NM_181882.3(PRX):c.3769G>A (p.Gly1257Arg) AND not provided
- Germline classification:
- Uncertain significance (3 submissions)
- Last evaluated:
- May 13, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000236523.19
Allele description [Variation Report for NM_181882.3(PRX):c.3769G>A (p.Gly1257Arg)]
NM_181882.3(PRX):c.3769G>A (p.Gly1257Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 10, 2024