SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs893926 | snp | A/C | 0.0633504 | 0.166319 | intron-variant | RNF40 | GRCh38.p7 | 16:30793841 | CTGGCCTGACGGTGG[A/C]CTCTGCAGCCTCCCC | 9810 |
rs893927 | snp | C/T | 0.0629771 | 0.165899 | utr-variant-3-prime, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30781124 | TGGGGGCTCCAGAGC[C/T]CCTGGTCACTTATTT | 9810 |
rs1048622 | snp | C/T | 0 | 0 | utr-variant-3-prime, intron-variant | RNF40 | GRCh38.p7 | 16:30774125 | GCTGAACCTGAAACT[C/T]AGGGGACTCTGGAAC | 9810 |
rs1057734 | snp | A/C | 0 | 0 | intron-variant | RNF40 | GRCh38.p7 | 16:30767360 | AGGAAGATAGGAAGT[A/C]TCAGGAGAAAGGGTG | 9810 |
rs1530201 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | RNF40 | GRCh38.p7 | 16:30767324 | tgttagctcttgaca[A/G]ataggaaagtaaagc | 9810 |
rs1550477 | snp | C/T | 0.0187849 | 0.0950767 | upstream-variant-2KB, utr-variant-5-prime | CCDC189, RNF40 | GRCh38.p7 | 16:30762501 | ACCGCCTCCTCCCGT[C/T]TGACGCCCCTCAGGG | 9810 |
rs3747486 | snp | C/T | 0.494733 | 0.0510469 | utr-variant-3-prime, intron-variant | RNF40 | GRCh38.p7 | 16:30775606 | ATCGGGACACCTCAG[C/T]TGGGTGACTTCCCTC | 9810 |
rs3812998 | snp | A/G | 0.000676132 | 0.0183741 | intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30784379 | AGGGGCTGCGGTCCC[A/G]GCAAGACGGTGGTCC | 9810 |
rs3812999 | snp | A/C | 0.494976 | 0.0498674 | upstream-variant-2KB, utr-variant-5-prime | CCDC189, RNF40 | GRCh38.p7 | 16:30762284 | TGGACGCCACTGCCC[A/C]CCCCCCAACGGTGCG | 9810 |
rs4617878 | snp | C/T | 0.0626037 | 0.165477 | utr-variant-3-prime, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30780142 | CTGAAGGTTTCTGGC[C/T]AAGGAGGAGAGGGGA | 9810 |
rs4889488 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | RNF40 | GRCh38.p7 | 16:30799112 | ccaagggtcaagcaa[C/T]cctcccacttcatcc | 9810 |
rs4889489 | snp | A/G | 0.495483 | 0.0473088 | | | GRCh38.p7 | 16:30801641 | ttacaggcatgaacc[A/G]ccgcgcccagccAGA | 9810 |
rs4889505 | snp | A/G | 0.0275918 | 0.114169 | utr-variant-3-prime, intron-variant, upstream-variant-2KB | PHKG2, CCDC189, RNF40 | GRCh38.p7 | 16:30760719 | TTACCTATCATGACA[A/G]GGCTGTGACAGCTAG | 9810 |
rs4889506 | snp | A/G | 0.0121731 | 0.0770609 | synonymous-codon | RNF40 | GRCh38.p7 | 16:30769507 | GACTGTGCAGAAGCT[A/G]GAGGAGAAGGAGCGA | 9810 |
rs4889507 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | RNF40 | GRCh38.p7 | 16:30771399 | gaggcgggcagatca[C/T]gaggtcaggagatct | 9810 |
rs4889508 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30785444 | GTGAGACTCATGCTC[A/G]TGGGAGGCTGGCAGG | 9810 |
rs4889509 | snp | C/T | 0.0905309 | 0.192535 | downstream-variant-500B | RNF40 | GRCh38.p7 | 16:30800448 | CCATGTGAATTCTTT[C/T]TCTTTCTCTTTCTTT | 9810 |
rs6565202 | snp | A/G | 0 | 0 | intron-variant | RNF40 | GRCh38.p7 | 16:30767258 | TGGAGCAACATTCTG[A/G]TAGAAGACAGACTAG | 9810 |
rs7188698 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF40 | GRCh38.p7 | 16:30767348 | gtaaagcagaaaagg[A/G]agataggaagtatca | 9810 |
