SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13449376 | snp | A/G | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | Rnf182 | Rn_Celera | 17:24291418 | CTCCAGGGTCCTTCA[A/G]TCTCATCTTCTTGGG | 498726 |
rs13449377 | snp | A/G | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | Rnf182 | Rn_Celera | 17:24291502 | CTGAGAGGTTTGCAC[A/G]AGGAGTTAGACCTCA | 498726 |
rs13449378 | snp | A/G | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | Rnf182 | Rn_Celera | 17:24291228 | GCGTCCCATGATTGT[A/G]GGTAGATGTCAGAGG | 498726 |
rs13449381 | snp | A/G | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | Rnf182 | Rn_Celera | 17:24291270 | AAAGCACGTGGGAGC[A/G]CCCCTCATTTTCCTG | 498726 |
rs13449382 | snp | C/T | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | Rnf182 | Rn_Celera | 17:24291275 | ACGTGGGAGCGCCCC[C/T]CATTTTCCTGGCGCT | 498726 |
rs13457532 | snp | A/T | 0.352532 | 0.228007 | missense | Rnf182 | Rn_Celera | 17:24290504 | TTGGTGATCACCATC[A/T]TGGAGGTACAGAGGG | 498726 |
rs13457533 | snp | A/C | 0 | 0 | synonymous-codon | Rnf182 | Rn_Celera | 17:24290656 | GACGTCCATCCGGGT[A/C]CTGGTGTGGTTGCTA | 498726 |
rs13457534 | snp | C/G | 0 | 0 | synonymous-codon | Rnf182 | Rn_Celera | 17:24290740 | GAAGGTCACCCTGGG[C/G]GTGGTCTTTGTTAGC | 498726 |
rs13457535 | snp | C/T | 0 | 0 | utr-variant-3-prime | Rnf182 | Rn_Celera | 17:24290962 | CCTCAATGAAGCCCT[C/T]GGCCATGCGTCTGCG | 498726 |
rs13457536 | snp | A/G | 0.353823 | 0.227422 | synonymous-codon | Rnf182 | Rn_Celera | 17:24290693 | AGATCCCTAAGGGCA[A/G]GGAGCTGAAGTACAG | 498726 |
rs13457537 | snp | C/T | 0 | 0 | synonymous-codon | Rnf182 | Rn_Celera | 17:24290611 | GGTGCAGTTCCACAC[C/T]GTCCAATTGTGGGAC | 498726 |
rs104907433 | snp | G/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24265749 | CACGCACACACACAC[G/T]CACACACACATGCAC | 498726 |
rs104970714 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24259860 | CAAAGGGTGCTTCAA[C/T]ATCCAGGCTCCAGAA | 498726 |
rs105008180 | snp | G/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24245641 | TCACCATGGCCAGCC[G/T]CTCCCCACCTGTTCT | 498726 |
rs105034929 | snp | A/T | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | Rnf182 | Rn_Celera | 17:24291037 | AGTGAACTTTTTTTT[A/T]TTTTTATTTTTCAGA | 498726 |
rs105061788 | snp | A/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24263902 | AACAAGAGAGATTTA[A/T]CTCTGGAAAGGGACG | 498726 |
rs105074171 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24265906 | ACATGCACACACACA[C/T]GCACACACACATGCA | 498726 |
rs105109592 | snp | A/C | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24277780 | GAACGGCATCTCCAG[A/C]TGCCATTGACATTTC | 498726 |
rs105119134 | snp | G/T | 0 | 0 | upstream-variant-2KB | Rnf182 | Rn_Celera | 17:24241333 | TTACCAATAGAGGAG[G/T]CCCCGTGTATTAACT | 498726 |
rs105121177 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24250633 | TTCTCTTGAGATTGC[C/T]TGTGATGCATTACTT | 498726 |
rs105137650 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24258306 | AGGGGTTGCAATTTG[A/G]TGGGAAAGGGTATTT | 498726 |
rs105143007 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24258502 | AATCAAACACGGTGA[C/T]TCTACGATGTGCATG | 498726 |
rs105146694 | snp | C/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24262973 | AGAGCACTGACTGCT[C/G]TTCCAGAGGTCCTGA | 498726 |
rs105198892 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24279438 | CTTATATGTTTGAAT[A/G]GTGTTTCCCGGCTGG | 498726 |
rs105241363 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24250336 | TGGGAACCCTCTTGC[C/T]GGTTCATAAGTGTTA | 498726 |
rs105246122 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24277712 | CCGACCCCAGGAAGG[A/G]CTAATTGTTGATTAA | 498726 |
rs105252095 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24264439 | ATAAATACTGGGAGG[A/G]GGTCAATGCATAGAA | 498726 |
rs105270346 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24274498 | CTTAAGAGTTCATTC[C/T]TCCCTCTCCCCAAAC | 498726 |
rs105284973 | snp | A/C | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24259862 | CGCAAAGGGTGCTTC[A/C]ACATCCAGGCTCCAG | 498726 |
rs105287635 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24283074 | TAAGAATTCTGCATG[C/T]TTTTCCTTTTTAAAC | 498726 |
rs105307845 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24252408 | TATTTAGGTCTTCGA[A/G]TTTCCACTAAGTTAC | 498726 |
rs105314828 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24257774 | GAAAGAGCATTCGAC[A/G]TCATTTATTGGGTAA | 498726 |
