| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193592327 | snp | A/G | | | synonymous-codon | ? | WS195 | II:14151693 | AGCCCGGAGCCTCTT[A/G]ACCGGATAAAGCTCA | 175069 |
| rs193592328 | snp | A/G | | | missense | ? | WS195 | II:14151976 | GTGATCAGCTTCTTG[A/G]CGAGCACACAACGAG | 175069 |
| rs193592329 | snp | C/T | | | missense | ? | WS195 | II:14152226 | TCGGCATCTTCAGCA[C/T]CAGCTTCTCCTTCGA | 175069 |
| rs353096354 | in-del | -/T | | | intron-variant | ? | WS195 | II:14152702 | ATTGAGAATTTTTGG[-/T]TTTTTTTTTTGGACA | 175069 |
| rs353114224 | snp | A/G | | | utr-variant-3-prime | ? | WS195 | II:14151125 | AGTTTTGACTTGACA[A/G]TTAGGTTTCAAATAA | 175069 |
| rs353118666 | snp | G/T | | | intron-variant | ? | WS195 | II:14152616 | TTGTGGGGTGAAAAA[G/T]TGGGATTTTTCGGGA | 175069 |
| rs353149562 | snp | A/T | | | intron-variant | ? | WS195 | II:14151378 | GAAAGTGAAAAAATT[A/T]TGGAAAATACATTTT | 175069 |
| rs353164958 | in-del | -/T | | | intron-variant | ? | WS195 | II:14151629 | TCTTTATTTTCGACG[-/T]TTTTTTTTCAATTTT | 175069 |
| rs353174127 | snp | C/T | | | intron-variant | ? | WS195 | II:14151553 | AAAAAAAAATGCCTT[C/T]TGCAGTTTTCGACGT | 175069 |
| rs353179535 | snp | A/T | | | intron-variant | ? | WS195 | II:14153856 | GAAAAAAATTAAAAA[A/T]ATTAATATAAAATTA | 175069 |