NM_000179.3(MSH6):c.1950C>T (p.Gly650=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Apr 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000583517.5
Allele description [Variation Report for NM_000179.3(MSH6):c.1950C>T (p.Gly650=)]
NM_000179.3(MSH6):c.1950C>T (p.Gly650=)
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
-
solute carrier family 35 member E1 [Homo sapiens]
solute carrier family 35 member E1 [Homo sapiens]gi|164607128|ref|NP_079157.3|Protein
-
dehydrogenase/reductase SDR family member 6 isoform X4 [Homo sapiens]
dehydrogenase/reductase SDR family member 6 isoform X4 [Homo sapiens]gi|2217351526|ref|XP_047271942.1|Protein
-
troponin T, cardiac muscle isoform 2 [Homo sapiens]
troponin T, cardiac muscle isoform 2 [Homo sapiens]gi|48255879|ref|NP_001001430.1|Protein
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See more...Assertion and evidence details
Last Updated: May 7, 2024