SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs64214340 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108597749 | TGAAGGAAATCAGGA[C/T]AGGAACTCAGACAGT | 303735 |
rs64534095 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108597618 | AAAACTTGGGGAACA[A/G]AATGACCTCAGGTTC | 303735 |
rs104906137 | snp | C/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108544715 | CACAGGCAAATCTGC[C/G]ATAGACACAAAACGA | 303735 |
rs104929987 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108610343 | CTGGGCTTACTCCTT[A/G]TACAAACATTCTTCT | 303735 |
rs104943010 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108546099 | AATGAAACCAGAAGG[C/T]CCTGACAGGTTCTGG | 303735 |
rs104976227 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108613118 | ATTTATTAATTTATC[A/G]TATGTGTCTTCGTGC | 303735 |
rs105008135 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108590960 | AACCCAGGGCCTTGC[A/G]CTTCCTAGGCAAGCG | 303735 |
rs105140524 | snp | A/C | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108620000 | CCACCTTCTGCATCT[A/C]AGTCCCTCAGAGACA | 303735 |
rs105180119 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108589992 | GGTGTGACTCTCGGT[G/T]ATGTGCTCCTGCTGG | 303735 |
rs105295474 | snp | A/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108597458 | CACGCGAGCGCGCGC[A/T]CACACACACACACAC | 303735 |
rs105339342 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108543732 | GGAGCTGGCTTTCTG[G/T]TTCAGAGGGTCGGTC | 303735 |
rs105422860 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108589931 | GCTGGTGTGACTCTC[A/G]GTGAGGTGCTCCTGC | 303735 |
rs105431421 | snp | A/T | 0 | 0 | synonymous-codon | Rnf213 | Rn_Celera | 10:108581886 | TAACCGGGTGAAGGT[A/T]TGCATGGAGACAGGG | 303735 |
rs105531445 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108542464 | TGCTGAGGGGAAGGC[G/T]CTGTAGCAGAGAAGA | 303735 |
rs105535362 | snp | A/C | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108541224 | AGGAAGGCTGCTGAG[A/C]TGAGCCACAGCTAGG | 303735 |
rs105559544 | snp | C/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108613340 | AACCCAGGGCCTTGC[C/G]CTTGCTAGGCAAGCG | 303735 |
rs105564882 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108606505 | CCAACCTCACTCAGA[C/T]CTGAAGAAGGCTAGC | 303735 |
rs105564984 | snp | C/G | 0.5 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108574111 | TGCTTTTTACACACA[C/G]ACACACACACACACA | 303735 |
rs105565838 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108610280 | TGGTCCTAACCACAA[C/T]ATGGCTGGCATATGA | 303735 |
rs105654903 | snp | A/C | 0 | 0 | missense | Rnf213 | Rn_Celera | 10:108568456 | CTTCAGTGTTCTTAA[A/C]CCGTTGTTAAACTTT | 303735 |
rs105712535 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108585400 | GTACCAGTGCTAGGG[A/G]GGAGGAGCCAGATGA | 303735 |
rs105719629 | snp | C/T | 0 | 0 | missense | Rnf213 | Rn_Celera | 10:108582544 | GACCATCATGAATGC[C/T]GGGCTGTCTTCACAG | 303735 |
rs105726869 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108545770 | AGGGCCTGTCTCCCT[G/T]GAGCTCCCATGCTAG | 303735 |
rs105730072 | snp | A/C | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108618435 | TCTAGCAGAGCATCA[A/C]AACAGGATGTGCTGT | 303735 |
rs105742821 | snp | A/C | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108596527 | AGATGACTCTGGGGT[A/C]GAGAGTGCTCACTGT | 303735 |
rs105766421 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108589478 | GCTGGTGTGACTCTC[A/G]GTGATGTGCTCCTGC | 303735 |
rs105772428 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108584977 | TTCAAGGAATTCCTT[C/T]ATCCATTTTTCTGGA | 303735 |
rs105788767 | snp | A/C | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108603716 | GTGATCCTGGCACAG[A/C]TAAGCACTACAGTAG | 303735 |
rs105799255 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108557109 | TGTTTGTGTGTCTTT[C/T]GCCCGTCTCAGTCTA | 303735 |
rs105835810 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108541251 | TAGGTGTGGCCGTGG[G/T]CAGGACCAGATGCAT | 303735 |
rs105845706 | snp | C/T | 0 | 0 | synonymous-codon | Rnf213 | Rn_Celera | 10:108608458 | AGACCTGCTGGTTCA[C/T]GCCAAGTTTTGGGAG | 303735 |
rs105872614 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108598951 | TTCTGGGACAAGAGT[G/T]ACATTAATTAACCTC | 303735 |
rs105912693 | snp | C/G | 0 | 0 | missense | Rnf213 | Rn_Celera | 10:108581699 | ACCCTGACCTGCAGG[C/G]ATCCAGCAGGGGCCT | 303735 |
