NM_001393500.2(TOMT):c.110G>A (p.Arg37Gln) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 22, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001195335.4
Allele description [Variation Report for NM_001393500.2(TOMT):c.110G>A (p.Arg37Gln)]
NM_001393500.2(TOMT):c.110G>A (p.Arg37Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024