NM_000535.7(PMS2):c.1602C>T (p.Asp534=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003187298.2
Allele description [Variation Report for NM_000535.7(PMS2):c.1602C>T (p.Asp534=)]
NM_000535.7(PMS2):c.1602C>T (p.Asp534=)
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: spastin [Bos indicus]
PREDICTED: spastin [Bos indicus]gi|1131156004|ref|XP_019825011.1|Protein
-
LOC102782924 [Neolamprologus brichardi]
LOC102782924 [Neolamprologus brichardi]Gene ID:102782924Gene
-
102782924[uid] AND (alive[prop]) (1)
Gene
-
RecName: Full=Protein Wnt-9b; AltName: Full=Protein Wnt-14b; AltName: Full=Prote...
RecName: Full=Protein Wnt-9b; AltName: Full=Protein Wnt-14b; AltName: Full=Protein Wnt-15; Flags: Precursorgi|30316345|sp|O35468.2|WNT9B_MOUSEProtein
-
RAD54L [Vulpes vulpes]
RAD54L [Vulpes vulpes]Gene ID:112914769Gene
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See more...Assertion and evidence details
Last Updated: May 1, 2024