NM_000210.4(ITGA6):c.148A>G (p.Met50Val) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000885969.6
Allele description [Variation Report for NM_000210.4(ITGA6):c.148A>G (p.Met50Val)]
NM_000210.4(ITGA6):c.148A>G (p.Met50Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024