NM_003799.3(RNMT):c.1045G>C (p.Gly349Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004203355.1
Allele description [Variation Report for NM_003799.3(RNMT):c.1045G>C (p.Gly349Arg)]
NM_003799.3(RNMT):c.1045G>C (p.Gly349Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 26, 2024