Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.80108386_80108456delCA2695227076GAAc.1052_1076-33del
17g.80108396C>ACA16620645GAAc.1062C>A (p.Tyr354Ter)
ClinVar dbSNP
17g.80108396C=CA2277812710GAAc.1062C= (p.Tyr354=)
17g.80108396C>GCA401364789GAAc.1062C>G (p.Tyr354Ter)
17g.80108396C>TCA502402325GAAc.1062C>T (p.Tyr354=)
ClinVar dbSNP
17g.80108397C>ACA401364791GAAc.1063C>A (p.Leu355Met)
17g.80108397C>GCA401364792GAAc.1063C>G (p.Leu355Val)
17g.80108397C>TCA502402327GAAc.1063C>T (p.Leu355=)
17g.80108398T>ACA401364793GAAc.1064T>A (p.Leu355Gln)
17g.80108398T>CCA8815136GAAc.1064T>C (p.Leu355Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.80108398T>GCA401364795GAAc.1064T>G (p.Leu355Arg)
dbSNP gnomAD v4
17g.80108398T=CA2277812711GAAc.1064T= (p.Leu355=)
17g.80108399G>ACA502402332GAAc.1065G>A (p.Leu355=)
ClinVar dbSNP
17g.80108399G>CCA502402328GAAc.1065G>C (p.Leu355=)
17g.80108399G>TCA502402329GAAc.1065G>T (p.Leu355=)
17g.80108400G>ACA401364801GAAc.1066G>A (p.Asp356Asn)
17g.80108400G>CCA401364799GAAc.1066G>C (p.Asp356His)
17g.80108400G>TCA401364797GAAc.1066G>T (p.Asp356Tyr)
17g.80108401A>CCA401364803GAAc.1067A>C (p.Asp356Ala)
17g.80108401A>GCA401364804GAAc.1067A>G (p.Asp356Gly)
17g.80108401A>TCA401364806GAAc.1067A>T (p.Asp356Val)
17g.80108402C>ACA401364809GAAc.1068C>A (p.Asp356Glu)
17g.80108402C=CA2277812712GAAc.1068C= (p.Asp356=)
17g.80108402C>GCA401364810GAAc.1068C>G (p.Asp356Glu)
17g.80108402C>TCA8815137GAAc.1068C>T (p.Asp356=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.80108403G>ACA8815138GAAc.1069G>A (p.Val357Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.80108403G>CCA401364814GAAc.1069G>C (p.Val357Leu)
17g.80108403G=CA2277812713GAAc.1069G= (p.Val357=)
17g.80108403G>TCA198782GAAc.1069G>T (p.Val357Phe)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.80108404T>ACA401364816GAAc.1070T>A (p.Val357Asp)
17g.80108404T>CCA401364818GAAc.1070T>C (p.Val357Ala)
17g.80108404T>GCA401364819GAAc.1070T>G (p.Val357Gly)
17g.80108405T>ACA502402340GAAc.1071T>A (p.Val357=)
17g.80108405T>CCA502402342GAAc.1071T>C (p.Val357=)
ClinVar dbSNP COSMIC
17g.80108405T>GCA502402344GAAc.1071T>G (p.Val357=)
17g.80108405T=CA2277812714GAAc.1071T= (p.Val357=)
17g.80108406G>ACA401364823GAAc.1072G>A (p.Val358Met)
gnomAD v4
17g.80108406G>CCA401364825GAAc.1072G>C (p.Val358Leu)
17g.80108406G>TCA401364822GAAc.1072G>T (p.Val358Leu)
17g.80108407T>ACA401364831GAAc.1073T>A (p.Val358Glu)
17g.80108407T>CCA401364827GAAc.1073T>C (p.Val358Ala)
17g.80108407T>GCA401364829GAAc.1073T>G (p.Val358Gly)
17g.80108408G>ACA502402345GAAc.1074G>A (p.Val358=)
COSMIC
17g.80108408G>CCA8815139GAAc.1074G>C (p.Val358=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.80108408G=CA2277812715GAAc.1074G= (p.Val358=)
17g.80108408G>TCA502402348GAAc.1074G>T (p.Val358=)
17g.80108409G>ACA401364835GAAc.1075G>A (p.Gly359Arg)
ClinVar
17g.80108409G>CCA401364836GAAc.1075G>C (p.Gly359Arg)
17g.80108409G=CA2277812716GAAc.1075G= (p.Gly359=)
17g.80108409G>TCA16620646GAAc.1075G>T (p.Gly359Ter)
ClinVar dbSNP

Number of alleles fetched