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VEP run statistics

VEP version (API) 113.0 (113)
Annotation sourcesCache: /tmp/nxf.XXXXWolsvr/113_GRCh38/homo_sapiens/113_GRCh38
Specieshomo_sapiens
Command line options
--assembly GRCh38 --cache  --cache_version 113 --compress_output bgzip --dir_cache /tmp/nxf.XXXXWolsvr/113_GRCh38 --everything --filter_common --fork 4 --format vcf --input_file 1029_BFKM-T1-TDNA-1_23FC2GLT4_s28_vs_1029_BFKM-N1-BDNA-1_2375WFLT3_s28.mutect2.filtered_custom.ann_snpEff.ann.vcf.gz --offline --output_file 1029_BFKM-T1-TDNA-1_23FC2GLT4_s28_vs_1029_BFKM-N1-BDNA-1_2375WFLT3_s28.mutect2.filtered_custom.ann_snpEff_VEP.ann.vcf.gz --per_gene --species homo_sapiens --stats_file 1029_BFKM-T1-TDNA-1_23FC2GLT4_s28_vs_1029_BFKM-N1-BDNA-1_2375WFLT3_s28.mutect2.filtered_custom.ann_snpEff_VEP.ann.summary.html --total_length --vcf
Start time2026-02-04 07:09:35
End time2026-02-04 07:10:27
Run time52 seconds
Input file
1029_BFKM-T1-TDNA-1_23FC2GLT4_s28_vs_1029_BFKM-N1-BDNA-1_2375WFLT3_s28.mutect2.filtered_custom.ann_snpEff.ann.vcf.gz
Output file
1029_BFKM-T1-TDNA-1_23FC2GLT4_s28_vs_1029_BFKM-N1-BDNA-1_2375WFLT3_s28.mutect2.filtered_custom.ann_snpEff_VEP.ann.vcf.gz

Data version

1000genomesphase3
COSMIC99
ClinVar202404
HGMD-PUBLIC20204
assemblyGRCh38.p14
dbSNP156
gencodeGENCODE 47
genebuildGENCODE47
gnomADev4.1
gnomADgv4.1
polyphen2.2.3
regbuild1.0
sift6.2.1

General statistics

Lines of input read28671
Variants processed28671
Variants filtered out0
Novel / existing variants0 (0.0) / 28671 (100.0)
Overlapped genes15448
Overlapped transcripts15882
Overlapped regulatory features773

Variant classes

 
 

Consequences (most severe)

 
 

Consequences (all)

 
 

Coding consequences

 
 

SIFT summary

 
 

PolyPhen summary

 
 

Variants by chromosome

 
 

Position in protein