SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs193343529 | snp | C/T | 0.487619 | 0.0776999 | missense | R09A1.2 | WS195 | V:1020763 | TTGTGATCGTTGAGA[C/T]GACGCTCGTAGATCC | 178603 |
rs193343530 | snp | A/C | 0.00999975 | 0.0699991 | missense | R09A1.2 | WS195 | V:1020778 | TGACGCTCGTAGATC[A/C]ACTTCAACGACATAT | 178603 |
rs193343531 | snp | A/G | 0.18 | 0.24 | missense | R09A1.2 | WS195 | V:1020844 | GCCGACAGACATGTG[A/G]TCACCGTGTTCGTCG | 178603 |
rs193343532 | snp | A/G | 0.02955 | 0.117906 | synonymous-codon | R09A1.2 | WS195 | V:1020906 | ATTGGTCGAGTATGT[A/G]TCGTGAAGGATCGAG | 178603 |
rs193343533 | snp | A/C | 0.180804 | 0.240233 | missense | R09A1.2 | WS195 | V:1022195 | CCTCTTGCAACGTGA[A/C]AATTTCAAAGTAGGA | 178603 |
rs193343534 | snp | G/T | 0.00995 | 0.0698283 | intron-variant | R09A1.2 | WS195 | V:1022281 | AAAGTAGGTACGAGG[G/T]AGGCCTAGGCGGAAA | 178603 |
rs193615129 | snp | C/T | | | missense | R09A1.2 | WS195 | V:1018446 | TCTTCTTCGATTTTT[C/T]GATTCCAAGACGTTT | 178603 |
rs193615130 | snp | A/G | | | intron-variant | R09A1.2 | WS195 | V:1018844 | AAAAATACTGTACGA[A/G]GTCTTGAAACGAAAA | 178603 |
rs193615131 | snp | A/T | | | intron-variant | R09A1.2 | WS195 | V:1019554 | AGAGTACTCCAATTA[A/T]TACCCTGGCGCGAAA | 178603 |
rs193615132 | snp | A/C | | | intron-variant | R09A1.2 | WS195 | V:1020234 | CAACAAGAGAAACTA[A/C]AGTACTCATTAAATT | 178603 |
rs193615133 | snp | A/G | | | synonymous-codon | R09A1.2 | WS195 | V:1020726 | CGAGCCGAGCGTCAG[A/G]CCTTGCAGAATCTTG | 178603 |
rs193615134 | snp | G/T | | | synonymous-codon | R09A1.2 | WS195 | V:1020978 | AGATGGAGAATGCGG[G/T]ATCTGGAAAAAAAAG | 178603 |
rs193615135 | snp | C/T | | | intron-variant | R09A1.2 | WS195 | V:1021396 | ATTTGTGTGCGCTGG[C/T]GCAGTGGGATGCGCC | 178603 |
rs193615136 | snp | A/G | | | intron-variant | R09A1.2 | WS195 | V:1021775 | TCTGTCGCCGTTGCC[A/G]CCGCTACCGCCCACT | 178603 |
rs193615137 | snp | A/T | | | intron-variant | R09A1.2 | WS195 | V:1021981 | GACCAGCTATTTGCC[A/T]GCTGCTCATCGCCCG | 178603 |
rs193615138 | snp | C/T | | | intron-variant | R09A1.2 | WS195 | V:1022025 | AAAAAATCAATATTT[C/T]CAGAGAGGCTTGTTC | 178603 |
rs193615139 | snp | C/G | | | missense | R09A1.2 | WS195 | V:1022436 | GCGGCGAGCATCACC[C/G]AGTGTGCCGGAATCG | 178603 |
rs193615140 | snp | A/T | | | missense | R09A1.2 | WS195 | V:1022834 | ACTCGGCCACCATTT[A/T]CAAACAAAAAATTGC | 178603 |