| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193600667 | snp | A/G | | | utr-variant-3-prime | rnf-113 | WS195 | III:10755525 | AAAAAAATCATATTT[A/G]GTTTACTCACAGACA | 176507 |
| rs193600668 | snp | A/G | | | synonymous-codon | rnf-113 | WS195 | III:10755751 | GTGATCATGATGATG[A/G]TGATCGTCGCATTCG | 176507 |
| rs193600669 | snp | C/G | | | intron-variant | rnf-113 | WS195 | III:10756118 | GCGGAACGTAATTTT[C/G]CAACCAATTTTGCAA | 176507 |
| rs193600670 | snp | C/T | | | intron-variant | rnf-113 | WS195 | III:10756441 | CTCTCTTTCTAGTTA[C/T]AATGTCTTATTATTG | 176507 |
| rs193600671 | snp | A/T | | | missense | rnf-113 | WS195 | III:10756605 | TGCGGTATTCATAAT[A/T]TTCTCAGTATTCTGC | 176507 |
| rs353098836 | in-del | -/T | | | intron-variant | rnf-113 | WS195 | III:10756289 | GCGAATTAAATTTGA[-/T]TTTTTTTCTCGTAAA | 176507 |
| rs353107939 | snp | A/T | | | intron-variant | rnf-113 | WS195 | III:10756451 | AGTTATAATGTCTTA[A/T]TATTGTCCAAAAAAT | 176507 |
| rs353111212 | snp | C/T | | | missense | rnf-113 | WS195 | III:10755741 | GCTCATCTTCGTGAT[C/T]ATGATGATGGTGATC | 176507 |
| rs353117019 | snp | C/T | | | intron-variant | rnf-113 | WS195 | III:10756040 | TTTGAACTATTTTCG[C/T]TGATTCTCTTCCAAC | 176507 |
| rs353128706 | snp | A/T | | | utr-variant-3-prime | rnf-113 | WS195 | III:10755561 | CGTACAGAAATATTT[A/T]AAAAAAAAATAAAAA | 176507 |
| rs353131186 | snp | A/T | | | utr-variant-3-prime | rnf-113 | WS195 | III:10755560 | CCGTACAGAAATATT[A/T]AAAAAAAAAATAAAA | 176507 |
| rs353133074 | snp | A/T | | | intron-variant | rnf-113 | WS195 | III:10755882 | AAAATTTAAAAATTA[A/T]TTTTTTTTTGCCACA | 176507 |
| rs353156479 | in-del | -/T | | | intron-variant | rnf-113 | WS195 | III:10756168 | TTTTCTTTTTTGGGG[-/T]TTTTTCCATAAAAGT | 176507 |
| rs353163355 | snp | A/C | | | intron-variant | rnf-113 | WS195 | III:10755997 | ACTTCACCCGGACAA[A/C]TGTGAGTTATTGGCT | 176507 |
| rs353179505 | snp | A/T | | | missense | rnf-113 | WS195 | III:10757138 | CCTGGGCATCGTGTG[A/T]ATAGTCTGTGTCCAC | 176507 |