NM_001048174.2(MUTYH):c.1460C>T (p.Ser487Phe) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Benign (6 submissions)
- Last evaluated:
- Nov 15, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000132436.21
Allele description [Variation Report for NM_001048174.2(MUTYH):c.1460C>T (p.Ser487Phe)]
NM_001048174.2(MUTYH):c.1460C>T (p.Ser487Phe)
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
-
cytochrome c oxidase subunit 2 (mitochondrion) [Clavispora lusitaniae]
cytochrome c oxidase subunit 2 (mitochondrion) [Clavispora lusitaniae]gi|533206670|ref|YP_008475004.1|Protein
-
transcriptional regulator [Azospirillum thiophilum]
transcriptional regulator [Azospirillum thiophilum]gi|933523903|gnl|PRJNA292868|AL072_ |gb|ALG74092.1|Protein
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024