NM_005261.4(GEM):c.751C>T (p.Arg251Trp) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004626883.1
Allele description [Variation Report for NM_005261.4(GEM):c.751C>T (p.Arg251Trp)]
NM_005261.4(GEM):c.751C>T (p.Arg251Trp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens kinesin family member 18A (KIF18A), transcript variant X...
PREDICTED: Homo sapiens kinesin family member 18A (KIF18A), transcript variant X1, mRNAgi|2217284882|ref|XM_017018379.2|Nucleotide
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Last Updated: Aug 11, 2024