Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.80656687C>T | CA123185 | CD36 | c.268C>T (p.Pro90Ser) c.241+27C>T (n.241+27C>T) c.40C>T (p.Pro14Ser) n.447C>T c.166C>T (p.Pro56Ser) c.-184-4376C>T (n.-184-4376C>T) c.-215C>T (n.-215C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.80656687C= | CA1720369396 | CD36 | c.268C= (p.Pro90=) c.241+27C= (n.241+27C=) c.40C= (p.Pro14=) n.447C= c.166C= (p.Pro56=) c.-184-4376C= (n.-184-4376C=) c.-215C= (n.-215C=) | dbSNP |