SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11693 | snp | A/G | 0.34146 | 0.23267 | utr-variant-3-prime, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38362951 | ATTCAGTTTACATGC[A/G]TTATTGGTTTATAAT | 51569 |
rs950556 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UFM1 | GRCh38.p7 | 13:38352830 | TTTAAATCGGAGACT[C/T]GGAAATGTCCTTACA | 51569 |
rs1011484 | snp | A/T | 0.201727 | 0.245295 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38348675 | CCATAGAAGATCAGT[A/T]GGCTGCAAAATTATT | 51569 |
rs1032753 | snp | A/G | 0.0158469 | 0.0875917 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38347932 | TTTTTTAACTTTGTG[A/G]AGGGATTTGCAATTG | 51569 |
rs1330959 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | UFM1 | GRCh38.p7 | 13:38350749 | AGCATGAAATGTAGC[A/G]AAGAACAGGATTACA | 51569 |
rs1553300 | snp | A/C | 0.275999 | 0.248644 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38349426 | GCGCGGAAAAGCTTA[A/C]TTGGTGCTCCAGAAG | 51569 |
rs2019516 | snp | G/T | 0.177503 | 0.239258 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38347874 | CTTCAACATTTTAAC[G/T]TTTCAGTAAAAGAGA | 51569 |
rs2019520 | snp | A/G | 0.295854 | 0.245759 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38347906 | GGTCCTTGTTTTGCT[A/G]TAAAATTTTCCAATT | 51569 |
rs2150468 | snp | G/T | 0.275999 | 0.248644 | intron-variant | UFM1 | GRCh38.p7 | 13:38353751 | TTTTGAACATGATTA[G/T]TAAGAGTACACAGAA | 51569 |
rs2150469 | snp | A/G | 0.081446 | 0.184634 | intron-variant | UFM1 | GRCh38.p7 | 13:38357927 | TGCATATGTCATTCA[A/G]GGGTCAGCTGTACTT | 51569 |
rs2150470 | snp | A/G | 0.375 | 0.216506 | intron-variant | UFM1 | GRCh38.p7 | 13:38358057 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAT | 51569 |
rs2231319 | snp | C/T | 0.0644693 | 0.167566 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38349071 | AAGTTGGTTGTTAAA[C/T]TGAATAAATGTGGTC | 51569 |
rs2231320 | snp | A/C | 0.0244538 | 0.107838 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38349078 | TTGTTAAATTGAATA[A/C]ATGTGGTCAGTGATT | 51569 |
rs2231321 | snp | C/G | 0 | 0 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38349262 | TCGTACTTGATAGCT[C/G]TCTTACTTAACCGAA | 51569 |
rs2231322 | snp | C/G | | | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38349526 | CCCAAGTCCATCTCG[C/G]TCTTCATCCGACTAC | 51569 |
rs2231323 | snp | A/G | 0.275999 | 0.248644 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38349545 | TCATCCGACTACCCC[A/G]TACCCTTACTTCCGC | 51569 |
rs2231324 | snp | A/C | 0.0170251 | 0.090679 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38349572 | CCGCCCCAACCTGCC[A/C]ACTGGAACCTAGGGT | 51569 |
rs2231325 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38349593 | AACCTAGGGTCCTAC[A/G]CTCTATGCCCACGCT | 51569 |
rs2231326 | snp | A/C | 0 | 0 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38349709 | ATATAAACGCAAAAG[A/C]ACAAGATATTTGTAA | 51569 |
