Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.80107816A=CA2277812404GAAc.875A= (p.Tyr292=)
17g.80107816A>CCA401363867GAAc.875A>C (p.Tyr292Ser)
17g.80107816A>GCA16041886GAAc.875A>G (p.Tyr292Cys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.80107816A>TCA401363865GAAc.875A>T (p.Tyr292Phe)
17g.80107817C>ACA401363869GAAc.876C>A (p.Tyr292Ter)
17g.80107817C=CA2277812405GAAc.876C= (p.Tyr292=)
17g.80107817C>GCA401363871GAAc.876C>G (p.Tyr292Ter)
ClinVar dbSNP
17g.80107817C>TCA8815080GAAc.876C>T (p.Tyr292=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.80107818G>ACA116622GAAc.877G>A (p.Gly293Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.80107818G>CCA401363876GAAc.877G>C (p.Gly293Arg)
ClinVar dbSNP
17g.80107818G=CA2277812406GAAc.877G= (p.Gly293=)
17g.80107818G>TCA401363875GAAc.877G>T (p.Gly293Trp)
gnomAD v4
17g.80107819G>ACA401363879GAAc.878G>A (p.Gly293Glu)
17g.80107819G>CCA401363881GAAc.878G>C (p.Gly293Ala)
17g.80107819G=CA2277812407GAAc.878G= (p.Gly293=)
17g.80107819G>TCA401363883GAAc.878G>T (p.Gly293Val)
dbSNP
17g.80107820G>ACA502402736GAAc.879G>A (p.Gly293=)
ClinVar dbSNP gnomAD v4
17g.80107820G>CCA502402737GAAc.879G>C (p.Gly293=)
17g.80107820G>TCA502402738GAAc.879G>T (p.Gly293=)
17g.80107821T>ACA401363885GAAc.880T>A (p.Ser294Thr)
17g.80107821T>CCA401363887GAAc.880T>C (p.Ser294Pro)
17g.80107821T>GCA401363889GAAc.880T>G (p.Ser294Ala)
17g.80107822C>ACA401363891GAAc.881C>A (p.Ser294Tyr)
17g.80107822C>GCA401363894GAAc.881C>G (p.Ser294Cys)
17g.80107822C>TCA401363892GAAc.881C>T (p.Ser294Phe)
17g.80107823T>ACA502402739GAAc.882T>A (p.Ser294=)
17g.80107823T>CCA502402740GAAc.882T>C (p.Ser294=)
17g.80107823T>GCA502402741GAAc.882T>G (p.Ser294=)
17g.80107824C>ACA8815081GAAc.883C>A (p.His295Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.80107824C=CA2277812408GAAc.883C= (p.His295=)
17g.80107824C>GCA401363897GAAc.883C>G (p.His295Asp)
17g.80107824C>TCA401363899GAAc.883C>T (p.His295Tyr)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.80107825A>CCA401363901GAAc.884A>C (p.His295Pro)
17g.80107825A>GCA401363903GAAc.884A>G (p.His295Arg)
17g.80107825A>TCA401363905GAAc.884A>T (p.His295Leu)
17g.80107826C>ACA401363907GAAc.885C>A (p.His295Gln)
17g.80107826C>GCA401363908GAAc.885C>G (p.His295Gln)
17g.80107826C>TCA502402742GAAc.885C>T (p.His295=)
17g.80107827C>ACA401363910GAAc.886C>A (p.Pro296Thr)
17g.80107827C>GCA401363912GAAc.886C>G (p.Pro296Ala)
gnomAD v4
17g.80107827C>TCA401363914GAAc.886C>T (p.Pro296Ser)
17g.80107828C>ACA401363920GAAc.887C>A (p.Pro296His)
17g.80107828C>GCA401363918GAAc.887C>G (p.Pro296Arg)
17g.80107828C>TCA401363916GAAc.887C>T (p.Pro296Leu)
17g.80107829T>ACA502402743GAAc.888T>A (p.Pro296=)
gnomAD v4
17g.80107829T>CCA502402744GAAc.888T>C (p.Pro296=)
17g.80107829T>GCA502402745GAAc.888T>G (p.Pro296=)
17g.80107830T>ACA401363922GAAc.889T>A (p.Phe297Ile)
17g.80107830T>CCA401363924GAAc.889T>C (p.Phe297Leu)
17g.80107830T>GCA401363926GAAc.889T>G (p.Phe297Val)

Number of alleles fetched