Y32H12A.8
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs193332726snpA/C0.03920.1344intron-variant?WS195III:5389310ACGAAACACTGAAAA[A/C]TCTAAGCAAAAAAAA175742
rs193332727snpG/T0.01980.0975088missense?WS195III:5389605ACGGGATACCCATCA[G/T]TTCAAGAACTTCTGC175742
rs193332728snpC/T0.02009840.0982103synonymous-codon?WS195III:5394306GTAAACCTCTTTGAG[C/T]ACAAATTCCCTATCT175742
rs193598704snpA/Gsynonymous-codon?WS195III:5395023TTTCAGTGGCTGCAG[A/G]GGCTTGGGATACTGC175742
rs193598705snpA/Cmissense?WS195III:5398270AGGTGTATCCCAATC[A/C]TCGCAAGGAACCTCG175742
rs193598706snpC/Gintron-variant?WS195III:5400015ATTTTTCGTATTTCT[C/G]GTGCAAAAATCGCAA175742
rs193598707snpA/Gintron-variant?WS195III:5403524AAGTGACAAATAAAT[A/G]GAACAAAAACTTTAA175742
rs353113995snpA/Cutr-variant-3-prime?WS195III:5385671AATTTTGAAAAAAAT[A/C]ATGGGAGAACAATTG175742
rs353120403snpA/Gintron-variant?WS195III:5392479CCATAAGTCTTCCCT[A/G]AAATTATGGATGAGA175742
rs353127391in-del-/Aintron-variant?WS195III:5396177AGTTTGAATATTCAG[-/A]AAAAAAAAAAATTTA175742
rs353140901in-del-/Tintron-variant?WS195III:5402242CCCATCTGAAATTTG[-/T]TTTTTTTTTTTTCAA175742
rs353149322snpG/Tintron-variant?WS195III:5389154TCCAATTTCCAAAAT[G/T]TGAATCTATAGGTTT175742
rs353153973snpA/Tintron-variant?WS195III:5397229TTTCATAATTTTTTT[A/T]AGAGAAATTTTAAAA175742
rs353154818snpA/Gintron-variant?WS195III:5402876GTTATGGAGGATGTG[A/G]TTGTAAACGTTATAA175742
rs353155776snpC/Tsynonymous-codon?WS195III:5393808TTGATCTTCAGACAA[C/T]GGAGGTACCACTACA175742
rs353172619snpA/Gintron-variant?WS195III:5390487ATGTGAAAATGTAAA[A/G]ATTTCGACTCAAAAC175742
rs353174215snpA/Gmissense?WS195III:5395688CGGGTCTGGAACGGG[A/G]TGGGCGGCCAGTTAT175742
rs353180269snpC/Tintron-variant?WS195III:5394098TTTGGAAATTTGAAT[C/T]ATTAAGAAAATAGTT175742