| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193327837 | snp | C/T | 0.0198 | 0.0975088 | synonymous-codon | mat-2 | WS195 | II:11115746 | AATTCCGCCGGAAAT[C/T]CATGAGAAATTTGTT | 174698 |
| rs353104964 | snp | C/T | | | intron-variant | mat-2 | WS195 | II:11117945 | CACTAAAATCTAGAC[C/T]GCAAAAAATGATTTT | 174698 |
| rs353114314 | snp | C/T | | | missense | mat-2 | WS195 | II:11118484 | TGATGTTCATGAAGA[C/T]GAATAATGAGTTTAT | 174698 |
| rs353125928 | in-del | -/A | | | intron-variant | mat-2 | WS195 | II:11114301 | TTTCCCCTTTTCCTG[-/A]AAAAAAAAATTCACG | 174698 |
| rs353150776 | in-del | -/A | | | intron-variant | mat-2 | WS195 | II:11115476 | AAAATTATTTTGAAC[-/A]AAAAAAAAAATTTTC | 174698 |
| rs353160519 | snp | A/T | | | intron-variant | mat-2 | WS195 | II:11119995 | GTATTTCTAGATTAT[A/T]GGATATTTTATTCAA | 174698 |
| rs353171858 | snp | A/G | | | intron-variant | mat-2 | WS195 | II:11116658 | TTTGAAAATAAAATT[A/G]TTTTTTTAGAAAAAT | 174698 |