NM_003079.5(SMARCE1):c.1078G>C (p.Gly360Arg) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001009863.4
Allele description [Variation Report for NM_003079.5(SMARCE1):c.1078G>C (p.Gly360Arg)]
NM_003079.5(SMARCE1):c.1078G>C (p.Gly360Arg)
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 LIM homeobox transcription factor 1, alpha, mRNA (cDNA clone IMAGE:...
Homo sapiens LIM homeobox transcription factor 1, alpha, mRNA (cDNA clone IMAGE:40119207), complete cdsgi|111185588|gb|BC119744.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024