NM_000251.3(MSH2):c.1106A>G (p.Asp369Gly) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 26, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002426288.2
Allele description [Variation Report for NM_000251.3(MSH2):c.1106A>G (p.Asp369Gly)]
NM_000251.3(MSH2):c.1106A>G (p.Asp369Gly)
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
-
ABC transporter substrate-binding protein [Paraburkholderia phenoliruptrix]
ABC transporter substrate-binding protein [Paraburkholderia phenoliruptrix]gi|503352322|ref|WP_013586983.1|Protein
-
ubiquitin carboxyl-terminal hydrolase MINDY-1 isoform 11 [Homo sapiens]
ubiquitin carboxyl-terminal hydrolase MINDY-1 isoform 11 [Homo sapiens]gi|1776842924|ref|NP_001363600.1|Protein
-
pyruvate, phosphate dikinase [Clostridioides difficile]
pyruvate, phosphate dikinase [Clostridioides difficile]gi|497576428|ref|WP_009890612.1|Protein
-
glutathione synthase [Synechococcus sp. Minos11]
glutathione synthase [Synechococcus sp. Minos11]gi|500469829|ref|WP_011936663.1|Protein
-
PREDICTED: Homo sapiens solute carrier family 12 member 7 (SLC12A7), transcript ...
PREDICTED: Homo sapiens solute carrier family 12 member 7 (SLC12A7), transcript variant X5, mRNAgi|2462489494|ref|XM_054328661.1|Nucleotide
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Last Updated: May 1, 2024