NM_005445.4(SMC3):c.969+14C>T AND Cornelia de Lange syndrome 3
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003502084.1
Allele description [Variation Report for NM_005445.4(SMC3):c.969+14C>T]
NM_005445.4(SMC3):c.969+14C>T
Condition(s)
-
Homo sapiens valosin-containing protein (VCP), mRNA
Homo sapiens valosin-containing protein (VCP), mRNAgi|6005941|ref|NM_007126.1|Nucleotide
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Last Updated: Feb 20, 2024