Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.66177389G>T | CA371344654 | CRH | c.89C>A (p.Pro30Gln) | dbSNP gnomAD v4 |
8 | g.66177389G>A | CA371344655 | CRH | c.89C>T (p.Pro30Leu) | dbSNP gnomAD v4 |
8 | g.66177389G>C | CA238539 | CRH | c.89C>G (p.Pro30Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.66177389G= | CA1790382233 | CRH | c.89C= (p.Pro30=) | dbSNP |