NM_001063.4(TF):c.954C>T (p.Ala318=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003864060.2
Allele description [Variation Report for NM_001063.4(TF):c.954C>T (p.Ala318=)]
NM_001063.4(TF):c.954C>T (p.Ala318=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Sep 29, 2024