Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.77917992A=CA1177620261NEXNc.252A= (p.Glu84=)
c.60A= (p.Glu20=)
1g.77917992A>CCA340886278NEXNc.252A>C (p.Glu84Asp)
c.60A>C (p.Glu20Asp)
1g.77917992A>GCA418708998NEXNc.252A>G (p.Glu84=)
c.60A>G (p.Glu20=)
dbSNP gnomAD v2 gnomAD v4
1g.77917992A>TCA340886279NEXNc.252A>T (p.Glu84Asp)
c.60A>T (p.Glu20Asp)
1g.77917993G>ACA340886281NEXNc.253G>A (p.Asp85Asn)
c.61G>A (p.Asp21Asn)
1g.77917993G>CCA340886283NEXNc.253G>C (p.Asp85His)
c.61G>C (p.Asp21His)
1g.77917993G>TCA340886284NEXNc.253G>T (p.Asp85Tyr)
c.61G>T (p.Asp21Tyr)
1g.77917994A=CA1177620262NEXNc.254A= (p.Asp85=)
c.62A= (p.Asp21=)
1g.77917994A>CCA340886287NEXNc.254A>C (p.Asp85Ala)
c.62A>C (p.Asp21Ala)
1g.77917994A>GCA340886288NEXNc.254A>G (p.Asp85Gly)
c.62A>G (p.Asp21Gly)
ClinVar dbSNP gnomAD v3 gnomAD v4
1g.77917994A>TCA340886289NEXNc.254A>T (p.Asp85Val)
c.62A>T (p.Asp21Val)
1g.77917995T>ACA340886290NEXNc.255T>A (p.Asp85Glu)
c.63T>A (p.Asp21Glu)
dbSNP gnomAD v2 gnomAD v4
1g.77917995T>CCA418709000NEXNc.255T>C (p.Asp85=)
c.63T>C (p.Asp21=)
1g.77917995T>GCA918601NEXNc.255T>G (p.Asp85Glu)
c.63T>G (p.Asp21Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.77917995T=CA1147150066NEXNc.255T= (p.Asp85=)
c.63T= (p.Asp21=)
1g.77917996G>ACA340886294NEXNc.256G>A (p.Val86Ile)
c.64G>A (p.Val22Ile)
dbSNP gnomAD v2 gnomAD v4
1g.77917996G>CCA340886295NEXNc.256G>C (p.Val86Leu)
c.64G>C (p.Val22Leu)
1g.77917996G=CA1177620263NEXNc.256G= (p.Val86=)
c.64G= (p.Val22=)
1g.77917996G>TCA340886296NEXNc.256G>T (p.Val86Leu)
c.64G>T (p.Val22Leu)
dbSNP gnomAD v2 gnomAD v4
1g.77917997T>ACA340886300NEXNc.257T>A (p.Val86Glu)
c.65T>A (p.Val22Glu)
1g.77917997T>CCA340886298NEXNc.257T>C (p.Val86Ala)
c.65T>C (p.Val22Ala)
ClinVar dbSNP gnomAD v4 COSMIC
1g.77917997T>GCA340886299NEXNc.257T>G (p.Val86Gly)
c.65T>G (p.Val22Gly)
1g.77917997T=CA1177620264NEXNc.257T= (p.Val86=)
c.65T= (p.Val22=)
1g.77917998A>CCA418709002NEXNc.258A>C (p.Val86=)
c.66A>C (p.Val22=)
1g.77917998A>GCA418709003NEXNc.258A>G (p.Val86=)
c.66A>G (p.Val22=)
1g.77917998A>TCA418709004NEXNc.258A>T (p.Val86=)
c.66A>T (p.Val22=)
1g.77917999T>ACA340886301NEXNc.259T>A (p.Ser87Thr)
c.67T>A (p.Ser23Thr)
gnomAD v4
1g.77917999T>CCA340886303NEXNc.259T>C (p.Ser87Pro)
c.67T>C (p.Ser23Pro)
1g.77917999T>GCA340886304NEXNc.259T>G (p.Ser87Ala)
c.67T>G (p.Ser23Ala)
1g.77918000C>ACA340886305NEXNc.260C>A (p.Ser87Tyr)
c.68C>A (p.Ser23Tyr)
1g.77918000C>GCA340886311NEXNc.260C>G (p.Ser87Cys)
c.68C>G (p.Ser23Cys)
1g.77918000C>TCA340886312NEXNc.260C>T (p.Ser87Phe)
c.68C>T (p.Ser23Phe)
COSMIC COSMIC
1g.77918001T>ACA418709007NEXNc.261T>A (p.Ser87=)
c.69T>A (p.Ser23=)
1g.77918001T>CCA418709008NEXNc.261T>C (p.Ser87=)
c.69T>C (p.Ser23=)
1g.77918001T>GCA418709006NEXNc.261T>G (p.Ser87=)
c.69T>G (p.Ser23=)
1g.77918002T>ACA340886314NEXNc.262T>A (p.Ser88Thr)
c.70T>A (p.Ser24Thr)
1g.77918002T>CCA340886316NEXNc.262T>C (p.Ser88Pro)
c.70T>C (p.Ser24Pro)
1g.77918002T>GCA340886317NEXNc.262T>G (p.Ser88Ala)
c.70T>G (p.Ser24Ala)
1g.77918003C>ACA340886321NEXNc.263C>A (p.Ser88Tyr)
c.71C>A (p.Ser24Tyr)
1g.77918003C>GCA340886322NEXNc.263C>G (p.Ser88Cys)
c.71C>G (p.Ser24Cys)
1g.77918003C>TCA340886323NEXNc.263C>T (p.Ser88Phe)
c.71C>T (p.Ser24Phe)
1g.77918004T>ACA418709012NEXNc.264T>A (p.Ser88=)
c.72T>A (p.Ser24=)
1g.77918004T>CCA418709011NEXNc.264T>C (p.Ser88=)
c.72T>C (p.Ser24=)
1g.77918004T>GCA418709010NEXNc.264T>G (p.Ser88=)
c.72T>G (p.Ser24=)
1g.77918005A>CCA340886324NEXNc.265A>C (p.Lys89Gln)
c.73A>C (p.Lys25Gln)
1g.77918005A>GCA340886326NEXNc.265A>G (p.Lys89Glu)
c.73A>G (p.Lys25Glu)
gnomAD v4
1g.77918005A>TCA340886325NEXNc.265A>T (p.Lys89Ter)
c.73A>T (p.Lys25Ter)
gnomAD v4
1g.77918006A>CCA340886327NEXNc.266A>C (p.Lys89Thr)
c.74A>C (p.Lys25Thr)
gnomAD v4
1g.77918006A>GCA340886328NEXNc.266A>G (p.Lys89Arg)
c.74A>G (p.Lys25Arg)
1g.77918006A>TCA340886329NEXNc.266A>T (p.Lys89Ile)
c.74A>T (p.Lys25Ile)

Number of alleles fetched