NM_000179.3(MSH6):c.2137G>T (p.Asp713Tyr) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 24, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004017947.1
Allele description [Variation Report for NM_000179.3(MSH6):c.2137G>T (p.Asp713Tyr)]
NM_000179.3(MSH6):c.2137G>T (p.Asp713Tyr)
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
-
Tssr2509 AND (alive[prop]) (0)
Gene
-
Homo sapiens isolate Assyrian_C165_W3b mitochondrion, complete genome
Homo sapiens isolate Assyrian_C165_W3b mitochondrion, complete genomegi|1765886760|gb|MK217237.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024