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OncoKB Gene Panel: Listing of All Nonsynonymous Variants in Genes of Interest; Variant May or May Not Play a Role in Cancer Predisposition
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Patient ID
292921
Open Patient
Specimen ID
168-R
Open Specimen
Sample ID
WS1V43
Open Sample
OncoKB Version
v3.14
Chr
chr17
Chr Start
7577551
Chr End
7577551
Ref Allele
C
Alt Allele
A
HGVS cDNA Change
c.730G>T
HGVS Protein Change
p.G244C
Existing Variant
TP53_g.13367G>T,COSM10941,COSM11524,COSM1646853,COSM1716873,COSM3355992,COSM3733384,COSM3970348,COSM3970349,COSM44221,COSM44940,COSM673602,COSM673603,COSM673604,COSM984898,COSM984900,COSM984901,COSM99683,COSM99684,COSM99685
Variant Class
Missense_Mutation
Total Reads
167
PolyPhen
probably_damaging(1)
Oncogenicity
Likely Oncogenic
Predicted
Functional Effect
Likely Loss-of-function