NM_001370259.2(MEN1):c.1314C>G (p.Thr438=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 23, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002383842.2
Allele description [Variation Report for NM_001370259.2(MEN1):c.1314C>G (p.Thr438=)]
NM_001370259.2(MEN1):c.1314C>G (p.Thr438=)
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
-
AGENCOURT_78602491 NICHD_XGC_skin_m Xenopus laevis cDNA clone IMAGE:8640658 5', ...
AGENCOURT_78602491 NICHD_XGC_skin_m Xenopus laevis cDNA clone IMAGE:8640658 5', mRNA sequencegi|95017462|gnl|dbEST|39159635|gb|E 46.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024