NM_003126.4(SPTA1):c.7132C>T (p.Gln2378Ter) AND See cases
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Dec 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003156096.1
Allele description [Variation Report for NM_003126.4(SPTA1):c.7132C>T (p.Gln2378Ter)]
NM_003126.4(SPTA1):c.7132C>T (p.Gln2378Ter)
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
Assertion and evidence details
Last Updated: Apr 1, 2023