGCTGCGG[C/T]CGGAGCCGCCTCTTC | 81550 |
rs544084701 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456519 | TTCTTTTGATTTTTT[C/T]TTATTACTAATACAA | 81550 |
rs544101987 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530661 | GGTTTCACCATGTTG[A/G]CCAGGCTGGTTTTGA | 81550 |
rs544108871 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494084 | AGCTGGATTTAGAAC[C/T]CAACTCTCAAGGCAG | 81550 |
rs544142414 | snp | C/T | 1.83172e-05 | 0.00302626 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485813 | GAAGTGTGTATCTCA[C/T]GTCCAAGTGGATAGC | 81550 |
rs544163446 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435854 | CTCCATACTGTTTTC[C/T]GTAGTGGTTGTAGCA | 81550 |
rs544176540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483956 | GAGGTTATGGAGTTA[C/T]TTGGAAATATGAAGT | 81550 |
rs544200756 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445048 | CATTACAATGACCTT[C/T]TCTTACCTTTCAATT | 81550 |
rs544239889 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426380 | AGGACTAAAGTTATT[A/T]AAATTAGAGATTTTT | 81550 |
rs544243377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475874 | TCATGTCCTTTGCCT[A/G]TTCTTTAATGAGGTT | 81550 |
rs544245276 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60449079 | CTCAAAACCTCAGCA[A/G]TACTGACATCAACCA | 81550 |
rs544251018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553783 | TCCAATCACCTCCCA[C/T]CAGGTCCCTCCATTG | 81550 |
rs544261561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403232 | ATAAAAAGAAACTTG[C/T]TACCTCAGCAGGTTG | 81550 |
rs544285881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462115 | ATTTGTTGACATTGT[A/G]ATTATATTCTCTTCT | 81550 |
rs544287064 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60442582 | AAGTTGTCTTTATAG[C/T]GTGAATTTAGGGCAT | 81550 |
rs544314988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454019 | ACATATTTACAAACA[C/T]AACTTTATATTCAGG | 81550 |
rs544337644 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419548 | GAAAAACCAAACACC[A/T]TGTGTTCTCACTCAT | 81550 |
rs544415137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507357 | GGACCTAATAGACAT[C/G]TACAGAACTCTCCAC | 81550 |
rs544420855 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60510496 | AAAAAAATTACTTAA[A/G]AGATGTAGACTATAC | 81550 |
rs544458215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494153 | GTCTTCATAATGCTT[A/G]TAGTATTTTCTTCTC | 81550 |
rs544479919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513883 | TGTCTTTATCAGCAG[C/T]AAGAAAATGAACTAA | 81550 |
rs544484130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402649 | ATTCGAATCATTAAA[A/G]CACTTTTTTAGATGC | 81550 |
rs544496239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489319 | TTCTTAACCAGTGAG[A/T]TTGAAATTGTTTCCT | 81550 |
rs544506627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461492 | AAACTTTCACTAGAC[A/G]TTTGCAGCCCTCCTC | 81550 |
rs544507868 | in-del | -/CCT | 0.00398564 | 0.0444627 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394939 | ATAACAACACTCCTA[-/CCT]CCTCAGATTGTGACA | 81550 |
rs544525577 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565112 | CCAGGCCGGAGTGCC[A/G]TGGCACTGTCTGGGC | 81550 |
rs544529357 | in-del | -/TGAAAATGAATTCAGAATTA | 0.0158469 | 0.0875917 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460133 | TTTCTCATTACCTTC[-/TGAAAATGAATTCAGAATTA]TGAAAATGAATTCAG | 81550 |
rs544534732 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538050 | AGTTAATACCTTGTT[A/G]TATGGAAAATTAAAA | 81550 |
rs544590450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521837 | GGGAGGTGGAGGTTG[C/T]GGTGAGCCGAGATCG | 81550 |
rs544592530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469194 | AGCTTAATAGTTCTA[C/T]ATAAACAGCCAAGTT | 81550 |
rs544596372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417605 | CCTCGGCCTCCCAAA[A/G]TGTTGGGATTACAGG | 81550 |
rs544598002 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516018 | ATCTTATTTATGTTC[A/T]TATTAGCAGCATCAT | 81550 |
rs544609304 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426955 | GTACAGCATGTTATC[A/G]TACTGAATACTGTGG | 81550 |
rs544622581 | snp | A/G | 0.00014834 | 0.00861092 | missense, synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567543 | GAAGAAGGCACCTAC[A/G]ATCAAACTCTGGAGT | 81550 |
rs544632135 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457361 | AATAACTTTATTACT[C/G]ATTAAAATGTATTTT | 81550 |
rs544648881 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407996 | TTCAGGGGTTTCCGC[A/T]TTTGTTTCTTCCTCA | 81550 |
rs544656807 | in-del | -/ACA | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435906 | GTAAACCACATCATG[-/ACA]ACATCTATGGTTTTT | 81550 |
rs544676332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519835 | GTTTTTTAATTATGT[C/G]AGAAATTTTACTAAA | 81550 |
rs544703168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467722 | ATATGTATACCTGTC[C/T]TATCTACAGACACAC | 81550 |
rs544720540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537223 | GGTTGTTGACGTTTT[A/G]TGAATTTGCGTAGGT | 81550 |
rs544723217 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420903 | GAGCCGAGATCACGT[A/C]ACTGTGCTCCAACCT | 81550 |
rs544733022 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416889 | CCTTTCTCATCATTC[A/G]TTGTCTTTTTATGAT | 81550 |
rs544768731 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452819 | CACTGTTCTTAGTTT[G/T]TTTTTTTTTTAATTA | 81550 |
rs544803301 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571676 | TTTATATTGTAATTT[C/G]CACATTCTTTGATTA | 81550 |
rs544807197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569826 | ACATTGGAGTGATGA[C/T]AGTCTCTCCAATAAA | 81550 |
rs544827467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514635 | TATGTATACAGGCAT[A/G]GAGGCATCAGAGCAC | 81550 |
rs544833012 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446999 | GATACAGGACAACAG[C/T]TGGCAAACAGAATAT | 81550 |
rs544836450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561609 | AATAAATAATAAAAA[A/T]ATATAAATCTGCTCT | 81550 |
rs544894014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469943 | TTTCAGTGGCATTAA[A/G]AACATTCGCATTGTT | 81550 |
rs544914303 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451873 | AATCAAATGATTAAG[A/T]CTCTTAAAAATATCA | 81550 |
rs544934848 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560088 | CTGTAGAAAAAAGTT[C/G]CTGATAGAAAACTAT | 81550 |
rs544941860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401065 | TCTGAGGGGTGATCC[C/T]ATTAGAATCAAATAA | 81550 |
rs544945032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560606 | CTGTATTTGCTTCTA[C/G]TGTCATTTAAAAATT | 81550 |
rs544954026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410101 | TTTTCTCTTGCCATC[A/G]CCATGAAAGAAGTGC | 81550 |
rs544962780 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459458 | ATATAATACAGCATT[A/C]GATTTAATATCGAAG | 81550 |
rs545051388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399351 | TTTATGTTTCTCCCA[C/T]CTGTCTGTGCTGCTT | 81550 |
rs545073922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474287 | CTCACACTCCTTACC[C/T]TGCCCCCTTGTCTTG | 81550 |
rs545100886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519244 | TTTATTGAGCATCTG[C/G]TATGTGCCAGGACTA | 81550 |
rs545103211 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466982 | TGTGTGTGTTTTTTT[G/T]TTTTTTTGTTTTAAG | 81550 |
rs545124232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503884 | TTGGTTTAAATGAAA[A/C]CTTATAGACGATTCC | 81550 |
rs545126092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511093 | CTTGTGAAATTGATA[C/T]ATCTCTTCTTTCTCC | 81550 |
rs545133188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434863 | GTGTGCACAGGGACC[A/G]TAACTGGAGTGCCTG | 81550 |
rs545140684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474708 | ACGTTTTAATTTTTT[C/T]CCCTTAAATGGTTTT | 81550 |
rs545166404 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464894 | ATAATAGGGTGACTA[C/T]AGTTAACAGTAATTT | 81550 |
rs545168231 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544852 | CAATAGATGTATACT[A/C]TAAGTACCTTCTCTT | 81550 |
rs545178681 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498863 | AATGTCACTGTGGTC[C/T]TCCAGTTAAAGTAGG | 81550 |
rs545211732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424595 | GGCAGGAGAATTGCT[C/T]GAACCCAGGAGGCAG | 81550 |
rs545214449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506064 | TTGAGAAGAGCAACC[C/T]CAAGACACATAATCA | 81550 |
rs545251753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489091 | ATTTTTACTTGTGTG[C/T]CTGTGTTTTTGAGGT | 81550 |
rs545263747 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394464 | GCGGATCACGAGGTC[A/G]CAAGATCCAGACCAT | 81550 |
rs545283151 | in-del | -/CTTTCTTTCTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541169 | TTTCTTTCTTTCTTT[-/CTTTCTTTCTTT]TTTTGAGACGGAGCC | 81550 |
rs545341406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533822 | TACTGAAAGATTGTT[C/G]CAATCAGATGACCTA | 81550 |
rs545344511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497740 | TGGGTGGGCCCTGAT[A/G]AAGCTGGGGACACTG | 81550 |
rs545357219 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428029 | AGAGGCTTTAGGGGA[C/G]AATCAGTAACTTACC | 81550 |
rs545373715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487309 | TAGCAAAACCCTGTC[C/T]CCACTAAAATTATAA | 81550 |
rs545384584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449828 | TCCTTTGCTGCATAT[G/T]AATATCATTTGAAAA | 81550 |
rs545392254 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60483324 | TATTATACACTATAA[C/T]AATCTGTTCTCTTTA | 81550 |
rs545401169 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552570 | AGGATGGTGGCCCTT[C/T]TCTCACAGCTTCACT | 81550 |
rs545428915 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478601 | TGAGCTACCGTGCCC[A/G]GTCCACAGTCTGTCA | 81550 |
rs545432660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479698 | TGGGTATATACATAT[G/T]TAGGATAGCTAAGTC | 81550 |
rs545434353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487907 | TACATAAGAGTTCTT[C/T]TTTCTTCACATCCTC | 81550 |
rs545456141 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409465 | TGGGAGGAAGGCTGT[A/G]TCCTGTAAAGCCACA | 81550 |
rs545494173 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430672 | GCCACTATACTATGT[A/C]ATATATCAATTATGG | 81550 |
rs545516208 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558636 | AAGAAGTTAATCATG[C/T]TAATTTATTTTTTGC | 81550 |
rs545541820 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407001 | AAAATTAATAAAGGT[A/G]GATTTTGTAAAATAC | 81550 |
rs545548326 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520054 | TGGCTTTTCTCAGTT[G/T]TCTTTTAAAAGGGGC | 81550 |
rs545589316 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526982 | TGAGATTACAGGTGT[A/G]CACCACCACACCCAG | 81550 |
rs545591967 | in-del | -/TG | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561871 | CAGGTTTTTTGTTGT[-/TG]TTGTTGTTGTTGTTG | 81550 |
rs545593250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481246 | TATCCTGTTTGGTTT[C/T]CAGTGAACTTTTTTG | 81550 |
rs545601847 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566656 | GAGCTAATTTTTTCT[C/T]TCTCTAATAGGGCAC | 81550 |
rs545608915 | snp | G/T | 1.64972e-05 | 0.00287199 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510691 | CCTGGGAAATGCAAG[G/T]CCATCAGCACCAAGC | 81550 |
rs545621764 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499718 | AAAATTTCTAGGGGT[C/T]CAGTGGTGTGGGGCG | 81550 |
rs545651104 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488630 | CCAGGGTGGAGTGCA[C/G]TGGCGCGATCTTGGC | 81550 |
rs545656303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482040 | GTTTTTAGTCTGCAT[A/G]GTCTGATCTGGCTGG | 81550 |
rs545656857 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493178 | CCGTCTCGGCCTCCC[-/A]AAGTGCTAGGATTAC | 81550 |
rs545659117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439488 | ACACAATAGCTCTTT[A/G]AGGGTACAAAAGAAA | 81550 |
rs545722573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431962 | TAAATTTTTAAGCTA[A/G]CATTGATTCAAGTCC | 81550 |
rs545734641 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430000 | ACATGCTGTCTCCTC[A/G]TTTATTCTTAGAAAA | 81550 |
rs545751495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523951 | AAATGTTACCCATTT[C/T]TACTTGTGCTTTTTT | 81550 |
rs545784921 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504744 | CTGAGGTACCTGGCT[C/T]ATCTCATTGGAACTG | 81550 |
rs545787074 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498871 | TGTGGTCCTCCAGTT[A/G]AAGTAGGGGCTTATG | 81550 |
rs545793586 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474356 | ACTACCGGTCTCCGC[C/G]CCTTGGTGGTAGTGG | 81550 |
rs545799019 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506806 | ATCAGCTAAAGGGCA[A/G]AATAACCAGCTAGCA | 81550 |
rs545830137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462403 | GAAAAAATTAATCGT[C/T]GTATGCTCTTCACTC | 81550 |
rs545840934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549319 | CTCTCAGCCCATTTT[C/T]AGTAGAGGTTCTCAT | 81550 |
rs545843941 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525104 | AAAAAAAAAAAAAAA[A/C]AAAAACCCCACAATT | 81550 |
rs545878479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403417 | TTTCAGTTAAGTGCC[A/G]TCAGTCTAGAAATTC | 81550 |
rs545880882 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501193 | ATCATTCCCCCCGCT[A/G]GAGTGGTAACTCTAA | 81550 |
rs545881048 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471579 | TTTGATAAGGATTAT[A/G]TTGACTCTATTGACC | 81550 |
rs545911432 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549786 | ACCATTTTATGAAAA[A/G]CAATTTTTCTAACAT | 81550 |
rs545951879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446603 | ATTGTCTTCACCAGT[A/G]TTAATGAAGATGTTT | 81550 |
rs545952242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530589 | GGGACTACAGAAATG[C/T]GCTACCATGCCCAGC | 81550 |
rs545954331 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542450 | CTTGTTGAATACACA[C/G]ACACACCTGTTTCAG | 81550 |
rs545961493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456451 | AGTTAGACATGCTTA[C/T]CTGGAGGTGCAATGA | 81550 |
rs545968881 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541159 | CTATTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 81550 |
rs545975429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517332 | AGGAAGGAAACTAGG[C/T]CGAGACAAGAGAGAA | 81550 |
rs545990460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522584 | TTTCACCTAAGGTTA[C/G]AGAACTAGTAAGTGG | 81550 |
rs546004806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470030 | TCTGTACCCATTAAA[C/T]AGTAACTCTGCATTC | 81550 |
rs546038206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565237 | ATTTTTTGTATTTTT[A/G]GTAGAGACGAGGTTT | 81550 |
rs546038669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445056 | TGACCTTTTCTTACC[C/T]TTCAATTTTATTTAC | 81550 |
rs546040067 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60573847 | GAATTTTTCTTCTGC[C/T]GTCAATAAAACCATT | 81550 |
rs546062403 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60449654 | TTCAGGGAATCTTAC[A/G]TTTGCAAAAACCTAT | 81550 |
rs546088020 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524542 | AAATAAAAAAAGAGA[A/G]AAGAAAAGAACGATT | 81550 |
rs546093033 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532760 | TTTTCGTCAACTGAA[A/C]TATTACAACAACCTC | 81550 |
rs546093665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472801 | ATTCTACTTATGTGA[A/G]GTACTGAAAGTAGCA | 81550 |
rs546101430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548480 | GCCACTTACATGAGC[C/T]GCTTGCCATTAATGC | 81550 |
rs546116493 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542715 | TATGTATGTCTCTAC[-/T]TTAATACTATTTCTC | 81550 |
rs546149572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414249 | AGAAAGAAAGATTAT[A/G]TAGCTTTATCCTAAG | 81550 |
rs546175448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523215 | TGATTTTCTACTACA[A/C]AATGCAGGTACAACT | 81550 |
rs546179602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412619 | TTTTATGTATTTTGT[A/G]ACTTTCTTATACTTT | 81550 |
rs546209243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545619 | AAAAGACTTAATAAG[A/G]CTGAAAATAATGTGG | 81550 |
rs546213443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555605 | TGGAGGTAAATGATA[C/G]CAACGTACTTGAGAA | 81550 |
rs546214534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470614 | TTTTTTTTTTTGATA[C/T]GGAGTGTTGCCCAGG | 81550 |
rs546244150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433792 | CCCCCTTTAGCTCAG[C/T]CAGCTGATGTGTAGT | 81550 |
rs546252037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515460 | GTACAAATAGCTAGA[C/T]GATAAAGTGATACAC | 81550 |
rs546275700 | in-del | -/T | 0.00538044 | 0.0515875 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510804 | TTTCTTTTCTTTCTT[-/T]TTTTTTTTTTTTTAG | 81550 |
rs546280281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477649 | TAGTTTTTGTTGTTA[A/C]TTCTGTTTATGTGGT | 81550 |
rs546285728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531225 | CCACTTCCTGGCTAT[C/T]AGGAAGACTTGAAAA | 81550 |
rs546322688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544980 | TATATTCCTGGTGGT[C/T]ACCTTTATTACTGAA | 81550 |
rs546341021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418993 | AGTTTTTGGTTATTA[G/T]GAATAAGGCTTGGAG | 81550 |
rs546341750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478373 | GCAGTGATGCAATCT[C/T]GGCTCACTGCAGCCT | 81550 |
rs546374809 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552734 | TACATCCTCTGAAAT[A/C]TAAGTGGAGGCTCCC | 81550 |
rs546381682 | snp | A/G | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502777 | CCAGTTCTCTCCATG[A/G]GAATTTTATTGTCTC | 81550 |
rs546397117 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396981 | CGCCACACTTTTGCT[C/G]TACGAAGAACCTCCT | 81550 |
rs546399824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556166 | TATTTCTTTTAACCT[A/G]TTATTCCATTGCTAA | 81550 |
rs546402523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419637 | GGCCTGTTGTGGGGG[C/T]GGGGGGCAAAGGGAG | 81550 |
rs546405832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499038 | CCCTCACACTGGCTC[C/T]CTGACTGGTAGGGTG | 81550 |
rs546411335 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509572 | CAGAGAATACTCAAG[C/G]CACAACCCCACATAT | 81550 |
rs546424381 | in-del | -/AT | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551969 | GGTCTCTCCCTCGAC[-/AT]GTGGGGATTACGATT | 81550 |
rs546451523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537642 | AACTGTAACTGATAA[A/G]TCATACTAGAAAAAT | 81550 |
rs546463317 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454908 | ATCCCACCTCTATTG[A/C]TTGATTGGTTGATTG | 81550 |
rs546475726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462972 | AAATCCACATACTTA[C/T]AGCCAACTCACTTTC | 81550 |
rs546495766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410462 | GTTAGGACATAAAGC[A/T]TGTAAAATGGGCTCC | 81550 |
rs546527367 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426596 | ATTCTAAAAACCTAT[A/T]TGAAATGGGTAGTTT | 81550 |
rs546531487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418385 | AGGTCCTTTAACATT[C/T]TGTCTCTAGCTCATT | 81550 |
rs546539050 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451767 | TGAGCCATATCTTTT[A/G]TGGCACTTGATCAAA | 81550 |
rs546548364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509137 | TCAAGAAATTTCTTC[A/G]TAGGATATGTTTATA | 81550 |
rs546574239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482403 | ACAGTTGTTTCTTAC[A/G]CATTGTTAAGATTGT | 81550 |
rs546574324 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518542 | AAACTGGTGAGTGAA[A/G]AACACCTTGTCCTGC | 81550 |
rs546581855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508027 | TGCCATTCACAATTG[C/T]TACAAAGAGAATACC | 81550 |
rs546623778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483660 | ATGGAAGGCCTTTTT[C/T]TTTCCTATTTCTTAT | 81550 |
rs546660941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526827 | AATGGATTTTTTTGG[A/G]CCACTTTGAGTCTTT | 81550 |
rs546663810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441209 | TTGCTTAAAAATATT[A/G]TAAAGGACTCTTCTT | 81550 |
rs546689943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417183 | CACCCCACATGGCCA[A/G]TTTTTTATTTTAGTA | 81550 |
rs546780184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400653 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 81550 |
rs546797070 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452181 | CTGGGTATATCTCTT[C/T]CTTTATTTTTCCCAT | 81550 |
rs546832438 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528185 | TGACTAAGAAAACTG[C/T]ACATTAGAAATGCAG | 81550 |
rs546850748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434076 | GACTTCTGAACACGA[C/T]GTGAAGACAGTTAAG | 81550 |
rs546860067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519384 | TAAAGCAAAAATAAC[A/G]TAAGGTTATTTCTAA | 81550 |
rs546860224 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455155 | TGACCTCAGGTGATC[C/T]GCCCACCTCAGCCTC | 81550 |
rs546871898 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546204 | TCATAAATGGAAAGA[C/G]TTTTAGAGACTGACT | 81550 |
rs546883028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484108 | ACTAATTAAAATAGG[A/G]TGGGAGAGGGTTTTT | 81550 |
rs546885796 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516114 | ATATATTTAGGGTTT[-/A]AAAAGTTTGTTTTTC | 81550 |
rs546923004 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526013 | AATCAAATTCTGCCA[A/C]ATCTGCCAAGCCTGG | 81550 |
rs546950669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474091 | GTTCCACCCTGTACA[A/C]CTGGCTCCACCTTTT | 81550 |
rs546972604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424777 | AGAACATTTAACCCG[A/G]TATGCATTGGCATCA | 81550 |
rs546977803 | in-del | -/TT | 0.00517822 | 0.0506191 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60573620 | TTTTAAAGTAGACTC[-/TT]TGTGAAGAAACGAGC | 81550 |
rs546983879 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434130 | ATCTCATAAATAGAA[A/G]CATTTACTAAAGGAA | 81550 |
rs546989916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407485 | TGCAGGAAATAGCCT[C/G]TTATAGAAAGCTTTC | 81550 |
rs547004498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408054 | GTGCCTTTCACGTCC[C/T]GCCATGATTCTGAGG | 81550 |
rs547025235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457468 | GTAGAAGTGCCAATC[C/T]GGTGAGGAGGCTGAA | 81550 |
rs547035994 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465097 | AAAAATAAAAATTTA[G/T]CCCCTAATTCCTTTT | 81550 |
rs547052427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464599 | ATACACACACACACA[C/T]ATACACTGGAATATT | 81550 |
rs547060905 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490520 | CTATTGTAAAGACAT[G/T]GTACTTCATTCAAGG | 81550 |
rs547072822 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457619 | AGTAGTTATCTGAGG[A/C]TGCTGTAACAAATTA | 81550 |
rs547087025 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396229 | GTCTTCTTCCCCTGA[C/G]CTGGCAGATGGGGAC | 81550 |
rs547091466 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432113 | AAACAAAATAAAAGA[C/G]CTCTTTTTTCATTTT | 81550 |
rs547145609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524848 | TCACACCTGTAATCC[A/G]AGCACTTTGGGAGGC | 81550 |
rs547154544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424383 | AATTCACCTCTTTAA[A/G]GTGTACAGTTCTGGC | 81550 |
rs547180645 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552145 | TTAAAATTCCAAGTC[A/G]AAAGTCTCATCTGAG | 81550 |
rs547185581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567882 | GCATCCACCACCATG[C/T]CCAGCTGATTTTTTT | 81550 |
rs547203119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415415 | CATCAGAATCTTTAC[A/G]CTTCAGCCAACCACT | 81550 |
rs547214313 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551786 | AGGAAACTTACAATA[C/T]GGTAAAAGGTGAAGG | 81550 |
rs547239960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60439963 | TATTAATATCTGTTA[C/T]ACAGAATCCAATGAA | 81550 |
rs547240697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451276 | TTACACACAAAAAAG[A/C]GGGACCTGTGGAGAA | 81550 |
rs547295830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567083 | TGGCTCTTCAACCCC[C/T]TTTCTTTATTCTACC | 81550 |
rs547341264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565334 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 81550 |
rs547341822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458855 | GGCTAAAAATATGGG[A/C]TACCAAAATAAACAG | 81550 |
rs547353069 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493139 | TAGCCAAGATGGTCT[C/T]GATCTCCTGACCTCG | 81550 |
rs547360598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418672 | AGTTGTGTACGTTTA[A/G]GTAACCCCCATTCTA | 81550 |
rs547405121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504488 | TAGCAAACCTAGTAT[C/T]TGACTTGTATGATTT | 81550 |
rs547411586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549601 | GCACGTGTATGTGCA[C/T]GTGGACAAACGTGAG | 81550 |
rs547412063 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429971 | TACTGTATTCCAAGC[A/G]TATGCTAGGTATTAC | 81550 |
rs547430364 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563661 | GCAGATAGCTCTCAC[-/T]TTGAGAACTCTTTCC | 81550 |
rs547432306 | in-del | -/A | 0.188629 | 0.24235 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471543 | TTTTCTATTTCTGCA[-/A]AAAAAAAAAATCATT | 81550 |
rs547474057 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523961 | CATTTCTACTTGTGC[-/T]TTTTTTTTTCCACCT | 81550 |
rs547484577 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497899 | TGTGGGATAATGGTG[C/G]AAGCAACATTGAGTT | 81550 |
rs547484761 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555856 | CCTATTTCTTTCTTT[C/T]TTTTTTTTTTTTGAG | 81550 |
rs547486000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516755 | GCAGCAGATGCAACA[A/G]CATCCTCCACTCACC | 81550 |
rs547492686 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540782 | ACTATATGTAAAAAC[A/G]TATTTAAAAGGTTTC | 81550 |
rs547521321 | snp | C/G | 0.00612552 | 0.0550021 | utr-variant-5-prime, intron-variant | TDRD3 | GRCh38.p7 | 13:60397339 | CCCACCCCAGCCCCC[C/G]ACCACCCCCGGCCTA | 81550 |
rs547521357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548738 | GGAAAAAATGAAATC[A/C]TAATACTTACGCTGG | 81550 |
rs547563211 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445721 | GAAAAGTAGGCAACA[A/G]TCTTGACTAGGTGTG | 81550 |
rs547587711 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401168 | TAAGGTTTAAGAATA[C/T]AGTTGGCCCTCCATA | 81550 |
rs547601209 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407782 | CTTTTCTTTTTGATA[C/T]TTCAGAATTGCTTAC | 81550 |
rs547622949 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451423 | GCTTGCCGTGTGCTG[A/G]ATCCAGCTTGTTCCA | 81550 |
rs547630740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572060 | AGTCCAACCAAAACT[C/T]TGTGCGTTTGGAGAG | 81550 |
rs547632431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542751 | TCTTACTTTTATCGT[C/G]TTATGAGTCATCTCT | 81550 |
rs547642914 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526254 | GACCTTAGTTTACCT[A/C]TCTCTGTTAAGCCTC | 81550 |
rs547654478 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566522 | AAGATAAAGTAAGGA[A/G]GAGAAAAAATAGGAT | 81550 |
rs547660045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449229 | AAAATAATATGTTTC[C/G]TATATGTTAGTCTGT | 81550 |
rs547663247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60437738 | CATTACATACTATTT[C/T]CCTCTTGTGTAGGAG | 81550 |
rs547665057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429336 | TTGTCTTAACTGCCT[A/G]TGATAATTGAAGTAG | 81550 |
rs547709167 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550875 | TTGAACACTCAACTT[G/T]GTACCAGACATTATT | 81550 |
rs547713358 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445880 | AAAAGATGCTGAGAA[C/T]TCACCTCTGCTACAA | 81550 |
rs547727945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430217 | TTTTGTAATACCTTA[C/T]ATTTATAAATAGCAT | 81550 |
rs547731304 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531724 | TATATTCTCTCTGCC[A/G]GTAGAAAATGTAACT | 81550 |
rs547746138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551654 | TTCTTTTCTGTTTCA[A/G]TGTGTATTAGTCCGT | 81550 |
rs547750151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542096 | GCTGGAATTGTTCAG[A/G]TGATCTTATTTTTCC | 81550 |
rs547764892 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522166 | AAACAGTATTAGAGT[A/T]TGATTTTGATTTTCT | 81550 |
rs547781240 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525393 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 81550 |
rs547792714 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432739 | AAAAATATCCTTTAA[A/T]AGAAGTTATTTTTTA | 81550 |
rs547822004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486888 | GATTATGTCACTTAA[C/T]GTAATGTCCTTCAGG | 81550 |
rs547863536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477179 | AGTATGATGTTGGCT[A/C]TACGTTTGTTATAGA | 81550 |
rs547874047 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446930 | CCGTTACTTACTAAC[A/G]TTATGTAAGTTATAG | 81550 |
rs547874480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505452 | CAGCCAGGGGATTAT[A/G]GATAAAACTCCCATG | 81550 |
rs547892004 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411200 | CAATTAAAAGACACT[C/G]TCATATAATTAGATG | 81550 |
rs547902734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502058 | CGCAAGTGTTGTGTA[G/T]TACATAATTTCCATC | 81550 |
rs547904998 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60513465 | ATGGGATTTTCTTTT[C/G]TATCACATTGTCAGT | 81550 |
rs547930926 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410843 | TGACTGCCTTTTCTG[A/G]TTGTGGATTTTTTGC | 81550 |
rs547935103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538497 | TATTAACTGGATAAA[C/T]GCTCTTATTTATCTC | 81550 |
rs547948228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485264 | TTTTTAGGCAGTGAT[A/G]CCTTTTTTTTTACTT | 81550 |
rs547955197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479910 | ACTTGTGAGATGGGT[C/G]CCTTGGAGACAGCAA | 81550 |
rs547974854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515726 | ACAAAAACAGTTGAG[A/G]CAAGCTACTGAATTG | 81550 |
rs547979764 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486992 | AGTCAGCTCTCCATA[A/T]TTGTGGATTCAACTC | 81550 |
rs547982990 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396685 | GGCATTTTCACTGTG[A/G]TGTCCGACTGGGGCA | 81550 |
rs547984472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414413 | AGTAGTTGTGACAGA[A/C]ATCAAATATTGTAGG | 81550 |
rs547989193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554748 | GCTTCATCCTTGAAC[A/G]AGAAGAATATAACAC | 81550 |
rs547993966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524091 | CTGTGCTGTCCATTG[C/G]TATCTAATGTAGTTT | 81550 |
rs547993975 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60472282 | CTGGTTTTTCATTGA[C/T]GATAGATTACTTTTT | 81550 |
rs548016923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533512 | CAGGTGTAGTAGCAC[A/G]TGCCTGTAATCCCAG | 81550 |
rs548041109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500043 | GAGCCTTTCGCAGGC[C/T]GCCATAGGTGAATCA | 81550 |
rs548050176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522716 | TTCTGCGTTAATAGA[A/C]AGAGATTATTAATTT | 81550 |
rs548050663 | in-del | -/AAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440231 | AAAACAGAAAAGCAA[-/AAT]AAGAAAATTAAATCT | 81550 |
rs548051140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563058 | ACATGATGAAACCCC[A/G]TCTCTACAAAACTAC | 81550 |
rs548069063 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557270 | TTCTAGTGAAGGATG[C/G]AAACCAATGGAGTTG | 81550 |
rs548100572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501594 | AAACTTTCCTACTTG[C/T]CCTAAACATCCTTCT | 81550 |
rs548113246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532330 | TTAGATGTGTACTTT[C/G]AGTTGTAGTGAGGAA | 81550 |
rs548120312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455279 | TTGACAGAGAAAGTA[G/T]GTAAAAAAGAGGTCG | 81550 |
rs548162995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428394 | TGGGGGATGTAGTCA[A/C]ATTATGTTTTCTAAG | 81550 |
rs548211164 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460850 | TCTCTACAAAATACA[A/G]GAATTAGCCAGGCAT | 81550 |
rs548217335 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418420 | TATAATTGTTTATAT[A/G]TTTGTCTCCTCAAGT | 81550 |
rs548218528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477939 | ATGGAACAGTTTCGG[C/T]AGGATTGGTATCAGT | 81550 |
rs548256188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469551 | AGTATTTCTTGTTAG[A/G]GAGTGATAAAAATTT | 81550 |
rs548262558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568728 | AACATAGTTGAATAA[A/G]ATAGAAGTACTAGCT | 81550 |
rs548273933 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481255 | TGGTTTTCAGTGAAC[C/T]TTTTTGATCTATGAG | 81550 |
rs548282396 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60414886 | GACAACAGACAGTGG[-/T]TTTTTTTTTTCTGTT | 81550 |
rs548295356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468775 | CTCTGAACTTTACAT[A/G]TAATAGATGTTATAA | 81550 |
rs548297225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460109 | TATAACTGTTTTCCT[A/C]GGGTTTTCTTTTCTC | 81550 |
rs548312392 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463363 | CAAAATTCTGGCTCA[-/A]AAAAAAAAAAAAAAA | 81550 |
rs548327585 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564152 | TGATAACATGGGTGA[A/G]GTAAGCAAAAGTCTT | 81550 |
rs548346322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427627 | TCCTGGTTTACCCAC[C/T]ATCCTTTTCTGTATA | 81550 |
rs548370535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491873 | GAAGTGAGGAGAATG[A/T]GTAAAATAGTGGTCT | 81550 |
rs548373677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505147 | AGTAGTCTAGCTCAG[C/T]GGATCCCACCCCCAC | 81550 |
rs548378038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418284 | TTCTCCATTTAAGTT[A/T]GTTAATTATTGTCCA | 81550 |
rs548383778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509375 | CATTTTTGGAGAGGT[G/T]CTGTATGAATTACAT | 81550 |
rs548396766 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565284 | ATGGTCTTGATCTCC[A/T]GACCTCGTGATCCGC | 81550 |
rs548403723 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60531826 | AAAAGTTATGAGCCA[C/T]AGTTAAAAAAAACAA | 81550 |
rs548438308 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463213 | ACTAGCTGGGCGAAC[A/C/G]TGGTGAAACATGGTG | 81550 |
rs548466885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470283 | TTATCCATCAATGGA[C/T]ATTAGGGTTGTTTTC | 81550 |
rs548467500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541093 | ATTAAAAATATTAAA[C/T]ATTAGGTTAGCATAA | 81550 |
rs548547729 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500938 | TTATATTCCAATGTG[C/T]CCATGAACAAAGTGG | 81550 |
rs548562490 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410290 | ATTTCATGCTAGGGC[A/C]TTTAATGAGGCAAAG | 81550 |
rs548564444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401498 | CTGAGGGATGACTGT[A/C]TCTGAAAAAGTGGGA | 81550 |
rs548592051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552576 | GTGGCCCTTCTCTCA[C/T]AGCTTCACTAGGCAG | 81550 |
rs548605810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443169 | GGCTAACATTTATTG[A/C]GTGCTTACTCTGTGC | 81550 |
rs548635865 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478983 | TGATTTTTTTTTTGT[A/G]TTTTTAGTAGACAGG | 81550 |
rs548637237 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395080 | AGTGATGTGTATGTC[C/T]AGTTGCATTACATCA | 81550 |
rs548648043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567942 | GGGTTTCACCATGTT[A/G]GCCAGGCTGGTCTTG | 81550 |
rs548668739 | snp | G/T | 1.65405e-05 | 0.00287576 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528725 | TTTTAAAAAAAGAGA[G/T]AACTCTATGCAAAGC | 81550 |
rs548704126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400563 | AAAATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 81550 |
rs548707624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521247 | CTTAGCTAAGCCCAG[A/G]TAATGGTGTTAAACA | 81550 |
rs548710822 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418919 | TATTGTTGAGTAGTA[A/G/T]TTCCTGTTTGAGTAT | 81550 |
rs548731625 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444324 | AAAAACATACTATGT[A/G]TATGTATTCAAAAGC | 81550 |
rs548747643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409354 | TGTGAGAAGAAGGCC[A/G]CTGTCCTCCAGACTT | 81550 |
rs548748290 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484405 | GATGCCATCAAAATT[C/T]AGCGGTTGGTAATCT | 81550 |
rs548845743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441848 | GAAGCCCTCTGAAGA[C/T]TAATACCCAAGGCCT | 81550 |
rs548863019 | snp | G/T | 0.114387 | 0.210022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561864 | ATGGGCCCAGGTTTT[G/T]TGTTGTTGTTGTTGT | 81550 |
rs548870268 | in-del | -/TT | 0.00690705 | 0.0583594 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510803 | TCTTTCTTTTCTTTC[-/TT]TTTTTTTTTTTTTAG | 81550 |
rs548874025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433761 | TGCTTTACTAGTCCT[C/T]GTGCAGACATGGCTG | 81550 |
rs548875990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425797 | CTCAACATGAAGACA[A/G]TGAGGATGAAGACCT | 81550 |
rs548892275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483605 | TTGCCTAATTATTGA[A/G]GTTAAGAATAATATA | 81550 |
rs548897667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507419 | CACTATGTCATACTT[C/T]AAAATTGACCACATA | 81550 |
rs548898925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553409 | CTGTTGTATCCTCCG[C/T]CTGTTACCCAGTTCC | 81550 |
rs548935709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545808 | GACATATCAAGGGGT[C/T]GAGAGTATTGGTACT | 81550 |
rs548946385 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525097 | CTCTCAAAAAAAAAA[A/C]AAAAAAAAAAAACCC | 81550 |
rs548951197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475402 | CCTCCAGATGCATCC[A/G]TATTGCTGCAAAGGA | 81550 |
rs548961279 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511620 | CTAGGCACAGCTTCA[C/T]TGGGGCCTCTGTTTA | 81550 |
rs549049481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536232 | AGTAATAATGTTTTG[A/G]GCCATGGATCTTTAT | 81550 |
rs549055589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450511 | TATTTAGTAAATACA[A/G]ATAATCCTAGGGTAC | 81550 |
rs549061515 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60573496 | AAAATTCTAGTTAAG[A/G]TCTATTTATACAAAC | 81550 |
rs549071701 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559563 | TTTATAGTAGCTTCA[C/T]GGCTGAAGCCATCCG | 81550 |
rs549087673 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534079 | ACTTTGGGAGGCCAA[C/G]TAGAGAAGATCACTT | 81550 |
rs549128224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407261 | AAGCATTTAGCACGA[C/T]GTAAGGTGCACAGTA | 81550 |
rs549177462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559280 | TGCCTATGATGTGGT[A/G]GAATCTAAACCCAGA | 81550 |
rs549178806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528067 | TTAATGTTTTAGGAA[A/G]TGATTTACCAGAATA | 81550 |
rs549233709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482770 | ACTCTTAATTATCTT[C/T]ATAAAATATACAGTG | 81550 |
rs549272943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490691 | AGTAATCTAGGATTT[A/T]AAAAAAAATGATGAT | 81550 |
rs549273013 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455341 | GCTTTTAAAGCAGCT[A/G]TAGGCAGAATTAGTA | 81550 |
rs549299148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425162 | GTCATCTTTGAAACA[G/T]AATACATTAAAAATA | 81550 |
rs549341119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512398 | GCCCCTCCCAAATAT[C/T]ATGTCCTCACATTTC | 81550 |
rs549361806 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520503 | GGGCTCACCTAAACC[C/G]CATTTCTCCACAGAC | 81550 |
rs549394379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424311 | CAGGCGTGAGCCACC[A/G]CCCCCAGACAGTGGT | 81550 |
rs549403806 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60435943 | TTTTACTTTTTAATT[A/G]TGGCCTTTCTTAGAG | 81550 |
rs549411408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542051 | ATATTCTTAAGGAAG[C/G]ATCATCGGTGAGAGC | 81550 |
rs549413993 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405228 | CCTGTCCCGGCCTCC[C/T]AGAGTCCTGGGATTA | 81550 |
rs549431518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488300 | GGATGTGGTGATCTG[A/G]TTAATTTTAGTTCTT | 81550 |
rs549464703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431228 | GAAACCTTTAAGCTA[A/G]TTTAGTATCTCTTCA | 81550 |
rs549485583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471972 | GGAAACACCTTCAGT[C/T]CTTCACTATTGAATA | 81550 |
rs549529667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566076 | TCAGTGATGATAGGC[C/T]CCTCAGGATGATCAT | 81550 |
rs549576647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399866 | ATGTGATCTTCAGGG[A/G]GGTACAGAAGATCTA | 81550 |
rs549579368 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524336 | ATATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 81550 |
rs549586875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458229 | CTATTCCTGCCCTGT[A/G]TTTGCATCAATGGCA | 81550 |
rs549613239 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473800 | CAAGGCCACTAGAGG[A/G]CTCCCTGGGCTAGCA | 81550 |
rs549653731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422268 | AACTACACAGGTGGA[A/G]GATTCATAATATGCC | 81550 |
rs549656312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473988 | TGAAAGGCCTGACTG[A/C]TGGCAGGCTTGTCCT | 81550 |
rs549717354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466467 | CAAGTGAAGACTAAA[C/G]CTCATTTCTTTGTCA | 81550 |
rs549741874 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449149 | CTCTTGCCCTTGGAT[A/C]GTCTAGAAATCGGAT | 81550 |
rs549742239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516668 | ACCTATTGTAGGGCT[A/T]CAAGGTCGTTGGGAA | 81550 |
rs549751156 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509582 | TCAAGGCACAACCCC[A/G]CATATCATACAGATT | 81550 |
rs549759712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404556 | ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 81550 |
rs549764829 | in-del | -/TCTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501967 | TAGCAATGGAAACTC[-/TCTG]TCTGATATTCCAGTT | 81550 |
rs549770869 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509859 | AACAACTTAGAAGCA[C/G]CACTGAACGTACTTC | 81550 |
rs549791308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464490 | CACAATACCCACGAT[A/G]TGGAATCAACCTAAG | 81550 |
rs549804930 | in-del | -/T | 0.0252325 | 0.109451 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541920 | TTAGTAGAGACAGGG[-/T]TTCTCCATGTTGGTC | 81550 |
rs549808802 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60531636 | ATCATACCCTGGGTA[A/G]TAACTGCAAAATTAA | 81550 |
rs549816835 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60510063 | CCAGTTTGGGAACCA[C/T]AGAGACATTTGTAGT | 81550 |
rs549830191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421781 | CAATCTTGTCCCACT[C/T]GTGGGGCTTTGGTGA | 81550 |
rs549851645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60562709 | TGCTGATGTATGTAT[C/T]GTGACTACTATACAA | 81550 |
rs549869785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532208 | GCATCTAAAAAACAG[C/T]ACCTAACAATTCAGT | 81550 |
rs549869975 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552286 | AGAAATCAGCCAAAA[C/T]AAAGGGGCCACAGGC | 81550 |
rs549890611 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554720 | GCTACAGCTGAATGG[A/C]AAAGGAGAAATAGCT | 81550 |
rs549917529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493712 | ACCAAATGTTTCATA[C/T]TGTACAGGTAACAAC | 81550 |
rs549921596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547772 | AAACAGTTAAGTATT[A/C]TAAGAATGTAAAACC | 81550 |
rs550002835 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543530 | TATTATACAATGTCT[A/G]CAGGAAATACTTGGA | 81550 |
rs550014495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550712 | AGCTAGTTTCGCATT[C/T]TGTGTTAGGTTAACT | 81550 |
rs550040535 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396036 | AAAAATCTGTATTAA[C/G]GAATTTTAGCTCCAC | 81550 |
rs550057868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436174 | TCTAGTCCTTTTTGC[A/G]TAGTTTGCAAATATT | 81550 |
rs550063784 | in-del | -/TTTAC | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555440 | AAACAAATATTAATG[-/TTTAC]TTTACACACTAGGAA | 81550 |
rs550082691 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398132 | TGCGAAATTAGGCAG[C/T]TTCTGGAATTGCGGC | 81550 |
rs550135606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538291 | GCCAAAATTGTGTTT[C/T]GATTATGATTAAATT | 81550 |
rs550163286 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540063 | CCTATGTGACCCTAG[C/T]CCAGAAGATTTTTCA | 81550 |
rs550205241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462556 | GTGAAACAACTCTCT[A/G]GATGGGATAAACCAG | 81550 |
rs550208777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429222 | TATTGTGCTTTTTAT[A/G]TGCCTCTTTCATTTT | 81550 |
rs550208841 | in-del | -/AATGTTTAGAATTTCTAAACCATGAA | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436354 | TCCGAAGAGTTTTCC[-/AATGTTTAGAATTTCTAAACCATGAA]AATGTTTAGAATTTT | 81550 |
rs550272528 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449496 | GTGGAAATTGTCAAA[C/T]GATACACTGGGAAAA | 81550 |
rs550280822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403510 | GGAAGAAGAATACTG[A/G]ATGCCCAGAAATTTT | 81550 |
rs550298969 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537688 | CTGCAGGGAAATGGT[G/T]AGAGAGGCCTTAGCA | 81550 |
rs550335102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486807 | ACTATGCTGCTCTTC[A/T]ATGAGACAACTTTTT | 81550 |
rs550355132 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545668 | TTTTTTTCTCAAGGT[G/T]ATCAGATAATATAAA | 81550 |
rs550362175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561993 | CTCCCATGGGCACCA[A/G]GGTTGTCTGTAATCT | 81550 |
rs550377226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531632 | AAAGATCATACCCTG[A/G]GTAGTAACTGCAAAA | 81550 |
rs550377487 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491729 | ATAAAGTATGACCAT[G/T]CATTTACCAACAGTG | 81550 |
rs550400708 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548608 | ACTTATGCTCAATAT[A/G]GTTTCTTGCTGAAGT | 81550 |
rs550412256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434208 | GGTGTGGTGGCTCAT[A/G]CCTGCAATCCTAGCA | 81550 |
rs550446735 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415678 | TATGCAAATAAAATT[C/G]CTTTCTTTTCTCAAA | 81550 |
rs550465708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569594 | AAATTTATATGGAAC[C/T]ACAAAAGTCCCAGAA | 81550 |
rs550468297 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441197 | TAGTTAATTCTATTG[C/T]TTAAAAATATTATAA | 81550 |
rs550491995 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514347 | AAAACACATGATAAA[A/C/G]GTTTGGAAAATTTAT | 81550 |
rs550493130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540594 | ATAGCTAAGCCTAAC[A/G]GAATATTATGAAAAA | 81550 |
rs550493968 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60479524 | GTCCAATTGATTGGG[C/T]GTTGAGTTTCAGTCC | 81550 |
rs550510159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419785 | GCACATGTATCCCAG[A/T]ACTTAAAGTAAAATA | 81550 |
rs550545358 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461728 | CTAATTAAGTAGGCA[C/T]GTAGGCATACAAATA | 81550 |
rs550602542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522057 | TTTTACTTTTTAAAT[A/G]TTTCTTAGCATTTTT | 81550 |
rs550608185 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423956 | GAATAGAAAAACAGT[A/C]AATCTAGCAAATAAG | 81550 |
rs550613631 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532192 | TTCAAAATGTCATGT[A/G]GCATCTAAAAAACAG | 81550 |
rs550624465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483447 | TAGCTTTATGCTTTA[A/G]AATGGAATTCTGTTA | 81550 |
rs550656694 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417314 | AGCCATTGTACTTGA[C/T]CCAGTCTCATTTGCT | 81550 |
rs550741586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522705 | AGTTTAGGTTTTTCT[A/G]CGTTAATAGAAAGAG | 81550 |
rs550774600 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469506 | TGTTTAATTATATGT[C/G]TCTGCACTTGACTTC | 81550 |
rs550783436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425134 | TATGTAAAATAAGAA[A/G]TAACAAAGAGAAGTC | 81550 |
rs550784856 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507781 | TGGCCAGGGCATTCA[A/G]GCAACAGAAAGAAAT | 81550 |
rs550835385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470133 | GTGGAATCATACAGT[A/G]TATATCTTTTTTGTG | 81550 |
rs550846686 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568620 | TATATGACAAACCCA[C/T]AGCTAGACTCATACT | 81550 |
rs550859987 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476934 | CTGAATTTGTTTATC[A/G]GCTCTAGAAGCCTTC | 81550 |
rs550907888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553326 | CATTTTGGTCAACAC[C/T]ATTCAACAAGTCTCT | 81550 |
rs550911946 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542082 | CACAACTGAACGGGG[C/T]TGGAATTGTTCAGGT | 81550 |
rs550946757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459872 | GTAATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 81550 |
rs550952125 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418021 | AAATCTGTCTTTTCT[A/G]TAGGTGTTAGAATGA | 81550 |
rs550996792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567924 | GTATTTTTAGTAGCA[A/G]TGGGGTTTCACCATG | 81550 |
rs551015043 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457528 | TAGGCTAGATCTCAA[A/G]AGGAAGATGAGTGAG | 81550 |
rs551026058 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451499 | ATAACCTCCAGTTGA[C/T]GGTTGTGGTTGGCCA | 81550 |
rs551054609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519432 | AGTCTAGTGCCTCGT[A/T]TATAAATACCTGTTT | 81550 |
rs551083612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399783 | TATTGTTAAATCTGT[A/T]CTATAGGCTTCACCT | 81550 |
rs551097255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527778 | ACTCTTAATTACTTT[A/G]ACAGATCAAGAAAAT | 81550 |
rs551101873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425681 | ACAGTACGGATTTGA[A/G]CTGTGTGAGTTCACT | 81550 |
rs551107956 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60540021 | AGTGTGGTTTTGCCA[A/G]TTAGTATTTAGTAAA | 81550 |
rs551127505 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425143 | TAAGAAATAACAAAG[A/G]GAAGTCATCTTTGAA | 81550 |
rs551148917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402117 | TCCACAGATGAAGGG[A/C]TTCTTTTCACATTCC | 81550 |
rs551166059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482596 | TAGTCTTTGTTTAAT[A/G]TTTAAATTAAGGAAA | 81550 |
rs551216865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407216 | CTTCTGTAAGGGAAA[A/G]ATCAAGTCTTCATAT | 81550 |
rs551228575 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60442044 | TGTAAGCTGGCCTTT[C/T]TAAAGATAGCTGCCT | 81550 |
rs551257741 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60413028 | TGGTATTCCCTGCAG[C/T]ATCCCTGTACTCCCA | 81550 |
rs551260621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440003 | AATGAAATTAACATC[C/T]CTTTTTTTCACCCAC | 81550 |
rs551261764 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432891 | TTGGATATCATGTGC[C/G]GGGGCTAGTAACCTC | 81550 |
rs551268507 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513475 | CTTTTCTATCACATT[G/T]TCAGTCTGCAAATTT | 81550 |
rs551276094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489610 | ACCTACTTCATATGT[A/G]AGAATTAAAACATTT | 81550 |
rs551285755 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560410 | TATCATTTGGAATTT[A/C]ATAAGGGTGACTTCT | 81550 |
rs551318114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452483 | ATATTCTTACATTAT[G/T]CTGTATATTCTTTTG | 81550 |
rs551322551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560951 | GCATTTTTTTCTCTT[C/T]TGCCATAAAATGTTT | 81550 |
rs551340275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532509 | AGTGTTTTTTAGGCA[A/G]AGACAAGGGTAGACA | 81550 |
rs551347165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504557 | CCATCCTTAAGACAT[G/T]TTGTTTCTTAAATAT | 81550 |
rs551353376 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462532 | GTTTATAGTTATCTT[A/G]GAAGGAAGGTGAAAC | 81550 |
rs551429201 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544093 | TAGTCTAAGCCAAAA[C/G]CTGAAATTCCTTTTT | 81550 |
rs551488499 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422873 | AACCAAAACAATTGA[A/G]AAGAGCTGATATCTA | 81550 |
rs551500186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541401 | TGAACTCCTGACCTC[A/C]GGTGATCCGCCTGCT | 81550 |
rs551518688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415506 | TGTAAGCAATAATAG[G/T]CAAATGCCATTATTG | 81550 |
rs551538745 | snp | C/G | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511674 | ATTTTGGTTGGAGCG[C/G]TGATGTTATCAGAGA | 81550 |
rs551562057 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406376 | ACAGTACTAAAAATG[A/C]GTGTAAGGATCTCAG | 81550 |
rs551608110 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565615 | GTGTATTTTATTAAT[-/A]AAATACAGATTTTTA | 81550 |
rs551623639 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550601 | GAAGAAAAATGAACA[G/T]TTTGTGAATGACAAG | 81550 |
rs551647013 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401355 | GTAGTCTAGAGATGA[C/T]TTCAGGTATGCAGGA | 81550 |
rs551665914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432327 | ATTGATTTTATTTTT[A/G]ACAGGTTATCTGAAG | 81550 |
rs551704347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423486 | GATAAGAGAAAATAC[G/T]CATTTTCTTAAGTGC | 81550 |
rs551723746 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430398 | CCTTTTGAACTGATA[C/T]ATGGTTTTATAGCCA | 81550 |
rs551731367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478880 | GCAATCTTGGCTCAC[A/T]GCAACCTCTGCTTCT | 81550 |
rs551743398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515032 | AAGCTCACTGTCTAG[C/T]GTGTGAGACAGAAGA | 81550 |
rs551750671 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524417 | GAGGCTGAGGCAGGA[G/T]AATCACTTGAACCCG | 81550 |
rs551773122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431041 | TAGATGTAGAAGAGA[C/T]GGGAAGAGAAAATTG | 81550 |
rs551823143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486720 | CTTATTCCTCCTAAC[G/T]GTAATTTAATTCCCA | 81550 |
rs551840631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412312 | GAATTGGTGTGAGTA[A/C]ATGAGGCTCTATTTT | 81550 |
rs551862833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470378 | AGCTTTCAATTCTTT[C/T]GTGTGATCTAGAAGT | 81550 |
rs551865216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60437908 | CTAGGATATTATTCC[C/T]AGAAGGTGCTTCACA | 81550 |
rs551877276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60495680 | ATATTAGTGAAACTG[G/T]TCTCGAACTCCTGAC | 81550 |
rs551891835 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60547197 | AAAGTATAACCAAAA[A/C]AAATCTCATGACATT | 81550 |
rs551906273 | snp | A/T | 1.70787e-05 | 0.00292217 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509690 | TTTTAGTTAAAAGAC[A/T]GTAAGTAGTTAAAAG | 81550 |
rs551924180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60573255 | GGAGGCGGTTAGGAT[A/G]GGGAAAGACGTGGTT | 81550 |
rs551925784 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462671 | TGCCCCTTGCTAGTT[A/T]TTATTATTATTATTA | 81550 |
rs551925959 | in-del | -/TTTG | 0.00755907 | 0.0610114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401680 | TACTCCAGGTTTTGT[-/TTTG]TTTGTTTGTTTTGAG | 81550 |
rs551946465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530992 | GATGTTGCCTGATGA[C/T]AGAATAAGGAGGAGT | 81550 |
rs551947264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397422 | TAAGTGGCGAGTCCC[A/G]CCGGCTGCCGGGCCG | 81550 |
rs551971570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406140 | GATGTTAGGCATTAG[A/G]AAATACCAATCTTGC | 81550 |
rs551983005 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438174 | CATAATATTTATGAA[A/G]GTGAATTTATAAGAT | 81550 |
rs551984668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473144 | CCAGGGCCTTCCTGC[A/T]GCATCATAACATGGT | 81550 |
rs551997077 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497406 | CTTCTGTTTTTGCCT[A/G]ATTAGCATTTTAGTG | 81550 |
rs552021719 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516518 | TAATGAAAAGGACAG[A/T]GTACTGGAGCAGATA | 81550 |
rs552036464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502288 | TGCAAGAGATCACCA[C/T]TTGATTCACAGGAAT | 81550 |
rs552053070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524948 | AAAAATTAGCCAGAC[A/G]TGGTGGCAGGCGCCT | 81550 |
rs552081077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405108 | CTTTTGTAAATTGCC[C/T]GGTCTCAGGTATGTC | 81550 |
rs552137632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523479 | AACTCATATAGCATT[A/C]TTTGATTAGTTTTCT | 81550 |
rs552144270 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561616 | AATAAAAAAATATAA[A/G]TCTGCTCTGTTAGAT | 81550 |
rs552147008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475140 | AGGCTTCTTAACATG[A/G]GTAAATTGTGTGTCA | 81550 |
rs552154382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421470 | TACAATTCGAGATGA[G/T]ATTTGGGTGGGGACA | 81550 |
rs552178099 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454290 | ACTTGTTCCTATTGG[G/T]TTTAAAGTTTTGTAT | 81550 |
rs552188470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471133 | CTTTTCACTGTGTTG[C/G]TAGTGTCTTTTGATG | 81550 |
rs552196793 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410658 | GTAATAATGAGATTT[C/T]TCAGGATCGTTTTGA | 81550 |
rs552197974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516574 | TCACAGCTCTTGTAT[A/G]CTAGTTGTATGTCTT | 81550 |
rs552202636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460935 | TTGAACCTGGTAGGC[A/G]GAGGTTGCAGTGAGC | 81550 |
rs552222226 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60556315 | TCTTCTAACTTCCAC[C/T]CAGTTTGTAAAAATA | 81550 |
rs552245525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569480 | AGAAGAATCGATAGT[A/G]TTAAAATGACAGTAC | 81550 |
rs552267609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461571 | CAGCTCGGGCTCCTC[C/T]AAGCTTTTTCACTTA | 81550 |
rs552278978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428499 | ATTAATAGCAGAGGC[A/T]TGCAAAATTAATTTT | 81550 |
rs552295827 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443909 | TTTATGAGTACTGAC[A/G]GTTTTCCTGTGAACA | 81550 |
rs552303893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500896 | ATTCTGTGGACACCA[C/T]CTCAACCTCTGTTCC | 81550 |
rs552341199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485415 | ACATATGTATATTGT[A/G]GTATAATATGGAAAT | 81550 |
rs552346359 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559013 | AAGAATACCCTCACA[A/G]TAAGCTAAGTTCCTG | 81550 |
rs552348054 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531550 | AGCAGAAGTAAGAGA[C/T]TGGAATTCACGTTCA | 81550 |
rs552356945 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60528269 | GATTTTAGAATAGTA[A/G]TTTGATAATTTTGTA | 81550 |
rs552359566 | snp | A/G | 5.46363e-05 | 0.00522639 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485971 | ATCAAATCATTACAC[A/G]TTTTATTTCTTATCA | 81550 |
rs552401516 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463335 | CCATTGCGCTCCAGT[C/T]GGTGTGACAAGAGCA | 81550 |
rs552420699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561923 | ACAAATATTAAAGTG[A/G]AATTTTTTTAAACAA | 81550 |
rs552428185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456713 | ACTTTTTTTGAGACA[C/T]CTTTTTGTGTGTATG | 81550 |
rs552436630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447000 | ATACAGGACAACAGT[C/T]GGCAAACAGAATATT | 81550 |
rs552452124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455077 | TGCCACCACGCCCGG[A/C]TAATTTTGTATTTTT | 81550 |
rs552540049 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419799 | AACTTAAAGTAAAAT[-/A]AAAAAAAAAAGAATA | 81550 |
rs552557165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507496 | TAACAGTCTGTCAGA[A/C]CACAGTGCAATGAAA | 81550 |
rs552582447 | in-del | -/CTA | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541122 | AACTATTTGAAAAAT[-/CTA]CAGCATTCTTTTTGT | 81550 |
rs552592430 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469437 | ACACACACACACATA[C/T]ACACACACACACACA | 81550 |
rs552606936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435453 | AGTCCCCAAAGTCCA[C/T]TATATCACTCTATAT | 81550 |
rs552609452 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395920 | TATCTAAACAATATA[C/T]TTGGGAGCAAATCTC | 81550 |
rs552613895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521958 | CAAAACTGAATAATT[A/G]CTATATCTGGAAGTG | 81550 |
rs552620867 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492949 | TTTGAGACGGAGTCT[A/C]GCTGTATCTCCCAGG | 81550 |
rs552638994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432619 | AACAGTTTAGGCAGA[C/G]TGAACAGAGAGATCT | 81550 |
rs552646861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544341 | CCCAGCTACTGAGGA[A/G]TCTGAGATGGGAGGA | 81550 |
rs552676611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513600 | TCTTGAATTCCCACA[C/T]GTTGTGGGAGGCACT | 81550 |
rs552685576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535384 | TAAGATTTTAATTCA[A/G]TGCTTACACTGAATG | 81550 |
rs552694439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474679 | TACTTTACATTCGTT[A/G]CGAAGGTCACAACAC | 81550 |
rs552698357 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445209 | CATTTTGCAGTACAC[A/C]CATATGTATTCGTGT | 81550 |
rs552701767 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436076 | TTTTGAGAAATGTCT[A/G]TTTCCATCCTTTGCC | 81550 |
rs552716720 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468918 | AATCTTGCCTGTTTT[A/G]TAAAGTCAGCCAAAG | 81550 |
rs552720178 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417593 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGT | 81550 |
rs552726691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459215 | TCTATCATTTCACAT[G/T]TCTCTTTGCTGAAAA | 81550 |
rs552749829 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517987 | CCTGGTCTTTCACTA[C/T]AGTAAGTTTGAAATG | 81550 |
rs552776869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427824 | GCCTTTCAAAATAAT[A/G]TTTTTTATTTAATTA | 81550 |
rs552828237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567497 | GGAGCCATTTTGAAC[A/G]TGTAAAATCACTACT | 81550 |
rs552835224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445240 | TATGAATTTTTTTGC[A/G]TCAGCAAACTTTAAT | 81550 |
rs552848224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455865 | CTGAGGTCCAGAGTT[C/T]GAGACCAGCCTGGCC | 81550 |
rs552863193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501397 | CAGCCATTCCGATGG[A/G]TTGTAATACTGGTTT | 81550 |
rs552868722 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396506 | CGAAGGGCATCGGCG[A/G]GGAAGCGGCTGTGGT | 81550 |
rs552913536 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477879 | ATCAGGATGATGCTG[A/G]CTTTGTGCAAAGAAG | 81550 |
rs552922305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474244 | GTGGACACGTGACTC[A/G]CATGACCTTACCTAT | 81550 |
rs552944456 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538744 | AACGAATTCCAGGAA[A/G]CCAGTAAAAAGATGC | 81550 |
rs552957946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467527 | AGAAACTATCTTTGT[C/T]TAAGTGTATTGTTTC | 81550 |
rs552972227 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417530 | TATGTTTAGTAGAGA[A/T]GGAGTTTCACCATGT | 81550 |
rs552991876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464336 | AACCACCATGGAAAA[C/T]GGTATGGCGGTTCCT | 81550 |
rs553030655 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534838 | GAGGTTGAGATGGGA[G/T]GATCGCTTGGGCTGG | 81550 |
rs553067660 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526485 | AAATCTTTACTCCTG[A/G]GCAGTAAACAATGCC | 81550 |
rs553086040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409489 | AGCCACAAGGGCAGA[A/G]CTGTCCAAGACCATG | 81550 |
rs553152319 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525439 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGGG | 81550 |
rs553160050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60543339 | TTAGTTCCACTTCAT[G/T]GTTAAACAAATTTGG | 81550 |
rs553220197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401717 | AGAGATGGGATGGAG[A/G]GGATAAACAAAGGTC | 81550 |
rs553241933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551368 | ATTGAATGTTTGAAA[G/T]GCTTGGCACACAGGT | 81550 |
rs553267174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519799 | GGATGTTATAACTGT[A/G]CTCTGAGGTAAGCTC | 81550 |
rs553282038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520558 | CCCCACTCCTCCTAG[G/T]TTTTTCATAAGTTGA | 81550 |
rs553286991 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482953 | TATTAAGTAACAACT[A/G]GTAAGACAAATGTAT | 81550 |
rs553300554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565519 | TAAACACAATAGATA[G/T]AAATAGATTTTCAAA | 81550 |
rs553317655 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440342 | TTCCATAATTGTATT[A/G]GCTTTTGGGTTTTTT | 81550 |
rs553353935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509252 | ATTGGGGTATAGCTG[C/T]CAAAGCATCATAGAT | 81550 |
rs553370455 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496094 | TATGGCTACAATATA[A/C]ACAGGTAGAAAAATG | 81550 |
rs553379112 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465562 | CTTTATTGAGATAGC[A/G]TTGGTGTATAAAAAT | 81550 |
rs553382040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559347 | CAGTGCTGTGATATA[A/G]TATCTCTTAAGGAAA | 81550 |
rs553409654 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566269 | ATAATAGTTCTTTTT[G/T]TTTTTTTAAGACTAC | 81550 |
rs553414670 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450559 | AAATTAAAGAACTTA[G/T]GTAAAGATCCTGCTA | 81550 |
rs553423509 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458921 | TTTAATTTAAATGTC[C/T]TTATTTTAATGGCAT | 81550 |
rs553443238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503468 | ACATTCGACTTTTAG[A/G]AATTCCATACAATAT | 81550 |
