NM_001370259.2(MEN1):c.1823A>C (p.Lys608Thr) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004522711.1
Allele description [Variation Report for NM_001370259.2(MEN1):c.1823A>C (p.Lys608Thr)]
NM_001370259.2(MEN1):c.1823A>C (p.Lys608Thr)
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
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Eucalyptus elliptica psbA-trnH intergenic spacer, partial sequence; chloroplast
Eucalyptus elliptica psbA-trnH intergenic spacer, partial sequence; chloroplastgi|925711239|gb|KT632278.1|Nucleotide
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Homo sapiens mRNA; cDNA DKFZp686L21216 (from clone DKFZp686L21216)
Homo sapiens mRNA; cDNA DKFZp686L21216 (from clone DKFZp686L21216)gi|34365117|emb|BX640841.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024