NM_000551.4(VHL):c.364G>A (p.Ala122Thr) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 31, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000564632.4
Allele description [Variation Report for NM_000551.4(VHL):c.364G>A (p.Ala122Thr)]
NM_000551.4(VHL):c.364G>A (p.Ala122Thr)
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
-
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1-like [Anopheles funestu...
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1-like [Anopheles funestus]gi|2273283397|ref|XP_049285244.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024