SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs193344268 | snp | C/T | 0.327163 | 0.237794 | synonymous-codon, intron-variant | W02G9.3, kel-8 | WS195 | V:2673644 | GTAATCTCCGACACA[C/T]TGAAGGCAGACGGCA | 3565011 |
rs193344269 | snp | A/C | 0.0198985 | 0.097741 | intron-variant, synonymous-codon | kel-8, W02G9.3 | WS195 | V:2673727 | TGTGGCGAAGAATTC[A/C]GTGCTCCAAATGGTC | 3565011 |
rs193344270 | snp | C/G | 0.0198985 | 0.097741 | missense, intron-variant | W02G9.3, kel-8 | WS195 | V:2673734 | AAGAATTCCGTGCTC[C/G]AAATGGTCGATGACG | 3565011 |
rs193344271 | snp | C/T | 0.30272 | 0.244378 | intron-variant | kel-8, W02G9.3 | WS195 | V:2673794 | GTTAGCCTAAATCGT[C/T]AGTGTCTCTAAAAAT | 3565011 |
rs193344272 | snp | C/T | 0.318773 | 0.240354 | intron-variant | kel-8 | WS195 | V:2675409 | GAGAACTGGTACTCT[C/T]AAAAACGACACCTTC | 3565011 |
rs193616813 | snp | C/T | | | intron-variant | W02G9.3, kel-8 | WS195 | V:2672250 | CAAACACCTAGCGGG[C/T]CATGGTGCGGGGGCC | 3565011 |
rs193616814 | snp | C/T | | | intron-variant | kel-8, W02G9.3 | WS195 | V:2672515 | AAATTGTTCGGGATA[C/T]ATACTTATTATACAT | 3565011 |
rs193616815 | snp | A/G | | | synonymous-codon, intron-variant | W02G9.3, kel-8 | WS195 | V:2672741 | TTCAAGTTTCGCTGT[A/G]AAGAACCGCCTCTTT | 3565011 |
rs193616817 | snp | A/G | | | intron-variant, synonymous-codon | kel-8, W02G9.3 | WS195 | V:2673527 | AGTTTACCCGGTGGA[A/G]CATACTTTAGCTGTG | 3565011 |
rs193616818 | snp | A/C | | | intron-variant | kel-8 | WS195 | V:2673985 | TAAGTCTCTTCTTCG[A/C]CCTTTTTCCCCCTTT | 3565011 |
rs193616819 | snp | A/G | | | intron-variant | kel-8 | WS195 | V:2674281 | AAAAAACGTGCAACC[A/G]ACCCGAAAATCTAGC | 3565011 |
rs193616820 | snp | A/T | | | intron-variant | kel-8 | WS195 | V:2674349 | TCGCTCTCTCGCAGC[A/T]CTTCCAAATTGTCAA | 3565011 |
rs193616821 | snp | C/T | | | intron-variant | kel-8 | WS195 | V:2674394 | TACACGCACCCCCCG[C/T]CGAAACTCGGGAGCA | 3565011 |
rs193616822 | snp | A/C | | | intron-variant | kel-8 | WS195 | V:2674414 | ACTCGGGAGCATTCA[A/C]TCTGGCCTGGTTTTC | 3565011 |
rs193616823 | snp | A/G | | | intron-variant | kel-8 | WS195 | V:2674464 | GGACTATTGTAAATT[A/G]TTTGTGAAAAAGGTC | 3565011 |
rs193616825 | snp | A/C | | | intron-variant | kel-8 | WS195 | V:2674852 | TACTGTAGTTTGGAA[A/C]TTTCGTTGCTGCCGG | 3565011 |
rs193616826 | snp | C/G | | | intron-variant | kel-8 | WS195 | V:2674964 | ATTGAAATTTTAAAA[C/G]TACAGAACTCTTTCG | 3565011 |
rs193616827 | snp | A/C | | | intron-variant | kel-8 | WS195 | V:2675107 | AACATAGTTGACGCG[A/C]AAAATATATCTCGTA | 3565011 |
rs193616828 | snp | C/T | | | intron-variant | kel-8 | WS195 | V:2675114 | TTGACGCGCAAAATA[C/T]ATCTCGTAGCGAAAA | 3565011 |