rs2231327 | snp | C/T | 0.0573587 | 0.15934 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38349716 | CGCAAAAGCACAAGA[C/T]ATTTGTAATTTAAAA | 51569 |
rs2231328 | snp | C/T | 0.275999 | 0.248644 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38349726 | CAAGATATTTGTAAT[C/T]TAAAAGCGCCATCTA | 51569 |
rs2231329 | snp | A/C | 0.000971425 | 0.0220175 | intron-variant | UFM1 | GRCh38.p7 | 13:38349925 | CGGCACCACCATGTA[A/C]GTGTTTGCTTACCGA | 51569 |
rs2231330 | snp | A/T | 0.112936 | 0.209078 | intron-variant | UFM1 | GRCh38.p7 | 13:38349946 | TGCTTACCGACTGCC[A/T]TAATTCCTGGTCCAG | 51569 |
rs2231331 | snp | C/G | 0.0405878 | 0.136558 | intron-variant | UFM1 | GRCh38.p7 | 13:38349980 | CCCGACCCTGACTCT[C/G]TCCCGCTCTTTTCCT | 51569 |
rs2231332 | snp | C/T | 0.11138 | 0.208063 | intron-variant, synonymous-codon | UFM1 | GRCh38.p7 | 13:38350126 | GGGGATGATCCGAGC[C/T]TTTCCAACAACTACC | 51569 |
rs2231333 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UFM1 | GRCh38.p7 | 13:38354370 | GTCTTTAAGAGTTGC[A/G]TGCACTTTGACCCAT | 51569 |
rs2231334 | snp | A/G | 0.0240553 | 0.107 | intron-variant | UFM1 | GRCh38.p7 | 13:38359382 | GGGTTATATATGTCA[A/G]TTGACACTGAATAGT | 51569 |
rs2231335 | snp | A/G | 0.0228947 | 0.104514 | intron-variant, utr-variant-3-prime | UFM1 | GRCh38.p7 | 13:38360608 | TGAGCTTTTGTACCC[A/G]TTTTACTGTTTACTA | 51569 |
rs2231336 | snp | C/T | 0.0228947 | 0.104514 | utr-variant-3-prime, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38360931 | CCTTTTTGTTGTCCA[C/T]ACTCTTCCTATGAAG | 51569 |
rs2455409 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | UFM1 | GRCh38.p7 | 13:38355162 | CTTAACTACATTAAT[A/G]AAAAATAGCTTAACA | 51569 |
rs2455410 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UFM1 | GRCh38.p7 | 13:38356646 | TATGTAATGATTATA[A/G]ATGCCTAGAGTAGTG | 51569 |
rs2455411 | snp | C/T | 0.0437281 | 0.141251 | utr-variant-3-prime, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38361698 | AAGTGCTAAGATCAG[C/T]CACCCATGTGAATAA | 51569 |
rs2481878 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | UFM1 | GRCh38.p7 | 13:38352837 | ACATTTCCAAGTCTC[C/T]GATTTAAAAGTGAAT | 51569 |
rs2481879 | snp | C/G | 0.251578 | 0.249995 | intron-variant | UFM1 | GRCh38.p7 | 13:38355897 | TGGATTTAAATCCCT[C/G]GTAAAATTGCCTTAG | 51569 |
rs2481880 | snp | C/T | 0.232067 | 0.249356 | intron-variant | UFM1 | GRCh38.p7 | 13:38356756 | ACTGGTCAAAAAATA[C/T]GAGAAACACTTCATT | 51569 |
rs2481881 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | UFM1 | GRCh38.p7 | 13:38359785 | ATTCAGATCTTCAAA[C/T]TGTTAAATTTATACA | 51569 |
rs2481882 | snp | C/T | 0.0554779 | 0.157039 | utr-variant-3-prime, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38361637 | CAAGGAAATACAGAT[C/T]GGAAGTGCTGATGAG | 51569 |
rs2485783 | snp | C/T | 0.232359 | 0.249377 | utr-variant-3-prime, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38362173 | ATGAAAGCCACTACA[C/T]TTCCAGCTCTAAAAA | 51569 |
