NM_000465.4(BARD1):c.154C>A (p.Arg52Ser) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 23, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001525157.2
Allele description [Variation Report for NM_000465.4(BARD1):c.154C>A (p.Arg52Ser)]
NM_000465.4(BARD1):c.154C>A (p.Arg52Ser)
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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Collomia heterophylla voucher BRY:94-020 internal transcribed spacer 1, partial ...
Collomia heterophylla voucher BRY:94-020 internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene, complete sequence; and internal transcribed spacer 2, partial sequencegi|345523296|gb|HQ116841.1|Nucleotide
-
Homo sapiens mitochondrial trans-2-enoyl-CoA reductase (MECR), transcript varian...
Homo sapiens mitochondrial trans-2-enoyl-CoA reductase (MECR), transcript variant 10, non-coding RNAgi|1700447977|ref|NR_146212.2|Nucleotide
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Last Updated: Dec 24, 2023