NM_000179.3(MSH6):c.112C>G (p.Pro38Ala) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002324478.2
Allele description [Variation Report for NM_000179.3(MSH6):c.112C>G (p.Pro38Ala)]
NM_000179.3(MSH6):c.112C>G (p.Pro38Ala)
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
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Homo sapiens leukocyte specific transcript 1 (LST1), transcript variant 5, mRNA
Homo sapiens leukocyte specific transcript 1 (LST1), transcript variant 5, mRNAgi|45580735|ref|NM_205840.1|Nucleotide
-
Homo sapiens leukocyte specific transcript 1 (LST1), mRNA
Homo sapiens leukocyte specific transcript 1 (LST1), mRNAgi|6005740|ref|NM_007161.1|Nucleotide
-
U exon, partial [Human adenovirus 2]
U exon, partial [Human adenovirus 2]gi|56160508|ref|AP_000189.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024