NM_000249.4(MLH1):c.410C>T (p.Ala137Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 29, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000165129.3
Allele description [Variation Report for NM_000249.4(MLH1):c.410C>T (p.Ala137Val)]
NM_000249.4(MLH1):c.410C>T (p.Ala137Val)
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
-
Homo sapiens eukaryotic translation initiation factor 3, subunit 6 48kDa, mRNA (...
Homo sapiens eukaryotic translation initiation factor 3, subunit 6 48kDa, mRNA (cDNA clone IMAGE:4106529)gi|13543582|gb|BC005944.1|Nucleotide
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Last Updated: Sep 29, 2024