Ensembl
VEP
Links

VEP run statistics

VEP version (API) 113.0 (113)
Annotation sourcesCache: /tmp/nxf.XXXX5WOwdO/113_GRCh38/homo_sapiens/113_GRCh38
Specieshomo_sapiens
Command line options
--assembly GRCh38 --cache  --cache_version 113 --compress_output bgzip --dir_cache /tmp/nxf.XXXX5WOwdO/113_GRCh38 --everything --filter_common --fork 4 --format vcf --input_file 1029_BBCQ-T1-TDNA-1_23FC2GLT4_s21_vs_1029_BBCQ-N1-BDNA-1_2375WFLT3_s21.strelka.somatic_snvs_custom.ann_snpEff.ann.vcf.gz --offline --output_file 1029_BBCQ-T1-TDNA-1_23FC2GLT4_s21_vs_1029_BBCQ-N1-BDNA-1_2375WFLT3_s21.strelka.somatic_snvs_custom.ann_snpEff_VEP.ann.vcf.gz --per_gene --species homo_sapiens --stats_file 1029_BBCQ-T1-TDNA-1_23FC2GLT4_s21_vs_1029_BBCQ-N1-BDNA-1_2375WFLT3_s21.strelka.somatic_snvs_custom.ann_snpEff_VEP.ann.summary.html --total_length --vcf
Start time2026-02-02 23:48:59
End time2026-02-02 23:49:46
Run time47 seconds
Input file
1029_BBCQ-T1-TDNA-1_23FC2GLT4_s21_vs_1029_BBCQ-N1-BDNA-1_2375WFLT3_s21.strelka.somatic_snvs_custom.ann_snpEff.ann.vcf.gz
Output file
1029_BBCQ-T1-TDNA-1_23FC2GLT4_s21_vs_1029_BBCQ-N1-BDNA-1_2375WFLT3_s21.strelka.somatic_snvs_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 read26633
Variants processed26633
Variants filtered out0
Novel / existing variants0 (0.0) / 26633 (100.0)
Overlapped genes17026
Overlapped transcripts17616
Overlapped regulatory features666

Variant classes

 
 

Consequences (most severe)

 
 

Consequences (all)

 
 

Coding consequences

 
 

SIFT summary

 
 

PolyPhen summary

 
 

Variants by chromosome

 
 

Position in protein