rs553449572 | in-del | -/TAAAG | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419789 | ATGTATCCCAGAACT[-/TAAAG]TAAAATAAAAAAAAA | 81550 |
rs553467049 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464955 | GATTCATAATGTTCT[C/G/T]GCAAAGAAAAGATAA | 81550 |
rs553471417 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60569462 | ACTCCATGTTCATGG[A/T]TTAGAAGAATCGATA | 81550 |
rs553476111 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405903 | AGCAGATCGACTTGA[C/G]AGATATTTGGAAGGT | 81550 |
rs553479632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423782 | ATCATAATTTATGTG[G/T]TATATTTAAAGCAGT | 81550 |
rs553528913 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399612 | TGACTGAAGGGCTTT[C/T]ACCAACTCATTTTAG | 81550 |
rs553574453 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401061 | TTATTCTGAGGGGTG[A/T]TCCTATTAGAATCAA | 81550 |
rs553607163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504207 | TTCATGCTTTCTGAT[A/G]ATCTTTTACTAAAAA | 81550 |
rs553654066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458486 | GTATGGATTGAATAA[C/G]GGTGCCATGGTTGCT | 81550 |
rs553679937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487744 | TAAATATGGGAGATA[C/T]CTCTTTGACCCACTG | 81550 |
rs553687378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480805 | GGGGTATTATAGCCA[A/G]CATGATGGGGAGTGC | 81550 |
rs553709701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533366 | CTATTATTGGCTGGG[C/T]GCAGTGGCTCATGTC | 81550 |
rs553755795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437222 | ACCTCTGCCTCCCGG[A/G]TTCAAGCAATTATCC | 81550 |
rs553771056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438178 | ATATTTATGAAAGTG[A/T]ATTTATAAGATTATT | 81550 |
rs553772885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549031 | TCTGCTGGATGAACT[A/G]TTATACACCTGTGAT | 81550 |
rs553809095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509515 | TAACATATCATAAAA[C/T]TTATTTTTTGTGTGT | 81550 |
rs553811534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550114 | GTCACTAAGAGTAGA[C/G]AGAGCTTAGAAAGAT | 81550 |
rs553839208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435603 | AAAGACATTATTTCA[A/G]TTCGTTTTTGTGGCT | 81550 |
rs553843333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547870 | TCACCTTTCTTCTTT[A/G]ATATTCCCAGAATTA | 81550 |
rs553844587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420443 | TTGTTGCCTACTTCA[A/G]GTTTGTGAAGGTACT | 81550 |
rs553851226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436218 | TGGGTTGTCTGTTTA[C/T]TCTGCTGATGATTTC | 81550 |
rs553903328 | in-del | -/GTTG | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561866 | GGGCCCAGGTTTTTT[-/GTTG]TTGTTGTTGTTGTTG | 81550 |
rs553919327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485560 | TTTAAATATGTGCCC[C/T]GTTTAGATAGCCACA | 81550 |
rs553922723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480201 | TGGTGGTAATAAATC[C/T]CCTTAGCATTTGCAT | 81550 |
rs553925862 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518370 | ACACACTGTCCTCAC[C/T]GTGCCTTTTCTGAAT | 81550 |
rs553932974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462955 | ATAGAGAACCCAGAA[A/G]TAAATCCACATACTT | 81550 |
rs553934817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472683 | TAAACCCAAAAGAAT[A/G]GAAAACAGGTCTTGA | 81550 |
rs553936167 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397757 | TGCAGCGCCGTCCGC[C/G]CGGCTTCTCCGGGGA | 81550 |
rs553974291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539092 | TACAATACACATCAT[C/T]TTGGCCAGTAATTCT | 81550 |
rs553987597 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401815 | CCATGCTAACATCCT[C/T]TGGCCCAAGTGCATA | 81550 |
rs553993328 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543958 | TATCGTTTTTGTAAT[A/G]TAGCTGTTTTTTTTT | 81550 |
rs553993787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463864 | GTTTGGATATTTGAC[C/T]CTCTAAACCCTATAT | 81550 |
rs554007045 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60456985 | ACAGGTGTGAGTCAC[C/T]GCACCCAGCCTTAAG | 81550 |
rs554024756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60570595 | ATCAGGGTATTTTAT[G/T]TCTTTTTAATTGCTT | 81550 |
rs554029940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563330 | AGCAAATAGAGCCCC[C/T]GCCAAATTTCTATAG | 81550 |
rs554058852 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471349 | ATTATTTGGCCATAT[A/G]TGAACAAATTTATTT | 81550 |
rs554107169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541496 | ATTTTTTTTTGTATA[C/T]GTGAATAATACCAGA | 81550 |
rs554111439 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430651 | CAACATAGTTAGGTT[A/G]CCATTGCCACTATAC | 81550 |
rs554115242 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467469 | TGAGTAAAATTAGTT[A/C]TTTGTGTCGGAGTTG | 81550 |
rs554126911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513694 | TCTCATGAGATCTGA[C/T]GGCTTTATAAAGTGG | 81550 |
rs554131712 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480631 | GGAATGTCAGAGTTG[-/T]TATGTTTGGTCTCTT | 81550 |
rs554133519 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495413 | AGCTATCGTGAGAGA[C/G]TGGAGTTTTATTATA | 81550 |
rs554185419 | in-del | -/T | 0.19594 | 0.244085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398865 | ATCTCTTCTTTCAGT[-/T]TTTTTTACCCACAAG | 81550 |
rs554202312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520879 | TCTAATTCCAAACGC[G/T]TTGTTTGGGCCCAGG | 81550 |
rs554214346 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502930 | CAAACTACTATATTG[C/T]GATAACTTAAGAGTA | 81550 |
rs554312399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561552 | ATATAGGAATTCTAC[A/G]TGAGATTTCATTTGA | 81550 |
rs554312766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554139 | TTTTTCAGCCAGTCC[C/T]GCTGTCAGTGTACCT | 81550 |
rs554331165 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396136 | GTTCCGCAGTCTCTG[C/T]TCCAAGTCTGTTTTT | 81550 |
rs554336433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485695 | TGTAGGCTTTTAGCT[A/G]TTGTAAAAGATACAA | 81550 |
rs554343343 | in-del | -/CTGA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474019 | CAGCCATCCAGAGGC[-/CTGA]CTGTCTCCCTGTGAT | 81550 |
rs554343525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441562 | CAAATTTATCATCTT[G/T]TAATAAAATTTAGGC | 81550 |
rs554344787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418643 | CTTAAGTGTTTAGCA[A/T]GATAGGTTTTGATAG | 81550 |
rs554351496 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547038 | GTCTAGATTGAAAAA[A/T]AATAATTTCAAAGTT | 81550 |
rs554358763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403977 | AAGCACTGTGTTGCT[C/G]AGCTATGATGTACAA | 81550 |
rs554420148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404692 | TCACTGTAACCTCCA[C/T]CTCCCAGGTTCAAGA | 81550 |
rs554421980 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396927 | CTCCTCAGGCCTTAT[C/T]CTGCCCTCTCTGAGG | 81550 |
rs554479823 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475784 | GATTTACATTTCTCT[A/G]ATGATTAGTGATAAT | 81550 |
rs554493056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412566 | ACTAGTATGACACAT[C/T]AAGAAATGGATGCTT | 81550 |
rs554501219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410592 | CCTAGGAATTGGCCA[C/T]GATCTTTTCTCTAGG | 81550 |
rs554506349 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514101 | TAATGATATGGACAA[A/T]GAAATCCAGGCTGAG | 81550 |
rs554528935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453731 | GAGGTACTGTAGAGC[C/T]ATGTGAACAAACACC | 81550 |
rs554547233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506917 | AGACTGGCAAATTGG[A/T]TAAAGAGTCAAGACC | 81550 |
rs554551086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523689 | TCAAGCAATTCGCCT[A/G]CCTCAGCCTCCTGAA | 81550 |
rs554607325 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444206 | TTCCAGTGGTATTGT[A/G]TCCTGGGATATTGTA | 81550 |
rs554653918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461267 | TTTCCTAGGAAATGA[C/T]TGAAGTCAGGGAGGT | 81550 |
rs554686243 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426832 | TGTTCTCAAGCAACT[A/T]TGTCACTGTGGGAAC | 81550 |
rs554691576 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419312 | GCTAAAGATGTTGAG[G/T]ACTTTTTAATGTGAC | 81550 |
rs554696905 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533231 | ATACCTTTGTAATAT[C/T]AAATATACTAGTTAA | 81550 |
rs554726540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459001 | CTTGTTAACAGTTTC[A/G]GACTTGCTTCAACTT | 81550 |
rs554730594 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412085 | GGCCTAGCTCAGTGA[C/T]TCTCAAACAAACAAC | 81550 |
rs554767714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462187 | TTCAAATTCCTATGA[C/T]GAATTCAGTCACACC | 81550 |
rs554775377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444881 | ACAGGTCACAAAGTC[A/G]TTGTTATGGTGACTT | 81550 |
rs554808442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505392 | ACTGCGTCTCTGGAT[C/T]CTTCCTCTCTGGGGA | 81550 |
rs554819536 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560117 | ATGTGAAGCAAGAAA[-/T]GGAAATATATACCGT | 81550 |
rs554871431 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454673 | CTCTTAGTTGCAGTG[G/T]TGTTACTGCCAGAAG | 81550 |
rs554873908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475730 | TTGACTTTTTAATAA[C/T]AGCCATTCTGTTATG | 81550 |
rs554876716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491066 | TTGTGGTGAGTCAAG[A/G]TTGTGCTATTGCACT | 81550 |
rs554884183 | snp | C/T | 1.6684e-05 | 0.00288821 | stop-gained, utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528378 | TCAGAACCTAAATCA[C/T]AGCCACAGCAGCTTC | 81550 |
rs554885488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500652 | AAATGGCGAAATGTG[C/T]GATTATATACTGATT | 81550 |
rs554896074 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60519013 | TTGTAGGGTTTGCAT[A/G]TTAAATCTACATTGT | 81550 |
rs554921648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560519 | GTGCTTAACCTGCCA[A/G]AAATAGCTTATTTAC | 81550 |
rs554925336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416201 | TTCAATAATTAAGGT[G/T]TCTCTAAGTGTAAAG | 81550 |
rs554970687 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60491637 | AATTAATATAGAATC[A/G]AGGAAGTTGTTTATT | 81550 |
rs555035906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439381 | TTAAGTCGAGATTAT[A/G]TTTGTATAATAGCAA | 81550 |
rs555041965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551750 | AATTGACTCACAGTT[C/G]TGCATAGCTGGAGAG | 81550 |
rs555042587 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443538 | CTGTAGGGATTATAC[A/T]ACTTATATTCTCATT | 81550 |
rs555049677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440123 | TACATAGAAACTCTA[A/G]CTAGGTTATAGCTTT | 81550 |
rs555049722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431880 | TACATGCTGGTACTT[A/G]GAAGTACTTTAAATA | 81550 |
rs555080260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481813 | GATGCTGGACATTGT[G/T]ATGTTGGTAGTTGTT | 81550 |
rs555088764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534651 | GAATTGTTGGCTGGG[C/T]GCAGTGGCTCACACC | 81550 |
rs555092745 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514522 | TGTGGGGAGGGCACA[C/G]TGACAGATTCAGGAA | 81550 |
rs555126522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400886 | AGAGCCCAGATGTCT[A/G]GAATAAAGATTCAGT | 81550 |
rs555152639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484409 | CCATCAAAATTTAGC[A/G]GTTGGTAATCTGTCT | 81550 |
rs555164608 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537851 | GGAAAACTCTTGTTT[C/T]CCTAAATGTAGCAGT | 81550 |
rs555301869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545158 | AGAAGGTATGTTTTC[C/T]TCCCTTCAGAAGCCA | 81550 |
rs555311580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424044 | TTTTGTTTTTTGAGA[G/T]GGAGTCTTACTCTGT | 81550 |
rs555313507 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414784 | TAGAACTTTCCATTA[C/T]ATCCTAGGGCAGATA | 81550 |
rs555320729 | in-del | -/CTTCA | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516785 | ATGTATCATTTCCAC[-/CTTCA]CTTCACTGCCCTACT | 81550 |
rs555353656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424493 | ACCAGCCTGGCCAAC[A/G]TGGCAAAACCCCTTC | 81550 |
rs555395362 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532583 | ATCTTCTTAATTGCA[C/T]TGTAATGATATTTTG | 81550 |
rs555399268 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523802 | GACTAGTTTTGAACT[C/G]CTGACCTCAAGTGAT | 81550 |
rs555414515 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452492 | CATTATTCTGTATAT[G/T]CTTTTGAGTTTTCTC | 81550 |
rs555414956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416714 | GTACCAGTGACCTTC[C/T]AGTTGTGAGATATCT | 81550 |
rs555436335 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542202 | CTTATAGATACTTTT[A/G]AAGCTATAATTTTAG | 81550 |
rs555472750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488605 | TTTTGACAGAGTCTT[G/T]CTCTGTTGCCCAGGG | 81550 |
rs555483541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524469 | CCGAGACTGCACCAC[G/T]GTACTCCAGCCTGGG | 81550 |
rs555491278 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417406 | CCCAGGCTGGAGGCT[A/C]TCCCAGCTCACTGCA | 81550 |
rs555505689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512334 | ACATGTGGGCATTCA[A/G]GATGAGATTTGGGTG | 81550 |
rs555517350 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60573682 | TTGACAGACCTTCCA[C/T]TTTCTCTTCAGAATA | 81550 |
rs555532641 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497532 | GTCGGCCTAGGAAAT[A/C]CAGCTAGTCCTGTCT | 81550 |
rs555553226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407739 | CTATTTCTTTCACAT[C/T]TGATGTTTTATGAGA | 81550 |
rs555553305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551214 | ATGAATTTTAGAGTC[C/T]ACATACCTTGGGAAA | 81550 |
rs555574656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430558 | TGTAAATTATAACCC[C/T]AATGAAAGTAAAAAT | 81550 |
rs555577558 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425266 | TATGAAAAGGTGCTC[A/C]AGATCACGAATGATC | 81550 |
rs555627123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557311 | AAAGCCAGAGAGCTC[C/T]CTTCACCAGAGTTAT | 81550 |
rs555675429 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421599 | TAGTAAATAACTTCC[C/T]AAAATCTTTCCCCCA | 81550 |
rs555693836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572428 | TGCAGCTGGATGTAG[A/G]ATGGATTATAGCACC | 81550 |
rs555699282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501821 | TATAACCTTATTTGC[A/G]TAGCCAGGGTGTGAC | 81550 |
rs555727574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402326 | CAGCATCAGTACAAC[C/T]TCTGCAGTAGCAGTA | 81550 |
rs555742664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518824 | TTTCAGAACTAGTCT[C/T]TGTAAAATACCATGA | 81550 |
rs555750584 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542848 | TTACCTCTGGTGAGT[A/G]GTATCTTTTGATGTA | 81550 |
rs555751831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517688 | ATTCGTTTTGAAGTG[C/T]AAATGTACCCCAAAT | 81550 |
rs555781368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472609 | GAAAACAGTATGGCA[C/G]TTCCTCAAAAAATTA | 81550 |
rs555806961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457571 | ATACAGTATTTTCTT[C/T]GCAATCAGGTAACTC | 81550 |
rs555808700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422071 | TTAAAGGGATAGATT[C/G]TATTTAAATGGGTAA | 81550 |
rs555813183 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488397 | GAAAGTTTCAGATTT[C/T]AAGATCAGAAGGGTC | 81550 |
rs555842993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464872 | ATAAGATTTAGTGTT[C/T]AGTGGCATAATAGGG | 81550 |
rs555845252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509457 | AAATTTTCATTAAGT[A/G]GTTTTCTCCTCACTG | 81550 |
rs555871540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471717 | CTGTGTTGATTTTGC[A/G]TACTCCAACTTTATT | 81550 |
rs555896623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548164 | AAGACATAAGAATTT[A/G]GTGGCTATTTGTTTG | 81550 |
rs555910488 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397532 | CCCCCGGCCTCTCCC[C/T]GGGCCCTTCGGGCCG | 81550 |
rs555929385 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463003 | AACAAAGGCATCAAG[A/G]ACATACATTGGCAAA | 81550 |
rs555934761 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60540954 | TTAAAGTTATTTTAA[C/T]AATAATGCATCTGTT | 81550 |
rs555953340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504139 | CTTAATTACCTCTAG[C/G]TTTATCTTATCAAAT | 81550 |
rs556007319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510321 | ATGGTCAAGTTTCTT[A/T]TGTGGTCCCAGTCCT | 81550 |
rs556020232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548623 | GGTTTCTTGCTGAAG[C/T]AGCAGTGTCATCTTT | 81550 |
rs556041834 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448529 | GATGCAAAAGTTTCA[G/T]AAAAATTTAAAAAGT | 81550 |
rs556073325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398536 | ATTTTGTGAATAAAG[A/T]TTTTGATCAGTAGAG | 81550 |
rs556099000 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495719 | ATCCACCCGCTTCTT[C/T]GGCCTCCCAAGGTGC | 81550 |
rs556100930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541469 | ACCTTGCCCAGTCCA[C/T]GGCATTCTTTTATTT | 81550 |
rs556131154 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464129 | TGAAACCCTCACCAG[A/T]ATTGGATGCTGATGC | 81550 |
rs556169738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563892 | TACAGTAATGAGAGA[C/T]TGAAGATGATATGCA | 81550 |
rs556170731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435566 | TAGAATAATGGCCTC[C/T]AGCTCCATCCAAGTT | 81550 |
rs556181453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462741 | CAATGAAAATATTAA[C/T]CAAAATATACTTTCT | 81550 |
rs556195431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443534 | GAATCTGTAGGGATT[A/G]TACAACTTATATTCT | 81550 |
rs556224952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446361 | CCTAGTAACTGAGAC[C/T]ACAGACAGGTGCATG | 81550 |
rs556253277 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544443 | AAGACCATATCTCTT[A/T]AAAAAAAAAAAAAAA | 81550 |
rs556258713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444831 | AATTACTTTTTGTCA[A/G]TAAAGACTGCAATTG | 81550 |
rs556278916 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446987 | ATCTGTGCATAAGAT[A/T]CAGGACAACAGTTGG | 81550 |
rs556279836 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412489 | CTATAATAGTAGGTA[G/T]TATGGACTGTATTTG | 81550 |
rs556281607 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563262 | AGGCAAGGCGATTCA[A/T]TAAGTAAAAATGAAC | 81550 |
rs556282817 | snp | A/T | 0.00106766 | 0.0230801 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484746 | AGTCCTATGGTGTGA[A/T]CCATGTTGATGGTTG | 81550 |
rs556315587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426970 | GTACTGAATACTGTG[A/G]GCAATTGTAACACAA | 81550 |
rs556315704 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501646 | TTTTAGGACAAGTGT[A/T]TACCATCCATAAAAT | 81550 |
rs556322148 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478226 | TGTAATACCATATTT[G/T]TGATTTCTGATTGTA | 81550 |
rs556343278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403884 | AATAAGTAAGGCATA[A/T]ACAGAGAAATATGTA | 81550 |
rs556401490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434904 | CAGTTGCTTTCTTTC[C/T]TGATTACCTCAATTA | 81550 |
rs556419407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548984 | AAGCTACTTAAGCAT[C/G]CAACAGTAGGAGAAT | 81550 |
rs556441289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569870 | ACTGGATATCCGTAT[A/G]TGGATGAATGAAACT | 81550 |
rs556455906 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541011 | TAATTTAAGCCTCAA[A/T]TTATTTAACTATTAC | 81550 |
rs556459771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514672 | CCTGTGCCTGGGAAT[A/G]TATGGTAGAGGTAGT | 81550 |
rs556502007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437196 | CAATGGCATGATCTC[A/G]GCTCACTGCAACCTC | 81550 |
rs556513645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418492 | CCATGGTTTTTTCAT[C/T]TTTGAATTCTTGGGA | 81550 |
rs556537881 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538869 | AAAACATTGTTGGGT[C/T]CTCATTTTCCATATA | 81550 |
rs556593521 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475497 | ATCCAGTTCTGTGTC[A/G]ATGGACCTCTTCACT | 81550 |
rs556595280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527287 | AGTTTTGATAGTCAA[A/C]ATCCCTGGGGATGCT | 81550 |
rs556595314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536677 | TATGTTATTTACTTC[C/T]TACTTTTTAGAAGAC | 81550 |
rs556607724 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437623 | ATAATATAAATAATC[-/T]ATTATAATTTAAATT | 81550 |
rs556645803 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498183 | CAGCTGGGAGGGTCC[A/G]GAAGATATACCCTTG | 81550 |
rs556649554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417628 | ATTACAGGTGTGAGC[C/T]GCCACACTGGCCGAT | 81550 |
rs556676352 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469339 | CAACTCTAATACCTT[A/G]TATAATTTTCCCACA | 81550 |
rs556680437 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528304 | TAGAATAAAGCATTT[A/T]AAAATAATTATTAAT | 81550 |
rs556702604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561473 | AAGTGAGGAAGAGGA[A/G]GCCAAAGGGGTACTG | 81550 |
rs556730176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501005 | GCAACATGGAACTCC[A/C]CTCACCAAGGCTGAC | 81550 |
rs556739665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553599 | ACGGTTCTGCATGGC[C/T]CGAGAGGTCTCTGGA | 81550 |
rs556813457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427881 | GAATTTGTAATGGGT[A/G]TATTTATTTCCTGTG | 81550 |
rs556823464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560681 | GCTTTACTAAGAAGA[G/T]CTTATAATAAAACCC | 81550 |
rs556839034 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394480 | CAAGATCCAGACCAT[C/G]CTGGCAAACACGGTG | 81550 |
rs556848954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530178 | GTATCTTTTTGCACT[A/G]CCATGATATTAAGTT | 81550 |
rs556886325 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447070 | TTGGTATAAAATGAT[A/G]TTTTCTAGTTTTCTT | 81550 |
rs556896884 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504808 | CAGAAGCAGAGTGGG[A/G]CGTTGCCTCACCTGG | 81550 |
rs556933335 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460242 | ATAATATATAATTTC[A/C]GTTTCAATCTTAATT | 81550 |
rs557007582 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418608 | TGCAGCACAATTAAT[G/T]TACATTAAAATGCAC | 81550 |
rs557012161 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502986 | GGAACCAGGCAGAGA[-/G]GAAACAAACATGCTC | 81550 |
rs557026507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426074 | GTGACTTGTATTTAC[A/G]ATGGGATATAATTGA | 81550 |
rs557031597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400086 | TGATTTGAACTTGAA[A/T]GTTCCAGGGCTTTCT | 81550 |
rs557040768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468221 | TTCCACATAGATCTT[C/G]TTGTAGCCAAATGGA | 81550 |
rs557059202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458586 | CTCCTACATTTGAAT[A/G]GAAGTGCGGTGCCTA | 81550 |
rs557076480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402328 | GCATCAGTACAACCT[C/T]TGCAGTAGCAGTAAT | 81550 |
rs557088943 | in-del | -/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508883 | TACAAAGCCTACAAA[-/G]AGGCAGGAAAATTTA | 81550 |
rs557115311 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444944 | TGACTTTTCAACATT[-/A]AAAAAAAAAGCAACC | 81550 |
rs557139375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518669 | AGGTATGTGCGAGTT[C/G]TAGGCTTCATCTTTT | 81550 |
rs557141619 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395432 | CACTCCGAAGAAATT[C/T]AATGTGTTTCATCAA | 81550 |
rs557153055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506781 | AACATCGACACTATG[A/G]AGAAACTGCATCAGC | 81550 |
rs557164095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453603 | ACCGAGGTTCTTGAC[A/T]AAGTTAAGCATCCCA | 81550 |
rs557184846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521609 | GTTAAAAATGAAAGT[A/G]TATGGGCCGGGTGCG | 81550 |
rs557196897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568969 | TGTTTTTTTTCCCCC[C/T]TTTTCTTCTTCTTTT | 81550 |
rs557225374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513654 | AGGGCAAGTCTTTCC[C/T]GAGATGTTCTTGTGA | 81550 |
rs557250302 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476154 | CCTAGGGTTTCTTCT[A/G]GGGTTTTTATTGTTT | 81550 |
rs557259439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468873 | AACTGATTACTCCTC[A/G]AGCTGAAATGTATTC | 81550 |
rs557268926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498695 | AGGAAAGACCCCACC[A/G]ACAGTTTATGCAGTG | 81550 |
rs557312927 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512574 | TTCCTAGATACAATG[A/G]GGGTACAGGCATTAG | 81550 |
rs557338972 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506104 | CCAAGGTTGAAATGA[A/C]GGAAAAAATATTAAG | 81550 |
rs557343630 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400812 | TGTGCATATGAAGAA[A/G]CTGAAGCACAGAGAG | 81550 |
rs557355326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559450 | TCTATTTAATCTTTA[A/G]AAATGGGTTTCAGAG | 81550 |
rs557369661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534645 | ATATAAGAATTGTTG[C/G]CTGGGCGCAGTGGCT | 81550 |
rs557409630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406443 | GTTAAAATAATTATT[A/G]AATTAATTTCACCTG | 81550 |
rs557421062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497081 | AGCCTGATTGGGAGC[A/G]GCAGCTGGCACCCCA | 81550 |
rs557422989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557915 | GCAACCTCCACCTCC[C/T]GGGTTCAAGTGATTC | 81550 |
rs557436423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450697 | TAGGGATGTAGAGAT[C/G]AAGATAGCCTCTGTC | 81550 |
rs557453348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449425 | AACTATTCAACTTAC[C/T]TTTTTCTGTTTTTGG | 81550 |
rs557459557 | in-del | -/AAGT | 0.000188775 | 0.00971348 | splice-donor-variant | TDRD3 | GRCh38.p7 | 13:60485947 | TTGCAAAGAGCAAGG[-/AAGT]AAGAAATCAAATCAT | 81550 |
rs557467216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566364 | GGATTTGACCAAATT[A/T]TCTTACCATCTTTGT | 81550 |
rs557484367 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488400 | AGTTTCAGATTTTAA[C/G]ATCAGAAGGGTCAAT | 81550 |
rs557503230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439253 | TGAGAAGATAATGTG[A/G]GAAAGTCCAGAGAGA | 81550 |
rs557521059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473762 | CCGGACAGGGCCACT[A/G]GAGGGCTCCCTGGTC | 81550 |
rs557541804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491009 | ATAATCCCAGCTACT[C/T]GGGAGCCTGAGGCAG | 81550 |
rs557543379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545044 | CAGTTTAATATGATA[A/G]CTTTTCAACAAATAT | 81550 |
rs557566418 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60439956 | AGCAAGTTATTAATA[-/TC]TGTTATACAGAATCC | 81550 |
rs557598594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551042 | TAGCATATAAATTAT[A/T]TCTACTTTGTTTTAC | 81550 |
rs557599453 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483065 | TAGAAAGACTTTATC[A/C]TGTGAGAAATTGCTT | 81550 |
rs557623449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60543597 | TTACATTTCTCATTC[A/G]TAACATGGGTAAAGA | 81550 |
rs557646380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451399 | CTGGTACAAGAAATA[C/G]TGTTAGATGCTTGCC | 81550 |
rs557659239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480834 | GCTGCAAGCGAGGGG[A/G]CCACATGCAGGAAAT | 81550 |
rs557704207 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421888 | TGACCACCAGAAAGA[A/T]CAAATCCACCCTAAA | 81550 |
rs557766608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431749 | AATGTATATTTATGA[C/T]GGCAAAGAAATCATA | 81550 |
rs557769696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571578 | AGGTTTTCTTTTTAT[A/G]TTTTGAGTACTTCAC | 81550 |
rs557782036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540928 | TTACCTAACACATGC[C/T]GTCACTCTTTTTAAA | 81550 |
rs557799855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542151 | CCTAAAACTTGTTCT[C/G]CTGGAAGTGCAAATT | 81550 |
rs557821586 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550199 | ACACAATACTATGAG[A/G]TTTATCAAATTATGA | 81550 |
rs557854246 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438498 | CTCATTTTGTTAACA[A/T]TCTTGGTTTGACTTA | 81550 |
rs557894620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564728 | ATGAAATTAAAATTA[C/T]TTTTTTGAGTTGTAA | 81550 |
rs557918281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541766 | CGGAGTTTTGCTCTT[C/G]TTGCCCAGGATGGTG | 81550 |
rs557938153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465856 | ATTTACCTTAGAAGT[A/G]CTATTTGCAGTACTT | 81550 |
rs557953218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415903 | AGACAAACTTCATCA[A/G]TATATCTTTTTCTTA | 81550 |
rs557957471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424416 | GGCGCAGTGGCTCAC[A/G]CGTGTAATCCCAGCA | 81550 |
rs557959456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526096 | ATACTTAGTTACTCT[C/T]GTGATGACTTAATAT | 81550 |
rs557970579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456879 | TTTTGTATTTTTTGT[A/G]GAGATGGGGTCTCCC | 81550 |
rs557974709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447275 | GCATTAAATGATACG[A/G]ACCAGGAACAGATTA | 81550 |
rs557980291 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429492 | TGTTTTAAATTTTGA[C/T]ATAAATGGCAGGTTG | 81550 |
rs558007214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572227 | GAGGGAAGCAGAGTC[C/T]ACAGCAAGTGGCTCT | 81550 |
rs558013370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413430 | TGCCACAGATTAGCT[A/G]TAACCTTGGGCACAT | 81550 |
rs558021207 | snp | G/T | | | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460519 | GCACAGCAGTAGAAT[G/T]TAGTTATATGTCAAA | 81550 |
rs558035410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533410 | CTTTGGAAGGCAGAG[A/G]CGGGCAGATCACTTG | 81550 |
rs558043780 | in-del | -/GATA | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420045 | AATACATCATGTAAT[-/GATA]GATATACTAGATTAT | 81550 |
rs558071823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525519 | TTTATAAATTTTACT[C/G]TCACTATATTATCTC | 81550 |
rs558093246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507897 | TCAGTTCAAAATCTC[C/T]TTAAGCTGATAAGCA | 81550 |
rs558096594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423863 | AACTAAATTTTCAGC[A/G]AAACTAAAAAAGATC | 81550 |
rs558108432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523733 | AGGTGCATGCCACCA[C/T]GCCCAGCTAATTTTT | 81550 |
rs558123275 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534188 | CATGGTTGTATGCAC[A/C]TGTAGACCCAGCTAC | 81550 |
rs558137799 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517652 | TTTCTTCCTGTAAAG[C/T]TGATTCCTTTTTACC | 81550 |
rs558160415 | in-del | -/CTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541177 | TTTCTTTCTTTCTTT[-/CTTT]TTTTGAGACGGAGCC | 81550 |
rs558167380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516825 | CATCAAGGCTTTCAT[C/T]GGCTTTCACTGTTTT | 81550 |
rs558193383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513786 | TCCTTGCCTTCTGCC[A/G]TGATTGTGAGGCTTC | 81550 |
rs558224660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552129 | TCGTTCCAGCATTAA[C/G]TTAAAATTCCAAGTC | 81550 |
rs558232969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428820 | AAGGAAAGGACCAGT[A/G]GTAATTTTCTTCTTT | 81550 |
rs558284009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403842 | AAATAGCAGTATAGT[A/G]CTCTTGAATTATAAT | 81550 |
rs558309490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487005 | TATTTGTGGATTCAA[C/T]TCTTCCTAACTATGG | 81550 |
rs558338518 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469645 | GATTTGGTAGCCACA[A/G]CAATGTAGGAAACAG | 81550 |
rs558344437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540326 | ACTTAGGGATTCCAT[A/G]CAGTATCTTTAAGCT | 81550 |
rs558345590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510178 | ATTTAACAAGGTTGT[C/T]ATGAGTAATAGAGAA | 81550 |
rs558353398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410716 | TTGGGGATGGATAGG[G/T]TAGGGTTAGTTCTCA | 81550 |
rs558386820 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457871 | CTTTATACTCTGTCT[A/G]TGTTTGTTTCCCCTT | 81550 |
rs558393277 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516236 | AAGTCAGAATTTAGC[A/G]CAGTAAGCCTTGGCT | 81550 |
rs558393966 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471284 | GTTTTCCCAGCACTA[C/T]TTTTTGAAAATAGTG | 81550 |
rs558395381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464181 | AGAACTATGAGCCAA[A/G]TAAACCTTTCTTTAT | 81550 |
rs558406576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508739 | TGAAAAAAGTTTAGA[A/G]AAGTCACTAAGCAAA | 81550 |
rs558407145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503575 | TAAACATGCCAAACA[A/C]TCCTGTTTATCTCTT | 81550 |
rs558413823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402536 | TTAAAATCTAGAATT[A/G]TGATATACCTTTAAT | 81550 |
rs558448983 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490908 | AGATCACCTGAGGTC[A/G]GGAGTTTGAGACCAG | 81550 |
rs558472615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491237 | GTGTGAGGGGAGGAG[A/G]ATCTGGTGCTCCATT | 81550 |
rs558476218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404913 | CTTTCCCATGCTGTT[C/T]TCGTGATAGTGAATG | 81550 |
rs558482737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403108 | AACTGTGCAAGTGTT[C/T]AGGTTTCAAGGTGCT | 81550 |
rs558502971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462032 | TCTGGTGTCTGCCTC[C/T]GGTAAATGAGGCCCC | 81550 |
rs558529308 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482979 | TGTATGTATATATTA[A/G]TACCTCAAAACCAAA | 81550 |
rs558529503 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511799 | CTTTATCTCCTAAAA[G/T]CTGCCTTCAGATTAT | 81550 |
rs558537548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509574 | GAGAATACTCAAGGC[A/G]CAACCCCACATATCA | 81550 |
rs558542361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483873 | TGTGTTGGCAGATGA[A/G]TTTAAATTAGGAAAA | 81550 |
rs558544698 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554308 | GAATTTGACTATTGT[A/G]TCATGCATTTTGTAC | 81550 |
rs558547508 | in-del | -/TCTC | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545890 | TGTTCTTCCTCTGTT[-/TCTC]TCTTTTTTCTCTTTA | 81550 |
rs558549359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501194 | TCATTCCCCCCGCTG[A/G]AGTGGTAACTCTAAC | 81550 |
rs558583340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522386 | GCACCTTATTTTCTG[A/T]TTTTTTGTCTTTCCT | 81550 |
rs558584970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469688 | TACTTGAGCAGCTGG[C/G]AGTGATATACATAGA | 81550 |
rs558601282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435638 | AGTATTCTATGGTGT[A/C]TATATGCCACATTTT | 81550 |
rs558619310 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493214 | TGAGCCACCGCGCCC[A/G]GCCTCAAATAATTTT | 81550 |
rs558626281 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454868 | TGTATGTGACAAATC[A/T]GACTTTATTTTTTTC | 81550 |
rs558652761 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461433 | TGTCCCCTCTATTCT[G/T]GATATTTCCATTTGG | 81550 |
rs558664824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569805 | TGACATAGGTGCCAA[A/G]AACATACATTGGAGT | 81550 |
rs558749780 | snp | C/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438132 | TCTTGTTACTGATTT[C/T]ACACAATACTTTTCA | 81550 |
rs558800426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486364 | GATGAATAAAAATCA[A/G]CGGATCTGTCACTGT | 81550 |
rs558807619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554908 | AGGTTACTAAAATAC[A/G]GTTTATGAATTTCAA | 81550 |
rs558841009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455334 | CTTTCAGGCTTTTAA[A/G]GCAGCTATAGGCAGA | 81550 |
rs558843707 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60548059 | CTAGTCCATTCATTT[A/T]CTCTGTGGGAAAGGA | 81550 |
rs558846723 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526990 | CAGGTGTGCACCACC[A/T]CACCCAGCTAATTTT | 81550 |
rs558849699 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501734 | AACATCCCTCTTTTA[A/G]ACAACCAACTATTCT | 81550 |
rs558850623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444995 | CTATGGCATGCTTAC[A/G]TGAACGGTGAGACTT | 81550 |
rs558874727 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565887 | TTTTATGATTTTCTT[A/T]CTTTTAATTGCTTTG | 81550 |
rs558924472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492206 | ATCCAGAAGATGGGA[C/G]TATTTCACTGGCACC | 81550 |
rs558951808 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411755 | CAGCAGCATTGATAT[A/C]ACCTGGTAGCTTGTT | 81550 |
rs558977736 | in-del | -/TTA/TTATTA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477197 | GTTTGTTATAGATGG[-/TTA/TTATTA]TTATTATTATTATTA | 81550 |
rs559020204 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424138 | GCCATTCTCCTGTCT[C/T]AGCCTCCCGAGTAGC | 81550 |
rs559036949 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557734 | TTATAATTATCTCTC[C/T]TACCACTCCAAGTTT | 81550 |
rs559044283 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TDRD3 | GRCh38.p7 | 13:60574225 | ATGCATCTGGTTGCA[A/G]GTACCAGAAAACCCA | 81550 |
rs559048932 | in-del | -/ACAA | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568877 | AAACTATTAAAACTG[-/ACAA]ACAAATTCAGTAAAG | 81550 |
rs559057129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407064 | GAAAAACTTGCTAAA[C/T]AAATTAAGCCAGTAT | 81550 |
rs559071375 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505971 | CTTCAGGATATTGTC[C/T]GGAAGAACTTCCCCA | 81550 |
rs559084154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530088 | CTACTTACATTATTC[G/T]CTTAATCAGTGCCTT | 81550 |
rs559107557 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450913 | TAGATGCCCCATATC[A/G]GGCGTATTTAAAATC | 81550 |
rs559114685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405786 | AATCATGATGTGAGG[A/G]TTATGGTGGGAATAA | 81550 |
rs559124164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545251 | TGGGTCTTGATTATA[C/G]TTTTACATGATAACA | 81550 |
rs559166455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419367 | TTTGAGTCTTTTGTC[C/T]GTTAAGAATTTGGAT | 81550 |
rs559177918 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439019 | TTCCTTCAGATTCAG[A/T]AATCTCTTTACTCTT | 81550 |
rs559187250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458702 | AACTCTGTGCTCTCC[A/G]TATATAGAACACTTG | 81550 |
rs559192053 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416108 | TTTGGAAGTTGATAA[A/G]GTATTGATTTTAGAT | 81550 |
rs559213660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473868 | GGACCTTGGCCTAGC[A/G]GTAGCGTCAGTACCT | 81550 |
rs559228678 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554668 | CTAATACAGAGACTT[C/T]GTGCTTTCCTAACTT | 81550 |
rs559235303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569083 | AAGACGTCCTGCCAT[C/T]TCAGCCTCCCTAGTA | 81550 |
rs559247556 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537926 | GTCAAAAAAGCCTGC[A/T]TATAAGCCAAAAGCC | 81550 |
rs559275855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398766 | TATGCGTTATTGTTG[C/T]TACAGTTTTTTCGCA | 81550 |
rs559303194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466911 | GTGCATTTTGAAGAA[C/T]CTGATTAGGTCATAA | 81550 |
rs559304196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426879 | ACACAAACCTTAATG[A/G]TATTGCCGACTACGC | 81550 |
rs559305255 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60414396 | GTGCTACAGGAGCAA[A/G]GAGTAGTTGTGACAG | 81550 |
rs559332049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440897 | ACAAGGAACATTTAA[A/G]ACATAAATAAATGTA | 81550 |
rs559339484 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559081 | GAAGTAGGTAAACAA[A/G/T]CTCATGTGTTTTGAA | 81550 |
rs559344219 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480860 | GAAATGCTCCTTTGG[A/T]AACAGCTGGGGCACT | 81550 |
rs559366952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511648 | TTAAAGTCTCAGATG[C/G]TGATGTTAAGATTTT | 81550 |
rs559404947 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444870 | TCTGGAGGTGAACAG[A/G]TCACAAAGTCATTGT | 81550 |
rs559410453 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509657 | GAATGACATTTTTAC[A/C/T]TAAGTATGGGATGTA | 81550 |
rs559510681 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453334 | AGGAAAACGAGTAAC[-/AT]GTAGTTTTTCTTTTC | 81550 |
rs559528136 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518360 | TCTGAGAGGGACACA[C/T]TGTCCTCACTGTGCC | 81550 |
rs559555865 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431903 | TTTAAATAGTACGTA[C/T]CTTTATTTATCTGAT | 81550 |
rs559557347 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422433 | AAATTTGCACGCAAA[C/T]CTAGGAAAATTCTTT | 81550 |
rs559557563 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423442 | AAGGTTGATCTTCTG[G/T]GTATACTGTATATTG | 81550 |
rs559571616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405030 | CTTGTCCCTCTTTGC[C/T]ATCTGCCATGATTGT | 81550 |
rs559573620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565161 | CCCGGGTTCACGCCA[C/T]TCTCCTGCCTCAGTC | 81550 |
rs559576828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407793 | GATATTTCAGAATTG[C/T]TTACAGCTTAGCACT | 81550 |
rs559584866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504496 | CTAGTATCTGACTTG[C/T]ATGATTTAGACCACA | 81550 |
rs559594456 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60543977 | CTGTTTTTTTTTTTT[G/T]TGTGATTCTTACCTT | 81550 |
rs559619499 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487491 | CAAAAAATAAAAATT[-/A]AAAAAAAAAGTATGC | 81550 |
rs559639268 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533955 | TGGATGGGATGATCT[C/G]TACTGAAAGATTACT | 81550 |
rs559642602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430899 | GCTGTATTTTGATGT[C/G]ACAGAAAAGCAATTA | 81550 |
rs559648438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542342 | GTTTTGTCTTATTTC[G/T]ATGGTCTCAGAGATG | 81550 |
rs559654045 | in-del | -/AC | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416328 | GAACAGATTTACAAA[-/AC]AGTGATTATTGAAAG | 81550 |
rs559674981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486650 | TAGCTATTTTGAAAT[A/G]TACAATAAATTATTG | 81550 |
rs559685020 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568157 | CTGGTTAAAAATTAG[A/T]TCTGCCATCCTAAGT | 81550 |
rs559685812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447838 | AAGAAGCAAAGAGTT[A/G]AAAAGCAACATGTTG | 81550 |
rs559694830 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559147 | TGAGACTAATAGCCA[A/G]CACTGCCTATTTGTG | 81550 |
rs559711503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533779 | CAACATTCAGACCTA[C/G]AATTTCTGTCCTGAA | 81550 |
rs559726559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400225 | TAGATAACAATTTTA[C/T]TCACTCTGCATTTTT | 81550 |
rs559744462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60437812 | TTATCACCCATATCC[C/T]TTTGTGTACTGTTGC | 81550 |
rs559757600 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438782 | ATGAGCTTGAGTTAG[A/T]TCTCTTAGACTAGCA | 81550 |
rs559771680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496694 | GTTGGTTGCTTCTAA[A/G]TTTGGTGGACAAAGT | 81550 |
rs559792698 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493432 | TTTGGGAGGGCAAGG[G/T]GGATAGATCATCTCA | 81550 |
rs559797107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503048 | TATTAAAGGCTGTAA[A/G]TCGTTCAAAATAAGT | 81550 |
rs559819487 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565231 | CGGCTAATTTTTTGT[A/T]TTTTTAGTAGAGACG | 81550 |
rs559847101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504769 | GAACTGGTTAGACAG[C/T]GTGTGCAGCCCATGG | 81550 |
rs559853480 | snp | C/T | 1.68009e-05 | 0.00289831 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485927 | GACGGCTGCTATTGC[C/T]GAAGTTGCAAAGAGC | 81550 |
rs559857705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494297 | TATTCAAAAGGAGTA[A/G]GTTAATATTTTATTT | 81550 |
rs559882210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404374 | GGAGTGCAGTGGCGG[C/G]ATCTCGGCTCACTGC | 81550 |
rs559910259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524866 | CACTTTGGGAGGCCT[A/T]GGCGGGTAGATCATG | 81550 |
rs559916233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473111 | CCAGAAGTACAATAA[C/T]ATGGCTTTGGTATCT | 81550 |
rs559942473 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480503 | TATGTCACAGAGGTT[C/T]TTTGAATTTCTTCAG | 81550 |
rs559950395 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497336 | AATGCCTGGGTTTAG[A/G]TCCCGATCATTGTCC | 81550 |
rs559962355 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490394 | GGCTCTAAAGCAGGA[A/G]CACAGAGAAACAGCG | 81550 |
rs560004892 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436495 | CTTCTACATGTGGCT[G/T]GCCAGTTTTCCCAGC | 81550 |
rs560052601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515764 | GCTCATTTTAAGATA[A/G]CATGTATTTTTAATT | 81550 |
rs560057400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414091 | AGGATTTCACTTAAA[C/G]AATAATGTGTTGCCC | 81550 |
rs560087599 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476445 | TATATTTTTGTACCA[A/G]TACCATTCTGTTTTG | 81550 |
rs560104051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531471 | CTCCTGTGAAAGGTT[A/G]AGGTGAGGATGGAAA | 81550 |
rs560105012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469302 | ATCAGTAGAGATTTT[C/T]TAAAGTGTGGTAAAA | 81550 |
rs560107008 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552347 | TCATGAAATTTTACA[C/G]CTCCAAAATAATCTC | 81550 |
rs560162820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540519 | AAATGTATTCCATAT[A/G]CATAAATGTTACCTT | 81550 |
rs560173313 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541426 | CCTGCTTTGGCCTCC[A/G]AAAGTGCTGGGATTA | 81550 |
rs560185563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532067 | TAATAAAGGTCTAAT[C/G]TTAATTGTAATTGTA | 81550 |
rs560187838 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400581 | CTCTACTAAAAATAC[-/A]AAAAAATTAGCCAGG | 81550 |
rs560201227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427285 | GTGTTCCATTTTTTC[A/G]TTCTTTGTATGTTGG | 81550 |
rs560202011 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417019 | CAGTCTCTCTCTCTC[-/T]TTTTTTTTTTTTTTT | 81550 |
rs560215142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479693 | AGTGTTGGGTATATA[A/C]ATATTTAGGATAGCT | 81550 |
rs560217954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429073 | CATTTTAAAGAAATG[G/T]AAATGAGAATTACTA | 81550 |
rs560225396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523852 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCATAG | 81550 |
rs560243547 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569305 | AAAGGAAACCAAGAA[A/C]GTAATCCCAATTAAA | 81550 |
rs560251479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435941 | TTTTTTACTTTTTAA[C/T]TATGGCCTTTCTTAG | 81550 |
rs560288398 | in-del | -/TTTAC | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470456 | CCATACTGTTTTATA[-/TTTAC]TTTACACTCATTTCC | 81550 |
rs560320603 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489267 | CTTTTAGACTGATAA[A/G]AAATTTTAGGTCATA | 81550 |
rs560322916 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525714 | TTTGTTAAATAATAA[-/G]CTGTTCAGGAATTTT | 81550 |
rs560327975 | snp | G/T | 0.276267 | 0.248616 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561872 | AGGTTTTTTGTTGTT[G/T]TTGTTGTTGTTGTTG | 81550 |
rs560336326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564356 | GTTTGGTCAAGGCGG[A/G]ACAACTTGAAGCGGG | 81550 |
rs560371963 | snp | A/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395054 | AACCATTTTGGCAAG[A/T]ATACTTCTTAAGTGA | 81550 |
rs560373129 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511189 | TTTATATACTTTAGT[A/G]ATTACTATATTGAAA | 81550 |
rs560374915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418971 | CTCCTTTTGATAGAC[A/G]ATAACCAGTTTTTGG | 81550 |
rs560378017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462258 | GCCATGTAATGGCTC[A/G]TTCTCTGATTTTATG | 81550 |
rs560385762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421343 | CTTTATAAAACAATC[A/G]GATCTCATGAGGCTT | 81550 |
rs560422445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471017 | TTTTTAATCAGGTCA[C/G]CTGTTGTTGTTGTTA | 81550 |
rs560466166 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422191 | GCGTTTCCTTTGGCA[A/G]TTGGATAATGAAGAG | 81550 |
rs560490649 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431062 | GAGAAAATTGTCTTA[A/G]TATATCTAATGGTGA | 81550 |
rs560496159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522495 | CTGTCCTAAGTACTT[C/T]ACATATGTTAATCCT | 81550 |
rs560496443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60442539 | GTCATCGTCCTAGCA[A/G]TCCTGATACAATGGC | 81550 |
rs560498536 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465202 | AACTTGACTACATAG[C/G]TCTTAGGTAAATGAT | 81550 |
rs560500967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401914 | CAAAATGTAGAACTG[A/G]AAAACAACCATGGGA | 81550 |
rs560521622 | in-del | -/T | 0.22805 | 0.249035 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510804 | CTTTCTTTTCTTTCT[-/T]TTTTTTTTTTTTTAG | 81550 |
rs560568778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555358 | ATTGGAATGCTTATT[A/G]TGTGCTTGACACCAT | 81550 |
rs560586935 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454279 | CTTGAGAAGATACTT[C/G]TTCCTATTGGGTTTA | 81550 |
rs560602938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521883 | GCCTGGGCAACAAGA[A/G]TGAAACTCCGTTTCA | 81550 |
rs560604832 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461212 | TAGTGTGTTCATCAC[A/G]CTGTTTAATGTTCTT | 81550 |
rs560605101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411698 | CATCTTATTGCTTTG[A/T]TGTCCCCTCACCCCT | 81550 |
rs560613253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507467 | CCTCAGCAAATGCAA[A/G]AGAACGAAAATAATA | 81550 |
rs560626107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408886 | CCCCAAGACCATGGA[A/G]AAAATGTCTCTCCAG | 81550 |
rs560663291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476763 | TAATTCTCATTGTAG[A/T]GATCTTTCGCCTCTT | 81550 |
rs560697263 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451926 | GCATTGAATCTGCGC[A/G]TTAGCTTAAAAACAA | 81550 |
rs560702522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554577 | CTTATGGATAAACTT[A/G]GAATTTTTAAAAAGT | 81550 |
rs560712602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455049 | CTCCCAAGTAGCTGG[A/G]ATTACAGGCGCCTGC | 81550 |
rs560720042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546443 | AGTCTAAATTTTGTT[A/G]TAGAAGTTTAATTAT | 81550 |
rs560736771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438600 | CTTCTGTACTGTTCT[A/G]ACTATTCACATTTCT | 81550 |
rs560760114 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572849 | TCTGGTCCAGCATCA[A/G]TGTCAGGAAAATGAT | 81550 |
rs560761407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441867 | TACCCAAGGCCTTTA[A/T]TGGGCTGCCCGCAAA | 81550 |
rs560768421 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546290 | CCAGTCCATTTATGT[G/T]GTATTCTTTAGAAAT | 81550 |
rs560780273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512870 | TAAATGGTGCAAGCT[C/G]TTGGTGGATCTACCA | 81550 |
rs560787842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445192 | CATTTGTCTATTGCA[A/G]TCATTTTGCAGTACA | 81550 |
rs560804054 | in-del | -/GTGT | 0.00636936 | 0.0560724 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403771 | ATTGGATGGATGTGA[-/GTGT]GTGTATGTACTTTTC | 81550 |
rs560808404 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395861 | AACACTGCATACTAC[C/T]GCACATTGCAGCGAA | 81550 |
rs560808852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403357 | CTTTTTTGGCTTATG[C/T]TTTCTCCTTTTGACA | 81550 |
rs560811259 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418158 | TGCTCCTACCTCTCC[A/G]GCAGTTTATGCTCTA | 81550 |
rs560837702 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475673 | AGCAACTGTGTATGT[A/G]TATTTTCCTTTCTTG | 81550 |
rs560839857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560255 | TAAAATGGTGAGATT[A/G]ATTCAAAGCCTTATT | 81550 |
rs560842878 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508207 | CCCAAAGTAATGTAT[A/T]GATTCAGTGCTATCC | 81550 |
rs560897971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560740 | ATATCCTGTAGAATC[A/G]TAAACAATTTTAATA | 81550 |
rs560910742 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557941 | GATTCTTCTGCCTCA[C/G]CCTCCTGAGTAGCTG | 81550 |
rs560925040 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407949 | TGCTATTCTTGTGAT[A/G]GTGAATACGTCTCGT | 81550 |
rs560940349 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459644 | TTGTTGTGTTGAGAC[A/G]GAGTCTCGCTCTGTC | 81550 |
rs560994078 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450103 | GAACAACACAGAAAA[A/T]ATAAACTATTATAGC | 81550 |
rs561019976 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492437 | AAATATCCCAATGAG[G/T]TAGGTTTTCTAATCC | 81550 |
rs561025720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497294 | AAAATGGGAGGGGAC[C/G]CAAAGGGGGTTGTCA | 81550 |
rs561046471 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555882 | TTGAGATGGAATCTC[A/G]CTCTGTCGCCCAGGC | 81550 |
rs561083155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513347 | GGGTTCCATGAAGAC[C/T]TCTGACATGCCCTGA | 81550 |
rs561088057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488672 | TCTGCCTCCCAGGTT[C/T]AAGCTATTCTCCAGC | 81550 |
rs561112922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408026 | ATTTTCTCTTGCCGC[C/T]GCCATGTAAGAAGTG | 81550 |
rs561138603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534973 | TACTAATGTGACTCA[A/G]AAGGGTTCCAAAGGT | 81550 |
rs561209925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491487 | TTGAACTTAGAGCCT[A/G]GATGGCAGAAGTGGA | 81550 |
rs561212966 | in-del | -/TT | 0.263509 | 0.249635 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452817 | ATCACTGTTCTTAGT[-/TT]TTTTTTTTTTTAATT | 81550 |
rs561242305 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410608 | GATCTTTTCTCTAGG[C/T]TGCCTGCTGATTCCC | 81550 |
rs561245902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526676 | TATTTGAAATCTTAT[A/G]TCTTAGAAAAATCTT | 81550 |
rs561275562 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503218 | TCCTGTACCTTTTTC[A/T]CTATTCCAGTGTTAC | 81550 |
rs561344991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472875 | GGGAGGAGAGAATGG[A/G]GGAGTTATTGTTTAA | 81550 |
rs561350535 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551969 | GGTCTCTCCCTCGAC[A/C/G]TGTGGGGATTACGAT | 81550 |
rs561355691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567785 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 81550 |
rs561357297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473797 | GGACAAGGCCACTAG[A/C]GGGCTCCCTGGGCTA | 81550 |
rs561380844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432022 | TATTCAATGTGGGAT[A/G]GGAAGTGGCTACTTT | 81550 |
rs561385729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450841 | AGGGTATTAGGTTGC[C/T]TTTCTTGCTAGACTG | 81550 |
rs561400206 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500068 | GAATCACAGCAGAAG[C/T]CTCTAGGATTTTGGA | 81550 |
rs561411552 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424765 | CTATCTAATTCAAGA[A/C]CATTTAACCCGATAT | 81550 |
rs561412997 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428417 | TTTCTAAGTTAATAT[A/T]GGGGCCAAGGGAAAA | 81550 |
rs561414420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504839 | GAAGCACAAGGGGTC[A/G]GGGAACTGTCTCCCA | 81550 |
rs561416280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542721 | ATGTCTCTACTTAAT[A/G]CTATTTCTCTTTAGT | 81550 |
rs561529799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475061 | TCTTTTCTTTATCTA[C/T]TTTTAAGTCTTTTCC | 81550 |
rs561621531 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465977 | TGTTTTCCTTTGCCA[C/G]AGGGTTAAGAGGGTA | 81550 |
rs561631524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425467 | ACTCCTAAAGAAATT[A/G]AAAATAGAACTACAG | 81550 |
rs561665168 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501744 | TTTTAAACAACCAAC[G/T]ATTCTCTTTAGGACA | 81550 |
rs561666655 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417224 | CTTGCTATGTTGTCC[A/T]GGCTGGTCTGAAACT | 81550 |
rs561667953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480389 | TGGGATTCTTTTTGT[A/T]AGGCCCCTTTTCTCT | 81550 |
rs561687196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517372 | ATTAGGCTAGATGTT[A/T]TTGTGAGGGATTTCC | 81550 |
rs561688987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525578 | ATTATTAACAAAATT[A/G]CTTGTTTTATTCTGT | 81550 |
rs561698530 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404967 | TAAAAATGGGAGGTG[A/C]CCTGCACAAGCTCTC | 81550 |
rs561700785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504452 | GTCTGTAAAGCAGGC[A/G]GTTTACAACCTTAAA | 81550 |
rs561704405 | snp | C/T | 0.478603 | 0.101197 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555848 | AAAACCAACCTATTT[C/T]TTTCTTTTTTTTTTT | 81550 |
rs561717953 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457903 | TCTTCTAAGGACACT[C/T]GTCATTGGCTTTAGG | 81550 |
rs561718502 | in-del | -/TTTTTT | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556017 | ACCATGCCCAGCTAA[-/TTTTTT]TTGTATTTTTAGTAG | 81550 |
rs561720031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572895 | TGTTACAGAACTCCA[C/T]GATGCCAGCAGAACA | 81550 |
rs561725598 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455441 | TGAATAATTTAGTCA[A/G]AAACCTCCCTTGAAA | 81550 |
rs561746944 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404188 | AGGAAAAAACAAGGC[A/G]CTGTATATGTTTTCT | 81550 |
rs561755051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565301 | ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 81550 |
rs561794560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556498 | TTAGGTTGGGAAAAT[A/T]ATTCTCTACAAATTT | 81550 |
rs561802862 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445683 | GTTTTCCAGGAGATG[G/T]AGAGTTCTAGGAAGG | 81550 |
rs561815001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450671 | TCTGAATGTGTATTT[A/G]TGCCAAGAGATAGGG | 81550 |
rs561816142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422328 | TATATAGCATGGATT[C/G]ACTGGTAGGAAAGGG | 81550 |
rs561825357 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412802 | AATGGTTTACCTTAT[C/G]GCAGTAGCTTTCATT | 81550 |
rs561849700 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504634 | AAAAAATATTTGATT[C/T]GGTGGTGGCTGGCAA | 81550 |
rs561885564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404221 | AAATATTGTGTCTTC[C/T]GATATTTGGCTAAGG | 81550 |
rs561908358 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551629 | TCCTTTTATTTTTTC[A/T]GTTAAAATTTTCTTT | 81550 |
rs561910348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559494 | TAAAAATTATATATT[C/T]GTTCCTGTACTTAAC | 81550 |
rs561920786 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518236 | CTAGTCTGTAAGTGC[A/T]CCCAGCCCTGGCCCT | 81550 |
rs561921982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550430 | TTTTCTTCTCAATAG[G/T]CATGTTCTTGGAGGA | 81550 |
rs561938607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406049 | TGTTAGAAGACGGTC[A/G]CATTTTTGGGGGTTG | 81550 |
rs561953073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397910 | CGCTGCGGCCGGAGC[C/T]GCCTCTTCTTACCCC | 81550 |
rs561989272 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551736 | TTAAGAAGAGGTTTA[A/C]TTGACTCACAGTTCT | 81550 |
rs561990954 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457312 | CTTGCTTTTGAACCA[A/G]TTAACAAGTACAAGA | 81550 |
rs562002907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406635 | CCTGCTAGTTAGGGG[A/G]AAAAGCTTTAGAATG | 81550 |
rs562061525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437649 | AAATTAATTAATCTA[C/T]TCTAGTTTATCTGAC | 81550 |
rs562066616 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60397261 | ACCAGAGGAGTTTTT[C/T]CTTTTCTTTTCTTTT | 81550 |
rs562077959 | in-del | -/A/AAAA | 0.353371 | 0.227628 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563232 | ACTCCATATCAATTT[-/A/AAAA]AAAAAAAAAAAAAAA | 81550 |
rs562079992 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423485 | CGATAAGAGAAAATA[C/T]TCATTTTCTTAAGTG | 81550 |
rs562098895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455984 | CTGAGGAAGGAGAAT[C/T]ACTTGAACCTGGGAG | 81550 |
rs562110561 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513167 | AGGCTTGAGGCATGC[A/G]CCATCTGCAGTCACG | 81550 |
rs562140185 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537703 | TAGAGAGGCCTTAGC[A/G]CAATTACACTATGGA | 81550 |
rs562150811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541804 | ACAATCTCGGCTCAC[C/G]ACAACCTCCGCCTCC | 81550 |
rs562184442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463167 | TTTGGGAAGTCAAGG[C/T]GGGCGGATCACCTGA | 81550 |
rs562190574 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507571 | GTGGAAACTGAACAA[C/T]CTTCTCCTGAATGAC | 81550 |
rs562200190 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525790 | GCATGAGAGTGCTTG[A/C]GTACATAAATGAAAG | 81550 |
rs562217091 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509311 | CTCAAGTACTAGTTT[A/T]AAAAAAAAAGCTCCT | 81550 |
rs562222146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496619 | GAGGCAAGGAGTTTA[A/G]TGACTCTATACATAA | 81550 |
rs562231424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563559 | GGGCTGTCCTGTGCA[C/T]TGTAGGATATTTAGC | 81550 |
rs562268850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487407 | CTTGAACTCGGAAGG[C/T]GGAGGTTGCAGTGAG | 81550 |
rs562277427 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541186 | TTCTTTCTTTTTTTG[A/T]GACGGAGCCTTGCTC | 81550 |
rs562287328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501241 | TGGACGATGACTCTT[C/T]TGGCTACTTCCTGCT | 81550 |
rs562376171 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400138 | AATAATGCACTAAAT[-/G]GTACCTTGTAAAGCT | 81550 |
rs562402492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454982 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAACCT | 81550 |
rs562414554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60495243 | ATTCAGCAGTATAAC[A/C]ATATTAGGGCATTTG | 81550 |
rs562423877 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60545941 | CATTCTCCTCCTCTT[G/T]TATTTTGTTTTCTAT | 81550 |
rs562432675 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568496 | GGACTTTGGCAACTT[C/T]GTGTTGTATAAGACA | 81550 |
rs562435583 | in-del | -/G | 0.304438 | 0.244001 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60397287 | TTTTTTTTTTTTTAA[-/G]GGGGGGGGGTCTCAA | 81550 |
rs562462979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493398 | CAGGCATGGTGGCTC[A/G]TGCCTGTAACTTCAG | 81550 |
rs562465945 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525196 | TTTTTTTTTTTGAGA[C/T]GAGATCTCTGTCTGT | 81550 |
rs562474434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522707 | TTTAGGTTTTTCTGC[A/G]TTAATAGAAAGAGAT | 81550 |
rs562476606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531366 | TATTTCTCCTTCATG[A/G]TGGAGGCAAGAAAAA | 81550 |
rs562479017 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547510 | AGTTACCTAATATCT[A/C]TGGGTCCCAGTTTCA | 81550 |
rs562490392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492851 | AGTGCTCATCCAACA[C/T]TTTAAAAAAGTTTTC | 81550 |
rs562491225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538181 | CTCCTTTTCGTGTGG[A/G]TATGTATTTTTACTT | 81550 |
rs562492648 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396288 | AATACGGGACGCCGC[A/T]GAGGTGAAAGACCAA | 81550 |
rs562513189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539443 | GGTTATTATTCCATA[C/T]TAGTTTAAAGATAAA | 81550 |
rs562523196 | snp | A/C/G | 3.44182e-05 | 0.00414827 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485852 | TGATCGAAGAAAAAC[A/C/G]TTGCAAGTTACAATG | 81550 |
rs562523496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444057 | AGCCTTGTTTTTGTT[A/G]GTCCTTATATTTTCC | 81550 |
rs562541384 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478645 | CTTTCAAAGAACCAT[A/C]TTTTTGTTCCATTGA | 81550 |
rs562558608 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554462 | TCATTGATACTCCAG[G/T]GTACCTTTCTCTTTG | 81550 |
rs562587905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435271 | TTTATAGGCCTTATT[A/G]TTTTCTTATTTCAAT | 81550 |
rs562588008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445050 | TTACAATGACCTTTT[A/C]TTACCTTTCAATTTT | 81550 |
rs562604846 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571430 | CAGCCATTTGACTTC[C/G]AGCAAATATAAGCAT | 81550 |
rs562636061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540407 | CTCATCTATCACCCA[A/G]CCTTTTACCATTTTT | 81550 |
rs562644097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429032 | TCAAAAATGTAAGCA[A/G]CACTAAGCACTTTGT | 81550 |
rs562657523 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492855 | CTCATCCAACATTTT[A/C/T]AAAAAGTTTTCATGT | 81550 |
rs562673135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470142 | TACAGTATATATCTT[C/T]TTTGTGCCTGACTTA | 81550 |
rs562718982 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464712 | CCAGGCACAGAAAGA[A/C]AAATATTGCATGTTC | 81550 |
rs562728723 | in-del | -/T | 0.302936 | 0.244331 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558965 | CAAAGACATTTTTGC[-/T]TTTTTTTTTTTTTTT | 81550 |
rs562812556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469199 | AATAGTTCTACATAA[A/G]CAGCCAAGTTTGTGA | 81550 |
rs562840505 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431268 | CTTCAACAGGAGTAT[A/G]ATATTTTACTTGTGA | 81550 |
rs562894322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489431 | TTTGGTTGTTCTTCC[C/T]GCAATGTCTTTCTGT | 81550 |
rs562906846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559680 | ACTTATATGTGGAAT[A/C]TAAAATAGTCAAACT | 81550 |
rs562919177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408675 | GTATCTAGCAGAAGA[A/C]ATTTCTAAGCAGCAT | 81550 |