rs2485784 | snp | C/G/T | 0.0437281 | 0.141251 | utr-variant-3-prime, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38361944 | TGTTGACAAGGCCAG[C/G/T]AGATACTTTGTTTTC | 51569 |
rs2485785 | snp | A/C | 0.279195 | 0.248289 | intron-variant | UFM1 | GRCh38.p7 | 13:38358544 | ATTATATACCTAAAA[A/C]GGAATAAAATTCTCA | 51569 |
rs2485786 | snp | A/G | 0.278664 | 0.248351 | intron-variant | UFM1 | GRCh38.p7 | 13:38358511 | ATTGCAAGCCTACAA[A/G]AAACAATTTTCTATC | 51569 |
rs2485787 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | UFM1 | GRCh38.p7 | 13:38353963 | ATTTCTAACACTTTC[A/G]TACATGTAAGTCTAG | 51569 |
rs2485788 | snp | A/T | 0.234692 | 0.249531 | intron-variant | UFM1 | GRCh38.p7 | 13:38352253 | AAAATTAGCTGGGCA[A/T]GGTGGCACACACCTG | 51569 |
rs2485789 | snp | C/T | 0.234692 | 0.249531 | intron-variant | UFM1 | GRCh38.p7 | 13:38350847 | GGCTGAGAGGTTGTA[C/T]GGATCATGGATTGGT | 51569 |
rs2496455 | snp | A/G | 0.0103295 | 0.0711199 | utr-variant-3-prime, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38361238 | TTAAATATATAGGTT[A/G]TGATGAAGTGAATAG | 51569 |
rs7327308 | snp | A/C | 0.0916144 | 0.193427 | intron-variant | UFM1 | GRCh38.p7 | 13:38354811 | CCAAAATTATTAGAA[A/C]TATCTATAATGCAAC | 51569 |
rs7330234 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | UFM1 | GRCh38.p7 | 13:38351552 | aatgacttcactcct[A/G]tgaaaaaccacttga | 51569 |
rs9532209 | snp | A/G | 0.34146 | 0.23267 | intron-variant | UFM1 | GRCh38.p7 | 13:38358812 | TCTGCATTCTGTCAC[A/G]TTGAAGTGTTTCTCT | 51569 |
rs9548317 | snp | A/G | 0 | 0 | intron-variant | UFM1 | GRCh38.p7 | 13:38352458 | TTACCTGTGGACTTA[A/G]TCTTTATAATAATTC | 51569 |
rs9548318 | snp | C/T | 0.34146 | 0.23267 | intron-variant | UFM1 | GRCh38.p7 | 13:38357007 | CCATACCACATTTCA[C/T]TGATTTAAAAAACAC | 51569 |
rs9566338 | snp | C/G | | | intron-variant | UFM1 | GRCh38.p7 | 13:38356592 | TTGATTCTTCAATTT[C/G]TAATTTAAAATAAGC | 51569 |
rs9576514 | snp | A/T | 0.492582 | 0.0604491 | intron-variant | UFM1 | GRCh38.p7 | 13:38358071 | TGTATATATATATAT[A/T]TTTTTTTTTCCTTCT | 51569 |
rs9576515 | snp | A/G | | | intron-variant | UFM1 | GRCh38.p7 | 13:38358404 | AAATAACTTTATTTA[A/G]CAAGTTTTTTTTTTT | 51569 |
rs9888482 | snp | A/C | 0.168135 | 0.236216 | intron-variant | UFM1 | GRCh38.p7 | 13:38354839 | AACTTTTTGGACATG[A/C]CACTTGAAAAAGTAG | 51569 |
rs10507470 | snp | C/T | 0.18989 | 0.242666 | intron-variant | UFM1 | GRCh38.p7 | 13:38355963 | GTAAGTAATGAATTG[C/T]TGAAACCTGCAAAGA | 51569 |
rs11363787 | in-del | -/T | 0.0573587 | 0.15934 | intron-variant | UFM1 | GRCh38.p7 | 13:38351412 | TTAAAAATTTCAAAC[-/T]TTCCACAGCTGCTGT | 51569 |
rs11381230 | in-del | -/T | 0.239902 | 0.249796 | intron-variant | UFM1 | GRCh38.p7 | 13:38358408 | CAAGTTTTTTTTTTT[-/T]ATTAAGTAAAGTTGT | 51569 |
rs11540728 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38361508 | TCAATCTCTTTTGAT[A/T]CAACATTTAAAACAA | 51569 |
rs11840717 | snp | A/C | 0 | 0 | intron-variant | UFM1 | GRCh38.p7 | 13:38356699 | ACACAAATTAGTACC[A/C]CCAAAAAAAAAAAAA | 51569 |
