Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.30611036A>T | CA10184523 | TCN2 | n.401A>T c.230A>T (p.Lys77Met) c.221A>T (p.Lys74Met) n.559A>T c.155A>T (p.Lys52Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.30611036A>G | CA411206449 | TCN2 | n.401A>G c.230A>G (p.Lys77Arg) c.221A>G (p.Lys74Arg) n.559A>G c.155A>G (p.Lys52Arg) | ClinVar dbSNP gnomAD v3 gnomAD v4 |