NM_001048174.2(MUTYH):c.1219C>T (p.His407Tyr) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Jan 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000129005.15
Allele description [Variation Report for NM_001048174.2(MUTYH):c.1219C>T (p.His407Tyr)]
NM_001048174.2(MUTYH):c.1219C>T (p.His407Tyr)
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
-
irregular chiasm C-roughest protein-like [Nymphalis io]
irregular chiasm C-roughest protein-like [Nymphalis io]gi|2293907480|ref|XP_050357957.1|Protein
-
Pseudomonas aeruginosa strain 10-03740 Flagellin (fliC) gene, partial cds
Pseudomonas aeruginosa strain 10-03740 Flagellin (fliC) gene, partial cdsgi|2174817087|gb|OL354412.1|Nucleotide
-
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See more...Assertion and evidence details
Last Updated: Jun 29, 2024