NM_007255.3(B4GALT7):c.297G>T (p.Val99=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 21, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000441342.1
Allele description [Variation Report for NM_007255.3(B4GALT7):c.297G>T (p.Val99=)]
NM_007255.3(B4GALT7):c.297G>T (p.Val99=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024