ClinVar Miner

Variants studied for Pancreatic adenocarcinoma

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
0 242 373 197 34 846

Gene and significance breakdown #

Total genes and gene combinations: 18
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Gene or gene combination likely pathogenic uncertain significance likely benign benign total
CBR4, PALLD 0 203 107 10 320
PALLD 0 170 90 24 284
TP53 175 0 0 0 175
PIK3CA 14 0 0 0 14
HRAS, LRRC56 10 0 0 0 10
CTNNB1, LOC126806658 9 0 0 0 9
SMAD4 9 0 0 0 9
CDKN2A 7 0 0 0 7
GNAS 3 0 0 0 3
POLE 3 0 0 0 3
MAP2K2 2 0 0 0 2
MED12 2 0 0 0 2
RXRA 2 0 0 0 2
U2AF1 2 0 0 0 2
ERBB2 1 0 0 0 1
KRAS 1 0 0 0 1
MYCN, MYCNOS 1 0 0 0 1
SF3B2 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 2
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Submitter likely pathogenic uncertain significance likely benign benign total
Labcorp Genetics (formerly Invitae), Labcorp 0 373 197 34 604
Database of Curated Mutations (DoCM) 242 0 0 0 242

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