NM_004281.4(BAG3):c.1299G>A (p.Gln433=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001432233.6
Allele description
NM_004281.4(BAG3):c.1299G>A (p.Gln433=)
Condition(s)
-
PREDICTED: Homo sapiens WRN RecQ like helicase (WRN), transcript variant X1, mRN...
PREDICTED: Homo sapiens WRN RecQ like helicase (WRN), transcript variant X1, mRNAgi|2462620955|ref|XM_054361180.1|Nucleotide
-
PREDICTED: Homo sapiens WRN RecQ like helicase (WRN), transcript variant X4, mis...
PREDICTED: Homo sapiens WRN RecQ like helicase (WRN), transcript variant X4, misc_RNAgi|2217373143|ref|XR_949472.4|Nucleotide
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Last Updated: May 1, 2024