Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.52766224G>C | CA1910256990 | MBL2 | c.*1913C>G (n.*1913C>G) | dbSNP |
10 | g.52766224G>A | CA10631783 | MBL2 | c.*1913C>T (n.*1913C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.52766224G= | CA1910256989 | MBL2 | c.*1913C= (n.*1913C=) | dbSNP |