NM_000548.5(TSC2):c.5331T>C (p.Pro1777=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 24, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001703960.1
Allele description [Variation Report for NM_000548.5(TSC2):c.5331T>C (p.Pro1777=)]
NM_000548.5(TSC2):c.5331T>C (p.Pro1777=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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PREDICTED: Canis lupus familiaris pleiotrophin (PTN), transcript variant X2, mRNAgi|1952689390|ref|XM_532732.6|Nucleotide
-
RPCI-11-165F1.TJ RPCI-11 Homo sapiens genomic clone RPCI-11-165F1, genomic surve...
RPCI-11-165F1.TJ RPCI-11 Homo sapiens genomic clone RPCI-11-165F1, genomic survey sequencegi|4474297|gnl|dbGSS|536269|gb|AQ41 1|Nucleotide
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Last Updated: Sep 29, 2024