F43G6.8
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs193589292snpC/Tintron-variant?WS195II:11813318TTTCTGTAGGTCAAA[C/T]AGTTTGAAAACTAGA174815
rs353111713snpA/Csynonymous-codon?WS195II:11812651TCTCTCAGTCTCCAC[A/C]GTTTTCATATAACGA174815
rs353112686in-del-/Autr-variant-5-prime?WS195II:11813963CAAATTTTAATGGAT[-/A]AAAAATATCGAATAG174815
rs353113678snpC/Tintron-variant?WS195II:11813448CCGTTTAGCATTGCA[C/T]CTCCACTAGTTCACT174815
rs353115192snpA/Gintron-variant?WS195II:11813512ATCAGTTAACTATTA[A/G]CTACAAAATTTTAGA174815
rs353130565snpC/Tintron-variant?WS195II:11813420AATTGAATTTGTGCA[C/T]AAAATTTGTGTACCG174815
rs353132538in-del-/AGACintron-variant?WS195II:11812910TTTTGCATAGGTACG[-/AGAC]AGACATAAGTAGGCT174815
rs353138692snpC/Tsynonymous-codon?WS195II:11812492ACCCAACACACGTGG[C/T]ACATACTCATCACTG174815
rs353141602snpA/Tintron-variant?WS195II:11813407AAATTGTTTTGACAA[A/T]TGAATTTGTGCATAA174815
rs353143530snpA/Cintron-variant?WS195II:11813472GTTCACTTTGAAAAG[A/C]TATATCTCAGTTCAT174815
rs353145750snpG/Tintron-variant?WS195II:11813641AAATTAAAATAAAAT[G/T]TTCAATGTTTATTTC174815
rs353147484in-del-/Aintron-variant?WS195II:11813657TTCAATGTTTATTTC[-/A]AAAACATTCCATCAC174815
rs353168741snpG/Tmissense?WS195II:11812572CTCCAGTCACCTCCT[G/T]CTGCTCAAACTGCAG174815
rs353170983snpC/Tintron-variant?WS195II:11813441TTGTGTACCGTTTAG[C/T]ATTGCACCTCCACTA174815
rs353172933snpC/Tintron-variant?WS195II:11813485AGATATATCTCAGTT[C/T]ATTTTGAAGTTATCA174815
Full records
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