NM_014850.4(SRGAP3):c.3036C>T (p.Pro1012=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000963813.4
Allele description [Variation Report for NM_014850.4(SRGAP3):c.3036C>T (p.Pro1012=)]
NM_014850.4(SRGAP3):c.3036C>T (p.Pro1012=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024