NM_001048174.2(MUTYH):c.585T>C (p.Ile195=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 10, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002367125.2
Allele description [Variation Report for NM_001048174.2(MUTYH):c.585T>C (p.Ile195=)]
NM_001048174.2(MUTYH):c.585T>C (p.Ile195=)
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
-
Scarus dimidiatus voucher FDP_IGCS_2110_003A cytochrome oxidase subunit 1 (COI) ...
Scarus dimidiatus voucher FDP_IGCS_2110_003A cytochrome oxidase subunit 1 (COI) gene, partial cds; mitochondrialgi|2722342200|gnl|uoguelph|MINDA192 OI-5P|gb|OR524637.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024