Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.103937424C>T | CA16428102 | PDGFD | c.772+6028G>A (n.772+6028G>A) c.754+6028G>A (n.754+6028G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.103937424C>G | CA1996762775 | PDGFD | c.772+6028G>C (n.772+6028G>C) c.754+6028G>C (n.754+6028G>C) | dbSNP |