rs7188927 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | RNF40 | GRCh38.p7 | 16:30776976 | CTGATGTAGACCGCT[C/G]TCTTCTCAAAACTTC | 9810 |
rs7195142 | snp | A/G | 0 | 0 | missense | RNF40 | GRCh38.p7 | 16:30768395 | CCAAGCGGGAGCTTC[A/G]GGAACGGGAAGGTCC | 9810 |
rs7195583 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | RNF40 | GRCh38.p7 | 16:30776861 | GGGCCCACCCCGACC[G/T]TGGCTGTCTTCTTGG | 9810 |
rs7195669 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | RNF40 | GRCh38.p7 | 16:30796643 | gctggagtgcaatgg[C/T]atcatcttggctcac | 9810 |
rs8045484 | snp | C/T | 0.0633504 | 0.166319 | upstream-variant-2KB, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30788035 | CAGTTCAACACACTG[C/T]ATTATTATTCCTGGG | 9810 |
rs8045877 | snp | A/G | 0.0629771 | 0.165899 | | | GRCh38.p7 | 16:30800920 | GAAAAAGAGTggcca[A/G]acggggtggctcacg | 9810 |
rs8047004 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | RNF40 | GRCh38.p7 | 16:30794372 | gcgtgcgccatctca[C/T]gcccagctaattttt | 9810 |
rs8047780 | snp | A/G | 0.0532157 | 0.154195 | | | GRCh38.p7 | 16:30800921 | AAAAAGAGTggccag[A/G]cggggtggctcacgc | 9810 |
rs8048328 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30785598 | CTGGTCTGCACCCAT[A/G]AGCTGGAACCATACT | 9810 |
rs8048656 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30785064 | AGGACTGGGGCACTT[C/T]CCTGTTATCCAAGCA | 9810 |
rs8050578 | snp | A/T | 0.0490535 | 0.14873 | upstream-variant-2KB, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30788083 | GGGTGGGCATACCTC[A/T]GAGATGCATGGAAAT | 9810 |
rs8050758 | snp | C/G | 0.00191732 | 0.0309028 | missense, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30782209 | TCCCACTTAAGAAGG[C/G]GCTGGGCCCTGCGCC | 9810 |
rs8051418 | snp | C/T | 0.0532157 | 0.154195 | | | GRCh38.p7 | 16:30801056 | aaaattagccaggca[C/T]ggtggcacatgcctg | 9810 |
rs8056105 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | RNF40 | GRCh38.p7 | 16:30770970 | ccgccttggcctccc[A/G]aagtgttgggattac | 9810 |
rs8058961 | snp | A/G | 0.468349 | 0.121752 | intron-variant | RNF40 | GRCh38.p7 | 16:30797742 | GATGCACAGGGCCAC[A/G]TCTTCAACCCCATCC | 9810 |
rs9921630 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | RNF40 | GRCh38.p7 | 16:30772656 | ACAGCAGATGTGGAC[A/G]CTTGAGCGGAGGGGT | 9810 |
rs9921835 | snp | A/G | 0.470908 | 0.117046 | downstream-variant-500B | RNF40 | GRCh38.p7 | 16:30800570 | aacctctgcctcccg[A/G]gttcaagcaattctc | 9810 |
rs9939243 | snp | A/T | 0.499879 | 0.0077866 | intron-variant | RNF40 | GRCh38.p7 | 16:30789862 | taataataataattt[A/T]aaaaaaaaTTAggcc | 9810 |
rs11556799 | snp | A/G/T | 4.94279e-05 | 0.00497107 | missense, stop-gained | RNF40 | GRCh38.p7 | 16:30769372 | AAGGATGAGTTGGGC[A/G/T]AGCAGGTCCTTGGCC | 9810 |
rs11556800 | snp | G/T | | | missense | RNF40 | GRCh38.p7 | 16:30768450 | CTCCGCTCTCTCAAG[G/T]GCTGATCGGGAGAAG | 9810 |
rs11556801 | snp | A/G | 0.005305 | 0.0512285 | missense | RNF40 | GRCh38.p7 | 16:30766835 | AGTATGAGATGCTGC[A/G]CATCGAGTTTGAGCA | 9810 |
rs11640414 | snp | C/T | 0.0490535 | 0.14873 | utr-variant-3-prime, intron-variant | RNF40 | GRCh38.p7 | 16:30775394 | CCCGGTCTGACCACG[C/T]CCTTGGCTGTCATGG | 9810 |
rs11642466 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | RNF40 | GRCh38.p7 | 16:30770621 | TGTCTAGCTTTGGCT[A/G]AAGGCTTAAGATTAA | 9810 |
rs11642862 | snp | C/T | 0.106633 | 0.204807 | utr-variant-3-prime, intron-variant | RNF40 | GRCh38.p7 | 16:30774503 | CTCGCTCCCTGCCTA[C/T]TGGCTCACAAATGAG | 9810 |
rs11645175 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | RNF40 | GRCh38.p7 | 16:30791978 | TCAGATGGGCCCAAG[C/T]GTGTCTGGGACCCAA | 9810 |
rs11648654 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | RNF40 | GRCh38.p7 | 16:30797246 | GAATTATAACATGAA[A/G]CTAGTGTTGGTACAC | 9810 |
rs12232385 | snp | A/G | | | intron-variant | RNF40 | GRCh38.p7 | 16:30792693 | tggtgggcgcctgta[A/G]tcccagctacttggg | 9810 |
rs12447534 | snp | C/T | 0.495483 | 0.0473088 | intron-variant | RNF40 | GRCh38.p7 | 16:30792936 | agacccctgacctgg[C/T]gatggatgaataaag | 9810 |
rs12447824 | snp | A/G | 0.0535932 | 0.154675 | upstream-variant-2KB, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30789061 | aaaaaaaagaaagac[A/G]acaacaacaacaaaa | 9810 |
rs12448366 | snp | G/T | 0 | 0 | synonymous-codon | RNF40 | GRCh38.p7 | 16:30768324 | AGAGGACTTCCAGGG[G/T]ATAACCCCTGGGGCC | 9810 |
rs12596394 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | RNF40 | GRCh38.p7 | 16:30795923 | CTATAGAAAATCATA[C/T]ATAAATGGGTAAATA | 9810 |
rs12598056 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | RNF40 | GRCh38.p7 | 16:30798012 | GAAAAAAAGGAGGGG[A/G]TCTGACAGATGACTT | 9810 |
rs12931844 | snp | G/T | 0.0629771 | 0.165899 | intron-variant | RNF40 | GRCh38.p7 | 16:30796981 | TATTTAAAGAACACC[G/T]TTAAGTGGGTCCCAT | 9810 |
rs12933849 | snp | C/G | 0.0588605 | 0.161139 | intron-variant | RNF40 | GRCh38.p7 | 16:30794767 | ACTCCCGGTCTGTAA[C/G]TCCTGACCTCAAGTG | 9810 |
rs28853644 | snp | C/T | 0.470132 | 0.118498 | intron-variant | RNF40 | GRCh38.p7 | 16:30789706 | AGCTGGGCATGGTGG[C/T]GTGCACCTGTAATCC | 9810 |
rs34121355 | in-del | -/T | | | frameshift-variant, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30781871 | TGAGGGCGAGACCCC[-/T]TACCCCCACAGAGAG | 9810 |
rs34348206 | in-del | -/T | | | upstream-variant-2KB, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30787460 | AATCTGAGATAGGGC[-/T]TTTCCGGGCGCGGCC | 9810 |
rs34405457 | in-del | -/A | 0.375 | 0.216506 | downstream-variant-500B, intron-variant | RNF40 | GRCh38.p7 | 16:30776397 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 9810 |
rs34418731 | in-del | -/C | | | frameshift-variant | RNF40 | GRCh38.p7 | 16:30769475 | GCAGCTGGGCATCCA[-/C]CTAAGGACCAGAGGA | 9810 |
rs34480360 | snp | C/T | 0.455263 | 0.142713 | upstream-variant-2KB, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30787368 | TCTCCCAGATGCCCA[C/T]GCTGCCTGCTCCCAC | 9810 |
rs34599648 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF40 | GRCh38.p7 | 16:30765700 | TTTTGACCTCTATTT[C/T]GTTCTCGCCAATATG | 9810 |
