NM_001048174.2(MUTYH):c.495G>A (p.Val165=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 2, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000582375.3
Allele description [Variation Report for NM_001048174.2(MUTYH):c.495G>A (p.Val165=)]
NM_001048174.2(MUTYH):c.495G>A (p.Val165=)
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
-
PREDICTED: Homo sapiens golgi SNAP receptor complex member 2 (GOSR2), transcript...
PREDICTED: Homo sapiens golgi SNAP receptor complex member 2 (GOSR2), transcript variant X12, mRNAgi|2217314901|ref|XM_047437112.1|Nucleotide
-
Golgi SNAP receptor complex member 2 isoform X6 [Homo sapiens]
Golgi SNAP receptor complex member 2 isoform X6 [Homo sapiens]gi|2462558976|ref|XP_054173870.1|Protein
-
H2_input
H2_inputGEO DataSets
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Last Updated: Dec 24, 2023