NM_004360.5(CDH1):c.221G>T (p.Arg74Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001014835.3
Allele description [Variation Report for NM_004360.5(CDH1):c.221G>T (p.Arg74Leu)]
NM_004360.5(CDH1):c.221G>T (p.Arg74Leu)
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
-
transcription elongation factor SPT6 isoform X1 [Homo sapiens]
transcription elongation factor SPT6 isoform X1 [Homo sapiens]gi|2217313408|ref|XP_047292556.1|Protein
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OLR1 [Chlorocebus sabaeus]
OLR1 [Chlorocebus sabaeus]Gene ID:103218575Gene
-
HS3ST6 [Gracilinanus agilis]
HS3ST6 [Gracilinanus agilis]Gene ID:123248629Gene
-
Mixture/Component Compounds for PubChem Compound (Select 572) (23)
PubChem Compound
-
Taxonomy Links for Nucleotide (Select 1160688532) (1)
Taxonomy
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024