NM_001099221.2(TIFAB):c.118C>T (p.Arg40Trp) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 17, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004467271.1
Allele description [Variation Report for NM_001099221.2(TIFAB):c.118C>T (p.Arg40Trp)]
NM_001099221.2(TIFAB):c.118C>T (p.Arg40Trp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024