rs17057848 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | UFM1 | GRCh38.p7 | 13:38350506 | TACTTGAACATTTGT[G/T]ATTCCGCGGCTTCTG | 51569 |
rs17057850 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | UFM1 | GRCh38.p7 | 13:38350825 | GACTGATAAATTTCA[A/G]TGATTTACCAATCCA | 51569 |
rs17057855 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | UFM1 | GRCh38.p7 | 13:38352398 | CACCCCTTCTGGCCA[A/G]AGATTTTTCTAATTG | 51569 |
rs17057857 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | UFM1 | GRCh38.p7 | 13:38353273 | AGCTGGTATTGAGAC[A/G]CTTAAGAACAATACA | 51569 |
rs17057900 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | UFM1 | GRCh38.p7 | 13:38358522 | GTTTCTTGTAGGCTT[C/G]CAATAATGAGAATTT | 51569 |
rs17232348 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | UFM1 | GRCh38.p7 | 13:38351055 | TCTACAACGTTTCAT[G/T]TAATCCATTAATCAC | 51569 |
rs17297815 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38348689 | TTGGCTGCAAAATTA[C/T]TGTAAAGATGAATTT | 51569 |
rs17298046 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | UFM1 | GRCh38.p7 | 13:38350734 | ATTGCAGTTGGAAGT[A/C]GCATGAAATGTAGCA | 51569 |
rs34361128 | in-del | -/G | | | intron-variant | UFM1 | GRCh38.p7 | 13:38359911 | TTTAAAATGTAATCT[-/G]CTTAGGCTTATAATC | 51569 |
rs34489703 | in-del | -/TT | 0 | 0 | intron-variant | UFM1 | GRCh38.p7 | 13:38357513 | CAGGGTTTTTTTTTT[-/TT]ACAGATAAAGCATAT | 51569 |
rs35105286 | in-del | -/AA | 0.496746 | 0.040204 | intron-variant | UFM1 | GRCh38.p7 | 13:38356701 | CAAATTAGTACCACC[-/AA]AAAAAAAAAAAAAAA | 51569 |
rs35578075 | in-del | -/T | | | intron-variant | UFM1 | GRCh38.p7 | 13:38359292 | TGATTTTACAACTTA[-/T]TTTTCTAGATGGAAT | 51569 |
rs35695251 | in-del | -/A | | | upstream-variant-2KB | UFM1 | GRCh38.p7 | 13:38348236 | TTTTATACATACAAT[-/A]AAAGCTCTCTGATTA | 51569 |
rs35784291 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38359326 | ATAAATCCTGCACAG[-/C]ACTGCTGGTGAGTAT | 51569 |
rs35879418 | in-del | -/T | 0 | 0 | intron-variant | UFM1 | GRCh38.p7 | 13:38352103 | TTTTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 51569 |
rs41292241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UFM1 | GRCh38.p7 | 13:38359462 | TTTTAGGGATTATAT[A/G]CCAGTCTTTACCTGT | 51569 |
rs41292243 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38361256 | ATGAAGTGAATAGAC[A/G]TATCAGTGAACAGTT | 51569 |
rs41292745 | snp | C/T | 0.0150606 | 0.0854603 | utr-variant-3-prime, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38361501 | TCCTTTATCAATCTC[C/T]TTTGATACAACATTT | 51569 |
rs56807983 | snp | A/T | | | intron-variant | UFM1 | GRCh38.p7 | 13:38351311 | GGAGGGTTTACATTA[A/T]ATTCATGACTACAAT | 51569 |
rs61947646 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | UFM1 | GRCh38.p7 | 13:38359940 | TCTAAAGTTTTAAAA[G/T]TAGGCATGCTTTAAT | 51569 |
rs67284300 | in-del | -/A | 0.461161 | 0.133832 | intron-variant | UFM1 | GRCh38.p7 | 13:38358071 | TGTATATATATATAT[-/A]TTTTTTTTTCCTTCT | 51569 |