rs105324983 | snp | C/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24249196 | GATGGCCCCTCTCTT[C/G]CCTACCTCCTGAGGT | 498726 |
rs105327922 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24281035 | TTCGGAGCTGGGGAC[C/T]GAACCCAGGGCCTTG | 498726 |
rs105381520 | snp | C/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24274550 | ATCACCCCTCAGAGG[C/G]CAGCTCATTCTGAAA | 498726 |
rs105427959 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24250543 | CCTAATATGTATTCA[A/G]TTAATCCTTACAACT | 498726 |
rs105453803 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24284467 | CCATATTAAAAGTAC[A/G]ATTTGAAAAATCAAA | 498726 |
rs105502499 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24285589 | TCAGATCCCTGTTCT[A/G]CATCTCAGCGACTGA | 498726 |
rs105518210 | snp | A/G | 0 | 0 | utr-variant-5-prime | Rnf182 | Rn_Celera | 17:24242681 | CCGGAGGATCGATGG[A/G]AGGACCGAGAGCCAC | 498726 |
rs105522877 | snp | C/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24279881 | ACACACACACACACA[C/G]GCACACACGTGCATA | 498726 |
rs105527799 | snp | A/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24257388 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGGGGG | 498726 |
rs105541856 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24246204 | TTTAAGGGAAGAAGC[A/G]GGAATCTAGCCTAAG | 498726 |
rs105577415 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24277110 | TTGGTTCTTTTTTTC[A/G]GAGCTGGGGACCGAA | 498726 |
rs105671863 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24279426 | AATAGTGTTTCCCGG[C/T]TGGTGGAACTGTTCA | 498726 |
rs105753489 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24289577 | AATTTGTACCAAATG[C/T]TGGTCTCTTTGACCA | 498726 |
rs105759896 | snp | C/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24281964 | CACACTTCTGCTGTC[C/G]TCTCTTTCAGCCTTG | 498726 |
rs105798353 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24257777 | CGTGAAAGAGCATTC[A/G]ACGTCATTTATTGGG | 498726 |
rs105854220 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24282671 | GTACACACGCACACA[C/T]GCACACACGCGTGCA | 498726 |
rs105893019 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24275241 | GAACAGGAGGCAGTC[A/G]CTGATTCCAGTGCTT | 498726 |
rs105912770 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24258607 | AGAAACGGAATTGGA[C/T]GGAGGGCTGTGTTGG | 498726 |
rs105924682 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24287959 | GTTCATCTGAGTACA[C/T]AAATTCTTTATCCAG | 498726 |
rs105940571 | snp | A/G | 0 | 0 | missense | Rnf182 | Rn_Celera | 17:24290138 | CATCTGAGACCTGAA[A/G]CTCTGCAGGCTCTTC | 498726 |
rs105943145 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24288010 | TCTTTCTGGTCAAAT[C/T]TGGACACATATCTGA | 498726 |
rs105981486 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24289763 | AACAGATTAAATCCC[C/T]TCCTCTTTCCCCACT | 498726 |
rs106066676 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24286628 | AGCCTAGATATGACC[A/G]TACAGTGTAATGGTT | 498726 |
rs106070927 | snp | A/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24258462 | GACATTAGAAATAGG[A/T]TAAAAGGAACCAAAA | 498726 |
rs106089338 | snp | A/C | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24244824 | TGGGCAGTGTATTCA[A/C]TCCGTGGCTGTTTAC | 498726 |
rs106126883 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24248691 | TTGAGAACAAGGGGA[C/T]ACGTGTATTGGGCGA | 498726 |
rs106140661 | snp | A/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24244561 | CAGTGTGGCTTTCAT[A/T]CAGCTACAGGTACAG | 498726 |
rs106226161 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24275262 | ACGGGGAAGCTGGAC[A/G]CATGAGAACAGGAGG | 498726 |
rs106231641 | snp | G/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24244570 | TAGAATTCCCAGTGT[G/T]GCTTTCATACAGCTA | 498726 |
rs106231881 | snp | C/T | 0 | 0 | utr-variant-5-prime | Rnf182 | Rn_Celera | 17:24290075 | GCAATCTTCTGTAGA[C/T]GTGCCTGGCTGAGCG | 498726 |
rs106265114 | snp | A/G | 0 | 0 | upstream-variant-2KB | Rnf182 | Rn_Celera | 17:24241799 | GATTAAACTGCTAAA[A/G]CACCTACCCGGACAC | 498726 |
rs106284159 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24245166 | CCAGACTGTGTTCTA[C/T]GACTTAGACCAAAAA | 498726 |
rs106293383 | snp | C/T | 0 | 0 | utr-variant-5-prime | Rnf182 | Rn_Celera | 17:24290091 | ATCTTGAATTATGGA[C/T]GCAATCTTCTGTAGA | 498726 |
rs106314567 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24257098 | GTGTGTGTGTGTGTG[C/T]GCCACGTGTGTACAC | 498726 |
