Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.204159399C>ACA344337528RENc.689G>T (p.Arg230Ile)
c.575G>T (p.Arg192Ile)
gnomAD v4
1g.204159399C=CA1141581509RENc.689G= (p.Arg230=)
c.575G= (p.Arg192=)
1g.204159399C>GCA344337535RENc.689G>C (p.Arg230Thr)
c.575G>C (p.Arg192Thr)
1g.204159399C>TCA122848RENc.689G>A (p.Arg230Lys)
c.575G>A (p.Arg192Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.204159400delCA2650014142RENc.688del (p.Arg230GlufsTer?)
c.574del (p.Arg192GlufsTer?)
gnomAD v4
1g.204159400T>ACA344337540RENc.688A>T (p.Arg230Ter)
c.574A>T (p.Arg192Ter)
1g.204159400T>CCA344337543RENc.688A>G (p.Arg230Gly)
c.574A>G (p.Arg192Gly)
1g.204159400T>GCA422837316RENc.688A>C (p.Arg230=)
c.574A>C (p.Arg192=)
1g.204159401G>ACA1344864RENc.687C>T (p.Asn229=)
c.573C>T (p.Asn191=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.204159401G>CCA1344865RENc.687C>G (p.Asn229Lys)
c.573C>G (p.Asn191Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.204159401G=CA2482057058RENc.687C= (p.Asn229=)
c.573C= (p.Asn191=)
1g.204159401G>TCA344337549RENc.687C>A (p.Asn229Lys)
c.573C>A (p.Asn191Lys)
gnomAD v4
1g.204159402T>ACA344337552RENc.686A>T (p.Asn229Ile)
c.572A>T (p.Asn191Ile)
1g.204159402T>CCA344337554RENc.686A>G (p.Asn229Ser)
c.572A>G (p.Asn191Ser)
gnomAD v4
1g.204159402T>GCA344337557RENc.686A>C (p.Asn229Thr)
c.572A>C (p.Asn191Thr)
gnomAD v4
1g.204159403T>ACA1344867RENc.685A>T (p.Asn229Tyr)
c.571A>T (p.Asn191Tyr)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.204159403T>CCA1344866RENc.685A>G (p.Asn229Asp)
c.571A>G (p.Asn191Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.204159403T>GCA344337565RENc.685A>C (p.Asn229His)
c.571A>C (p.Asn191His)
gnomAD v4
1g.204159403T=CA1149074997RENc.685A= (p.Asn229=)
c.571A= (p.Asn191=)
1g.204159404G>ACA422837318RENc.684C>T (p.Tyr228=)
c.570C>T (p.Tyr190=)
1g.204159404G>CCA344337568RENc.684C>G (p.Tyr228Ter)
c.570C>G (p.Tyr190Ter)
gnomAD v4
1g.204159404G>TCA344337571RENc.684C>A (p.Tyr228Ter)
c.570C>A (p.Tyr190Ter)
1g.204159405delCA2573985050RENc.683del (p.Tyr228SerfsTer?)
c.569del (p.Tyr190SerfsTer?)
1g.204159405T>ACA344337574RENc.683A>T (p.Tyr228Phe)
c.569A>T (p.Tyr190Phe)
1g.204159405T>CCA344337575RENc.683A>G (p.Tyr228Cys)
c.569A>G (p.Tyr190Cys)
dbSNP gnomAD v3 gnomAD v4
1g.204159405T>GCA344337576RENc.683A>C (p.Tyr228Ser)
c.569A>C (p.Tyr190Ser)
gnomAD v4
1g.204159405T=CA2482057059RENc.683A= (p.Tyr228=)
c.569A= (p.Tyr190=)
1g.204159406A>CCA344337577RENc.682T>G (p.Tyr228Asp)
c.568T>G (p.Tyr190Asp)
1g.204159406A>GCA344337579RENc.682T>C (p.Tyr228His)
c.568T>C (p.Tyr190His)
1g.204159406A>TCA344337581RENc.682T>A (p.Tyr228Asn)
c.568T>A (p.Tyr190Asn)
1g.204159407G>ACA422837320RENc.681C>T (p.Tyr227=)
c.567C>T (p.Tyr189=)
1g.204159407G>CCA344337582RENc.681C>G (p.Tyr227Ter)
c.567C>G (p.Tyr189Ter)
1g.204159407G>TCA344337585RENc.681C>A (p.Tyr227Ter)
c.567C>A (p.Tyr189Ter)
1g.204159408T>ACA344337589RENc.680A>T (p.Tyr227Phe)
c.566A>T (p.Tyr189Phe)
1g.204159408T>CCA344337593RENc.680A>G (p.Tyr227Cys)
c.566A>G (p.Tyr189Cys)
gnomAD v4 COSMIC
1g.204159408T>GCA344337596RENc.680A>C (p.Tyr227Ser)
c.566A>C (p.Tyr189Ser)
1g.204159409A>CCA344337605RENc.679T>G (p.Tyr227Asp)
c.565T>G (p.Tyr189Asp)
1g.204159409A>GCA344337602RENc.679T>C (p.Tyr227His)
c.565T>C (p.Tyr189His)
gnomAD v4
1g.204159409A>TCA344337601RENc.679T>A (p.Tyr227Asn)
c.565T>A (p.Tyr189Asn)
1g.204159410G>ACA422837321RENc.678C>T (p.Phe226=)
c.564C>T (p.Phe188=)
1g.204159410G>CCA344337609RENc.678C>G (p.Phe226Leu)
c.564C>G (p.Phe188Leu)
1g.204159410G>TCA344337612RENc.678C>A (p.Phe226Leu)
c.564C>A (p.Phe188Leu)
1g.204159411A>CCA344337616RENc.677T>G (p.Phe226Cys)
c.563T>G (p.Phe188Cys)
1g.204159411A>GCA344337618RENc.677T>C (p.Phe226Ser)
c.563T>C (p.Phe188Ser)
1g.204159411A>TCA344337622RENc.677T>A (p.Phe226Tyr)
c.563T>A (p.Phe188Tyr)
1g.204159413delCA2650014143RENc.677del (p.Phe226SerfsTer?)
c.563del (p.Phe188SerfsTer?)
gnomAD v4
1g.204159412A>CCA344337625RENc.676T>G (p.Phe226Val)
c.562T>G (p.Phe188Val)
1g.204159412A>GCA344337626RENc.676T>C (p.Phe226Leu)
c.562T>C (p.Phe188Leu)
1g.204159412A>TCA344337629RENc.676T>A (p.Phe226Ile)
c.562T>A (p.Phe188Ile)
1g.204159413A>CCA422837322RENc.675T>G (p.Ser225=)
c.561T>G (p.Ser187=)

Number of alleles fetched