NM_001048174.2(MUTYH):c.1173C>A (p.Ala391=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Aug 12, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000584206.6
Allele description [Variation Report for NM_001048174.2(MUTYH):c.1173C>A (p.Ala391=)]
NM_001048174.2(MUTYH):c.1173C>A (p.Ala391=)
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
-
hypothetical protein M876_01130 [Elizabethkingia anophelis FMS-007]
hypothetical protein M876_01130 [Elizabethkingia anophelis FMS-007]gi|822870945|gnl|PRJNA210135|M876_0 gb|AKH93169.1|Protein
-
LOC126593231 [Malus sylvestris]
LOC126593231 [Malus sylvestris]Gene ID:126593231Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024