rs193616829 | snp | G/T | | | intron-variant | kel-8 | WS195 | V:2675732 | CGTGGTAGGCAAATT[G/T]CGTACCACTTCTCGG | 3565011 |
rs193616830 | snp | C/G | | | intron-variant | kel-8 | WS195 | V:2675881 | TTTTTAATACGCGCA[C/G]ATAGAAAAGGAGAGG | 3565011 |
rs193616832 | snp | C/T | | | intron-variant | kel-8 | WS195 | V:2677395 | AGGCCTGGGCTCATT[C/T]TTAGGCTTCGGATTA | 3565011 |
rs193616833 | snp | G/T | | | intron-variant | kel-8 | WS195 | V:2677557 | AAAATTCAGAATTTA[G/T]TGCTCCCGTAATATT | 3565011 |
rs193616834 | snp | C/T | | | intron-variant | kel-8 | WS195 | V:2677891 | AATTTAAGGCTCGAT[C/T]TTTTTTCTTTCATAT | 3565011 |
rs193616835 | snp | A/G | | | intron-variant | kel-8 | WS195 | V:2678424 | TTAGGAAAATTCATA[A/G]GGTGCGTACAACTTT | 3565011 |
rs193616836 | snp | C/T | | | intron-variant | kel-8 | WS195 | V:2680053 | GGTTCCTCAACTCAA[C/T]CATTTTTGCTCCAAT | 3565011 |
rs193616837 | snp | A/T | | | intron-variant | kel-8 | WS195 | V:2680597 | AATTGGAAAAAAAAT[A/T]TTTTTAGATTTTTCG | 3565011 |
rs193616838 | snp | A/C | | | intron-variant | kel-8 | WS195 | V:2681350 | TTTAAGGCCCTCCAG[A/C]TTTTCAAAAGCATTT | 3565011 |
rs193616839 | snp | C/T | | | intron-variant | kel-8 | WS195 | V:2682262 | AAAACTTTCATAATT[C/T]TATAGATTTTTTATT | 3565011 |
rs193616840 | snp | A/G | | | missense | kel-8 | WS195 | V:2684068 | GATGATGTGCTCAAT[A/G]GAAAACTGGCACGTG | 3565011 |
rs193616841 | snp | C/G | | | intron-variant | kel-8 | WS195 | V:2684247 | CATTTTTTTGTAGAT[C/G]AAACTGTTATGAGAC | 3565011 |
rs193616842 | snp | A/G | | | intron-variant | kel-8 | WS195 | V:2685640 | GGATTTCACGCCAAA[A/G]TGCACATCTGGGAAA | 3565011 |
rs193616843 | snp | G/T | | | intron-variant | kel-8 | WS195 | V:2685649 | GCCAAAATGCACATC[G/T]GGGAAACGCCGCTCC | 3565011 |
rs193616844 | snp | A/G | | | synonymous-codon | kel-8 | WS195 | V:2686156 | AATGGTTCTCGATGC[A/G]ATGACACCGTCAAAA | 3565011 |
rs193616845 | snp | G/T | | | intron-variant | kel-8 | WS195 | V:2687327 | GAAAATAATGGAAAT[G/T]CTCCGCCCTAAAACT | 3565011 |
rs193616847 | snp | A/G | | | intron-variant | kel-8 | WS195 | V:2687844 | GAAAAATTTTTACGG[A/G]TTTTCACCGCCAAAT | 3565011 |
rs193616848 | snp | A/T | | | intron-variant | kel-8 | WS195 | V:2687896 | GGGGGCGGAGTGTTT[A/T]CACTTGACCGTGGAG | 3565011 |
rs193616849 | snp | A/C | | | intron-variant | kel-8 | WS195 | V:2688012 | ACGCGGGAATTTTTC[A/C]ATGCAAAATCAGTTG | 3565011 |
rs193616850 | snp | A/C | | | intron-variant | kel-8 | WS195 | V:2688176 | AAATAATAAAAAAAT[A/C]ATTTTCAGCTATCTC | 3565011 |
rs193616851 | snp | A/T | | | utr-variant-3-prime | kel-8 | WS195 | V:2688378 | ATTTGAGCCCTAAAC[A/T]TTTTATTTTTGAATT | 3565011 |
rs353149293 | in-del | -/A | | | intron-variant | kel-8 | WS195 | V:2685049 | TCTACGTAGATCTAC[-/A]AAAAAATGTGGCAGG | 3565011 |