Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.80105781G>ACA502177515GAAc.579G>A (p.Val193=)
ClinVar dbSNP
17g.80105781G>CCA8814934GAAc.579G>C (p.Val193=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.80105781G=CA2277811233GAAc.579G= (p.Val193=)
17g.80105781G>TCA502177517GAAc.579G>T (p.Val193=)
gnomAD v4
17g.80105781dupCA2576660839GAAc.579dup (p.Pro194AlafsTer?)
17g.80105782C>ACA401362156GAAc.580C>A (p.Pro194Thr)
17g.80105782C>GCA401362158GAAc.580C>G (p.Pro194Ala)
17g.80105782C>TCA401362160GAAc.580C>T (p.Pro194Ser)
gnomAD v4
17g.80105784dupCA2965194585GAAc.582dup (p.Glu196GlyfsTer?)
17g.80105784delCA2965194593GAAc.582del (p.Leu195TrpfsTer26)
c.582del (p.Leu195TrpfsTer?)
17g.80105783C>ACA401362161GAAc.581C>A (p.Pro194His)
gnomAD v4
17g.80105783C=CA2277811234GAAc.581C= (p.Pro194=)
17g.80105783C>GCA401362163GAAc.581C>G (p.Pro194Arg)
17g.80105783C>TCA401362165GAAc.581C>T (p.Pro194Leu)
dbSNP gnomAD v2 gnomAD v4
17g.80105784C>ACA502177523GAAc.582C>A (p.Pro194=)
17g.80105784C=CA2277811235GAAc.582C= (p.Pro194=)
17g.80105784C>GCA8814935GAAc.582C>G (p.Pro194=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.80105784C>TCA502177525GAAc.582C>T (p.Pro194=)
17g.80105785T>ACA401362168GAAc.583T>A (p.Leu195Met)
17g.80105785T>CCA502177528GAAc.583T>C (p.Leu195=)
ClinVar dbSNP
17g.80105785T>GCA401362170GAAc.583T>G (p.Leu195Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.80105785T=CA2277811236GAAc.583T= (p.Leu195=)
17g.80105786dupCA2965194608GAAc.584dup (p.Leu195PhefsTer?)
17g.80105786delCA2965194632GAAc.584del (p.Leu195TrpfsTer26)
c.584del (p.Leu195TrpfsTer?)
17g.80105786T>ACA401362172GAAc.584T>A (p.Leu195Ter)
ClinVar
17g.80105786T>CCA401362176GAAc.584T>C (p.Leu195Ser)
gnomAD v4
17g.80105786T>GCA401362173GAAc.584T>G (p.Leu195Trp)
17g.80105787G>ACA502177532GAAc.585G>A (p.Leu195=)
17g.80105787G>CCA401362178GAAc.585G>C (p.Leu195Phe)
17g.80105787G>TCA401362180GAAc.585G>T (p.Leu195Phe)
17g.80105787_80105788delCA2840238209GAAc.585_586del (p.Glu196AspfsTer?)
17g.80105788delCA2965194656GAAc.586del (p.Glu196ArgfsTer25)
c.586del (p.Glu196ArgfsTer?)
17g.80105788G>ACA401362183GAAc.586G>A (p.Glu196Lys)
17g.80105788G>CCA401362184GAAc.586G>C (p.Glu196Gln)
dbSNP gnomAD v2 gnomAD v4
17g.80105788G=CA2277811237GAAc.586G= (p.Glu196=)
17g.80105788G>TCA401362187GAAc.586G>T (p.Glu196Ter)
gnomAD v4
17g.80105790_80105791delCA2965194662GAAc.588_589del (p.Glu196AspfsTer?)
17g.80105789delCA2580095298GAAc.587del (p.Glu196GlyfsTer25)
c.587del (p.Glu196GlyfsTer?)
ClinVar
17g.80105789A>CCA401362189GAAc.587A>C (p.Glu196Ala)
17g.80105789A>GCA401362191GAAc.587A>G (p.Glu196Gly)
17g.80105789A>TCA401362192GAAc.587A>T (p.Glu196Val)
17g.80105790G>ACA502177537GAAc.588G>A (p.Glu196=)
17g.80105790G>CCA401362194GAAc.588G>C (p.Glu196Asp)
17g.80105790G>TCA401362196GAAc.588G>T (p.Glu196Asp)
17g.80105791A>CCA401362201GAAc.589A>C (p.Thr197Pro)
17g.80105791A>GCA401362200GAAc.589A>G (p.Thr197Ala)
17g.80105791A>TCA401362198GAAc.589A>T (p.Thr197Ser)
17g.80105792C>ACA8814936GAAc.590C>A (p.Thr197Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.80105792C=CA2277811238GAAc.590C= (p.Thr197=)
17g.80105792C>GCA401362205GAAc.590C>G (p.Thr197Ser)

Number of alleles fetched