rs562991310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433892 | CTTTCAAAGAAATGG[A/G]TCAAAAGAAAATTGG | 81550 |
rs562995958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513532 | ATAACTTCATGATTT[A/G]GGAGACACTATAGAA | 81550 |
rs563003474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426428 | TAGCTGCCCTTGTCA[C/T]ACACAAAAAGTAACT | 81550 |
rs563004285 | snp | A/T | 1.65293e-05 | 0.00287479 | stop-gained, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528714 | AGTGATGGTGCTTTT[A/T]AAAAAAGAGATAACT | 81550 |
rs563011931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460731 | AATATATGGCCAGGC[A/G]TGGTGGCTCAAGCCT | 81550 |
rs563030216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483966 | AGTTATTTGGAAATA[C/T]GAAGTTCAAGGAATT | 81550 |
rs563067097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566948 | CATGAAGCTTTCTTT[A/G]TATGTAAATTGTATT | 81550 |
rs563110537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400468 | TATCTTCTGGCTGGG[C/T]GCAGTGGTGGCTCAT | 81550 |
rs563115876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553032 | TAGAGACATTTTCCC[C/T]ATTGTCTTGGCTGTT | 81550 |
rs563119138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458797 | CTACATGTGGCTGGA[A/G]GATTGTATTGGACAG | 81550 |
rs563123837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60562213 | AGCTACTCGGGAGGC[C/T]GAGACAGAAGAATAG | 81550 |
rs563125951 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553786 | AATCACCTCCCACCA[C/G]GTCCCTCCATTGACA | 81550 |
rs563171172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419561 | CCATGTGTTCTCACT[C/T]ATAGGTGGGAGTTGA | 81550 |
rs563173081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410105 | CTCTTGCCATCGCCA[C/T]GAAAGAAGTGCCTTT | 81550 |
rs563174360 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60442690 | TATATATGTATGGCA[C/G]TTTAGAAATTATGTA | 81550 |
rs563189535 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499169 | CAGAGATTAGTGCCA[C/T]CATCAAGGACCTGAA | 81550 |
rs563192377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519246 | TATTGAGCATCTGCT[A/G]TGTGCCAGGACTATG | 81550 |
rs563198896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451875 | TCAAATGATTAAGAC[C/T]CTTAAAAATATCATG | 81550 |
rs563200068 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552490 | CACAGTCTGGTGTTG[A/G]GTGCCTGTGGCTTTT | 81550 |
rs563209708 | snp | G/T | 0.0456336 | 0.143994 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466990 | TTTTTTTGTTTTTTT[G/T]TTTTAAGTTTCAGGG | 81550 |
rs563250447 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471172 | TGTTGAAGAGTTTTT[A/T]TAGGTTTAGCTTTTA | 81550 |
rs563273274 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512810 | TACAGCCTCCCTCCC[A/C]GCTGCTTTAATGGGC | 81550 |
rs563275597 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410593 | CTAGGAATTGGCCAC[A/G]ATCTTTTCTCTAGGC | 81550 |
rs563297551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490658 | AGAATTGGAAACCAA[A/C]AAGTAGAGAATTATT | 81550 |
rs563299427 | snp | A/C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502006 | GTGGTAACGTGTATA[A/C/G]CCCTACTGCAAATAG | 81550 |
rs563301337 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530972 | GAGGTATAAGCAGAG[C/T]GTTAGATGTTGCCTG | 81550 |
rs563311904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544879 | TCTTTTAAATCTTGA[C/T]AGTATCAGAATTTTA | 81550 |
rs563316495 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439139 | AGAGATAGGAAAAGT[A/G]AAAGATGTATTGTAA | 81550 |
rs563341114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459473 | AGATTTAATATCGAA[G/T]TTAAAGTTTTTATTT | 81550 |
rs563350091 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524869 | TTTGGGAGGCCTAGG[C/T]GGGTAGATCATGAGG | 81550 |
rs563362460 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503914 | CATCTAATCTTAACC[A/T]GTTTGACCATAAATG | 81550 |
rs563367081 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433645 | ATGTGTTTAATAAGT[A/T]CAAAGTACATGTACC | 81550 |
rs563394042 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555473 | AAAACTACAAATATG[C/G]GTTCAGAGCTGTTAA | 81550 |
rs563431948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499714 | CAGGAAAATTTCTAG[A/G]GGTCCAGTGGTGTGG | 81550 |
rs563439078 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519916 | ATGCATTTTACATGG[A/G]ACTAAACAGGGCAAT | 81550 |
rs563474093 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413107 | CAACAGGAAGTTAGC[A/C]TGTGAAAATGCTGCC | 81550 |
rs563483522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536213 | AAACAAAAAACCTAA[C/T]AGTAGTAATAATGTT | 81550 |
rs563495744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497196 | GGTGGATGGCAAGCG[A/G]AAGCTCAGCTTGAGT | 81550 |
rs563499454 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551500 | TTAATTGCAGCAGCA[A/G]CCACTGATTGAAATT | 81550 |
rs563508124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545438 | CCTCTTGGTCATGAT[A/T]ATTAAAGAGTTTATT | 81550 |
rs563537218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542620 | TGAACCTTGATGGTG[A/G]TGGACTAAAAGTGGA | 81550 |
rs563556244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526521 | AAACTAAAAGTGACC[A/C]TTTTTCTTCTCTCTA | 81550 |
rs563556618 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498316 | AGTCACTCAACTACA[A/T]AATTTAACTGCAGTG | 81550 |
rs563557028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505561 | TCTGAAGCAAGCAGC[A/G]GATCTCTCAGCACAG | 81550 |
rs563572783 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425079 | GTTAACAAAATAGAC[-/A]AAACCATTAGCTAAC | 81550 |
rs563592207 | in-del | -/T | 0.00177082 | 0.0297031 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510765 | TGGAAGGTAAGCTAA[-/T]TTAAAGTTGATTCCT | 81550 |
rs563617006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398940 | CCCATTTCTCATTAG[C/G]TTGAGCGTTGATCCT | 81550 |
rs563655865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438947 | GTTGATTTTAGAATT[A/G]TTGAGTTTATCAAAG | 81550 |
rs563665296 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541955 | TGGTCTCGAACTCCC[A/G]ACCTCAGGTGATCCA | 81550 |
rs563668553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534906 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACCC | 81550 |
rs563668864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525820 | GTGTTAATTGTTAGT[A/G]AAAACAATAATAAAA | 81550 |
rs563727734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448917 | TCAGCTACTCGAGGA[A/C]CTTATGTACTGCTAT | 81550 |
rs563747112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431113 | TAAATGAGTTTTTTT[A/T]AAACCCTGAGTGATC | 81550 |
rs563788175 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431964 | AATTTTTAAGCTAGC[A/G]TTGATTCAAGTCCTG | 81550 |
rs563848669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424273 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGCGCT | 81550 |
rs563853422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496817 | GTCTTATTGTTACTG[A/G]AGGGTCCTTGTTCTT | 81550 |
rs563860091 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520086 | TTGAAACACCAAAAA[A/G]TTAGTTGTTTGAACA | 81550 |
rs563866113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473926 | CAGGAAAGGGAGTCT[C/G]CCTTTCCCTGGGGGA | 81550 |
rs563880083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474321 | CCAATAAATAACAGC[A/C]TAGCTAGGCATTCGG | 81550 |
rs563900219 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446152 | TTCCTCATTGATTAT[A/G]TTTTTTCCTTTCATT | 81550 |
rs563911726 | snp | A/C | 4.96184e-05 | 0.00498063 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510758 | TTGAATGTGGAAGGT[A/C]AGCTAATTTAAAGTT | 81550 |
rs563984886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437409 | GGGGTTAGAGGCGTG[A/C]GCCACTGTGCCCAGC | 81550 |
rs563989263 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442868 | TGGGATGGATCAAAG[C/T]TTAGGATTTTTGTCT | 81550 |
rs564046689 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489152 | ATCCTGAACAACAAA[A/C]CCCTCTCTCTTATAT | 81550 |
rs564090466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60562638 | ACTCATTAACATTTC[A/G]TGGTTCAAAATATCC | 81550 |
rs564100089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405976 | CAGGAGTTGTTAAAG[A/G]CTTGATTTCTAGGTT | 81550 |
rs564103059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422250 | CCCTGTGAGACAAAA[C/T]AGAACTACACAGGTG | 81550 |
rs564127224 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60509130 | CTTTGGTTCAAGAAA[C/T]TTCTTCGTAGGATAT | 81550 |
rs564133916 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503544 | ATTGCACATCATTTC[A/G]GAAATCCAATGTGAC | 81550 |
rs564145522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455204 | AGGTGTGTGCCACCA[C/T]ACCTGGCTTATATTT | 81550 |
rs564162494 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541171 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTTTTTGA | 81550 |
rs564166571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429163 | ATTGTTTAGTATTTA[C/G]CTGTTTAGTGACACA | 81550 |
rs564169696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457177 | GTTTACTCATAGAAT[A/G]TTTCTGAATTGTGGA | 81550 |
rs564179851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524548 | AAAAAGAGAAAAGAA[A/G]AGAACGATTGCCTCT | 81550 |
rs564200630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532144 | AAATTAAAAAAAATC[A/G]AAGTACCAAATTTAT | 81550 |
rs564211753 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565211 | CAGGCGCCCGCCACC[A/G]CGCCCGGCTAATTTT | 81550 |
rs564240060 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420585 | ATACAGATATTCAGG[C/T]ATTTCAGTGACATTT | 81550 |
rs564254147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569962 | GAAACTATGACACTC[A/G]TAGATGACAACACTG | 81550 |
rs564265388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517333 | GGAAGGAAACTAGGC[C/T]GAGACAAGAGAGAAT | 81550 |
rs564276954 | snp | C/T | 0.00305386 | 0.0389564 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528327 | TTATTAATGCAGAGT[C/T]TTCATCTTAATTTGC | 81550 |
rs564279453 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398040 | GCTCGGTAGAACTTT[C/T]CTTGAAAGGATGGTG | 81550 |
rs564300414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515474 | ACGATAAAGTGATAC[A/G]CACACACATATATAT | 81550 |
rs564322002 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446613 | CCAGTATTAATGAAG[A/T]TGTTTTGAAAAATAA | 81550 |
rs564328754 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426505 | ACTATCTATATGTAT[A/C]CTGTAACATCATGTT | 81550 |
rs564334251 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547732 | CTCTTCATATTGAAA[A/T]TATTATTTCTATCCT | 81550 |
rs564363521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554669 | TAATACAGAGACTTC[A/G]TGCTTTCCTAACTTG | 81550 |
rs564364562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486741 | TTAATTCCCATTAAT[C/T]AACCTCTCCCACTGT | 81550 |
rs564367556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423106 | TCAAGCTTTTCAAAA[C/T]CAATATATAAAGCAA | 81550 |
rs564375365 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464456 | GCATCTGCACTCCCA[G/T]TTTTATTGTAGCACT | 81550 |
rs564384248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415259 | TTTAGATTTGTGTTC[C/T]GAAACTTTGAGAATT | 81550 |
rs564389515 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534733 | GAGTTTGAGACCAGC[C/T]TGGGCGACATGGTGA | 81550 |
rs564396708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564459 | ATCTCAGAATCTTAG[A/G]CGAAGATGACATTGG | 81550 |
rs564406628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455856 | GTGGATCACCTGAGG[C/T]CCAGAGTTCGAGACC | 81550 |
rs564406805 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60397851 | GAACGCGGCCGGAGC[C/T]CGCGGGCCCATAGGA | 81550 |
rs564408597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445315 | TCTTCTTTGTCTTTC[A/G]TCAGGAGAAATGGAG | 81550 |
rs564422945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411041 | TGTGCCTGTGTTTAC[A/G]TTGTTGTTAGTGCAA | 81550 |
rs564445172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508409 | CAGCATGATATTGGT[A/G]CCAAAACAAATATAT | 81550 |
rs564461942 | snp | A/G | 3.34778e-05 | 0.00409119 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485915 | TGAAAAGCAAAGGAC[A/G]GCTGCTATTGCTGAA | 81550 |
rs564497657 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395639 | AATTCTGATGATTGG[C/T]ACAACATATTTTCAT | 81550 |
rs564498135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462427 | TTCACTCATCATTGA[A/G]GCAGCATGCCTACTT | 81550 |
rs564503782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545636 | TGAAAATAATGTGGA[C/G]AATGTACACGAATGT | 81550 |
rs564525677 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549354 | AACCTGCCATTTGAA[A/T]ATCTGTGTCATCATA | 81550 |
rs564539080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546567 | ATTTAAAGTGGTCAT[A/G]AAAAGACTGAATATG | 81550 |
rs564606782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404036 | CTGTTATTTTACTTG[A/C]AAGATTTTGTTGAAA | 81550 |
rs564610870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501399 | GCCATTCCGATGGGT[C/T]GTAATACTGGTTTGC | 81550 |
rs564611509 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411855 | CACATTAAAGTGATT[C/G]TTTTGCACATTAAGG | 81550 |
rs564617012 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553519 | TCTGCTCTAGAGATA[-/T]CTACCTGAGACTGGG | 81550 |
rs564640415 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572395 | AGTGATATGATCAAA[A/T]TTAAGCTTAGGAAAT | 81550 |
rs564674279 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426547 | ATATACACAATAAAA[A/T]TTTTTTTAAATGTCA | 81550 |
rs564684353 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516027 | ATGTTCATATTAGCA[A/G]CATCATTTATTTGGG | 81550 |
rs564685636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491602 | AGGCAATTGAAAAGT[C/T]ACATAAGATGAGGAC | 81550 |
rs564733603 | snp | G/T | | | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467366 | ACCTTATTGAGAAAT[G/T]GGAGTTACAGAGAGT | 81550 |
rs564735007 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447750 | ACTAAGTTCCAAGCC[C/T]ATCTGATATTACCAT | 81550 |
rs564745145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436591 | TGGCTGTATTTGGCT[G/T]TATTTCGAGGTTCTC | 81550 |
rs564752670 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396508 | AAGGGCATCGGCGGG[G/T]AAGCGGCTGTGGTTG | 81550 |
rs564803401 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553300 | TACCCTAAATCATCA[C/T]TCACTATCAGCATTT | 81550 |
rs564814817 | in-del | -/TTA | 0.0236746 | 0.106192 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462671 | GCCCCTTGCTAGTTT[-/TTA]TTATTATTATTATTA | 81550 |
rs564815607 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60545896 | TCCTCTGTTTCTCTC[G/T]TTTTTCTCTTTATCT | 81550 |
rs564816159 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60397003 | GAACCTCCTCGCGAC[C/T]TTCCAAGGTGTGCAA | 81550 |
rs564817408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501957 | CAAAATACTATAGCA[A/G]TGGAAACTCTCTGTC | 81550 |
rs564852755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453919 | TTTTTTGTTTTTTTT[C/T]CAGTTCTCTTTAAGG | 81550 |
rs564855735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427409 | AAAGGTACTTTTTTT[G/T]TGTGGGGAGGCTGGG | 81550 |
rs564861867 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539121 | CTGGAAGGTGATAGG[C/T]AAATTGTTATCGTCT | 81550 |
rs564879824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499869 | TACTCTGGCGGATTT[A/T]TCAAGTGACCCAAAA | 81550 |
rs564918920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492693 | TATTTTTTTTTTTGC[G/T]GGGATTCCATAAACC | 81550 |
rs564940193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453098 | TTTAAGATATACCAA[A/G]GAAACTATGCAATAC | 81550 |
rs564940864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469440 | CACACACACATACAC[A/G]CACACACACACACAC | 81550 |
rs564949757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521997 | TAAGCAGAAGGTGGA[A/G]CTTTCTTCTATACAT | 81550 |
rs565035968 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548811 | TGCTGAAAATTAGTA[C/T]GATCCTTTTGATTAT | 81550 |
rs565063545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529675 | TAACATATAAGTTAA[G/T]TATTTATTTTATAAT | 81550 |
rs565070375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476834 | CATTGTAAATGGGTT[C/T]GCATTCTTGATTTGA | 81550 |
rs565075867 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422176 | CAAAAAGGAGGGAAG[G/T]CGTTTCCTTTGGCAA | 81550 |
rs565076760 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404425 | ACGCCATTCTCCTGC[C/T]TCAGCCTCCCAAGTA | 81550 |
rs565113698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513454 | TTTCTCAGAAAATGG[G/T]ATTTTCTTTTCTATC | 81550 |
rs565145887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435097 | CCCAAATTATTGTTA[A/C]TTTAGGCTCAGTCCT | 81550 |
rs565147805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527683 | TTGGACATTATAGGC[A/G]GTATTATGCTTAGTA | 81550 |
rs565196418 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432776 | CTTTTATGTTTTTTC[A/C/G]CTCTCTTGTCCCACC | 81550 |
rs565213763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485010 | GTTATAAAGTTCATT[C/T]TGAAAAAATTCTTGT | 81550 |
rs565276324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512951 | TGCCCAGTGGTGAAC[G/T]CTGTGTGGGGACTCT | 81550 |
rs565329317 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457489 | GGAGGCTGAATAAGT[A/G]CCCCCTCCCTCATGT | 81550 |
rs565356310 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498841 | ATGTTGATTCCAGGG[G/T]ACCCAAAATGTCACT | 81550 |
rs565365471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535015 | TAAAGAATATTACAC[A/G]TTGGAACACTTTAAA | 81550 |
rs565371323 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544802 | CACTTGAGAGATTTC[A/T]AAGTGAGTTCATGCA | 81550 |
rs565377511 | in-del | -/TGTT | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441162 | TTTATGACTAAAAAC[-/TGTT]TGTCTTGCACTGAAA | 81550 |
rs565392139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520215 | ATTTGAATAATTATA[C/T]AAATTATAATTGAAA | 81550 |
rs565403065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433557 | TTATACTATCTGAGG[C/T]ACACTTACGGCACAA | 81550 |
rs565403904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424837 | TCTCATCTGCTTTCT[A/G]TCTCTATGGATTTTT | 81550 |
rs565421388 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60435433 | CTCCAAACCTACCCC[A/G]GTAGAGTCCCCAAAG | 81550 |
rs565446461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409022 | GCCTAGGGACTTGGT[A/G]CCCTGTGTCCCAGCC | 81550 |
rs565468708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468618 | TCTTGCATCTGTATC[C/T]CAAGTTATCCTCCTA | 81550 |
rs565468761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467832 | CTAATATTTTTCCCC[A/G]TTTATATTAACAATA | 81550 |
rs565482635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460637 | GTAGGAATGGACCCT[C/T]AATTGTGTGTTACAG | 81550 |
rs565490900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557856 | TTGAGACAGAGTCTC[A/G]CTCTGTCACCAGGCT | 81550 |
rs565497876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480807 | GGTATTATAGCCAGC[A/G]TGATGGGGAGTGCTG | 81550 |
rs565502209 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500455 | CAGTTGACAGAGGAA[C/G]AGAAGACTGGGGCCT | 81550 |
rs565527948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410787 | TGTGCAAGAGCTGGA[C/T]GTACGTTTTCCCTTA | 81550 |
rs565559417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555452 | ATGTTTACTTTACAC[A/G]CTAGGAAAACTACAA | 81550 |
rs565567044 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554376 | TGAACTTTCCTAGTC[-/T]TTTTTTATTTCTCTT | 81550 |
rs565572764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417847 | GTTTTAGAGGTGGTA[C/G]ACTCATCTCACCATT | 81550 |
rs565602294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475827 | CATATGTTTGTTGGC[C/T]ATTTGTATGTCTTCT | 81550 |
rs565635404 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405449 | GGAATTAGCCTTTTC[A/T]TGGTGGTCAGAGAAT | 81550 |
rs565684564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488350 | TGAGTGTCATTTCCT[A/G]AGGAAAGAACTCAGA | 81550 |
rs565688584 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444023 | TCAGAATTTCCTTTT[C/T]TTATGTCATGAATGC | 81550 |
rs565779265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510074 | ACCATAGAGACATTT[A/G]TAGTCTCAGTCTCAT | 81550 |
rs565780024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503538 | AAGAAGATTGCACAT[C/T]ATTTCGGAAATCCAA | 81550 |
rs565780189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557005 | AGGTCGGGAGTTCGA[G/T]ACCAGCCTGACCAAC | 81550 |
rs565787359 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398266 | AACGGCTCTCTGCAA[C/T]TACTGCTTTAGGAGA | 81550 |
rs565803351 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415575 | CAATGCAATCTTTAT[A/G]ACTCATTCACACACT | 81550 |
rs565806432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439105 | GGGCAAATAAGACAA[A/T]GCGTAAAAAAAACTG | 81550 |
rs565815598 | snp | C/T | 0.000197609 | 0.00993808 | utr-variant-5-prime, intron-variant | TDRD3 | GRCh38.p7 | 13:60397361 | CCCGGCCTAAGCAGC[C/T]ACCATGGCCCAGGTG | 81550 |
rs565851587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60439974 | GTTATACAGAATCCA[A/G]TGAAAAAGGAAAAAA | 81550 |
rs565862641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431659 | TTTTTTTTTGCATAT[A/T]AATCCTTTCACCAGC | 81550 |
rs565862996 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467006 | TTTAAGTTTCAGGGT[-/AC]ACATGTGTAGGATGT | 81550 |
rs565923908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572119 | CTAGATACTAATTAG[G/T]AGGAGCAGCCCTTAG | 81550 |
rs565926728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423815 | TTAGAGGAAAATTTA[C/T]TTTACTGCTTTTATT | 81550 |
rs565941015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551667 | CAATGTGTATTAGTC[C/T]GTTTTCACACTGCTG | 81550 |
rs565948926 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464608 | CACACACATACACTG[G/T]AATATTATTCCGCCA | 81550 |
rs565960864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60573078 | CTGGAGCATACAAGT[C/G]TTCTCTCGCCATTTA | 81550 |
rs565967523 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525916 | ATATAGTTCTCCAGT[A/G]TAGTTCCATAGACCC | 81550 |
rs565967912 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446228 | TATTATTCACAGAAT[C/T]ATTATTTTTTCTGAG | 81550 |
rs565970187 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60556334 | TTTGTAAAAATAAAG[G/T]CTGACAAGTCACCAA | 81550 |
rs565993974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421812 | TCCAAGGCAGACCTC[A/G]AAAAAAACTACAGAA | 81550 |
rs565995663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430334 | GTAGGCAGCAATGCT[A/G]TGAGTGCAGTAGTCA | 81550 |
rs566008520 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486952 | TTCTTTTATATAACT[-/G]AATAATAATCCATTA | 81550 |
rs566030435 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502062 | AGTGTTGTGTAGTAC[A/C/G]TAATTTCCATCTAAA | 81550 |
rs566044233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486971 | AATAATCCATTATGT[G/T]TAGACAGTCAGCTCT | 81550 |
rs566144822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514476 | CACTACATACAGGAA[A/G]CAAAATTTTTAATCT | 81550 |
rs566168846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493905 | TACAGACTTAAAAGC[C/T]TTTATATGCAGTCGG | 81550 |
rs566174267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414447 | GCCTGCAATATTTAC[C/T]ATCTGGTTCTTTACA | 81550 |
rs566206385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485266 | TTTAGGCAGTGATGC[C/T]TTTTTTTTTACTTTA | 81550 |
rs566256113 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522250 | GTTTTTATTAAAGCA[G/T]TCTTCCTGCCCTGTT | 81550 |
rs566269132 | in-del | -/TTC | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417810 | CCTCCATCTCCCAAG[-/TTC]TTCTTCTCTTTACAC | 81550 |
rs566290961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516759 | CAGATGCAACAGCAT[C/G]CTCCACTCACCATGT | 81550 |
rs566298813 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396713 | GCAACTCGATCTGCC[A/C]GCGGGGACTCAAAAA | 81550 |
rs566300322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477960 | TGGTATCAGTTCTTC[A/T]TTGTATGTCTTAAAG | 81550 |
rs566306744 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508308 | AGGAGCCCATGTAGC[A/G]AAGACAATCCTAAGC | 81550 |
rs566342737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479223 | CATTAATTTCAGATA[A/G]TTTTTTGATTTCTGC | 81550 |
rs566353098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523705 | CCTCAGCCTCCTGAA[C/T]AGCTGGGACTACAGG | 81550 |
rs566361412 | in-del | -/TTTA | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408581 | TGACTCTTGTTATGT[-/TTTA]TTTAGCAAGGAGACT | 81550 |
rs566373708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547963 | ATTTTGGCAGAGGGA[A/T]GTCCCTTGAATCCTG | 81550 |
rs566380065 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514945 | ATAAATGCAGTATTT[A/T]ATTTAGTATTTAAAA | 81550 |
rs566383508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413363 | ATGGCTGGTGTTTAC[C/G]AGCATGGGCTCTTGA | 81550 |
rs566404099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471430 | ACTGTTTTGATTACT[A/G]TAACTTTTTATTAAG | 81550 |
rs566425173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403083 | CGAAAAATGACTGGA[C/T]GTTTTGTTAAACTGT | 81550 |
rs566437413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403695 | AAAGGAGGAAAGAAC[C/T]GCATAGACAGAGAGC | 81550 |
rs566466725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569733 | AAAACAAACAGACCA[A/G]TGGAACAGAATGGAG | 81550 |
rs566471793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530808 | GGATGTGCCTATGAG[A/T]GTGTGTGGCTAAAGG | 81550 |
rs566502087 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60570141 | CCACCCACAGAATGG[A/G]AGAAGATATTTTCAA | 81550 |
rs566532378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427710 | TTAAGCTAACCAATA[A/G]GGTTCACTGAAAGTA | 81550 |
rs566540143 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482666 | ATTAGATTAATATCT[A/T]AAATATAGGTTTTAA | 81550 |
rs566549851 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532704 | TGGGAACTTCTGGAA[A/G]GTTCTTCTTCCTGTA | 81550 |
rs566573858 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425120 | AAAAAATGCATAACT[A/C]TGTAAAATAAGAAAT | 81550 |
rs566575790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509378 | TTTTGGAGAGGTGCT[A/G]TATGAATTACATTTC | 81550 |
rs566581783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527660 | TTCTATATTTATCAC[A/G]TTATTTCTTGGACAT | 81550 |
rs566584533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419852 | GAAAAGGAATAATCT[A/G]AAGTAAATATGGTAA | 81550 |
rs566617480 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554764 | AGAAGAATATAACAC[A/G]TATTTGATATGATCA | 81550 |
rs566622473 | in-del | -/A | 0.245346 | 0.249957 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421193 | GACTGGGTAATTAAT[-/A]AAAAAAAAAGAGGTT | 81550 |
rs566633989 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455211 | TGCCACCACACCTGG[C/T]TTATATTTATTTATT | 81550 |
rs566649608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412235 | ACACTTGAAGTAGGT[C/T]ATATTTGACATATTT | 81550 |
rs566650459 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460133 | TTTTCTCATTACCTT[A/C]TGAAAATGAATTCAG | 81550 |
rs566686012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501632 | CAACCAAAGATTCTT[C/T]TTAGGACAAGTGTTT | 81550 |
rs566748757 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482109 | AGCTTACAACTCTCA[A/G]TTGTTTTTTGCTCAG | 81550 |
rs566773979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563091 | AAATTAGCTAGGCAT[C/G]ATGGCTGGTACCTGT | 81550 |
rs566791237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571090 | TGGATTCCTGACATC[A/T]ATAAAAAAAAATTGG | 81550 |
rs566821982 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452276 | TATCTATTTTTGTTA[C/T]TGTAAATGGTGTTTA | 81550 |
rs566825853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492035 | GCTCATAAAGGGCAA[C/T]ACCAGTTACCTTATG | 81550 |
rs566855333 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410396 | GCTAAACAGAGTTTA[A/C]TCTTGTTATCTTGCA | 81550 |
rs566860117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453326 | GACAGCTTAGGAAAA[C/T]GAGTAACATGTAGTT | 81550 |
rs566865536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505934 | AAGTGACAGGAAGAA[G/T]GGAACCAAGTTGGAA | 81550 |
rs566867612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560535 | AAATAGCTTATTTAC[A/G]TTATATTAATGTGTA | 81550 |
rs566888083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544215 | ACACTTTGGGAGGCC[A/G]AGACAGGAGGGTCAT | 81550 |
rs566888820 | snp | A/G | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396239 | CCTGACCTGGCAGAT[A/G]GGGACGCTGCCCCTT | 81550 |
rs566915758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537890 | AGTGAAGATTTTTTT[A/T]AACTAGTTTGCAGAA | 81550 |
rs566948762 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409386 | AGAATGGTAGAGCCA[A/C]TGACAGCTTGCACTG | 81550 |
rs566972196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433031 | TCCAGATATCTTCTT[A/C]TTTTTTTTGACATAG | 81550 |
rs566973163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568784 | TAAAGAACATCCAAA[C/T]TGGAAAGGAAGAGTC | 81550 |
rs566976811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401509 | CTGTATCTGAAAAAG[G/T]GGGACACTGTATTGT | 81550 |
rs566983193 | in-del | -/TCTC | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60566920 | GTCTTACTCTGGTGA[-/TCTC]TCTATCTTGCATGAA | 81550 |
rs566997703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440232 | AAACAGAAAAGCAAA[A/C]TAAGAAAATTAAATC | 81550 |
rs566999900 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459509 | AGGAAAATGTGAAAA[A/T]ATGTCAATTACAACT | 81550 |
rs567001945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400602 | ATTAGCCAGGCGTGG[C/T]GGCAGGCCCCTGTAA | 81550 |
rs567007447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513578 | CTGTGTCCCCACCCA[A/G]ATCTCATCTTGAATT | 81550 |
rs567053075 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514333 | TCAGTTTTAAAGGGA[A/G]AACACATGATAAAAG | 81550 |
rs567058480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60434244 | GGAGGCCGAGGTGGG[C/T]GGATTGTTGGAGCTC | 81550 |
rs567061793 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462921 | GCATAAAAACAGACA[A/C]ATAGACCAATGGAAC | 81550 |
rs567083828 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454976 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 81550 |
rs567119468 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435428 | ACCCTCTCCAAACCT[A/T]CCCCAGTAGAGTCCC | 81550 |
rs567126972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443313 | TCCAAGTGAAAAGGC[A/G]TACAACGTGAGGTAC | 81550 |
rs567127212 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436292 | TTTTTATTTTTGTTG[C/T]ATTTGTTTTTGGGGT | 81550 |
rs567137055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467942 | TGCAGTCAAATCTCG[C/T]ATCACTTCCTTGCTC | 81550 |
rs567144628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432659 | TAATTTTTAAAAAAT[A/G]TCTTTACAACATTGA | 81550 |
rs567148227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553851 | GGGACACAGAGTCAA[A/G]CTATATCACAATGTT | 81550 |
rs567172712 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402022 | CTCTATTCCACATTA[C/G]TTTGAAGATAGCTAC | 81550 |
rs567204774 | in-del | -/AA | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438958 | ATTGTTGAGTTTATC[-/AA]AAAGAGTTTCAAAAT | 81550 |
rs567238539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425821 | AAGACCTTAATGATG[G/T]TCTCTTTCCACATAA | 81550 |
rs567239714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441114 | AAGACTAATTTTTTA[A/G]TAATAAGCATTAGCT | 81550 |
rs567297712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525301 | ACTTCACCCTCCCGA[A/G]TAGCTGGGATTACAG | 81550 |
rs567332163 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490564 | TTTGGAATGTTTTGA[A/G]CACAGCAATAACCTC | 81550 |
rs567333357 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517728 | GTACTTTAAGCTTAA[C/T]TTGAATTAATTATTT | 81550 |
rs567344560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505067 | TCATACCCCAGTGAC[A/G]CCTGGAATGCCAGTG | 81550 |
rs567371338 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498418 | GCTACTGTAATGGAC[A/G]GTAGAAGCAAAACGG | 81550 |
rs567376770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567960 | CAGGCTGGTCTTGAA[C/T]TCCTGAGCTCAGGTA | 81550 |
rs567409081 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425226 | AACTTTTCCCCAAAG[A/C]AGACATAAAAATGTC | 81550 |
rs567425708 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431579 | AAGGCATTTCATATT[-/G]TTTTGCATCATCAGA | 81550 |
rs567428023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528074 | TTTAGGAAATGATTT[A/G]CCAGAATAGCATATG | 81550 |
rs567437836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527145 | TGGCCTGACCACTTT[G/T]AGTCTTGATCTTTAA | 81550 |
rs567464947 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417482 | GAGTAGCTGGGATTA[C/T]AGGCTCCTGCCACCA | 81550 |
rs567482646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418327 | ATAACTGTCATCTGT[G/T]ATAAGAAGTCTTCCC | 81550 |
rs567611429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406236 | TGGTGCATGGATAAG[A/G]TCATCTAAGGCTGCA | 81550 |
rs567614781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473417 | ATGAATTGCATTTTT[A/T]AAATGATTCTGTTAT | 81550 |
rs567617310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518512 | TGGCCTCACCTAGAA[C/T]TGTGATTTAAAAAAA | 81550 |
rs567618187 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498045 | AATGTGGATTAAAAG[A/G]TGGCCCACTGTGAGC | 81550 |
rs567625467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407270 | GCACGATGTAAGGTG[C/T]ACAGTAGACACTTAA | 81550 |
rs567634192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488304 | GTGGTGATCTGGTTA[A/G]TTTTAGTTCTTTGAT | 81550 |
rs567647311 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395852 | TATGACTTAAACACT[A/G]CATACTACTGCACAT | 81550 |
rs567668870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423764 | ATGACAGTGACACTT[C/T]ATATCATAATTTATG | 81550 |
rs567677524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424320 | GCCACCGCCCCCAGA[C/G]AGTGGTTTTTAAAAA | 81550 |
rs567693356 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480753 | GTGTGGGGTGCTGCA[A/G]GTGGGAGTGCTCCAG | 81550 |
rs567709751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559330 | GTTGAGCTCTTACAT[G/T]CCAGTGCTGTGATAT | 81550 |
rs567717394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464543 | TAAAGAAAACATATG[C/T]ATGTATGTATATGTG | 81550 |
rs567718607 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60408714 | AAAGGTGACTTGGGT[A/G]CTGTTAAAAGCATTC | 81550 |
rs567791761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504671 | TGAATAGGAACAGCT[C/T]CGGCCTGCAGCTCCT | 81550 |
rs567860023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458805 | GGCTGGAGGATTGTA[C/T]TGGACAGCATAGGCT | 81550 |
rs567932303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60473924 | ACCAGGAAAGGGAGT[A/C]TCCCTTTCCCTGGGG | 81550 |
rs567932314 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420158 | ACTTGTAATTATTTC[C/G]ATAAAGGTTAATGTT | 81550 |
rs567942043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416306 | TTTTTAACTAAGGAA[C/G]TTTTAAGAACAGATT | 81550 |
rs567959340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564615 | CTCTCTTGGTTTATA[A/G]ACTCATCTGTCGAAT | 81550 |
rs567969085 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468608 | TGTGCTGGGATCTTG[C/T]ATCTGTATCTCAAGT | 81550 |
rs567975976 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456783 | TCACTGTAGCCTCCA[C/T]CTCCCAGGCTCAAGA | 81550 |
rs568019400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60495974 | AGTATTGATCCTGAG[C/T]GTGTCTGTGAGGGTG | 81550 |
rs568035797 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456351 | GATGACAGAGGTATT[C/T]GTCTACCTCAGGAGA | 81550 |
rs568090124 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TDRD3 | GRCh38.p7 | 13:60445662 | CAAGAATTTGCATTT[C/T]GAACAGTTTTCCAGG | 81550 |
rs568097452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516679 | GGCTACAAGGTCGTT[A/G]GGAAGATCAAATTAG | 81550 |
rs568124682 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541936 | TCTCCATGTTGGTCA[-/T]GGCTGGTCTCGAACT | 81550 |
rs568128389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505201 | CTGGCTTGAAATTCT[C/T]GCTGCCAGCACCACA | 81550 |
rs568156643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436182 | TTTTTGCATAGTTTG[A/C]AAATATTTTCTCCTG | 81550 |
rs568157703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524034 | TGCTGACTGTACAGA[A/G]AAATATCTTAGTATA | 81550 |
rs568162062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414351 | ACACAGCCAGAACCA[A/C]TCATACACCTACTGT | 81550 |
rs568163416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509458 | AATTTTCATTAAGTA[A/G]TTTTCTCCTCACTGT | 81550 |
rs568166185 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404590 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 81550 |
rs568178233 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557088 | GCACATGCCTGTAAT[C/G]CCAGCTACTCTGGAG | 81550 |
rs568184920 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456854 | GCACACACCACCACG[C/G]TTGGCTAATTTTTGT | 81550 |
rs568193268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403511 | GAAGAAGAATACTGA[A/G]TGCCCAGAAATTTTC | 81550 |
rs568196590 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415105 | TTTATATAAGAAATT[A/G]AACTTATGAAAAAAA | 81550 |
rs568197983 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397845 | AGGGACGAACGCGGC[C/T]GGAGCCCGCGGGCCC | 81550 |
rs568207741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541482 | CACGGCATTCTTTTA[C/T]TTTTTTTTGTATACG | 81550 |
rs568213936 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476045 | GCTCTTTAGTTTAAT[A/T]GGGTCCCACTTCTTA | 81550 |
rs568215899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487652 | GATGACTGTATACCA[C/T]GTTTTCTTTATCCCT | 81550 |
rs568218883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550772 | CTCAAACCAGTAAAA[G/T]AAAAACTGTTTATGT | 81550 |
rs568221862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449160 | GGATAGTCTAGAAAT[C/T]GGATGTTTTTAAAAA | 81550 |
rs568235327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60554741 | AGAAATAGCTTCATC[C/T]TTGAACGAGAAGAAT | 81550 |
rs568236464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541535 | CATTAATCTTTTATC[A/G]ACTAAATCTCCCCTT | 81550 |
rs568240837 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398154 | AATTGCGGCCATTAC[G/T]GTTGTAATCATCCCG | 81550 |
rs568247385 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444511 | TATACTTTAAACAAC[A/G]TATTATGGGACACTG | 81550 |
rs568330516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471299 | CTTTTTGAAAATAGT[A/G]TTCTTAATGAATGAT | 81550 |
rs568335622 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498391 | CAACCATCAAAGGCA[A/T]GGTTAAGCGTGGCTA | 81550 |
rs568344911 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60535508 | CAAAAATTTGTATGC[C/G]TGAAATGGGTTTTTA | 81550 |
rs568349638 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502374 | TGGAATTTAATGACA[A/C]ATGTATAAGCTTTGG | 81550 |
rs568366903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436754 | GACTTATGTGGATAA[A/T]GGCAAGTTTCCAAAC | 81550 |
rs568376249 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560588 | GGACAATGATGAATA[C/G]TACTGTATTTGCTTC | 81550 |
rs568386583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557627 | CCTGTCATTTTTATA[C/T]TTCTTAACTCTCATT | 81550 |
rs568429850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493731 | ACAGGTAACAACTGG[C/T]GATGCTTTTCAGTTA | 81550 |
rs568455179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508515 | CAAAAACAAGCAATG[A/G]GGAAAGGATTTCCTA | 81550 |
rs568481958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546980 | TTATAAACTTTCTGA[A/G]TTTTTCAGATGTCTT | 81550 |
rs568482521 | snp | A/C/T | 5.01065e-05 | 0.00500507 | missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528932 | TGAAAAACATTTTAA[A/C/T]GTAAATACTGATTAT | 81550 |
rs568489600 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484612 | TTTTGTAAGATATAC[G/T]CTCACTTAAATAAGT | 81550 |
rs568490583 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540066 | ATGTGACCCTAGTCC[A/G]GAAGATTTTTCATTT | 81550 |
rs568499630 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396598 | GGGGGAGGGCAACAG[A/G]AAAAACAAGCACTGA | 81550 |
rs568500236 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486019 | TATTTGTGATCGTTA[C/T]TGTCTTTTCATATAA | 81550 |
rs568512807 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465292 | TTATTTTTATTTATC[C/T]TTGTACAATGACTGT | 81550 |
rs568520457 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529922 | GAGCAAGAAAGGGAA[A/G]GGGACAGAGGGACCA | 81550 |
rs568520694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521617 | TGAAAGTGTATGGGC[C/T]GGGTGCGGTGGCTCA | 81550 |
rs568558410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501076 | GCTACCTGTTGGCAC[A/G]TTGATTATATTGCAC | 81550 |
rs568585310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60421786 | TTGTCCCACTTGTGG[A/G]GCTTTGGTGATCCAA | 81550 |
rs568621596 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527236 | TTTACCAGATACCTT[C/T]TGGCCTCCAGTGGCT | 81550 |
rs568629229 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501110 | TTCCATCATGGAAAG[A/G]GCAGAGGTTTGTTCT | 81550 |
rs568633134 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506111 | TGAAATGAAGGAAAA[A/G]ATATTAAGGGAAGCC | 81550 |
rs568665803 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565479 | CCATTTACTTGGATC[A/T]GGTTAGTTCAGTTCG | 81550 |
rs568668555 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564153 | GATAACATGGGTGAG[A/G]TAAGCAAAAGTCTTT | 81550 |
rs568669722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571403 | CATCTAAAAAAAGAT[A/G]AACATTGTAGCCAGC | 81550 |
rs568670079 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553347 | ACAAGTCTCTAGGAA[A/G]TTCCAAACTTTCCCA | 81550 |
rs568673523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403006 | GGTAATAAGCCTTGC[C/T]GACTTTCTGTCTCAA | 81550 |
rs568674320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429265 | AATGTACAGGGAATC[A/G]TTATGCTATTAGATT | 81550 |
rs568681187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523636 | GGCTAGAATGCAGAG[A/G]TGCCATCTTCCCTCA | 81550 |
rs568687698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428637 | ATTTTAAGGTGAAAA[A/G]TGATTTTTAGGGGAA | 81550 |
rs568700886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486820 | TCTATGAGACAACTT[C/T]TTTATCTCTCACATA | 81550 |
rs568706453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60562046 | CTGGGTGCAGTGGCT[C/T]ATGCCTGTAATCCCA | 81550 |
rs568729717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538374 | TTGTTCTAGCTAGAT[G/T]TCACCTGTATTTTTT | 81550 |
rs568732810 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562953 | GATAAAGTGGGCTAG[A/G]CATGGTGGCTCACAC | 81550 |
rs568748827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420837 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 81550 |
rs568749944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494405 | AAATGCTGTCTACAT[A/G]CCTCTCTTTTATCTT | 81550 |
rs568750061 | in-del | -/T | 0.00134529 | 0.0259005 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398865 | AATCTCTTCTTTCAG[-/T]TTTTTTACCCACAAG | 81550 |
rs568808704 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522073 | TTTCTTAGCATTTTT[A/C]ATATAGAAAAAAATT | 81550 |
rs568810393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60426104 | AGCCTTTAAAAAGAA[C/G]GAGATCCTGCCGTTT | 81550 |
rs568812837 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411167 | AGTTATAAAGACTTA[G/T]TTAGCTATGATAGTT | 81550 |
rs568838056 | snp | A/G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511036 | CTGTGTAAACAGGTT[A/G/T]TTGTGTTGGAAATTT | 81550 |
rs568895513 | snp | C/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476939 | TTTGTTTATCGGCTC[C/T]AGAAGCCTTCTGGTG | 81550 |
rs568902199 | in-del | -/AC | 0.00953873 | 0.0683987 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453093 | TAGGTTTTAAGATAT[-/AC]CAAAGAAACTATGCA | 81550 |
rs568915731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537760 | GTGCACTATATATGT[A/G]CACTACAATTTTTTT | 81550 |
rs568916003 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60435931 | GGTTTTTTTTTTTTT[-/A]ACTTTTTAATTATGG | 81550 |
rs568941086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505370 | TTGGCAAATCTGCTG[C/T]AGCCAGACTGCGTCT | 81550 |
rs568980445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484303 | TTCAGCATCAAATTG[A/T]TTCTCAACAATCTTC | 81550 |
rs568991483 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568773 | AGAGAAAGAAATAAA[G/T]AACATCCAAATTGGA | 81550 |
rs569033593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60461745 | TAGGCATACAAATAT[G/T]GTAAGACATATATAA | 81550 |
rs569044098 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454404 | TTTAATAATTTTTTT[A/T]AATATTTCTCAATCT | 81550 |
rs569045246 | snp | C/G/T | 1.65184e-05 | 0.00287384 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467407 | TATGGCTTGAACTTT[C/G/T]GAAACATTACACTCT | 81550 |
rs569047403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475274 | AGTCCCCAGTGTCTC[C/T]TGTTCCCATCTCTGT | 81550 |
rs569050352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419797 | CAGAACTTAAAGTAA[A/T]ATAAAAAAAAAAGAA | 81550 |
rs569062441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507656 | GAGAACAAAGACAAA[A/G]AATACCAGAATCTCT | 81550 |
rs569113604 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487895 | TCCCACCAACAGTAC[A/G]TAAGAGTTCTTCTTT | 81550 |
rs569156681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458914 | CCTGTGATTTAATTT[A/G]AATGTCCTTATTTTA | 81550 |
rs569165917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514386 | TCTCAGGGACACCTG[C/T]TCCTTGGATGAGCAC | 81550 |
rs569215089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506586 | ACATGGTGAAAGCCC[A/G]TCTCTACTAAAAATA | 81550 |
rs569231433 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60540001 | GAGGATTAGAATTAT[A/G]TAACAGTGTGGTTTT | 81550 |
rs569231528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567926 | ATTTTTAGTAGCAAT[C/G]GGGTTTCACCATGTT | 81550 |
rs569240107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409205 | AGGATGTATGGAAAT[A/G]CCTGGATGCCCAGGC | 81550 |
rs569245248 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459918 | GAGCTACCACACCCG[G/T]TCCAGAGAGCATTCT | 81550 |
rs569253429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513102 | GGTTCCCAATCCCCA[A/G]TTCTTAACTTCTGTG | 81550 |
rs569266474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405256 | TTACAGATGTGAGCC[A/G]CAGTGTCCAGCCTCA | 81550 |
rs569294582 | in-del | -/A | 0.00199481 | 0.0315187 | downstream-variant-500B | TDRD3 | GRCh38.p7 | 13:60574346 | CTCGGGGATGTCATG[-/A]AAGACTGATTCTTTT | 81550 |
rs569308375 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463105 | CATATACAAAAATCA[A/T]CCTAAATGTGGCTGG | 81550 |
rs569318528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491031 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGCA | 81550 |
rs569324234 | in-del | -/ATTTTTTGT | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530607 | TACCATGCCCAGCTA[-/ATTTTTTGT]ATTTTTTTTTTTTTT | 81550 |
rs569336654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453234 | AGAACTTACTGAAGG[A/G]TAACATACATAAAAT | 81550 |
rs569351798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440034 | TGATCAGTCATAGAC[C/T]TTTTTAACATTTACA | 81550 |
rs569382996 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543116 | TGGCTGAGAGCTCCA[C/T]TCAGAAGGGAAAGGA | 81550 |
rs569390122 | snp | A/G | | | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494502 | ATGCTGCTGGTAACC[A/G]AAATAGGGAAGTTTT | 81550 |
rs569399636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60536692 | TTACTTTTTAGAAGA[C/G]TTAGTAAGAGATTAA | 81550 |
rs569408635 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401247 | TTTGGAAAAATAAAA[A/C]AAAATAAAAATAACA | 81550 |
rs569409279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407256 | ATTCCAAGCATTTAG[C/G]ACGATGTAAGGTGCA | 81550 |
rs569456720 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433686 | TGAGCCCTGTTTTGT[C/T]TGGCTTGTACACTGC | 81550 |
rs569464097 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456155 | AGTTAAGAAAAAAAA[A/C]TTGTTTTAAGTGTTT | 81550 |
rs569498779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452486 | TTCTTACATTATTCT[G/T]TATATTCTTTTGAGT | 81550 |
rs569511808 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433841 | TTATCTATACATTAT[A/T]GCCAGTGAGTAAGTT | 81550 |
rs569513367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551710 | TACTACCTGAGACTG[C/T]GTAATTTATTTTAAG | 81550 |
rs569524188 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478244 | ATTTCTGATTGTACC[A/G]ATTTGGATCTTCTCT | 81550 |
rs569548447 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561636 | CTCTGTTAGATTTAT[C/T]TCCAGTTCCCCTGCA | 81550 |
rs569591578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552848 | GCCACAGCCCAAGTT[C/G]CATCTTGGCCCCTTT | 81550 |
rs569599384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60542933 | TGTTTATTCTAGCAT[C/T]GTGTATAATGGGTTT | 81550 |
rs569640987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497465 | TGTGAACTAAGCTCC[A/G]TGTTTAAAGGTGGGT | 81550 |
rs569649166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399054 | CATTTTTTAGGTCCC[A/G]AACACGTGTTGACTT | 81550 |
rs569669714 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60558057 | TGATCTCTTGACCTC[A/G]TGATCTGCCCACCTC | 81550 |
rs569685191 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411519 | ATTTTTCCAATGCTT[-/A]AAAAAAAATGCCCTG | 81550 |
rs569703428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532534 | TAGACATTTAAGAAA[A/G]GGAATTGAGTGTAAC | 81550 |
rs569703942 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60458059 | TATTTAACCCACTAA[A/C]AGAGGTGGAGAGGCC | 81550 |
rs569719743 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533271 | ATTTTGAGGGTAACT[C/G]ATTTTTTAGAAGGAT | 81550 |
rs569726816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511683 | GGAGCGGTGATGTTA[G/T]CAGAGACTTGAGTTC | 81550 |
rs569744919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399829 | GGAAATATTTAGTGC[G/T]GAAAAGTTTACAATT | 81550 |
rs569757287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551082 | TATGTATTTAAAATG[C/T]GAGTGAGATGGAAAG | 81550 |
rs569774113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504599 | GAACTAAAAAGCATT[A/G]CAGCTTTTATCTTTC | 81550 |
rs569793992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482719 | CTTTAAATTATTCTT[C/T]GCTCAATAAACTGAA | 81550 |
rs569799524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541425 | GCCTGCTTTGGCCTC[C/T]GAAAGTGCTGGGATT | 81550 |
rs569807245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432361 | ATCTTGTGCCCCAAT[C/T]CTTACTAGCATTTTT | 81550 |
rs569815501 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406771 | ATATTGGAGACTCAG[A/G]GCACCTTTTAAAACA | 81550 |
rs569859002 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500358 | ATGAGGAAGTGGCTC[A/G]AATGTCCATGGTCTC | 81550 |
rs569861562 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425151 | AACAAAGAGAAGTCA[A/T]CTTTGAAACAGAATA | 81550 |
rs569874898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526944 | GGTTCAAGCGATTCT[C/G]TTGCCTCAGCTTTCC | 81550 |
rs569893033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416577 | TAATGTTTAGCACAT[A/G]TATGACTGTGTTCAT | 81550 |
rs569914060 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565423 | GACATCAAGTTATGA[A/G]TTACGTGAAAGAAAT | 81550 |
rs569945845 | in-del | -/TATT | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423531 | CAAAAACTGATTATA[-/TATT]ATGTCATAAGGAAAA | 81550 |
rs569948595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432962 | AAACTGCATGAAGCC[A/T]TTTGATTTGGGTTTT | 81550 |
rs569951109 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565978 | GGGATATAGGGAAAG[C/G]AAAACTCATCTGGAA | 81550 |
rs569970058 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475077 | TTTTAAGTCTTTTCC[-/T]TTTTTTTTTCTTCCT | 81550 |
rs569974343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423493 | GAAAATACTCATTTT[A/C]TTAAGTGCCTATGGC | 81550 |
rs569979327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489638 | TTTAGAGCTAATACT[A/G]CTGCTACTTGGCACA | 81550 |
rs570028207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479962 | ATCCAACTTGCCATC[A/G]TATTCCTTTTAAGTG | 81550 |
rs570033419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60495698 | TCGAACTCCTGACCT[C/T]AGATGATCCACCCGC | 81550 |
rs570036596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415601 | ACACTTAAAGAATAT[A/G]AGAATTTTGAAGAGT | 81550 |
rs570049528 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441210 | TGCTTAAAAATATTA[A/T]AAAGGACTCTTCTTG | 81550 |
rs570085053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429515 | GCAGGTTGAACAAAA[A/G]CAATAGCAGTTCATT | 81550 |
rs570094477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487616 | GGGAGTCCTAGAACC[A/G]ATCCCTCACGGATAC | 81550 |
rs570145592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60465451 | TCTACTTAAGGGTTA[A/G]GTTAGGTAAGGCTGT | 81550 |
rs570146649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508827 | TCTGACTTTCAGTTA[C/T]CTAATTACAGGATTC | 81550 |
rs570162561 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475804 | TAGTGATAATGAGCA[-/T]TTTTTTTCATATGTT | 81550 |
rs570163113 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457532 | CTAGATCTCAAGAGG[A/T]AGATGAGTGAGGCTG | 81550 |
rs570189591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406142 | TGTTAGGCATTAGGA[A/G]ATACCAATCTTGCAC | 81550 |
rs570285144 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443322 | AAAGGCGTACAACGT[C/G]AGGTACGGTTTATAT | 81550 |
rs570293825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511015 | ATATCTAGATGACAG[A/C]TATAACTGTGTAAAC | 81550 |
rs570330964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405586 | TGCAAAAGTCATAGG[A/G]CACTAGGGAGCATGG | 81550 |
rs570349544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471203 | TGCTTAGGTCTTTGA[C/T]CCATTTTGAGTTAAT | 81550 |
rs570424212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462697 | TATTATTATTACAAT[A/G]AAGTGAGATTAAAGG | 81550 |
rs570460892 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571108 | AAAAAAAAATTGGTG[G/T]GGGACAGTGCCATGA | 81550 |
rs570462460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403847 | GCAGTATAGTGCTCT[C/T]GAATTATAATATCTT | 81550 |
rs570463332 | in-del | -/GGC | 0.00517822 | 0.0506191 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397628 | GCGGCCTGGGCCCCG[-/GGC]GGCGGCGGGCCTGGG | 81550 |
rs570481904 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523578 | ATACATTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 81550 |
rs570499642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563805 | ACCAATTTATGATGA[A/G]CTTTTATAACACGGC | 81550 |
rs570506790 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454336 | GGCTTATTATTTTGT[A/G]GTCTGTGTTTGATAC | 81550 |
rs570518788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444538 | ACTGTTACTTGAAAG[A/G]TTGATAATACATGTA | 81550 |
rs570519426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522822 | GATTTCTACATCTCA[C/T]CAGAAATGAACAGAT | 81550 |
rs570520332 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60420816 | GGGCGTGATGGCGGG[C/T]GCCTGTAGTCCCAGC | 81550 |
rs570524689 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486277 | CCTATTAGTAGTTGG[A/G]CTAGTTGCCACTTTT | 81550 |
rs570527475 | snp | A/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439342 | CTCAATCTCTTTTTA[A/T]GATCTTATGGTATTA | 81550 |
rs570556229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515042 | TCTAGTGTGTGAGAC[A/C]GAAGAAGTCATAAAC | 81550 |
rs570570848 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451724 | TGTATCAACTATGTT[A/G]CCTTCAGTATTGTAT | 81550 |
rs570580712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453541 | GAATATCAGCTCTTA[C/T]TGGAATAGCACTTGG | 81550 |
rs570585475 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412380 | ATTCTTCTACTTTTT[A/T]AAAAATAGTGATATC | 81550 |
rs570586599 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505752 | ACAAGTATCAATAGC[C/T]GAATTGATAAAGTGG | 81550 |
rs570593644 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565754 | TTTCAGTTAATATGC[-/AG]AGTTTCAAATGTTGT | 81550 |
rs570602341 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549827 | TTTGAATGAGAAAAA[A/T]TTTTTTTAGTGCTCA | 81550 |
rs570625528 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561946 | TTAAACAAGGATAAT[C/T]GGTAAAGTTCAGTAT | 81550 |
rs570641617 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447002 | ACAGGACAACAGTTG[G/T]CAAACAGAATATTTG | 81550 |
rs570654800 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404552 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 81550 |
rs570668522 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477327 | TCAAGGGATCCTCCT[G/T]CCTCAGTCTCCTGAG | 81550 |
rs570669845 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568084 | GTCTTGTGATATTTC[C/T]GCTGGGCAGCACTGT | 81550 |
rs570724208 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396768 | CGTCCGGGCGGACCA[A/G]AAGGCGAGGTGAAGG | 81550 |
rs570728935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456174 | TTTTAAGTGTTTATC[C/T]AGATGTGATTATACT | 81550 |
rs570732210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478020 | ATTTTTTTGGTTAAG[A/C]GATTTTTTTTTATTA | 81550 |
rs570746090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60555985 | CCTCCTTAGTAGCTG[A/G]GACTACAGGCGCCCG | 81550 |
rs570773642 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534180 | TAGCCAGGCATGGTT[C/G]TATGCACCTGTAGAC | 81550 |
rs570806329 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60479525 | TCCAATTGATTGGGT[A/G]TTGAGTTTCAGTCCA | 81550 |
rs570814207 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453067 | ACTCATTAGTTTTAT[C/T]TTTTCAAAAATAGGT | 81550 |
rs570830766 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395924 | TAAACAATATACTTG[A/G]GAGCAAATCTCAATA | 81550 |
rs570860417 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564277 | GGTGGTCGGGATGCA[C/G]CTTGGTTTTATATAC | 81550 |
rs570864740 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546839 | TATTTCCTCTTAATT[A/T]GGATGGATGTTGATT | 81550 |
rs570865934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500217 | ACCTGAACTGCCTAT[C/T]ATGAACTGGGTGCTT | 81550 |
rs570881847 | in-del | -/AAAAAAAAAAAA | 0.13446 | 0.221699 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431704 | AAGACTATCTTTACC[-/AAAAAAAAAAAA]AAAAAAAAAGGTGGA | 81550 |
rs570882187 | in-del | -/T | 0.453412 | 0.14534 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452818 | TCACTGTTCTTAGTT[-/T]TTTTTTTTTTTAATT | 81550 |
rs570884728 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420800 | ACAAAAAAAATTAGC[C/T]GGGCGTGATGGCGGG | 81550 |
rs570939532 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436109 | CTTTTGGATGGGTTG[G/T]TTTTTTTTTTTTCTT | 81550 |
rs570954974 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506765 | AACAAACAAAAAAAA[A/G]AACATCGACACTATG | 81550 |
rs570955397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425950 | TATGTTATTGGTAAG[C/G]CTTCTGGTCAGCAGT | 81550 |
rs570967456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507562 | CACAAATAGGTGGAA[A/G]CTGAACAACCTTCTC | 81550 |
rs570986247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544983 | ATTCCTGGTGGTCAC[C/T]TTTATTACTGAAAAG | 81550 |
rs571024611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530089 | TACTTACATTATTCT[C/T]TTAATCAGTGCCTTA | 81550 |
rs571024944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518281 | TATGTGAATCTTTAG[A/G]TGATTCTGGTGCTGG | 81550 |
rs571033848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60547735 | TTCATATTGAAAATA[C/T]TATTTCTATCCTCTG | 81550 |
rs571051727 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566178 | ATGCAAAACCGAAAG[A/G]TACTACTGTCTTAGA | 81550 |
rs571058165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488058 | CTAGATCCTGCTGCT[C/T]ACTGCACAGTAAGCC | 81550 |
rs571069192 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60540541 | TGTTACCTTAAAATT[C/G]GTTCGTATCTAACTC | 81550 |
rs571111898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492967 | TGTATCTCCCAGGTT[A/G]GAGTGCAGTGGCGCG | 81550 |
rs571134758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569512 | ACCCAAAGCAATCTA[C/T]AGATTTAATGAAATC | 81550 |
rs571145681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561343 | AGTTCTGGCTCTTCC[A/G]CTAGCTCATTTTATT | 81550 |
rs571151538 | in-del | -/TTTTCTTTCTTTC | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541178 | TCTTTCTTTCTTTCT[-/TTTTCTTTCTTTC]TTTTTTGAGACGGAG | 81550 |
rs571203544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433798 | TTAGCTCAGTCAGCT[A/G]ATGTGTAGTTTGCCT | 81550 |
rs571241412 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489967 | TTTATTGGAGCATAG[A/T]TAACCTATTATAATG | 81550 |
rs571283523 | in-del | -/GTCTCA | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514120 | ATCCAGGCTGAGGTG[-/GTCTCA]GATGGAGATGAGGAA | 81550 |
rs571284590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475557 | GCTGCAATGAACAAA[A/C]AAGTGCATGTGTCTT | 81550 |
rs571286585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484155 | AAAGTAAGAAGACAA[A/T]AATACATCATAATTT | 81550 |
rs571386224 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481570 | TTCATTGTTGGTGGT[G/T]TTTTTCTTTTATAGA | 81550 |
rs571427239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460958 | CAGTGAGCTGAGATC[A/G]TGCCATTGCACTTCA | 81550 |
rs571455819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410473 | AAGCATGTAAAATGG[A/G]CTCCTCAGTATCCTT | 81550 |
rs571505537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466588 | AGGTCATGAGTTGGA[G/T]ACCACCCTGGCCAAC | 81550 |
rs571511157 | snp | A/G | 1.66059e-05 | 0.00288144 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528810 | GGATCTGTAGATTAT[A/G]ATAATCAAAAACGTG | 81550 |
rs571546001 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429919 | AAACAAGGGCACCAT[A/G]TTTAAGAAGGAAGAA | 81550 |
rs571547319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544347 | TACTGAGGAGTCTGA[A/G]ATGGGAGGATTGCCT | 81550 |
rs571571905 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474379 | GGTAGTGGCCCCCCC[C/G]GGGCCCAGCTGTCCT | 81550 |
rs571593118 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399329 | ACTTTATATTGCAAC[G/T]TAACTGTTTATGTTT | 81550 |
rs571602110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476348 | CAAAGATCAGGCGTT[C/T]GTAGTTGTATCACTT | 81550 |
rs571602727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400078 | GATTTTGCTGATTTG[A/C]ACTTGAATGTTCCAG | 81550 |
rs571639749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525996 | CCTTTTAGAAGAATT[A/G]AAATCAAATTCTGCC | 81550 |
rs571694509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567096 | CCTTTTCTTTATTCT[A/G]CCAAAACACTTTTCC | 81550 |
rs571701032 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417215 | AGATGGGCTCTTGCT[A/G]TGTTGTCCAGGCTGG | 81550 |
rs571707131 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571614 | GATGAATGACACATG[A/G]TAGCTGTTCAGTAAG | 81550 |
rs571724369 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60550691 | CTTTGTAAAGTGCCA[G/T]TTAAGAGCTAGTTTC | 81550 |
rs571732609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424386 | TCACCTCTTTAAAGT[A/G]TACAGTTCTGGCTGG | 81550 |
rs571739724 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526889 | ACCCAGGCTGGAGAG[C/T]AGTGGCACAATCTCG | 81550 |
rs571754726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60441270 | AAAGAGATTTTATGA[C/T]AATTTGCTGGGGTTT | 81550 |
rs571762618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560358 | GTTTCAAGTTGTAAA[C/T]TCATGTGTTTTCAAA | 81550 |
rs571847968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60552803 | ACACCACGTGGAAGC[C/T]GCTAAGGCTTGGGTC | 81550 |
rs571860542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559786 | GAAGTTTCAGTTATG[C/G]CAGATGAATGGGTTC | 81550 |
rs571863884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451300 | TGGAGAATCCTGTCA[A/G]TAATAGTTGAAGTTG | 81550 |
rs571871516 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469708 | ATATACATAGAAATT[A/G]TAAACCATAAAGCTA | 81550 |
rs571940292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60437241 | AAGCAATTATCCTGC[C/T]TCAGCCTCCCGAGTA | 81550 |
rs571960142 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503021 | CTTTGTTCACAGAAT[A/G]CCTTATTCAATTATT | 81550 |
rs571980416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496140 | GCCTAGGCTCCCAGC[C/G]TACATCTTTATCCTG | 81550 |
rs571996657 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496987 | GTCACGGAAGAAAAC[C/T]GTGGAACCCAGCAAC | 81550 |
rs572010677 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467548 | GTATTGTTTCTCTAA[A/T]GTAGATATACTTTTT | 81550 |
rs572016050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438267 | GGATAATAAATTATT[A/G]TAGCCATTTTGAGTT | 81550 |
rs572018402 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497599 | GAAAAACAGACACAA[A/G]CTCTTATCATGTGAG | 81550 |
rs572018694 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466567 | CTGAGGCAGGTGGAT[C/T]ACCTGAGGTCATGAG | 81550 |
rs572024792 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541146 | TCTTTTTGTTTTTCT[A/T]TTCTTTCTTTCTTTC | 81550 |
rs572035646 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522723 | TTAATAGAAAGAGAT[A/T]ATTAATTTTAGGTCA | 81550 |
rs572042700 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502768 | GGTATGAGGCCAGTT[A/C]TCTCCATGGGAATTT | 81550 |
rs572048220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532124 | ATAGCTGTGGTGAAA[A/G]AATTAAATTAAAAAA | 81550 |
