NM_000075.4(CDK4):c.888T>G (p.His296Gln) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 27, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002376010.2
Allele description [Variation Report for NM_000075.4(CDK4):c.888T>G (p.His296Gln)]
NM_000075.4(CDK4):c.888T>G (p.His296Gln)
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
-
Macrochelys suwanniensis isolate rMacSuw1 chromosome 4, whole genome shotgun seq...
Macrochelys suwanniensis isolate rMacSuw1 chromosome 4, whole genome shotgun sequencegi|2618199855|gb|CM065778.1||gnl|WG FKX|SUPER_4Nucleotide
-
Macrochelys suwanniensis isolate rMacSuw1 chromosome 6, whole genome shotgun seq...
Macrochelys suwanniensis isolate rMacSuw1 chromosome 6, whole genome shotgun sequencegi|2618199850|gb|CM065780.1||gnl|WG FKX|SUPER_6Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 1, 2024