Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.128360026T>A | CA685161739 | TMEM132C | c.86-54706T>A (n.86-54706T>A) c.26-54706T>A (n.26-54706T>A) n.319-54706T>A | dbSNP gnomAD v3 gnomAD v4 |
12 | g.128360026T>C | CA15754163 | TMEM132C | c.86-54706T>C (n.86-54706T>C) c.26-54706T>C (n.26-54706T>C) n.319-54706T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |