NM_000465.4(BARD1):c.835T>C (p.Ser279Pro) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000378845.4
Allele description [Variation Report for NM_000465.4(BARD1):c.835T>C (p.Ser279Pro)]
NM_000465.4(BARD1):c.835T>C (p.Ser279Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens tRNA methyltransferase 2 homolog B (TRMT2B), transcript variant 2, ...
Homo sapiens tRNA methyltransferase 2 homolog B (TRMT2B), transcript variant 2, mRNAgi|1890346385|ref|NM_001167970.2|Nucleotide
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Last Updated: Sep 29, 2024