NM_001164508.2(NEB):c.22005G>A (p.Thr7335=) AND not specified
- Germline classification:
- Likely benign (3 submissions)
- Last evaluated:
- Nov 21, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000174430.11
Allele description [Variation Report for NM_001164508.2(NEB):c.22005G>A (p.Thr7335=)]
NM_001164508.2(NEB):c.22005G>A (p.Thr7335=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jan 19, 2025