rs572078772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60447257 | CTGATTGAGGGTGGA[A/G]AGGCATTAAATGATA | 81550 |
rs572080112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429952 | CTAATACTTATTTAG[C/G]ACCTACTGTATTCCA | 81550 |
rs572105288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472725 | TGTACCCTTGTTTAC[A/G]GCGGCAGAGGGCATT | 81550 |
rs572177337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428079 | GCTGACATTCCTTGG[A/C]TTGAGGCATCATCAG | 81550 |
rs572186074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549308 | TAACAGTTAACCTCT[C/T]AGCCCATTTTCAGTA | 81550 |
rs572195340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415009 | GTAAAATATAGGAGG[A/C]GTTTGTTCTTAGATA | 81550 |
rs572214034 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408564 | AACTTGTTGGGAACT[A/G]GGTGACTCTTGTTAT | 81550 |
rs572242051 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524489 | TCCAGCCTGGGCCAC[A/G]GAGTGAGGCTCCATC | 81550 |
rs572256096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572690 | GTATTCCCAGTTTCA[C/T]GTGTTAGTCAGAAAC | 81550 |
rs572261772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463976 | TTGGTGCCATCCTTG[A/C]AGTGAGTGAGTTCTT | 81550 |
rs572287825 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415551 | CAATGTTAGCTAACT[-/A]AAACAGACCAATGCA | 81550 |
rs572311694 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411756 | AGCAGCATTGATATC[A/G]CCTGGTAGCTTGTTA | 81550 |
rs572316010 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478290 | AGCTAGCAGTCTACC[A/G]ATTTTTTTTTTTTTT | 81550 |
rs572340149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430669 | ATTGCCACTATACTA[C/T]GTAATATATCAATTA | 81550 |
rs572363796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470006 | TTTTTCATCTTCCCA[A/G]ACTTAAACTCTGTAC | 81550 |
rs572367375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60570631 | AAAGTTTTAAATTGT[A/G]GCCAAAGATTGTCAA | 81550 |
rs572489586 | snp | C/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438372 | CCTACCATCTATTCA[C/T]TCTTACTGACTCATC | 81550 |
rs572536019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564102 | GTATAAAAGCTCATA[C/T]TGAGTATTAGTTATT | 81550 |
rs572539730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60402406 | TTATGCATATAATAA[A/G]AGGGTATTAGAAGTT | 81550 |
rs572578782 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454886 | CTTTATTTTTTTCTC[C/T]CTTCCTATCCCACCT | 81550 |
rs572578907 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530302 | ATTAGTTAATTCTGG[A/G]GAGAGCAATTACATA | 81550 |
rs572579226 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556162 | AACCTATTTCTTTTA[A/T]CCTATTATTCCATTG | 81550 |
rs572593388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513374 | CTGAAGACATTTTCC[C/T]CATTGTCTTGGGGAT | 81550 |
rs572608097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60412608 | TGATGCCTTCTTTTT[A/C]TGTATTTTGTAACTT | 81550 |
rs572619065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446568 | ATATAAGAATATATA[C/T]TATTCTCACAGAATT | 81550 |
rs572625830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401987 | AAAGTGATTATTGCA[C/T]TCTTGTATTCAAGGG | 81550 |
rs572627150 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501461 | AATGGAACATTCCTT[C/T]TGGGATAAGTAGCAT | 81550 |
rs572630166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513738 | AAGCTCTCTCTTGGC[C/T]TGCTGCCATCCACAT | 81550 |
rs572635957 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546128 | CATACCTGGTTGATC[C/T]TTTGTATGCCCTGAT | 81550 |
rs572636133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501880 | AGACTCAGTGATAGT[A/G]AAATTTTTATGCTTC | 81550 |
rs572665653 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506689 | TGGAACCTGGGAGGC[A/G]GAGTTTGCAGTGAGC | 81550 |
rs572697175 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435067 | TTATAAAAATGAAAA[G/T]ATTAATTTGTAAATC | 81550 |
rs572711639 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396940 | ATCCTGCCCTCTCTG[A/G]GGTGGCCGCCTGTGG | 81550 |
rs572712756 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527001 | ACCACACCCAGCTAA[-/T]TTTTTGTATTTTTAG | 81550 |
rs572713712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509532 | TATTTTTTGTGTGTT[A/G]CTTTTGCAGTGTTAC | 81550 |
rs572766735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515360 | ACCAGGACCTGATTG[C/T]ACCATTACTAGTAGC | 81550 |
rs572788337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561567 | GTGAGATTTCATTTG[A/C]AACAAGAGTGCTGAA | 81550 |
rs572795806 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395587 | CCTTACTGAATCACA[A/C]GACATGTGAGAACAA | 81550 |
rs572803351 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516224 | TAGTACCTCTAGAAG[G/T]CAGAATTTAGCGCAG | 81550 |
rs572808197 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396181 | AAGCAGGGGCAGCGG[C/T]AAGCGGCGGAGATAG | 81550 |
rs572811246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419330 | TTTTTAATGTGACTA[C/T]TAGCTCTTCATAAAG | 81550 |
rs572812727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453878 | TCATGATATAAAAGA[C/T]AACTTCTTAATTCAA | 81550 |
rs572814969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568333 | TGTCCCTAATGCAAG[G/T]TCATCAAGTAAACAG | 81550 |
rs572832884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60506995 | CATAGGCTCAAAATA[C/T]GGGGATGGAGGAATA | 81550 |
rs572851634 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60409849 | TGATTGGTTTTGAAA[C/T]GTGAGGGCATGAGAT | 81550 |
rs572928576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60490408 | AGCACAGAGAAACAG[C/T]GGAGTGGCCAGTGGA | 81550 |
rs572948615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444935 | AACTTTTGGTGACTT[C/T]TCAACATTAAAAAAA | 81550 |
rs572953958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468567 | TCTTAAGTTCTGCAC[G/T]TATCTGTTGAACAAT | 81550 |
rs572960865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435606 | GACATTATTTCAATT[C/T]GTTTTTGTGGCTGAG | 81550 |
rs572976203 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477129 | CCTTGTCTTGTTTCA[A/G]TTATCAAGGAGAATG | 81550 |
rs573015265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498760 | GGCCTTTTACCAGGG[C/T]AACTGTGCATTGGGG | 81550 |
rs573047723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493197 | TGCTAGGATTACAGG[C/T]GTGAGCCACCGCGCC | 81550 |
rs573077407 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445031 | CAGATGTAATTGGCA[C/T]TCATTACAATGACCT | 81550 |
rs573091692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500586 | GGGTAATCTTCCCAG[C/T]GGGCAGAACTTCAAG | 81550 |
rs573102362 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468319 | ATTTTTACATTATTC[A/G]TCTTGTTTTTTCTCT | 81550 |
rs573105176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520910 | AGAAAGCAGTTTTAT[A/G]TATATTTTCAAATTG | 81550 |
rs573125556 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443692 | AGTGTTTTCTCCTTA[A/T]GTCTAACAAAAATTT | 81550 |
rs573161008 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447819 | AGCATTTGGCCCAGT[A/G]TTTAAGAAGCAAAGA | 81550 |
rs573166048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60442442 | GTAGATGCTTTGAAA[A/T]TTATTTTTAAAGTTT | 81550 |
rs573182535 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499432 | CACCCGAAGCAATTT[A/G/T]CCTTCAGCTGGCAAG | 81550 |
rs573183725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492439 | ATATCCCAATGAGGT[A/G]GGTTTTCTAATCCCA | 81550 |
rs573186379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492381 | CCATGTGCCAGCTAC[A/T]GAGATAATCACTTCA | 81550 |
rs573192066 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60483512 | AAGACTGTTTTCTCC[C/T]TAGGGGAATGGCCTG | 81550 |
rs573194641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535938 | TCTGTGAAGTTTTTC[A/G]TACTTCTTTCATTTC | 81550 |
rs573203898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60454764 | GGATGACATTGGGAA[C/T]GTTTCTGAAATTTCT | 81550 |
rs573230580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544603 | GCTCTTTTATTAATA[A/G]GCTACTGTGTTGTCT | 81550 |
rs573286898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432584 | GGTGTATTACAATCA[A/G]TTTACACTATGGAGA | 81550 |
rs573303739 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488728 | ACAGGTGTGCACCAC[C/T]GTGTCTGGCTAATTC | 81550 |
rs573316605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545183 | AAGCCACCTAATATT[G/T]TTAAGGCTACCATGA | 81550 |
rs573369401 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404937 | GTGAATGGGTCTCAC[A/G]AGATCTGATGGTTTT | 81550 |
rs573374512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431898 | AGTACTTTAAATAGT[A/G]CGTACCTTTATTTAT | 81550 |
rs573397957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531725 | ATATTCTCTCTGCCA[A/G]TAGAAAATGTAACTG | 81550 |
rs573449133 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483183 | GTTGGATTTGGAAGC[C/T]TATTTTTAGTTAATG | 81550 |
rs573449897 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428230 | GGACCTGCCTGGATT[A/G]TCTAGTATGATTTTC | 81550 |
rs573483141 | snp | C/T | 3.29712e-05 | 0.00406011 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60483803 | ACAATAGAAGCAATA[C/T]TGGAACTGAAGGTGG | 81550 |
rs573483185 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486183 | AGTTACTCTTGCTGG[C/T]AAATTACCCTCCTTT | 81550 |
rs573540851 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399725 | TATGTACTTAGTTAC[C/T]TGTAGAAGCTAAAAA | 81550 |
rs573541859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424082 | GCTGGAGTGCAGTGG[C/G]GCCATCTTGGCTCAC | 81550 |
rs573546761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534703 | GGCCAAGGCAGGCAG[A/T]TCACTTGAGCTCAGG | 81550 |
rs573548945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481854 | ATTTTGCTATTTTCC[C/T]TTAATGAGTATAAGA | 81550 |
rs573600152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416080 | ACTTTGTTGGATGGC[C/T]CAAAAATTGTGTTTT | 81550 |
rs573629025 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60424504 | CAACATGGCAAAACC[C/G]CTTCTCTACTAAAAA | 81550 |
rs573629394 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450979 | ACACAGATCACGCAT[-/AC]ACACACACACTATAT | 81550 |
rs573632694 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533617 | CTGCACTCCAGCCTG[C/G]GTGACAGAGGACGAC | 81550 |
rs573642055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60525615 | ATGTACATCATCATC[A/G]ATTCAGTAACTGAAA | 81550 |
rs573659730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60543189 | CATATAGTTTAATAA[A/G]AGTAAACATAATGAA | 81550 |
rs573671211 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512283 | GGAAAGACCTGCCCC[C/T]ATGATTTACTTACCT | 81550 |
rs573671715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517000 | TTTTTATGGTGTTCC[A/G]TTATTTTTATTTTCT | 81550 |
rs573674722 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464151 | TGCTGATGCCATGCT[A/G]CTTGTACAGTCTGCA | 81550 |
rs573680953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526468 | CACTGCTATTCTTCC[C/T]GAAATCTTTACTCCT | 81550 |
rs573703498 | in-del | -/CT | 0.00398564 | 0.0444627 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396836 | ATGGGCTGGGGACAC[-/CT]CTGAGTTTTGCTGCC | 81550 |
rs573709158 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460329 | GAAAACACAGCCCTG[A/G]ATAGAGTTTCATGAC | 81550 |
rs573771966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567386 | CTTCCCCTTGCCTCC[C/G]TCTGTTGTAAAAGTT | 81550 |
rs573775026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450882 | GAGATGTGATTTTCA[A/G]TGAAGGAATAGTGGG | 81550 |
rs573783390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516447 | CATAATTCTAGTTGA[C/T]GTTTTTATTAATATT | 81550 |
rs573785014 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60489326 | CCAGTGAGATTGAAA[C/T]TGTTTCCTTTATTCA | 81550 |
rs573792565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512733 | CTCACATCTAGGTTA[C/T]ACGGATGAAAGAGGA | 81550 |
rs573837774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416765 | CTCTGTTACTTTGGA[C/T]GGTTTATGTCTATCT | 81550 |
rs573876670 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512336 | ATGTGGGCATTCAAG[A/T]TGAGATTTGGGTGGG | 81550 |
rs573911044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60408393 | AGAACTGGGTAACAG[G/T]CAGAGGTTGGAACAG | 81550 |
rs573913339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400189 | CTTCACGGGGAGAAG[A/C]AATTTGACTCTGAAT | 81550 |
rs573925388 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411292 | CAGTGTAGTGGTATA[C/T]ACTTTTACAGTTACA | 81550 |
rs573953540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509619 | TGCCTCTTGTAAAAA[A/T]TCAGCAAGAGAATGT | 81550 |
rs573964563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456940 | GGTTCAAGCGAGCCA[C/G]CCACCTCCATCCTCC | 81550 |
rs573988436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510413 | TTATATGAACAAATT[C/T]GGACTTCTGAATAGA | 81550 |
rs574004292 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407767 | AGATAGCAACAAATT[A/C/T]TTTTCTTTTTGATAT | 81550 |
rs574009979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558235 | GTTTTAGCATTAAAA[A/G]CATTCTGGCATTATG | 81550 |
rs574011926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550528 | TGATGACTGTATTTG[A/G]TAAACTGGTAGGATT | 81550 |
rs574048807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466734 | CAGAGGTTTCAGTGA[A/G]TCAAAATTGTGCCAC | 81550 |
rs574083100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564353 | TTGGTTTGGTCAAGG[C/T]GGGACAACTTGAAGC | 81550 |
rs574097013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414820 | CCTTCATTGGTTTCA[A/G]TTGAGCATTCCTATC | 81550 |
rs574120879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494178 | CTTCTCTATAGTTGT[A/G]CACTCATTTTCATGA | 81550 |
rs574122579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502581 | ACAAGGAACCTCAGA[C/T]AAGATCTTTTAAAGC | 81550 |
rs574128993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541813 | GCTCACCACAACCTC[C/T]GCCTCCTGGGTTCAA | 81550 |
rs574147868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501266 | CCTGCTTAAGAGAGG[C/T]ATTGTGTGGGGAACA | 81550 |
rs574158409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471734 | ACTCCAACTTTATTG[A/G]ATTTAGTATTCTAAC | 81550 |
rs574175950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449600 | GAGCAACTTATGTGC[C/T]CTACTGTTATTTTGA | 81550 |
rs574202102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503790 | AGGCAAAAGCCTTTC[A/G]TTAGCCTTTACTATT | 81550 |
rs574223768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60472652 | CCATATGATCCATCA[A/G]TTCCACTTCTGGCTA | 81550 |
rs574226932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511044 | ACAGGTTGTTGTGTT[A/G]GAAATTTATTATAAT | 81550 |
rs574235553 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60403925 | ATAATATGTGCACTG[A/G]AATACATTTAGTAAA | 81550 |
rs574287223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448566 | AGTTGGACAATCACA[A/G]TTTTTTCCAGGCTTC | 81550 |
rs574309351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497154 | GTGGAAGTCAACGGC[A/G]GGTCTGGGACGGCGG | 81550 |
rs574401554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496644 | ACATAATACCTTTGA[C/T]CATATGTGGAGAACC | 81550 |
rs574402731 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60508896 | AAAAGGCAGGAAAAT[G/T]TAGCCCATTCACAAG | 81550 |
rs574413631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60540435 | TTTGTGGGAGGTTGC[A/G]GATTATACAAAAACA | 81550 |
rs574440575 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60556097 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 81550 |
rs574453266 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396847 | ACACCTCTGAGTTTT[C/G]CTGCCCGCAACGTGA | 81550 |
rs574472725 | in-del | -/TT | 0.223819 | 0.248625 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561860 | TACTATGGGCCCAGG[-/TT]TTTTGTTGTTGTTGT | 81550 |
rs574473762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455742 | GTTAGGTATACAGAT[A/T]GAGAAATTTCTTTCT | 81550 |
rs574492139 | snp | A/G/T | 0.00239401 | 0.0345304 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497165 | CGGCGGGTCTGGGAC[A/G/T]GCGGTGAACAGCAGT | 81550 |
rs574508437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531981 | TACTGCTATGTGCCA[A/G]GTGATTGGGGCATAT | 81550 |
rs574556261 | in-del | -/TTTC | 0.000874126 | 0.0208878 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510786 | GTTGATTCCTTTTTT[-/TTTC]TTTCTTTTCTTTCTT | 81550 |
rs574562779 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402395 | AAAATATGAGTTTAT[G/T]CATATAATAAGAGGG | 81550 |
rs574583844 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517517 | AAATGGTTGCTATGT[A/G]AGTAAAGTCATCAAC | 81550 |
rs574601221 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453687 | GGCTAGATCACAAGA[A/C]CCTGCAGGATACTGG | 81550 |
rs574624362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60532622 | TAATACATTAGTATA[C/T]ATATTGCTTAAAAAA | 81550 |
rs574638034 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416224 | TGTAAAGTGTAAAGA[-/T]TTTTTAGAGGAAGAT | 81550 |
rs574653506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531371 | CTCCTTCATGGTGGA[A/G]GCAAGAAAAAGTGAA | 81550 |
rs574662754 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429893 | TATGTTTTGAAAATA[C/T]TTTGTAGAATAAACA | 81550 |
rs574669955 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470646 | TGGAGTACAATGGCA[C/T]GATTTCGGCTTACTG | 81550 |
rs574682360 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60478707 | ACTTAGTTCTCTGAT[G/T]TTAGTTATTTCTTTT | 81550 |
rs574704077 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539020 | CATTGTTCAGCTATT[A/T]TTTCAACTAGAAAAA | 81550 |
rs574748916 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444510 | GTATACTTTAAACAA[C/T]GTATTATGGGACACT | 81550 |
rs574753545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427001 | TTTAGTATTGTGTAC[A/G]TATTTATGTATTTAA | 81550 |
rs574757977 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429055 | CACTTTGTATTTAAG[A/T]TGCATTTTAAAGAAA | 81550 |
rs574768438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469237 | ATTTCCTGGAGAAAC[C/T]ACCCATTTCATGTGA | 81550 |
rs574786049 | in-del | -/AC | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460649 | CCTTAATTGTGTGTT[-/AC]AGTTTTTCAGATGAA | 81550 |
rs574799554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60533411 | TTTGGAAGGCAGAGG[C/T]GGGCAGATCACTTGA | 81550 |
rs574815735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419606 | TGGACACAGAGAGGG[G/T]AACATCACACACTGA | 81550 |
rs574899577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60538179 | TTCTCCTTTTCGTGT[A/G]GATATGTATTTTTAC | 81550 |
rs574904742 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506602 | TCTCTACTAAAAATA[C/T]AAAAACTAGCTGGGC | 81550 |
rs574936615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60530231 | CTCTGGTTTCCGTCT[A/G]TAGTCTTGCTTCTTT | 81550 |
rs574936712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521852 | CGGTGAGCCGAGATC[A/G]CACCATTGCACTCCA | 81550 |
rs574946157 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477937 | TTATGGAACAGTTTC[A/G/T]GTAGGATTGGTATCA | 81550 |
rs574950413 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60417641 | GCCGCCACACTGGCC[A/G]ATTTAAACTAATTTC | 81550 |
rs575010148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60477604 | TGAATTTTATTGAAG[A/G]CCTTTTCTGCATCTA | 81550 |
rs575080046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459572 | TTGTATGCTTCATGT[A/G]TACCAGGAGAGGGAG | 81550 |
rs575083571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60442716 | ATGTAAACTTTGAGC[A/G]TGTAGTCTTTTTTTA | 81550 |
rs575084463 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503584 | CAAACAATCCTGTTT[A/G]TCTCTTCTCTGGATG | 81550 |
rs575091436 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469355 | TATAATTTTCCCACA[A/G]CCCAGTCCCATAGCC | 81550 |
rs575098145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60443536 | ATCTGTAGGGATTAT[A/G]CAACTTATATTCTCA | 81550 |
rs575102819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471919 | GTGTTGAATGGAAGT[G/T]ATGAAAATGACATCC | 81550 |
rs575103467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60512829 | GCTTTAATGGGCTGG[C/T]GAGGAGTGTCTGTGG | 81550 |
rs575117163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403315 | CATAGTAACATTTTA[A/G]GAACCATAAAAATAT | 81550 |
rs575139892 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410848 | GCCTTTTCTGGTTGT[G/T]GATTTTTTGCTTTGG | 81550 |
rs575146687 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452536 | TTTCTTGGTATTTCA[C/T]GTGAATGGAATCACA | 81550 |
rs575159045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568198 | TTTTCATCTGTTCTA[A/T]CCCTCAGCTTCTCAT | 81550 |
rs575163691 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493200 | TAGGATTACAGGCGT[A/G]AGCCACCGCGCCCGG | 81550 |
rs575165822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560713 | TGAGTTAGGTATTCA[C/G]ATGATTTCATGATAT | 81550 |
rs575170503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522446 | AATTTTAATGCTAAT[G/T]AAACATTTATTGGGT | 81550 |
rs575183054 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60553137 | ATGCTCACACTGCAA[A/C]TTTTCCAAATCTTTA | 81550 |
rs575186031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60514911 | ATAGTTGTATGTGTT[A/G]TGGGGAATTATTCAT | 81550 |
rs575204174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60513309 | CATTTTTTCCTCCTA[G/T]GCCTCCTGGCTTGTG | 81550 |
rs575220188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460265 | TCTTAATTGAAGTTA[C/T]TATAAATCATAAAGC | 81550 |
rs575247104 | in-del | -/ACTGCATACT | 0.0023933 | 0.0345097 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395849 | ACGTATGACTTAAAC[-/ACTGCATACT]ACTGCACATTGCAGC | 81550 |
rs575248811 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481405 | TTAGACTGCTGGTAA[-/T]TTTCCAACCAGTCAC | 81550 |
rs575262470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60468245 | AAATGGAGTTGCTTC[A/G]TCTTTCTTTGATGCT | 81550 |
rs575266434 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419263 | TGGTGTGAAATGGTA[C/T]CTCATTGTGGTTTTA | 81550 |
rs575287482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504417 | CCAGCATCTAACTCC[A/G]TATGTCCCAGGACTT | 81550 |
rs575302906 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482568 | AAGTTGAAATGATTT[A/G]TAGCTGTTTGAATAG | 81550 |
rs575312174 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395436 | CCGAAGAAATTCAAT[C/G]TGTTTCATCAATTAT | 81550 |
rs575345094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453685 | TTGGCTAGATCACAA[A/G]ACCCTGCAGGATACT | 81550 |
rs575449774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467776 | AGAATTTCACTGTAA[C/T]GGAGGAGTTCTTGTT | 81550 |
rs575451332 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400145 | CACTAAATGGTACCT[G/T]GTAAAGCTTAATTAT | 81550 |
rs575454079 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60448719 | TTTTTCTTGGATATT[A/G]CAAAGTCCTAGGACT | 81550 |
rs575484846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401824 | CATCCTCTGGCCCAA[A/G]TGCATACATAACTCC | 81550 |
rs575495665 | snp | G/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394661 | CCTGGGCGGCAGAGC[G/T]AGACTCCCGTCTCAA | 81550 |
rs575496936 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394603 | TCGCTTGAACCGGGA[G/T]GCCGAGGTTGCAGTG | 81550 |
rs575521359 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486316 | AATTTCCCCTTATTA[A/G]TAGCAACTTATGAGA | 81550 |
rs575532176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60452927 | ACTCTTGTCAGTTAT[C/T]AGTTTCATTAGTCTT | 81550 |
rs575543513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551965 | GCCAGGTCTCTCCCT[C/T]GACATGTGGGGATTA | 81550 |
rs575639494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399433 | CTATCTTTCTAGGAA[C/T]TGTGAGTTTCATGTA | 81550 |
rs575696921 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400107 | AGGGCTTTCTACAGA[G/T]TAGTGATAATGTTTA | 81550 |
rs575697431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438504 | TTGTTAACATTCTTG[A/G]TTTGACTTAAATATA | 81550 |
rs575705060 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525023 | ACCCGGGAGGTGGAG[G/T]TTGCAGTGAGCCAAG | 81550 |
rs575712329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440523 | CCATCTCTAGCATAG[A/G]TACAAAAATTAGCTG | 81550 |
rs575760953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483085 | AGAAATTGCTTTTGC[C/T]AGAAGATTTTCTTTC | 81550 |
rs575769387 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60433323 | ATAAGTAGTCCTCAA[A/G]GTCTGAAGTAAGCAT | 81550 |
rs575772582 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405907 | GATCGACTTGACAGA[C/T]ATTTGGAAGGTAAAT | 81550 |
rs575778711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558798 | AGAAAAAGAGGCCAC[C/T]CCACCTCTCCCCAAA | 81550 |
rs575797171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407683 | TAGGGTCTTTGAAAT[A/G]TTCTGTTTCAAGGTA | 81550 |
rs575810271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432701 | TTTGCAGTAGGTCAG[C/T]TACTTCCATATTTGC | 81550 |
rs575833934 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439306 | AACAGTGTTTATTTT[A/G]GTTTTATTTTTATAA | 81550 |
rs575834213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450101 | CAGAACAACACAGAA[A/G]ATATAAACTATTATA | 81550 |
rs575849141 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60482108 | CAGCTTACAACTCTC[A/C]GTTGTTTTTTGCTCA | 81550 |
rs575914178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544490 | GAAAAGAAAAAATTG[C/T]CAAAACTAGTAAATT | 81550 |
rs575916801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60480837 | GCAAGCGAGGGGGCC[A/G]CATGCAGGAAATGCT | 81550 |
rs575923724 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430735 | TGCTCAGCTGTTACA[A/T]TTTTTTTAATACCAA | 81550 |
rs575929361 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518903 | ATTAGGGGCGTTTCT[A/G]AATTCAGATGATCCT | 81550 |
rs575939160 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60522410 | CTTTCCTGATGTGTC[A/T]TCAATTAAGTTTATT | 81550 |
rs575942031 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492881 | CATGTATACTTCTTT[A/G]TATTTTCTTCCGTTT | 81550 |
rs575956072 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486968 | AATAATAATCCATTA[-/T]GTGTAGACAGTCAGC | 81550 |
rs575965241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488441 | ACAAAAAAACTGTCT[A/G]TGGGACTATTGGGCT | 81550 |
rs575988926 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455007 | CAACCTCTCCTTCCC[A/G]GATTTAAGCGATTCT | 81550 |
rs575992440 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545462 | GTTTATTATACAAAG[A/C]AAGATATTAGAAGTC | 81550 |
rs575997335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60423219 | TATTAAGGCCATATA[A/G]AAATAGTTTTCATCA | 81550 |
rs576011603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571457 | GCATGAATTCTAATA[C/T]ATGCTGAAATTTTCT | 81550 |
rs576031202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431816 | ATAGTTGATTAATGA[C/G]TAAAATAAATCTTAT | 81550 |
rs576054922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60413442 | GCTATAACCTTGGGC[A/G]CATTTCTTAACTGCT | 81550 |
rs576059564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488056 | GTCTAGATCCTGCTG[C/T]TCACTGCACAGTAAG | 81550 |
rs576081873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60541785 | CCCAGGATGGTGCAA[C/T]GGCACAATCTCGGCT | 81550 |
rs576112593 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531811 | GTCTAATATCCTTTA[A/G]AAAGTTATGAGCCAT | 81550 |
rs576126626 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60518028 | TGTTGTTAGGACATT[A/C/G]CAGTCTCTGGATTTA | 81550 |
rs576145236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422013 | TGGGTCAGGCATGTA[A/G]CTTAAAATAGACACA | 81550 |
rs576152367 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524627 | CTCAGTTTCAAAATA[C/T]TTACTTTATATATGA | 81550 |
rs576181540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457868 | GGTCTTTATACTCTG[C/T]CTGTGTTTGTTTCCC | 81550 |
rs576198129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511228 | AAGTATGGTAAATAT[G/T]CAGCCTTTTTCTAAG | 81550 |
rs576231751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60448494 | TCTGTCTTTTCTCCA[C/T]AAAGTTTCCCCAGAA | 81550 |
rs576286459 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565713 | AATTACTTCATCTCC[C/T]ACAGTACCAAATATA | 81550 |
rs576312014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60437910 | AGGATATTATTCCTA[C/G]AAGGTGCTTCACACT | 81550 |
rs576327681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523734 | GGTGCATGCCACCAC[A/G]CCCAGCTAATTTTTG | 81550 |
rs576330255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406456 | TTAAATTAATTTCAC[C/T]TGTTTTTACTTTTTA | 81550 |
rs576342099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60571612 | GTGATGAATGACACA[C/T]GGTAGCTGTTCAGTA | 81550 |
rs576345249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60463081 | AAGAATGAAATTCCC[A/G]TCTCTCACCATATAC | 81550 |
rs576354927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415301 | TCTGTGGACATTCAT[A/G]TCAACCGGGATCCAG | 81550 |
rs576355356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60515648 | TCTTGTTGACCTGCT[C/T]ACACTACTCAGTGCC | 81550 |
rs576366577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516305 | AATTTGTCAGGCTGG[A/T]TGGAAAAAAATATAT | 81550 |
rs576380605 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60464209 | TATAAATTACCCAGC[C/T]TCAGGTATTCCTTTA | 81550 |
rs576411930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404080 | AGTTAACCCAGACTT[C/G]GGAAGGTTGGAAGCC | 81550 |
rs576417612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415923 | TCTTTTTCTTAAGGA[A/T]AAGTGAAGAAAGGGA | 81550 |
rs576459576 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406344 | TATAAATGTAAAATA[C/T]GCACTGAATTTGGAA | 81550 |
rs576464928 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466985 | GTGTGTTTTTTTGTT[C/T]TTTTGTTTTAAGTTT | 81550 |
rs576467746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60471596 | TGACTCTATTGACCA[A/C]TCAGTATTGATATCT | 81550 |
rs576506948 | in-del | -/ACAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469432 | CCAACACACACACAC[-/ACAT]ACACACACACACACA | 81550 |
rs576520529 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409463 | GCTGGGAGGAAGGCT[C/G]TATCCTGTAAAGCCA | 81550 |
rs576521827 | in-del | -/TCTGG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434740 | AGTAAACAAGAACCC[-/TCTGG]TCTGGTGTCAGTTTC | 81550 |
rs576549004 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60507962 | GCAAAAATCACAAGC[A/T]TTCCTATACACTGGT | 81550 |
rs576554893 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395654 | TACAACATATTTTCA[G/T]AGTTAACAGGTTACA | 81550 |
rs576577016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60456883 | GTATTTTTTGTAGAG[A/G]TGGGGTCTCCCTATG | 81550 |
rs576581752 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416346 | GTGATTATTGAAAGA[C/T]GGTGATACTTGCTCT | 81550 |
rs576582621 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60562922 | TGGGAAAATGCTGAA[-/G]GGAATGGTAATATAA | 81550 |
rs576591536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550259 | ATTCTAGTGATAAAT[C/T]CTTTGGTAAATTTAG | 81550 |
rs576596814 | in-del | -/AAC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557509 | TCACTGAAGAGAAAT[-/AAC]AAACTATGGGTTGTT | 81550 |
rs576653985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404915 | TTCCCATGCTGTTCT[C/T]GTGATAGTGAATGGG | 81550 |
rs576657693 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60470652 | ACAATGGCACGATTT[C/T]GGCTTACTGCAACCT | 81550 |
rs576659678 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479358 | CACTGTGGTCCAAAT[A/G/T]TGTGCTTGGTATGAT | 81550 |
rs576663669 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397901 | CACAGCCCGCGCTGC[G/T]GCCGGAGCCGCCTCT | 81550 |
rs576671091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60531278 | ATCCAGATTCTTATT[A/C]TTCCAACTCAGACTA | 81550 |
rs576685087 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60403859 | TCTTGAATTATAATA[A/T]CTTTACAATAATAAG | 81550 |
rs576720190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501740 | CCTCTTTTAAACAAC[C/G]AACTATTCTCTTTAG | 81550 |
rs576745546 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524960 | GACGTGGTGGCAGGC[A/G]CCTGTAATCCCAGGT | 81550 |
rs576765976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509579 | TACTCAAGGCACAAC[A/C]CCACATATCATACAG | 81550 |
rs576795847 | snp | A/G | 1.65015e-05 | 0.00287237 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483877 | TTGGCAGATGAATTT[A/G]AATTAGGAAAAAGTG | 81550 |
rs576800721 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396242 | GACCTGGCAGATGGG[C/G]ACGCTGCCCCTTAGA | 81550 |
rs576826387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60502858 | CCTTGATAAAATAAC[C/T]GGTTTTTCTAATTGT | 81550 |
rs576826697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510204 | GAGAAAATATGTGAC[G/T]GGTTCTATTATTTCT | 81550 |
rs576849096 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525283 | GGTTCAAGCAATTCT[C/T]CCACTTCACCCTCCC | 81550 |
rs576887833 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403145 | AGTGATTTTTTTTTT[A/T]TTTCTGGTGACTAAC | 81550 |
rs576932383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486421 | ACTTTATTTTATTTA[A/G]TGTATAGTAAAAAAT | 81550 |
rs576940497 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60436371 | TGTTTAGAATTTCTA[A/T]ACCATGAAAATGTTT | 81550 |
rs576949232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428192 | CTGCCTCTCTCCTAT[A/G]AAAACACTTGTCATT | 81550 |
rs576958166 | in-del | -/TAT | 0.00233569 | 0.0340939 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529236 | TGGATGCTTTAAAGA[-/TAT]TATACACTAATATTA | 81550 |
rs576972596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411348 | TAAATAATACATGAC[A/G]GAAATTATGGTGTGC | 81550 |
rs576975103 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467679 | TATAATTCTTTCTGC[-/A]AAAAAACAAAAGTGC | 81550 |
rs576976915 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518921 | TTCAGATGATCCTAA[A/T]ATACTTTGCTGTGAA | 81550 |
rs576983016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561599 | TTATCCTCAAAATAA[A/G]TAATAAAAAAATATA | 81550 |
rs576985193 | in-del | -/TG/TTGTGATG | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60418645 | AAGTGTTTAGCATGA[-/TG/TTGTGATG]TAGGTTTTGATAGTT | 81550 |
rs576996109 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430648 | TAACAACATAGTTAG[A/G]TTACCATTGCCACTA | 81550 |
rs576998433 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482863 | TTAACTTTGTCACCT[A/G]TTTTACATATTTTAA | 81550 |
rs577007736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60428847 | CTTTGAAGAGTCTGG[A/G]GTTTAAGCAGATAAG | 81550 |
rs577013314 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526937 | TCTCCCAGGTTCAAG[C/T]GATTCTCTTGCCTCA | 81550 |
rs577034758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435786 | TTGGGTAGATACCCA[A/G]TAGTAGGATTGCTGG | 81550 |
rs577046737 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60453927 | TTTTTTTTCAGTTCT[C/T]TTTAAGGCTATCAAT | 81550 |
rs577060863 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544255 | GCTTGGGCAAACATA[A/G]CAAGACCCTTACTTT | 81550 |
rs577063483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60493244 | TCTAATGTTATTGTA[A/T]TATATATAATTTATA | 81550 |
rs577072491 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427894 | GTATATTTATTTCCT[A/G]TGGCTGCGGTAGCAA | 81550 |
rs577075832 | snp | A/G | 1.90134e-05 | 0.00308323 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485800 | ACTTGTTTTACTAGA[A/G]GTGTGTATCTCATGT | 81550 |
rs577081992 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483319 | CTCCATATTATACAC[C/T]ATAACAATCTGTTCT | 81550 |
rs577107225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60475866 | ATGTTCGTTCATGTC[C/T]TTTGCCTATTCTTTA | 81550 |
rs577113021 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546243 | AACTTATTACAAAAA[-/G]ATCTAGAAATGATAA | 81550 |
rs577133283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60492285 | ATTTAATTTGGAGCA[C/G]GTGAGATTCCAGACT | 81550 |
rs577153893 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398496 | CTACACAAGATCTAT[A/G]TGGTTCGTGAAAGAT | 81550 |
rs577167368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60476700 | TCTGTGGGCATGGAA[C/T]GTTTCCATTTTTTTG | 81550 |
rs577176891 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60446201 | ATTAATAAACTAATA[C/G]TTTTCTAGAATTATT | 81550 |
rs577202254 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416882 | CTTCATTCCTTTCTC[A/T]TCATTCGTTGTCTTT | 81550 |
rs577203999 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533660 | AAAAAGAGAGATGCT[A/G]TTAGAGTAGATAGTG | 81550 |
rs577220880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60561306 | GAAAGGCTCTGAACT[C/T]AGAGCCAGAGGCCTG | 81550 |
rs577264869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60499499 | ATATCAACTCTCTGG[C/T]TTTGTGTCATAATTG | 81550 |
rs577267646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537209 | TTTTATAATCAAGTG[A/G]TTGTTGACGTTTTAT | 81550 |
rs577274511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60491288 | GTACTTATCAGACAT[A/G]CATGTAGTAATAATG | 81550 |
rs577290201 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563160 | TTGAACCTGGAAGGC[A/G]GAGGTTGCCTTGAGC | 81550 |
rs577297779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535450 | CTTGTATAATGTTTT[A/G]TTGTATTATGCTTTG | 81550 |
rs577337992 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521821 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 81550 |
rs577357539 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537951 | AAAGCCTTTGTAGAA[A/G]ATTAGTTGCTTGTGT | 81550 |
rs577386138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60469745 | GAAGTGAAGAAGCAC[C/T]AAGCATTCAGTAAAC | 81550 |
rs577394889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410730 | GGTAGGGTTAGTTCT[C/T]AGGCTACATGAGAAT | 81550 |
rs577407063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60451750 | TGTATATGAGATTCA[A/G]TTGAGCCATATCTTT | 81550 |
rs577469696 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567943 | GGTTTCACCATGTTG[A/G]CCAGGCTGGTCTTGA | 81550 |
rs577497858 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60569100 | CAGCCTCCCTAGTAG[C/G]TGGGACCACAGGTGC | 81550 |
rs577525804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466980 | TGTGTGTGTGTTTTT[G/T]TGTTTTTTTGTTTTA | 81550 |
rs577528097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568088 | TGTGATATTTCTGCT[A/G]GGCAGCACTGTCCTA | 81550 |
rs577531354 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60527275 | ATGTTTGGGGAAAGT[A/T]TTGATAGTCAACATC | 81550 |
rs577548738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459338 | AAGTTGCCACTTTAG[A/T]TAAATTTACTTTTCA | 81550 |
rs577572073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60519812 | GTACTCTGAGGTAAG[C/T]TCATTTGGTTTTTTA | 81550 |
rs577588342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467557 | CTCTAAAGTAGATAT[A/G]CTTTTTCAGTATTTG | 81550 |
rs577614372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60407834 | GGTGTGGCTGTGTTC[C/T]GACCCAAATCTCAAC | 81550 |
rs577627828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419368 | TTGAGTCTTTTGTCC[A/G]TTAAGAATTTGGATT | 81550 |
rs577644395 | snp | A/G | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60526486 | AATCTTTACTCCTGG[A/G]CAGTAAACAATGCCA | 81550 |
rs577651270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399320 | GCATTTGCTACTTTA[C/T]ATTGCAACTTAACTG | 81550 |
rs577679497 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464465 | CTCCCATTTTTATTG[C/T]AGCACTATTCACAAT | 81550 |
rs577706915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60517983 | AAACCCTGGTCTTTC[A/G]CTACAGTAAGTTTGA | 81550 |
rs577726237 | in-del | -/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396694 | CTGTGGTGTCCGACT[-/G]GGGGCAACTCGATCT | 81550 |
rs577736909 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511073 | ATCTTATATAACTTA[C/T]TTTGCTTGTGAAATT | 81550 |
rs577789206 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512844 | CGAGGAGTGTCTGTG[G/T]CTTTTCCAGGTAAAT | 81550 |
rs577793227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60498857 | ACCCAAAATGTCACT[G/T]TGGTCCTCCAGTTAA | 81550 |
rs577795724 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544357 | TCTGAGATGGGAGGA[G/T]TGCCTGAGCTCAGGA | 81550 |
rs577856863 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TDRD3 | GRCh38.p7 | 13:60534839 | AGGTTGAGATGGGAG[G/T]ATCGCTTGGGCTGGG | 81550 |
rs577868574 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60560130 | AATGGAAATATATAC[A/C/T]GTATGATGCAATGAA | 81550 |
rs577945043 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505972 | TTCAGGATATTGTCC[A/G]GAAGAACTTCCCCAA | 81550 |
rs577956414 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478493 | CATTTTTAGTAGAGA[C/T]GGGGTTTCAGAATGT | 81550 |
rs577956495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558573 | ACTGGTTTCTTTTTA[A/T]GGGATATCTTAAAAT | 81550 |
rs577985280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504327 | TGGTGAAAAACCTGG[G/T]TAGTAAGCAGTTTTA | 81550 |
rs578013620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60505508 | AGGGGCGGCTGTGGG[C/G]ACAGCTTCAGCAGAC | 81550 |
rs578017183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60415870 | AGCAAAGACAATTTA[C/T]GGAAAAACATTCTTT | 81550 |
rs578052733 | in-del | -/ACTAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460284 | AAATCATAAAGCATG[-/ACTAT]TAAGGAAAAGAGAAA | 81550 |
rs578066182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457720 | TTAAAGTGTCAGCAG[C/G]GTTGGTTCCTTTTGG | 81550 |
rs578074304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60449703 | TTTCTTAATTATAAG[G/T]AATTTATTAAATGTT | 81550 |
rs578094689 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431946 | AAGCCACAGAGAAAA[C/T]TAAATTTTTAAGCTA | 81550 |
rs578097231 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TDRD3 | GRCh38.p7 | 13:60524534 | AAATAAATAAATAAA[A/T]AAAGAGAAAAGAAAA | 81550 |
rs578116988 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60573797 | AAAAAAATACTGAGT[G/T]AAATTAAGCAAATAC | 81550 |
rs578119779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440405 | GTAAGTAAACAGGCT[C/G]GGCATGGTGGCCCAC | 81550 |
rs578126152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565180 | CCTGCCTCAGTCTCC[C/T]GAGTAGCTGGGACTA | 81550 |
rs578167134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60457007 | AGCCTTAAGATGATT[G/T]TAGATTCAGGATTTA | 81550 |
rs578195206 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TDRD3 | GRCh38.p7 | 13:60504747 | AGGTACCTGGCTCAT[C/T]TCATTGGAACTGGTT | 81550 |
rs578199139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60489068 | GTTTGATATAATCTC[A/G]TTTGTCTATTTTTAC | 81550 |
rs578205694 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60497701 | GGAAAAGAGTAGGAC[C/T]TTGTAGCTTGGAATG | 81550 |
rs578207471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60551818 | GAAACAAGCACCTTC[C/T]TCATGAGGCAGCAGG | 81550 |
rs578246837 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463847 | AGAAGATAACTGCTA[C/T]AGTTTGGATATTTGA | 81550 |
rs578251843 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488626 | TTGCCCAGGGTGGAG[G/T]GCAGTGGCGCGATCT | 81550 |
rs745306387 | in-del | -/AT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571547 | TCACTTTTAAAAAAC[-/AT]AATTTCACAGTCATA | 81550 |
rs745331760 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486224 | TTTTTTTATACAATG[A/T]AGTAACTGAACACAC | 81550 |
rs745368111 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445998 | TCTTTAAGATTTCCT[A/T]TGAATGTAGCTAGCA | 81550 |
rs745422713 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60472187 | TGATTTTTATATGTC[A/G]AAGCATTCTTGTATT | 81550 |
rs745462114 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423443 | AGGTTGATCTTCTGG[G/T]TATACTGTATATTGA | 81550 |
rs745487945 | snp | A/G | 1.78328e-05 | 0.00298598 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510601 | GTTTTTGCATATACA[A/G]TACATATTTCTTGCT | 81550 |
rs745536591 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516976 | ATTCAGACTACATTA[A/T]TTATATTGTTTTTAT | 81550 |
rs745543131 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60449241 | TTCCTATATGTTAGT[C/T]TGTGTTAAGTAATAC | 81550 |
rs745571646 | in-del | -/AGAATTGTTGA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471152 | TGTCTTTTGATGCAC[-/AGAATTGTTGA]AGAGTTTTTATAGGT | 81550 |
rs745575030 | snp | A/G | 1.65285e-05 | 0.00287471 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509904 | CAGAAACCTGTTATG[A/G]GTCCTCCTCTGAGAG | 81550 |
rs745585868 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425295 | TCAGGGACATGCAAA[C/T]TGAAACCACTATGAT | 81550 |
rs745586728 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405866 | GACTATGAAATAGAT[A/G]GTGATGGTTGAGATA | 81550 |
rs745588036 | snp | A/G | 1.64928e-05 | 0.00287161 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494534 | CAGAAAGAAAAGTCA[A/G]CCAAATCAGAGGGAA | 81550 |
rs745597303 | snp | C/T | 3.33973e-05 | 0.00408626 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528893 | ACAAACAATAAATAA[C/T]GAAGCTTTCAGTGGT | 81550 |
rs745613614 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544497 | AAAAATTGTCAAAAC[C/T]AGTAAATTCCATTGG | 81550 |
rs745630747 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60528196 | ACTGTACATTAGAAA[A/T]GCAGGACTCCAAGGA | 81550 |
rs745686943 | snp | A/C | 1.65941e-05 | 0.00288041 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528794 | AAATCCACTTCCTCA[A/C]GGATCTGTAGATTAT | 81550 |
rs745688130 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445368 | TAAATAATTATATAC[A/G]TGAAGACATAAATGT | 81550 |
rs745718538 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555334 | TTAGAGTTTCAAAAC[A/G]TGATTACCATTGGAA | 81550 |
rs745727648 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498747 | CAAGGAGACCTCCGG[C/T]CTTTTACCAGGGTAA | 81550 |
rs745728465 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518346 | CTGGAGGCTCCACAT[A/C]TGAGAGGGACACACT | 81550 |
rs745774305 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407134 | TTTGAGAGAGAAATA[C/G]GGACATATGTTAAGT | 81550 |
rs745777970 | snp | G/T | | | downstream-variant-500B | TDRD3 | GRCh38.p7 | 13:60573921 | TCTTTCTTGTTCATC[G/T]GGTATTAACCCCATA | 81550 |
rs745778171 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429968 | ACCTACTGTATTCCA[A/G]GCATATGCTAGGTAT | 81550 |
rs745803238 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446958 | TAGTTCTTGTTTAAA[G/T]CAACTTTGTTTGAAT | 81550 |
rs745806277 | snp | C/T | 1.66371e-05 | 0.00288414 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483734 | CTGGAAATATATTTT[C/T]TATGTATAACTGCTC | 81550 |
rs745883369 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433873 | GATTCACCGATTTTA[C/G]CTGCTTTCAAAGAAA | 81550 |
rs745900232 | snp | C/G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538731 | CTTTAAACTCTAAAA[C/G/T]GAATTCCAGGAAACC | 81550 |
rs745902337 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555525 | AGCTAGTAAGTTGCA[A/G]AGCTGATAGTCAGGT | 81550 |
rs745904840 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488821 | TGACCTCAGGTGATC[C/T]GCTCACTTTGGCCTT | 81550 |
rs745962557 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401726 | ATGGAGAGGATAAAC[A/T]AAGGTCTCCTTCTTA | 81550 |
rs745981528 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431304 | GGTTGTCATCTAGTG[A/G]TGCTTTCAAGTAGTA | 81550 |
rs745989254 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554138 | GTTTTTCAGCCAGTC[C/T]TGCTGTCAGTGTACC | 81550 |
rs745994785 | snp | A/G | 1.65012e-05 | 0.00287234 | splice-acceptor-variant | TDRD3 | GRCh38.p7 | 13:60567523 | CTACTCTTTGCAAAT[A/G]GGAGGAAGAAGGCAC | 81550 |
rs746006256 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530617 | AGCTAATTTTTTGTA[-/T]TTTTTTTTTTTTTTT | 81550 |
rs746009307 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475519 | CTCTTCACTGATTCC[A/G]TGTCTTTGCTGTTGT | 81550 |
rs746010147 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514578 | ATGACATCTAGTTAA[C/G]ACTGAGGGGAAGTGT | 81550 |
rs746076570 | snp | C/T | 0.000102801 | 0.00716869 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60444715 | TGGCAAGAAATTCCT[C/T]CCCAGTGACATCAAT | 81550 |
rs746092691 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424054 | TGAGATGGAGTCTTA[C/T]TCTGTCGCCCAGGCT | 81550 |
rs746100100 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60513204 | GCTCTACATTGGTCC[C/T]TTTCAGCAATGGCTA | 81550 |
rs746101853 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530987 | TGTTAGATGTTGCCT[A/G]ATGATAGAATAAGGA | 81550 |
rs746105989 | in-del | -/GAGA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398376 | CTGTGGAATGGGAGG[-/GAGA]GTTACTTTCCTAAAG | 81550 |
rs746142033 | snp | C/T | 0.00184077 | 0.030282 | utr-variant-5-prime, intron-variant | TDRD3 | GRCh38.p7 | 13:60397334 | TCACCCCCACCCCAG[C/T]CCCCCACCACCCCCG | 81550 |
rs746187356 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442177 | TTGAAATCCAGCATG[C/T]AAGTTTTACGTTCAA | 81550 |
rs746205470 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481683 | TAATAGCTGTTTAAC[A/G]CCCTATTTATTAGTT | 81550 |
rs746242117 | in-del | -/A | 1.6492e-05 | 0.00287154 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528566 | CAGTGGATTACCTAG[-/A]AATAGAGGTTCTGAA | 81550 |
rs746258381 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507697 | TAAAGCAATTTGTAG[-/A]GGGAAAGACTGGCAC | 81550 |
rs746265527 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415171 | ATAACAGTGTTTAGG[A/G]AACTAGGCATGAAGG | 81550 |
rs746277012 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428386 | AAGAGGTATGGGGGA[C/T]GTAGTCAAATTATGT | 81550 |
rs746293526 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466681 | TAATCCCAGCTACTC[A/G]AAAGGCTGAGACAGG | 81550 |
rs746329018 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454794 | AACAATGTATATTTC[-/T]TTTTTTTTTTTTATT | 81550 |
rs746355575 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416122 | AGGTATTGATTTTAG[A/G]TTTAACATGGTACAA | 81550 |
rs746372583 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451608 | GCACACATATAACAG[C/T]TTCCCTAAGGAATAT | 81550 |
rs746386486 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502203 | TGACAGAATTTGCAG[A/G]ATAATTGTCCAGAAC | 81550 |
rs746393972 | snp | C/G/T | 9.88756e-05 | 0.00703062 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509818 | TCAGTAAGGAAGCAT[C/G/T]GAGGCAAGCTCTTAT | 81550 |
rs746393974 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488587 | TTTTTTGTTTTTTTT[-/T]ATTTTTGACAGAGTC | 81550 |
rs746426423 | snp | C/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438219 | ACAGATACAGTTGGA[C/T]AATTTTTCATTATTC | 81550 |
rs746443311 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400268 | CAGAGGTTCATTCTC[C/T]TTTAGGATGATATCC | 81550 |
rs746459457 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428657 | TTTTAGGGGAATTCA[A/G]TGGGCTTGGAGAACA | 81550 |
rs746467246 | snp | A/T | 1.65102e-05 | 0.00287312 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509897 | CAATAAACAGAAACC[A/T]GTTATGGGTCCTCCT | 81550 |
rs746470277 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498576 | TCTAATGGACAAAAG[A/G]CTAATTTGAATTATG | 81550 |
rs746473942 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549818 | GAGCACACTTTTGAA[C/T]GAGAAAAAATTTTTT | 81550 |
rs746476183 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60531393 | AAAAGTGAAGTAATT[A/G]GAAAGCAGTGTTTGT | 81550 |
rs746493835 | snp | A/G | | | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60483815 | ATATTGGAACTGAAG[A/G]TGGACCACCGCCTTT | 81550 |
rs746522274 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423688 | CAACTTTTTAAAAAG[C/T]ATTTTAAAAAATTGT | 81550 |
rs746544727 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429830 | TTTCTTTCTCATTAG[A/C]GAAATTGTATTCTCT | 81550 |
rs746549596 | snp | A/G | 5.11723e-05 | 0.00505802 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529182 | ATGTGGAAACCTGGA[A/G]ATGAATGTTTTGCAC | 81550 |
rs746563959 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548244 | GTCCTAGCCCACCCT[C/T]AGCCAAACTAAACTT | 81550 |
rs746572679 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467006 | TTTTAAGTTTCAGGG[C/T]ACATGTGTAGGATGT | 81550 |
rs746648024 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444339 | TATGTATTCAAAAGC[-/T]TGTCATTTGATTTTG | 81550 |
rs746665953 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469544 | CCACATTAGTATTTC[C/T]TGTTAGGGAGTGATA | 81550 |
rs746668726 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504019 | TTATTTCAATGCTCA[A/G]TTTATGAAAAGATCA | 81550 |
rs746691638 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522433 | AGTTTATTTGCTTAA[C/T]TTTAATGCTAATTAA | 81550 |
rs746705425 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402011 | TCAAGGGCCCACTCT[A/G]TTCCACATTACTTTG | 81550 |
rs746706366 | in-del | -/GTTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561872 | AGGTTTTTTGTTGTT[-/GTTG]TTGTTGTTGTTGTTG | 81550 |
rs746713847 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434848 | AGGTCCACCAGGTGG[G/T]TGTGCACAGGGACCG | 81550 |
rs746726013 | snp | A/G | 1.65026e-05 | 0.00287246 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528670 | ATGACAGAACTAAAG[A/G]TACTTCATATCCTTT | 81550 |
rs746751421 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422400 | AAAAATGAACAAAAT[A/G]TTTCTAAATCAGGAA | 81550 |
rs746785521 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507567 | ATAGGTGGAAACTGA[A/G]CAACCTTCTCCTGAA | 81550 |
rs746815951 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498642 | GCCAGTTTACAGACC[C/G]AGAATCCCTTGAATG | 81550 |
rs746832363 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459647 | TTGTGTTGAGACGGA[C/G]TCTCGCTCTGTCATC | 81550 |
rs746838457 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532111 | CTGTCCATCAGTAAT[-/A]GCTGTGGTGAAAAAA | 81550 |
rs746840953 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572007 | ACAGCTTGGAAATAT[A/G]AGCAGATATAAAATA | 81550 |
rs746868464 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534144 | AGCAATACCCTGTCT[C/G]TATGAAAAATTTTTA | 81550 |
rs746875434 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508866 | CACTTCCCAACAAAA[A/C]ATTACAAAGCCTACA | 81550 |
rs746888993 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60449987 | TTTTTAGTGAATTCT[A/G]ATAATTCTTGTTCTT | 81550 |
rs746897442 | snp | A/G | 1.64912e-05 | 0.00287147 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467343 | AGTTCTTGGTGGTGA[A/G]GTGGAACACCTTATT | 81550 |
rs746930938 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570271 | AATAGGCATTTCTCA[A/G]TAGAAGACATACAGA | 81550 |
rs746934545 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544667 | AAGCTTGTTATTCAG[A/T]ACCTTCTAAAAAACA | 81550 |
rs746934999 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442738 | CTTTTTTTAGCCTGA[C/T]AACAACTTTGTGAGA | 81550 |
rs746978412 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60479616 | AATCTCTCACTATTA[C/T]TGTGTTTGTCTAAGT | 81550 |
rs746982728 | snp | C/G | | | downstream-variant-500B | TDRD3 | GRCh38.p7 | 13:60574244 | CCAGAAAACCCATCT[C/G]AAACCAGCTTAAACA | 81550 |
rs746989004 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497983 | TTAATATTGCAGCTC[A/G]GGGGGTTAAAAAAAA | 81550 |
rs747004506 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410335 | GTATCTTGCAGTCTA[A/T]GTTGTCATAGAGTTC | 81550 |
rs747020549 | snp | A/G | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535201 | GAAGAGGTGCTACTG[A/G]GCAATATCAAGCCCA | 81550 |
rs747032190 | snp | C/T | 1.67024e-05 | 0.0028898 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467209 | TTCTCAGCTTCAATA[C/T]GTTTTTAACACTTTT | 81550 |
rs747068358 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501183 | TAACTCCTGTATCAT[C/T]CCCCCCGCTGGAGTG | 81550 |
rs747123526 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567390 | CCCTTGCCTCCCTCT[A/G]TTGTAAAAGTTGACA | 81550 |
rs747182026 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432841 | TTTCTTTGTGGCTAA[G/T]CAAGAATTCATTTAT | 81550 |
rs747243290 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546059 | AGTCTAAATAAATAG[A/T]GCATCATTTAAAGTT | 81550 |
rs747260881 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526773 | ATTTTAAAAGTATTT[A/G]AAGCCTTTTGGCTTC | 81550 |
rs747266808 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474172 | AGAAGAAATAATGGC[A/G]TAAGCTGTCCTCTCT | 81550 |
rs747296272 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60539908 | ATAAAATTAGGCTCC[A/G]TCTAGTTTTATTTGA | 81550 |
rs747301476 | snp | C/T | 1.68131e-05 | 0.00289935 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494389 | TTTTAGAACTATTTT[C/T]AAATGCTGTCTACAT | 81550 |
rs747326393 | snp | C/T | 1.65836e-05 | 0.0028795 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528786 | GCAAAAGAAAATCCA[C/T]TTCCTCAAGGATCTG | 81550 |
rs747339843 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520612 | GCTTTAAGCTACATT[A/G]TTTGTTCTTTTTACC | 81550 |
rs747342443 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457994 | AGCCTTGTTCCCAAA[C/T]GAGGTCATATTTATA | 81550 |
rs747371086 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495226 | GTTACAAGTGTTGGT[A/G]AATTCAGCAGTATAA | 81550 |
rs747402827 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572947 | ACCCGACGCTCTGTA[-/T]TTTTCTAAGCAGGAG | 81550 |
rs747403505 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440735 | CTGCAATTACCCTCT[A/G]ATTGTTTTTCTATGT | 81550 |
rs747460471 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538307 | GATTATGATTAAATT[A/C]TAATTATCTTCAAAA | 81550 |
rs747468621 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60480183 | GCTCTTGTAAGGCAG[A/G]TCTGGTGGTAATAAA | 81550 |
rs747478871 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565689 | GTATTCCATTCTAAT[A/T]CCTGAAATAATTACT | 81550 |
rs747490841 | snp | G/T | 3.29544e-05 | 0.00405908 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567589 | ATGGCCAGCCAAGAC[G/T]ATCCACTCGGCCAAC | 81550 |
rs747491717 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427255 | ATTTGATTGATTTTG[C/T]TTTTTCTTCAGAATG | 81550 |
rs747518352 | snp | A/G | 0.000102875 | 0.00717127 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60444709 | AACAATTGGCAAGAA[A/G]TTCCTCCCCAGTGAC | 81550 |
rs747524303 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412528 | AAGGGATTACAAGCC[G/T]TGTTGGTTTAATCAT | 81550 |
rs747539619 | in-del | -/AGG | 4.95054e-05 | 0.00497496 | splice-acceptor-variant | TDRD3 | GRCh38.p7 | 13:60567523 | CTACTCTTTGCAAAT[-/AGG]AGGAAGAAGGCACCT | 81550 |
rs747546785 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553757 | CAGCATGGGGGAAAC[C/T]GACCCCATGATCCAA | 81550 |
rs747578902 | snp | C/T | 1.65718e-05 | 0.00287848 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567500 | GCCATTTTGAACATG[C/T]AAAATCACTACTCTT | 81550 |
rs747586273 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508651 | TTAAATGTAAGACCT[A/C]AAACCATAAAAATCC | 81550 |
rs747590494 | in-del | -/GCACA | 1.65206e-05 | 0.00287403 | frameshift-variant, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460504 | ATGGTCATATAAGTT[-/GCACA]GCAGTAGAATTTAGT | 81550 |
rs747606287 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562257 | GGTGGAGGTTGCAGC[A/G]AGCCAAGATTGCACC | 81550 |
rs747615550 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441381 | ATTTGTGCTGTGTTC[A/G]TAAGAGGTGCATGCT | 81550 |
rs747623255 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409220 | GCCTGGATGCCCAGG[A/C]AAAAGTTTGCTGCTG | 81550 |
rs747640735 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546590 | TGAATATGTGAATTT[C/T]CTATCTATTCTAATG | 81550 |
rs747643628 | snp | G/T | 1.66123e-05 | 0.00288199 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528959 | TTATCAGAATCCAGT[G/T]CGAAGTAATAGTTTC | 81550 |
rs747674324 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497782 | TCTGATGAATTTTTT[C/T]TTGCTAGAAGAAACA | 81550 |
rs747703111 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442577 | TAATAAAGTTGTCTT[C/T]ATAGTGTGAATTTAG | 81550 |
rs747721436 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520486 | CACATTTCTTCTCAT[A/T]AGGGCTCACCTAAAC | 81550 |
rs747722139 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481867 | CCTTTAATGAGTATA[A/C]GAATTAGCTTTGGTC | 81550 |
rs747761648 | snp | G/T | 4.9507e-05 | 0.00497504 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483880 | GCAGATGAATTTAAA[G/T]TAGGAAAAAGTGTTT | 81550 |
rs747765442 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534928 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 81550 |
rs747866543 | in-del | -/TTAAATA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504565 | AAGACATTTTGTTTC[-/TTAAATA]TTAAAGTCACATGAA | 81550 |
rs747883611 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432930 | AGCAGATAATCAGGT[C/G]TAGGTTAGAACCCCA | 81550 |
rs747927164 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561062 | TCTTCAATATATTTT[-/C]TTCTAAAGGGGAATT | 81550 |
rs747937447 | in-del | -/TT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470592 | TCATTATAGTTGGGT[-/TT]TTTTTTTTTTTTTTT | 81550 |
rs747941202 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532564 | CTATCATTAAGATAC[C/T]ATAATCTTCTTAATT | 81550 |
rs747947947 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60531160 | CTTTTTCTCTGGAAA[A/T]GCAAAAGCCTTCCCA | 81550 |
rs747950257 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473995 | CCTGACTGATGGCAG[C/G]CTTGTCCTCAGCCAT | 81550 |
rs747970046 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421220 | GGTTTAATGGACTCA[C/T]AGTTCCATATGGCTC | 81550 |
rs748053987 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422156 | GCTTCTGGGGGAGAA[A/G]GAAACAAAAAGGAGG | 81550 |
rs748076907 | in-del | -/TTTAG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453486 | TCTAGCAACACTTTC[-/TTTAG]CTTTAATCAGTTGAA | 81550 |
rs748134064 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463575 | CAAAGTGAGGAGACT[A/G]CCTACAGAATGGGAG | 81550 |
rs748140219 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526469 | ACTGCTATTCTTCCC[A/G]AAATCTTTACTCCTG | 81550 |
rs748143649 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507524 | AAATTAAAACTCAGG[A/G]TTAAGAAACTCACTC | 81550 |
rs748162174 | in-del | -/TA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527615 | CAGAATAAAAATCAC[-/TA]TGTGAAATACAGTCA | 81550 |
rs748172883 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433423 | AGTGTGATGTAAACA[A/G]CTCACCAGAGAACAT | 81550 |
rs748178461 | snp | C/T | 3.77188e-05 | 0.00434258 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485984 | ACGTTTTATTTCTTA[C/T]CATTATGTTCTATTT | 81550 |
rs748186389 | in-del | -/TTAG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60413211 | ACATTTATATTAGAA[-/TTAG]TTAATTATAATTAAT | 81550 |
rs748226361 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544204 | CTATAATCCCAACAC[A/T]TTGGGAGGCCGAGAC | 81550 |
rs748259217 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412295 | TTACGGTAAATTTGA[A/G]TGAATTGGTGTGAGT | 81550 |
rs748320794 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508617 | TTGTACAAAAATTAA[C/G]TCAAGATGGATTAAA | 81550 |
rs748340309 | snp | G/T | 1.64993e-05 | 0.00287218 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528657 | CCGTATTCTAGATAT[G/T]ACAGAACTAAAGATA | 81550 |
rs748349166 | snp | A/C | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396272 | AAGCCTTTTTCCCCG[A/C]AATACGGGACGCCGC | 81550 |
rs748370276 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60414594 | GTCAAAAATAACTTG[A/C]CAAGAAAACCACAAT | 81550 |
rs748377837 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559268 | AGATTAGTAACGTGC[C/T]TATGATGTGGTAGAA | 81550 |
rs748389015 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501041 | TATGGCCAGTGACTA[G/T]TCCTTGGGGTGATCA | 81550 |
rs748401061 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60449064 | GTAGGAGTGACTGGT[C/T]TCAAAACCTCAGCAA | 81550 |
rs748404994 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542236 | GTCCTGAATTTTACC[A/G]TTCTTTCGCAAATAT | 81550 |
rs748412466 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534863 | GGCTGGGGAGGCGGA[A/G]GTTGCAGTGAGCCAA | 81550 |
rs748414118 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553716 | AACCATCAGCTCTCA[A/T]GAGAACTCACTCACT | 81550 |
rs748421422 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486448 | AAATAATTTTATCTT[C/T]ACATTATATGTCTAT | 81550 |
rs748427994 | snp | A/G | 3.29875e-05 | 0.00406112 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528534 | GACTCCCAAAATTCA[A/G]AGTCAGTTTTAGAAG | 81550 |
rs748467015 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454904 | TCCTATCCCACCTCT[A/G]TTGATTGATTGGTTG | 81550 |
rs748480342 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537013 | CTGAACTACAGCAAT[A/G]CTTTCATATTCTTCC | 81550 |
rs748498433 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490471 | ATAAAGTCAAGAGAG[A/G]TAATAGAGGTTACCT | 81550 |
rs748556417 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60403440 | AGAAATTCATTCTTT[A/C]TGAAAGGTCTAGGAT | 81550 |
rs748576723 | snp | C/T | 3.29723e-05 | 0.00406018 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535176 | TAAATTCATTGACTA[C/T]GGAAACTATGAAGAG | 81550 |
rs748581338 | snp | C/G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512925 | CCTCTTCTTATAGCT[C/G/T]CACTGAGCAGTGCCC | 81550 |
rs748585924 | snp | C/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439391 | ATTATATTTGTATAA[C/T]AGCAAAGAGCAGCTT | 81550 |
rs748597703 | in-del | -/AAGAC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463386 | AAAAAAAAAAAAGAT[-/AAGAC]CTAAAACTATGAAAT | 81550 |
rs748657557 | in-del | -/TA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469338 | TCAACTCTAATACCT[-/TA]TATAATTTTCCCACA | 81550 |
