Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.33263767C>TCA5466933NRP1c.537G>A (p.Val179=)
c.-7G>A (n.-7G>A)
c.537G>A (p.Ala179=)
n.878G>A
n.640G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.33263767C>GCA205486469NRP1c.537G>C (p.Val179=)
c.-7G>C (n.-7G>C)
c.537G>C (p.Ala179=)
n.878G>C
n.640G>C
dbSNP COSMIC COSMIC COSMIC
10g.33263767C=CA1900699821NRP1c.537G= (p.Val179=)
c.-7G= (n.-7G=)
c.537G= (p.Ala179=)
n.878G=
n.640G=
dbSNP dbSNP
10g.33263767C>ACA468981496NRP1c.537G>T (p.Val179=)
c.-7G>T (n.-7G>T)
c.537G>T (p.Ala179=)
n.878G>T
n.640G>T
dbSNP gnomAD v4

Number of alleles fetched