rs34628363 | in-del | -/A | | | downstream-variant-500B | RNF40 | GRCh38.p7 | 16:30800485 | GAGCGAGATTCCATC[-/A]AAAAAAAAAAAAAAA | 9810 |
rs34730253 | in-del | -/G | | | intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30786137 | TACCGCTCTTTGGCA[-/G]GGGTGCAGCCAGTCT | 9810 |
rs35033286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF40 | GRCh38.p7 | 16:30797366 | ACAGGCTTGAGCCAC[C/T]GTGTCCGGCCTGGAC | 9810 |
rs35083725 | in-del | -/G | | | frameshift-variant, intron-variant | RNF40 | GRCh38.p7 | 16:30774060 | GGCCGCGTTGCACTT[-/G]GGGGCACTTCCTCTG | 9810 |
rs35207681 | in-del | -/T | | | intron-variant | RNF40 | GRCh38.p7 | 16:30793181 | GATCTTAAAACTAAC[-/T]TTTTGATGTACCAGA | 9810 |
rs35289287 | in-del | -/G | | | intron-variant | RNF40 | GRCh38.p7 | 16:30772738 | GTACCGCACTCTTCA[-/G]GGAGGTGACACGGCC | 9810 |
rs35408241 | in-del | -/A | | | frameshift-variant, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30784062 | ATCCCTTGGACCACC[-/A]AGATCCCCCTGGACC | 9810 |
rs35446957 | in-del | -/TT | 0.497824 | 0.0329157 | utr-variant-3-prime, intron-variant, upstream-variant-2KB | PHKG2, CCDC189, RNF40 | GRCh38.p7 | 16:30760684 | CGGCCACCAATACTC[-/TT]TTTCTTTTACTATAA | 9810 |
rs35589507 | in-del | -/C | | | | | GRCh38.p7 | 16:30802254 | AATCCCAGATACTCC[-/C]AGAGGCTGAGGCGGG | 9810 |
rs35662051 | in-del | -/A | | | intron-variant | RNF40 | GRCh38.p7 | 16:30799221 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 9810 |
rs35676536 | in-del | -/C | | | utr-variant-3-prime, intron-variant | RNF40 | GRCh38.p7 | 16:30774130 | ATGGTGTTCCAGAGT[-/C]CCCTGAGTTTCAGGT | 9810 |
rs35695082 | snp | A/G | 0.121369 | 0.214369 | utr-variant-3-prime, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30781068 | GAAAAGGTCCCACTC[A/G]CTGCACTGGGGTCCT | 9810 |
rs35698207 | in-del | -/T | | | upstream-variant-2KB, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30789246 | GTGCCCTGCCCGGAC[-/T]TTTTTTTTTTTTTTT | 9810 |
rs55733443 | in-del | -/TAAATAAA/TAAATAAATAAA | 0 | 0 | intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30785894 | AAATAAATAAATAAA[-/TAAATAAA/TAAATAAATAAA]AACAGCCAGCTGTCA | 9810 |
rs56038936 | snp | C/G/T | 0.0414363 | 0.137845 | intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30785141 | TGCATCTGCAGGAAC[C/G/T]GCCCAGAGGAAGAGA | 9810 |
rs56656810 | snp | A/C | 0.464203 | 0.128908 | intron-variant | RNF40 | GRCh38.p7 | 16:30777438 | TCAGGTCACTTTCCC[A/C]GGAAAGCTTCCTGAC | 9810 |
rs57331958 | snp | C/G/T | | | intron-variant | RNF40 | GRCh38.p7 | 16:30796031 | TGGAGGTCAGGAATT[C/G/T]GAGACCAGACTAGCC | 9810 |
rs58257924 | in-del | -/G | 0.0532157 | 0.154195 | intron-variant | RNF40 | GRCh38.p7 | 16:30799701 | TTTTTAGTAGAGACA[-/G]GGGTTTCACCATGTT | 9810 |
rs58318211 | snp | C/G | | | intron-variant | RNF40 | GRCh38.p7 | 16:30795988 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCCGAGG | 9810 |
rs59129131 | in-del | -/AAAAAAAA/AAAAAAAAAAAAAAAAAAAAAA | 0 | 0 | intron-variant | RNF40 | GRCh38.p7 | 16:30797654 | AAAAAAAAAAAAAAA[lengthTooLong]TACTGGGTCCACACT | 9810 |
