NM_000051.4(ATM):c.2075G>T (p.Arg692Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 12, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000567410.3
Allele description [Variation Report for NM_000051.4(ATM):c.2075G>T (p.Arg692Leu)]
NM_000051.4(ATM):c.2075G>T (p.Arg692Leu)
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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Amelanchier nantucketensis voucher 583-91B ribosomal protein L2 (rpl12) gene, pa...
Amelanchier nantucketensis voucher 583-91B ribosomal protein L2 (rpl12) gene, partial cds; and rpl2-trnH intergenic spacer, partial sequence; chloroplastgi|379643806|gb|JQ392067.1|Nucleotide
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Last Updated: Nov 3, 2024