NM_002528.7(NTHL1):c.336C>T (p.Asp112=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 16, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002455313.2
Allele description [Variation Report for NM_002528.7(NTHL1):c.336C>T (p.Asp112=)]
NM_002528.7(NTHL1):c.336C>T (p.Asp112=)
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
-
2695857[uid] (1)
Taxonomy
-
1RIN (7)
Protein
-
Aponogeton[orgn] (0)
GEO DataSets
-
PREDICTED: Biomphalaria glabrata polypeptide N-acetylgalactosaminyltransferase 1...
PREDICTED: Biomphalaria glabrata polypeptide N-acetylgalactosaminyltransferase 11-like (LOC106055667), transcript variant X3, mRNAgi|2502133474|ref|XM_013212028.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024