NM_000548.5(TSC2):c.5383C>T (p.Arg1795Cys) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jan 15, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000163344.13
Allele description [Variation Report for NM_000548.5(TSC2):c.5383C>T (p.Arg1795Cys)]
NM_000548.5(TSC2):c.5383C>T (p.Arg1795Cys)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
JGI_CABC8005.rev NIH_XGC_tropFat1 Xenopus tropicalis cDNA clone IMAGE:7804140 3'...
JGI_CABC8005.rev NIH_XGC_tropFat1 Xenopus tropicalis cDNA clone IMAGE:7804140 3', mRNA sequencegi|71495330|gnl|dbEST|30359099|gb|D 76.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024