NM_153700.2(STRC):c.4563G>A (p.Arg1521=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 22, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000215654.4
Allele description [Variation Report for NM_153700.2(STRC):c.4563G>A (p.Arg1521=)]
NM_153700.2(STRC):c.4563G>A (p.Arg1521=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Dec 24, 2022