SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7639 | snp | C/T | 0.0821764 | 0.185298 | utr-variant-3-prime | UBE2H | GRCh38.p7 | 7:129833591 | ATGTTTTCTCTCCTG[C/T]GTATGTTAAGAGGAA | 7328 |
rs8485 | snp | C/T | 0 | 0 | utr-variant-3-prime | UBE2H | GRCh38.p7 | 7:129833335 | GATTATTTAATTTTT[C/T]TTTTTGACGTGTGTT | 7328 |
rs8673 | snp | A/C/G/T | 0 | 0 | utr-variant-3-prime | UBE2H | GRCh38.p7 | 7:129834860 | ATATTCATATTTAAA[A/C/G/T]AAAGCAATTTTTTTT | 7328 |
rs10486 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2H | GRCh38.p7 | 7:129834496 | AATGGAGAGGAAAAA[C/G]TTGGGGAGGAAGAGG | 7328 |
rs12690 | snp | A/G | 0.0799831 | 0.183287 | utr-variant-3-prime | UBE2H | GRCh38.p7 | 7:129831121 | TGGGATGAGTGGGAG[A/G]AAGCCCTTTGAGAAG | 7328 |
rs718925 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | UBE2H | GRCh38.p7 | 7:129857658 | TCAAGAGAAATACTT[C/T]TAATAGATCTGTGAA | 7328 |
rs718926 | snp | C/G | 0.078151 | 0.181571 | intron-variant | UBE2H | GRCh38.p7 | 7:129857841 | ACAGACCTTGTGTGT[C/G]TCTGAATGTGATACC | 7328 |
rs873664 | snp | C/T | 0.134802 | 0.221877 | downstream-variant-500B | UBE2H | GRCh38.p7 | 7:129830327 | CCTGCTGGGACTGAT[C/T]TGCCTAAACAGGTGG | 7328 |
rs923231 | snp | G/T | 0.113685 | 0.209567 | intron-variant | UBE2H | GRCh38.p7 | 7:129851851 | TACACCTCATCTGAA[G/T]ATTTCCAAGCAGACA | 7328 |
rs1045894 | snp | A/G | 0.0836354 | 0.186609 | intron-variant, utr-variant-5-prime | UBE2H | GRCh38.p7 | 7:129952702 | TCCCCCGTGCGGGGG[A/G]CGGCGGCGGCGGCTG | 7328 |
rs1045896 | snp | C/T | 0.239037 | 0.24976 | intron-variant, utr-variant-5-prime | UBE2H | GRCh38.p7 | 7:129952677 | CGGCTGACGGGACCG[C/T]CGGGACCGCGGGGGT | 7328 |
rs1045897 | snp | A/C | 0.289165 | 0.246913 | intron-variant, utr-variant-5-prime | UBE2H | GRCh38.p7 | 7:129952670 | CGGGACCGCCGGGAC[A/C]GCGGGGGTGTTGCCA | 7328 |
rs1046691 | snp | A/G | 0.257732 | 0.24988 | utr-variant-3-prime | UBE2H | GRCh38.p7 | 7:129833899 | GAGAAGACGACCCAC[A/G]TGGTGACTGCAAAGC | 7328 |
rs1057928 | snp | A/G | 0 | 0 | intron-variant | UBE2H | GRCh38.p7 | 7:129947470 | TACTCTTTAATTTGT[A/G]TTCAAAGGGTAGACA | 7328 |
rs1062977 | snp | A/C | | | intron-variant, utr-variant-5-prime | UBE2H | GRCh38.p7 | 7:129952585 | CCGTGACAGACGGGC[A/C]GAGGAAGGGAGAGAG | 7328 |
rs1405239 | snp | C/T | 0.00623047 | 0.0554654 | intron-variant | UBE2H | GRCh38.p7 | 7:129923994 | AGGTCAGACTTTGGC[C/T]TACTCTGTGAATGAA | 7328 |
rs1464970 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | UBE2H | GRCh38.p7 | 7:129948107 | TCAGGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 7328 |
rs1464971 | snp | A/G | 0.081446 | 0.184634 | intron-variant | UBE2H | GRCh38.p7 | 7:129916273 | GGAAACTGTTTTCCT[A/G]TTTTTCTTAGATACC | 7328 |
rs1464972 | snp | A/G | 0.081446 | 0.184634 | intron-variant | UBE2H | GRCh38.p7 | 7:129916173 | GTGTTTAGGATGTTA[A/G]AGTCCTGGAATGAAT | 7328 |
