Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.45645389C>ACA359707446HCN1c.645G>T (p.Met215Ile)
dbSNP gnomAD v2 COSMIC
5g.45645389C=CA1543790554HCN1c.645G= (p.Met215=)
5g.45645389C>GCA359707444HCN1c.645G>C (p.Met215Ile)
5g.45645389C>TCA359707445HCN1c.645G>A (p.Met215Ile)
COSMIC
5g.45645390A>CCA359707447HCN1c.644T>G (p.Met215Arg)
gnomAD v4
5g.45645390A>GCA359707449HCN1c.644T>C (p.Met215Thr)
gnomAD v3 gnomAD v4
5g.45645390A>TCA359707448HCN1c.644T>A (p.Met215Lys)
5g.45645391T>ACA359707450HCN1c.643A>T (p.Met215Leu)
COSMIC
5g.45645391T>CCA118324608HCN1c.643A>G (p.Met215Val)
ClinVar dbSNP gnomAD v4 COSMIC
5g.45645391T>GCA359707451HCN1c.643A>C (p.Met215Leu)
5g.45645391T=CA1543790557HCN1c.643A= (p.Met215=)
5g.45645392C>ACA359707452HCN1c.642G>T (p.Lys214Asn)
COSMIC
5g.45645392C>GCA359707453HCN1c.642G>C (p.Lys214Asn)
5g.45645392C>TCA444401806HCN1c.642G>A (p.Lys214=)
5g.45645393T>ACA359707454HCN1c.641A>T (p.Lys214Met)
5g.45645393T>CCA118324609HCN1c.641A>G (p.Lys214Arg)
dbSNP
5g.45645393T>GCA359707455HCN1c.641A>C (p.Lys214Thr)
5g.45645393T=CA1543790559HCN1c.641A= (p.Lys214=)
5g.45645394T>ACA359707456HCN1c.640A>T (p.Lys214Ter)
5g.45645394T>CCA359707457HCN1c.640A>G (p.Lys214Glu)
5g.45645394T>GCA359707458HCN1c.640A>C (p.Lys214Gln)
5g.45645395G>ACA444401807HCN1c.639C>T (p.Ile213=)
5g.45645395G>CCA359707459HCN1c.639C>G (p.Ile213Met)
5g.45645395G=CA1543790564HCN1c.639C= (p.Ile213=)
5g.45645395G>TCA3259425HCN1c.639C>A (p.Ile213=)
ClinVar dbSNP ExAC gnomAD v2
5g.45645396A>CCA359707462HCN1c.638T>G (p.Ile213Ser)
5g.45645396A>GCA359707461HCN1c.638T>C (p.Ile213Thr)
5g.45645396A>TCA359707460HCN1c.638T>A (p.Ile213Asn)
5g.45645397T>ACA359707463HCN1c.637A>T (p.Ile213Phe)
COSMIC
5g.45645397T>CCA359707464HCN1c.637A>G (p.Ile213Val)
5g.45645397T>GCA359707465HCN1c.637A>C (p.Ile213Leu)
5g.45645398C>ACA3259426HCN1c.636G>T (p.Val212=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.45645398C=CA1543790569HCN1c.636G= (p.Val212=)
5g.45645398C>GCA444401808HCN1c.636G>C (p.Val212=)
5g.45645398C>TCA3259427HCN1c.636G>A (p.Val212=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
5g.45645399A>CCA359707466HCN1c.635T>G (p.Val212Gly)
5g.45645399A>GCA359707467HCN1c.635T>C (p.Val212Ala)
5g.45645399A>TCA359707468HCN1c.635T>A (p.Val212Glu)
ClinVar dbSNP
5g.45645400C>ACA359707469HCN1c.634G>T (p.Val212Leu)
5g.45645400C>GCA359707470HCN1c.634G>C (p.Val212Leu)
5g.45645400C>TCA359707471HCN1c.634G>A (p.Val212Met)
5g.45645401T>ACA359707472HCN1c.633A>T (p.Lys211Asn)
5g.45645401T>CCA444401809HCN1c.633A>G (p.Lys211=)
5g.45645401T>GCA359707473HCN1c.633A>C (p.Lys211Asn)
5g.45645402T>ACA359707475HCN1c.632A>T (p.Lys211Ile)
gnomAD v4
5g.45645402T>CCA359707476HCN1c.632A>G (p.Lys211Arg)
5g.45645402T>GCA359707474HCN1c.632A>C (p.Lys211Thr)
5g.45645403T>ACA359707477HCN1c.631A>T (p.Lys211Ter)
5g.45645403T>CCA3259428HCN1c.631A>G (p.Lys211Glu)
dbSNP ExAC gnomAD v2
5g.45645403T>GCA359707478HCN1c.631A>C (p.Lys211Gln)

Number of alleles fetched