NM_020949.3(SLC7A14):c.1796T>C (p.Leu599Pro) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001207574.7
Allele description [Variation Report for NM_020949.3(SLC7A14):c.1796T>C (p.Leu599Pro)]
NM_020949.3(SLC7A14):c.1796T>C (p.Leu599Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 8, 2024