Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.90149169G>C | CA709836001 | KCNK13 | c.335-34942G>C (n.335-34942G>C) | dbSNP |
14 | g.90149169G>T | CA965843276 | KCNK13 | c.335-34942G>T (n.335-34942G>T) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.90149169G>A | CA264910053 | KCNK13 | c.335-34942G>A (n.335-34942G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |