NM_006473.4(TAF6L):c.1847A>T (p.Tyr616Phe) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 16, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004468866.1
Allele description [Variation Report for NM_006473.4(TAF6L):c.1847A>T (p.Tyr616Phe)]
NM_006473.4(TAF6L):c.1847A>T (p.Tyr616Phe)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024