NM_000179.3(MSH6):c.664G>T (p.Asp222Tyr) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 14, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002366851.2
Allele description [Variation Report for NM_000179.3(MSH6):c.664G>T (p.Asp222Tyr)]
NM_000179.3(MSH6):c.664G>T (p.Asp222Tyr)
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
-
Profile neighbors for GEO Profiles (Select 131296292) (200)
GEO Profiles
-
GEO Profile Links for Gene (Select 9267) (2843)
GEO Profiles
-
ATP1B2 ATPase Na+/K+ transporting subunit beta 2 [Homo sapiens]
ATP1B2 ATPase Na+/K+ transporting subunit beta 2 [Homo sapiens]Gene ID:482Gene
-
Gene Links for GEO Profiles (Select 131296296) (1)
Gene
-
DDX53 DEAD-box helicase 53 [Homo sapiens]
DDX53 DEAD-box helicase 53 [Homo sapiens]Gene ID:168400Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024