Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.133837662T>C | CA12249917 | LINC01312,TARID | n.659T>C n.478+8215A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.133837662T>G | CA452310603 | LINC01312,TARID | n.659T>G n.478+8215A>C | dbSNP |
6 | g.133837662T>A | CA452310602 | LINC01312,TARID | n.659T>A n.478+8215A>T | dbSNP gnomAD v4 |