NM_001040616.3(LINS1):c.1415G>C (p.Ser472Thr) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 9, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001644786.9
Allele description [Variation Report for NM_001040616.3(LINS1):c.1415G>C (p.Ser472Thr)]
NM_001040616.3(LINS1):c.1415G>C (p.Ser472Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 9, 2024