NM_000179.3(MSH6):c.2021G>T (p.Gly674Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 2, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000480051.1
Allele description [Variation Report for NM_000179.3(MSH6):c.2021G>T (p.Gly674Val)]
NM_000179.3(MSH6):c.2021G>T (p.Gly674Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Mar 26, 2023