rs748663076 | snp | A/T | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494483 | AGAAGTAATCTCAAT[A/T]TGAATGCTGCTGGTA | 81550 |
rs748671261 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512371 | CAGCCAAACCATATC[A/G]TTCCACCCCCAGCCC | 81550 |
rs748675174 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60491382 | ACATATGGATGGTAT[C/T]GAAAATTATGAGGCC | 81550 |
rs748683088 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567007 | TCTGTCTCTAGATGT[A/C]AGGTTCTTAACAGTG | 81550 |
rs748712936 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423181 | AATTTGGGATTTTAT[A/G]TCTAGCCAAGCTGCT | 81550 |
rs748714015 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532974 | TCATAAGTCAAAAAT[-/A]ACATATATCTTAGTC | 81550 |
rs748754194 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566647 | AAAACTGAGAGCTAA[-/T]TTTTTTCTCTCTCTA | 81550 |
rs748766161 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473846 | GGGAAGGTGCCGATT[A/G]CCTAGTGGACCTTGG | 81550 |
rs748769023 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420875 | CATGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG | 81550 |
rs748804818 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517569 | AAGAAATGTGTAGCT[A/G]TCTACCCACAGCCTA | 81550 |
rs748820094 | in-del | -/TAAC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473238 | ATCCCACTCCCAAGA[-/TAAC]TAACCCATTCCTGTG | 81550 |
rs748856194 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458124 | CTTGCTTGGAAATCG[G/T]CATTTGGGGGCAGGT | 81550 |
rs748863686 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407796 | ATTTCAGAATTGCTT[A/G]CAGCTTAGCACTTCA | 81550 |
rs748867310 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507370 | ATCTACAGAACTCTC[C/T]ACCTCTAATCAAGAG | 81550 |
rs748867557 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495352 | ATAAAGCTGATTTAT[C/G]AAGACAGGGGAATTG | 81550 |
rs748872329 | snp | C/T | 3.31846e-05 | 0.00407323 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483745 | TTTTTTATGTATAAC[C/T]GCTCTTTTGTGACTG | 81550 |
rs748887294 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60536627 | GTTCCCAGTTGTTTT[C/T]AGCCATAGCAGTCAA | 81550 |
rs748896680 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534713 | GGCAGATCACTTGAG[C/T]TCAGGAGTTTGAGAC | 81550 |
rs748903244 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445312 | ATGTCTTCTTTGTCT[C/T]TCATCAGGAGAAATG | 81550 |
rs748937437 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475158 | AAATTGTGTGTCACT[A/G]AGGCTTGGTGTATCA | 81550 |
rs748950013 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552448 | TGCCCCTGTGGCTCT[G/T]CAGGGTGCAGCCCTT | 81550 |
rs748957370 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496957 | GCAGTGTTATAGCTC[C/T]GTTAGAAGCGGTGGG | 81550 |
rs748984426 | snp | A/C/T | 0.000214506 | 0.0103545 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444791 | TAATTAATTTAGTTA[A/C/T]AATAAATATGAACTA | 81550 |
rs749003263 | in-del | -/T | 0.000801165 | 0.0199985 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510779 | TTTAAAGTTGATTCC[-/T]TTTTTTTTTCTTTCT | 81550 |
rs749010366 | snp | C/T | 3.29875e-05 | 0.00406112 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467365 | CACCTTATTGAGAAA[C/T]GGGAGTTACAGAGAG | 81550 |
rs749022302 | in-del | -/TT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60437121 | TTTGATAAATTAAAC[-/TT]TTTTTTTTTTTTTTT | 81550 |
rs749028045 | in-del | -/TTT/TTTT/TTTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557820 | TTTTTTTTTTCCTGA[-/TTT/TTTT/TTTTT]TTTTTTTTTTTTTTT | 81550 |
rs749039185 | in-del | -/TAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406641 | GTTAGGGGAAAAAGC[-/TAA]TTTAGAATGCATTAT | 81550 |
rs749041497 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396145 | TCTCTGCTCCAAGTC[C/T]GTTTTTGATGATGCC | 81550 |
rs749044387 | snp | A/G | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509763 | CTTTATTCCTTCCAG[A/G]TTGATGAGAAAGCTC | 81550 |
rs749050202 | snp | A/G | 0.000113193 | 0.0075222 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529255 | ATACACTAATATTAC[A/G]AAATGTAACATTCTA | 81550 |
rs749059852 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522916 | GCAGCTTGGCATAAT[A/G]GAAAAATCATGTGTT | 81550 |
rs749067281 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60547602 | CTATAGAAATATAAA[C/T]TCTTATTATCATAGG | 81550 |
rs749122046 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431281 | ATAATATTTTACTTG[C/T]GAAACAAGGTTGTCA | 81550 |
rs749123949 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60448596 | CCAGATTTTCTTATA[G/T]GCACTTCATATTTGA | 81550 |
rs749172682 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419496 | GGACATGGATGCAGC[C/T]GGAAACCATCATTCT | 81550 |
rs749185187 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400867 | AAATGGCAGAACCAA[A/G]AATAGAGCCCAGATG | 81550 |
rs749206104 | snp | A/G | 1.73564e-05 | 0.00294583 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509661 | GACATTTTTACATAA[A/G]TATGGGATGTAATTT | 81550 |
rs749208176 | snp | C/T | 1.6525e-05 | 0.00287441 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529031 | AAGACGAATAGGACC[C/T]ATTAAGCCAGCAGGA | 81550 |
rs749213443 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498204 | TATACCCTTGAGCAA[C/T]GCCTTGCAAAATAGA | 81550 |
rs749243259 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60472452 | TACTACCCTACAGCC[A/G]TTATCCATTACAATG | 81550 |
rs749251150 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526582 | AAAATAAGACATTGT[G/T]TTATGTTTATTAGGC | 81550 |
rs749259872 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487417 | GAAGGCGGAGGTTGC[A/G]GTGAGCCAAGATTGC | 81550 |
rs749268770 | snp | A/G | 4.9489e-05 | 0.00497414 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528503 | AAGAAATGAAAAACC[A/G]CCTCGTTTTCAAAGA | 81550 |
rs749272792 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436700 | TTTTAAGTCTAGCAA[C/T]GTGATGTATGGGCCT | 81550 |
rs749289126 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476988 | AGATATAGAATGATA[G/T]CATCAGCAAAGAGAG | 81550 |
rs749289501 | in-del | -/AG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443119 | CAGATGATTAAAAAA[-/AG]TACATGTTTTATACT | 81550 |
rs749337849 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527555 | TAGACATGCTATGTG[-/A]AATTATGGAGGAAGA | 81550 |
rs749385989 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461764 | AGACATATATAAACT[A/G]AGAGGTCTAAGAGTC | 81550 |
rs749396179 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476590 | TTTTTCTAATTCTGT[A/G]AAGAATAACATTGAT | 81550 |
rs749416275 | snp | C/G/T | 3.3082e-05 | 0.00406696 | missense, utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528421 | ACAGATCATCAAATA[C/G/T]TGAGCAAAATGGAGT | 81550 |
rs749441051 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478356 | TCCCAGGCTGGAGTA[A/G]TGCAGTGATGCAATC | 81550 |
rs749468236 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484937 | TTTGAAGTGTGTTTT[A/G]TAGCTTCTTAGGGGT | 81550 |
rs749473471 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453844 | CTGCTTTGCTTCTTG[A/G]GCTGGCTTGGAGTGC | 81550 |
rs749503010 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426217 | TATATGTGCAATATT[A/G]TAAACCAAAAAAGAG | 81550 |
rs749518611 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555609 | GGTAAATGATACCAA[C/T]GTACTTGAGAATTTT | 81550 |
rs749519407 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571572 | AGTCATAGGTTTTCT[G/T]TTTATGTTTTGAGTA | 81550 |
rs749532862 | snp | A/G | 1.66874e-05 | 0.0028885 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460420 | TTCAAAAAATTCGCA[A/G]TGTTGCTGCACCAAA | 81550 |
rs749543256 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515758 | TTTTCAGCTCATTTT[A/C]AGATAGCATGTATTT | 81550 |
rs749581626 | snp | A/C | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395422 | TTTTTGGTGGCACTC[A/C]GAAGAAATTCAATGT | 81550 |
rs749602278 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429702 | CTCAGTGAACTCCAT[A/G]TGAGTAGCCTGCTAG | 81550 |
rs749611648 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468018 | CCTGGACTGCTGTAT[G/T]AGCCTTCTGACTGTC | 81550 |
rs749613433 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559495 | AAAAATTATATATTC[A/G]TTCCTGTACTTAACT | 81550 |
rs749618635 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551926 | AGCATGGGGGAAACT[A/G]TCCCCATGATTCAGT | 81550 |
rs749644505 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463667 | ATAATAGCAAAAAAC[-/A]AAAAAAACAAAAAAT | 81550 |
rs749675645 | in-del | -/TT | 1.65214e-05 | 0.0028741 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467414 | TGAACTTTTGAAACA[-/TT]ACACTCTTTTTTATT | 81550 |
rs749677214 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400375 | ATTTTTCTCTTCCAT[C/T]TCCTCCTTTGTTTGT | 81550 |
rs749711873 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453008 | TTTATTTTTCTTCTA[A/C]CTGATTTGAACTCAC | 81550 |
rs749725948 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511312 | AAAAGTTAAGGAAAT[A/G]TACTTTTAAATTCAG | 81550 |
rs749734872 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60435212 | AATTATGGAGTAAAC[C/T]TATAAGGCTTAAGTT | 81550 |
rs749757909 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454546 | TTTTGTTTTTAGAAG[A/G]GATATGTGCTTCTTT | 81550 |
rs749765109 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401875 | GAACAACTAAGAAAG[C/G]CTACAGCTTATTAAG | 81550 |
rs749796265 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563935 | TTGTAACTTGTCAAA[C/T]GCACATTATAGATGA | 81550 |
rs749829192 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490392 | AAGGCTCTAAAGCAG[A/G]AGCACAGAGAAACAG | 81550 |
rs749845225 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60448248 | AGAAGACCAGCTAAT[C/T]CTGGACATATTGAAT | 81550 |
rs749852875 | snp | C/G | 1.64811e-05 | 0.00287059 | missense, synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567552 | ACCTACGATCAAACT[C/G]TGGAGTTCCGTAGGG | 81550 |
rs749857393 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552393 | TTACATCCAGGGCAC[A/G]CTAATGCAAGGGGTA | 81550 |
rs749865843 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396392 | AGCGTGAGTCACGGA[C/T]GCCCAATCGCGCGGT | 81550 |
rs749908219 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396954 | GAGGTGGCCGCCTGT[A/G]GGCGCTGCAAACGCC | 81550 |
rs749909027 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568048 | TTTAATGTGGCTACT[A/C]GAAAATTTAAAATTA | 81550 |
rs749973737 | snp | G/T | | | intron-variant, missense | TDRD3 | GRCh38.p7 | 13:60527471 | CAGCTGCATGTTGAT[G/T]ATGATGTATGACAAA | 81550 |
rs749998654 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566219 | CAAAGTCACAAAGCT[C/T]TCCCAAGCTTCAGTA | 81550 |
rs750023793 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512112 | GGATTTACAGTTCCA[C/T]GTGGCTGGGGAAGCC | 81550 |
rs750042452 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452806 | TGGACATTTTGATCA[A/C]TGTTCTTAGTTTTTT | 81550 |
rs750059542 | snp | A/C | 6.68527e-05 | 0.00578117 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535269 | ACAAAGGCATAAACT[A/C]TTTTGAAGAAAATAT | 81550 |
rs750068673 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433473 | GTTCTTTGCTCTCCC[A/C]GTGCGTACAAAGTGA | 81550 |
rs750089469 | snp | C/T | 0.000218818 | 0.0104576 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397431 | AGTCCCGCCGGCTGC[C/T]GGGCCGCGGGTGCGG | 81550 |
rs750099014 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488109 | TTGCCAGGAAAGAAG[G/T]CTTTATTTGGGTGCT | 81550 |
rs750105533 | snp | G/T | 1.65987e-05 | 0.00288082 | splice-donor-variant | TDRD3 | GRCh38.p7 | 13:60494576 | GTCTATAGAGAACTG[G/T]TAAGGCTAAAGAACT | 81550 |
rs750114662 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481009 | TAATAGGGTGGCAGG[A/G]ATTCAGCAGGTGGGA | 81550 |
rs750137983 | in-del | -/ATTC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541146 | TCTTTTTGTTTTTCT[-/ATTC]TTTCTTTCTTTCTTT | 81550 |
rs750171882 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478080 | CTGGTCAGGTTTTCA[C/G]TCCCTTCCTGGTTCA | 81550 |
rs750178515 | snp | C/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438665 | TCTACTTCTTAAAGG[C/T]ACTTTTTTTTGGTTG | 81550 |
rs750266895 | in-del | -/TT | 0.00011568 | 0.0076044 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444635 | GAGGTTAGATTTAAA[-/TT]TACTCTTTTCTATAA | 81550 |
rs750268678 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440373 | CAAGAGTTATAAAAG[C/T]TGTTTGAAATAAAAA | 81550 |
rs750339291 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60536016 | TCAACAAATATGTTG[A/G]TATTTTCCTAAAATA | 81550 |
rs750344240 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434352 | GAGTGCCTGTAATCC[C/T]AGCTATTTGGGGGAC | 81550 |
rs750346760 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411853 | TGCACATTAAAGTGA[A/T]TCTTTTGCACATTAA | 81550 |
rs750349832 | snp | G/T | 1.64827e-05 | 0.00287073 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60483834 | ACCACCGCCTTTTGT[G/T]CCTTTTGGACAGGTA | 81550 |
rs750355896 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464487 | ATTCACAATACCCAC[A/G]ATATGGAATCAACCT | 81550 |
rs750358714 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426893 | GGTATTGCCGACTAC[A/G]CGCATAGGCTATATG | 81550 |
rs750359698 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560332 | AATAAGCATTCATAC[A/T]CCTTTTTGCTGTTTC | 81550 |
rs750364083 | snp | G/T | 1.76502e-05 | 0.00297066 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528328 | TATTAATGCAGAGTC[G/T]TCATCTTAATTTGCA | 81550 |
rs750386193 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60413953 | AATTTGAGAGAGGAA[A/G]CTGTCAATATTCAGT | 81550 |
rs750395505 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404311 | TGTTGGTTTGTTTGC[-/T]TTTTTTTTTTTTTTT | 81550 |
rs750425254 | snp | A/G/T | 0.000100764 | 0.00709744 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460417 | AAATTCAAAAAATTC[A/G/T]CAATGTTGCTGCACC | 81550 |
rs750450146 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60485997 | TATCATTATGTTCTA[C/T]TTAGATTATTTGTGA | 81550 |
rs750470597 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571198 | GTTTGAAGAAAATTT[G/T]ACTTAGTTTTGCATT | 81550 |
rs750474692 | snp | A/G | 3.2975e-05 | 0.00406035 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509864 | CTTAGAAGCAGCACT[A/G]AACGTACTTCTTACA | 81550 |
rs750505583 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533871 | GATAAATAGAGCTAT[A/G]TATTAGTTATTGAAC | 81550 |
rs750508375 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470998 | TATTCAAGTCCTTTG[C/T]CCATTTTTAATCAGG | 81550 |
rs750516756 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418120 | GTATGCATAGCCTCT[C/T]GTTTCTTTGTGGCAT | 81550 |
rs750546884 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490899 | GAGGTGGGCAGATCA[C/T]CTGAGGTCGGGAGTT | 81550 |
rs750571391 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454447 | TCCTTGTAAGTCTCA[C/T]GATAGTTTGTTATGA | 81550 |
rs750582967 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60550775 | AAACCAGTAAAAGAA[A/T]AACTGTTTATGTTGT | 81550 |
rs750593741 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532294 | CTGAATGATCTTCTA[C/T]GATGGCTACTTTGAT | 81550 |
rs750604840 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402542 | TCTAGAATTATGATA[C/T]ACCTTTAATTACCAT | 81550 |
rs750618445 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60491456 | AAGCTAATAATGAAC[A/C]CTGTAACACTTCAAT | 81550 |
rs750633017 | in-del | -/TTGT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515739 | AGGCAAGCTACTGAA[-/TTGT]TTTTCAGCTCATTTT | 81550 |
rs750643450 | in-del | -/TT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452816 | GATCACTGTTCTTAG[-/TT]TTTTTTTTTTTTAAT | 81550 |
rs750646404 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60509327 | AAAAAAAAAGCTCCT[A/G]GGGGGTATCATTTTG | 81550 |
rs750650862 | snp | A/G | 1.65886e-05 | 0.00287993 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529133 | TAAGCCAGAAAAAAT[A/G]CTAGAATCATCTATT | 81550 |
rs750666321 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505753 | CAAGTATCAATAGCC[A/G]AATTGATAAAGTGGA | 81550 |
rs750694214 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405122 | CCGGTCTCAGGTATG[G/T]CTTTATCAGCAGCAT | 81550 |
rs750703449 | snp | A/C/T | 3.29953e-05 | 0.00406162 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528642 | ATCAAATGTGATAGA[A/C/T]CGTATTCTAGATATG | 81550 |
rs750738821 | snp | A/G | 1.65315e-05 | 0.00287498 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529015 | AAATGCCACTGAAAG[A/G]AAGACGAATAGGACC | 81550 |
rs750751582 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543691 | ATTAATAGAGATTAA[A/G]TATATAAACAGCAAT | 81550 |
rs750777900 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537407 | TGTGTGCATATAGAT[G/T]TAAAAAAACCCTGAA | 81550 |
rs750785433 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444103 | TACTTCTGCATTTTC[A/G]TAGTTATTTGTTTAC | 81550 |
rs750841585 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541521 | ACCAGAAGCTATTAC[A/G]TTAATCTTTTATCAA | 81550 |
rs750841600 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498417 | GGCTACTGTAATGGA[C/T]GGTAGAAGCAAAACG | 81550 |
rs750841684 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60558684 | AGACTTTATAGCGTG[C/T]CTGTAACTTTTGATT | 81550 |
rs750877136 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429477 | CTTTCTTGACATTAT[G/T]GTTTTAAATTTTGAC | 81550 |
rs750901796 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60573004 | CTGTTTGTATGCAGC[C/T]GCAGGAACTCCACTA | 81550 |
rs750917550 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440405 | GTAAGTAAACAGGCT[-/G]GGCATGGTGGCCCAC | 81550 |
rs750921906 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446638 | AAATAATTTAAATAA[A/G]CATTTTAGAAGCTGG | 81550 |
rs750929585 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557398 | AGGGAAGATCAGAGC[A/G]GTGACTGCTGGAGTA | 81550 |
rs750935133 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565511 | GAATTCTTTAAACAC[A/C]ATAGATAGAAATAGA | 81550 |
rs750996243 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417088 | GTGGCATAATCATAG[C/G]TCACTGCAGCCTCAA | 81550 |
rs751017632 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500673 | TATACTGATTTATGG[G/T]CTGTAGCCAATGGTT | 81550 |
rs751064901 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484196 | CATTAAAAACATTAG[-/A]GGGGGAGAGAAAAAT | 81550 |
rs751068468 | in-del | -/TTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470591 | ATCATTATAGTTGGG[-/TTT]TTTTTTTTTTTTTTT | 81550 |
rs751100312 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543214 | AATGAAGAGGTTCTA[A/G]TAAACAACCCAGACC | 81550 |
rs751160594 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395943 | CAAATCTCAATAGCA[C/T]TCCATCTAACGAAAG | 81550 |
rs751174437 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499421 | TCCATAAGGTCCACC[C/T]GAAGCAATTTGCCTT | 81550 |
rs751226852 | snp | C/T | 1.65438e-05 | 0.00287605 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528728 | TAAAAAAAGAGATAA[C/T]TCTATGCAAAGCAGA | 81550 |
rs751230904 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486158 | CCAGATCTCCATGGT[A/T]GTTCCAGTAAGTTAC | 81550 |
rs751241071 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541402 | GAACTCCTGACCTCA[G/T]GTGATCCGCCTGCTT | 81550 |
rs751242269 | snp | A/C | 1.65633e-05 | 0.00287774 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494427 | TTTTATCTTTCTCTT[A/C]TGTAAAGACCAAGAC | 81550 |
rs751259679 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552617 | GGGACTCTGTATGTG[C/G]GCTGGAGCCCCACAT | 81550 |
rs751265167 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396854 | TGAGTTTTGCTGCCC[C/G]CAACGTGACCTTTTT | 81550 |
rs751314304 | snp | A/T | 1.77253e-05 | 0.00297697 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528324 | TAATTATTAATGCAG[A/T]GTCTTCATCTTAATT | 81550 |
rs751316376 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60489528 | ACACCTTTGGATGGT[A/T]ACTCAGCTTTTTTGT | 81550 |
rs751326256 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60535613 | TCTCTGTTGGATGTG[C/G]AATGTCATTTATTAT | 81550 |
rs751329014 | snp | C/T | 4.95995e-05 | 0.00497969 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467420 | TTTGAAACATTACAC[C/T]CTTTTTTATTGCATT | 81550 |
rs751331984 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453957 | TTTTTCTTCTAGCAC[C/T]GATTTAACTATACTC | 81550 |
rs751383761 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571091 | GATTCCTGACATCAA[-/T]TAAAAAAAAATTGGT | 81550 |
rs751406096 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60491330 | GTAAGACTGAAGAGT[G/T]AGCTTTATAATAGAT | 81550 |
rs751419619 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438446 | TCATTTATCATTGTG[A/G]TTTAACAGTGTCATG | 81550 |
rs751472561 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537167 | TCACTAAATCTTTTG[G/T]AGATTCTGGTATTTC | 81550 |
rs751473464 | snp | C/G | 4.95029e-05 | 0.00497484 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510725 | TTATTTGATTTCTTG[C/G]AATCTAAAATGGGAA | 81550 |
rs751498110 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477774 | CTGGATTAGTTTGCT[A/T]GTATTTTATTGAAGA | 81550 |
rs751503991 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551692 | CTGCTGTCAACATAA[A/G]GATACTACCTGAGAC | 81550 |
rs751521409 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425879 | TTTTTGTAACATTTT[A/C]TTTTTATTGTAGGAA | 81550 |
rs751551460 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410653 | TTTGAGTAATAATGA[A/G]ATTTCTCAGGATCGT | 81550 |
rs751557211 | in-del | -/AG | 1.67562e-05 | 0.00289444 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460332 | AACACAGCCCTGAAT[-/AG]AGTTTCATGACTAGA | 81550 |
rs751561725 | snp | A/G/T | 9.30681e-05 | 0.00682103 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510592 | TCTCTTTTTGTTTTT[A/G/T]CATATACAGTACATA | 81550 |
rs751563276 | snp | A/G | 4.99189e-05 | 0.00499569 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535256 | ATACATATTCTGTAC[A/G]AAGGCATAAACTATT | 81550 |
rs751570043 | in-del | -/TG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442375 | TAGGGATTTTATGTG[-/TG]TGTGTGTGTGTGTGT | 81550 |
rs751572386 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443377 | GAGGTTGTAAAAAGC[A/G]TAAGTCTAAAGCATT | 81550 |
rs751578007 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511840 | GCCACCCCATAGGCA[A/G]TTTACATATTGTTTG | 81550 |
rs751586749 | snp | A/G | 1.68801e-05 | 0.00290512 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494604 | ACTAACCACAAATTT[A/G]AAGTGTTATTTCTTA | 81550 |
rs751605548 | snp | G/T | 1.65526e-05 | 0.00287681 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528991 | TTGGTGTTCCAAATG[G/T]AGAAGTAGAAATGCC | 81550 |
rs751632368 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484394 | CTTCTCCTGATGATG[C/G]CATCAAAATTTAGCG | 81550 |
rs751655489 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549143 | TAGTGGTGGTTTTAG[A/C]GTCAAGTCTCTGGGT | 81550 |
rs751659742 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530750 | GTGAGCCACCACGCC[C/T]GGCCCAAAATAAATA | 81550 |
rs751697761 | snp | A/G | 6.66467e-05 | 0.00577225 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528865 | TTCCTGATTATTTTT[A/G]TGACAGGAAATCACA | 81550 |
rs751714000 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562943 | GGTAATATAAGATAA[A/G]GTGGGCTAGGCATGG | 81550 |
rs751738006 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496502 | AAACTGCTATGGACT[C/G]TACTTCTAATAGTGT | 81550 |
rs751749603 | snp | A/C | | | intron-variant, missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60547478 | TCTGCCACTTACTAC[A/C]TATGTGACTTTGGGT | 81550 |
rs751796240 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424178 | AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 81550 |
rs751809416 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60521108 | AGTTTACTTTTTGTG[G/T]GTTGTGCAATCTTTT | 81550 |
rs751816880 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452448 | ATAATTTTTAAAACA[A/C]CATTTACAACAAGAA | 81550 |
rs751871049 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417760 | ATCCCAGGGGCACCT[C/T]GAACTCCTCATGCCT | 81550 |
rs751885167 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557066 | AAAAAATTAGCCGGG[C/T]ATGGTGGCACATGCC | 81550 |
rs751886639 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534927 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 81550 |
rs751921365 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555228 | CATACATTTAAGCAT[A/G]TTGCACAAAATCAGC | 81550 |
rs751936787 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516704 | AATTAGATAATGTAT[A/T]TGAAGTGCTAAGCCT | 81550 |
rs751943643 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515619 | TCTTTAGCAGGTATC[A/G]TTGTGTTACTTTCTC | 81550 |
rs751966698 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570976 | AACTTAAACATCACA[A/G]TTTTGGTGGTTTTCT | 81550 |
rs752048798 | snp | C/T | 1.69037e-05 | 0.00290716 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460414 | TGCAAATTCAAAAAA[C/T]TCGCAATGTTGCTGC | 81550 |
rs752054990 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60569866 | GAAAACTGGATATCC[A/G]TATATGGATGAATGA | 81550 |
rs752089801 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542821 | TTTTAATTTTTAAAT[C/T]TCTTTTTCTTTTTAC | 81550 |
rs752093390 | snp | G/T | 0.000413746 | 0.0143771 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460353 | TCATGACTAGAAAGT[G/T]ATTTTTATTCTTTTC | 81550 |
rs752097113 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476345 | TGTCAAAGATCAGGC[A/G]TTTGTAGTTGTATCA | 81550 |
rs752115615 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523802 | GACTAGTTTTGAACT[-/C]CTGACCTCAAGTGAT | 81550 |
rs752115708 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497330 | AGCTCGAATGCCTGG[A/G]TTTAGATCCCGATCA | 81550 |
rs752124682 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428282 | AATTACTTCTGTAAA[A/G]ACTGTCTCTAAATAA | 81550 |
rs752133096 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60531987 | TATGTGCCAGGTGAT[G/T]GGGGCATATCAGATA | 81550 |
rs752156077 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458151 | AGGTGTTCCTCCTTA[G/T]CCTTCATTCCCCAGA | 81550 |
rs752163783 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477615 | GAAGGCCTTTTCTGC[A/G]TCTATTAAGATGATT | 81550 |
rs752164802 | in-del | -/CAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554442 | GCTTTACAATATAGA[-/CAT]CATCATTGATACTCC | 81550 |
rs752216551 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425041 | TTCATTTATCGGATG[A/C]ACAGTCTTGGTGTTT | 81550 |
rs752281409 | in-del | -/TCC | 1.65321e-05 | 0.00287502 | cds-indel, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509906 | GAAACCTGTTATGGG[-/TCC]TCCTCTGAGAGGTAT | 81550 |
rs752292525 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460879 | ATGATGGCGGGTGCC[A/G]GTAATCCCAGCTACT | 81550 |
rs752318568 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431628 | AGATTCTTAAATAGT[A/G]TTAAGTAATTAAAAA | 81550 |
rs752357314 | in-del | -/ACACAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469430 | CACCAACACACACAC[-/ACACAT]ACACACACACACACA | 81550 |
rs752372274 | snp | C/T | 1.64947e-05 | 0.00287177 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528623 | AGTATGGGCTGAAGA[C/T]AGAATCAAATGTGAT | 81550 |
rs752383674 | snp | C/T | 7.41922e-05 | 0.00609021 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485809 | ACTAGAAGTGTGTAT[C/T]TCATGTCCAAGTGGA | 81550 |
rs752388593 | snp | C/T | 0.000102833 | 0.00716979 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60444711 | CAATTGGCAAGAAAT[C/T]CCTCCCCAGTGACAT | 81550 |
rs752394192 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411315 | CAGTTACAGGGTAAT[C/G]AGAATGGACTTAATA | 81550 |
rs752404305 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498420 | TACTGTAATGGACGG[C/T]AGAAGCAAAACGGCA | 81550 |
rs752405281 | snp | C/T | 1.65045e-05 | 0.00287263 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528479 | TCCTCGAAATGATAC[C/T]AGGCAGCCAAGAAAT | 81550 |
rs752436762 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394790 | CAAATATCACCTATA[C/T]GTCCTTTACATTTCT | 81550 |
rs752449835 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551380 | AAATGCTTGGCACAC[A/T]GGTTGTTAATTAATG | 81550 |
rs752450491 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60414050 | TTGCATTGTTATTAA[A/G]TATTTGCCTTATATT | 81550 |
rs752455414 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461461 | TGGCCATTCTGAGCT[C/G]TGTTTTCTGAGGTGG | 81550 |
rs752486883 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467742 | TACAGACACACATAC[A/G]TGCAAGTAAAAGTAA | 81550 |
rs752535858 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538675 | AGGGGCAAAGAAAAC[C/T]TGCTACTTGTGTTTC | 81550 |
rs752538924 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416635 | TTATAGCTACTGTTT[C/G]TTTGGGCTGTCTGCT | 81550 |
rs752542180 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399388 | GGCAGTGACTCATAA[A/G]GGCAGTAGTAATCTG | 81550 |
rs752579587 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60489420 | TGTTCTTGAATTTTG[A/G]TTGTTCTTCCCGCAA | 81550 |
rs752606824 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434598 | TAGCCTTTTAATGCC[C/G]TGCTTGTCAGTAAAA | 81550 |
rs752635414 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563321 | AGTATTTTCAGCAAA[C/T]AGAGCCCCCGCCAAA | 81550 |
rs752640590 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436239 | TGATGATTTCTTTTG[C/T]TGTGCAGAAGCTTTT | 81550 |
rs752645043 | in-del | -/AG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464934 | TTCAAAATAATTAAA[-/AG]AGTAGATTCATAATG | 81550 |
rs752646678 | snp | A/G | 1.66707e-05 | 0.00288705 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529152 | GAATCATCTATTCCT[A/G]TGGAGTATGCAAAAA | 81550 |
rs752661681 | snp | A/T | 1.66161e-05 | 0.00288232 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535091 | TGTCATATTTAAAAC[A/T]CCTTTTGCCTCCTCA | 81550 |
rs752704962 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440537 | GATACAAAAATTAGC[C/T]GGGCGTGGTAGTGTG | 81550 |
rs752707693 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523758 | ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 81550 |
rs752709167 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458558 | TAAACATTAAATAAA[A/G]GCAAATGTTTCCCTC | 81550 |
rs752783169 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496600 | TTTGATTCATCACTC[A/C]TGAGAGGCAAGGAGT | 81550 |
rs752784065 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60545839 | TACTCTAAATTTTCA[A/G]TCTATTTTAGGTGAA | 81550 |
rs752787384 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562137 | CTAACATGGTGAAAC[C/T]CCATCTCTACTGAAA | 81550 |
rs752795102 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441695 | TGTACGTACCCACAC[A/G]TGCATAGCTAATTAT | 81550 |
rs752824855 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60437405 | TGCTGGGGTTAGAGG[C/T]GTGAGCCACTGTGCC | 81550 |
rs752832774 | in-del | -/ATTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487994 | ATGAGATAATATCTC[-/ATTTT]GTTTTGATTTGCATT | 81550 |
rs752855126 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466463 | TTTGCAAGTGAAGAC[C/T]AAACCTCATTTCTTT | 81550 |
rs752863654 | snp | A/C | 4.94931e-05 | 0.00497434 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510687 | AGGACCTGGGAAATG[A/C]AAGGCCATCAGCACC | 81550 |
rs752864374 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471109 | TATTTTTCCCATCCC[A/G]TGTGTTGCCTTTTCA | 81550 |
rs752886159 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518088 | TCAGAGTAACAAGGC[C/T]AGGCAGGTAGTTTAA | 81550 |
rs752890116 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562706 | ATATGCTGATGTATG[C/T]ATTGTGACTACTATA | 81550 |
rs752909866 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537453 | TTGCTGTCAGTACAT[A/G]CAATGTAGAGTTCAT | 81550 |
rs752916630 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415950 | GGGAGAACTCTGGTT[G/T]GCCGTCAGTGTCCTT | 81550 |
rs752920598 | in-del | -/ACTC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570311 | GGTATATGAAAAAAT[-/ACTC]AACATCATTAATCAT | 81550 |
rs752981780 | snp | C/T | 1.64901e-05 | 0.00287137 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467313 | ATTCCTGCTCTTGAA[C/T]GACTCTAACACCACA | 81550 |
rs753001436 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551255 | ATTTTTTAACTTTAG[-/T]TTTGTTTTCTTCTAT | 81550 |
rs753029597 | in-del | -/TTA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477198 | GTTTGTTATAGATGG[-/TTA]TTATTATTATTATTG | 81550 |
rs753040242 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514240 | TTAAACTTGAGAGAG[A/T]TGATTTAGGGTATCT | 81550 |
rs753043454 | snp | A/G | 0.000112568 | 0.00750143 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439658 | ATTTTGATTTTAGAT[A/G]ATATTAAGCCATTTA | 81550 |
rs753058015 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60569643 | GCATAAAGAAGAAAG[C/G]TGGAGGCATCAGACT | 81550 |
rs753060081 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471900 | GGCTAAAACTTTTAA[C/T]ATAGTGTTGAATGGA | 81550 |
rs753068092 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506228 | GGTGGCCACTATTCA[A/G]CATTCTTAAAGAAGA | 81550 |
rs753103542 | snp | G/T | 3.35847e-05 | 0.00409771 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509707 | TAAGTAGTTAAAAGT[G/T]TATGCCTTGCCTTAT | 81550 |
rs753122802 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433373 | TTTGTAAAATATTTA[C/T]GTCAATGACCAGACT | 81550 |
rs753132446 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493858 | TAATGTCACATATAT[A/G]TTTATTCAAAAAAGA | 81550 |
rs753169406 | snp | C/T | | | utr-variant-3-prime, stop-gained, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60573632 | CTCTTTGTGAAGAAA[C/T]GAGCCAGTGACTGAA | 81550 |
rs753173006 | in-del | -/TGGTGAG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542840 | TTTTCTTTTTACCTC[-/TGGTGAG]TGGTATCTTTTGATG | 81550 |
rs753209941 | snp | A/G | 1.66527e-05 | 0.00288549 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528859 | CATCTATTCCTGATT[A/G]TTTTTATGACAGGAA | 81550 |
rs753214492 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424545 | ATCTGGGCATAGTGG[A/G]ATGCTCCTGTAGTCC | 81550 |
rs753243899 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488227 | TGCAGGAAAATAGGA[A/G]CTAAGGAGGGGTAAG | 81550 |
rs753247875 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438731 | AGAATCAGTCTAGTG[-/A]TTGAGAGTTGATGGT | 81550 |
rs753251677 | snp | A/G | 1.65064e-05 | 0.00287279 | missense, utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528460 | ATAATCATCTGAGAC[A/G]TCCTCCTCGAAATGA | 81550 |
rs753281587 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452116 | GGAATTAGGAAGAAA[C/T]GTACATAAAAAGTTT | 81550 |
rs753283337 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433545 | TGGCTATGAATGTTA[C/T]ACTATCTGAGGTACA | 81550 |
rs753311286 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421831 | AAAACTACAGAAAAG[C/T]AGAGGAGAGATGCAA | 81550 |
rs753352621 | snp | G/T | 1.64901e-05 | 0.00287137 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483861 | GGTAATGACTTTTGT[G/T]TTGGCAGATGAATTT | 81550 |
rs753365342 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554836 | ATTACTCTCCAGATT[A/G]TAATCAGTTCCCCCA | 81550 |
rs753425312 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514054 | TTGGAACTCCCTAGA[A/G]ACTTGTTGAATGGCT | 81550 |
rs753432412 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60489315 | ACATTTCTTAACCAG[A/T]GAGATTGAAATTGTT | 81550 |
rs753447190 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474755 | TTTTTAAAAGATATT[G/T]TTGTCTTTCTACACA | 81550 |
rs753489200 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424718 | CATTCAGTAGCTTTT[C/T]GTATATTCACAGAGA | 81550 |
rs753499687 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423110 | GCTTTTCAAAACCAA[A/T]ATATAAAGCAAGGCA | 81550 |
rs753507805 | snp | C/T | 1.75841e-05 | 0.00296509 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528334 | TGCAGAGTCTTCATC[C/T]TAATTTGCATATGGT | 81550 |
rs753520794 | snp | A/G | 1.65356e-05 | 0.00287533 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567684 | AGTGGTTTTCATATA[A/G]AGAAAGATGAAATTC | 81550 |
rs753534952 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458697 | GGTCTAACTCTGTGC[C/T]CTCCATATATAGAAC | 81550 |
rs753540088 | in-del | -/TAAG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418670 | ATAGTTGTGTACGTT[-/TAAG]TAACCCCCATTCTAA | 81550 |
rs753586351 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60408804 | AGAAAAGAAAAACCC[A/G]TTTTCTAGGGAGAAA | 81550 |
rs753589055 | in-del | -/TTAATGGC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463953 | GGGGCAGAGCCCTCA[-/TTAATGGC]TTGGTGCCATCCTTG | 81550 |
rs753612813 | snp | C/T | 3.29571e-05 | 0.00405924 | synonymous-codon, missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567563 | AACTCTGGAGTTCCG[C/T]AGGGGAGGTGATGGC | 81550 |
rs753621177 | snp | A/C/G/T | 6.65609e-05 | 0.00576863 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529146 | ATACTAGAATCATCT[A/C/G/T]TTCCTATGGAGTATG | 81550 |
rs753640284 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419183 | CAACAGTGTATGAGA[A/G]ATCTGGTTTCTCCAC | 81550 |
rs753667296 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515687 | TAGGTGAGCTGGGGT[A/G]TATTGTAAAATAAAC | 81550 |
rs753697255 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427576 | ATCCCCTCTCTACGT[C/T]TTTCCTTTGACTGAT | 81550 |
rs753704037 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466150 | TGCATAAATAACTTT[C/G]ATTTGATCTTTGACT | 81550 |
rs753714062 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562206 | TAATTCCAGCTACTC[A/G]GGAGGCTGAGACAGA | 81550 |
rs753730495 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500792 | TGAGTGGTCAAAAAC[C/T]GTGAAGATGTTTGTA | 81550 |
rs753733579 | snp | A/G | 1.92944e-05 | 0.00310593 | splice-acceptor-variant | TDRD3 | GRCh38.p7 | 13:60485797 | CTTACTTGTTTTACT[A/G]GAAGTGTGTATCTCA | 81550 |
rs753738760 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60521371 | TTGCCTGATTCTGTC[A/G]TAGCTAAGCACTGGA | 81550 |
rs753764070 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450465 | TGAGTGACCACTGGT[A/G]AAGTACTTTATCCTC | 81550 |
rs753768256 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399098 | CTCTTATGCTTTTCC[A/G]GGGCAGGGAAGTGAG | 81550 |
rs753785603 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415730 | CCTTGATGGATCTTC[C/T]GGGAACTACCATGTC | 81550 |
rs753804543 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555146 | TTGGAAAGAGAATAA[A/T]TCTTTTTAAAAGAGA | 81550 |
rs753840662 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564484 | CATTGGACAGTTCCC[A/G]TTTATGAAAATTATT | 81550 |
rs753846965 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60539229 | ACATCTCTTAGTTGT[C/T]GGGCACTGTTCTAGG | 81550 |
rs753934244 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517849 | TCAGTGCTGAAATTG[A/G]GAGTGTTTAGAAACC | 81550 |
rs753987591 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438837 | AGAATGTCTGCAATG[A/G]TGATGGTACCATTAG | 81550 |
rs754011208 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60479904 | ATCATTACTTGTGAG[A/G]TGGGTCCCTTGGAGA | 81550 |
rs754015671 | snp | A/C | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467290 | GGCATTGTTGACATA[A/C]AAAATGGATTCCTGC | 81550 |
rs754020195 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444064 | TTTTTGTTAGTCCTT[A/G]TATTTTCCTTGTTGA | 81550 |
rs754025835 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60494090 | ATTTAGAACCCAACT[A/C]TCAAGGCAGTAGTCA | 81550 |
rs754096974 | in-del | -/TCT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532430 | GATGGAATTAGTTAA[-/TCT]TCTGAAACCACAAAT | 81550 |
rs754099788 | snp | C/T | 3.35003e-05 | 0.00409256 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509953 | TGTGCCAGATAGTAT[C/T]GTTTGCTTTTCAGAG | 81550 |
rs754103685 | snp | A/T | 1.70872e-05 | 0.00292289 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460558 | GATTGGCACTTTATT[A/T]TGTGTATTTGTTACA | 81550 |
rs754109465 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499249 | TGGCCTGTGCAGAAG[A/C]CAGATGGATCTTGGA | 81550 |
rs754113074 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470555 | TTGATAGTAGCCATT[C/G]TAACATGGGTAAAAT | 81550 |
rs754113425 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494457 | CATTTGGAGGAGGTG[A/G]TGGTGGTGCTAGAAG | 81550 |
rs754113525 | in-del | -/GT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484532 | AATAAGGTTTATCGT[-/GT]GTGTGTGTGTGTCCA | 81550 |
rs754116086 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495853 | CAGTTTGTGGAGGGT[C/G]AGAATCTTGTAGCCT | 81550 |
rs754118001 | snp | A/G | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509880 | AACGTACTTCTTACA[A/G]GCAATAAACAGAAAC | 81550 |
rs754173250 | in-del | -/TGA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560479 | ATGGATGCAGCTTTT[-/TGA]TGTTTTCACTGAATT | 81550 |
rs754175986 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527644 | TCATTAAAAATTACC[C/T]TTCTATATTTATCAC | 81550 |
rs754181586 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426957 | ACAGCATGTTATCGT[A/G]CTGAATACTGTGGGC | 81550 |
rs754226330 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522133 | GAATGTTTATAGATA[C/T]ACTATATTTTAAGTG | 81550 |
rs754231238 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425029 | ATTTTGTTTATATTC[A/G]TTTATCGGATGAACA | 81550 |
rs754243716 | in-del | -/AC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469424 | CCTTCTCACCAACAC[-/AC]ACACACACATACACA | 81550 |
rs754266916 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418416 | GTGCTATAATTGTTT[A/G]TATGTTTGTCTCCTC | 81550 |
rs754278919 | snp | A/G | 1.65466e-05 | 0.00287628 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528734 | AAGAGATAACTCTAT[A/G]CAAAGCAGATCAGGA | 81550 |
rs754335600 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432521 | TCTCTGACTAGGTAT[A/T]GTATAGTAAGAGTCT | 81550 |
rs754356832 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426794 | CTGTCATTCATCACT[G/T]TATGGGGTATGTTCT | 81550 |
rs754361356 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399267 | GTCCCACCCTGCTTC[C/G]TTATATTGTTATAAA | 81550 |
rs754380854 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543810 | GTCATTAGTAATACT[A/G]TTTTATTGCATACAA | 81550 |
rs754416192 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504950 | CACAACCTGCACACC[A/G]GGAGATTCCCTTGGG | 81550 |
rs754425636 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420105 | ATAGATATCATTTAC[A/G]TCAAGTTAATCAGTG | 81550 |
rs754447694 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434371 | TATTTGGGGGACTGA[A/G]CCATGAGAATTGCTT | 81550 |
rs754448812 | in-del | -/AAAG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503522 | ACCAAAATATAACTT[-/AAAG]AAGATTGCACATCAT | 81550 |
rs754453745 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60456423 | CTAGCAGATACTTAA[C/T]ATTGTTTGTTAGAGT | 81550 |
rs754469085 | snp | A/C | 1.64944e-05 | 0.00287175 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483867 | GACTTTTGTGTTGGC[A/C]GATGAATTTAAATTA | 81550 |
rs754471655 | in-del | -/TT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522631 | GCTATGTAGTCTTTC[-/TT]TTGCTATTTCTAAGT | 81550 |
rs754472726 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421962 | AGTAAGGACAGGTGC[C/G]AAGTAAAGGGCCAGA | 81550 |
rs754477719 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60539391 | ACAAAATATGAGTAG[A/G]GAAAATCTTACTGAA | 81550 |
rs754497661 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423208 | TGCTTTTTAAATATT[A/T]AGGCCATATAAAAAT | 81550 |
rs754507582 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501309 | CCTCCTAGGATCAAT[C/T]TAAAGGTCCTCAGCA | 81550 |
rs754520913 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474772 | TGTCTTTCTACACAT[G/T]TACCATTTCCGTCCC | 81550 |
rs754522441 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400373 | GAATTTTTCTCTTCC[A/T]TCTCCTCCTTTGTTT | 81550 |
rs754541857 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551228 | CCACATACCTTGGGA[A/G]AGATATAGAATATTT | 81550 |
rs754542662 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508500 | CTTTGACAAACCTGA[C/G]AAAAACAAGCAATGG | 81550 |
rs754563544 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537960 | GTAGAAAATTAGTTG[C/T]TTGTGTTGTCTTTTA | 81550 |
rs754581519 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409123 | CTTGGCAGCTTCCAT[A/G]TGGTGTTGAGCCTGT | 81550 |
rs754606735 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476054 | TTTAATTGGGTCCCA[C/T]TTCTTATTTTTGTTT | 81550 |
rs754608634 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458773 | AATTTTAAGTGAAAA[C/T]TTAAATAGCTACATG | 81550 |
rs754623977 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514064 | CTAGAGACTTGTTGA[A/G]TGGCTTTGAACAAAA | 81550 |
rs754630468 | snp | A/T | 1.75336e-05 | 0.00296082 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528339 | AGTCTTCATCTTAAT[A/T]TGCATATGGTATACT | 81550 |
rs754652932 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568159 | GGTTAAAAATTAGTT[C/G]TGCCATCCTAAGTGA | 81550 |
rs754670939 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497505 | TTCCCCAGCTAGGCT[C/T]AGGAATTCTTAGTCG | 81550 |
rs754698380 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460713 | TGTATAAAAATAGTT[A/G]AGAATATATGGCCAG | 81550 |
rs754704234 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466325 | AGCTAAAGCTCAGAG[A/G]GAAAAAATGTCAAAT | 81550 |
rs754712079 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60437208 | CTCGGCTCACTGCAA[A/C]CTCTGCCTCCCGGGT | 81550 |
rs754744830 | in-del | -/CCCTTTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464082 | GTGATCTGCATATAC[-/CCCTTTG]CCTTCTGCCATGAGT | 81550 |
rs754747151 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60547788 | TAAGAATGTAAAACC[C/T]AGTTGGTTAAATTAA | 81550 |
rs754787376 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409961 | CCACGTGTTGTGGGA[-/G]GGACCCAGGGGGAGG | 81550 |
rs754800382 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544448 | CATATCTCTTTAAAA[-/A]AAAAAAAAAAAGAAA | 81550 |
rs754820512 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487444 | TTGCACCATTGCGCT[C/G]CAGCCTGGGCAATAA | 81550 |
rs754835385 | snp | A/G | 6.59261e-05 | 0.00574097 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509780 | TGATGAGAAAGCTCT[A/G]AAGCACATAACGGAA | 81550 |
rs754860034 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415743 | TCCGGGAACTACCAT[C/G]TCCAGAGATTTATTG | 81550 |
rs754868877 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434765 | AGTTTCTTCTTTTGT[A/G]TCAATGCCCTTGGGT | 81550 |
rs754875414 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562219 | TCGGGAGGCTGAGAC[A/G]GAAGAATAGCTTGAA | 81550 |
rs754893220 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501876 | TAGCAGACTCAGTGA[C/T]AGTAAAATTTTTATG | 81550 |
rs754905286 | snp | A/T | 3.30491e-05 | 0.00406491 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529032 | AGACGAATAGGACCT[A/T]TTAAGCCAGCAGGAC | 81550 |
rs754925239 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433580 | CGGCACAACACTGTA[G/T]GTCAGAGACAACTTG | 81550 |
rs754944401 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543936 | TGTTATTTATGAAGA[C/T]TCCCATTATCGTTTT | 81550 |
rs754951066 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399221 | CCAGTCAGAATTCTC[C/T]GGGCAGGGCCTCTGC | 81550 |
rs754954345 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405304 | AGCATATTGTGGCAG[A/G]CACTTTCTTAGTATA | 81550 |
rs754957365 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511060 | GAAATTTATTATAAT[A/C]TTATATAACTTATTT | 81550 |
rs754960025 | in-del | -/C | 1.65086e-05 | 0.00287298 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509759 | TTCTCTTTATTCCTT[-/C]CAGGTTGATGAGAAA | 81550 |
rs754982036 | in-del | -/TC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453485 | TCTCTAGCAACACTT[-/TC]CTTTAATCAGTTGAA | 81550 |
rs754985315 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438964 | TGAGTTTATCAAAGA[A/G]TTTCAAAATGTCCAT | 81550 |
rs754997821 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60413884 | AAAGATAAAAGGTAC[A/G]GGTAGAATATTTCAC | 81550 |
rs755056518 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517993 | CTTTCACTACAGTAA[A/G]TTTGAAATGTTCTGG | 81550 |
rs755089153 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60491366 | CACTTGAGAGTTGTA[A/G]ACATATGGATGGTAT | 81550 |
rs755139598 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440479 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGTCA | 81550 |
rs755140789 | snp | C/T | 3.29777e-05 | 0.00406051 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467305 | AAAAATGGATTCCTG[C/T]TCTTGAATGACTCTA | 81550 |
rs755183267 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481153 | GGCAGGGACTCTTAG[A/C]GGAGTGTTTTCTTTA | 81550 |
rs755194676 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557666 | GAAAACATCAGCAAA[C/G]AACTATTTTTGTATC | 81550 |
rs755219103 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517015 | ATTATTTTTATTTTC[A/T]GTGGATTTTGTGAGA | 81550 |
rs755229618 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426995 | ACACAATTTAGTATT[C/G]TGTACGTATTTATGT | 81550 |
rs755243549 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465823 | CATTTCAGAATAATT[G/T]TCTAATTTATCCTAA | 81550 |
rs755256233 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464903 | TGACTATAGTTAACA[A/G]TAATTTATTGAATAT | 81550 |
rs755304399 | snp | C/T | 1.71384e-05 | 0.00292727 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460563 | GCACTTTATTTTGTG[C/T]ATTTGTTACAGAATG | 81550 |
rs755304408 | snp | A/G | 1.6757e-05 | 0.00289452 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509954 | GTGCCAGATAGTATT[A/G]TTTGCTTTTCAGAGT | 81550 |
rs755324079 | in-del | -/TTC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541159 | CTATTCTTTCTTTCT[-/TTC]TTTCTTTCTTTCTTT | 81550 |
rs755346604 | in-del | -/TCTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457864 | AAATGGTCTTTATAC[-/TCTG]TCTGTGTTTGTTTCC | 81550 |
rs755366000 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477637 | AAGATGATTATGTAG[A/T]TTTTGTTGTTAATTC | 81550 |
rs755367734 | in-del | -/AT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445211 | TTTTGCAGTACACAC[-/AT]ATGTATTCGTGTTAT | 81550 |
rs755370785 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527750 | CACTTTTCTGTATTT[C/T]CAAGTAGTACCCACT | 81550 |
rs755380917 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566702 | GTTAATTCAAAAACA[C/T]TTAAATAACAGGGTG | 81550 |
rs755388778 | in-del | -/ATTCCTACTCTCATCATAAGC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60569888 | GATGAATGAAACTAG[-/ATTCCTACTCTCATCATAAGC]AAAAATCAAAATGGA | 81550 |
rs755435054 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420198 | ACAACAACAACAACA[A/C]AAAGAAATTGGATTG | 81550 |
rs755453966 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475038 | GTAATCTTTTTTTAT[A/G]TAATGTATCTTTTCT | 81550 |
rs755486119 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492903 | TTCCGTTTCAAATAA[-/T]TTTTCTTTCTTTTCT | 81550 |
rs755493778 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455911 | ATCTCTACTAAAAAA[G/T]ATAGAAAAATTAGCT | 81550 |
rs755500040 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504971 | TTCCCTTGGGTGCTC[A/C]TGCCACCAGGACCCT | 81550 |
rs755504094 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60403102 | TTGTTAAACTGTGCA[A/G]GTGTTCAGGTTTCAA | 81550 |
rs755512827 | in-del | -/TTTTT | 1.89116e-05 | 0.00307497 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510580 | TTAGTATATATTCTC[-/TTTTT]TTTTTGTTTTTGCAT | 81550 |
rs755519612 | snp | A/C/G | 3.30946e-05 | 0.00406773 | missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528737 | AGATAACTCTATGCA[A/C/G]AGCAGATCAGGAAAA | 81550 |
rs755531109 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420202 | CAACAACAACAAAAA[G/T]AAATTGGATTGTTGG | 81550 |
rs755539423 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527087 | CAATACACCTGCTTC[A/C]GCCTTCCAAAGTGCT | 81550 |
rs755576008 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560343 | ATACTCCTTTTTGCT[C/G]TTTCAAGTTGTAAAC | 81550 |
rs755582260 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60536420 | ATCATCAATATCTAA[G/T]TTACATCTTTCTTTT | 81550 |
rs755590957 | snp | A/G | 1.65433e-05 | 0.002876 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510760 | GAATGTGGAAGGTAA[A/G]CTAATTTAAAGTTGA | 81550 |
rs755591335 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450366 | ATGTAACAAATATTA[C/T]CATACTTTTAGAATA | 81550 |
rs755603255 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463457 | TGGTCTGGGCAAAAA[-/T]TTTTTTGGATAAGAC | 81550 |
rs755613802 | snp | C/T | 3.32674e-05 | 0.0040783 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483735 | TGGAAATATATTTTT[C/T]ATGTATAACTGCTCT | 81550 |
rs755663376 | snp | C/T | 4.94393e-05 | 0.00497164 | missense, synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567561 | CAAACTCTGGAGTTC[C/T]GTAGGGGAGGTGATG | 81550 |
rs755669487 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552406 | ACGCTAATGCAAGGG[C/G]TAGGCTCCTAAGGCC | 81550 |
rs755682145 | snp | C/T | 5.01383e-05 | 0.00500666 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535270 | CAAAGGCATAAACTA[C/T]TTTGAAGAAAATATA | 81550 |
rs755731106 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421811 | ATCCAAGGCAGACCT[C/T]GAAAAAAACTACAGA | 81550 |
rs755762646 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473784 | TCCCTGGTCTAGCGG[A/T]CAAGGCCACTAGAGG | 81550 |
rs755766293 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568963 | CGCAATTGTTTTTTT[-/T]CCCCCCTTTTCTTCT | 81550 |
rs755784220 | snp | G/T | 0.000231616 | 0.0107589 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397440 | GGCTGCCGGGCCGCG[G/T]GTGCGGGCCGGGGCC | 81550 |
rs755793130 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566240 | AGCTTCAGTATTCTT[C/T]ATATAAAGTGGAAAT | 81550 |
rs755846315 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60479711 | ATTTAGGATAGCTAA[G/T]TCTTCTTATTGAGTT | 81550 |
rs755856065 | in-del | -/TTA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398609 | TTAAAGGCACTTGTG[-/TTA]TTATACACCCCATTT | 81550 |
rs755880210 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561229 | AATTATAAAATGAGA[C/T]ATTTAATTTATAGGA | 81550 |
rs755891938 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564556 | ATGGCCCTGGTTTGG[A/C]CTCTTCCTCTAATTA | 81550 |
rs755914607 | in-del | -/ATTTCTTA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515514 | ATTTTGCCTGTAGCT[-/ATTTCTTA]ATTTCTTATATTCTC | 81550 |
rs755941378 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60519693 | AGGTTAATACTGGGG[C/T]CTGGAATCTACTCAG | 81550 |
rs756002980 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60414168 | TGTGAGACAATGTAC[A/G]TTTTTTTTTAAGTCC | 81550 |
rs756010364 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511338 | TTCAGTTTCTCATTC[A/T]GATATATTTTGAATC | 81550 |
rs756014383 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60510785 | AGTTGATTCCTTTTT[C/T]TTTCTTTCTTTTCTT | 81550 |
rs756023832 | in-del | -/TGTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60456719 | TTTGAGACACCTTTT[-/TGTG]TGTATGTGTGTCACC | 81550 |
rs756064433 | in-del | -/TTT | 0.00360241 | 0.0422875 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510803 | TCTTTCTTTTCTTTC[-/TTT]TTTTTTTTTTTTAGC | 81550 |
rs756069809 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60448294 | TAAGACGCATCAGAG[C/G]CCTTCAGAAAGGCGT | 81550 |
rs756084205 | snp | C/T | 1.67094e-05 | 0.0028904 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460531 | AATTTAGTTATATGT[C/T]AAAAATAAGGTGATT | 81550 |
rs756096498 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60483840 | GCCTTTTGTGCCTTT[C/T]GGACAGGTAATGACT | 81550 |
rs756126824 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454493 | TCTTTCTCTGTGAGA[A/C]TCCTGGCCACTTGAA | 81550 |
rs756127014 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493295 | TAATCATTTTAAAAC[A/G]TATTTTAAAATATTG | 81550 |
rs756139549 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401778 | CTTTGGGGTTATCTC[C/T]ATTTGATTATTGGTG | 81550 |
rs756150950 | in-del | -/AAAAG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562733 | TATACAAATTCTGTT[-/AAAAG]AAACAAATGATTCAA | 81550 |
rs756165400 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571270 | AAATATCTCTTTGAC[A/G]TACTATCTTTGAATG | 81550 |
rs756185866 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533997 | ACCTATTCCTAGTTA[A/T]TTAACAGATAAATTT | 81550 |
rs756262662 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504870 | TAGCCAAGATAAGCC[A/G]TGAGGTATTGTGCCA | 81550 |
rs756270804 | in-del | -/ATACC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560126 | AAGAAATGGAAATAT[-/ATACC]GTATGATGCAATGAA | 81550 |
rs756283079 | snp | C/T | 9.89218e-05 | 0.00703215 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509867 | AGAAGCAGCACTGAA[C/T]GTACTTCTTACAAGC | 81550 |
rs756383808 | in-del | -/CTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60437549 | ACATCTCTAGGACTC[-/CTT]CATCTGTAAAGTTGA | 81550 |
rs756387404 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537515 | AAGTGTTAATGTTGG[A/G]GTCTTTGAGTACTTT | 81550 |
rs756397959 | snp | A/G | 1.65726e-05 | 0.00287855 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509735 | TATCTGTGGGCTATC[A/G]GCCAGCTTTTCTCTT | 81550 |
rs756404098 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405368 | AATTACATATTCAAA[-/C]ATACTGCATCTATAA | 81550 |
rs756409339 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525710 | TTTATTTGTTAAATA[A/G]TAAGCTGTTCAGGAA | 81550 |
rs756421980 | snp | C/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438754 | TTGATGGTGGAATTG[C/G]TGTTCATCAAAAATG | 81550 |
rs756464540 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60483567 | TGAATATGTGTTTTG[G/T]TAAGGGGAGGTGAGG | 81550 |
rs756475676 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525992 | TTTTCCTTTTAGAAG[-/A]ATTGAAATCAAATTC | 81550 |
rs756500442 | in-del | -/AT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461006 | CTGTGTCTCAAAAAT[-/AT]ATATATATATAAAAT | 81550 |
rs756501511 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543733 | CACATTCCAAGCCTC[G/T]TCCTTTCTGTGAGTA | 81550 |
rs756514305 | in-del | -/AG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423284 | CTGGCTTTCTGAAAC[-/AG]AAACTTCAGGAGTTT | 81550 |
rs756522649 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515995 | GACAGCTAATGAAGA[A/G]AGTTAAGATCTTATT | 81550 |
rs756524797 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394754 | GGATTTATGTGCCTG[C/T]GTCTTCATGTTTAAC | 81550 |
rs756532876 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524041 | TGTACAGAAAAATAT[C/G]TTAGTATATTTATTA | 81550 |
rs756542543 | snp | A/C | 1.77059e-05 | 0.00297533 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485960 | GGAAGTAAGAAATCA[A/C]ATCATTACACGTTTT | 81550 |
rs756563539 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429522 | GAACAAAAACAATAG[C/T]AGTTCATTTTGCATT | 81550 |
rs756586029 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467903 | CCTCTACTTTGCTTC[C/T]AACAACCATTTCTGT | 81550 |
rs756651634 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477123 | GGGCATCCTTGTCTT[A/G]TTTCAATTATCAAGG | 81550 |
rs756685213 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492917 | ATTTTCTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 81550 |
rs756744286 | snp | A/G | 0.000116561 | 0.00763327 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535259 | CATATTCTGTACAAA[A/G]GCATAAACTATTTTG | 81550 |
rs756746589 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411567 | GCTAGGCTGATGTAA[G/T]AGAAGCCTGGAGAAC | 81550 |
rs756756578 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475217 | AGTACCCTATAGGTA[A/G]CCTTCCAACTTATTT | 81550 |
rs756758914 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446927 | GATCCGTTACTTACT[A/G]ACATTATGTAAGTTA | 81550 |
rs756760639 | snp | A/G | 1.64985e-05 | 0.0028721 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535123 | TTTTACCGGGCAGAA[A/G]TTGAAGCCCTCCATT | 81550 |
rs756768892 | in-del | -/ATTAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406440 | TTTGTTAAAATAATT[-/ATTAA]ATTAATTTCACCTGT | 81550 |
rs756774278 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60448061 | AGACGAGTCTTCAAA[A/C]TTCATCTCCTGAAAG | 81550 |
rs756805510 | snp | A/G | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395947 | TCTCAATAGCATTCC[A/G]TCTAACGAAAGCATC | 81550 |
rs756822949 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499423 | CATAAGGTCCACCCG[A/T]AGCAATTTGCCTTCA | 81550 |
rs756837141 | in-del | -/TA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470765 | TTTTTGTATTTTTAG[-/TA]GAGACGGGGTTTCAC | 81550 |
rs756847849 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523830 | GATCCACCCACCTTG[G/T]CATCCCAAAGTGCTG | 81550 |
rs756855860 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544168 | CAAAAAAAGTGTTGG[A/G]TTGGGCATGGTGGCT | 81550 |
rs756867709 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60510144 | CAAAACAAAAACAAA[A/G]TGGGTCTAACAATAC | 81550 |
rs756868984 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467680 | TATAATTCTTTCTGC[-/A]AAAAACAAAAGTGCA | 81550 |
rs756885914 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430878 | CGATCATTTTAAAAT[C/T]GTCATGCTGTATTTT | 81550 |
rs756886730 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409390 | TGGTAGAGCCACTGA[C/G]AGCTTGCACTGTGCA | 81550 |
rs756972167 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432592 | ACAATCAATTTACAC[A/T]ATGGAGAGAGAAACA | 81550 |
rs757016955 | in-del | -/GT | 1.66058e-05 | 0.00288143 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528434 | ACTGAGCAAAATGGA[-/GT]GTAAAAGATAATAAT | 81550 |
rs757021268 | snp | A/G | 4.96808e-05 | 0.00498377 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467428 | ATTACACTCTTTTTT[A/G]TTGCATTAAAGAGCT | 81550 |
rs757036576 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476671 | CATTTTAATGATATT[A/G]GTTCTTGCCAATATC | 81550 |
rs757048313 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425254 | GTCTAAGAGGTGTAT[A/G]AAAAGGTGCTCAAGA | 81550 |
rs757071732 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490550 | GAGAAATGGGAGCCT[G/T]TGGAATGTTTTGAGC | 81550 |
rs757077075 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60535706 | CTGCATATATATTGA[C/T]GTATATATGTACAGA | 81550 |
rs757077479 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436316 | TTGGGGTCTTAGTCA[C/T]GAATTCTTTGCCTAT | 81550 |
rs757078586 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461480 | TTTCTGAGGTGGAAA[C/T]TTTCACTAGACATTT | 81550 |
rs757101065 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60519085 | CTTTTTTTGGTACTT[A/G]GATCTGTAGAAGATG | 81550 |
rs757119602 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432251 | TCAACTAACTGCTGG[G/T]GTTCCATTTTATATT | 81550 |
rs757120118 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478011 | TGGTCTAGGATTTTT[C/T]TGGTTAAGAGATTTT | 81550 |
rs757152239 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430020 | TTCTTAGAAAAACTC[C/T]GTAGATCAGTATTTT | 81550 |
rs757226185 | snp | A/G | 4.95937e-05 | 0.0049794 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510752 | GGAACTTTGAATGTG[A/G]AAGGTAAGCTAATTT | 81550 |
rs757258094 | snp | A/G | 1.6492e-05 | 0.00287154 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467349 | TGGTGGTGAAGTGGA[A/G]CACCTTATTGAGAAA | 81550 |
rs757271737 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462502 | AAACAATTTGGAAGA[C/T]ATTATACAAAATAAG | 81550 |
rs757275129 | snp | C/T | 1.66579e-05 | 0.00288595 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509718 | AAGTTTATGCCTTGC[C/T]TTATCTGTGGGCTAT | 81550 |
rs757295970 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441175 | ACTGTTTGTCTTGCA[C/T]TGAAATTAGTTAATT | 81550 |
rs757296911 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538977 | TTTAAAAGTTCATAG[C/T]ATCTGCTTCTTGGTA | 81550 |
rs757335051 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400026 | CGGACTTAAAATAAT[A/T]TTTGTTCTTCAATGG | 81550 |
rs757368539 | snp | G/T | 1.69384e-05 | 0.00291014 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494608 | ACCACAAATTTAAAG[G/T]GTTATTTCTTAAAAT | 81550 |
rs757381117 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416870 | TGTTCTTGTTCTCTT[C/T]ATTCCTTTCTCATCA | 81550 |
rs757381289 | snp | C/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438058 | ATGTATTGTGTTATA[C/T]TGTATAGCAGACTGT | 81550 |
rs757423649 | in-del | -/TATC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60545907 | TCTCTTTTTTCTCTT[-/TATC]TAAGCTCCTCCTCCT | 81550 |
rs757443017 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530907 | CCTTTAATAAGGATG[C/T]TGTAGGATTTGGGGT | 81550 |
rs757527587 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60547513 | TACCTAATATCTCTG[G/T]GTCCCAGTTTCAGTA | 81550 |
rs757530139 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440752 | TTGTTTTTCTATGTA[A/G]CTTTATAATAAGCTA | 81550 |
rs757563015 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562187 | GTTTGGTGGTGCGTG[A/C]CTGTAATTCCAGCTA | 81550 |
rs757616737 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508107 | GAAACCATTGCTCAA[A/G]GAAATAAGAGAGGAT | 81550 |
rs757616829 | in-del | -/TCAG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440022 | TTTTTCACCCACTGA[-/TCAG]TCATAGACTTTTTTA | 81550 |
rs757623366 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546179 | TACTTGGCCATACTG[G/T]TGGTGGTTCTCATAA | 81550 |
rs757650105 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407648 | AACATTTCTTTGCCC[A/G]AGACAACCAGCTGTC | 81550 |
rs757668926 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567594 | CAGCCAAGACGATCC[A/G]CTCGGCCAACCCAAC | 81550 |