rs59538019 | snp | G/T | | | intron-variant | RNF40 | GRCh38.p7 | 16:30796094 | AAAAATTAGCCAGGT[G/T]TGGTAGCTCAGGCCT | 9810 |
rs60196227 | snp | A/G | | | intron-variant | RNF40 | GRCh38.p7 | 16:30796028 | CACTGGAGGTCAGGA[A/G]TTCGAGACCAGACTA | 9810 |
rs61729947 | snp | C/T | 0.0460887 | 0.144638 | synonymous-codon, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30782300 | CTGATGCTGGAGGAG[C/T]ACAGAGCGATCCAGG | 9810 |
rs61741652 | snp | A/T | 0.00819451 | 0.0634831 | missense, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30781848 | TTTTGCCCTTCCCCA[A/T]GGCTGCTGCTCTCTG | 9810 |
rs61754473 | snp | C/T | 0.00249112 | 0.0352044 | synonymous-codon | RNF40 | GRCh38.p7 | 16:30772145 | GAAGGTGGAGGTCTA[C/T]GCAGATGCCGACGAA | 9810 |
rs62057185 | snp | A/G | 0.030665 | 0.119967 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CCDC189, RNF40 | GRCh38.p7 | 16:30761991 | CACGCCAGTGGGAGC[A/G]AAGAGAACGCGCAGA | 9810 |
rs62057223 | snp | G/T | 0.495368 | 0.0478996 | intron-variant | RNF40 | GRCh38.p7 | 16:30790666 | ACTCTGGAGGCTGAG[G/T]CATGAGAATTGCTTG | 9810 |
rs62057224 | snp | A/G | | | intron-variant | RNF40 | GRCh38.p7 | 16:30792732 | GCAGGAGAATCACTT[A/G]AACCCAGGAGGCAGA | 9810 |
rs62057225 | snp | G/T | | | intron-variant | RNF40 | GRCh38.p7 | 16:30792748 | AACCCAGGAGGCAGA[G/T]GTTGCAGTGAGCCAA | 9810 |
rs62057226 | snp | A/C/T | 0.5 | 0 | intron-variant | RNF40 | GRCh38.p7 | 16:30796727 | AGCGGGGATTACAGG[A/C/T]GTGCGCCACCATGCC | 9810 |
rs62057227 | snp | C/T | | | intron-variant | RNF40 | GRCh38.p7 | 16:30799461 | ATGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 9810 |
rs62622830 | snp | A/G | 0.251199 | 0.249997 | utr-variant-3-prime, intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | PHKG2, CCDC189, RNF40 | GRCh38.p7 | 16:30759629 | CCTGGAACATTCTGG[A/G]AACTTTACCCATCCC | 9810 |
rs71149050 | in-del | -/GGATTTTTTTTTTTTTTTTTT | 0 | 0 | intron-variant | RNF40 | GRCh38.p7 | 16:30770120 | AAAAAAACAAAAGAT[-/GGATTTTTTTTTTTTTTTTTT]TTTTGAGTTGGAGTC | 9810 |
rs71149051 | in-del | -/T | | | intron-variant | RNF40 | GRCh38.p7 | 16:30799534 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 9810 |
rs71149052 | in-del | -/G | 0 | 0 | | | GRCh38.p7 | 16:30801607 | ATCTGCCCGCCTCGG[-/G]CCTCCCAAAGTGCTG | 9810 |
rs71380412 | multinucleotide-polymorphism | AG/GA | 0 | 0 | | | GRCh38.p7 | 16:30800920 | GAAAAAGAGTGGCCA[AG/GA]CGGGGTGGCTCACGC | 9810 |
rs71389478 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF40 | GRCh38.p7 | 16:30797928 | TTGTGGGGGCCAAGG[A/C]AAGAGGATTGCTTGA | 9810 |
rs72793383 | snp | A/G | 0.0201023 | 0.0982194 | utr-variant-3-prime, intron-variant | RNF40 | GRCh38.p7 | 16:30774146 | ACTCTGGAACACCAT[A/G]GACCCTGGGGGCTGT | 9810 |
rs73540514 | snp | G/T | 0.0123036 | 0.0774623 | utr-variant-3-prime, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30778890 | CAGTGCCTTCCAGAC[G/T]CAGTTGTGGTGAGCA | 9810 |
rs73540515 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime, intron-variant | ZNF629, RNF40 | GRCh38.p7 | 16:30780536 | CTCCCTCTCCACTGA[A/G]GACAGAATTTGAGGA | 9810 |