NM_004360.5(CDH1):c.442G>A (p.Gly148Ser) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Mar 28, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001182395.3
Allele description [Variation Report for NM_004360.5(CDH1):c.442G>A (p.Gly148Ser)]
NM_004360.5(CDH1):c.442G>A (p.Gly148Ser)
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
-
Homo sapiens glutamyl-tRNA(Gln) amidotransferase, subunit C homolog (bacterial),...
Homo sapiens glutamyl-tRNA(Gln) amidotransferase, subunit C homolog (bacterial), mRNA (cDNA clone IMAGE:5588592)gi|40555869|gb|BC064523.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024