NM_000264.5(PTCH1):c.672C>T (p.Tyr224=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 31, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002363455.2
Allele description [Variation Report for NM_000264.5(PTCH1):c.672C>T (p.Tyr224=)]
NM_000264.5(PTCH1):c.672C>T (p.Tyr224=)
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
-
NR5A1 nuclear receptor subfamily 5 group A member 1 [Bos taurus]
NR5A1 nuclear receptor subfamily 5 group A member 1 [Bos taurus]Gene ID:281948Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024