rs1464973 | snp | C/T | 0.487495 | 0.0780784 | intron-variant | UBE2H | GRCh38.p7 | 7:129916117 | GCTGAAGTCATTTGA[C/T]GAAAAGTTAACAAGT | 7328 |
rs1471874 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | UBE2H | GRCh38.p7 | 7:129884661 | GCAGTAGCATGATCA[C/T]GGCTCACTGCAGTCT | 7328 |
rs1471875 | snp | A/T | 0.428484 | 0.175052 | intron-variant | UBE2H | GRCh38.p7 | 7:129884752 | ccacacccagctaat[A/T]tttttagtttttgta | 7328 |
rs1471876 | snp | A/G | 0.376394 | 0.215696 | intron-variant | UBE2H | GRCh38.p7 | 7:129885992 | AAGGCAGGTTAAAAT[A/G]ACAAAAATAATGATC | 7328 |
rs1471877 | snp | C/G | 0.0803491 | 0.183626 | intron-variant | UBE2H | GRCh38.p7 | 7:129886046 | CTGGGAGACTGGTGG[C/G]ACTCACTAGAAGATT | 7328 |
rs1486830 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBE2H | GRCh38.p7 | 7:129868185 | AAAAGCTAGAGGTCA[C/T]CCAATACAGAGTAGG | 7328 |
rs1486831 | snp | C/G | 0.324619 | 0.238604 | intron-variant | UBE2H | GRCh38.p7 | 7:129872253 | AAACTCCTCTCTACT[C/G]CAAATACTGGCCCAT | 7328 |
rs1526323 | snp | A/T | 0.270351 | 0.24917 | intron-variant | UBE2H | GRCh38.p7 | 7:129870468 | AAAAATGCAAAAAAA[A/T]TAGCCAAGCGTGGTG | 7328 |
rs1723727 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | UBE2H | GRCh38.p7 | 7:129937297 | tcacacaactgcact[C/T]cggcctgggcaacag | 7328 |
rs1723728 | snp | C/T | 0.202959 | 0.245534 | intron-variant | UBE2H | GRCh38.p7 | 7:129951933 | AACAGGAGGGACTGA[C/T]TGAAAACACACAGAG | 7328 |
rs1725077 | snp | A/G | 0.487621 | 0.0776941 | intron-variant | UBE2H | GRCh38.p7 | 7:129930157 | aaaTACAGAGTGTAA[A/G]GCGTGCTGAGACCAG | 7328 |
rs1725078 | snp | C/T | 0.489201 | 0.0726845 | intron-variant | UBE2H | GRCh38.p7 | 7:129941498 | CCAAAACAGTCTACT[C/T]ACCAAACATACTATC | 7328 |
rs1725079 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | UBE2H | GRCh38.p7 | 7:129942060 | ACGAAAAATACAAAA[A/G]TAAGCCAGGTGTGGT | 7328 |
rs1965567 | snp | C/T | 0.081446 | 0.184634 | intron-variant | UBE2H | GRCh38.p7 | 7:129916994 | gctgaagtgcagtgg[C/T]gtgatctcggctcac | 7328 |
rs1965568 | snp | A/G | 0.079617 | 0.182947 | intron-variant | UBE2H | GRCh38.p7 | 7:129916872 | ttttttgtatttttg[A/G]tagagatggggtttc | 7328 |
rs2037720 | snp | C/T | 0.271702 | 0.249056 | intron-variant | UBE2H | GRCh38.p7 | 7:129866708 | AAAATAGCACATGTA[C/T]CCCAAAAATGTGTGT | 7328 |
rs2255639 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | UBE2H | GRCh38.p7 | 7:129871812 | TATTAGAGAAGTACA[C/T]AGGTGATCTGAATGG | 7328 |
rs2280680 | snp | C/T | 0.197082 | 0.244335 | intron-variant | UBE2H | GRCh38.p7 | 7:129909328 | TCTGATGAATACCTA[C/T]CCCCTGCCTGCCCCT | 7328 |
rs2402980 | snp | A/G | 0.427575 | 0.175975 | intron-variant | UBE2H | GRCh38.p7 | 7:129904358 | ctcctggccttaagc[A/G]atcctcttgccttgg | 7328 |
rs2464894 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | UBE2H | GRCh38.p7 | 7:129894817 | TTTTTTTTTTAACTT[C/G]TTTTCTCAAAGTACA | 7328 |