rs105971697 | snp | G/T | 0 | 0 | missense | Rnf213 | Rn_Celera | 10:108541035 | GTTTTTGTAGATGCT[G/T]CAGAGGACACAGCTG | 303735 |
rs106037959 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108597456 | TGCACGCGAGCGCGC[A/G]CTCACACACACACAC | 303735 |
rs106057374 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108576807 | GAGCCCTTCCATCCC[A/G]CTTTATTTATTTGTT | 303735 |
rs106076940 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108600871 | ACGGGTGTTTTGTCT[A/G]CTTGTATGCCTGGCA | 303735 |
rs106119072 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108613398 | CAAGAATGACTTTTT[C/T]TTAACTAAAAGACAA | 303735 |
rs106144830 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108589878 | TGTGACTCTCGGTGA[G/T]GTGCTCCTGCTGGTG | 303735 |
rs106188791 | snp | G/T | 0.5 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108573211 | CACATGTGCTCGGGG[G/T]TGGGGGGGAAGGGGG | 303735 |
rs106248944 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108589907 | TGTGACTCTCGGTGA[G/T]GTGCTCCTGCTGGTG | 303735 |
rs106285835 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108618469 | CACACTGCTCTGGTG[C/T]TCAGTGTTGCCCGTC | 303735 |
rs106314020 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108542616 | CCTGCCTGGCTCTCT[C/T]TTTTTTTTTAAAGGT | 303735 |
rs106384084 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108605091 | CTGTAGTCTGTCATG[A/G]TGGGATTACAGAGAA | 303735 |
rs106398457 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108610978 | TGTCTACAGCACAAT[A/G]GATTCTGGTGCTTCT | 303735 |
rs106433530 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108618454 | AGGATGTGCTGTGCA[C/T]ACACTGCTCTGGTGT | 303735 |
rs106536418 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108569182 | TAGGGTTTTACTGCT[A/G]TGAACAGACACCATG | 303735 |
rs106551188 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108577213 | GAAGAAGAAGAAGAA[A/G]AAAAGAAAATCCCTC | 303735 |
rs106610737 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108605914 | ACTCCATAGAGTGCT[A/G]TGAGTGGAGAAAACA | 303735 |
rs106633024 | snp | A/G | 0 | 0 | synonymous-codon | Rnf213 | Rn_Celera | 10:108614546 | TTTTACTGAAGTATT[A/G]TCAACCAAAGGATGC | 303735 |
rs106687790 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108571802 | GCATATTCTTTACCA[G/T]CTGAGCCTTGGCCAT | 303735 |
rs106717944 | snp | C/T | 0 | 0 | missense | Rnf213 | Rn_Celera | 10:108607557 | GCTCCTAAGATCAAC[C/T]GCTTTGCAAAATCGC | 303735 |
rs106741476 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108587176 | AGAGTCACCGTGGAC[A/G]CTCTTAAAGAGATTA | 303735 |
rs106767833 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108573869 | TTAATACAGCTATGC[C/T]GTGGTTCTGCAGGAT | 303735 |
rs106931389 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108569278 | CATTATTATCAAGAC[A/G]GGAGCATGGCAGCAC | 303735 |
rs106965247 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108577949 | TGCTGAGCCTGTTTC[C/T]CAGGCTTGCAGCTGA | 303735 |
rs106971292 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108594339 | TTCTGTTAAAGGACT[A/G]ACAATGTGGCTCAGT | 303735 |
rs106987270 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108605550 | GCGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 303735 |
rs106999992 | snp | C/T | 0 | 0 | missense | Rnf213 | Rn_Celera | 10:108557509 | TTGGTGAGGACCACC[C/T]TCCAGGAGGCCCTGA | 303735 |
rs107061597 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108559815 | GTCAAAGTTCTTGTG[C/T]GATGCCCTTAGAAGA | 303735 |
rs107086530 | snp | C/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108588035 | GGATGCAGAGCCACT[C/G]TGCTGTTCCAGCCCC | 303735 |
rs107144544 | snp | A/C | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108600293 | TTGTCATCTTTGACA[A/C]CTCGCGCCCGGTAAT | 303735 |
rs107162783 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108573458 | TCTCAAAGTCCTGGT[A/G]CACTTTTGTATGGCC | 303735 |
rs107213981 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108592668 | GGGCCTGACCCTGTG[G/T]GGCTCCAGGATGTAG | 303735 |
rs107222301 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108544717 | CAGGCAAATCTGCCA[C/T]AGACACAAAACGATA | 303735 |
rs107222827 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108589994 | TGTGACTCTCGGTGA[G/T]GTGCTCCTGCTGGTG | 303735 |
rs107253606 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108589981 | GTGCTCCTGCTGGTG[G/T]GACTCTCGGTGATGT | 303735 |
