NM_006517.5(SLC16A2):c.447C>T (p.Leu149=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Apr 14, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000503612.6
Allele description [Variation Report for NM_006517.5(SLC16A2):c.447C>T (p.Leu149=)]
NM_006517.5(SLC16A2):c.447C>T (p.Leu149=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024