rs2466981 | snp | A/C | 0.5 | 0 | intron-variant | UBE2H | GRCh38.p7 | 7:129867723 | AAAAAAAAAAGAAAA[A/C]CAAAAAAAAAAAAAA | 7328 |
rs2466987 | snp | C/T | | | intron-variant | UBE2H | GRCh38.p7 | 7:129868683 | CCTTAGAGGTGGCAG[C/T]CTGGGGAATGGGGTG | 7328 |
rs2466989 | snp | A/T | 0.5 | 0 | intron-variant | UBE2H | GRCh38.p7 | 7:129886768 | TTTTTGTTTTTTGGT[A/T]aaaaaaaaaaaaaaa | 7328 |
rs2631601 | snp | A/G | 0.163564 | 0.234582 | intron-variant | UBE2H | GRCh38.p7 | 7:129888122 | ATCAGGAGCCTTTCT[A/G]TTGGACATGACCATT | 7328 |
rs2631602 | snp | A/C | 0.495855 | 0.045338 | intron-variant | UBE2H | GRCh38.p7 | 7:129883529 | atgctttgtaatttt[A/C]ttttgggtgactata | 7328 |
rs2631603 | snp | A/G | 0.427575 | 0.175975 | intron-variant | UBE2H | GRCh38.p7 | 7:129882535 | ATATCTCTTGTGGAT[A/G]CTCAGGGCTCTTGAG | 7328 |
rs2631604 | snp | G/T | 0.0629771 | 0.165899 | intron-variant | UBE2H | GRCh38.p7 | 7:129854870 | TTGCATGTATCGGAA[G/T]TTCTTATGGCTGAAT | 7328 |
rs2631605 | snp | C/T | | | intron-variant | UBE2H | GRCh38.p7 | 7:129854086 | CGCCAACCCCTGCCC[C/T]GCCaaaaaaaaaaaa | 7328 |
rs2631606 | snp | A/G | 0.283947 | 0.247685 | intron-variant | UBE2H | GRCh38.p7 | 7:129840282 | GGGAGGTTGGCTTGA[A/G]CCCAAGAGTTTGAAG | 7328 |
rs2631607 | snp | A/G | 0 | 0 | intron-variant | UBE2H | GRCh38.p7 | 7:129839645 | TACCTTTCAGAGTGG[A/G]GGGTTTTGTAAGCTG | 7328 |
rs2692442 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB | UBE2H | GRCh38.p7 | 7:129953977 | TATACTAGGGGGCTG[C/T]GTAAATTTAGTCTTT | 7328 |
rs2692443 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | UBE2H | GRCh38.p7 | 7:129931865 | ctgggtgacagagct[A/G]gactccgtctcaaaa | 7328 |
rs2693721 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE2H | GRCh38.p7 | 7:129844772 | TCAGTCTGATCTTAC[A/G]TTAATGTTAAAATTA | 7328 |
rs2693722 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | UBE2H | GRCh38.p7 | 7:129858660 | ACTACTGTTTGCTGG[A/G]TAACAAGAAAAATGA | 7328 |
rs2693723 | snp | C/T | 0.197703 | 0.244469 | intron-variant | UBE2H | GRCh38.p7 | 7:129865947 | CCAATTGAGTAAGGG[C/T]GGGGGGGTGCTGCCA | 7328 |
rs2693724 | snp | C/T | 0.488302 | 0.0755777 | intron-variant | UBE2H | GRCh38.p7 | 7:129872043 | TATTTTTAGTAGACA[C/T]GGGGTTTCACCATAT | 7328 |
rs2693725 | snp | A/C | 0.488118 | 0.0761554 | intron-variant | UBE2H | GRCh38.p7 | 7:129932066 | tgaccacgtgatccg[A/C]ctgcctcggcctccc | 7328 |
rs2693740 | snp | C/T | 0.081446 | 0.184634 | intron-variant | UBE2H | GRCh38.p7 | 7:129923406 | ATATTGCAGAACAAA[C/T]TCTGGGTTGGTAGTA | 7328 |
rs2693741 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | UBE2H | GRCh38.p7 | 7:129920818 | TTTGTTTATTACATT[G/T]TTTTCAATGACAAAA | 7328 |
rs2693742 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | UBE2H | GRCh38.p7 | 7:129918570 | GGGCACTTGAGCCTG[A/G]CCAACATGGCAAAAC | 7328 |
rs2693743 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | UBE2H | GRCh38.p7 | 7:129914533 | ATCTGATTTACAAAG[A/G]TCTTTTTATTTCTTG | 7328 |
rs2693744 | snp | A/T | 0.145978 | 0.227331 | intron-variant | UBE2H | GRCh38.p7 | 7:129913646 | CAGTTAAAGGCTCTT[A/T]ACCCTTCTGAGGCTC | 7328 |
rs2693746 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | UBE2H | GRCh38.p7 | 7:129887905 | GTTTTTTTGTTTTTG[C/T]TTTTGTTTTGTTTTG | 7328 |
rs2693747 | snp | C/T | 0.0818113 | 0.184966 | intron-variant | UBE2H | GRCh38.p7 | 7:129886474 | TTAAGGCCCAGACAT[C/T]GCCTTTGGCTTCCTT | 7328 |
rs2708637 | snp | C/T | 0.487871 | 0.076925 | intron-variant | UBE2H | GRCh38.p7 | 7:129867102 | TATGATTTACATATG[C/T]TTCCCATAACTCTGT | 7328 |
rs2708641 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | UBE2H | GRCh38.p7 | 7:129881406 | ACCCGCCTAGGCCTC[C/T]CAAACTGTTGGGATT | 7328 |
rs2708648 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE2H | GRCh38.p7 | 7:129914407 | CCTGACCTCAAGTGA[C/T]CCACACACCTTGGCC | 7328 |
rs2708649 | snp | A/G | 0.487432 | 0.0782705 | intron-variant | UBE2H | GRCh38.p7 | 7:129918438 | ATCAAGACTCACTGC[A/G]ACCTCTGCCTCCTGG | 7328 |
rs2708650 | snp | A/G | 0 | 0 | intron-variant | UBE2H | GRCh38.p7 | 7:129876833 | AATGAGTGGGTATTC[A/G]AAATAGTGGCATAGC | 7328 |
rs2708651 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | UBE2H | GRCh38.p7 | 7:129907108 | AAAGGTTTATCATCA[C/T]CAAAAGCCATTTATT | 7328 |
rs2708653 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | UBE2H | GRCh38.p7 | 7:129910837 | cagtgagcagagagc[A/G]caccaccgtactcca | 7328 |
rs2727458 | snp | A/T | 0.141934 | 0.225437 | intron-variant | UBE2H | GRCh38.p7 | 7:129847031 | ATTATTATTATTATT[A/T]TTTTTTGAGACGGAG | 7328 |
rs2727459 | snp | C/T | 0.081446 | 0.184634 | intron-variant | UBE2H | GRCh38.p7 | 7:129849604 | AATAAAATAATAAAA[C/T]AATTAATTTGAACTC | 7328 |
rs2727460 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | UBE2H | GRCh38.p7 | 7:129849999 | CAAAATAAAAAAACA[A/G]AAACAGGTGAAAACA | 7328 |
rs2727461 | snp | A/C | 0.0626037 | 0.165477 | intron-variant | UBE2H | GRCh38.p7 | 7:129852123 | AATTAATCATCCATG[A/C]AGACACATACATGTA | 7328 |
rs2727462 | snp | C/T | 0.495252 | 0.0484902 | intron-variant | UBE2H | GRCh38.p7 | 7:129854942 | AACAGTCACAAAAGA[C/T]CACATATTATATAAT | 7328 |
rs2727463 | snp | A/C | | | intron-variant | UBE2H | GRCh38.p7 | 7:129855855 | tgagctattatcgca[A/C]cactgcattccagcc | 7328 |
rs2727464 | snp | A/G | 0.489837 | 0.0705577 | intron-variant | UBE2H | GRCh38.p7 | 7:129862621 | GCCACCTGGTACCAA[A/G]AGGAGAGGAGAAGGT | 7328 |
rs2727465 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | UBE2H | GRCh38.p7 | 7:129868898 | tttttggtgacaata[C/T]agaccatactcctga | 7328 |
rs2727466 | snp | G/T | 0.376989 | 0.215346 | intron-variant | UBE2H | GRCh38.p7 | 7:129870586 | CCACATGTCTTCACA[G/T]CGGTGTATGTCTAGA | 7328 |
rs2727467 | snp | G/T | 0.0916144 | 0.193427 | intron-variant | UBE2H | GRCh38.p7 | 7:129871245 | TGGAAGGATGATGTA[G/T]GCCACAGCCAAAGCC | 7328 |
