NM_003476.5(CSRP3):c.108C>T (p.His36=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 28, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000439429.2
Allele description [Variation Report for NM_003476.5(CSRP3):c.108C>T (p.His36=)]
NM_003476.5(CSRP3):c.108C>T (p.His36=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 5, 2024