Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.80663151A>GCA161069325CD36c.591A>G (p.Thr197=)
c.*103A>G (n.*103A>G)
c.363A>G (p.Thr121=)
c.430-1255A>G (n.430-1255A>G)
n.770A>G
c.489A>G (p.Thr163=)
c.126A>G (p.Thr42=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.80663151A>CCA161069324CD36c.591A>C (p.Thr197=)
c.*103A>C (n.*103A>C)
c.363A>C (p.Thr121=)
c.430-1255A>C (n.430-1255A>C)
n.770A>C
c.489A>C (p.Thr163=)
c.126A>C (p.Thr42=)
 dbSNP
7g.80663151A>TCA4315245CD36c.591A>T (p.Thr197=)
c.*103A>T (n.*103A>T)
c.363A>T (p.Thr121=)
c.430-1255A>T (n.430-1255A>T)
n.770A>T
c.489A>T (p.Thr163=)
c.126A>T (p.Thr42=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched