Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.36461009C>A | CA512324390 | CLDN14,CLDN14-AS1 | c.687G>T (p.Thr229=) n.468+15002C>A | dbSNP gnomAD v2 gnomAD v4 |
21 | g.36461009C>T | CA133533 | CLDN14,CLDN14-AS1 | c.687G>A (p.Thr229=) n.468+15002C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.36461009C= | CA2388017387 | CLDN14,CLDN14-AS1 | c.687G= (p.Thr229=) n.468+15002C= | dbSNP |
21 | g.36461009C>G | CA512324388 | CLDN14,CLDN14-AS1 | c.687G>C (p.Thr229=) n.468+15002C>G | dbSNP gnomAD v4 |