NM_152490.5(B3GALNT2):c.169G>A (p.Val57Met) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 1, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001200565.16
Allele description [Variation Report for NM_152490.5(B3GALNT2):c.169G>A (p.Val57Met)]
NM_152490.5(B3GALNT2):c.169G>A (p.Val57Met)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024