NM_198994.3(TGM6):c.1025G>A (p.Arg342Gln) AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Sep 18, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000502237.8
Allele description [Variation Report for NM_198994.3(TGM6):c.1025G>A (p.Arg342Gln)]
NM_198994.3(TGM6):c.1025G>A (p.Arg342Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 20, 2024