NM_145292.4(GALNTL5):c.11C>T (p.Ala4Val) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004154080.1
Allele description [Variation Report for NM_145292.4(GALNTL5):c.11C>T (p.Ala4Val)]
NM_145292.4(GALNTL5):c.11C>T (p.Ala4Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024