Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.50626877G>C | CA412177162 | ARSA | c.641C>G (p.Ala214Gly) c.383C>G (p.Ala128Gly) n.1145C>G | dbSNP |
22 | g.50626877G>A | CA340036 | ARSA | c.641C>T (p.Ala214Val) c.383C>T (p.Ala128Val) n.1145C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.50626877G>T | CA10324959 | ARSA | c.641C>A (p.Ala214Asp) c.383C>A (p.Ala128Asp) n.1145C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |