Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.80108513G>ACA401364953GAAc.1100G>A (p.Trp367Ter)
ClinVar dbSNP gnomAD v2
17g.80108513G>CCA401364954GAAc.1100G>C (p.Trp367Ser)
17g.80108513G=CA2277812794GAAc.1100G= (p.Trp367=)
17g.80108513G>TCA401364955GAAc.1100G>T (p.Trp367Leu)
17g.80108514G>ACA401364958GAAc.1101G>A (p.Trp367Ter)
17g.80108514G>CCA401364957GAAc.1101G>C (p.Trp367Cys)
17g.80108514G>TCA401364956GAAc.1101G>T (p.Trp367Cys)
17g.80108515G>ACA8815170GAAc.1102G>A (p.Gly368Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.80108515G>CCA401364959GAAc.1102G>C (p.Gly368Arg)
17g.80108515G=CA2277812795GAAc.1102G= (p.Gly368=)
17g.80108515G>TCA294892167GAAc.1102G>T (p.Gly368Cys)
dbSNP
17g.80108516G>ACA294892175GAAc.1103G>A (p.Gly368Asp)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.80108516G>CCA401364960GAAc.1103G>C (p.Gly368Ala)
17g.80108516G=CA2277812796GAAc.1103G= (p.Gly368=)
17g.80108516G>TCA8815171GAAc.1103G>T (p.Gly368Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.80108517C>ACA502402383GAAc.1104C>A (p.Gly368=)
dbSNP gnomAD v2 gnomAD v4
17g.80108517C=CA2277812797GAAc.1104C= (p.Gly368=)
17g.80108517C>GCA502402384GAAc.1104C>G (p.Gly368=)
17g.80108517C>TCA502402385GAAc.1104C>T (p.Gly368=)
gnomAD v4
17g.80108518dupCA2580095322GAAc.1105dup (p.Leu369ProfsTer?)
ClinVar
17g.80108518C>ACA401364961GAAc.1105C>A (p.Leu369Met)
17g.80108518C>GCA401364962GAAc.1105C>G (p.Leu369Val)
gnomAD v4
17g.80108518C>TCA502402386GAAc.1105C>T (p.Leu369=)
ClinVar dbSNP gnomAD v4
17g.80108519T>ACA401364963GAAc.1106T>A (p.Leu369Gln)
ClinVar
17g.80108519T>CCA401364964GAAc.1106T>C (p.Leu369Pro)
ClinVar dbSNP gnomAD v4
17g.80108519T>GCA401364965GAAc.1106T>G (p.Leu369Arg)
17g.80108519T=CA2277812798GAAc.1106T= (p.Leu369=)
17g.80108520G>ACA502402387GAAc.1107G>A (p.Leu369=)
ClinVar
17g.80108520G>CCA502402388GAAc.1107G>C (p.Leu369=)
ClinVar
17g.80108520G=CA2277812799GAAc.1107G= (p.Leu369=)
17g.80108520G>TCA8815172GAAc.1107G>T (p.Leu369=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.80108521G>ACA401364966GAAc.1108G>A (p.Gly370Ser)
17g.80108521G>CCA401364968GAAc.1108G>C (p.Gly370Arg)
17g.80108521G>TCA401364967GAAc.1108G>T (p.Gly370Cys)
17g.80108522G>ACA401364969GAAc.1109G>A (p.Gly370Asp)
ClinVar dbSNP
17g.80108522G>CCA401364971GAAc.1109G>C (p.Gly370Ala)
17g.80108522G=CA2277812800GAAc.1109G= (p.Gly370=)
17g.80108522G>TCA401364970GAAc.1109G>T (p.Gly370Val)
17g.80108523C>ACA502402390GAAc.1110C>A (p.Gly370=)
17g.80108523C=CA2277812801GAAc.1110C= (p.Gly370=)
17g.80108523C>GCA8815173GAAc.1110C>G (p.Gly370=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.80108523C>TCA502402389GAAc.1110C>T (p.Gly370=)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.80108524T>ACA401364972GAAc.1111T>A (p.Phe371Ile)
17g.80108524T>CCA401364973GAAc.1111T>C (p.Phe371Leu)
17g.80108524T>GCA401364974GAAc.1111T>G (p.Phe371Val)
17g.80108525T>ACA401364975GAAc.1112T>A (p.Phe371Tyr)
17g.80108525T>CCA401364976GAAc.1112T>C (p.Phe371Ser)
17g.80108525T>GCA401364977GAAc.1112T>G (p.Phe371Cys)
17g.80108526C>ACA401364978GAAc.1113C>A (p.Phe371Leu)
17g.80108526C>GCA401364979GAAc.1113C>G (p.Phe371Leu)

Number of alleles fetched