rs757680580 | snp | A/G | 4.95111e-05 | 0.00497525 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528481 | CTCGAAATGATACCA[A/G]GCAGCCAAGAAATGA | 81550 |
rs757713222 | snp | A/T | 1.72603e-05 | 0.00293766 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528352 | ATTTGCATATGGTAT[A/T]CTTTTACCTTTCAGA | 81550 |
rs757726978 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571005 | CTATGTTCCCTGAGT[G/T]AAAACTTCCATCGAC | 81550 |
rs757728879 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481634 | TCTTTACTAGTTGAA[C/T]TTATGTTTTCTTTTA | 81550 |
rs757735226 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555445 | AATATTAATGTTTAC[C/T]TTACACACTAGGAAA | 81550 |
rs757737926 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60408611 | TGGCAACATTTTGCC[C/T]CTGCCCTAGAGATTT | 81550 |
rs757750054 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522356 | TGGTGGTAGTGGGAA[C/T]GTATAAATAGGGAAG | 81550 |
rs757816938 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60569877 | ATCCGTATATGGATG[A/C]ATGAAACTAGATTCC | 81550 |
rs757851659 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425182 | CATTAAAAATAATTT[G/T]ATTAAAAAATGGGCA | 81550 |
rs757853830 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409319 | CACAGAGTCCCTACT[A/G]GGGCACTGCCTAGTA | 81550 |
rs757914501 | in-del | -/ATAAAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466113 | CTTAAAAATTAGCAT[-/ATAAAA]ATCCTTTTAAAGTTA | 81550 |
rs757916310 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462444 | CAGCATGCCTACTTT[G/T]GGTGCCGTAAAAATG | 81550 |
rs757924149 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523763 | TGTATTTTTAGTAGA[C/G]ATGGGGTTTCACCAT | 81550 |
rs757925968 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60547192 | TGGCAAAGTATAACC[-/A]AAAAAAAATCTCATG | 81550 |
rs757926941 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497922 | ATTGAGTTGGATCAG[C/G]CTGAATTTATTGATT | 81550 |
rs757941618 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410595 | AGGAATTGGCCACGA[A/T]CTTTTCTCTAGGCTG | 81550 |
rs757985585 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394813 | ACATTTCTTCTTACA[C/T]CTAGACCTTAGCATT | 81550 |
rs758001452 | snp | A/G | 0.000171274 | 0.00925244 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485944 | AAGTTGCAAAGAGCA[A/G]GGAAGTAAGAAATCA | 81550 |
rs758044680 | snp | A/G | 0.000107152 | 0.00731879 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444797 | ATTTAGTTACAATAA[A/G]TATGAACTAAATTAC | 81550 |
rs758063597 | snp | G/T | 1.64928e-05 | 0.00287161 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467335 | AACACCACAGTTCTT[G/T]GTGGTGAAGTGGAAC | 81550 |
rs758082923 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484820 | TAAACATTCTAATAA[C/G]TTATATTTGAAAATA | 81550 |
rs758105746 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60539866 | GTCCTAGATAAAGGT[C/T]GTGTTAGTAATTTTA | 81550 |
rs758127583 | in-del | -/AAC | 0.000104915 | 0.007242 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444764 | GTAAAGAAAATCAAT[-/AAC]TTCTTACATTAATTA | 81550 |
rs758147924 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534093 | AGTAGAGAAGATCAC[C/T]TGAGGCCAAGAGTTT | 81550 |
rs758153296 | snp | C/T | 0.000189084 | 0.00972144 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510580 | ATTAGTATATATTCT[C/T]TTTTTGTTTTTGCAT | 81550 |
rs758178598 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433794 | CCCTTTAGCTCAGTC[A/C]GCTGATGTGTAGTTT | 81550 |
rs758181824 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434617 | TTGTCAGTAAAATGT[A/T]TTCAGATGTTGTCAT | 81550 |
rs758187492 | in-del | -/AAAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553554 | TTATTTTTTTTAAAT[-/AAAA]AAAAAAAAAAGAGGT | 81550 |
rs758192440 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563806 | CCAATTTATGATGAA[-/C]TTTTATAACACGGCT | 81550 |
rs758213651 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551632 | TTTTATTTTTTCTGT[G/T]AAAATTTTCTTTTCT | 81550 |
rs758295757 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400988 | AAAAATTGAAAATTG[G/T]GTTGAAGCATTTTGT | 81550 |
rs758301788 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549696 | AAGAAAGTAAGAAAA[C/T]GTAGAAAATAATTTT | 81550 |
rs758321874 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505449 | CCTCAGCCAGGGGAT[G/T]ATAGATAAAACTCCC | 81550 |
rs758326488 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462794 | TGAAGGTGATAGTAA[A/G]AATTGTATTAAAATT | 81550 |
rs758365874 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427146 | GTGGAGTGTGACTGT[A/G]TTGAAAACTTTTTTT | 81550 |
rs758375350 | snp | A/C | 1.66114e-05 | 0.00288192 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535092 | GTCATATTTAAAACT[A/C]CTTTTGCCTCCTCAG | 81550 |
rs758388996 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419915 | AGCAGGAATTTTTAA[A/G]AATTATTTTTAATGT | 81550 |
rs758389353 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476397 | CCTGTTCCATTGGTC[C/T]GTGAGTCTGTTTTTG | 81550 |
rs758396240 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563333 | AAATAGAGCCCCCGC[C/G]AAATTTCTATAGAGA | 81550 |
rs758403754 | snp | G/T | 3.30087e-05 | 0.00406242 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509891 | TACAAGCAATAAACA[G/T]AAACCTGTTATGGGT | 81550 |
rs758407063 | snp | C/T | 6.59217e-05 | 0.00574078 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509791 | CTCTGAAGCACATAA[C/T]GGAAATGGGCTTCAG | 81550 |
rs758407549 | snp | C/T | 1.66538e-05 | 0.00288559 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528860 | ATCTATTCCTGATTA[C/T]TTTTATGACAGGAAA | 81550 |
rs758435263 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434391 | GAGAATTGCTTGAGC[A/C]CAGGCAGTTCAGGCT | 81550 |
rs758453606 | in-del | -/AT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470112 | TTGACGAAGTAACTC[-/AT]ATGTGTGGAATCATA | 81550 |
rs758454172 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60414639 | TTATTTGTAGTGACT[A/G]GTATGAATAGGGCTG | 81550 |
rs758471917 | snp | A/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494489 | AATCTCAATATGAAT[A/G]CTGCTGGTAACCGAA | 81550 |
rs758476751 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444477 | TTAAGGCCTTATGTG[G/T]TACTGTTCATCTTAC | 81550 |
rs758488719 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60547212 | AAAATCTCATGACAT[C/T]GTTCACCACTTTTGC | 81550 |
rs758526686 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542440 | AAAAGGCATCCTTGT[G/T]GAATACACACACACA | 81550 |
rs758541724 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481391 | CAATTACACATACAT[C/T]AGACTGCTGGTAATT | 81550 |
rs758630603 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466525 | AGGTACAGTGGCTCA[C/T]GCATATAATCCTAGC | 81550 |
rs758635584 | in-del | -/TCCACT | 1.65778e-05 | 0.002879 | cds-indel, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528782 | AGAGGCAAAAGAAAA[-/TCCACT]TCCTCAAGGATCTGT | 81550 |
rs758663582 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560983 | GTTTAAATAAAATGT[G/T]CTGGATGAGGTACAT | 81550 |
rs758665875 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450762 | AACCAGCCGTGTCAA[C/T]GTAGTGAAACAAATG | 81550 |
rs758682119 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422478 | CGTGAACTATAACTC[G/T]AAGTTCATACTCCAA | 81550 |
rs758693631 | snp | A/G | 2.21266e-05 | 0.00332608 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460383 | CTGTTTTGACAGCTC[A/G]AAGGTCCATGTGTTT | 81550 |
rs758742800 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60456297 | CAACCATTTAAATCT[G/T]ATATTTCATATCCGT | 81550 |
rs758753342 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559308 | AGACTCAGATCTGAC[C/T]TAAGAGGTTGAGCTC | 81550 |
rs758765200 | in-del | -/TTA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552208 | AAAATCAAAAGCAAC[-/TTA]GTTACTTTCAAGATA | 81550 |
rs758777246 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60569720 | TAGTACTGACATAAA[A/T]ACAAACAGACCAATG | 81550 |
rs758782881 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506908 | AAAAGGCACAGACTG[G/T]CAAATTGGATAAAGA | 81550 |
rs758794371 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60472579 | GTGGGAATATAAAAT[A/G]GCATAGTTGCTACAG | 81550 |
rs758794489 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506340 | CAGACAAGAAAATGC[A/T]GAGAGATTTTATCAC | 81550 |
rs758805131 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553728 | TCATGAGAACTCACT[C/G]ACTATCACGAGAACA | 81550 |
rs758811199 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402691 | GAGGAAACCAATTGC[-/T]TTTTTTTTTTTTTTT | 81550 |
rs758824807 | snp | C/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567566 | TCTGGAGTTCCGTAG[C/G]GGAGGTGATGGCCAG | 81550 |
rs758830759 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457880 | CTGTCTGTGTTTGTT[C/T]CCCCTTCTCTTCTAA | 81550 |
rs758833380 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405489 | ACTAAAGGGGAGTTC[A/G]TGTTTTCATGGTGGT | 81550 |
rs758839221 | snp | C/T | 1.69006e-05 | 0.00290689 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535284 | ATTTTGAAGAAAATA[C/T]ATAGCTCTAAAGAAT | 81550 |
rs758886086 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421774 | CCTGTGCCAATCTTG[A/T]CCCACTTGTGGGGCT | 81550 |
rs758899274 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568413 | GGTATTTTTCTTACG[G/T]CATGGAATAACTGGT | 81550 |
rs758908413 | snp | C/T | 1.64955e-05 | 0.00287184 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528616 | TATCTGAAGTATGGG[C/T]TGAAGACAGAATCAA | 81550 |
rs758916373 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440641 | AGCCGAGATCATGCC[A/G]CTGCACTCCAGCCTG | 81550 |
rs758926437 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453372 | AATTCAGTTCTACTT[A/T]GATAAATCTGGTTAC | 81550 |
rs758956945 | snp | C/G/T | 3.37247e-05 | 0.00410627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494601 | AGAACTAACCACAAA[C/G/T]TTAAAGTGTTATTTC | 81550 |
rs759008412 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516159 | AATCAAACCTTTCTT[A/G]CTTCTGTGTTTTGTA | 81550 |
rs759023932 | in-del | -/G | | | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396716 | ACTCGATCTGCCCGC[-/G]GGGACTCAAAAAAGC | 81550 |
rs759050636 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60556294 | TGTTACCCTTTTAGA[C/T]GGTAGTCTTCTAACT | 81550 |
rs759093881 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436053 | GTTGGCTGTTTTTAT[A/G]TATCTTCTTTTGAGA | 81550 |
rs759098094 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515108 | TCATCATTTACTTAA[C/T]GTAAAACAAAACAGT | 81550 |
rs759101958 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418560 | ACAAATGTTTATTGA[A/G]TAAATAAACTGAATG | 81550 |
rs759124765 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461337 | AATGATTTTCCAAAC[C/G]CTTTGTTTGGTTATT | 81550 |
rs759146832 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554843 | TCCAGATTGTAATCA[C/G]TTCCCCCAACCTCTG | 81550 |
rs759157467 | snp | A/G | 3.32408e-05 | 0.00407668 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467219 | CAATATGTTTTTAAC[A/G]CTTTTCTCTTTGCTT | 81550 |
rs759161850 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490791 | TTAGGGTTACTGAGA[C/T]TGGATATAGGGTACA | 81550 |
rs759182255 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424776 | AAGAACATTTAACCC[A/G]ATATGCATTGGCATC | 81550 |
rs759199891 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427770 | CATTTTAAGTTGAAT[A/G]GAAAATGTCCTTCTA | 81550 |
rs759243233 | snp | A/T | 1.65007e-05 | 0.00287229 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460482 | ATGCTGCGATTACAG[A/T]TGACTGATGGTCATA | 81550 |
rs759245072 | in-del | -/TC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60536504 | GATGGCTATTTTCAT[-/TC]TCTCTTTTCCATTAA | 81550 |
rs759259678 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564217 | ATATGAGTGATCATG[G/T]CCCATGACACAGCCC | 81550 |
rs759282455 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477448 | TCAAACTCCTAGCCT[C/T]AAGCAATCCTCCTTG | 81550 |
rs759286068 | in-del | -/T/TT | 0.104196 | 0.203905 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510802 | TCTTTCTTTTCTTTC[-/T/TT]TTTTTTTTTTTTTTT | 81550 |
rs759323984 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442870 | GGATGGATCAAAGTT[G/T]AGGATTTTTGTCTAG | 81550 |
rs759330199 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60509407 | TCCCTTCTAGTATGG[A/G]GAAGTATCAAAAAAT | 81550 |
rs759336839 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442618 | GATTTGGTAGATCAT[A/T]TTCATCTTGCTAAAA | 81550 |
rs759364254 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537168 | CACTAAATCTTTTGG[A/T]GATTCTGGTATTTCT | 81550 |
rs759369138 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401139 | TCTGAAAATCTGGTA[A/T]ATTCTGTATTTTTTA | 81550 |
rs759387567 | in-del | -/AG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60529801 | GCTAAAGGCAAAGAA[-/AG]AAATTGTAGGGGAAA | 81550 |
rs759418148 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523432 | AATTAAAATCTTGTA[A/C]TAATAGGAATGTTTT | 81550 |
rs759438608 | snp | C/G | | | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467347 | CTTGGTGGTGAAGTG[C/G]AACACCTTATTGAGA | 81550 |
rs759473004 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484038 | TTGACGTTTGCGAGA[A/G]CTGTTAACCCAAAGA | 81550 |
rs759529854 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416575 | TGTAATGTTTAGCAC[A/G]TGTATGACTGTGTTC | 81550 |
rs759536432 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452119 | ATTAGGAAGAAATGT[A/G]CATAAAAAGTTTTTG | 81550 |
rs759549340 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570051 | ACAGGCAACCAAAGC[-/A]AAAATGAACAAATGG | 81550 |
rs759556391 | in-del | -/TG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538671 | ATTAGGGGCAAAGAA[-/TG]AACCTGCTACTTGTG | 81550 |
rs759563495 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422496 | GTTCATACTCCAACA[G/T]AATTAAATTTACTCC | 81550 |
rs759591514 | snp | G/T | 1.65233e-05 | 0.00287426 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528704 | TTCTCAGCATAGTGA[G/T]GGTGCTTTTAAAAAA | 81550 |
rs759599897 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421615 | AAAATCTTTCCCCCA[A/G]ACTATACGGATGACT | 81550 |
rs759614182 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60519189 | ATTAATTGTCCGTTC[A/G]CTTATACATTTATTA | 81550 |
rs759618908 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398004 | GAGCTAAGAATGACC[G/T]CAATGTCAACTCGTG | 81550 |
rs759632404 | snp | A/C | 1.65187e-05 | 0.00287386 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467410 | GGCTTGAACTTTTGA[A/C]ACATTACACTCTTTT | 81550 |
rs759634296 | snp | C/T | 0.00266957 | 0.0364371 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510793 | CCTTTTTTTTTCTTT[C/T]TTTTCTTTCTTTTTT | 81550 |
rs759652333 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537507 | AGTATTGAAAGTGTT[A/C]ATGTTGGGGTCTTTG | 81550 |
rs759655336 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506788 | ACACTATGAAGAAAC[A/T]GCATCAGCTAAAGGG | 81550 |
rs759668159 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60535545 | TTTTGTTTTTTTCCC[A/G]GTTTGTTACTTTGAA | 81550 |
rs759672779 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458415 | AAGGTGTCATGTCAA[C/T]ACCCAGGGGACGTAG | 81550 |
rs759723351 | snp | C/G | 0.000115619 | 0.00760239 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510660 | GGGGGCGAATAAGAT[C/G]TGAAGATGAAGAGGA | 81550 |
rs759728825 | snp | A/G | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535222 | ATCAAGCCCATTCAA[A/G]CAGAGGCATGGGTAC | 81550 |
rs759744342 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552980 | GGCCTTCGGGCCTGT[C/G]ATGGAAGGGGATGTC | 81550 |
rs759749392 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572957 | TCTGTATTTTCTAAG[C/G]AGGAGACTGTTTACT | 81550 |
rs759753600 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482824 | AATATGCTTGAAAGT[A/G]CACATGGTGGTTGTT | 81550 |
rs759754463 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523139 | AATAAATATTAAGGC[A/C]TTTCTTCAGGTAGGT | 81550 |
rs759755515 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396578 | TAGGACACGGATGGT[-/C]CCCAGGGGGAGGGCA | 81550 |
rs759780132 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465138 | AACTTGAATTTAATC[C/T]GGTCAGACTATCAAT | 81550 |
rs759831779 | snp | A/T | 3.31625e-05 | 0.00407188 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528968 | TCCAGTTCGAAGTAA[A/T]AGTTTCATTGGTGTT | 81550 |
rs759840201 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530151 | ATATTTTTTGTTTTG[A/G]TTCTTGAATTGGTAT | 81550 |
rs759849983 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60547177 | ATGAATTTCACATAA[A/G]TGGCAAAGTATAACC | 81550 |
rs759882407 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533469 | AACATGGTAAAAACC[C/T]GTCTTTACTAAAAAT | 81550 |
rs759895098 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486849 | TATGAGAGAGAATAT[A/G]CAGTATTTGTCTTTC | 81550 |
rs759914572 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446394 | ACCACGCCTGGCTAA[-/T]TTTTGTATTTTTTAG | 81550 |
rs759917770 | snp | C/G | 3.32535e-05 | 0.00407746 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528840 | GGAAAAAGAGAAAGC[C/G]AAACATCTATTCCTG | 81550 |
rs759937327 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447803 | AGAGTGAGGATTGGA[A/G]AGCATTTGGCCCAGT | 81550 |
rs759966251 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520714 | TTTCATATAGAGTGA[C/T]TAGGAGAGCGTTGAC | 81550 |
rs760046296 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543965 | TTTGTAATATAGCTG[-/T]TTTTTTTTTTTTTGT | 81550 |
rs760048008 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415709 | TGGGCAAGCTTTGTA[C/T]AGATGCCTTGATGGA | 81550 |
rs760055979 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452170 | CCAGCACAACCCTGG[A/G]TATATCTCTTCCTTT | 81550 |
rs760058617 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60513976 | TGACTTGGGAACTGG[A/G]TAACAGGCAGAGGTT | 81550 |
rs760069664 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398585 | GCTTTGAAGAAGCCC[C/T]TCCTGATTTTAAAGG | 81550 |
rs760094922 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501547 | AATTATTAATCCCTC[A/C]ATGACTTACACAGAC | 81550 |
rs760112560 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487827 | TAGTTCTATTTTTAG[C/T]TTTTTTGAGCAACCT | 81550 |
rs760144503 | snp | A/G | 1.64969e-05 | 0.00287196 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467257 | AACACACCACCTGGA[A/G]CTAAAGTTAAGCTCT | 81550 |
rs760182789 | in-del | -/T | 1.66391e-05 | 0.00288431 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483737 | GAAATATATTTTTTA[-/T]GTATAACTGCTCTTT | 81550 |
rs760212167 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436748 | ATATTTGACTTATGT[-/G]GATAAAGGCAAGTTT | 81550 |
rs760224362 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60529862 | AGAAAGAGTGCAGTG[C/G]GTCAAGTAAAAGCCT | 81550 |
rs760243777 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492464 | ATCCCAGTTTTAAAG[A/T]TGAAAAACCTGAGGC | 81550 |
rs760251184 | in-del | -/TTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416553 | TACGAATGCCTTTTC[-/TTG]TTGTTGTAATGTTTA | 81550 |
rs760261726 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416494 | ATTTATTAAGCAAGA[C/T]TTTTTTCTCCAAAAT | 81550 |
rs760280894 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568083 | TGTCTTGTGATATTT[C/T]TGCTGGGCAGCACTG | 81550 |
rs760312308 | snp | C/T | | | intron-variant, synonymous-codon | TDRD3 | GRCh38.p7 | 13:60527492 | GTATGACAAAGGAAA[C/T]AAGACACATACACCA | 81550 |
rs760312885 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502478 | TAAACTTTAGTCTTA[C/T]ACTTGGCCTGATTAT | 81550 |
rs760328600 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453289 | CTAAACATTTTCCCA[A/G]TGACTGACTAAGCCT | 81550 |
rs760329968 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517312 | TGGTAATAGCTTAAT[C/T]GGAAAGGAAGGAAAC | 81550 |
rs760335864 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503161 | CCATTTAGTTAACTT[C/G]TGTTTTGCTTGATAC | 81550 |
rs760343675 | snp | A/T | 4.39088e-05 | 0.00468534 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460357 | GACTAGAAAGTGATT[A/T]TTATTCTTTTCTGTT | 81550 |
rs760361364 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549026 | ATTCATCTGCTGGAT[-/G]AACTATTATACACCT | 81550 |
rs760384199 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434103 | TAAGTGATTCTAAGA[C/T]GGAATTTTGACATCT | 81550 |
rs760431938 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60489222 | TTTGCTTATTTGTAA[C/T]AGGTGTTTTTCCTAG | 81550 |
rs760437110 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443096 | TTGATATGATGGTTA[C/T]GTATGTTCAGATGAT | 81550 |
rs760437488 | snp | A/T | 3.45829e-05 | 0.00415816 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509674 | AAGTATGGGATGTAA[A/T]TTTTAGTTAAAAGAC | 81550 |
rs760437511 | in-del | -/TC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400245 | TCTGCATTTTTGTTT[-/TC]TCTCTTCAGAGGTTC | 81550 |
rs760466346 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60521175 | ATGTGCTTTGCTGCA[A/G]ACTTCTCCTAAAGAA | 81550 |
rs760467244 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420913 | CACGTCACTGTGCTC[C/T]AACCTAGGTGACAGA | 81550 |
rs760468102 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541470 | CCTTGCCCAGTCCAC[A/G]GCATTCTTTTATTTT | 81550 |
rs760498268 | snp | C/T | 2.07157e-05 | 0.0032183 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485780 | TACTAAGTTGACTTA[C/T]TCTTACTTGTTTTAC | 81550 |
rs760501047 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495759 | AGGCGTGAGCCACCA[C/T]GCCCGGTGGGATAAA | 81550 |
rs760509438 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440384 | AAAGTTGTTTGAAAT[A/C]AAAATGTAAGTAAAC | 81550 |
rs760527058 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473620 | TAGTATTACTCTTTA[C/T]TCCAATATTATAATA | 81550 |
rs760554131 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60539180 | TTTCTGTAGAATACT[A/C]ATTTATTCAACAAAT | 81550 |
rs760585251 | in-del | -/GTAGGT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538678 | GCAAAGAAAACCTGC[-/GTAGGT]TACTTGTGTTTCCCA | 81550 |
rs760592971 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60480935 | GCCCTCTGGTATTGG[G/T]AGTTGGGTTGTCTTG | 81550 |
rs760634733 | in-del | -/T | 0.516955 | 0.202164 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484674 | AAAAAATAATGTTGA[-/T]TTTTTTTTTTTTACT | 81550 |
rs760657426 | in-del | -/CG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474353 | GTCACTACCGGTCTC[-/CG]CGCCTTGGTGGTAGT | 81550 |
rs760707149 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433094 | TTGGTTTTCTCATTG[A/G]CATTTTAAAGACTTT | 81550 |
rs760721023 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486602 | CCTCAAACATTTACC[A/T]TCTTTGTGTTGAGAA | 81550 |
rs760771471 | snp | A/G | 1.67103e-05 | 0.00289048 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509946 | TAAGCAGTGTGCCAG[A/G]TAGTATTGTTTGCTT | 81550 |
rs760774421 | in-del | -/ACACACAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469428 | CTCACCAACACACAC[-/ACACACAT]ACACACACACACACA | 81550 |
rs760782434 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419821 | AAAAGAATAGATGGA[C/T]GAAAGCAGAAAGGAA | 81550 |
rs760785921 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471414 | TCTATCTTTATGCCA[C/T]ACTGTTTTGATTACT | 81550 |
rs760793057 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551167 | AATTCTCTTCTTTAG[A/C]CTCTGTATCCACTGG | 81550 |
rs760793209 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421418 | TTCAATTACTTCCCA[C/T]TGGGTCCCTCCTGTG | 81550 |
rs760815433 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511672 | AGATTTTGGTTGGAG[C/T]GGTGATGTTATCAGA | 81550 |
rs760817783 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457212 | CTAACTTAAGGCTTG[A/G]TGATTCAAATTAAGA | 81550 |
rs760826790 | in-del | -/C | 0.000132122 | 0.0081267 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510793 | CCTTTTTTTTTCTTT[-/C]TTTTCTTTCTTTTTT | 81550 |
rs760841074 | in-del | -/TTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561869 | CCAGGTTTTTTGTTG[-/TTG]TTGTTGTTGTTGTTG | 81550 |
rs760861115 | snp | A/C | 1.67119e-05 | 0.00289062 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535066 | ATTGCCCTTTATAGA[A/C]AATACCAGTTGTCAT | 81550 |
rs760874207 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565637 | AGATTTTTAGATGTT[C/T]TCCAGCCAATTCTGC | 81550 |
rs760896764 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471376 | ATTTCTAGGTTATCT[A/G]TTCTGTTTCACTGGT | 81550 |
rs760942561 | snp | A/C/G | 4.96285e-05 | 0.00498118 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528732 | AAAAGAGATAACTCT[A/C/G]TGCAAAGCAGATCAG | 81550 |
rs760946445 | in-del | -/AT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415456 | AGGACTATAATTAAC[-/AT]ATTGGTAATAAGCAA | 81550 |
rs760967168 | in-del | -/TCTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484268 | CCCTTCTGACCAGTA[-/TCTT]TCTTGTGACTTCACT | 81550 |
rs760970684 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425672 | TGATCTTGAACAGTA[C/T]GGATTTGAACTGTGT | 81550 |
rs760970696 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60545276 | ATAACAGCATGTTAA[C/G]TGAATGAGATAATTT | 81550 |
rs761006536 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446684 | CATTTGGTTTGTCTT[C/T]AGCTAAAAATCCATA | 81550 |
rs761030774 | in-del | -/ATTCTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477214 | ATTATTATTATTATT[-/ATTCTT]GTTATTATTATTATT | 81550 |
rs761042518 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561710 | GGTACCACAGTGAGG[A/G]GCAGTCGGGCTTGTG | 81550 |
rs761059560 | snp | C/T | 1.64991e-05 | 0.00287215 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467385 | GTTACAGAGAGTAAG[C/T]GTAAACTATGGCTTG | 81550 |
rs761086472 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462203 | GAATTCAGTCACACC[C/T]CTTGCAAGGGAGCTC | 81550 |
rs761097386 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60510207 | AAAATATGTGACTGG[C/T]TCTATTATTTCTAGA | 81550 |
rs761109561 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499152 | CATCCCTGGAGGGAT[C/T]GCAGAGATTAGTGCC | 81550 |
rs761156794 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60480903 | CCATATGGGATGGGG[G/T]TGCACTCTGGTGGGA | 81550 |
rs761171662 | snp | A/G | 1.73462e-05 | 0.00294496 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509665 | TTTTTACATAAGTAT[A/G]GGATGTAATTTTTAG | 81550 |
rs761174508 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60519068 | ATATGATAATATTAT[C/T]ACTTTTTTTGGTACT | 81550 |
rs761176286 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463769 | ATGAAAAAATGCTCA[A/G]CATCACTAAAACTAC | 81550 |
rs761180115 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426886 | CCTTAATGGTATTGC[C/T]GACTACGCGCATAGG | 81550 |
rs761199680 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500186 | ATTTGACTATGGGTC[A/G]TCAAGTCACCATGCA | 81550 |
rs761264086 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517754 | TATTTCCAATTCTAT[C/T]TGTGGACAACTTGTT | 81550 |
rs761264440 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447606 | GATTCAATAAATAAG[G/T]TAAGGCAAATTGGTA | 81550 |
rs761265844 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60545025 | ACACCAAGCCTGTAC[A/G]TGACAGTTTAATATG | 81550 |
rs761305418 | in-del | -/AGAG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567428 | TTCCAGGGCAGCTTA[-/AGAG]AGAGAGATATTATTA | 81550 |
rs761306045 | snp | G/T | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467276 | AAGTTAAGCTCTCAG[G/T]CATTGTTGACATAAA | 81550 |
rs761314252 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60573058 | TGCATGAGGCTAAAA[G/T]AGGCCTGGAGCATAC | 81550 |
rs761323633 | snp | C/T | 4.96241e-05 | 0.00498092 | stop-gained, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510650 | GGAAAAGGCAGGGGG[C/T]GAATAAGATCTGAAG | 81550 |
rs761352240 | snp | C/G | 0.000193442 | 0.00983279 | synonymous-codon, intron-variant | TDRD3 | GRCh38.p7 | 13:60397400 | GGCGTTGTCCCAGGC[C/G]GGTTGGTAAGTGGCG | 81550 |
rs761384990 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467436 | CTTTTTTATTGCATT[A/G]AAGAGCTCTTTCAAT | 81550 |
rs761402483 | in-del | -/ATTCTTTCTTTC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541146 | TCTTTTTGTTTTTCT[-/ATTCTTTCTTTC]TTTCTTTCTTTCTTT | 81550 |
rs761421568 | in-del | -/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395331 | CTTGGAAAACTGTGA[-/T]TTTTTCTAATTCTAT | 81550 |
rs761439872 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559854 | AGTAGTGTATTGTAT[A/G]CTTGAAATTTGGTAA | 81550 |
rs761444311 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396902 | GTTCCCTCGCAGCCA[A/G]CCCGTCAGTCTCCTC | 81550 |
rs761459879 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402479 | ATATTTGTAGAGAAT[A/G]TTGGTAGTTCTTTAT | 81550 |
rs761467306 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495299 | TTCTCCTTAGTGTTA[G/T]GTAACTGCTCAATGG | 81550 |
rs761467956 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411830 | AGATTCTTATTAAAG[A/T]ATCTTATTGCACATT | 81550 |
rs761468543 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467017 | AGGGTACATGTGTAG[A/G]ATGTGCAGATTTGTT | 81550 |
rs761510746 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543218 | AAGAGGTTCTAGTAA[A/T]CAACCCAGACCATCA | 81550 |
rs761528450 | snp | C/G | 1.65652e-05 | 0.0028779 | missense, utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528433 | ATACTGAGCAAAATG[C/G]AGTAAAAGATAATAA | 81550 |
rs761531111 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450179 | TCACAGTTTTTTGTT[G/T]CTAGAGCACCTGAGT | 81550 |
rs761538953 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419624 | CATCACACACTGAGG[C/T]CTGTTGTGGGGGCGG | 81550 |
rs761540005 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568939 | ATGCTACTATTTCTA[A/T]ATGTCAACCGCAATT | 81550 |
rs761576156 | snp | C/T | 0.000116267 | 0.00762363 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528822 | TATAATAATCAAAAA[C/T]GTGGAAAAAGAGAAA | 81550 |
rs761593178 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501392 | GCTGTCAGCCATTCC[G/T]ATGGGTTGTAATACT | 81550 |
rs761618442 | snp | A/G | 1.77002e-05 | 0.00297486 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528325 | AATTATTAATGCAGA[A/G]TCTTCATCTTAATTT | 81550 |
rs761669070 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455336 | TTCAGGCTTTTAAAG[C/G]AGCTATAGGCAGAAT | 81550 |
rs761675759 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493606 | AGGTGGAGGTTGTAG[C/T]GAGCTGAGATTGCAC | 81550 |
rs761690423 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567633 | CAACCACCCCGGGCT[C/T]GGAACTAATAGGAAA | 81550 |
rs761700770 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405080 | GGAACTGTTAAGTCC[A/G]ATAAATGTCTTTCTT | 81550 |
rs761702711 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553042 | TTCCCCATTGTCTTG[A/G]CTGTTAACAAGTTAC | 81550 |
rs761727614 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566094 | TCAGGATGATCATTA[A/C]TTTTTGGCTATTGGC | 81550 |
rs761755041 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60513751 | GCCTGCTGCCATCCA[A/C]ATAAGATGTGACTTG | 81550 |
rs761756934 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60456836 | AAGTAGCTGCGGCTA[C/T]AAGCACACACCACCA | 81550 |
rs761792644 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567794 | AGTGGCGTGATCTCG[G/T]CTCACTGTAACTTCT | 81550 |
rs761807043 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557772 | TTTTTGTGGCATCAA[A/T]CTGGCCTGTATTTTA | 81550 |
rs761811078 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60529339 | GTACCTGTTTAAAAT[A/C]TTTGAACAGATTTAT | 81550 |
rs761844955 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512609 | ATATAGCCATTCCAA[A/G]TGGGAGAAATTGGCC | 81550 |
rs761848903 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440024 | TTTCACCCACTGATC[A/T]GTCATAGACTTTTTT | 81550 |
rs761850380 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447222 | TCAAGAAGCAGAGGA[A/G]GCATGGTTGTGGCAT | 81550 |
rs761872709 | snp | G/T | 5.03774e-05 | 0.00501858 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485886 | GTCAAACCTACAAAT[G/T]ATAATGATGAATTTG | 81550 |
rs761912448 | snp | A/T | 5.1402e-05 | 0.00506935 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460332 | AACACAGCCCTGAAT[A/T]GAGTTTCATGACTAG | 81550 |
rs761915691 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563063 | ATGAAACCCCATCTC[C/T]ACAAAACTACAAAAA | 81550 |
rs761922648 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60550665 | AGTAATCCAGATGAA[C/T]TGTAAAATCACTTTG | 81550 |
rs761930969 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430384 | AGGCTTCATGTAAGC[C/G]TTTTGAACTGATATA | 81550 |
rs761931865 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484414 | AAAATTTAGCGGTTG[A/G]TAATCTGTCTTGCAT | 81550 |
rs761942677 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523264 | GCAAAAAAGTATTAA[C/T]ATTTTAAGATGCCTG | 81550 |
rs761946260 | snp | A/G | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529116 | CGAAGATCTGGGCCA[A/G]TTAAGCCAGAAAAAA | 81550 |
rs761955543 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446656 | TTTTAGAAGCTGGCA[C/T]ACAGAAATTACTCAT | 81550 |
rs761962744 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470367 | CTTTGAGACCCAGCT[A/T]TCAATTCTTTTGTGT | 81550 |
rs761983298 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504728 | ATTTCTGCATTTTCA[A/G]CTGAGGTACCTGGCT | 81550 |
rs761994598 | snp | C/G | 1.6914e-05 | 0.00290805 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485873 | AGTTACAATGCCTGT[C/G]AAACCTACAAATGAT | 81550 |
rs761997416 | snp | C/G | 2.13299e-05 | 0.00326566 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485767 | TCTCTTTTGGAACTA[C/G]TAAGTTGACTTATTC | 81550 |
rs762012451 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549148 | GTGGTTTTAGAGTCA[A/G]GTCTCTGGGTATGTG | 81550 |
rs762012834 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571259 | GAAGTAGAATGAAAT[A/G]TCTCTTTGACATACT | 81550 |
rs762013025 | in-del | -/AGA | 1.93864e-05 | 0.00311333 | splice-acceptor-variant | TDRD3 | GRCh38.p7 | 13:60485797 | CTTACTTGTTTTACT[-/AGA]AGTGTGTATCTCATG | 81550 |
rs762014712 | snp | A/C | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395500 | CATTTCTCCAGTAAA[A/C]AACCCATTCTTTAAG | 81550 |
rs762021568 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500525 | AAAAGTGGACAGCTA[C/T]AGCCTACAGCCCCTT | 81550 |
rs762023046 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431547 | TGACCAGTGTGGATG[A/T]TAACCATGATGATAT | 81550 |
rs762043554 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444121 | GTTATTTGTTTACCA[C/T]CTTCTATTTCTGTAA | 81550 |
rs762053315 | snp | A/C | | | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528821 | TTATAATAATCAAAA[A/C]CGTGGAAAAAGAGAA | 81550 |
rs762058060 | in-del | -/CT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511078 | ATATAACTTATTTTG[-/CT]TGTGAAATTGATATA | 81550 |
rs762062193 | in-del | -/TC | 8.55377e-05 | 0.00653923 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510801 | TTTCTTTCTTTTCTT[-/TC]TTTTTTTTTTTTTTT | 81550 |
rs762105271 | snp | C/T | 1.65056e-05 | 0.00287272 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467246 | GCTTTAGCCTGAACA[C/T]ACCACCTGGAACTAA | 81550 |
rs762114088 | snp | G/T | 1.66178e-05 | 0.00288247 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509927 | TCTGAGAGGTATAAT[G/T]TATTAAGCAGTGTGC | 81550 |
rs762132435 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516771 | CATCCTCCACTCACC[A/G]TGTATCATTTCCACC | 81550 |
rs762191392 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572931 | CAGGTGAGGATTATA[A/G]TACCCGACGCTCTGT | 81550 |
rs762226920 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517668 | TGATTCCTTTTTACC[A/T]TTCCATTCGTTTTGA | 81550 |
rs762240812 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443687 | CATCTAGTGTTTTCT[C/G]CTTAAGTCTAACAAA | 81550 |
rs762261205 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429072 | GCATTTTAAAGAAAT[A/G]GAAATGAGAATTACT | 81550 |
rs762275570 | snp | G/T | 1.89529e-05 | 0.00307832 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529261 | TAATATTACGAAATG[G/T]AACATTCTAGTGGGA | 81550 |
rs762320696 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438138 | TACTGATTTCACACA[A/G]TACTTTTCACATAAG | 81550 |
rs762340645 | snp | A/G/T | 1.68732e-05 | 0.00290454 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460415 | GCAAATTCAAAAAAT[A/G/T]CGCAATGTTGCTGCA | 81550 |
rs762351146 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477706 | TTGAACCAACATTGC[A/G]TCCCAGGGATAAAGA | 81550 |
rs762393224 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461947 | GAACAGTGGGTATGC[A/G]AGAGGAAATGTGGTA | 81550 |
rs762401684 | snp | A/G | | | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510649 | AGGAAAAGGCAGGGG[A/G]CGAATAAGATCTGAA | 81550 |
rs762404189 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60558280 | CTCAGAGAAAGAATT[C/T]GTTAACTCATCTTAT | 81550 |
rs762412396 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537166 | ATCACTAAATCTTTT[C/G]GAGATTCTGGTATTT | 81550 |
rs762428354 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493243 | TTCTAATGTTATTGT[A/G]TTATATATAATTTAT | 81550 |
rs762431925 | snp | A/C | 1.64833e-05 | 0.00287078 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509858 | CAACAACTTAGAAGC[A/C]GCACTGAACGTACTT | 81550 |
rs762440083 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416786 | ATGTCTATCTTGGAA[-/T]TCACTGTTAAGACAT | 81550 |
rs762480761 | snp | A/G | 1.66355e-05 | 0.002884 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494416 | ACATACCTCTCTTTT[A/G]TCTTTCTCTTATGTA | 81550 |
rs762484472 | snp | A/T | 1.65965e-05 | 0.00288062 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528800 | ACTTCCTCAAGGATC[A/T]GTAGATTATAATAAT | 81550 |
rs762487473 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425761 | GACCAACCCCTCCTC[C/T]TCTTCCTCCTCCTCA | 81550 |
rs762535865 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530374 | GTAGTAAAAACGTAT[-/G]TAAGGGAGTTACAGA | 81550 |
rs762539688 | snp | C/T | 0.000108454 | 0.0073631 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60439708 | TTTCAGATGAAGGCA[C/T]TGAAGCTTGCACAAG | 81550 |
rs762541837 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412986 | TTTTTGTTATTTTCA[A/G]CTTGCTTTTTGCTGT | 81550 |
rs762571796 | snp | A/G | 1.65395e-05 | 0.00287567 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528724 | CTTTTAAAAAAAGAG[A/G]TAACTCTATGCAAAG | 81550 |
rs762576617 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411414 | GCCTTGACATTTTTA[C/T]TAGTTTCTACTTATG | 81550 |
rs762578695 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426702 | ATAGAGAAAATTAAG[G/T]AGAGATTACTCCATA | 81550 |
rs762594073 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416656 | GCTGTCTGCTACAGT[A/C]TGGCTTGTGCTTCTT | 81550 |
rs762635520 | in-del | -/TT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567892 | CCATGCCCAGCTGAT[-/TT]TTTTTTTTTTTTTTT | 81550 |
rs762645638 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418274 | TTGGATTTTTTTCTC[C/T]ATTTAAGTTAGTTAA | 81550 |
rs762648480 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60556962 | GTAATCCCAACACTT[C/T]AGGAGGCTGAGGCGG | 81550 |
rs762658414 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570767 | GTGAACATGAATGAG[A/G]GTGCAGCCAGATGAG | 81550 |
rs762683222 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464295 | GGGAATGCTCAAACA[A/C]CACTGATCGGAATGT | 81550 |
rs762731674 | snp | C/G | 1.64958e-05 | 0.00287187 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528625 | TATGGGCTGAAGACA[C/G]AATCAAATGTGATAG | 81550 |
rs762733884 | snp | A/G | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395222 | TAAGTTATGGCTTGA[A/G]ACTTTGAGACCATGT | 81550 |
rs762737773 | in-del | -/TAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416003 | AAAAATAGAATCAGT[-/TAA]TAATGTTTATTAGTG | 81550 |
rs762746365 | snp | A/T | 1.6593e-05 | 0.00288031 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535248 | GGTACGTGATACATA[A/T]TCTGTACAAAGGCAT | 81550 |
rs762746630 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560337 | GCATTCATACTCCTT[G/T]TTGCTGTTTCAAGTT | 81550 |
rs762796783 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512431 | AACCAATCATGCCTT[C/T]GCAACAGTCCGCCAA | 81550 |
rs762805293 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455075 | CCTGCCACCACGCCC[A/G]GCTAATTTTGTATTT | 81550 |
rs762814151 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468615 | GGATCTTGCATCTGT[A/G]TCTCAAGTTATCCTC | 81550 |
rs762814262 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60485721 | TACAAGATACTTTTG[A/C]AGAAGTATTACTTTC | 81550 |
rs762830927 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565709 | AAATAATTACTTCAT[C/G]TCCTACAGTACCAAA | 81550 |
rs762849514 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417691 | AATCTTTCTGGGCCT[C/G]AACTTCAAAATACAG | 81550 |
rs762910467 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505565 | AAGCAAGCAGCGGAT[C/T]TCTCAGCACAGTGCT | 81550 |
rs762926757 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60397766 | GTCCGCGCGGCTTCT[A/C]CGGGGAGGGGGTGTT | 81550 |
rs762928153 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442486 | TTTCCTGTATTATTA[-/T]TTTTTTGTTGTTCAA | 81550 |
rs762931494 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60509185 | GAATTCTATTCAGGT[C/T]TAGATTTTTAAAAGA | 81550 |
rs762973221 | snp | A/G | 8.24531e-05 | 0.00642026 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60483788 | AGAGCTTATCAAAAC[A/G]CAATAGAAGCAATAT | 81550 |
rs762979544 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522833 | CTCACCAGAAATGAA[C/G]AGATACAGGTGATAA | 81550 |
rs762981729 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460079 | ACAGCAATAAATATA[C/T]CTTTCATCCAGAAAT | 81550 |
rs763020009 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498186 | CTGGGAGGGTCCAGA[A/C]GATATACCCTTGAGC | 81550 |
rs763027341 | snp | C/T | 0.000133806 | 0.00817833 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484760 | ATCCATGTTGATGGT[C/T]GGTATTCTCCCAGTG | 81550 |
rs763041982 | snp | A/C | 1.65198e-05 | 0.00287395 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494556 | CAGAGGGAAAACATG[A/C]AGGTGTCTATAGAGA | 81550 |
rs763064350 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562844 | GAAGAGAATAATTGC[C/T]ATTCCCATTTCCCAC | 81550 |
rs763066243 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446902 | CATGACTCTAGAATC[A/G]GTCACTACTGATCCG | 81550 |
rs763069644 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443113 | TATGTTCAGATGATT[A/T]AAAAAAGTACATGTT | 81550 |
rs763072876 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60408398 | TGGGTAACAGGCAGA[A/G]GTTGGAACAGTTTGG | 81550 |
rs763072877 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424349 | AAACAACTTTATTGA[C/G]TTATAAATCACAGAA | 81550 |
rs763079493 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429169 | TAGTATTTACCTGTT[C/T]AGTGACACATTTAAA | 81550 |
rs763130293 | snp | C/T | 1.66106e-05 | 0.00288184 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510806 | TTCTTTTCTTTCTTT[C/T]TTTTTTTTTTTAGCG | 81550 |
rs763138900 | in-del | -/TT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402693 | AGGAAACCAATTGCT[-/TT]TTTTTTTTTTTTTTT | 81550 |
rs763145419 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571932 | AGATATGAGACTTTA[A/G]GGGAGATAGAGCCCA | 81550 |
rs763156061 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538936 | ATAAGAAGTGTTTTA[C/T]AGTGTGCTAATGTCT | 81550 |
rs763158844 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409967 | GTTGTGGGAGGGACC[C/T]AGGGGGAGGTAATTG | 81550 |
rs763176678 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518145 | AGTGAAAATATACTA[C/T]ACTGCTGCCTCCTCT | 81550 |
rs763179383 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515444 | ATGATAACACACATA[A/G]GTACAAATAGCTAGA | 81550 |
rs763193412 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477111 | AGTAGTGAAAGTGGG[C/T]ATCCTTGTCTTGTTT | 81550 |
rs763238798 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398851 | TTCTGTTCAATAGGA[A/T]TCTCTTCTTTCAGTT | 81550 |
rs763244660 | snp | C/T | 1.65364e-05 | 0.0028754 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529095 | TTTTACAATAGTGGG[C/T]CCAAACGAAGATCTG | 81550 |
rs763260943 | in-del | -/TAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458329 | TAAAACTAGGTAATG[-/TAA]TAATGCATGTGTCCA | 81550 |
rs763279034 | snp | A/G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434074 | GTGACTTCTGAACAC[A/G/T]ACGTGAAGACAGTTA | 81550 |
rs763294671 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484295 | CACTTGTCTTCAGCA[C/T]CAAATTGATTCTCAA | 81550 |
rs763294981 | snp | A/G | 1.66843e-05 | 0.00288823 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509941 | TTTATTAAGCAGTGT[A/G]CCAGATAGTATTGTT | 81550 |
rs763295450 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474376 | GGTGGTAGTGGCCCC[A/C]CCCGGGCCCAGCTGT | 81550 |
rs763328062 | snp | A/G | 6.69748e-05 | 0.00578644 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509711 | TAGTTAAAAGTTTAT[A/G]CCTTGCCTTATCTGT | 81550 |
rs763360223 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433394 | TGACCAGACTGAATG[A/G]TTTGATACTTTTTAG | 81550 |
rs763410858 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405423 | ATCATTCCAAATGCA[C/T]GTACTAAGGGGGAAT | 81550 |
rs763448678 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60550489 | GAGAGGAAAAAACTT[G/T]AACTTGCATGAATTT | 81550 |
rs763464907 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458559 | AAACATTAAATAAAA[A/G]CAAATGTTTCCCTCC | 81550 |
rs763469829 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60408201 | GTGCCTTTCACCTCC[C/T]GCCATGATTCTGAGG | 81550 |
rs763493533 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433832 | TCCGTTTCATTATCT[A/G]TACATTATAGCCAGT | 81550 |
rs763521296 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60479238 | ATTTTTTGATTTCTG[C/T]CTTGATTTCATTGTT | 81550 |
rs763531192 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475881 | CTTTGCCTATTCTTT[A/C]ATGAGGTTGTTTTTT | 81550 |
rs763543702 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441953 | GTTTATATGAATAAT[A/C]CATGCAGTGAATTAC | 81550 |
rs763544730 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548956 | TAGGATTATCATGGT[A/G]GTGAAAAACCAGAAG | 81550 |
rs763551689 | snp | A/C | 1.65592e-05 | 0.00287738 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528984 | AGTTTCATTGGTGTT[A/C]CAAATGGAGAAGTAG | 81550 |
rs763568156 | in-del | -/AA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60448495 | CTGTCTTTTCTCCAC[-/AA]AGTTTCCCCAGAACC | 81550 |
rs763576376 | in-del | -/G | 1.77732e-05 | 0.00298099 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528319 | AAAATAATTATTAAT[-/G]GCAGAGTCTTCATCT | 81550 |
rs763588093 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426769 | CTATAAAACCTTCAC[A/G]TACCATATACTGTCA | 81550 |
rs763598578 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432302 | TATATCTGTAAGCTG[C/T]ATTGAATATATTGAT | 81550 |
rs763618553 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504748 | GGTACCTGGCTCATC[C/T]CATTGGAACTGGTTA | 81550 |
rs763630921 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499405 | TTTTTCTCCATTCTG[G/T]TCCATAAGGTCCACC | 81550 |
rs763635330 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425856 | CAGTAAATATGTTTT[C/T]CATATGGTTTTTGTA | 81550 |
rs763656486 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411428 | ACTAGTTTCTACTTA[C/T]GTGAATAAGCATTTA | 81550 |
rs763668052 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462445 | AGCATGCCTACTTTT[C/G]GTGCCGTAAAAATGG | 81550 |
rs763718726 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486149 | GTTCTTTTTCCAGAT[A/C]TCCATGGTAGTTCCA | 81550 |
rs763724363 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399311 | TATATTGTAGCATTT[G/T]CTACTTTATATTGCA | 81550 |
rs763744390 | snp | A/G | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395925 | AAACAATATACTTGG[A/G]AGCAAATCTCAATAG | 81550 |
rs763757889 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60558281 | TCAGAGAAAGAATTC[A/G]TTAACTCATCTTATA | 81550 |
rs763760810 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60413385 | GGCTCTTGAAGACCA[A/G]TTCTCCTGAGCTGAG | 81550 |
rs763763257 | snp | C/G | 1.65987e-05 | 0.00288082 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494422 | CTCTCTTTTATCTTT[C/G]TCTTATGTAAAGACC | 81550 |
rs763765583 | snp | C/T | 1.6528e-05 | 0.00287467 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467417 | ACTTTTGAAACATTA[C/T]ACTCTTTTTTATTGC | 81550 |
rs763777478 | snp | G/T | 1.72513e-05 | 0.0029369 | splice-donor-variant | TDRD3 | GRCh38.p7 | 13:60485949 | GCAAAGAGCAAGGAA[G/T]TAAGAAATCAAATCA | 81550 |
rs763810375 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503063 | ATCGTTCAAAATAAG[G/T]TTCCTTGACTCTGAA | 81550 |
rs763849776 | snp | C/T | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510699 | ATGCAAGGCCATCAG[C/T]ACCAAGCACATTATT | 81550 |
rs763867847 | snp | C/T | 1.64961e-05 | 0.00287189 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528635 | AGACAGAATCAAATG[C/T]GATAGACCGTATTCT | 81550 |
rs763875268 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552181 | GCAAGTCCCATCTGC[C/T]TTTGAGCCTGTAAAA | 81550 |
rs763882572 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565807 | TTTTCACATTTAGCT[A/C]TAATACTTGAAAATC | 81550 |
rs763899556 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504641 | ATTTGATTCGGTGGT[A/G]GCTGGCAAGATGGCT | 81550 |
rs763914569 | snp | C/T | 1.65734e-05 | 0.00287862 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510807 | TCTTTTCTTTCTTTT[C/T]TTTTTTTTTTAGCGT | 81550 |
rs763932359 | snp | C/G | 1.64849e-05 | 0.00287092 | synonymous-codon, missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567539 | GGAGGAAGAAGGCAC[C/G]TACGATCAAACTCTG | 81550 |
rs763948860 | snp | A/G | 9.97059e-05 | 0.00705996 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535252 | CGTGATACATATTCT[A/G]TACAAAGGCATAAAC | 81550 |
rs763966409 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425190 | ATAATTTGATTAAAA[A/C]ATGGGCAAACGATCT | 81550 |
rs763969200 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555011 | GTCATTCAATTTTCC[-/T]TTATCTAAGTTGACA | 81550 |
rs763974420 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453876 | GTTCATGATATAAAA[G/T]ACAACTTCTTAATTC | 81550 |
rs763989268 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60491294 | ATCAGACATGCATGT[A/G]GTAATAATGTTTAAT | 81550 |
rs764002857 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512432 | ACCAATCATGCCTTC[A/G]CAACAGTCCGCCAAA | 81550 |
rs764024803 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60435314 | TACAGGTGGTTTTTG[G/T]TTACCTAGATAAGTT | 81550 |
rs764052304 | in-del | -/AC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451540 | CACAAATTACAGATT[-/AC]AGTGGCTTTTCCCCT | 81550 |
rs764077417 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493342 | AAAATTGTTTTAGCT[G/T]CTTCTTTTATTATAT | 81550 |
rs764080495 | snp | C/T | 0.00019656 | 0.00991168 | utr-variant-5-prime, intron-variant | TDRD3 | GRCh38.p7 | 13:60397364 | GGCCTAAGCAGCTAC[C/T]ATGGCCCAGGTGGCC | 81550 |
rs764092710 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511734 | CTAGCAGAATTCATT[G/T]TCTTGTGGAAATGAA | 81550 |
rs764095113 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562840 | CATTGAAGAGAATAA[G/T]TGCCATTCCCATTTC | 81550 |
rs764099202 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482618 | TTAAGGAAAGGGCCT[C/T]TTGATAATTTTATGC | 81550 |
rs764124147 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564315 | AGACGTGAGACTTCA[A/G]TCAAATACATTTAAG | 81550 |
rs764142608 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60510970 | CTGGGATTAGTAATC[-/T]TCACCAAACCAGTTT | 81550 |
rs764145229 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443188 | CTTACTCTGTGCAAG[A/T]CATTATACTGAGTGC | 81550 |
rs764154018 | in-del | -/ATATT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60540749 | ATATCTGATAATAAC[-/ATATT]ATAATCTATTTAAAC | 81550 |
rs764154425 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477753 | AATTAACTTTTTGAT[A/G]TGCTGCTGGATTAGT | 81550 |
rs764177348 | in-del | -/GGGCCGCGGGTGCGGGCCG | 0.000218818 | 0.0104576 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397431 | GTCCCGCCGGCTGCC[-/GGGCCGCGGGTGCGGGCCG]GGGCCGCGGGTGCGG | 81550 |
rs764186712 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524650 | ATATATGACTTTATG[A/G]TTTAACTAACCTAAG | 81550 |
rs764188548 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515531 | TTTCTTATATTCTCT[A/T]GGTTCTGTCTTCATG | 81550 |
rs764225606 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401339 | GTATTAGGTATTTTA[A/G]GTAGTCTAGAGATGA | 81550 |
rs764267983 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60521069 | CTCAGTGTTCTCTAG[G/T]GCAAATCAGAGATGG | 81550 |
rs764268443 | snp | C/T | | | intron-variant, synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60547477 | CTCTGCCACTTACTA[C/T]CTATGTGACTTTGGG | 81550 |
rs764268703 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562933 | CTGAAGGAATGGTAA[C/T]ATAAGATAAAGTGGG | 81550 |
rs764284281 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440999 | TTATGTCCTACACTG[A/G]GTCATCTTTTTTTCA | 81550 |
rs764295799 | snp | C/T | 3.33156e-05 | 0.00408126 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528864 | ATTCCTGATTATTTT[C/T]ATGACAGGAAATCAC | 81550 |
rs764313870 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497436 | GAGCTCTCTTTACTA[-/C]CTGATTGGTCGGGTG | 81550 |
rs764315589 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428695 | TGAGACATACGTCCT[C/T]GTGCATCCTGAGACA | 81550 |
rs764319470 | in-del | -/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395403 | AAGATTTTGTCCTCC[-/T]TCATTTTTGGTGGCA | 81550 |
rs764328249 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60483800 | AACACAATAGAAGCA[A/G]TATTGGAACTGAAGG | 81550 |
rs764333247 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430255 | GGAAACTTAACCAAG[C/T]ATGTGATCTCCTTGG | 81550 |
rs764358357 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562171 | TAAAAAAATTATCTG[A/G]GTTTGGTGGTGCGTG | 81550 |
rs764378010 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533557 | GAGGCAGGAGAATCA[C/T]TGGAACCCGAGAGGC | 81550 |
rs764411920 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416771 | TACTTTGGACGGTTT[A/G]TGTCTATCTTGGAAT | 81550 |
rs764419197 | snp | C/T | 1.65029e-05 | 0.00287248 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460490 | ATTACAGATGACTGA[C/T]GGTCATATAAGTTGC | 81550 |
rs764434473 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538990 | AGTATCTGCTTCTTG[A/G]TATCAGGAAATGATC | 81550 |
rs764460840 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468655 | TTTATAAGGGCTGTT[A/G]AATAACTTACTTTAT | 81550 |
rs764461447 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475913 | CTTGCTGATTTGTTT[A/T]AATTCCTTATAGATT | 81550 |
rs764488487 | in-del | -/AAATCATGGTGATGT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523361 | TTATTCTTGCATTTC[-/AAATCATGGTGATGT]AAAACATTGTAGTCA | 81550 |
rs764505323 | snp | C/T | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509833 | CGAGGCAAGCTCTTA[C/T]GGATAATGGCAACAA | 81550 |
rs764507185 | snp | A/C | 5.18077e-05 | 0.00508932 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460407 | TGTGTTTTGCAAATT[A/C]AAAAAATTCGCAATG | 81550 |
rs764514609 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505009 | CAGCACAAAACTGAT[-/G]GCCTTTTGGGCAGAC | 81550 |
rs764523642 | snp | C/G/T | 5.01419e-05 | 0.00500688 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509713 | GTTAAAAGTTTATGC[C/G/T]TTGCCTTATCTGTGG | 81550 |
rs764532614 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515599 | GTGTTGGTTGCCCTC[A/T]GGTATCTTTAGCAGG | 81550 |
rs764551155 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506960 | GTATTCAGGAGACCC[A/G]TCTCACGTGCAAAGA | 81550 |
rs764567370 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559799 | TGCCAGATGAATGGG[-/T]TCTGAAGATTTAATG | 81550 |
rs764576248 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497268 | TAATAGAGTGAAAAC[A/G]GAGCTCCCATAAAAT | 81550 |
rs764614286 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458571 | AAAGCAAATGTTTCC[C/T]TCCTACATTTGAATG | 81550 |
rs764632428 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422694 | ACCCAAGGGAAAATG[G/T]ACTAGAATGAAAAAT | 81550 |
rs764666093 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490843 | ATGAATCTAGCCAGG[C/T]GCAGTGGCTCACGCC | 81550 |
rs764722369 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60408416 | TGGAACAGTTTGGAG[A/G]GCTTAGAAGAAGACA | 81550 |
rs764732004 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522079 | GCATTTTTAATATAG[-/A]AAAAAAATTAAAGGA | 81550 |
rs764740939 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554858 | GTTCCCCCAACCTCT[C/G]TTGAACATCTCAGAT | 81550 |
rs764749057 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548971 | AGTGAAAAACCAGAA[A/G]CTACTTAAGCATCCA | 81550 |
rs764771909 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481004 | CATTCTAATAGGGTG[A/G]CAGGGATTCAGCAGG | 81550 |
rs764798546 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412347 | GCCTTTGATACTTTT[G/T]GATTTAGTTTACTTA | 81550 |
rs764801114 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60556365 | AATAACTTTTCAGAA[A/C]TACCTGATGTAATAT | 81550 |
rs764803275 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424811 | CCCTTTCCTCCTAGA[C/G]CCTGGCAACTTCTCA | 81550 |
rs764815661 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60472076 | GTATATTTTTATTAT[-/A]AAAGTGTGTTTGGTT | 81550 |
rs764818676 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410515 | TGTACTCAGAATGGC[A/G]AGTACTGGCAACCCT | 81550 |
rs764857603 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60531629 | CACAAAGATCATACC[A/C]TGGGTAGTAACTGCA | 81550 |
rs764879609 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467450 | TAAAGAGCTCTTTCA[A/G]TAATGAGTAAAATTA | 81550 |
rs764884890 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570663 | GCCCTCATTGCTGGA[A/C]GGCAGCCATTGTTTA | 81550 |
rs764894161 | snp | A/G | 1.64953e-05 | 0.00287182 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528620 | TGAAGTATGGGCTGA[A/G]GACAGAATCAAATGT | 81550 |
rs764910704 | in-del | -/TG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427665 | GGGCCACTGACACTC[-/TG]TGTAATTTGTATTTT | 81550 |
rs764914707 | snp | C/T | 1.68148e-05 | 0.0028995 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509961 | ATAGTATTGTTTGCT[C/T]TTCAGAGTAATATAT | 81550 |
rs764918920 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429048 | CACTAAGCACTTTGT[A/G]TTTAAGATGCATTTT | 81550 |
rs764926920 | snp | C/T | 3.30082e-05 | 0.00406239 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528476 | TCCTCCTCGAAATGA[C/T]ACCAGGCAGCCAAGA | 81550 |
rs764940854 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460740 | CCAGGCGTGGTGGCT[C/T]AAGCCTGTAATCCCA | 81550 |
rs764993428 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498745 | CCCAAGGAGACCTCC[A/G]GCCTTTTACCAGGGT | 81550 |
rs765026878 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462246 | GAAGAAAGACTTGCC[A/C]TGTAATGGCTCATTC | 81550 |
rs765032100 | snp | A/C/T | 3.34254e-05 | 0.00408801 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494404 | TAAATGCTGTCTACA[A/C/T]ACCTCTCTTTTATCT | 81550 |
rs765045534 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501889 | GATAGTAAAATTTTT[A/C]TGCTTCTTTTTTGTT | 81550 |
rs765054696 | snp | A/G | 4.95577e-05 | 0.00497759 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535230 | CATTCAAACAGAGGC[A/G]TGGGTACGTGATACA | 81550 |
rs765129921 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557965 | GTAGCTGGGACTATA[G/T]GCACACGCCACCACG | 81550 |
rs765135591 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502856 | AGCCTTGATAAAATA[A/G]CCGGTTTTTCTAATT | 81550 |
rs765177430 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468483 | CCTAGCACTAAAATT[A/G]TGTTCATTTCTCATC | 81550 |
rs765186352 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416609 | TGCACATTTGTTTGC[A/G]TTAGTCTTACTTATA | 81550 |
rs765188451 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399301 | TCAGCAATGTTATAT[G/T]GTAGCATTTGCTACT | 81550 |
rs765195694 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406409 | ATTTTTATATTGATC[A/G]TACTTTAAAATATAT | 81550 |
rs765222278 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440518 | AAACCCCATCTCTAG[C/T]ATAGATACAAAAATT | 81550 |
rs765241166 | in-del | -/AAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523165 | TAGGTGTATCAGAAT[-/AAA]ATGAGGATTAGTCTT | 81550 |
rs765257143 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453401 | ACCAATCAATACATA[C/T]ATAAATTAGAGTAAT | 81550 |
rs765285671 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60489361 | CTGTAATGAAGCTTA[C/G]CTTACAACTGCTTTC | 81550 |
rs765384369 | snp | A/G | 0.000198131 | 0.00995119 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483771 | GACTGGATTTTTTCC[A/G]CAGAGCTTATCAAAA | 81550 |
rs765394758 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560765 | TTAATATAACTTTAG[A/C]AAATATAGTATTTAA | 81550 |
rs765408059 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442906 | ATTTACTTTACAGTG[A/G]TGGCTCATTTTCACT | 81550 |
rs765414576 | snp | A/G | 6.60835e-05 | 0.00574781 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467411 | GCTTGAACTTTTGAA[A/G]CATTACACTCTTTTT | 81550 |
rs765426120 | in-del | -/TAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60545683 | ATCAGATAATATAAA[-/TAT]TATTATTATTAGGAA | 81550 |
rs765427132 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496382 | AAGAACCCTAATACA[G/T]ATTTTGGTACCAGGA | 81550 |
rs765438816 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441677 | ATTCTTATTGTGCAT[A/G]TATGTACGTACCCAC | 81550 |
rs765447280 | in-del | -/AGA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451177 | GAGTTTTGGTGGTAG[-/AGA]AGAAGAAAATGCCAG | 81550 |
rs765453201 | snp | A/G | 4.95225e-05 | 0.00497582 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510669 | TAAGATCTGAAGATG[A/G]AGAGGACCTGGGAAA | 81550 |
rs765454994 | in-del | -/ATTTTCATG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436390 | ATGAAAATGTTTAGA[-/ATTTTCATG]ATTTCAGGTCTTAGA | 81550 |
rs765461072 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518074 | CATGATAGCTTTTGT[C/T]AGAGTAACAAGGCCA | 81550 |
rs765492080 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60535610 | AAATCTCTGTTGGAT[A/G]TGCAATGTCATTTAT | 81550 |
rs765496141 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552995 | GATGGAAGGGGATGT[C/T]TCAAAGATCTCTGAA | 81550 |
rs765507725 | snp | A/G | 1.64901e-05 | 0.00287137 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467310 | TGGATTCCTGCTCTT[A/G]AATGACTCTAACACC | 81550 |
rs765521966 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481189 | GATTTCAACAATTCA[A/G]TTGTTTAATTATGAT | 81550 |
rs765524000 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497120 | GAAACACAGTGGACA[C/T]CCTGCTGGATCCGGA | 81550 |
rs765529470 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548872 | TTTTAAACCAGTAAT[A/C]CCATAGTTGCTAATG | 81550 |
rs765559281 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396806 | TGTTTATAAGAAAGT[A/T]AACTTTTGTGCAGAA | 81550 |
rs765613526 | snp | C/T | 0.000270673 | 0.0116303 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397449 | GCCGCGGGTGCGGGC[C/T]GGGGCCCCAGGGAGG | 81550 |
rs765615142 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482295 | CCTCTGTTTGCATCA[C/T]GGCTACAAGCAGAAA | 81550 |
rs765619708 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60449947 | TTTTTGGCACAAGCA[C/T]CTACCTTACCTAGGA | 81550 |
rs765642162 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530240 | CCGTCTGTAGTCTTG[C/T]TTCTTTCACAGTATA | 81550 |
rs765650006 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486919 | CTTATCCATGTTGCT[A/G]AGAATGGCAGGATTT | 81550 |
rs765661410 | snp | A/T | 1.65798e-05 | 0.00287917 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528969 | CCAGTTCGAAGTAAT[A/T]GTTTCATTGGTGTTC | 81550 |
rs765661501 | snp | C/G | 1.67279e-05 | 0.002892 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494590 | GGTAAGGCTAAAGAA[C/G]TAACCACAAATTTAA | 81550 |
rs765667166 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430755 | TTTAATACCAAATAA[A/G]CATTCTAGGGTGAAT | 81550 |
rs765677857 | snp | C/T | 4.99156e-05 | 0.00499553 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528847 | GAGAAAGCCAAACAT[C/T]TATTCCTGATTATTT | 81550 |
rs765678509 | in-del | -/TTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402692 | GAGGAAACCAATTGC[-/TTT]TTTTTTTTTTTTTTT | 81550 |
rs765696209 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473349 | GTTACAATGGCAATT[A/T]CATTTCAATATAAGT | 81550 |
rs765700958 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523655 | CATCTTCCCTCACTG[C/T]AGCCTCCACCTCCCA | 81550 |
rs765720495 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526617 | ATTCTTGGGGGAAAG[-/T]TTTTTTTTTTTTTTT | 81550 |
rs765726032 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60547185 | CACATAAATGGCAAA[C/G]TATAACCAAAAAAAA | 81550 |
rs765762092 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561872 | AGGTTTTTTGTTGTT[-/G]TTGTTGTTGTTGTTG | 81550 |
rs765772369 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433330 | GTCCTCAAAGTCTGA[A/C]GTAAGCATGGGTTCT | 81550 |
rs765781028 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402138 | TTCACATTCCATTAC[A/T]TAGAGGCTTCTTCTC | 81550 |
rs765786059 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457592 | CAGGTAACTCATTCC[A/G]TAAGTGGGTATAGTA | 81550 |
rs765786253 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474304 | GCCCCCTTGTCTTGT[A/G]TCCAATAAATAACAG | 81550 |
rs765793921 | snp | C/G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427505 | TGGGATGTTTGGAGT[C/G/T]GGCTTCGCACGTGTC | 81550 |
