Ensembl
VEP
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VEP run statistics

VEP version (API) 113.0 (113)
Annotation sourcesCache: /tmp/nxf.XXXXYtvYfq/113_GRCh38/homo_sapiens/113_GRCh38
Specieshomo_sapiens
Command line options
--assembly GRCh38 --cache  --cache_version 113 --canonical --compress_output bgzip --dir_cache /tmp/nxf.XXXXYtvYfq/113_GRCh38 --fasta Homo_sapiens_assembly38.fasta --flag_pick --fork 4 --format vcf --hgvs --input_file custom_Sig_18_tumor_normal.snv_indel.phased.vcf.gz --offline --output_file custom_Sig_18_tumor_normal.snv_indel.phased.vep.vcf.gz --species homo_sapiens --stats_file custom_Sig_18_tumor_normal.snv_indel.phased.vep.summary.html --vcf
Start time2026-06-08 20:55:35
End time2026-06-08 20:55:43
Run time8 seconds
Input file
custom_Sig_18_tumor_normal.snv_indel.phased.vcf.gz
Output file
custom_Sig_18_tumor_normal.snv_indel.phased.vep.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 read252
Variants processed252
Variants filtered out0
Novel / existing variants-
Overlapped genes169
Overlapped transcripts1031
Overlapped regulatory features-

Variant classes

 
 

Consequences (most severe)

 
 

Consequences (all)

 
 

Coding consequences

 
 

Variants by chromosome

 
 

Distribution of variants on chromosome chr21

 

Position in protein