NM_000276.4(OCRL):c.426_427delinsAC (p.Ser143Pro) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 28, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000193098.6
Allele description [Variation Report for NM_000276.4(OCRL):c.426_427delinsAC (p.Ser143Pro)]
NM_000276.4(OCRL):c.426_427delinsAC (p.Ser143Pro)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens VPS11 core subunit of CORVET and HOPS complexes (VPS11), transcript...
Homo sapiens VPS11 core subunit of CORVET and HOPS complexes (VPS11), transcript variant 9, non-coding RNAgi|1804894048|ref|NR_165449.1|Nucleotide
-
Homo sapiens thrombospondin type 1 domain containing 7A (THSD7A), mRNA
Homo sapiens thrombospondin type 1 domain containing 7A (THSD7A), mRNAgi|1519313347|ref|NM_015204.3|Nucleotide
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Last Updated: Apr 9, 2023