ClinVar Miner

Variants studied for Adenocarcinoma of stomach

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
0 360 1 0 0 361

Gene and significance breakdown #

Total genes and gene combinations: 33
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Gene or gene combination likely pathogenic uncertain significance total
TP53 157 0 157
PIK3CA 43 0 43
CTNNB1 21 0 21
ERBB2 14 0 14
FBXW7 14 0 14
NRAS 14 0 14
HRAS, LRRC56 13 0 13
SMAD4 9 0 9
RHOA 8 0 8
CDKN2A 7 0 7
B2M 5 0 5
ERBB3 5 0 5
MAP2K1 5 0 5
PTEN 5 0 5
CREBBP 4 0 4
FGFR2 4 0 4
BRAF 3 0 3
FGFR1 3 0 3
GNAS 3 0 3
PPP2R1A 3 0 3
ACVR1 2 0 2
CNOT9 2 0 2
KIT 2 0 2
KRAS 2 0 2
MAP2K2 2 0 2
MED12 2 0 2
MTOR 2 0 2
RAF1 2 0 2
AKT1 1 0 1
CDH1 0 1 1
MLH1 1 0 1
POLE 1 0 1
PTPN11 1 0 1

Submitter and significance breakdown #

Total submitters: 2
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Submitter likely pathogenic uncertain significance total
Database of Curated Mutations (DoCM) 360 0 360
3DMed Clinical Laboratory Inc 0 1 1

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