rs2727475 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | UBE2H | GRCh38.p7 | 7:129915367 | TTTTGTATTTTTAGT[A/G]GACGGGGTTCCACTG | 7328 |
rs2727476 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | UBE2H | GRCh38.p7 | 7:129907708 | CACATGTATACCTCG[C/T]CACAATGATGATATT | 7328 |
rs2727477 | snp | A/G | 0.487684 | 0.0775019 | intron-variant | UBE2H | GRCh38.p7 | 7:129900091 | CCAGGCTGGAGTGCA[A/G]TGATGTGATCTCGGG | 7328 |
rs2727478 | snp | A/G | 0 | 0 | intron-variant | UBE2H | GRCh38.p7 | 7:129899517 | AGCATGCTTTTCCCC[A/G]TGGGTCACCTAGCCA | 7328 |
rs2727479 | snp | A/T | 0.28578 | 0.247426 | intron-variant | UBE2H | GRCh38.p7 | 7:129896863 | TCCTCGTAAAATTTA[A/T]CTGCTTACTGTGAAT | 7328 |
rs2727480 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | UBE2H | GRCh38.p7 | 7:129896803 | TGAATAGAGATTTTT[A/G]TGCACTGACTTAGCT | 7328 |
rs2727481 | snp | A/G | 0.081446 | 0.184634 | intron-variant | UBE2H | GRCh38.p7 | 7:129896095 | cctgccttgaatccc[A/G]aagtgctgggattac | 7328 |
rs2727482 | snp | C/T | 0.427879 | 0.175668 | intron-variant | UBE2H | GRCh38.p7 | 7:129895261 | TGCTTCCCTTCATGC[C/T]ATAGCCCCCATGTGA | 7328 |
rs2727483 | snp | C/T | 0.496105 | 0.0439572 | intron-variant | UBE2H | GRCh38.p7 | 7:129894779 | GGTATGGGCCGGGCG[C/T]GGTGGCTCAGGCCTG | 7328 |
rs2727484 | snp | G/T | 0.5 | 0 | intron-variant | UBE2H | GRCh38.p7 | 7:129891814 | TGttttttttttttt[G/T]tttgtttttgttttt | 7328 |
rs2727485 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | UBE2H | GRCh38.p7 | 7:129875582 | AGATAAAACAGTGTT[A/G]GAAAAGGTATTATGA | 7328 |
rs2727486 | snp | C/G | | | intron-variant | UBE2H | GRCh38.p7 | 7:129875032 | TAGAAAGCCATCAGG[C/G]TTGGCCAGAATTCCC | 7328 |
rs2727487 | snp | G/T | 0.488057 | 0.0763479 | intron-variant | UBE2H | GRCh38.p7 | 7:129873980 | TACAGGTAACAAGTT[G/T]AGAAACCAATTTGTG | 7328 |
rs2727488 | snp | C/T | 0.488424 | 0.0751925 | intron-variant | UBE2H | GRCh38.p7 | 7:129873168 | agctgggcatggtgg[C/T]gggcgcctgtattcc | 7328 |
rs2727489 | snp | A/G | 0.496348 | 0.0425753 | intron-variant | UBE2H | GRCh38.p7 | 7:129873119 | aggcaggagaatggc[A/G]tgaacccgggaggcg | 7328 |
rs2727490 | snp | A/G | 0.49614 | 0.0437598 | intron-variant | UBE2H | GRCh38.p7 | 7:129871840 | TGAATTTTGGGGCTG[A/G]GGAGGCAAAATTCCA | 7328 |
rs2727491 | snp | C/G | 0.376989 | 0.215346 | intron-variant | UBE2H | GRCh38.p7 | 7:129870584 | TAGACATACACCGCT[C/G]TGAAGACATGTGGCT | 7328 |
rs2727492 | snp | C/T | 0.497722 | 0.0336691 | intron-variant | UBE2H | GRCh38.p7 | 7:129868443 | ACAGGCGCCCGCCAC[C/T]GCGCCTGGCTAATTT | 7328 |
rs2727493 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | UBE2H | GRCh38.p7 | 7:129863897 | gaatctcttgaaccc[A/G]ggaggcggaggttgc | 7328 |
rs2727494 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | UBE2H | GRCh38.p7 | 7:129862431 | TTTTTCTAAAGACCT[C/T]TCCTTACAGGTATTT | 7328 |