Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.116782048C>TCA10584670METc.*1188C>T (n.*1188C>T)
c.3637C>T (p.Leu1213Phe)
c.3583C>T (p.Leu1195Phe)
c.2293C>T (p.Leu765Phe)
c.3640C>T (p.Leu1214Phe)
n.3714C>T
ClinVar dbSNP COSMIC
7g.116782048C>ACA368991080METc.*1188C>A (n.*1188C>A)
c.3637C>A (p.Leu1213Ile)
c.3583C>A (p.Leu1195Ile)
c.2293C>A (p.Leu765Ile)
c.3640C>A (p.Leu1214Ile)
n.3714C>A
dbSNP COSMIC
7g.116782048C>GCA257006METc.*1188C>G (n.*1188C>G)
c.3637C>G (p.Leu1213Val)
c.3583C>G (p.Leu1195Val)
c.2293C>G (p.Leu765Val)
c.3640C>G (p.Leu1214Val)
n.3714C>G
ClinVar dbSNP COSMIC
7g.116782048C=CA1737012337METc.*1188C= (n.*1188C=)
c.3637C= (p.Leu1213=)
c.3583C= (p.Leu1195=)
c.2293C= (p.Leu765=)
c.3640C= (p.Leu1214=)
n.3714C=
dbSNP

Number of alleles fetched