Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.177095415C>GCA16602607FGFR4c.1605C>G (p.Asn535Lys)
c.1485C>G (p.Asn495Lys)
c.1401C>G (p.Asn467Lys)
n.591C>G
c.499C>G
c.1698C>G (p.Asn566Lys)
c.1287C>G (p.Asn429Lys)
n.1600C>G
ClinVar dbSNP COSMIC COSMIC
5g.177095415C>TCA447725470FGFR4c.1605C>T (p.Asn535=)
c.1485C>T (p.Asn495=)
c.1401C>T (p.Asn467=)
n.591C>T
c.499C>T
c.1698C>T (p.Asn566=)
c.1287C>T (p.Asn429=)
n.1600C>T
dbSNP gnomAD v3 gnomAD v4
5g.177095415C>ACA16602606FGFR4c.1605C>A (p.Asn535Lys)
c.1485C>A (p.Asn495Lys)
c.1401C>A (p.Asn467Lys)
n.591C>A
c.499C>A
c.1698C>A (p.Asn566Lys)
c.1287C>A (p.Asn429Lys)
n.1600C>A
ClinVar dbSNP COSMIC COSMIC

Number of alleles fetched