NM_000059.4(BRCA2):c.606C>T (p.Pro202=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 8, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000779925.3
Allele description [Variation Report for NM_000059.4(BRCA2):c.606C>T (p.Pro202=)]
NM_000059.4(BRCA2):c.606C>T (p.Pro202=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens regulatory factor X2 (RFX2), transcript variant 2, mRNA
Homo sapiens regulatory factor X2 (RFX2), transcript variant 2, mRNAgi|1675036438|ref|NM_134433.3|Nucleotide
-
EDEM3 [Capra hircus]
EDEM3 [Capra hircus]Gene ID:102174143Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024