SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs193328009 | snp | A/G | 0.0200984 | 0.0982103 | intron-variant, nc-transcript-variant | mdt-8, Y62F5A.11 | WS195 | II:11532168 | ATATGGAAATGACTT[A/G]AAACGTCGTAAAATC | 174763 |
rs193589096 | snp | A/T | | | synonymous-codon | mdt-8 | WS195 | II:11531632 | TCCTTCTCCAGTTAA[A/T]ATTGATTTTACGATT | 174763 |
rs193589097 | snp | G/T | | | intron-variant | mdt-8 | WS195 | II:11531736 | TTGAAATTTGGTGTT[G/T]TTGTTTTTCAATTTT | 174763 |
rs193589098 | snp | A/G | | | intron-variant | mdt-8 | WS195 | II:11532387 | AATGCCTATTGACTT[A/G]AAATCTATCTAAATA | 174763 |
rs193589099 | snp | A/T | | | intron-variant | mdt-8 | WS195 | II:11532566 | GCAATTAAAAAATTT[A/T]AAATTCTGCTCGGTT | 174763 |
rs353101730 | in-del | -/T | | | intron-variant | mdt-8 | WS195 | II:11531227 | ATCTTTTTTTTTCTA[-/T]TTTTTTTTTAAAGAA | 174763 |
rs353107915 | in-del | -/C | | | intron-variant | mdt-8 | WS195 | II:11530645 | AAAGAACCTTTGCCA[-/C]CCAAAAAGTTTGTCA | 174763 |
rs353136700 | snp | A/G | | | nc-transcript-variant, intron-variant | Y62F5A.11, mdt-8 | WS195 | II:11532101 | TGATGAAGATTCACT[A/G]GCTCTACGCGTTTCA | 174763 |
rs353138375 | snp | A/G | | | synonymous-codon | mdt-8 | WS195 | II:11533483 | CCCATAATCTTCGTG[A/G]CCGTGAGGCATTCCA | 174763 |
rs353151357 | snp | A/G | | | intron-variant | mdt-8 | WS195 | II:11528325 | AGGCTCTGCCTGATG[A/G]TCTGATCCTTCCGAT | 174763 |
rs353153807 | snp | A/G | | | intron-variant | mdt-8 | WS195 | II:11532414 | AATAAATTTATTAAA[A/G]CAAGATAAACTATTG | 174763 |
rs353164501 | in-del | -/GA | | | intron-variant | mdt-8 | WS195 | II:11527408 | GCATTTTTGATCTCT[-/GA]TTATTTCAACATTAT | 174763 |
rs353172571 | snp | C/T | | | intron-variant | mdt-8 | WS195 | II:11527448 | TGAAAGCAAGAGATA[C/T]AGAGAATTGAGGAGT | 174763 |