NM_000368.5(TSC1):c.1333+5A>G AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001729368.1
Allele description [Variation Report for NM_000368.5(TSC1):c.1333+5A>G]
NM_000368.5(TSC1):c.1333+5A>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
proton-coupled zinc antiporter SLC30A1 [Rattus norvegicus]
proton-coupled zinc antiporter SLC30A1 [Rattus norvegicus]gi|12408302|ref|NP_074044.1|Protein
-
Homo sapiens CUGBP Elav-like family member 1 (CELF1), transcript variant 2, mRNA
Homo sapiens CUGBP Elav-like family member 1 (CELF1), transcript variant 2, mRNAgi|1775678380|ref|NM_198700.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024