rs765826522 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502625 | GGGTTTGTATCTTCA[A/G]ATACCTGTGAGTTGG | 81550 |
rs765844505 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501622 | TCTTTTTAAACAACC[A/G]AAGATTCTTTTTAGG | 81550 |
rs765865328 | snp | C/T | 1.7607e-05 | 0.00296702 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528333 | ATGCAGAGTCTTCAT[C/T]TTAATTTGCATATGG | 81550 |
rs765872481 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451994 | GCTGGTAAAATGCTT[C/T]TCTGAAGAGCAAAAA | 81550 |
rs765881293 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399025 | GACCCCCCCTCCTTT[A/G]GAAAGATTAGTCTCA | 81550 |
rs765886374 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562070 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGTGTGT | 81550 |
rs765904594 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499136 | ATCAAAAACAATATT[G/T]CATCCCTGGAGGGAT | 81550 |
rs765910274 | snp | A/C | 0.000106298 | 0.00728957 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460368 | GATTTTTATTCTTTT[A/C]TGTTTTGACAGCTCG | 81550 |
rs765930908 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514000 | AGAGGTTGGAATGGT[G/T]TGGAGGGCTTAGAAG | 81550 |
rs765962563 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434215 | TGGCTCATGCCTGCA[A/G]TCCTAGCACTTTGGG | 81550 |
rs765973733 | snp | C/T | 1.65323e-05 | 0.00287505 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567682 | GAAGTGGTTTTCATA[C/T]AAAGAAAGATGAAAT | 81550 |
rs765976454 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496020 | AACATTTGAATCAGT[A/G]ACTTGGGAAAGGCAG | 81550 |
rs765980153 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553468 | TTTTTAGCAGTACCC[C/G]ACTCTGCTGGTACCA | 81550 |
rs765982168 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60569401 | TGAAAACTGTAAAAC[A/T]TTGATAAAAGAAATT | 81550 |
rs765993995 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459796 | CAGCTAATTTTTGTA[C/T]TTTTAGTAGAGACGG | 81550 |
rs766003499 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455912 | TCTCTACTAAAAAAG[A/G]TAGAAAAATTAGCTG | 81550 |
rs766040517 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440018 | CCTTTTTTTCACCCA[C/T]TGATCAGTCATAGAC | 81550 |
rs766054441 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60435864 | TTTTCCGTAGTGGTT[A/G]TAGCAATTTACATTT | 81550 |
rs766069283 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568098 | CTGCTGGGCAGCACT[A/G]TCCTAGAATGTGATA | 81550 |
rs766075148 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527540 | TTGGTAATCATGTTA[C/T]AGACATGCTATGTGA | 81550 |
rs766100482 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481002 | GGCATTCTAATAGGG[A/T]GGCAGGGATTCAGCA | 81550 |
rs766108541 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496288 | TACTTAACAAACTCC[C/T]ATATATATATATATA | 81550 |
rs766169958 | snp | C/G | 1.67461e-05 | 0.00289357 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485892 | CCTACAAATGATAAT[C/G]ATGAATTTGAAAAGC | 81550 |
rs766180388 | snp | A/G | 4.948e-05 | 0.00497369 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528574 | TACCTAGAAATAGAG[A/G]TTCTGAAAGACCAAG | 81550 |
rs766192791 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476025 | GTTTCCTTTGCTGTG[C/T]AGAAGCTCTTTAGTT | 81550 |
rs766207892 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541022 | TCAAATTATTTAACT[A/G]TTACTAAGTGGACAT | 81550 |
rs766228299 | in-del | -/ACTC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465627 | TATATAATCTATCTT[-/ACTC]TGTATGGGCTCTTTG | 81550 |
rs766230571 | in-del | -/C | 1.71773e-05 | 0.00293059 | frameshift-variant, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485855 | CGAAGAAAAACATTG[-/C]CAAGTTACAATGCCT | 81550 |
rs766259445 | snp | C/T | 2.06209e-05 | 0.00321092 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485782 | CTAAGTTGACTTATT[C/T]TTACTTGTTTTACTA | 81550 |
rs766263276 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465836 | TTTTCTAATTTATCC[C/T]AAGTATTTACCTTAG | 81550 |
rs766295855 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482148 | TCAGCAGTGACTCAA[A/G]GGAACTCCTTTGAGG | 81550 |
rs766320185 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537168 | CACTAAATCTTTTGG[-/A]GATTCTGGTATTTCT | 81550 |
rs766345741 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419974 | TAGAAGACAAAAAGA[G/T]ATGAAAAGGTATTTT | 81550 |
rs766350000 | snp | A/G | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467287 | TCAGGCATTGTTGAC[A/G]TAAAAAATGGATTCC | 81550 |
rs766357960 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60573225 | ACTCAATTCAGAGGC[C/G]TTCACAGAAGAACTG | 81550 |
rs766370508 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455752 | CAGATTGAGAAATTT[A/C]TTTCTCAAGAGAATT | 81550 |
rs766376598 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60535460 | GTTTTGTTGTATTAT[A/G]CTTTGGAAATAGGTG | 81550 |
rs766385709 | snp | A/G | | | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467284 | CTCTCAGGCATTGTT[A/G]ACATAAAAAATGGAT | 81550 |
rs766449352 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60472937 | TTACTTTTAATGGAA[C/T]TCAGTATGGAAAGTT | 81550 |
rs766449406 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546217 | GACTTTTAGAGACTG[A/G]CTTGTATTGGAACTT | 81550 |
rs766468717 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554770 | ATATAACACATATTT[C/G]ATATGATCATACATT | 81550 |
rs766511525 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405276 | GTCCAGCCTCAACAA[A/G]TAATTCTTAAACAGC | 81550 |
rs766536041 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418244 | CTGTACCATTTCTGA[-/T]CTTGTCCTTTCTGCT | 81550 |
rs766547169 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421456 | GGGATTATGGGAGCT[A/G]CAATTCGAGATGAGA | 81550 |
rs766556320 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520877 | AGTCTAATTCCAAAC[A/G]CTTTGTTTGGGCCCA | 81550 |
rs766571429 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457453 | CTTGTACACTCACTC[G/T]TAGAAGTGCCAATCC | 81550 |
rs766576245 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516967 | CAGGATAAAATTCAG[A/G]CTACATTATTTATAT | 81550 |
rs766581398 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498419 | CTACTGTAATGGACG[A/G]TAGAAGCAAAACGGC | 81550 |
rs766598381 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493770 | TGTCTTTCAAAACCA[A/G]TATTATTTATGTCCT | 81550 |
rs766601026 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406165 | TCTTGCACTCAGAAG[A/G]GAAGACTGGGCTAGA | 81550 |
rs766618877 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563102 | GCATGATGGCTGGTA[-/C]CTGTAATCCCAGTTG | 81550 |
rs766628908 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424177 | CAGGCGCCCGCCACC[A/G]TGCCCGGCTAATTTT | 81550 |
rs766632312 | snp | A/G | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394787 | GCTCAAATATCACCT[A/G]TACGTCCTTTACATT | 81550 |
rs766644699 | in-del | -/AA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60456069 | GTGAGACTATGTCTC[-/AA]AAAAAAAAAAAAAAA | 81550 |
rs766651856 | snp | A/C | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509878 | TGAACGTACTTCTTA[A/C]AAGCAATAAACAGAA | 81550 |
rs766667819 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440388 | TTGTTTGAAATAAAA[A/T]TGTAAGTAAACAGGC | 81550 |
rs766692318 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511713 | CCTCTTACAGGCTCA[C/T]CCATTCTAGCAGAAT | 81550 |
rs766728734 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405819 | TCATGGTTTTGAAGT[A/G]TCCTTGGACTGAAGA | 81550 |
rs766731219 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411307 | TACTTTTACAGTTAC[A/G]GGGTAATGAGAATGG | 81550 |
rs766737132 | snp | A/G | 6.61748e-05 | 0.00575178 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494431 | ATCTTTCTCTTATGT[A/G]AAGACCAAGACATTT | 81550 |
rs766742959 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572843 | TGACAATCTGGTCCA[G/T]CATCAATGTCAGGAA | 81550 |
rs766770569 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495822 | GCCAGTGAGCCAAGA[A/G]CACTGATCTTAGGAG | 81550 |
rs766788063 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499203 | CACAGGGGTGATGAT[A/T]CCCACCACATCCCCA | 81550 |
rs766798242 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60529409 | GGATGCCTAGGGACA[A/G]TCTGTCCCGTAAGAT | 81550 |
rs766823671 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432405 | TGTTATTCATTATGG[C/T]AAAATACTGTATTTT | 81550 |
rs766835503 | snp | A/G | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395791 | ATTCCTGGCTCCTGT[A/G]TATGATGGCCGATGA | 81550 |
rs766840322 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486033 | ATTGTCTTTTCATAT[A/T]AGCTAACTAATTCAA | 81550 |
rs766859888 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60560075 | GGAATAACATTGACT[A/G]TAGAAAAAAGTTCCT | 81550 |
rs766869990 | snp | A/G | 1.64999e-05 | 0.00287222 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467386 | TTACAGAGAGTAAGT[A/G]TAAACTATGGCTTGA | 81550 |
rs766926157 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471478 | GAGACCTTTTTCAGG[A/G]TTGTTTTGGCTATTC | 81550 |
rs766960725 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458123 | GCTTGCTTGGAAATC[A/G]GCATTTGGGGGCAGG | 81550 |
rs766984760 | snp | A/G | 1.66621e-05 | 0.00288631 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535262 | ATTCTGTACAAAGGC[A/G]TAAACTATTTTGAAG | 81550 |
rs767003331 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415432 | TTCAGCCAACCACTT[C/G]GGTGTATCAGGACTA | 81550 |
rs767018152 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465528 | TAAGCTTGGGGCCCT[C/G]AAAATAATTTTTTAA | 81550 |
rs767028145 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450354 | TCTGTTTTTAGTATG[C/T]AACAAATATTATCAT | 81550 |
rs767029888 | snp | G/T | 1.65847e-05 | 0.0028796 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494574 | GTGTCTATAGAGAAC[G/T]GGTAAGGCTAAAGAA | 81550 |
rs767035464 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60413880 | AATTAAAGATAAAAG[C/G]TACAGGTAGAATATT | 81550 |
rs767049775 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60448158 | TTTTCAGCATTTGGG[A/G]ACTTGAGAGTGGGAA | 81550 |
rs767066344 | snp | C/T | | | intron-variant, synonymous-codon | TDRD3 | GRCh38.p7 | 13:60527459 | TAAGAATAATTACAG[C/T]TGCATGTTGATTATG | 81550 |
rs767083567 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396909 | CGCAGCCAACCCGTC[A/G]GTCTCCTCAGGCCTT | 81550 |
rs767112251 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60545148 | TAAGAGAAGTAGAAG[A/G]TATGTTTTCTTCCCT | 81550 |
rs767115167 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548879 | CCAGTAATCCCATAG[-/T]TGCTAATGTCTCCTA | 81550 |
rs767117882 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433405 | AATGATTTGATACTT[C/T]TTAGTGTGATGTAAA | 81550 |
rs767125210 | snp | C/T | 1.66554e-05 | 0.00288573 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460344 | AATAGAGTTTCATGA[C/T]TAGAAAGTGATTTTT | 81550 |
rs767143251 | snp | A/G | 0.000212743 | 0.0103115 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397426 | TGGCGAGTCCCGCCG[A/G]CTGCCGGGCCGCGGG | 81550 |
rs767161683 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500644 | TTAAGGAGAAATGGC[A/G]AAATGTGCGATTATA | 81550 |
rs767187171 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405081 | GAACTGTTAAGTCCA[A/G]TAAATGTCTTTCTTT | 81550 |
rs767203983 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543244 | CATCATAAGAATACA[A/G]AAGTTATTATTTTTT | 81550 |
rs767232191 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493701 | AATATTGTTTAACCA[A/G]ATGTTTCATACTGTA | 81550 |
rs767251762 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487224 | AGAATGGCCAGGTGC[A/T]GTGGCTCATGCCTGT | 81550 |
rs767303723 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426051 | GCTGCTAACACCCGA[A/G]TTCAAGGGTGACTTG | 81550 |
rs767332341 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60513947 | GCAGAAAAGATAACC[C/T]GAAAATGTGGAAGTG | 81550 |
rs767343367 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471048 | TTGTATGAGTTATGT[A/G]TAGATTCTAGATATC | 81550 |
rs767345168 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499322 | CTGTACCAGATGTGG[-/T]TTCATTGCTTGAGCA | 81550 |
rs767363831 | snp | C/T | 8.24151e-05 | 0.00641878 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60483824 | CTGAAGGTGGACCAC[C/T]GCCTTTTGTGCCTTT | 81550 |
rs767410353 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511101 | ATTGATATATCTCTT[C/T]TTTCTCCCCATATTA | 81550 |
rs767463347 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509861 | CAACTTAGAAGCAGC[A/G]CTGAACGTACTTCTT | 81550 |
rs767473302 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416998 | TGTTCTTCTGACTTT[-/A]ACTGATCAGTCTCTC | 81550 |
rs767492561 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464433 | AAGGAAGTCAGCATA[C/T]TGAGGAAGCATCTGC | 81550 |
rs767498162 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60550728 | TGTGTTAGGTTAACT[C/T]ACTGGGATAAAATAG | 81550 |
rs767505318 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440325 | CTCTAGCTGTTTTTT[A/T]TTTCCATAATTGTAT | 81550 |
rs767506352 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468771 | GTAGCTCTGAACTTT[A/C]CATGTAATAGATGTT | 81550 |
rs767520657 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60521354 | TACTGAGTGCCACCT[A/G]TTTGCCTGATTCTGT | 81550 |
rs767522023 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426892 | TGGTATTGCCGACTA[C/T]GCGCATAGGCTATAT | 81550 |
rs767524983 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496741 | GAACTCAGGCATCCT[A/G]TCTCCTGGCTTCAGA | 81550 |
rs767621439 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538674 | TAGGGGCAAAGAAAA[C/T]CTGCTACTTGTGTTT | 81550 |
rs767653758 | in-del | -/TT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477211 | GTTATTATTATTATT[-/TT]ATTGTTATTATTATT | 81550 |
rs767654619 | in-del | -/TGAGAGATGTACAACA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426347 | GTAGGATGAACAAGT[-/TGAGAGATGTACAACA]TGAGGACTAAAGTTA | 81550 |
rs767660262 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418105 | GTCTGTCTTACAAAG[A/G]TATGCATAGCCTCTT | 81550 |
rs767666166 | in-del | -/AAAC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522293 | CAAATAAAAACAAAT[-/AAAC]AAGAAAACTAAAGCA | 81550 |
rs767702433 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505747 | CATACACAAGTATCA[A/G]TAGCCGAATTGATAA | 81550 |
rs767705603 | in-del | -/TTTTTTTTTTTTTTTTTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60435918 | TGACAACATCTATGG[-/TTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTAC | 81550 |
rs767715394 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467976 | AGTTCTTATTATTAC[C/T]GTAGTGTAGGTCTTT | 81550 |
rs767724646 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549276 | ATTATTAGTTTCTAG[C/G]TGCAAGAAAAGTTTG | 81550 |
rs767754176 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511590 | TTACCTTATAGTTTC[-/T]TTTGTGTCAGGAGTC | 81550 |
rs767779245 | snp | A/G | 1.65321e-05 | 0.00287502 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529013 | AGAAATGCCACTGAA[A/G]GGAAGACGAATAGGA | 81550 |
rs767781805 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398190 | TTCAGTAACGCTTTT[C/G]CCAGGCTTGCACAGG | 81550 |
rs767804125 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402532 | GTTTTTAAAATCTAG[A/C]ATTATGATATACCTT | 81550 |
rs767859025 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60558681 | CTCAGACTTTATAGC[A/G]TGTCTGTAACTTTTG | 81550 |
rs767860275 | snp | C/T | 1.6646e-05 | 0.00288491 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460526 | AGTAGAATTTAGTTA[C/T]ATGTCAAAAATAAGG | 81550 |
rs767860310 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462148 | TTGAAGAGTAGGATT[C/T]GTACTTTTGTGTAGA | 81550 |
rs767900072 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60455356 | ATAGGCAGAATTAGT[A/G]TTTCTTCTTCCAAGG | 81550 |
rs767959918 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506771 | CAAAAAAAAGAACAT[C/T]GACACTATGAAGAAA | 81550 |
rs767968842 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484425 | GTTGGTAATCTGTCT[C/T]GCATTTGCTCTTTAA | 81550 |
rs767978458 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473829 | AGTAACGCCCTCGCC[-/T]TGGGAAGGTGCCGAT | 81550 |
rs767983671 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498331 | AAATTTAACTGCAGT[A/G]GGAATAATTGGATCC | 81550 |
rs767992775 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410173 | TGGAACTGTAAGTCC[G/T]GTTAAACCTCTTTTT | 81550 |
rs767993589 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452817 | ATCACTGTTCTTAGT[-/T]TTTTTTTTTTTTAAT | 81550 |
rs768004400 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60573238 | GCGTTCACAGAAGAA[C/T]TGGAGGCGGTTAGGA | 81550 |
rs768004938 | in-del | -/GTTGTTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561872 | AGGTTTTTTGTTGTT[-/GTTGTTG]TTGTTGTTGTTGTTG | 81550 |
rs768013296 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572941 | TTATAGTACCCGACG[C/T]TCTGTATTTTCTAAG | 81550 |
rs768013706 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406002 | AGGTTTTGGACTTGT[A/G]TCCTCAAATCAATTA | 81550 |
rs768019005 | snp | A/G | 1.66214e-05 | 0.00288278 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509929 | TGAGAGGTATAATTT[A/G]TTAAGCAGTGTGCCA | 81550 |
rs768021400 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443985 | AGTCGTAAAATATTC[C/T]GCTTTTTATGTAGAT | 81550 |
rs768028055 | snp | G/T | 3.34074e-05 | 0.00408688 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528933 | GAAAAACATTTTAAT[G/T]TAAATACTGATTATC | 81550 |
rs768038034 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443614 | ATTATGGTAGGTGTT[-/A]AAAGAAGATGGTCCT | 81550 |
rs768043320 | in-del | -/TTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557826 | TTTTCCTGATTTTTT[-/TTTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 81550 |
rs768052927 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429442 | TGCAATATAATTTTA[A/G]ACTTTATTGCTTACT | 81550 |
rs768075419 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499046 | CTGGCTCCCTGACTG[A/G]TAGGGTGAGGGTGAT | 81550 |
rs768079147 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518687 | GGCTTCATCTTTTAT[C/G]AACCTTAAATTATGC | 81550 |
rs768102775 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516817 | CAGGCCTTCATCAAG[G/T]CTTTCATCGGCTTTC | 81550 |
rs768257900 | snp | G/T | 1.65293e-05 | 0.00287479 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494559 | AGGGAAAACATGAAG[G/T]TGTCTATAGAGAACT | 81550 |
rs768267915 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458128 | CTTGGAAATCGGCAT[C/T]TGGGGGCAGGTGTTC | 81550 |
rs768277671 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561794 | TAGCCTCTTAGTTTG[A/T]CTAACTGTTCTTTAC | 81550 |
rs768278917 | snp | A/G | 1.66015e-05 | 0.00288105 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528804 | CCTCAAGGATCTGTA[A/G]ATTATAATAATCAAA | 81550 |
rs768331855 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517571 | GAAATGTGTAGCTAT[C/T]TACCCACAGCCTATC | 81550 |
rs768334899 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572890 | ATAACTGTTACAGAA[A/C]TCCATGATGCCAGCA | 81550 |
rs768378805 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427481 | CTTTTCAAATCTTTT[G/T]TCTTCAGCTGGGATG | 81550 |
rs768397261 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465148 | TAATCTGGTCAGACT[A/G]TCAATTGTTTCAGTG | 81550 |
rs768399218 | snp | C/T | 1.65597e-05 | 0.00287743 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483752 | TGTATAACTGCTCTT[C/T]TGTGACTGGATTTTT | 81550 |
rs768483355 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470593 | CATTATAGTTGGGTT[-/T]TTTTTTTTTTTTTTT | 81550 |
rs768489074 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534738 | TGAGACCAGCCTGGG[C/T]GACATGGTGAAACCC | 81550 |
rs768495664 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486322 | CCCTTATTAATAGCA[A/G]CTTATGAGAAATAGC | 81550 |
rs768497413 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567776 | TTGCCCAGGCTGGAG[C/T]GCAGTGGCGTGATCT | 81550 |
rs768503879 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570997 | GTGGTTTTCTATGTT[C/T]CCTGAGTTAAAACTT | 81550 |
rs768535002 | snp | A/T | | | downstream-variant-500B | TDRD3 | GRCh38.p7 | 13:60574269 | TAAACATTAAAGGGA[A/T]TTTATTGGCTCACTT | 81550 |
rs768536759 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506618 | AAAAACTAGCTGGGC[A/G]TTGTGGTGCATGCCT | 81550 |
rs768566891 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419524 | TCTCAGCAAACTAAC[A/G]TAGGAACAGAAAAAC | 81550 |
rs768569855 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470018 | CCAAACTTAAACTCT[A/G]TACCCATTAAACAGT | 81550 |
rs768570013 | snp | C/T | 3.33433e-05 | 0.00408296 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460421 | TCAAAAAATTCGCAA[C/T]GTTGCTGCACCAAAG | 81550 |
rs768603967 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546539 | ATGATACACTTTCCT[A/G]TTTATTGAAAATATT | 81550 |
rs768609817 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505633 | AAGCTAAGAAACTTG[A/G]AAAAAGGTTAGAGGA | 81550 |
rs768617435 | in-del | -/CTAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399057 | TTTTAGGTCCCGAAC[-/CTAA]ACGTGTTGACTTTGT | 81550 |
rs768618896 | snp | A/C | 1.64819e-05 | 0.00287066 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485750 | TCTAACGAAAACTTG[A/C]ATCTCTTTTGGAACT | 81550 |
rs768643622 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407873 | TTTCTCCCAGAATTC[C/G]CATGTGTTGTGGGAG | 81550 |
rs768652235 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524278 | AGGGAGACCGAGGGC[A/G]GGTGGATCACTTGAG | 81550 |
rs768654794 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404977 | AGGTGCCCTGCACAA[C/G]CTCTCTTTTTGCCTG | 81550 |
rs768660132 | in-del | -/TACT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548742 | AAAATGAAATCATAA[-/TACT]TACGCTGGCAAGGAT | 81550 |
rs768679981 | in-del | -/C | 5.78642e-05 | 0.00537855 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510798 | TTTTTTCTTTCTTTT[-/C]TTTCTTTTTTTTTTT | 81550 |
rs768682391 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527164 | CTTGATCTTTAATCA[A/G]TGACCTGTTTTGTCA | 81550 |
rs768725833 | snp | C/T | 1.6495e-05 | 0.0028718 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528505 | GAAATGAAAAACCGC[C/T]TCGTTTTCAAAGAGA | 81550 |
rs768742358 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523155 | TTTCTTCAGGTAGGT[A/G]TATCAGAATAAAATG | 81550 |
rs768744622 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430641 | AGATGAATAACAACA[C/T]AGTTAGGTTACCATT | 81550 |
rs768757796 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502630 | TGTATCTTCAAATAC[C/T]TGTGAGTTGGGTGAT | 81550 |
rs768773755 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395435 | TCCGAAGAAATTCAA[C/T]GTGTTTCATCAATTA | 81550 |
rs768775799 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432890 | TTGGATATCATGTGC[-/G]GGGGGCTAGTAACCT | 81550 |
rs768809545 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446384 | GGTGCATGCCACCAC[A/G]CCTGGCTAATTTTTG | 81550 |
rs768812864 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60485740 | AGTATTACTTTCTAA[A/C]GAAAACTTGAATCTC | 81550 |
rs768876140 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417688 | CTAAATCTTTCTGGG[C/T]CTGAACTTCAAAATA | 81550 |
rs768890734 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453111 | AAAGAAACTATGCAA[A/T]ACAAAAGTTTAACGA | 81550 |
rs768899516 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447077 | AAAATGATATTTTCT[A/T]GTTTTCTTTTTATAT | 81550 |
rs768917519 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410920 | TCTTTATAAACATAT[G/T]AATTAGATGTTTCCC | 81550 |
rs768951615 | snp | A/C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401972 | GACAGTATAGGTTAT[A/C/G]AAGTGATTATTGCAC | 81550 |
rs768966325 | snp | C/T | 1.88663e-05 | 0.00307129 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529254 | TATACACTAATATTA[C/T]GAAATGTAACATTCT | 81550 |
rs768969234 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400498 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCTAA | 81550 |
rs768975677 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499874 | TGGCGGATTTATCAA[G/T]TGACCCAAAAGGCTG | 81550 |
rs768985609 | snp | A/G | 1.65712e-05 | 0.00287843 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509917 | TGGGTCCTCCTCTGA[A/G]AGGTATAATTTATTA | 81550 |
rs768998874 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527546 | TCATGTTATAGACAT[-/G]GCTATGTGAAATTAT | 81550 |
rs769000899 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564931 | TAAGAAGTGATTGTT[A/T]TGGGTAACCAGATTT | 81550 |
rs769005545 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412195 | ACAGTAACAGAGTTT[A/G]TGGATTGGCATTAAT | 81550 |
rs769041220 | snp | C/T | 6.59674e-05 | 0.00574277 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535142 | AAGCCCTCCATTCTT[C/T]GGGTATGACAGCAGT | 81550 |
rs769044910 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512282 | AGGAAAGACCTGCCC[C/T]CATGATTTACTTACC | 81550 |
rs769126010 | in-del | -/AG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425141 | AATAAGAAATAACAA[-/AG]AGAAGTCATCTTTGA | 81550 |
rs769134887 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511373 | CAAATAAGCTCAGAG[A/C]TAAAATGCTTTTATA | 81550 |
rs769138820 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488836 | CGCTCACTTTGGCCT[C/T]CCAAAGTGCTGGGAT | 81550 |
rs769143429 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454581 | CTTGAGCTAGTGGGG[A/G]TGCTACTTGACTTAC | 81550 |
rs769147355 | snp | C/T | 4.96216e-05 | 0.0049808 | stop-gained, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529101 | AATAGTGGGCCCAAA[C/T]GAAGATCTGGGCCAA | 81550 |
rs769150369 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60489081 | TCGTTTGTCTATTTT[C/T]ACTTGTGTGCCTGTG | 81550 |
rs769170716 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454985 | GTGGCGCGATCTCGG[C/T]TCACTGCAACCTCTC | 81550 |
rs769201809 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441731 | GGGAGGATAATCCAT[G/T]AACAAGTTTTCTTCT | 81550 |
rs769211492 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534305 | GCAACAGAGTGAGAA[C/G]TTGTCTCTAGAAATA | 81550 |
rs769220691 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60509199 | TCTAGATTTTTAAAA[C/G]AGATTTGGATTCTGG | 81550 |
rs769265000 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553802 | GTCCCTCCATTGACA[C/T]GTGGGGAATACAATT | 81550 |
rs769304378 | snp | C/T | 4.94776e-05 | 0.00497357 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467353 | GGTGAAGTGGAACAC[C/T]TTATTGAGAAATGGG | 81550 |
rs769308282 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505368 | GCTTGGCAAATCTGC[C/T]GTAGCCAGACTGCGT | 81550 |
rs769309782 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424374 | ACAGAAAAAAATTCA[C/T]CTCTTTAAAGTGTAC | 81550 |
rs769316631 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516299 | GACAGTAATTTGTCA[A/G]GCTGGTTGGAAAAAA | 81550 |
rs769333776 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60472333 | GTAAAATACACATAA[C/T]GTAAAATTTACCATC | 81550 |
rs769360552 | in-del | -/GTTGTTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561866 | GGGCCCAGGTTTTTT[-/GTTGTTG]TTGTTGTTGTTGTTG | 81550 |
rs769361765 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60396839 | GGCTGGGGACACCTC[G/T]GAGTTTTGCTGCCCG | 81550 |
rs769381176 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495244 | TTCAGCAGTATAACA[A/G]TATTAGGGCATTTGT | 81550 |
rs769392379 | snp | A/C | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467242 | CTTTGCTTTAGCCTG[A/C]ACACACCACCTGGAA | 81550 |
rs769398213 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506520 | GGAGGCCAGGGTGGG[C/T]GGATCGCAAGGTCAG | 81550 |
rs769445890 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516516 | TCTAATGAAAAGGAC[-/A]GTGTACTGGAGCAGA | 81550 |
rs769458249 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533304 | GAAAAATATGAATTT[G/T]TGTTGCCTGTAGCAT | 81550 |
rs769462817 | snp | A/G | 1.78883e-05 | 0.00299062 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494625 | TTATTTCTTAAAATG[A/G]TTCTTTTATTCTTTC | 81550 |
rs769490134 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60403920 | ATACAATAATATGTG[C/T]ACTGAAATACATTTA | 81550 |
rs769494458 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537162 | TAGAATCACTAAATC[-/T]TTTGGAGATTCTGGT | 81550 |
rs769507418 | in-del | -/AT | 3.34373e-05 | 0.00408871 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467206 | GTGTTCTCAGCTTCA[-/AT]ATGTTTTTAACACTT | 81550 |
rs769526283 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451445 | CTTGTTCCAGCTCGT[A/G]AAGTTCATTGTCGGC | 81550 |
rs769550308 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60550113 | TGTCACTAAGAGTAG[A/T]GAGAGCTTAGAAAGA | 81550 |
rs769554768 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445600 | TGGACCTCAAACAAC[C/G]TCTACTCCCATCTGA | 81550 |
rs769576228 | snp | C/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439513 | AAGAAAAGTATGCAC[C/T]GTTCATCTCTTCTAT | 81550 |
rs769578421 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405895 | TAGAGAGCAGCAGAT[C/T]GACTTGACAGATATT | 81550 |
rs769668626 | snp | A/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395107 | ATCAGTAAGCAGAAT[A/T]CATTAGATTGTCCCA | 81550 |
rs769678364 | in-del | -/TATT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548170 | TAAGAATTTGGTGGC[-/TATT]TGTTTGGTCAGTGCT | 81550 |
rs769700941 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460621 | TTAAGAATTTTGAAA[A/G]GTAGGAATGGACCCT | 81550 |
rs769718119 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498770 | CAGGGTAACTGTGCA[C/T]TGGGGAAAGAGAAAT | 81550 |
rs769718513 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484212 | GGGGGAGAGAAAAAT[A/G]AAGCCACACAGAGTG | 81550 |
rs769728591 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544512 | TAGTAAATTCCATTG[G/T]GTATGTGTACATTTT | 81550 |
rs769806180 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60485448 | AGCTCTTAATTACAA[A/T]ACCAAATTTATGTCT | 81550 |
rs769827933 | snp | C/T | 0.00527325 | 0.0510766 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510798 | TTTTTTCTTTCTTTT[C/T]TTTCTTTTTTTTTTT | 81550 |
rs769846135 | snp | A/G | 3.29821e-05 | 0.00406078 | synonymous-codon, missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567527 | TCTTTGCAAATAGGA[A/G]GAAGAAGGCACCTAC | 81550 |
rs769864965 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417629 | TTACAGGTGTGAGCC[A/G]CCACACTGGCCGATT | 81550 |
rs769872946 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555526 | GCTAGTAAGTTGCAG[A/G]GCTGATAGTCAGGTT | 81550 |
rs769890656 | snp | C/T | 1.65449e-05 | 0.00287614 | missense, utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528415 | GACAATACAGATCAT[C/T]AAATACTGAGCAAAA | 81550 |
rs769898314 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523484 | ATATAGCATTCTTTG[A/G]TTAGTTTTCTCATAT | 81550 |
rs769925838 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409887 | GGCCAGGGTTGGAAT[C/G]ATGTGGTTTGGCTGT | 81550 |
rs769928544 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567157 | AAATATTCAAGAAAA[-/T]TTGTCATTATAATGC | 81550 |
rs769961369 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422585 | GAAGTGGACAATAAA[C/T]AGGGACAAATGGGGG | 81550 |
rs769963074 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568898 | AAATTCAGTAAAGTT[G/T]CAGGATACAAAATCA | 81550 |
rs769966689 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554212 | GCATAAATTAGTGTT[C/T]AACCCTGGACAGGCT | 81550 |
rs769980401 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon, missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567608 | CACTCGGCCAACCCA[A/G]CAGTTTTACCAACCA | 81550 |
rs770014780 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532373 | AATAGATTACACCAC[C/G]CTTAACCATTGGGAA | 81550 |
rs770034371 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461701 | GATTTCAGCCTCTTA[A/G]TAGCTCATATGCTAA | 81550 |
rs770068922 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424108 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACG | 81550 |
rs770126897 | in-del | -/TG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518825 | TTCAGAACTAGTCTC[-/TG]TAAAATACCATGAAA | 81550 |
rs770133014 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451710 | TCTTGCAAAGCACTT[G/T]TATCAACTATGTTAC | 81550 |
rs770146747 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399204 | CCTTGGAATGCCCCT[-/G]GCCAGTCAGAATTCT | 81550 |
rs770201624 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498094 | CTCCCTTGGCTTAAT[A/G]TAGAGGAAGGGATAC | 81550 |
rs770204442 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398709 | GTGGAGTTGAATGTT[C/G]AGCACAGAGGGCCTG | 81550 |
rs770265930 | in-del | -/AAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60556106 | CTGCCTCGGCCTCCC[-/AAA]GTGCTGGGATTACAG | 81550 |
rs770292131 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400271 | AGGTTCATTCTCCTT[C/T]AGGATGATATCCCTG | 81550 |
rs770295855 | snp | A/G | 0.000107053 | 0.0073154 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485826 | CATGTCCAAGTGGAT[A/G]GCAGAGAACTTGATC | 81550 |
rs770333331 | snp | A/C/T | 3.33113e-05 | 0.00408102 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467215 | GCTTCAATATGTTTT[A/C/T]AACACTTTTCTCTTT | 81550 |
rs770350854 | in-del | -/TAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446802 | TTAGTAAAATAAGAC[-/TAA]TAATATAGTAAAAGC | 81550 |
rs770376404 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538642 | TTTCTATTTCCTACC[A/C]CTGTATGAGAAAACA | 81550 |
rs770379407 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562641 | CATTAACATTTCATG[A/G]TTCAAAATATCCTCA | 81550 |
rs770383707 | snp | G/T | 0.000133932 | 0.00818217 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484729 | GATAAAAGAAAGTGT[G/T]AAGTCCTATGGTGTG | 81550 |
rs770387736 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502297 | TCACCACTTGATTCA[C/T]AGGAATAAGCAGGGT | 81550 |
rs770391800 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60529294 | TTATAGAAGCTGTCA[C/T]TTTGGAACTATGAGT | 81550 |
rs770396170 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566810 | CTATACTCTTTATGC[-/T]ATTTAATCTGCTTAT | 81550 |
rs770399604 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520810 | ATCATCCCAATTTTA[C/G]AAGGTCACACAGCTG | 81550 |
rs770473022 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60485177 | TTCCTTTTTATTAAT[G/T]AGTTGAGAAAAAGTT | 81550 |
rs770484293 | in-del | -/TTGTTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561864 | ATGGGCCCAGGTTTT[-/TTGTTG]TTGTTGTTGTTGTTG | 81550 |
rs770504643 | in-del | -/AACTA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559507 | TTCGTTCCTGTACTT[-/AACTA]TACTATTTCAACAAA | 81550 |
rs770518951 | snp | A/G | 1.71452e-05 | 0.00292785 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529187 | GAAACCTGGAGATGA[A/G]TGTTTTGCACTTTAT | 81550 |
rs770533103 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416555 | CGAATGCCTTTTCTT[C/G]TTGTTGTAATGTTTA | 81550 |
rs770546173 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505288 | ACTAAGCCTTAGTAG[A/G]CAGTTTTCCCCTCAC | 81550 |
rs770594102 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566820 | TATGCTATTTAATCT[C/G]CTTATCCTAATTTCC | 81550 |
rs770667029 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562355 | AGAAAAGAAAAGCTG[A/G]TTCAGCTTTCAATTT | 81550 |
rs770670113 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407993 | TTTTTCAGGGGTTTC[C/T]GCTTTTGTTTCTTCC | 81550 |
rs770691663 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498300 | TAACAGTGTGAACTG[C/T]AGTCACTCAACTACA | 81550 |
rs770698497 | in-del | -/T | 0.000801165 | 0.0199985 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510780 | TTTAAAGTTGATTCC[-/T]TTTTTTTTCTTTCTT | 81550 |
rs770710929 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555848 | AAACCAACCTATTTC[-/T]TTTCTTTTTTTTTTT | 81550 |
rs770722900 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418480 | TTGAGGTCAGTACCA[C/T]GGTTTTTTCATCTTT | 81550 |
rs770733845 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522936 | AATCATGTGTTTTAG[C/T]TTCAGTTAGATTTCA | 81550 |
rs770749240 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459707 | CTCACTGCAACTTCC[A/G]TTTCCCGGATTCAAG | 81550 |
rs770758097 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409630 | CCCTGTAACCCCTTT[A/G]TTTTGGCCAACCTCA | 81550 |
rs770769232 | snp | C/G | 1.6507e-05 | 0.00287284 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528681 | AAAGATACTTCATAT[C/G]CTTTAGGTTCTCAGC | 81550 |
rs770819975 | snp | G/T | | | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60483825 | TGAAGGTGGACCACC[G/T]CCTTTTGTGCCTTTT | 81550 |
rs770830892 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442793 | TTATAGAGGAGTAAA[G/T]TAACTGGGTTTAGAG | 81550 |
rs770855657 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557962 | TGAGTAGCTGGGACT[A/G]TAGGCACACGCCACC | 81550 |
rs770896443 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60456763 | TGTAGTGGCGCAATC[A/G]TGGTTCACTGTAGCC | 81550 |
rs770900203 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469978 | AGCTGGTACCACCAT[C/T]CACTTCCCTAACTTT | 81550 |
rs770925976 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533202 | CTGGAAAGGAAACAC[C/T]GTGGATTCACTTAAT | 81550 |
rs770949856 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497985 | AATATTGCAGCTCGG[A/G]GGGTTAAAAAAAAAG | 81550 |
rs770951780 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60556142 | TGAGCCACCGCACCC[A/G]GCCCAACCTATTTCT | 81550 |
rs770966516 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60414758 | GTTTTGAAATGGTCT[A/G]CTAATTTTAATAGAA | 81550 |
rs770983320 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433835 | GTTTCATTATCTATA[C/T]ATTATAGCCAGTGAG | 81550 |
rs770990187 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398450 | GAGCTGCTGGAGATG[A/G]CACAGGGAAGCGCTT | 81550 |
rs771000037 | in-del | -/TA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60535707 | GCATATATATTGACG[-/TA]TATATATGTACAGAT | 81550 |
rs771001460 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487769 | CCACTGCTTTCCTTT[C/T]CTTTGGATAAATACC | 81550 |
rs771005453 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568681 | TATGATCTGGAACAA[C/G]ACAAAGATGTCCATT | 81550 |
rs771016863 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433178 | ATTTCAGGAAGTCAA[A/G]TTGCAGTTCAGATTT | 81550 |
rs771024705 | snp | A/G | 0.000364365 | 0.0134926 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567501 | CCATTTTGAACATGT[A/G]AAATCACTACTCTTT | 81550 |
rs771041808 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570553 | TCCAGCAATTCCACT[A/G]CTGTGTATTTATCCA | 81550 |
rs771054595 | in-del | -/AT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410916 | AAAGTCTTTATAAAC[-/AT]ATTAATTAGATGTTT | 81550 |
rs771065387 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454016 | TTTACATATTTACAA[A/T]CATAACTTTATATTC | 81550 |
rs771067426 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422428 | GAAACAAATTTGCAC[A/G]CAAACCTAGGAAAAT | 81550 |
rs771089072 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482314 | TACAAGCAGAAAGCC[A/G]TAGCTCACCTGTTTT | 81550 |
rs771093603 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567444 | AGAGAGATATTATTA[A/T]AATAGGGACCATACA | 81550 |
rs771094106 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458352 | TGTGTCCATTTAACT[A/G]TACAAAGAAAAGGCA | 81550 |
rs771111167 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451007 | TATTTAATGTTTTCT[A/G]TTACACAAAAAGCTC | 81550 |
rs771115644 | snp | A/G | 1.65386e-05 | 0.00287559 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510651 | GAAAAGGCAGGGGGC[A/G]AATAAGATCTGAAGA | 81550 |
rs771138959 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533115 | AAGAGGGGAGAGATA[G/T]GAAGGTATAACAAGA | 81550 |
rs771147210 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466656 | AGCTGGTCGTGGGGG[C/T]GCATGCCTGTAATCC | 81550 |
rs771185330 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475294 | CCCATCTCTGTGTCC[A/T]TGTGTACTCAGTGTT | 81550 |
rs771200018 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60480267 | AGCTTAGTTTGGTAG[G/T]ATATGAAATTCTTGG | 81550 |
rs771203453 | snp | A/G | 4.94645e-05 | 0.00497291 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535202 | AAGAGGTGCTACTGA[A/G]CAATATCAAGCCCAT | 81550 |
rs771204173 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561866 | GGGCCCAGGTTTTTT[G/T]TTGTTGTTGTTGTTG | 81550 |
rs771214596 | snp | A/G | 8.27287e-05 | 0.00643098 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483756 | TAACTGCTCTTTTGT[A/G]ACTGGATTTTTTCCG | 81550 |
rs771224525 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520620 | CTACATTATTTGTTC[C/T]TTTTACCTATTTGTT | 81550 |
rs771253026 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426649 | AAGTTGCCCCCATTA[G/T]AGTTAGAAAGCTTAA | 81550 |
rs771253487 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412672 | TTGAATTGGTGTTAT[A/G]AAACTTATCTGGGCC | 81550 |
rs771258271 | snp | A/G | 1.65231e-05 | 0.00287424 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529068 | ACAGCTGTACCCTGT[A/G]ATGATAAAATATTTT | 81550 |
rs771310371 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500284 | CAGCATTCCATTATC[A/C]AATGGAAGTTGTATA | 81550 |
rs771312408 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538472 | AACACACATGAGATG[C/T]ACAGCTTATTATTAA | 81550 |
rs771344372 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507581 | AACAACCTTCTCCTG[A/C]ATGACTACTGGGTAA | 81550 |
rs771362960 | in-del | -/AAAAAAA | 1.65244e-05 | 0.00287436 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467415 | AACTTTTGAAACATT[-/AAAAAAA]ACACTCTTTTTTATT | 81550 |
rs771391365 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505156 | GCTCAGCGGATCCCA[-/C]CCCCACAGAGCCCAA | 81550 |
rs771441620 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420811 | TAGCCGGGCGTGATG[A/G]CGGGCGCCTGTAGTC | 81550 |
rs771464099 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427520 | CGGCTTCGCACGTGT[C/T]ATTTGGAGGTCAGTC | 81550 |
rs771470564 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60414851 | ACACTTGGACAACTT[G/T]TGGATTCTGTAGAAT | 81550 |
rs771474082 | snp | A/G | 0.000115355 | 0.00759368 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509792 | TCTGAAGCACATAAC[A/G]GAAATGGGCTTCAGT | 81550 |
rs771487632 | in-del | -/GTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492753 | TTGGTAATTGAAGAT[-/GTG]GTTTTAATTTTGATT | 81550 |
rs771489783 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553832 | TTGGGAAAAGATTTT[C/G]GTGGGGACACAGAGT | 81550 |
rs771509883 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464992 | GAGGTAATAGATATC[C/T]CATTTTTACCCTGAT | 81550 |
rs771525668 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501185 | ACTCCTGTATCATTC[A/C]CCCCGCTGGAGTGGT | 81550 |
rs771527198 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446246 | TATTTTTTCTGAGAT[A/G]GAGTCTTGCTCTGTT | 81550 |
rs771583900 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562262 | AGGTTGCAGCGAGCC[A/C]AGATTGCACCACTGC | 81550 |
rs771593708 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60449577 | ATAATTACTTTGTGA[A/T]TGAATACGAGCAACT | 81550 |
rs771615809 | snp | A/T | 1.73225e-05 | 0.00294295 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509668 | TTACATAAGTATGGG[A/T]TGTAATTTTTAGTTA | 81550 |
rs771661683 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467162 | GCCTGACAGGCCCCG[A/G]TCTGTGTTGTTTCCC | 81550 |
rs771683042 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428567 | GTTTATACAATAGTG[C/T]AGTGGGGGTACAGAA | 81550 |
rs771701039 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515834 | TGAATCTCCACTTTG[A/G]TGGAAAATTTGGTTA | 81550 |
rs771738291 | snp | C/G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492331 | TTCTAGTATATTAAC[C/G/T]AAAATAGTAAATACC | 81550 |
rs771771180 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416309 | TTAACTAAGGAAGTT[C/T]TAAGAACAGATTTAC | 81550 |
rs771792522 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473479 | GCGGCAAGCCACCCA[C/G]GTGCCAAGGCAAGAG | 81550 |
rs771797752 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451763 | CAATTGAGCCATATC[A/T]TTTGTGGCACTTGAT | 81550 |
rs771833106 | snp | C/G | 1.6495e-05 | 0.0028718 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528536 | CTCCCAAAATTCAAA[C/G]TCAGTTTTAGAAGGC | 81550 |
rs771846282 | snp | A/G | 4.9525e-05 | 0.00497595 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567662 | AAAGGTAAACTTAAC[A/G]TTGTGAAGTGGTTTT | 81550 |
rs771870477 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507533 | CTCAGGATTAAGAAA[A/C]TCACTCAGAATGGCA | 81550 |
rs771872647 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570762 | AGGCAGTGAACATGA[A/G]TGAGGGTGCAGCCAG | 81550 |
rs771911265 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406048 | CTGTTAGAAGACGGT[C/T]GCATTTTTGGGGGTT | 81550 |
rs771918418 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506714 | GTGAGCTGAGATTGC[A/T]CTACGGCACTCCAGC | 81550 |
rs771926398 | in-del | -/AG | 0.000604305 | 0.017372 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528322 | AATAATTATTAATGC[-/AG]AGTCTTCATCTTAAT | 81550 |
rs771930120 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459523 | ATATGTCAATTACAA[A/C]TCATACTTCTTCAAC | 81550 |
rs771958620 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497006 | GAACCCAGCAACTAG[C/T]GTTCAGCTCAATTAG | 81550 |
rs771966533 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60529608 | AAAGTAAAATTCTGC[A/C]GATTTTCAGTTGAAG | 81550 |
rs772001017 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407957 | TTGTGATAGTGAATA[C/T]GTCTCGTGAGATCTG | 81550 |
rs772003953 | in-del | -/TTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561864 | ATGGGCCCAGGTTTT[-/TTG]TTGTTGTTGTTGTTG | 81550 |
rs772012217 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495711 | CTCAGATGATCCACC[A/C]GCTTCTTCGGCCTCC | 81550 |
rs772016675 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467205 | TGTGTTCTCAGCTTC[A/G]ATATGTTTTTAACAC | 81550 |
rs772074135 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458295 | TAAAGTGACATGTCC[A/G]CTTTGTGAGCAATAG | 81550 |
rs772082380 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568948 | TTTCTATATGTCAAC[C/T]GCAATTGTTTTTTTT | 81550 |
rs772102721 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541320 | TTACAGGCACCCGCC[A/G]CTATCCAGGCTAATT | 81550 |
rs772126078 | snp | C/T | | | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528910 | AAGCTTTCAGTGGTA[C/T]AAAAATTGAAAAACA | 81550 |
rs772142255 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486550 | TGATACGTGTATACA[A/C]TATGTAATGATGAAA | 81550 |
rs772151079 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412354 | ATACTTTTTGATTTA[C/G]TTTACTTAATATTCT | 81550 |
rs772154015 | snp | A/C | 1.91823e-05 | 0.0030969 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485986 | GTTTTATTTCTTATC[A/C]TTATGTTCTATTTAG | 81550 |
rs772156733 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524443 | ACCCGGGAGGCGGAG[G/T]TTGCACTGAGCCGAG | 81550 |
rs772164699 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511478 | TTTGAGAAAACAAAT[A/G]TTTGATGTGGGCAAG | 81550 |
rs772178046 | snp | A/G | 1.65239e-05 | 0.00287431 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460444 | CACCAAAGGATAATG[A/G]AGAATCTCAGGCTGC | 81550 |
rs772183727 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447270 | GAGAGGCATTAAATG[A/G]TACGGACCAGGAACA | 81550 |
rs772196123 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565493 | CTGGTTAGTTCAGTT[C/T]GTGAATTCTTTAAAC | 81550 |
rs772203438 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417271 | TTCTCCTGCCTCAGC[C/T]TCCCAAAGTGCTCGG | 81550 |
rs772209746 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432989 | TTTTATTCAGGGGCA[A/G]TTAAGAACACCATGT | 81550 |
rs772227085 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457120 | AGTATAAGAAACTGA[A/G]TATTGTAAGCAGAAT | 81550 |
rs772242656 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553621 | GTCTCTGGAAACTTA[A/G]AATCATGGCAGAAAG | 81550 |
rs772244042 | snp | C/G | 0.000115493 | 0.00759825 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528661 | ATTCTAGATATGACA[C/G]AACTAAAGATACTTC | 81550 |
rs772246082 | snp | A/C | 1.68778e-05 | 0.00290493 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485875 | TTACAATGCCTGTCA[A/C]ACCTACAAATGATAA | 81550 |
rs772247660 | snp | C/T | 1.8987e-05 | 0.0030811 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529264 | TATTACGAAATGTAA[C/T]ATTCTAGTGGGACTT | 81550 |
rs772273614 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431938 | TTATATATAAGCCAC[A/G]GAGAAAATTAAATTT | 81550 |
rs772314134 | snp | A/G | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467377 | AAATGGGAGTTACAG[A/G]GAGTAAGTGTAAACT | 81550 |
rs772325513 | snp | A/G | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396299 | CCGCAGAGGTGAAAG[A/G]CCAAGAAGGTGGAGC | 81550 |
rs772328384 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492172 | TCCATACAATGGAAA[A/G]AAAATTATAAGTAAA | 81550 |
rs772328765 | snp | A/G | 1.66247e-05 | 0.00288307 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510635 | GCATCTAAAGGTAGA[A/G]GAAAAGGCAGGGGGC | 81550 |
rs772334850 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434168 | CTAAAATCCCTTTTT[-/A]AAAAGTTTTGAGCAC | 81550 |
rs772355806 | in-del | -/TTTTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561861 | CTATGGGCCCAGGTT[-/TTTTTT]TTTTGTTGTTGTTGT | 81550 |
rs772384044 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425643 | ATGAATAAAGAAAAT[A/G]TGGTATATACAGTTG | 81550 |
rs772385358 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487726 | TTGTGACTAGTGCTG[C/T]AGTAAATATGGGAGA | 81550 |
rs772400988 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60437235 | GGGTTCAAGCAATTA[C/T]CCTGCCTCAGCCTCC | 81550 |
rs772416493 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398128 | ATTATGCGAAATTAG[G/T]CAGTTTCTGGAATTG | 81550 |
rs772460267 | in-del | -/AT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60535909 | ACAGGAATACAAGAC[-/AT]ATTAGAATTAGCTCT | 81550 |
rs772470378 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411108 | ATATCTAGCTGCTCT[C/T]TGCAACACAGACACC | 81550 |
rs772471668 | snp | A/C | 1.65737e-05 | 0.00287864 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510769 | AGGTAAGCTAATTTA[A/C]AGTTGATTCCTTTTT | 81550 |
rs772490405 | snp | C/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439394 | ATATTTGTATAATAG[C/G]AAAGAGCAGCTTATA | 81550 |
rs772570065 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433326 | GTAGTCCTCAAAGTC[-/T]TGAAGTAAGCATGGG | 81550 |
rs772578488 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415279 | CTTTGAGAATTACCA[A/G]TTCCACTCTGTGGAC | 81550 |
rs772590322 | in-del | -/TTTTCT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425875 | ATGGTTTTTGTAACA[-/TTTTCT]TTTTATTGTAGGAAT | 81550 |
rs772597266 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563976 | CTCCTTTTTGCATTG[G/T]TTTTTGTCTTTTGTT | 81550 |
rs772654923 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478959 | CAGGCACACACCACC[A/G]TGCCTAGCTGATTTT | 81550 |
rs772658927 | snp | C/T | 3.29734e-05 | 0.00406025 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535182 | CATTGACTACGGAAA[C/T]TATGAAGAGGTGCTA | 81550 |
rs772668023 | in-del | -/C | 0.000384106 | 0.013853 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510789 | GATTCCTTTTTTTTT[-/C]TTTCTTTTCTTTCTT | 81550 |
rs772673493 | in-del | -/A | 0.00028173 | 0.0118653 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484674 | TAAAAAATAATGTTG[-/A]TTTTTTTTTTTTACT | 81550 |
rs772694704 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548199 | GTGCTTTGAATATTA[C/T]CTGATTTGCCTCAGC | 81550 |
rs772720810 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482013 | TCCCTGTCCTGAATG[A/C]ATGTCCAAAGAGTTT | 81550 |
rs772740201 | snp | C/T | 1.7315e-05 | 0.00294231 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509671 | CATAAGTATGGGATG[C/T]AATTTTTAGTTAAAA | 81550 |
rs772743020 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463641 | AATATCCAGAATATA[C/T]AAGGAGCTCAAATAA | 81550 |
rs772762092 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60529720 | TAAACCATTGCTTCT[C/T]GGCCTTTTGGCTAAG | 81550 |
rs772776009 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537165 | AATCACTAAATCTTT[C/T]GGAGATTCTGGTATT | 81550 |
rs772779405 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400516 | TTTGGGAGGCTAAGG[C/T]GGGTGGTCAGGAGTT | 81550 |
rs772782969 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546670 | GGAAAAAAGTGGTCA[C/T]ACCAGGCTGCAGGTA | 81550 |
rs772786171 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415588 | ATAACTCATTCACAC[A/T]CTTAAAGAATATGAG | 81550 |
rs772830051 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451914 | TTGATTGAAATTGCA[C/T]TGAATCTGCGCATTA | 81550 |
rs772831358 | snp | G/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509800 | ACATAACGGAAATGG[G/T]CTTCAGTAAGGAAGC | 81550 |
rs772855484 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428653 | TGATTTTTAGGGGAA[A/T]TCAATGGGCTTGGAG | 81550 |
rs772863695 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469743 | TGGAAGTGAAGAAGC[A/G]CTAAGCATTCAGTAA | 81550 |
rs772870938 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561669 | TCTGAGATTTACGAT[A/G]CCTGTATTCCTTACC | 81550 |
rs772876718 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418250 | CATTTCTGATCTTGT[-/C]CTTTCTGCTTGGATT | 81550 |
rs772901953 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458299 | GTGACATGTCCACTT[G/T]GTGAGCAATAGTGAG | 81550 |
rs772921934 | snp | G/T | 8.24613e-05 | 0.00642058 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528554 | AGTTTTAGAAGGCAG[G/T]GGATTACCTAGAAAT | 81550 |
rs772932760 | in-del | -/CATT | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395505 | CTCCAGTAAAAAACC[-/CATT]CTTTAAGAGAATTTA | 81550 |
rs772999156 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502444 | AACAAATTATGATAG[A/G]ACTGTGTTTTTTGTA | 81550 |
rs773011474 | in-del | -/GA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60471499 | TGGCTATTCAGTATT[-/GA]GAGATTCCTTATGAA | 81550 |
rs773017834 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60480925 | CTGGTGGGAAGCCCT[C/T]TGGTATTGGTAGTTG | 81550 |
rs773062859 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495497 | AGATGGCATTTCACT[C/G]TTGTTGCCCAGGCTG | 81550 |
rs773073991 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407973 | GTCTCGTGAGATCTG[A/T]TGGGTTTTTCAGGGG | 81550 |
rs773122868 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TDRD3 | GRCh38.p7 | 13:60397157 | GAGCCCCACACCAGG[C/T]CGGCCCCTACGGCCG | 81550 |
rs773122882 | snp | A/T | 2.45354e-05 | 0.00350244 | missense, utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528442 | AAAATGGAGTAAAAG[A/T]TAATAATCATCTGAG | 81550 |
rs773142441 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552055 | TTCTCCCAAATCTCA[C/T]ATCCTTTTCACATTT | 81550 |
rs773147380 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562203 | CTGTAATTCCAGCTA[C/T]TCGGGAGGCTGAGAC | 81550 |
rs773151418 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498164 | TCTTTAGACCTACTC[A/C]TTCCAGCTGGGAGGG | 81550 |
rs773163121 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512379 | CCATATCGTTCCACC[C/T]CCAGCCCCTCCCAAA | 81550 |
rs773170374 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60531299 | ACTCAGACTACTTTC[C/T]AAAATTCAGGAACTG | 81550 |
rs773204546 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553541 | GAGACTGGGTAATTT[A/T]TTTTTTTTAAATAAA | 81550 |
rs773206494 | snp | G/T | 9.90688e-05 | 0.00703737 | intron-variant | TDRD3 | GRCh38.p7 | 13:60567665 | GGTAAACTTAACATT[G/T]TGAAGTGGTTTTCAT | 81550 |
rs773239265 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60522847 | ACAGATACAGGTGAT[A/T]AAATTGAAGGTAACA | 81550 |
rs773246039 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467459 | CTTTCAATAATGAGT[-/A]AAATTAGTTCTTTGT | 81550 |
rs773256701 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441458 | ATATGTGGTTAAATA[C/T]TGCAGTCCAAAGCTA | 81550 |
rs773286898 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410870 | TGCTTTGGTTTTATG[-/T]TTTTTTCCCTGTTTA | 81550 |
rs773315859 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486554 | ACGTGTATACAATAT[A/G]TAATGATGAAATCAG | 81550 |
rs773317947 | in-del | -/ACACAC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469420 | GTAACCTTCTCACCA[-/ACACAC]ACACACACATACACA | 81550 |
rs773344732 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427532 | TGTCATTTGGAGGTC[A/T]GTCAGGTGTAGGTAG | 81550 |
rs773360624 | snp | G/T | 1.95904e-05 | 0.00312966 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485993 | TTCTTATCATTATGT[G/T]CTATTTAGATTATTT | 81550 |
rs773385220 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419817 | AAAAAAAAGAATAGA[C/T]GGATGAAAGCAGAAA | 81550 |
rs773385909 | snp | C/T | 1.67072e-05 | 0.00289021 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535059 | CTCAAATATTGCCCT[C/T]TATAGACAATACCAG | 81550 |
rs773407969 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487741 | CAGTAAATATGGGAG[A/T]TATCTCTTTGACCCA | 81550 |
rs773440068 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433065 | CTATCCATTTGTGAA[A/G]AATGTTTTCACTCTT | 81550 |
rs773454099 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451572 | GTCCCTCTACCAGAA[A/G]TATTTTACCAACACA | 81550 |
rs773470891 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421397 | AGGAAAAACTTGCCT[G/T]CTTGATTCAATTACT | 81550 |
rs773532677 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559944 | TGAGGTGATGGATAT[A/G]TTAACCTTGATTGTG | 81550 |
rs773539459 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426636 | GTACAGATGACCAAA[A/G]TTGCCCCCATTAGAG | 81550 |
rs773551776 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532453 | AACCACAAATTGAAG[-/A]GGTGGCTTCTAAATG | 81550 |
rs773583533 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460860 | ATACAAGAATTAGCC[A/G]GGCATGATGGCGGGT | 81550 |
rs773621222 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60535392 | TAATTCAATGCTTAC[A/G]CTGAATGAACTACAA | 81550 |
rs773629924 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425646 | AATAAAGAAAATGTG[G/T]TATATACAGTTGATC | 81550 |
rs773679063 | snp | C/G | 3.29913e-05 | 0.00406135 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467378 | AATGGGAGTTACAGA[C/G]AGTAAGTGTAAACTA | 81550 |
rs773702534 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60519060 | TTCTTTGCATATGAT[A/G]ATATTATTACTTTTT | 81550 |
rs773705441 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537296 | CTTTCTTCTTTATCT[A/G]CATAAATAATTAACT | 81550 |
rs773717932 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411122 | TTTGCAACACAGACA[A/C]CTGCCATAGTACTCA | 81550 |
rs773765043 | snp | A/G | 1.65534e-05 | 0.00287688 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60510646 | TAGAGGAAAAGGCAG[A/G]GGGCGAATAAGATCT | 81550 |
rs773777718 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463659 | GGAGCTCAAATAATA[A/G]CAAAAAACAAAAAAA | 81550 |
rs773779672 | in-del | -/ATA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431266 | AGCTTCAACAGGAGT[-/ATA]ATATTTTACTTGTGA | 81550 |
rs773793131 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452015 | AGAGCAAAAAATAGC[C/T]CTGACACATAGCATT | 81550 |
rs773793408 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552659 | ATTGCCCTAGTAGAG[G/T]TTCTCCATGAGGGCT | 81550 |
rs773794473 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517710 | ACCCCAAATTTCTAG[A/C]TAGTACTTTAAGCTT | 81550 |
rs773795974 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495418 | TCGTGAGAGACTGGA[A/G]TTTTATTATACTCAA | 81550 |
rs773823813 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60489821 | CCAGAAATACATAAA[A/C]TTATGGAGTTTCAGA | 81550 |
rs773829214 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60463650 | AATATATAAGGAGCT[C/G]AAATAATAGCAAAAA | 81550 |
rs773852552 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465236 | ATTCATTAGCAATTT[C/T]TTTGGAGGTAAAGAG | 81550 |
rs773870173 | snp | A/G | 1.64871e-05 | 0.00287111 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535194 | AAACTATGAAGAGGT[A/G]CTACTGAGCAATATC | 81550 |
rs773887446 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544643 | TTGAATAGTATATTA[A/G]TTCATTAAAAGCTTG | 81550 |
rs773906818 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395594 | GAATCACACGACATG[C/T]GAGAACAAATGACTT | 81550 |
rs773942013 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450133 | CCTTCCCTTTTACTT[C/T]AGAGATAAGAGAATT | 81550 |
rs773955474 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60413494 | ATAAAATGGTGTCAA[A/T]ATTATACCTACTTCA | 81550 |
rs773956682 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486366 | TGAATAAAAATCAGC[C/G]GATCTGTCACTGTGT | 81550 |
rs773972093 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481808 | GCTTAGATGCTGGAC[A/G]TTGTGATGTTGGTAG | 81550 |
rs773985738 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442039 | AACCTTGTAAGCTGG[C/T]CTTTCTAAAGATAGC | 81550 |
rs773989104 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553014 | AAGATCTCTGAAATG[C/G]CCTAGAGACATTTTC | 81550 |
rs774009961 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60558375 | TTGTGATTAGTGCTC[A/T]TATGTCTTAACCATA | 81550 |
rs774043032 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415369 | TATTATTTTATTATC[A/T]GATTATATTATTCTG | 81550 |
rs774043203 | snp | A/G | 1.65329e-05 | 0.0028751 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494561 | GGAAAACATGAAGGT[A/G]TCTATAGAGAACTGG | 81550 |
rs774091877 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567631 | ACCAACCACCCCGGG[C/T]TCGGAACTAATAGGA | 81550 |
rs774160452 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60568932 | TACAAAAATGCTACT[A/G]TTTCTATATGTCAAC | 81550 |
rs774183380 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546556 | TTATTGAAAATATTT[A/G]AAGTGGTCATGAAAA | 81550 |
rs774215994 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470866 | GGGATTATAGGTGTA[A/C]GCCACCATGCCCGGC | 81550 |
rs774226567 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461817 | GTAACCAGGAGTGGG[G/T]TTAAAATATGAGTAG | 81550 |
rs774247565 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567541 | AGGAAGAAGGCACCT[A/G]CGATCAAACTCTGGA | 81550 |
rs774250895 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498244 | GCAGCACAGGCATCT[C/T]TGAAGATGCCCTGTA | 81550 |
rs774254333 | in-del | -/ATGT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562596 | TAGAATAAGTGGTTC[-/ATGT]ATGAATCACTGAAGG | 81550 |
rs774279549 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434465 | AGTGAGACCCTGTTT[-/A]AAAAAAAAAAAAAAA | 81550 |
rs774317378 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473332 | TCCTACCTCTTAACA[C/G]TGTTACAATGGCAAT | 81550 |
rs774317684 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60472681 | TATAAACCCAAAAGA[A/G]TGGAAAACAGGTCTT | 81550 |
rs774344137 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506680 | GATAATCACTGGAAC[A/C]TGGGAGGCGGAGTTT | 81550 |
rs774360701 | in-del | -/CGTTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538670 | CATTAGGGGCAAAGA[-/CGTTTT]AAACCTGCTACTTGT | 81550 |
rs774413537 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60439834 | TATTCATAAAAAAGT[C/T]TCAGAGTAAATTGGG | 81550 |
rs774448796 | snp | C/T | 0.000384763 | 0.0138648 | synonymous-codon, intron-variant | TDRD3 | GRCh38.p7 | 13:60397382 | GGCCCAGGTGGCCGG[C/T]GCGGCGTTGTCCCAG | 81550 |
rs774457171 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478801 | TGTTAATTTGAGGAC[-/T]TTTTTTTTTTTTTTT | 81550 |
rs774526722 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430318 | CCTCAGCATGGACTT[C/T]GTAGGCAGCAATGCT | 81550 |
rs774533582 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498950 | GTCCAGTGGGTACGC[A/G]GACTCATCCTGTGGT | 81550 |
rs774553588 | in-del | -/AA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557214 | CTGTCTCAAAAAAAA[-/AA]AAAAAAAAAAAAAGT | 81550 |
rs774562200 | in-del | -/G | 0.000308436 | 0.0124146 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460335 | ACAGCCCTGAATAGA[-/G]TTTCATGACTAGAAA | 81550 |
rs774567693 | snp | A/C | 3.30781e-05 | 0.00406669 | missense, utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528426 | TCATCAAATACTGAG[A/C]AAAATGGAGTAAAAG | 81550 |
rs774575819 | in-del | -/TTA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477200 | TGTTATAGATGGTTA[-/TTA]TTATTATTATTATTG | 81550 |
rs774599055 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426188 | CAGAAAGAAAAGTAT[C/T]ATGTGATCTTACTTA | 81550 |
rs774603024 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447196 | AAACTTAAAATATAC[A/G]ATAGACTATTTCAAG | 81550 |
rs774618576 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431499 | TCAATTTTTAAAATA[A/C]ATTTTTTGTTTGGCT | 81550 |
rs774621578 | snp | A/G | 1.74604e-05 | 0.00295464 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485842 | GCAGAGAACTTGATC[A/G]AAGAAAAACATTGCA | 81550 |
rs774625502 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485764 | GAATCTCTTTTGGAA[C/T]TACTAAGTTGACTTA | 81550 |
rs774648727 | snp | A/G | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395479 | TTGGATGCTCATGTT[A/G]TCCCACATTTCTCCA | 81550 |
rs774703612 | snp | A/G | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509856 | GGCAACAACTTAGAA[A/G]CAGCACTGAACGTAC | 81550 |
rs774722079 | snp | C/T | 1.65636e-05 | 0.00287776 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529114 | AACGAAGATCTGGGC[C/T]AATTAAGCCAGAAAA | 81550 |
rs774725363 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503867 | ATTAATGTTAACCCC[A/G]ATTGGTTTAAATGAA | 81550 |
