NM_003271.5(TSPAN4):c.638C>T (p.Ala213Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004200087.1
Allele description [Variation Report for NM_003271.5(TSPAN4):c.638C>T (p.Ala213Val)]
NM_003271.5(TSPAN4):c.638C>T (p.Ala213Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 8, 2024