rs107278040 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108543430 | TTTCCCCACATAGTG[C/T]AGCTCAGTGGACACT | 303735 |
rs107291328 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108613457 | TAATGCTGGGGCCAT[A/G]AACATGGCGGGCAAA | 303735 |
rs107378686 | snp | A/T | 0.5 | 0 | synonymous-codon | Rnf213 | Rn_Celera | 10:108581787 | GATCCTACAGCAGAC[A/T]TTCTTTGAGGGTCAG | 303735 |
rs107386196 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108618284 | AAACAGACCTTGGCT[A/G]TATTGTCATAGTTCT | 303735 |
rs107388989 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108614389 | CATCAGGGGCTGTTA[A/G]CATCCTTAGGGTGCT | 303735 |
rs107395583 | snp | C/T | 0 | 0 | synonymous-codon | Rnf213 | Rn_Celera | 10:108581505 | CCTCATCAAGATGGT[C/T]TTTGCCAAAGCCAAA | 303735 |
rs107399609 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108614941 | GGAGGCCAAATCCTA[C/T]AAGTACTGTTACGCT | 303735 |
rs107458954 | snp | A/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108614042 | TTGGAAGTACGATAA[A/T]AACAAGAAAGGGGCT | 303735 |
rs107511874 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108609281 | GGCTTCTAGCCCAGG[A/G]TTCCTCCATGCAGCA | 303735 |
rs107517329 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108589848 | TGTGACTCTCGGTGA[G/T]GTGCTCCTGCTGGTG | 303735 |
rs107521236 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108613501 | CTGTGCCAAGGAAAG[C/T]CCCGCAGTGATCTTT | 303735 |
rs107587147 | snp | C/G | 0 | 0 | missense | Rnf213 | Rn_Celera | 10:108582280 | ATCGGCTACCATTCC[C/G]ATGCCTGTGCCTCTG | 303735 |
rs197041091 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108584826 | TCTTCCCCTGCCCCC[A/G]ATACTCTATCCCACC | 303735 |
rs197055993 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108540532 | TTGTCGCTTCCTCTA[A/G]GGCTAGCGGGTTTGT | 303735 |
rs197088474 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108564497 | AGCAGGTGGAGTTAT[C/T]AGGGATCCCTGGTGG | 303735 |
rs197097472 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108544163 | GTGTGTGTGTGTGTG[C/T]GTCTGTGGGTCTGTG | 303735 |
rs197103238 | snp | C/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108615859 | TACTAATGTCATTTT[C/G]CTTCCTCAGTTTCTC | 303735 |
rs197104214 | snp | C/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108606433 | CTGGTGGCTGGAACT[C/G]GTGCTAACATTTGAG | 303735 |
rs197127717 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108596097 | CATGGAACACTCAGG[A/G]CCAGGCCCTCAACCT | 303735 |
rs197128257 | snp | C/T | 0 | 0 | synonymous-codon | Rnf213 | Rn_Celera | 10:108549482 | AGGGAAGAAGCAGGC[C/T]GCTGTGATCATGCTC | 303735 |
rs197173107 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108614749 | TTTCACTGCCCTCAA[C/T]GTACAGCTTGCTTGT | 303735 |
rs197176630 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108591026 | CCCCCATTTTAACAC[A/G]GAAATGCGTCCTCTG | 303735 |
rs197298541 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108573973 | CAGGAGGACCTATGA[C/T]CAGCTGTGGAGAAGA | 303735 |
rs197319867 | snp | C/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108540711 | CAAGCTCTGGAGGCC[C/G]GCCTGGCTTGGTTCT | 303735 |
rs197372316 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108587830 | GAGACTTTGTTCTTC[A/G]CAGGGCTATGGAGGT | 303735 |
rs197382330 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108557772 | ACATTGACAACCCAC[A/G]GCCACATGGGAAGTG | 303735 |
rs197414392 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108586718 | GTTTCTTACCCAGTC[A/G]CAGTTACCTGGGTAT | 303735 |
rs197489327 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108541975 | GTCTCCACTGAACGA[A/G]TGGGAAACAAGGCTC | 303735 |
rs197495227 | snp | G/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108572512 | ACCATGGTGAAACCT[G/T]GCCTATGGGAAAGTG | 303735 |
rs197515943 | snp | A/G | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108562531 | CGACATTCAGCTGAT[A/G]TGCTGATAAGGAAGA | 303735 |
rs197545678 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108588285 | GGGTATAAACCTAGG[C/T]AGTCTGGTCCTGCAG | 303735 |
rs197572978 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108602734 | TCCCAAAGTGAGTTC[C/T]CTTCTCCCCATGAAG | 303735 |
rs197639973 | snp | C/T | 0 | 0 | intron-variant | Rnf213 | Rn_Celera | 10:108563452 | GCGCCCATGCGTGCG[C/T]CCGTGCGTGCAATTG | 303735 |