SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs193320815 | snp | A/T | 0.0702582 | 0.173761 | intron-variant | duo-3 | WS195 | I:10466061 | TTAAAAATTACTTTT[A/T]TAAAAAAATCATAAA | 172925 |
rs193320816 | snp | A/T | 0.488473 | 0.0750361 | intron-variant | duo-3 | WS195 | I:10466062 | TAAAAATTACTTTTT[A/T]AAAAAAATCATAAAT | 172925 |
rs193320817 | snp | A/T | 0.0209401 | 0.100158 | intron-variant | duo-3 | WS195 | I:10466063 | AAAAATTACTTTTTT[A/T]AAAAAATCATAAATC | 172925 |
rs193320818 | snp | A/G | 0.0205106 | 0.0991697 | intron-variant | duo-3 | WS195 | I:10470609 | GAGAGTGTGATTTTA[A/G]GTTTGAGATTATTAC | 172925 |
rs193320819 | snp | C/T | 0.0494731 | 0.149295 | synonymous-codon | duo-3 | WS195 | I:10470946 | TCCGGGACACCTGAA[C/T]CTGATAGAATCCGAT | 172925 |
rs353096951 | in-del | -/A | | | intron-variant | duo-3 | WS195 | I:10470046 | TTTAGTTTTTTTTTT[-/A]AATTTATTTAGGCTG | 172925 |
rs353110477 | snp | A/G | | | intron-variant | duo-3 | WS195 | I:10470288 | ACTGCCATGTTCCTT[A/G]CTACTACACAAAGCT | 172925 |
rs353125369 | snp | C/T | | | missense | duo-3 | WS195 | I:10470869 | AATTTGGCTCCCGTA[C/T]GTGAATTATCCGCTA | 172925 |
rs353126071 | snp | A/T | | | intron-variant | duo-3 | WS195 | I:10470046 | GTTTAGTTTTTTTTT[A/T]AATTTATTTAGGCTG | 172925 |
rs353157202 | in-del | -/A | | | intron-variant | duo-3 | WS195 | I:10466289 | TGGGTCCAAAAAAAC[-/A]AAAAAAAAAGAAGTT | 172925 |
rs353168577 | snp | C/T | | | intron-variant | duo-3 | WS195 | I:10468696 | CCATCGCATTGAACA[C/T]TCAAAAAAAAATTAA | 172925 |
rs353182768 | snp | A/T | | | intron-variant | duo-3 | WS195 | I:10470801 | TATGATATTTCATTT[A/T]AAAAAAATTAAATCA | 172925 |