rs68091289 | in-del | -/A | 0.169086 | 0.236544 | intron-variant | UFM1 | GRCh38.p7 | 13:38358072 | TAGAAGGAAAAAAAA[-/A]TATATATATATATAC | 51569 |
rs71215987 | in-del | -/A/AA/AAA/TAT | 0.298311 | 0.275163 | intron-variant | UFM1 | GRCh38.p7 | 13:38358071 | TAGAAGGAAAAAAAA[-/A/AA/AAA/TAT]ATATATATATATACA | 51569 |
rs71673975 | in-del | -/GT | | | intron-variant | UFM1 | GRCh38.p7 | 13:38358049 | GTTTTGTGTGTGTGT[-/GT]GTGTGTGTATATATA | 51569 |
rs71720939 | in-del | -/TG | | | intron-variant | UFM1 | GRCh38.p7 | 13:38358038 | ATTATCTTATAGTTT[-/TG]TGTGTGTGTGTGTGT | 51569 |
rs73176729 | snp | A/G | | | intron-variant | UFM1 | GRCh38.p7 | 13:38351615 | GGTTAAAGTAGATGG[A/G]GTCCAGTGCCCCCTC | 51569 |
rs73176730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UFM1 | GRCh38.p7 | 13:38355378 | GGGACACAAATCTGA[A/G]TATAGCATTGTCATT | 51569 |
rs73460276 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | UFM1 | GRCh38.p7 | 13:38350593 | GATCACACCCTTCCT[A/G]TGCTGGGATTTAATA | 51569 |
rs73460277 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UFM1 | GRCh38.p7 | 13:38353080 | AAAGGGTAAAAATGA[A/T]ACCCATTTTCATCCT | 51569 |
rs73460280 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | UFM1 | GRCh38.p7 | 13:38353141 | GCAGCCAAGAAATCT[A/G]TTCACATTTCTATTA | 51569 |
rs73460282 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | UFM1 | GRCh38.p7 | 13:38357080 | ATCACTGTTGGCCAA[A/C]TGGCTTTCACTTAAT | 51569 |
rs73460283 | snp | A/G | 0.168135 | 0.236216 | intron-variant | UFM1 | GRCh38.p7 | 13:38357708 | AATATGTATTTTGTT[A/G]TGTGTATTATATACT | 51569 |
rs73460289 | snp | A/G | 0.147656 | 0.228091 | utr-variant-3-prime, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38362068 | CAAATCTTGAAAGAC[A/G]AAATCAAAGCCCATT | 51569 |
rs74047550 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | UFM1 | GRCh38.p7 | 13:38350422 | ATTAGAAAAGCGTTT[C/T]ACCGCTTTGGCCAGC | 51569 |
rs74047551 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | UFM1 | GRCh38.p7 | 13:38355601 | GAAAATCTTAACATA[A/C]AGTAGTGAATAAGAA | 51569 |
rs74047552 | snp | A/G | 0.0244538 | 0.107838 | utr-variant-3-prime, nc-transcript-variant | UFM1 | GRCh38.p7 | 13:38362235 | AATTATTATCTTAGC[A/G]TGTTTCAGTATCTTC | 51569 |
rs74047553 | snp | A/G | 0.0244538 | 0.107838 | downstream-variant-500B | UFM1 | GRCh38.p7 | 13:38363164 | TAGTAGTGATGTTTC[A/G]TCCAACAACAGACCG | 51569 |
rs74469165 | snp | A/T | | | intron-variant | UFM1 | GRCh38.p7 | 13:38358421 | AAGTTTTTTTTTTTA[A/T]TAAGTAAAGTTGTTT | 51569 |
rs74868151 | snp | C/G | 0.0640965 | 0.167152 | intron-variant | UFM1 | GRCh38.p7 | 13:38355916 | AAATTGCCTTAGTAA[C/G]CAATAATAAAATTTC | 51569 |
rs75307954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UFM1 | GRCh38.p7 | 13:38355248 | CTCAAAGCTCCTTGT[A/G]TTGTCAGGAATCACT | 51569 |
rs75575750 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | UFM1 | GRCh38.p7 | 13:38357468 | GTACACTTTTATAAT[C/T]AATGGTGTCCTAAAT | 51569 |