Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.67181354G>ACA392956232SMAD3c.187G>A (p.Asp63Asn)
c.457G>A (p.Asp153Asn)
c.772G>A (p.Asp258Asn)
n.475G>A
c.640G>A (p.Asp214Asn)
n.282+6770G>A
c.625G>A (p.Asp209Asn)
dbSNP COSMIC
15g.67181354G>CCA325318SMAD3c.187G>C (p.Asp63His)
c.457G>C (p.Asp153His)
c.772G>C (p.Asp258His)
n.475G>C
c.640G>C (p.Asp214His)
n.282+6770G>C
c.625G>C (p.Asp209His)
ClinVar dbSNP
15g.67181354G=CA2184414782SMAD3c.187G= (p.Asp63=)
c.457G= (p.Asp153=)
c.772G= (p.Asp258=)
n.475G=
c.640G= (p.Asp214=)
n.282+6770G=
c.625G= (p.Asp209=)
dbSNP

Number of alleles fetched