NM_001013627.3(NHSL2):c.3346G>C (p.Val1116Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004254513.1
Allele description [Variation Report for NM_001013627.3(NHSL2):c.3346G>C (p.Val1116Leu)]
NM_001013627.3(NHSL2):c.3346G>C (p.Val1116Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024