NM_172166.4(MSH5):c.1497C>G (p.Asp499Glu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 7, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004132084.1
Allele description [Variation Report for NM_172166.4(MSH5):c.1497C>G (p.Asp499Glu)]
NM_172166.4(MSH5):c.1497C>G (p.Asp499Glu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024