rs106371274 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24258361 | AAGACAGAGCATAGA[A/G]GGGGGAAAATTCCCA | 498726 |
rs106377480 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24274955 | TCCACTTGGCACTAA[C/T]GTAAAATCAGAGGTC | 498726 |
rs106382925 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24267772 | CATACACACACACGC[A/G]CACAGTTTCCTCGTT | 498726 |
rs106415146 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24278145 | ATGTTTGCCTCAAAC[A/G]CTAAGACAAGCAACC | 498726 |
rs106456225 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24256986 | GGAACTAAACCCAGG[C/T]GCTCCACAAAAGCAG | 498726 |
rs106466318 | snp | C/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24254120 | AAACAGCTGAACAAA[C/G]GAAGCAACCATTCTC | 498726 |
rs106572956 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24284347 | AACCAAAAAGAAAAA[A/G]AAAAAGAAAAAAGAA | 498726 |
rs106668400 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24258606 | GAAACGGAATTGGAC[A/G]GAGGGCTGTGTTGGC | 498726 |
rs106696108 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24245252 | AGTTAAACAAAATTC[C/T]TTGGCTTGCTTTGGT | 498726 |
rs106731875 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24259341 | CCAGAGAACTAAACC[A/G]AAAGAGAGCAGACGT | 498726 |
rs106743141 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24274003 | GTATGTCCCCCGTCA[C/T]GCACACAACCATGTA | 498726 |
rs106767947 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24285590 | TTCAGATCCCTGTTC[C/T]GCATCTCAGCGACTG | 498726 |
rs106798359 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24270481 | TGCCTGAGACAGCCC[A/G]TACTGTCAAAGCAAT | 498726 |
rs106803237 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24258489 | GACTCTACGATGTGC[A/G]TGTAAATGCCAGACA | 498726 |
rs106813173 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24249375 | TCTCTTTTCATCCTG[C/T]GCCCTTTCCAAAATA | 498726 |
rs106837419 | snp | A/G | 0 | 0 | upstream-variant-2KB | Rnf182 | Rn_Celera | 17:24241480 | TCCTGGTATTTGTCA[A/G]TCGCCAAAGAAGTCC | 498726 |
rs106891828 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24277162 | ATTCAACTGTGAAGG[C/T]GAGGATAAAGTAAAC | 498726 |
rs106923533 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24279215 | GCTCTCCACCATGAC[A/G]GTCATGGACTCTAAT | 498726 |
rs106926661 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24284278 | GAAGAATGCAGCCAA[A/G]ATGTTTGTGACACCT | 498726 |
rs106939517 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24284353 | AAAAAGAACCAAAAA[A/G]AAAAAAAAAAAGAAA | 498726 |
rs106958227 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24257087 | TGTGTGCCACGTGTG[C/T]ACACAGTGTCCAAGG | 498726 |
rs107032877 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24265750 | GCACGCACACACACA[C/T]TCACACACACATGCA | 498726 |
rs107042295 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24275276 | CAACCCAAGAGAAAA[C/T]GGGGAAGCTGGACAC | 498726 |
rs107052069 | snp | A/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24257390 | GTGTGTGTGTGTGTG[A/T]GTGAGAGAGAGAGGG | 498726 |
rs107056998 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24265806 | ACACATACACACACA[C/T]GCAGACACACACACA | 498726 |
rs107118740 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24257141 | GTTCTCTGCCTGCAT[A/G]TGTGTGTGTGTGTGT | 498726 |
rs107119663 | snp | A/T | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | Rnf182 | Rn_Celera | 17:24291031 | CTTTTTTTTATTTTT[A/T]TTTTTCAGAATCCAG | 498726 |
rs107124823 | snp | G/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24279402 | CTGTTCAGGAAGGAT[G/T]AGGAGGTGTGGTCTT | 498726 |
rs107221243 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24281786 | GCCCCGAGACACACA[C/T]GCCTAAACACCCCAC | 498726 |
rs107237643 | snp | C/G | 0 | 0 | upstream-variant-2KB | Rnf182 | Rn_Celera | 17:24241789 | CTAAAGCACCTACCC[C/G]GACACCAAGTGACAG | 498726 |
rs107239263 | snp | G/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24257839 | AGCATGGAAATCGAC[G/T]GTTATCTATAGAAAT | 498726 |
rs107282601 | snp | C/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24289515 | CAGCTAATTAATAAG[C/T]ACCTTCCGAGGGGCT | 498726 |
rs107344206 | snp | A/G | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24277982 | TCTGTGATTTCAAAC[A/G]CGGAAGAGCTGGTTA | 498726 |
rs107400322 | snp | G/T | 0 | 0 | intron-variant | Rnf182 | Rn_Celera | 17:24248729 | AAAGGCCCCTGAATT[G/T]GGAACTCTTAATCAC | 498726 |