Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.67165023C>TCA020077SMAD3c.20C>T (p.Ala7Val)
c.335C>T (p.Ala112Val)
c.203C>T (p.Ala68Val)
c.280C>T (p.Pro94Ser)
n.185C>T
c.188C>T (p.Ala63Val)
ClinVar dbSNP COSMIC COSMIC
15g.67165023C>GCA392954060SMAD3c.20C>G (p.Ala7Gly)
c.335C>G (p.Ala112Gly)
c.203C>G (p.Ala68Gly)
c.280C>G (p.Pro94Ala)
n.185C>G
c.188C>G (p.Ala63Gly)
dbSNP
15g.67165023C>ACA392954061SMAD3c.20C>A (p.Ala7Asp)
c.335C>A (p.Ala112Asp)
c.203C>A (p.Ala68Asp)
c.280C>A (p.Pro94Thr)
n.185C>A
c.188C>A (p.Ala63Asp)
ClinVar dbSNP
15g.67165023C=CA2184410374SMAD3c.20C= (p.Ala7=)
c.335C= (p.Ala112=)
c.203C= (p.Ala68=)
c.280C= (p.Pro94=)
n.185C=
c.188C= (p.Ala63=)
dbSNP

Number of alleles fetched