Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.177995888G>T | CA447993088 | PROP1 | c.46C>A (p.Arg16=) | ClinVar dbSNP gnomAD v4 |
5 | g.177995888G>C | CA3587654 | PROP1 | c.46C>G (p.Arg16Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.177995888G>A | CA214192 | PROP1 | c.46C>T (p.Arg16Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
5 | g.177995888G= | CA1603815359 | PROP1 | c.46C= (p.Arg16=) | dbSNP |