ClinVar Miner

Variants studied for cutaneous melanoma

Included ClinVar conditions (1):
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 protective total
0 279 0 0 0 1 280

Gene and significance breakdown #

Total genes and gene combinations: 37
Download table as spreadsheet
Gene or gene combination likely pathogenic protective total
TP53 92 0 92
CTNNB1, LOC126806658 23 0 23
BRAF 19 0 19
PIK3CA 18 0 18
NRAS 14 0 14
HRAS, LRRC56 11 0 11
CDKN2A 10 0 10
FBXW7 10 0 10
MAP2K1 8 0 8
EZH2 6 0 6
B2M 5 0 5
IDH1 5 0 5
SF3B1 5 0 5
CDK4 4 0 4
CNOT9 4 0 4
CREBBP 4 0 4
ERBB2 4 0 4
PTEN 4 0 4
ARAF 3 0 3
GNAS 3 0 3
MTOR 3 0 3
MYC 3 0 3
RAC1 3 0 3
KIT 2 0 2
KRAS 2 0 2
MAP2K2 2 0 2
PIK3R1 2 0 2
RAF1 2 0 2
AKT1 1 0 1
BCL2L12, LOC130064935 1 0 1
CRNKL1, LOC130065490 1 0 1
GNA11 1 0 1
KNSTRN 1 0 1
PPP6C 1 0 1
SF3B2 1 0 1
SLC45A2 0 1 1
STK19 1 0 1

Submitter and significance breakdown #

Total submitters: 2
Download table as spreadsheet
Submitter likely pathogenic protective total
Database of Curated Mutations (DoCM) 279 0 279
ClinVar Staff, National Center for Biotechnology Information (NCBI) 0 1 1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.