NM_199420.4(POLQ):c.69C>A (p.Ser23Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004055102.1
Allele description [Variation Report for NM_199420.4(POLQ):c.69C>A (p.Ser23Arg)]
NM_199420.4(POLQ):c.69C>A (p.Ser23Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens pleckstrin homology domain containing B2 (PLEKHB2), tran...
PREDICTED: Homo sapiens pleckstrin homology domain containing B2 (PLEKHB2), transcript variant X4, mRNAgi|2462574616|ref|XM_054342703.1|Nucleotide
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Last Updated: Oct 13, 2024