Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.7116952T>G | CA2320763821 | INSR | c.*104A>C (n.*104A>C) | dbSNP gnomAD v4 |
19 | g.7116952T>C | CA10643414 | INSR | c.*104A>G (n.*104A>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7116952T= | CA2320763819 | INSR | c.*104A= (n.*104A=) | dbSNP |
19 | g.7116952T>A | CA2580607727 | INSR | c.*104A>T (n.*104A>T) | dbSNP gnomAD v4 |