rs774758638 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60535756 | TTGCTAATTATTGGA[G/T]TAGTTTTGTTACCAA | 81550 |
rs774789059 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466680 | GTAATCCCAGCTACT[C/T]GAAAGGCTGAGACAG | 81550 |
rs774795339 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60435771 | AGGACTTCTTTTCCT[G/T]TGGGTAGATACCCAG | 81550 |
rs774804487 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60489166 | ACCCCTCTCTCTTAT[A/G]TTATTGATAGCCAAA | 81550 |
rs774817652 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475940 | GATTCGGGATAGTAG[A/G]CCTTTGTTGGATGTA | 81550 |
rs774819441 | snp | A/T | 1.66007e-05 | 0.00288098 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509923 | CTCCTCTGAGAGGTA[A/T]AATTTATTAAGCAGT | 81550 |
rs774839113 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534842 | TTGAGATGGGAGGAT[C/T]GCTTGGGCTGGGGAG | 81550 |
rs774839253 | in-del | -/T | 1.65359e-05 | 0.00287536 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467421 | TGAAACATTACACTC[-/T]TTTTTTATTGCATTA | 81550 |
rs774847492 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60509241 | TAGATTTTCTTATTG[G/T]GGTATAGCTGTCAAA | 81550 |
rs774877298 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60456561 | AGACATTAAAGAAGA[C/G]TTGGGTGATCAAGAT | 81550 |
rs774884466 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511433 | AATTGAAGCATGTTT[A/G]CTAGATTATATAGAA | 81550 |
rs774894092 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490464 | GTAGAAGATAAAGTC[A/G]AGAGAGATAATAGAG | 81550 |
rs774915477 | in-del | -/TTTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468535 | TCTGAGGTCAGAATT[-/TTTG]TTTGTATCATCTTTC | 81550 |
rs774931074 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533573 | TGGAACCCGAGAGGC[A/G]GAGGTTGCAGTGAGC | 81550 |
rs774933505 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505433 | CAAAGAAAGGCAGAT[G/T]CCTCAGCCAGGGGAT | 81550 |
rs774942217 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564957 | GATTTGCTCTCAACA[A/G]CTCTGCAGGATGAGT | 81550 |
rs774948846 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516404 | CAGCATTGACTTTTT[A/G]TTGTTATATCTTTAA | 81550 |
rs774960523 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506688 | CTGGAACCTGGGAGG[C/T]GGAGTTTGCAGTGAG | 81550 |
rs774961944 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60480393 | ATTCTTTTTGTAAGG[C/T]CCCTTTTCTCTAGCT | 81550 |
rs774965261 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439469 | CGTATGAATAATCCT[A/G]TTGACACAATAGCTC | 81550 |
rs774985977 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477037 | TTATTTGGATGTCAT[A/G]TATTTCTTTCTCTTG | 81550 |
rs774995771 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60479066 | ACTGCCTTGGCCTCT[C/G]AAAGAGCTGGGATTA | 81550 |
rs775008286 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570756 | GAGAGGAGGCAGTGA[A/G]CATGAATGAGGGTGC | 81550 |
rs775016836 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60550615 | ATTTTGTGAATGACA[A/G]GATTCTTAGTCTCTT | 81550 |
rs775023441 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492843 | TATCCATTAGTGCTC[A/G]TCCAACATTTTAAAA | 81550 |
rs775036522 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60558161 | GTATTATAGGTGTCC[A/G]TGGCATACTGTATCT | 81550 |
rs775038801 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533309 | ATATGAATTTTTGTT[G/T]CCTGTAGCATTTTCT | 81550 |
rs775054286 | snp | C/T | 1.64925e-05 | 0.00287158 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467357 | AAGTGGAACACCTTA[C/T]TGAGAAATGGGAGTT | 81550 |
rs775060860 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517563 | AAGCAGAAGAAATGT[G/T]TAGCTATCTACCCAC | 81550 |
rs775079099 | snp | C/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438099 | AGGGCAGGTGTTTAG[C/T]TTTCATCATTTTACT | 81550 |
rs775080573 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60425755 | CAGCAAGACCAACCC[C/T]TCCTCTTCTTCCTCC | 81550 |
rs775087456 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420812 | AGCCGGGCGTGATGG[C/T]GGGCGCCTGTAGTCC | 81550 |
rs775121970 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572721 | CTTAAAACCAATAGC[C/T]AAGCATAGACTACTA | 81550 |
rs775129487 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60517213 | TTCAAGTTTCAGGTC[A/G]CTTTGGATAGTTTGC | 81550 |
rs775142157 | snp | A/G | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467243 | TTTGCTTTAGCCTGA[A/G]CACACCACCTGGAAC | 81550 |
rs775143087 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567285 | AATTCTAATCTTACC[A/G]CTATAAATGATGTTT | 81550 |
rs775151177 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429994 | GGTATTACATGCTGT[A/C]TCCTCATTTATTCTT | 81550 |
rs775170737 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426665 | AGTTAGAAAGCTTAA[A/G]CAGACCAATGTTATA | 81550 |
rs775194154 | snp | A/T | 0.000200582 | 0.0100125 | utr-variant-5-prime, intron-variant | TDRD3 | GRCh38.p7 | 13:60397355 | ACCACCCCCGGCCTA[A/T]GCAGCTACCATGGCC | 81550 |
rs775239130 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417671 | CTATATACTGATGAT[A/T]CCTAAATCTTTCTGG | 81550 |
rs775265085 | in-del | -/ATTA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473589 | TTATATGTGAATATC[-/ATTA]ATTATTAGTTTGTAG | 81550 |
rs775366233 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475821 | TTTTTTCATATGTTT[A/G]TTGGCCATTTGTATG | 81550 |
rs775392936 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507768 | GTATTGGATGTTCTG[G/T]CCAGGGCATTCAGGC | 81550 |
rs775410328 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504608 | AGCATTACAGCTTTT[A/G]TCTTTCCTTAAAAAA | 81550 |
rs775440119 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60408325 | TATAGTAAATTAGTA[C/T]CAGTAGAGTGGGGCA | 81550 |
rs775445888 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457133 | GAATATTGTAAGCAG[A/C]ATAATGAAAAAAATC | 81550 |
rs775459084 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468503 | CATTTCTCATCTCCT[A/G]TAACAGATAGTATGC | 81550 |
rs775460997 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60485611 | TTATTTACTAGTTAC[A/G]TTTATTGAAAAGTTA | 81550 |
rs775461537 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475729 | TTTGACTTTTTAATA[A/G]TAGCCATTCTGTTAT | 81550 |
rs775463801 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446314 | TGCAACCTCCACCAC[C/T]TGGGTTCAGTTGATT | 81550 |
rs775468680 | snp | A/G | 3.30874e-05 | 0.00406726 | missense, utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528417 | CAATACAGATCATCA[A/G]ATACTGAGCAAAATG | 81550 |
rs775481395 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473465 | CAGCTATATTGTGGG[C/T]GGCAAGCCACCCAGG | 81550 |
rs775502020 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524554 | AGAAAAGAAAAGAAC[A/G]ATTGCCTCTCCCACA | 81550 |
rs775505704 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544517 | AATTCCATTGGGTAT[A/G]TGTACATTTTTAAAT | 81550 |
rs775546879 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469939 | TAAATTTCAGTGGCA[A/T]TAAGAACATTCGCAT | 81550 |
rs775549720 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60419359 | AGTATCTATTTGAGT[A/C]TTTTGTCCGTTAAGA | 81550 |
rs775563362 | snp | C/T | 1.65184e-05 | 0.00287384 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494554 | ATCAGAGGGAAAACA[C/T]GAAGGTGTCTATAGA | 81550 |
rs775571609 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460006 | CAAGGTGTCCCTTAA[C/T]GTAAAAGGAGGGAGA | 81550 |
rs775581339 | snp | A/T | 1.65957e-05 | 0.00288055 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528798 | CCACTTCCTCAAGGA[A/T]CTGTAGATTATAATA | 81550 |
rs775589533 | in-del | -/TGTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442997 | AATTTGTATGTATTC[-/TGTT]TCTCATTCATATTTA | 81550 |
rs775595641 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60542910 | ATTGAACTTTACTGG[A/T]CCTGTGCTGTTTATT | 81550 |
rs775653711 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500319 | ATTGGGCTTGAGCAG[G/T]TCCTGAAGGCACAAG | 81550 |
rs775657514 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60443025 | TATTTAAATATTTCA[A/G]CTTTTGGGTGACTTC | 81550 |
rs775659472 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461756 | ATATTGTAAGACATA[C/T]ATAAACTGAGAGGTC | 81550 |
rs775684929 | in-del | -/T | 0.229885 | 0.249189 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484675 | AAAAAATAATGTTGA[-/T]TTTTTTTTTTTACTG | 81550 |
rs775688978 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60509076 | AAACATGTTAACTAT[A/T]AGATGTATAAAAGTT | 81550 |
rs775734045 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409950 | TCCCAGAATTCCCAC[A/G]TGTTGTGGGAGGGAC | 81550 |
rs775736253 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60411817 | CTTAATTTTAGTAAG[A/G]TTCTTATTAAAGAAT | 81550 |
rs775741647 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498548 | TAATTTAGACAAGCA[A/G]AAAGCTTCTAGGTCT | 81550 |
rs775745757 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445702 | GTTCTAGGAAGGATA[C/T]TTAGAAAAGTAGGCA | 81550 |
rs775751185 | snp | C/T | 1.65007e-05 | 0.00287229 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60483777 | ATTTTTTCCGCAGAG[C/T]TTATCAAAACACAAT | 81550 |
rs775766312 | snp | G/T | 4.95319e-05 | 0.00497629 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510805 | TTTCTTTTCTTTCTT[G/T]TTTTTTTTTTTTAGC | 81550 |
rs775788545 | snp | C/T | 1.65282e-05 | 0.00287469 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529085 | TGATAAAATATTTTA[C/T]AATAGTGGGCCCAAA | 81550 |
rs775791754 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552231 | TTTCAAGATATAATG[A/G]AGGTACAGGCATTGG | 81550 |
rs775797444 | in-del | -/TT | 3.86974e-05 | 0.00439855 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510790 | ATTCCTTTTTTTTTC[-/TT]TCTTTTCTTTCTTTT | 81550 |
rs775809625 | snp | A/G | 0.0001036 | 0.00719648 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60444737 | GACATCAATAGTGGA[A/G]AGGTAGAAAAGGTAA | 81550 |
rs775850989 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488906 | TTTGTTTTGTTTAGT[G/T]TTGTTTTGCTTTTGA | 81550 |
rs775856457 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466838 | GTCTTCTCACTTCCT[C/G]TCTGGTGGTCTATTC | 81550 |
rs775913485 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60510206 | GAAAATATGTGACTG[C/G]TTCTATTATTTCTAG | 81550 |
rs775919413 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400359 | TCTCTGGACATTTTG[A/C]ATTTTTCTCTTCCAT | 81550 |
rs775946252 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451744 | CAGTATTGTATATGA[A/G]ATTCAATTGAGCCAT | 81550 |
rs775966408 | snp | G/T | 4.96907e-05 | 0.00498426 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528980 | TAATAGTTTCATTGG[G/T]GTTCCAAATGGAGAA | 81550 |
rs776030917 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469684 | CAGTTACTTGAGCAG[C/G]TGGCAGTGATATACA | 81550 |
rs776039523 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502313 | AGGAATAAGCAGGGT[G/T]AGTCTAAAATGTCAA | 81550 |
rs776051346 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504326 | TTGGTGAAAAACCTG[G/T]TTAGTAAGCAGTTTT | 81550 |
rs776061470 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60569447 | AAACACTGAAAAGAT[A/C]CTCCATGTTCATGGA | 81550 |
rs776068166 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563680 | AGAACTCTTTCCTTA[A/G]AGGACTGGTTTGTAT | 81550 |
rs776105525 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533216 | CCGTGGATTCACTTA[A/G]TACCTTTGTAATATT | 81550 |
rs776136142 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453368 | AGCCAATTCAGTTCT[A/G]CTTAGATAAATCTGG | 81550 |
rs776136612 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468214 | TAAATTCTTCCACAT[A/T]GATCTTGTTGTAGCC | 81550 |
rs776142902 | snp | A/G | 1.65004e-05 | 0.00287227 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460480 | GGATGCTGCGATTAC[A/G]GATGACTGATGGTCA | 81550 |
rs776143208 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490734 | CATAGCAGTTGTGTA[A/G]GTAGTGCAGAGTGGT | 81550 |
rs776156155 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562751 | AGAAACAAATGATTC[A/C]ATTTTATTAAATTAT | 81550 |
rs776163223 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60502738 | TCAGGAACCTTGTAC[A/T]GGATTATATATATAG | 81550 |
rs776171678 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548748 | AAATCATAATACTTA[C/T]GCTGGCAAGGATGCA | 81550 |
rs776175506 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570563 | CCACTACTGTGTATT[C/T]ATCCAAAGGAAAGGA | 81550 |
rs776197317 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60435442 | TACCCCAGTAGAGTC[C/T]CCAAAGTCCATTATA | 81550 |
rs776199378 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422640 | GAAATGGAAGAAAAT[A/G]TCAGAATTATTTTAG | 81550 |
rs776202581 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60536610 | GGTTTGCTATTTATT[A/G]TGTTCCCAGTTGTTT | 81550 |
rs776204323 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60531514 | ATTGGATAATGTGGG[C/G]TTACTGGTGACCTTG | 81550 |
rs776257563 | snp | A/G | 0.000214803 | 0.0103612 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509903 | ACAGAAACCTGTTAT[A/G]GGTCCTCCTCTGAGA | 81550 |
rs776272539 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409676 | TGTATTTACCCAATA[C/T]CTGTACCCTCATTGT | 81550 |
rs776273036 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417584 | TGACTTCAGGTGATC[C/T]ACCTGCCTCGGCCTC | 81550 |
rs776290272 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60533514 | GGTGTAGTAGCACGT[G/T]CCTGTAATCCCAGCT | 81550 |
rs776295496 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495225 | GGTTACAAGTGTTGG[C/T]AAATTCAGCAGTATA | 81550 |
rs776327654 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482215 | TCTGAAACAGCCCCA[C/T]AACTTCCAGTTGCAT | 81550 |
rs776331400 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559666 | ACTACATGATCTTAC[-/T]TTATATGTGGAATCT | 81550 |
rs776414600 | snp | A/T | | | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467317 | CTGCTCTTGAATGAC[A/T]CTAACACCACAGTTC | 81550 |
rs776422149 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446569 | TATAAGAATATATAT[A/T]ATTCTCACAGAATTA | 81550 |
rs776432685 | snp | C/T | 1.6507e-05 | 0.00287284 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528682 | AAGATACTTCATATC[C/T]TTTAGGTTCTCAGCA | 81550 |
rs776445368 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572239 | GTCCACAGCAAGTGG[C/G]TCTCAGTGGCTACAA | 81550 |
rs776481960 | snp | C/T | 0.000117591 | 0.00766691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467190 | CCCGCCCTGTGTCCA[C/T]GTGTTCTCAGCTTCA | 81550 |
rs776517421 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508936 | AATCCATAGAAACCA[C/T]ACCTCAAATAGCCCA | 81550 |
rs776519012 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497080 | TAGCCTGATTGGGAG[C/T]GGCAGCTGGCACCCC | 81550 |
rs776555170 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537445 | AGTCTGTGTTGCTGT[C/G]AGTACATGCAATGTA | 81550 |
rs776573563 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60421598 | GTAGTAAATAACTTC[C/T]CAAAATCTTTCCCCC | 81550 |
rs776592115 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520032 | TTTATGCTAACTTTT[A/T]AAAAATTGGCTTTTC | 81550 |
rs776607023 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498072 | GAGCAAGCTGGAAAT[A/G]CCTGATCTCCCTTGG | 81550 |
rs776629259 | snp | C/T | 0.000117101 | 0.00765093 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485914 | TTGAAAAGCAAAGGA[C/T]GGCTGCTATTGCTGA | 81550 |
rs776636358 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487781 | TTTCCTTTGGATAAA[C/T]ACCCAGTAGTGGGAT | 81550 |
rs776666495 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428733 | GTGGGCCCACAGAGA[A/G]GACAGTGGTTCTGTC | 81550 |
rs776672652 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492838 | TATGTTATCCATTAG[C/T]GCTCATCCAACATTT | 81550 |
rs776678843 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429962 | TTTAGCACCTACTGT[A/T]TTCCAAGCATATGCT | 81550 |
rs776732464 | in-del | -/TGTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436212 | GCTCTGTGGGTTGTC[-/TGTT]TACTCTGCTGATGAT | 81550 |
rs776768674 | in-del | -/TTC | 8.77982e-05 | 0.00662506 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510800 | TTTTCTTTCTTTTCT[-/TTC]TTTTTTTTTTTTTTT | 81550 |
rs776777345 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571057 | ACTGTTAACAGGAAA[C/T]ATATGATGCAGATAT | 81550 |
rs776788109 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459720 | CCATTTCCCGGATTC[A/G]AGTGATTCTTCTGCC | 81550 |
rs776798210 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464282 | GATGCAGAGAAAGGG[C/G]AATGCTCAAACACCA | 81550 |
rs776804619 | in-del | -/TTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567891 | ACCATGCCCAGCTGA[-/TTT]TTTTTTTTTTTTTTT | 81550 |
rs776815991 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475426 | CAAAGGACATTATTT[C/T]ATTCTTATTTATGGC | 81550 |
rs776838284 | snp | A/G | | | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528508 | ATGAAAAACCGCCTC[A/G]TTTTCAAAGAGACTC | 81550 |
rs776860883 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422456 | AATTCTTTTTCCCCA[A/G]AACAACCGTGAACTA | 81550 |
rs776893939 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458374 | GAAAAGGCAGTTTGT[C/T]ACAACACATTGAAAG | 81550 |
rs776901848 | snp | C/G | 4.94825e-05 | 0.00497381 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535214 | TGAGCAATATCAAGC[C/G]CATTCAAACAGAGGC | 81550 |
rs776907396 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506786 | CGACACTATGAAGAA[A/T]CTGCATCAGCTAAAG | 81550 |
rs776943144 | snp | A/G | 4.98716e-05 | 0.00499333 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528838 | GTGGAAAAAGAGAAA[A/G]CCAAACATCTATTCC | 81550 |
rs776953011 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503017 | CAAACTTTGTTCACA[A/G]AATACCTTATTCAAT | 81550 |
rs776953038 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512385 | CGTTCCACCCCCAGC[C/G]CCTCCCAAATATCAT | 81550 |
rs776973846 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60413090 | TATATGAACTAATAG[A/G]TCAACAGGAAGTTAG | 81550 |
rs776984177 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487066 | GGTGGGGGCGGGGAA[A/G]GATGGTTGCATCTGT | 81550 |
rs776997319 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507604 | CTGGGTAAATAAAAA[A/T]ATTAAGGCAAAAGTA | 81550 |
rs777037679 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60519169 | CATTATTTTCTTCCT[A/C]CTCAATTAATTGTCC | 81550 |
rs777079761 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465028 | CATTACACATTGTAT[A/G]TATGTGTCAAAATAT | 81550 |
rs777102232 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500305 | AAGTTGTATATGTGA[C/T]TGGGCTTGAGCAGGT | 81550 |
rs777112546 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561978 | GATAATAATACATGA[C/G]TCCCATGGGCACCAA | 81550 |
rs777117014 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486790 | CCCAGCCTCTAGTAA[C/T]TACTATGCTGCTCTT | 81550 |
rs777140929 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520674 | AAGCTCCACAGGATA[A/G]AGGGCAATGGGTCTT | 81550 |
rs777212069 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525320 | CTGGGATTACAGGGC[C/T]GCGCCACCAAGCCTG | 81550 |
rs777213948 | snp | A/G | 4.96216e-05 | 0.0049808 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483757 | AACTGCTCTTTTGTG[A/G]CTGGATTTTTTCCGC | 81550 |
rs777216124 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555981 | TCAGCCTCCTTAGTA[A/G]CTGGGACTACAGGCG | 81550 |
rs777226976 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538698 | TGTGTTTCCCACAGG[C/T]CCTTTCCAAATTGCT | 81550 |
rs777244634 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60449653 | TTTCAGGGAATCTTA[C/G]GTTTGCAAAAACCTA | 81550 |
rs777250240 | in-del | -/AGAGTG | 1.65217e-05 | 0.00287412 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467411 | CTTGAACTTTTGAAA[-/AGAGTG]CATTACACTCTTTTT | 81550 |
rs777265064 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60494404 | AAATGCTGTCTACAT[-/A]ACCTCTCTTTTATCT | 81550 |
rs777302209 | snp | C/T | 1.9204e-05 | 0.00309865 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510790 | ATTCCTTTTTTTTTC[C/T]TTCTTTTCTTTCTTT | 81550 |
rs777303985 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553847 | GGTGGGGACACAGAG[A/T]CAAACTATATCACAA | 81550 |
rs777332550 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433226 | TTCAATGGGTGGCAG[C/T]GGGTAAAAGAGAATA | 81550 |
rs777395587 | in-del | -/TGGAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60415720 | GTACAGATGCCTTGA[-/TGGAT]TGGATCTTCCGGGAA | 81550 |
rs777403156 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394844 | ACTGACATTCTGGGC[C/T]ACATCATTCTTTGGA | 81550 |
rs777417329 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562328 | CCTTCCCCCCACCCC[C/T]GGCAAAAAAAAAGAA | 81550 |
rs777456828 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484955 | GCTTCTTAGGGGTTA[A/G]AGAATATAATAAAAG | 81550 |
rs777464298 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469415 | TCCTAGTAACCTTCT[C/T]ACCAACACACACACA | 81550 |
rs777514892 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429766 | TATACACTTTTGACT[A/G]TTAGCTGTAGCCTTT | 81550 |
rs777515751 | snp | A/G | 3.34197e-05 | 0.00408763 | intron-variant | TDRD3 | GRCh38.p7 | 13:60467208 | GTTCTCAGCTTCAAT[A/G]TGTTTTTAACACTTT | 81550 |
rs777516628 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446917 | AGTCACTACTGATCC[A/G]TTACTTACTAACATT | 81550 |
rs777520167 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417476 | CCTCCTGAGTAGCTG[G/T]GATTACAGGCTCCTG | 81550 |
rs777526318 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60539872 | GATAAAGGTCGTGTT[A/G]GTAATTTTAATGGCA | 81550 |
rs777539649 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422298 | CCCCTAATGAAACCA[A/G]CCACTTCATTAAAGT | 81550 |
rs777544228 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476428 | TACCCAGTACTCATT[A/G]TTATATTTTTGTACC | 81550 |
rs777561518 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525341 | ACCAAGCCTGGCTAA[-/T]TTTTGCATTTTTAGT | 81550 |
rs777562483 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458414 | GAAGGTGTCATGTCA[A/G]CACCCAGGGGACGTA | 81550 |
rs777568508 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60489490 | CAGGCTCTGGAATCA[C/T]AGGCTGGAAGCATAT | 81550 |
rs777583957 | in-del | -/AA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518521 | CTAGAATTGTGATTT[-/AA]AAAAAAACTGGTGAG | 81550 |
rs777598548 | snp | A/C | 1.80748e-05 | 0.00300618 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60485818 | GTGTATCTCATGTCC[A/C]AGTGGATAGCAGAGA | 81550 |
rs777610832 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60520595 | TCATAGATTTTATTA[C/T]AGCTTTAAGCTACAT | 81550 |
rs777625536 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423463 | CTGTATATTGAATGC[C/T]ATACCTCGATAAGAG | 81550 |
rs777629701 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551668 | AATGTGTATTAGTCC[A/G]TTTTCACACTGCTGT | 81550 |
rs777633557 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532809 | TGAAACTTTATTCCT[A/T]TTAAATTTGTCCTCA | 81550 |
rs777634138 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461382 | TTAGAGCCATGCCCA[A/G]TGGAATGGACGAAAA | 81550 |
rs777642962 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475205 | TGTAGTGAGCATAGT[A/T]CCCTATAGGTAGCCT | 81550 |
rs777665158 | in-del | -/TTATTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60477210 | TGGTTATTATTATTA[-/TTATTG]TTATTATTATTATTA | 81550 |
rs777696179 | snp | C/T | 1.87443e-05 | 0.00306134 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510587 | TATATTCTCTTTTTG[C/T]TTTTGCATATACAGT | 81550 |
rs777705417 | snp | C/T | 1.6604e-05 | 0.00288127 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535093 | TCATATTTAAAACTC[C/T]TTTTGCCTCCTCAGT | 81550 |
rs777712187 | in-del | -/TTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429149 | TTGACAAAAAATTTA[-/TTG]TTTAGTATTTACCTG | 81550 |
rs777721524 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549780 | TTATTGACCATTTTA[A/T]GAAAAGCAATTTTTC | 81550 |
rs777737217 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484836 | TTATATTTGAAAATA[A/C]TAGTATATTTGTAAA | 81550 |
rs777760436 | snp | A/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60437761 | TGTAGGAGCTTGGAA[A/T]GCTGTGTTTTTGTAA | 81550 |
rs777789315 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416069 | AAGAATTAATAACTT[G/T]GTTGGATGGCTCAAA | 81550 |
rs777795656 | snp | A/G | 1.65737e-05 | 0.00287864 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528775 | CCTTTGCAGAGGCAA[A/G]AGAAAATCCACTTCC | 81550 |
rs777815656 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428108 | AGTCCAGTTTCTGCC[C/T]CCAGCTTCATATGGC | 81550 |
rs777846031 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60508677 | AATCCTAGAAGAAAA[C/T]CTAGGCAATACCATT | 81550 |
rs777850130 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468515 | CCTGTAACAGATAGT[A/G]TGCTTCTGAGGTCAG | 81550 |
rs777868788 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501103 | GCACATTTTCCATCA[C/T]GGAAAGGGCAGAGGT | 81550 |
rs777889929 | snp | C/T | 3.29712e-05 | 0.00406011 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494500 | GAATGCTGCTGGTAA[C/T]CGAAATAGGGAAGTT | 81550 |
rs777902408 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433819 | TAGTTTGCCTTGCTC[C/T]GTTTCATTATCTATA | 81550 |
rs777941433 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506360 | GATTTTATCACCACC[A/G]GGCCTGCCTTACAAG | 81550 |
rs778002579 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60519280 | GGTGCTTTGCATACT[A/G]TTAATTCATTTTATC | 81550 |
rs778006726 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457978 | AATTACATCTGAAAA[G/T]AGCCTTGTTCCCAAA | 81550 |
rs778071690 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60398197 | ACGCTTTTCCCAGGC[A/T]TGCACAGGCACATTC | 81550 |
rs778081444 | snp | A/G | 1.65012e-05 | 0.00287234 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528663 | TCTAGATATGACAGA[A/G]CTAAAGATACTTCAT | 81550 |
rs778087976 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546018 | TAGGTTGCATATTTT[C/T]CAACTCAGGACTAGT | 81550 |
rs778103298 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514343 | AGGGAAAACACATGA[C/T]AAAAGTTTGGAAAAT | 81550 |
rs778112658 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482265 | GACTGATATTCTAAA[C/G]TCAGCTCCCTATGAC | 81550 |
rs778116689 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60511348 | CATTCAGATATATTT[C/T]GAATCTAGCCAAATA | 81550 |
rs778172009 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544476 | AAAGAAAGAAAAAAG[A/T]AAAGAAAAAATTGTC | 81550 |
rs778175784 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561016 | AAAGAGATTATCTTA[C/G]AGCTGCTCTGGAGGG | 81550 |
rs778195113 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530717 | GCCTCGGCGTCCTAA[A/C]GTGCTGGGATTACAG | 81550 |
rs778202867 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440695 | CAAAAAAAAAAGTAA[A/G]TAAACAAATGTTCTT | 81550 |
rs778225123 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424692 | AAAAAATAAATAAAA[A/G]TAAAGCATATCATTC | 81550 |
rs778232287 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507473 | CAAATGCAAAAGAAC[A/G]AAAATAATAACAGTC | 81550 |
rs778257513 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60405716 | CTTGGACCTTGTTGG[C/T]CATGTTAGGATTTAT | 81550 |
rs778266281 | in-del | -/AAAAA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60544444 | AGACCATATCTCTTT[-/AAAAA]AAAAAAAAAAAGAAA | 81550 |
rs778292729 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427253 | AGATTTGATTGATTT[G/T]GTTTTTTCTTCAGAA | 81550 |
rs778302076 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561431 | GGTTTTTAATTTCTG[C/T]GGCTTGAGGGCTACA | 81550 |
rs778322271 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60406840 | ATTCCCCACAATCTT[C/T]CCCCAAATTCCTCTA | 81550 |
rs778322771 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496629 | GTTTAGTGACTCTAT[A/G]CATAATACCTTTGAC | 81550 |
rs778331455 | snp | A/C | 1.6669e-05 | 0.00288691 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510775 | GCTAATTTAAAGTTG[A/C]TTCCTTTTTTTTTCT | 81550 |
rs778333389 | snp | A/C | 1.64776e-05 | 0.00287028 | synonymous-codon, missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567584 | AGGTGATGGCCAGCC[A/C]AGACGATCCACTCGG | 81550 |
rs778405761 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410491 | CCTCAGTATCCTTGC[A/T]CAGTTCACTGTACTC | 81550 |
rs778419059 | snp | A/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396366 | TTCCGCCTGTTCCTC[A/T]CTGATTGGCCAGCGT | 81550 |
rs778429693 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496981 | CGGTGGGTCACGGAA[G/T]AAAACCGTGGAACCC | 81550 |
rs778494681 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464956 | ATTCATAATGTTCTC[A/G]CAAAGAAAAGATAAA | 81550 |
rs778561499 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60409219 | TGCCTGGATGCCCAG[A/G]CAAAAGTTTGCTGCT | 81550 |
rs778567147 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549502 | TCAGGCCTTCTAGAG[C/T]TCATCTTTATGCCAG | 81550 |
rs778576643 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458968 | AAAAGTTCATCCTGA[A/G]TTAGCAGCTTATCTA | 81550 |
rs778602786 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60449178 | ATGTTTTTAAAAAGA[A/G]AAGGAATTGAAAAAA | 81550 |
rs778619772 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60501040 | CTATGGCCAGTGACT[A/G]TTCCTTGGGGTGATC | 81550 |
rs778658029 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538080 | ATAAAAATCAAGTTA[A/G]TACTTTAAATCTAAG | 81550 |
rs778672420 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442527 | TTCTTGGACCCAGTC[A/G]TCGTCCTAGCAATCC | 81550 |
rs778675881 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60479607 | GTATGTTGAAATCTC[C/T]CACTATTATTGTGTT | 81550 |
rs778680336 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60428527 | TTTATCGTGCATAGC[A/C]CAAGGGAATTACAAG | 81550 |
rs778689249 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432834 | TCTTTATTTTCTTTG[C/T]GGCTAAGCAAGAATT | 81550 |
rs778689868 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488338 | TTTTGAAAGGCCTGA[A/G]TGTCATTTCCTGAGG | 81550 |
rs778698732 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430128 | AAAGGTAAGGCTGAG[A/G]TTTTCATCTAGTTTT | 81550 |
rs778702213 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432651 | GTATGGGTAATTTTT[-/A]AAAAAATATCTTTAC | 81550 |
rs778740818 | snp | A/G | 1.6525e-05 | 0.00287441 | | | GRCh38.p7 | 13:60529041 | GGACCTATTAAGCCA[A/G]CAGGACCTGTCACAG | 81550 |
rs778741892 | in-del | -/ACACACA | | | | | GRCh38.p7 | 13:60469428 | CTCACCAACACACAC[-/ACACACA]TACACACACACACAC | 81550 |
rs778743967 | snp | A/G/T | 5.20633e-05 | 0.0051019 | | | GRCh38.p7 | 13:60528348 | CTTAATTTGCATATG[A/G/T]TATACTTTTACCTTT | 81550 |
rs778744339 | snp | C/G | | | | | GRCh38.p7 | 13:60536998 | TTTAGTGATTCTGTT[C/G]TGAACTACAGCAATA | 81550 |
rs778748057 | snp | A/G | | | | | GRCh38.p7 | 13:60544313 | GCCAGGTGAGGTGGT[A/G]TGAACCTATAGTCCC | 81550 |
rs778761823 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60531105 | TCACATCTTTACTTA[A/C]GCCTGGAAAGAAGGG | 81550 |
rs778779705 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60474824 | ATCAAGTTCCTGCAT[C/G]GTGTGTCTTTTAGTT | 81550 |
rs778780512 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555240 | CATATTGCACAAAAT[C/G]AGCATTTATATAACA | 81550 |
rs778796761 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60487609 | GAGTGGTGGGAGTCC[C/T]AGAACCAATCCCTCA | 81550 |
rs778827830 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60397973 | TCTGCCTTCCGCGGC[A/G]CACACACAACTTCTG | 81550 |
rs778852021 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548044 | TATATAAATGTGCCT[C/G]TAGTCCATTCATTTT | 81550 |
rs778864982 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60422150 | TGCATAGCTTCTGGG[A/G]GAGAAAGAAACAAAA | 81550 |
rs778870842 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458949 | CATTAACAAAAGCCA[A/G]ATAAAAAGTTCATCC | 81550 |
rs778885817 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60527699 | GTATTATGCTTAGTA[A/G]TGTTTCTGACACTTT | 81550 |
rs778913891 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460431 | CGCAATGTTGCTGCA[C/T]CAAAGGATAATGAAG | 81550 |
rs778928155 | snp | A/G | 4.94393e-05 | 0.00497164 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509787 | AAAGCTCTGAAGCAC[A/G]TAACGGAAATGGGCT | 81550 |
rs778941412 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427013 | TACGTATTTATGTAT[C/T]TAAACATATTTGTAT | 81550 |
rs778962291 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60521547 | GAGATACTGTTCATT[C/T]TAAAACTGAATTGCA | 81550 |
rs779044012 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426348 | TAGGATGAACAAGTT[A/G]AGAGATGTACAACAT | 81550 |
rs779058934 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458167 | CCTTCATTCCCCAGA[C/T]CTTTGTTCTCATAGT | 81550 |
rs779065860 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60448849 | CTTTTTAAACCTAGG[C/T]GTAAAAGTTAATTAT | 81550 |
rs779102688 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399505 | TAGGCTTTCAGGTGG[C/T]TTCTACTAGGTCTTT | 81550 |
rs779132250 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418702 | AAATGTTATATAGAA[C/T]GTTTTCATCACCCAA | 81550 |
rs779183104 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504989 | CCACCAGGACCCTGG[G/T]TTTCCAGCACAAAAC | 81550 |
rs779184939 | snp | A/G | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60535145 | CCCTCCATTCTTCGG[A/G]TATGACAGCAGTTGT | 81550 |
rs779187361 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427084 | ACAGTATTTTAATCT[C/T]AGAGGACCACAGTCA | 81550 |
rs779218223 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412248 | GTCATATTTGACATA[C/T]TTGAATTTTTCATTC | 81550 |
rs779218341 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60559264 | GAAAAGATTAGTAAC[A/G]TGCCTATGATGTGGT | 81550 |
rs779219689 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60403319 | GTAACATTTTAAGAA[A/C]CATAAAAATATGACT | 81550 |
rs779219834 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60567003 | TTTTTCTGTCTCTAG[A/T]TGTAAGGTTCTTAAC | 81550 |
rs779230212 | snp | A/G | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494468 | GGTGGTGGTGGTGCT[A/G]GAAGTAATCTCAATA | 81550 |
rs779233820 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561541 | CCATATATTTTATAT[A/G]GGAATTCTACGTGAG | 81550 |
rs779250624 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436899 | TTTCCTGATCTTCTA[C/T]GATGCAGAAGGGAAC | 81550 |
rs779258976 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488514 | TTGACCATTTGTATG[A/G]TCTTTTGAAAAATGA | 81550 |
rs779266460 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454864 | AGGGTGTATGTGACA[A/C]ATCAGACTTTATTTT | 81550 |
rs779270823 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431703 | AAGACTATCTTTACC[-/A]AAAAAAAAAAAAAAA | 81550 |
rs779308451 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60414563 | CAAGTAGTATATGCT[A/G]TTGGTACCAGAATTT | 81550 |
rs779310058 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60573765 | TGGAAAAAACAGTCA[A/G]CTCACACAAAGAATG | 81550 |
rs779332617 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60485211 | TTTATACTATTTTTA[C/T]TGGTAAGATTGGACT | 81550 |
rs779348032 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512370 | ACAGCCAAACCATAT[C/T]GTTCCACCCCCAGCC | 81550 |
rs779352732 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468805 | AAAAATACTTGTGGT[A/G]TAAATGAATTACAAA | 81550 |
rs779360923 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423514 | TGCCTATGGCACATT[A/C]ACAAAAACTGATTAT | 81550 |
rs779370523 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438163 | CATAAGCGGGGCATA[A/G]TATTTATGAAAGTGA | 81550 |
rs779424754 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60536496 | TCTCATATGATGGCT[A/G]TTTTCATTCTCTCTT | 81550 |
rs779458295 | in-del | -/TTTTCTTTC | 1.70606e-05 | 0.00292062 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510785 | AGTTGATTCCTTTTT[-/TTTTCTTTC]TTTTCTTTCTTTTTT | 81550 |
rs779459207 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506212 | TACAAGCCAGAAGAG[C/T]GGTGGCCACTATTCA | 81550 |
rs779487922 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541158 | CTATTCTTTCTTTCT[-/A]TTCTTTCTTTCTTTC | 81550 |
rs779518183 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60526020 | TTCTGCCACATCTGC[C/G]AAGCCTGGCTGAACT | 81550 |
rs779546327 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60491771 | GTGGTCAAAATCTAT[A/G]TGAGTTCTTTAATGA | 81550 |
rs779580720 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60506521 | GAGGCCAGGGTGGGC[A/G]GATCGCAAGGTCAGG | 81550 |
rs779592621 | snp | A/G | 1.68735e-05 | 0.00290456 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510620 | ATATTTCTTGCTTTT[A/G]CATCTAAAGGTAGAG | 81550 |
rs779599179 | snp | A/G | 1.66158e-05 | 0.0028823 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483740 | ATATATTTTTTATGT[A/G]TAACTGCTCTTTTGT | 81550 |
rs779668957 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60495335 | CCTTACCCACTGCCT[A/C]AATAAAGCTGATTTA | 81550 |
rs779670872 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60507086 | ACAGGCTTTAAACTA[A/T]CAAAGATCAAAAGAG | 81550 |
rs779698546 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534609 | AAATAAATTACTCTA[C/T]AGTTATATATTCTGA | 81550 |
rs779717080 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60458042 | TCTTTTGGTGGAGCC[A/G]CTATTTAACCCACTA | 81550 |
rs779778526 | snp | G/T | 1.69123e-05 | 0.0029079 | intron-variant | TDRD3 | GRCh38.p7 | 13:60535282 | CTATTTTGAAGAAAA[G/T]ATATAGCTCTAAAGA | 81550 |
rs779790290 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552413 | TGCAAGGGGTAGGCT[C/G]CTAAGGCCTTGAGCA | 81550 |
rs779804856 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440767 | GCTTTATAATAAGCT[A/G]TAAACAATCAAATGT | 81550 |
rs779836515 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464768 | TTGATCTCCTGGAGA[C/T]AGTAAAATGGCAGCC | 81550 |
rs779837992 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60500674 | ATACTGATTTATGGG[C/T]TGTAGCCAATGGTTT | 81550 |
rs779838482 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447017 | GCAAACAGAATATTT[A/G]AATAAGTAATCTGCC | 81550 |
rs779875134 | in-del | -/TATAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503491 | TACAATATTGGAACA[-/TATAT]TAGTATTATTCACCA | 81550 |
rs779879013 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60397630 | CGGCCTGGGCCCCGG[G/T]CGGCGGGCCTGGGCC | 81550 |
rs779880273 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551908 | ACTTGCTATCATGAG[A/G]ACAGCATGGGGGAAA | 81550 |
rs779886914 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60412006 | CTGAGGAAGAGAGAC[A/G]TCGTATCCTTGGTTT | 81550 |
rs779888618 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60546211 | TGGAAAGACTTTTAG[A/T]GACTGACTTGTATTG | 81550 |
rs779903451 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518435 | GAATGTTCTTTTATG[C/T]CACTAAGTTTGAGTA | 81550 |
rs779913042 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60531856 | AAGAATGAATGAATG[A/G]CTATGAATGATTATC | 81550 |
rs779928504 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60448472 | CTTCTTAACATACTT[C/T]TCAATTTCTGTCTTT | 81550 |
rs779933437 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407699 | TTCTGTTTCAAGGTA[A/G]TATTAGTAGAAACTG | 81550 |
rs779969880 | in-del | -/GGCGGCGGCGGCGGCGGCCTGGGCCCCG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60397601 | CCTAGGTCCCCTGGA[-/GGCGGCGGCGGCGGCGGCCTGGGCCCCG]GGCGGCGGGCCTGGG | 81550 |
rs779982733 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396143 | AGTCTCTGCTCCAAG[C/T]CTGTTTTTGATGATG | 81550 |
rs779983859 | in-del | -/TT | 0.00010507 | 0.00724733 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444766 | AAGAAAATCAATAAC[-/TT]TTCTTACATTAATTA | 81550 |
rs780003088 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572255 | TCTCAGTGGCTACAA[C/T]AGAGAATATGAACCA | 81550 |
rs780003130 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431116 | ATGAGTTTTTTTTAA[A/C]CCCTGAGTGATCTTT | 81550 |
rs780007532 | in-del | -/AC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469437 | CACACACACACATAC[-/AC]ACACACACACACACA | 81550 |
rs780026167 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60491614 | AGTTACATAAGATGA[A/G]GACTTAGAATTAATA | 81550 |
rs780043411 | snp | A/T | 1.65282e-05 | 0.00287469 | synonymous-codon, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60529022 | ACTGAAAGGAAGACG[A/T]ATAGGACCTATTAAG | 81550 |
rs780043444 | snp | A/G | 8.67762e-05 | 0.00658639 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509660 | TGACATTTTTACATA[A/G]GTATGGGATGTAATT | 81550 |
rs780069201 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555581 | ATGAACCTTCACTTT[A/G]TCTGTAAATGGAGGT | 81550 |
rs780078372 | snp | A/G | 1.67061e-05 | 0.00289011 | missense, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60460419 | ATTCAAAAAATTCGC[A/G]ATGTTGCTGCACCAA | 81550 |
rs780084085 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60537797 | GAAATGGTATTGTAT[C/G]TTTCATTAAGATTTA | 81550 |
rs780092778 | snp | C/T | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438796 | GATCTCTTAGACTAG[C/T]AGTCTTGGATCCTTT | 81550 |
rs780115358 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60462849 | AGCTGGAGGTATCAC[A/G]TTACTTGATTTCAAA | 81550 |
rs780118586 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490367 | CCAGGCAGAAGGAAA[A/C]GCCATGGCAAAGGCT | 81550 |
rs780133944 | snp | A/G | 3.34325e-05 | 0.00408842 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528919 | GTGGTATAAAAATTG[A/G]AAAACATTTTAATGT | 81550 |
rs780165810 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557493 | TAGTTTTCTTTATAT[G/T]TCACTGAAGAGAAAT | 81550 |
rs780182686 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60410893 | CCTGTTTAATTACTC[A/G]TTCATCAAAAGTCTT | 81550 |
rs780186449 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532368 | CTCTAAATAGATTAC[A/G]CCACCCTTAACCATT | 81550 |
rs780207199 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60472430 | GTAAATCAAATACAG[C/T]GAGATATACTACCCT | 81550 |
rs780221390 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504914 | ACTTCGGCCCAGATA[C/T]TATGCTTTTCTCACA | 81550 |
rs780226927 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420013 | TTATAATTATTGTGG[A/T]TATGTGTTTTATATG | 81550 |
rs780239611 | snp | C/T | 3.29544e-05 | 0.00405908 | synonymous-codon, missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567614 | GCCAACCCAACAGTT[C/T]TACCAACCACCCCGG | 81550 |
rs780249466 | snp | A/C | 1.69063e-05 | 0.00290738 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460544 | GTCAAAAATAAGGTG[A/C]TTGGCACTTTATTTT | 81550 |
rs780271440 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60565644 | TAGATGTTCTCCAGC[A/C]AATTCTGCAGCCAAA | 81550 |
rs780281472 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60429699 | GTTCTCAGTGAACTC[C/T]ATGTGAGTAGCCTGC | 81550 |
rs780287094 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60436565 | TTTTGTATGCTTTGT[G/T]GAAGATCAGTTGGCT | 81550 |
rs780304322 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60467905 | TCTACTTTGCTTCCA[A/G]CAACCATTTCTGTTG | 81550 |
rs780339021 | snp | A/G | 1.77776e-05 | 0.00298136 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485961 | GAAGTAAGAAATCAA[A/G]TCATTACACGTTTTA | 81550 |
rs780369557 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60417260 | CCTCAAAGGGCTTCT[C/G]CTGCCTCAGCCTCCC | 81550 |
rs780379423 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515735 | GTTGAGGCAAGCTAC[G/T]GAATTGTTTTTCAGC | 81550 |
rs780388841 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60538157 | TGTCAGTAGACCAAA[A/T]ATTTATTTCTCCTTT | 81550 |
rs780390371 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60479798 | GTTTAAAGTCTGTTT[C/T]AGTTGACAGAAGAAT | 81550 |
rs780390540 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60459810 | ATTTTTAGTAGAGAC[A/G]GGGATTCACCATGTT | 81550 |
rs780394377 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452965 | ATAGACTTTGTTAAT[A/G]TTGTTATTGTATTTT | 81550 |
rs780417853 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484639 | AAGTCATTTTTGCAT[C/G]AAACCTATTTTGAAG | 81550 |
rs780471065 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514650 | GGAGGCATCAGAGCA[C/T]CAATTCCCTGTGCCT | 81550 |
rs780473242 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60555614 | ATGATACCAACGTAC[A/T]TGAGAATTTTTGTAT | 81550 |
rs780489220 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60524166 | TCTGACTGGGGAACC[A/G]AGGAGCTGCCTTTTC | 81550 |
rs780489249 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60543743 | GCCTCTTCCTTTCTG[G/T]GAGTAGAAGACAAAA | 81550 |
rs780502629 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60485210 | TTTTATACTATTTTT[A/C]CTGGTAAGATTGGAC | 81550 |
rs780538944 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564614 | CCTCTCTTGGTTTAT[A/G]GACTCATCTGTCGAA | 81550 |
rs780571011 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60401863 | CATTTCACCTTTGAA[C/G]AACTAAGAAAGCCTA | 81550 |
rs780578441 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60468940 | CAGCCAAAGGCCTAA[A/G]CAATATTTCAAGCTT | 81550 |
rs780580093 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60512092 | TACAGGAAAAAGAGT[A/G]TATTGGATTTACAGT | 81550 |
rs780633549 | snp | C/T | 1.64972e-05 | 0.00287199 | missense, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528502 | CAAGAAATGAAAAAC[C/T]GCCTCGTTTTCAAAG | 81550 |
rs780638084 | in-del | -/GTAGTGTGTGCCTGTA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60440545 | AATTAGCTGGGCGTG[-/GTAGTGTGTGCCTGTA]GTTCCAGCTACTCGG | 81550 |
rs780643975 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60418356 | CCTGATAGAAAGTAG[A/G]TACCCTTCTTCTGAG | 81550 |
rs780670603 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454495 | TTTCTCTGTGAGAAT[C/T]CTGGCCACTTGAATC | 81550 |
rs780698098 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503808 | AGCCTTTACTATTAC[A/G]TGAAAATCCTGTTGA | 81550 |
rs780726219 | snp | C/T | 3.67006e-05 | 0.00428357 | intron-variant | TDRD3 | GRCh38.p7 | 13:60510595 | CTTTTTGTTTTTGCA[C/T]ATACAGTACATATTT | 81550 |
rs780766293 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60473637 | CCAATATTATAATAA[G/T]TTTTGTTTTATAATT | 81550 |
rs780797105 | in-del | -/T | 4.06364e-05 | 0.00450739 | intron-variant | TDRD3 | GRCh38.p7 | 13:60460364 | AAGTGATTTTTATTC[-/T]TTTCTGTTTTGACAG | 81550 |
rs780832796 | snp | C/T | 1.79525e-05 | 0.00299599 | intron-variant | TDRD3 | GRCh38.p7 | 13:60529221 | GAAGACAACAAGGTA[C/T]GGATGCTTTAAAGAT | 81550 |
rs780834182 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60549932 | CAAGTAATCCTATTA[A/C]GAACATACTTTTATG | 81550 |
rs780872048 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486221 | CCTTTTTTTTATACA[A/G]TGTAGTAACTGAACA | 81550 |
rs780883604 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60456310 | CTGATATTTCATATC[C/T]GTTGGTATGACTAGT | 81550 |
rs780891565 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60505304 | CAGTTTTCCCCTCAC[A/G]GTGTAAACAAAGCCA | 81550 |
rs780895664 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400471 | CTTCTGGCTGGGCGC[A/G]GTGGTGGCTCATGCC | 81550 |
rs780904596 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430731 | ACTTGCTCAGCTGTT[-/A]ACAATTTTTTTAATA | 81550 |
rs780943995 | in-del | -/AAA | 1.64806e-05 | 0.00287054 | cds-indel, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60509837 | CAAGCTCTTATGGAT[-/AAA]AATGGCAACAACTTA | 81550 |
rs780951653 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60510314 | TCATTGCATGGTCAA[A/G]TTTCTTATGTGGTCC | 81550 |
rs780954289 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551556 | TCCAAATTACCTCTC[C/T]AGGAAGTAAACCCAA | 81550 |
rs780959917 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469091 | TACTAATGTGCTGTG[A/G]TTTGGGTTGCTGTAC | 81550 |
rs780971368 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60518344 | CACTGGAGGCTCCAC[A/G]TCTGAGAGGGACACA | 81550 |
rs780979757 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60478060 | TTTCAAAACTTGTTA[C/T]TGGTCTGGTCAGGTT | 81550 |
rs781017155 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466949 | CTGAATTCCAGTTTT[-/G]GGAAAGAGCTTCAAA | 81550 |
rs781038208 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446954 | GTTATAGTTCTTGTT[C/T]AAATCAACTTTGTTT | 81550 |
rs781045377 | snp | A/G | 1.66468e-05 | 0.00288498 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483727 | ATAAATGCTGGAAAT[A/G]TATTTTTTATGTATA | 81550 |
rs781059807 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497642 | AATGAAAGGTGCATG[C/T]ACAGTCTTGCCAGGT | 81550 |
rs781068906 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60465974 | CCTTGTTTTCCTTTG[A/C]CAGAGGGTTAAGAGG | 81550 |
rs781077248 | snp | C/T | 1.65883e-05 | 0.00287991 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60528791 | AGAAAATCCACTTCC[C/T]CAAGGATCTGTAGAT | 81550 |
rs781086731 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60413922 | TACATTATTTCACTT[A/G]TACAGGAAGAATAGA | 81550 |
rs781087922 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453484 | TCTCTAGCAACACTT[-/C]TCCTTTAATCAGTTG | 81550 |
rs781116781 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571340 | ACGGAATATATTCTT[-/G]AGATAAAAGATATTT | 81550 |
rs781126733 | snp | A/G | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395077 | TTAAGTGATGTGTAT[A/G]TCTAGTTGCATTACA | 81550 |
rs781135076 | snp | A/C/T | 0.000148419 | 0.00861332 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60467350 | GGTGGTGAAGTGGAA[A/C/T]ACCTTATTGAGAAAT | 81550 |
rs781139060 | snp | G/T | 3.30737e-05 | 0.00406642 | splice-donor-variant | TDRD3 | GRCh38.p7 | 13:60510756 | CTTTGAATGTGGAAG[G/T]TAAGCTAATTTAAAG | 81550 |
rs781142732 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445338 | AAATGGAGTACATCT[G/T]GTTACCTTCCTTTGT | 81550 |
rs781163003 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60503385 | TAAAAACATGACTGA[C/T]AAAGTTTAGTTATCT | 81550 |
rs781175105 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60566902 | AAAAATAAAATAGTT[C/T]GAGTCTTACTCTGGT | 81550 |
rs781201834 | snp | A/G | 1.70609e-05 | 0.00292065 | intron-variant | TDRD3 | GRCh38.p7 | 13:60494612 | CAAATTTAAAGTGTT[A/G]TTTCTTAAAATGATT | 81550 |
rs781231484 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553881 | TACTAATATAATGAG[A/G]TTTTATATTAGAAAT | 81550 |
rs781243512 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60547572 | ATGTAAATGTGCTCT[A/G]TAACCTCCCAAGAGC | 81550 |
rs781249092 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60489855 | TATTGAGAATATATT[G/T]TTTAAAATGATTATA | 81550 |
rs781257977 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481872 | AATGAGTATAAGAAT[G/T]AGCTTTGGTCAACAG | 81550 |
rs781261476 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434815 | CACATGGGAATTGAT[A/G]ATAATTCTCTTCTCT | 81550 |
rs781262797 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60498734 | TTCTATCCTTCCCCA[A/G]GGAGACCTCCGGCCT | 81550 |
rs781267773 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60433234 | GTGGCAGTGGGTAAA[A/G]GAGAATAAAACTTTA | 81550 |
rs781306298 | snp | C/T | 0.000102822 | 0.00716943 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60444712 | AATTGGCAAGAAATT[C/T]CTCCCCAGTGACATC | 81550 |
rs781322217 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400099 | AATGTTCCAGGGCTT[C/T]CTACAGAGTAGTGAT | 81550 |
rs781356119 | in-del | -/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426296 | GAGGGCAGAGGAAAT[-/G]GGGGAGATGTGGGTC | 81550 |
rs781364973 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60488694 | TTCTCCAGCCTCAGC[C/G]TCCCAGGTAGCTGGG | 81550 |
rs781391384 | snp | A/G/T | 3.3166e-05 | 0.00407211 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509732 | CCTTATCTGTGGGCT[A/G/T]TCAGCCAGCTTTTCT | 81550 |
rs781415012 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441997 | GAGTGGTCCAAGTGC[A/G]AAGTCCCTAGCTGCC | 81550 |
rs781425784 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452529 | TTTGCCTTTTCTTGG[C/T]ATTTCACGTGAATGG | 81550 |
rs781425793 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60514564 | GCTTCTTAGGGGAGA[G/T]GACATCTAGTTAAGA | 81550 |
rs781495038 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60540441 | GGAGGTTGCGGATTA[C/T]ACAAAAACACTTTGC | 81550 |
rs781496016 | snp | C/T | 3.29875e-05 | 0.00406112 | missense, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60494532 | TACAGAAAGAAAAGT[C/T]AACCAAATCAGAGGG | 81550 |
rs781513794 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530955 | TGTGCTCATTAAATA[A/G]TGAGGTATAAGCAGA | 81550 |
rs781513900 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60534629 | ATATATTCTGATTAG[C/T]ATATAAGAATTGTTG | 81550 |
rs781561745 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497463 | GGTGTGAACTAAGCT[C/T]CGTGTTTAAAGGTGG | 81550 |
rs781582892 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60540012 | TATGTAACAGTGTGG[-/T]TTTTGCCAATTAGTA | 81550 |
rs781607715 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60532275 | TGGAGCATTCTTAGG[A/G]TAACTGAATGATCTT | 81550 |
rs781624299 | in-del | -/GGCCTGGGCCCCGGGCGGCG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60397616 | GGCGGCGGCGGCGGC[-/GGCCTGGGCCCCGGGCGGCG]GGCCTGGGCCCCGGG | 81550 |
rs781644003 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60447855 | AAAGCAACATGTTGC[A/G]GGGAGGAGGGTGTCA | 81550 |
rs781695688 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60416100 | AATTGTGTTTTGGAA[A/G]TTGATAAGGTATTGA | 81550 |
rs781702867 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482905 | TCTGTAGTGATAACA[A/G]TTAAAATGCACAAAA | 81550 |
rs781722392 | snp | C/T | 1.65373e-05 | 0.00287548 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483895 | TTAGGAAAAAGTGTT[C/T]TTCATTAGCATTCAA | 81550 |
rs781735949 | snp | C/T | 3.29538e-05 | 0.00405904 | missense, stop-gained, nc-transcript-variant | TDRD3 | GRCh38.p7 | 13:60567601 | GACGATCCACTCGGC[C/T]AACCCAACAGTTTTA | 81550 |
rs781762699 | snp | C/T | 3.43077e-05 | 0.00414158 | intron-variant | TDRD3 | GRCh38.p7 | 13:60528356 | GCATATGGTATACTT[C/T]TACCTTTCAGAACCT | 81550 |
rs781763950 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423102 | AGCATCAAGCTTTTC[A/G]AAACCAATATATAAA | 81550 |
rs781778616 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60515689 | GGTGAGCTGGGGTAT[A/G]TTGTAAAATAAACAA | 81550 |
rs796083153 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60430342 | CAATGCTATGAGTGC[A/G]GTAGTCAGTGTAGTG | 81550 |
rs796088952 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475666 | CATTCCCAGCAACTG[A/T]GTATGTGTATTTTCC | 81550 |
rs796091588 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404312 | TGTTGGTTTGTTTGC[-/T]TTTTTTTTTTTTTTT | 81550 |
rs796092332 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523768 | TTTTAGTAGAGATGG[A/G]GTTTCACCATGTTGG | 81550 |
rs796101755 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399247 | TCTGCAGAAGCTTAG[A/G]TAGAGTCCCACCCTG | 81550 |
rs796104947 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60466979 | ATGTGTGTGTGTTTT[G/T]TTGTTTTTTTGTTTT | 81550 |
rs796114773 | in-del | CC/TCTTTAGA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453486 | TCTAGCAACACTTTC[CC/TCTTTAGA]TTAATCAGTTGAACT | 81550 |
rs796133888 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60452284 | TTTGTTATTGTAAAT[G/T]GTGTTTAAAAATTTT | 81550 |
rs796134914 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60476933 | ACTGAATTTGTTTAT[C/T]GGCTCTAGAAGCCTT | 81550 |
rs796137493 | in-del | -/AT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60464600 | TACACACACACACAC[-/AT]ACACTGGAATATTAT | 81550 |
rs796144666 | in-del | -/TTTTTTTTTTTTTTTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60541717 | TCCTTCAGCATAGTC[-/TTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 81550 |
rs796158516 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60490962 | GTCTCTACTAAAAAT[A/G]CAAAATTAGCTGGGC | 81550 |
rs796189945 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450405 | AAAGACAGGCTTTGG[C/T]ATGAGATAGATCCGA | 81550 |
rs796224262 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460926 | GAGAATAGCTTGAAC[A/C]TGGTAGGCGGAGGTT | 81550 |
rs796229274 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402845 | AGGCATGCGCCACCA[C/T]GCCTGGCTAGCCAAT | 81550 |
rs796237022 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60530226 | TGCCTCTCTGGTTTC[C/T]GTCTGTAGTCTTGCT | 81550 |
rs796240540 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60424662 | AGCCTGCGCAACAGA[A/G]GGCAACTCTGTCTGA | 81550 |
rs796259856 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60400738 | GCGAGACTGTGTCTC[-/A]AAAAAAAAAAAAAAA | 81550 |
rs796265441 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434694 | CTCCATTAGAGAGTG[A/C]AAAAAAAAAGTGTGC | 81550 |
rs796270383 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481670 | TTACACATAGTTTTA[A/C]TAGCTGTTTAACGCC | 81550 |
rs796271695 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60548136 | GCTTAACCTGAGGAG[-/T]TATAGTAGAGGGAAG | 81550 |
rs796288663 | in-del | -/AG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60557848 | TTTTTTTTTTGAGAC[-/AG]AGTCTCGCTCTGTCA | 81550 |
rs796293309 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60404165 | TCATGTCTTGTGCTC[C/T]TTGGCTAAGGAAAAA | 81550 |
rs796303113 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60536060 | GAAAATTATATCATC[C/T]AGAGTAACTTCATCA | 81550 |
rs796324007 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469630 | GGCTTTATAGTTTTT[G/T]ATTTGGTAGCCACAG | 81550 |
rs796325439 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60486765 | CCACTGTCCCTTAAC[A/G]TTCACCCTTCCCAGC | 81550 |
rs796334241 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60450754 | GATTGAGAAACCAGC[C/T]GTGTCAATGTAGTGA | 81550 |
rs796346605 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60407841 | CTGTGTTCCGACCCA[A/T]ATCTCAACTTGAATT | 81550 |
rs796347111 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60482652 | TGTTGTTGTGAAAAA[A/T]TAGATTAATATCTTA | 81550 |
rs796358951 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461428 | GAAATTGTCCCCTCT[A/C]TTCTTGATATTTCCA | 81550 |
rs796385989 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60552824 | GGCTTGGGTCTTGCA[C/T]CCTTTGAAGCCACAG | 81550 |
rs796394898 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426038 | TGCAGGGGTTGGTGC[C/T]GCTAACACCCGAGTT | 81550 |
rs796419363 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60446490 | CCTCAGCCTCCCAAA[A/G]TATTGGGATTACAGG | 81550 |
rs796424669 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60444398 | TTTACATAAATTAAG[-/T]TTTTGGATTTTAATA | 81550 |
rs796434541 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60479565 | TGTTATGTTTCTGCA[G/T]TGATGATTTGTCTAA | 81550 |
rs796460926 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60531018 | GGAGTACAGAGTGAA[A/T]CAGCTAGATGGCATA | 81550 |
rs796509168 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60516263 | GGCTTGGATGGACTT[C/G]TTATGTCATATCAGA | 81550 |
rs796527278 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60529280 | ATTCTAGTGGGACTT[C/T]ATAGAAGCTGTCACT | 81550 |
rs796528255 | multinucleotide-polymorphism | CA/TG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60563176 | AGGTTGCCTTGAGCC[CA/TG]GATTGCACCATTGCA | 81550 |
rs796533247 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60561875 | TTTTTTGTTGTTGTT[G/T]TTGTTGTTGTTGTTG | 81550 |
rs796537711 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60497471 | CTAAGCTCCGTGTTT[-/A]AAGGTGGGTGCAGTC | 81550 |
rs796540704 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60547033 | AAAATGTCTAGATTG[-/A]AAAAAAATAATTTCA | 81550 |
rs796550349 | in-del | -/AC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60469436 | CACACACACACACAT[-/AC]ACACACACACACACA | 81550 |
rs796562162 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445348 | CATCTGGTTACCTTC[C/G]TTTGTAAATAATTAT | 81550 |
rs796564618 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457201 | TTGTGGAACTACTAA[C/T]TTAAGGCTTGATGAT | 81550 |
rs796571780 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60403979 | GCACTGTGTTGCTGA[A/G]CTATGATGTACAAGA | 81550 |
rs796572727 | in-del | -/ATATATATATATATATATATATATATATATATATATATATATAT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60496289 | ACTTAACAAACTCCC[lengthTooLong]ATATATATATATCCT | 81550 |
rs796573158 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60402354 | GTAATGTAATTATAC[C/T]TTCTTATACTAGTGG | 81550 |
rs796581395 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60492454 | AGGTTTTCTAATCCC[A/G]GTTTTAAAGATGAAA | 81550 |
rs796603744 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60434540 | TTTGAAGGTAAAATT[A/G]GTGAGAAATATTTGT | 81550 |
rs796606666 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60480644 | TTGTATGTTTGGTCT[C/T]TTTACATAACCCCAT | 81550 |
rs796613407 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60499474 | ACCTTTACTGTCCTT[C/T]CTCAGGGGTATATCA | 81550 |
rs796632134 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60470771 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTATGT | 81550 |
rs796634266 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570427 | ATGCTAGCAAGGATG[G/T]GGAGAAAGGAGAACC | 81550 |
rs796640418 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60564545 | TCAGAAAGAAAATGG[C/G]CCTGGTTTGGACTCT | 81550 |
rs796656846 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60423032 | AGATTATTAAGATAA[C/T]AAAATCCTTAGGACC | 81550 |
rs796662720 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60453982 | ATACTCCTATATTTA[C/T]ATAGGAAATATATGT | 81550 |
rs796665829 | in-del | -/A | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60420943 | CTGAGACTCCGTCTC[-/A]AAAAAAAAAGAAAAT | 81550 |
rs796671189 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554824 | GATGATAAGCAAATT[A/T]CTCTCCAGATTGTAA | 81550 |
rs796672955 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562695 | CACTGAATTTCATAT[G/T]CTGATGTATGTATTG | 81550 |
rs796683136 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525666 | TGTAATGACTTTTCC[C/T]CTTTACTATCAGCAA | 81550 |
rs796724403 | in-del | -/GT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60484531 | ATAATAAGGTTTATC[-/GT]GTGTGTGTGTGTCCA | 81550 |
rs796744899 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60504659 | TGGCAAGATGGCTGA[A/G]TAGGAACAGCTCCGG | 81550 |
rs796748234 | snp | A/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525092 | ATTTTCTCTCAAAAA[A/C]AAAAAAAAAAAAAAA | 81550 |
rs796749990 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60431235 | TTAAGCTAGTTTAGT[A/G]TCTCTTCAGGGTCTT | 81550 |
rs796760057 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475889 | ATTCTTTAATGAGGT[G/T]GTTTTTTGCTTGCTG | 81550 |
rs796765642 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60523960 | CATTTCTACTTGTGC[-/T]TTTTTTTTTTCCACC | 81550 |
rs796782738 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60570809 | GTCCCCTTGACCCCT[-/T]CTTTAGTTTCTTTCA | 81550 |
rs796788367 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60457149 | ATAATGAAAAAAATC[A/G]TTATATTTACTGGTT | 81550 |
rs796795160 | in-del | -/TTAG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60441181 | TGTCTTGCACTGAAA[-/TTAG]TTAATTCTATTGCTT | 81550 |
rs796800024 | in-del | -/AT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461005 | GACTGTGTCTCAAAA[-/AT]ATATATATATAAAAT | 81550 |
rs796802235 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60399900 | AGACCAATCTGTTCA[A/G]GTTTACATTATTTTT | 81550 |
rs796806259 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60554853 | AATCAGTTCCCCCAA[C/G]CTCTGTTGAACATCT | 81550 |
rs796823358 | in-del | AA/CAAAAC | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60525099 | TCAAAAAAAAAAAAA[AA/CAAAAC]AAAAAAAACCCCACA | 81550 |
rs796837758 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60481350 | TCTTCCCTCTTTGTG[-/T]TTTTTTTTTTTTTGT | 81550 |
rs796840592 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60493341 | AAAAATTGTTTTAGC[G/T]TCTTCTTTTATTATA | 81550 |
rs796848510 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60491797 | AATGATTATTTCAGG[-/T]TTTTTTTTTTTTTAA | 81550 |
rs796850624 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60442000 | TGGTCCAAGTGCAAA[A/G]TCCCTAGCTGCCAGC | 81550 |
rs796854314 | in-del | -/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60454795 | AACAATGTATATTTC[-/T]TTTTTTTTTTTATTT | 81550 |
rs796875576 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60562944 | GTAATATAAGATAAA[A/G]TGGGCTAGGCATGGT | 81550 |
rs796902341 | snp | C/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60461896 | CTGACAACAGAAAGA[C/G]TGAGAAGTTACATTT | 81550 |
rs796917016 | snp | G/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60475644 | CCACAGTGGCTGGAC[G/T]AGTTTACATTCCCAG | 81550 |
rs796935043 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60553269 | GCTTTGCTGCTTAGA[A/G]ATTTCTTCAGCCAGA | 81550 |
rs796959589 | snp | A/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60572412 | TAAGCTTAGGAAATA[A/T]TGCAGCTGGATGTAG | 81550 |
rs796961493 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60571680 | TATTGTAATTTGCAC[A/G]TTCTTTGATTATCCT | 81550 |
rs796985071 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60460028 | GGAGGGAGAAGTGGG[A/G]TTTATGGGTATGATT | 81550 |
rs796989882 | snp | A/G | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60439070 | ATGCATGGCTGATTT[A/G]GACTGGATAAAAGAA | 81550 |
rs796997716 | snp | A/G | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60426154 | ATAGGATGTTATGCT[A/G]AGTGAAAAAAGCCAG | 81550 |
rs797005566 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60451038 | CTTTGTAGTGGAAAC[C/T]AAAGAATAAAAAATA | 81550 |
rs797008805 | snp | C/T | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60551743 | GAGGTTTAATTGACT[C/T]ACAGTTCTGCATAGC | 81550 |