Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.4862018C>G | CA1058778845 | MSX1 | c.470-683C>G (n.470-683C>G) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.4862018C>A | CA11677030 | MSX1 | c.470-683C>A (n.470-683C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.4862018C= | CA1435013222 | MSX1 | c.470-683C= (n.470-683C=) | dbSNP |