NM_000368.5(TSC1):c.774G>A (p.Glu258=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jul 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002258955.3
Allele description [Variation Report for NM_000368.5(TSC1):c.774G>A (p.Glu258=)]
NM_000368.5(TSC1):c.774G>A (p.Glu258=)
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
-
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Metapenaeopsis cytochrome oxidase subunit I (COX1) gene, partial cds; mitochondr...
Metapenaeopsis cytochrome oxidase subunit I (COX1) gene, partial cds; mitochondrial.PopSet: 1016883065PopSet
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024