SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs193589481 | snp | C/G | | | intron-variant | ? | WS195 | V:3756715 | TTTTTATTTAACAAA[C/G]AATTTCGTGTCGAGA | 178791 |
rs193618471 | snp | C/T | | | synonymous-codon | ? | WS195 | V:3750636 | GACGCGGCCGTGTTT[C/T]CGCTTGGTTTTGTCG | 178791 |
rs193618472 | snp | A/T | | | intron-variant | ? | WS195 | V:3750783 | CAATTTTACTGTAAT[A/T]TATTTCGTTGTCTTT | 178791 |
rs193618473 | snp | C/T | | | intron-variant | ? | WS195 | V:3750881 | GTGTCGATTTACGGG[C/T]CTTAATCAGTTTTGA | 178791 |
rs193618474 | snp | A/G | | | intron-variant | ? | WS195 | V:3750984 | GATATTTTGCGCGTC[A/G]GATATATTGTGCTGT | 178791 |
rs193618475 | snp | C/T | | | intron-variant | ? | WS195 | V:3751101 | TTTTTTCAAAAATTT[C/T]AACTAATCTTGAGAA | 178791 |
rs193618476 | snp | A/C | | | intron-variant | ? | WS195 | V:3751173 | CGAAATTACAGTACT[A/C]TTTAAAGGCGCACGC | 178791 |
rs193618477 | snp | A/T | | | intron-variant | ? | WS195 | V:3751243 | GTACCGTGTGTTTGG[A/T]GAAAAAAACGTTCTA | 178791 |
rs193618479 | snp | A/G | | | intron-variant | ? | WS195 | V:3751374 | TTCTAAAAAATGAAA[A/G]TCCGATATTTTCCGA | 178791 |
rs193618480 | snp | A/T | | | intron-variant | ? | WS195 | V:3751381 | AAATGAAAATCCGAT[A/T]TTTTCCGAAAGATCG | 178791 |
rs193618481 | snp | A/G | | | intron-variant | ? | WS195 | V:3751506 | GGAATATTTTCACAG[A/G]AAAATTGTGACGTCA | 178791 |
rs193618482 | snp | C/T | | | missense | ? | WS195 | V:3751681 | CGAAGACACCCTTGG[C/T]TGCTGAATAAGTGAA | 178791 |
rs193618483 | snp | A/T | | | synonymous-codon | ? | WS195 | V:3751728 | TCCAATCGAGCCTGT[A/T]GCAATGAAATTCTGA | 178791 |
rs193618484 | snp | A/T | | | intron-variant | ? | WS195 | V:3753317 | TGTGTCGAGACCAGG[A/T]ACCGTAGTTTTGACC | 178791 |
rs193618485 | snp | C/T | | | intron-variant | ? | WS195 | V:3754050 | CTGTAGCGCTTGTGT[C/T]AATTTACGGGCTCGA | 178791 |
rs193618486 | snp | A/G | | | synonymous-codon | ? | WS195 | V:3754784 | TTTGAAGCATTTAAC[A/G]ATATATGATCCATGC | 178791 |
rs193618487 | snp | C/G | | | intron-variant | ? | WS195 | V:3755023 | ATTGAAAAAAGACAT[C/G]CGCCTTAAAATTTCG | 178791 |
rs193618488 | snp | A/G | | | intron-variant | ? | WS195 | V:3755260 | AAAGAAACTTTAAAG[A/G]CGCACACCCGTTTTC | 178791 |
rs193618489 | snp | C/T | | | intron-variant | ? | WS195 | V:3755565 | ATGCGGGAGTTGAGA[C/T]GCATATTTCTCAACT | 178791 |
rs193618490 | snp | C/T | | | intron-variant | ? | WS195 | V:3755904 | AAAGAGTACTGTAGT[C/T]TAAAACTTTAGGTGC | 178791 |
rs193618491 | snp | A/T | | | intron-variant | ? | WS195 | V:3756251 | AAAAACTCCAAAAAA[A/T]TTTTTTTTCGCGCCG | 178791 |
rs193618492 | snp | C/G | | | intron-variant | ? | WS195 | V:3756731 | AATTTGTCGTGTTGA[C/G]ACCTGGTACAGTATC | 178791 |
rs353136141 | in-del | -/T | | | frameshift-variant | ? | WS195 | V:3750651 | CGCTTGGTTTTGTCG[-/T]TTTCGCGTAGCGATT | 178791 |