NM_003982.4(SLC7A7):c.1119G>A (p.Leu373=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Aug 29, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000616460.1
Allele description [Variation Report for NM_003982.4(SLC7A7):c.1119G>A (p.Leu373=)]
NM_003982.4(SLC7A7):c.1119G>A (p.Leu373=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 20, 2024