NM_003002.4(SDHD):c.411T>C (p.Ala137=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 4, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002324102.9
Allele description [Variation Report for NM_003002.4(SDHD):c.411T>C (p.Ala137=)]
NM_003002.4(SDHD):c.411T>C (p.Ala137=)
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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257976[uid] (1)
Taxonomy
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238237[uid] (1)
Taxonomy
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227824[uid] (1)
Taxonomy
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163626[uid] (1)
Taxonomy
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34544[uid] (1)
Taxonomy
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024