NM_000551.4(VHL):c.42C>G (p.Gly14=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 27, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002330296.2
Allele description [Variation Report for NM_000551.4(VHL):c.42C>G (p.Gly14=)]
NM_000551.4(VHL):c.42C>G (p.Gly14=)
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
-
110161[uid] (1)
Taxonomy
-
CD1.1
CD1.1gi|123910910|sp|Q4ADW0|Q4ADW0_CHICKProtein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024