SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8151751 | snp | C/T | | | missense | Herc4 | Rn_Celera | 20:26830661 | GTTTCTTTCTCTGTA[C/T]ATTTTGGGAGATCTA | 309758 |
rs8158006 | snp | A/G | | | intron-variant, utr-variant-3-prime | Herc4 | Rn_Celera | 20:26831073 | GAAAAATAATCAAAT[A/G]ACTATTGGCAGGCCC | 309758 |
rs8169649 | snp | G/T | | | intron-variant | Herc4 | Rn_Celera | 20:26796485 | AAAATGACAGTCAAT[G/T]AAATATTTAAATGAA | 309758 |
rs105850472 | snp | G/T | 0 | 0 | intron-variant | Herc4 | Rn_Celera | 20:26790900 | ATTTTTGATGTATTG[G/T]TCAGAAACGTTTGGT | 309758 |
rs107277266 | snp | A/C | 0 | 0 | intron-variant | Herc4 | Rn_Celera | 20:26822784 | ATGGCCATCGCAGGC[A/C]AGGCCTGACAGCCCA | 309758 |
rs197330979 | snp | A/C | 0 | 0 | intron-variant | Herc4 | Rn_Celera | 20:26810318 | CAGTGCACATTAAAA[A/C]CCAAAAAAAAAAAAA | 309758 |
rs197391164 | snp | C/T | 0 | 0 | intron-variant | Herc4 | Rn_Celera | 20:26771725 | ATTTTGTGTTTTGTA[C/T]ATTTATAAAGTTCAG | 309758 |
rs197791084 | snp | C/T | 0 | 0 | intron-variant | Herc4 | Rn_Celera | 20:26827888 | GTGTTTTTAGAGCCA[C/T]TTGCCATGCATTTTC | 309758 |
rs198248615 | snp | A/T | 0 | 0 | intron-variant | Herc4 | Rn_Celera | 20:26789839 | GCTCCGAAAAAAAGA[A/T]CCAAAAAAAAAAAAA | 309758 |