File Info

Filename
HCC1395_tumor_vs_HCC1395_BL.strelka.somatic_indels_custom.ann_snpEff.csv
Full Path
s3://natera-rnd-pltf-dev-nextflow-data-01/users/mipeters/semiproductionize/sarek/698115e9/test_regression_dev_b0193075/reports/raw_qc/snpeff/strelka/HCC1395_tumor_vs_HCC1395_BL/HCC1395_tumor_vs_HCC1395_BL.strelka.somatic_indels_custom.ann_snpEff.csv
Size
3.4 KB
Published
Feb 02, 2026 1:41 PM
# Summary table
Name , Value
Genome , GRCh38.105
Date , 2026-02-02 21:41
SnpEff_version , SnpEff 5.1d (build 2022-04-19 15:49), by Pablo Cingolani
Command_line_arguments , SnpEff GRCh38.105 -csvStats HCC1395_tumor_vs_HCC1395_BL.strelka.somatic_indels_custom.ann_snpEff.csv HCC1395_tumor_vs_HCC1395_BL.strelka.somatic_indels_custom.ann.vcf.gz
Warnings , 1
Number_of_lines_in_input_file, 6
Number_of_variants_before_filter, 6
Number_of_not_variants , 0
Number_of_variants_processed , 6
Number_of_known_variants (i.e. non-empty ID) , 0, 0%
Number_of_effects , 12
Genome_total_length ,63147197748
Genome_effective_length ,46709983
Change_rate , 7784997
# Change rate by chromosome
Chromosome , Length , Changes , Change_rate
21 , 46709983 , 6 , 7784997
# Variantss by type
Type , Count , Percent
DEL , 4 , 66.666667%
INS , 2 , 33.333333%
# Effects by impact
Type , Count , Percent
MODERATE , 3 , 25%
MODIFIER , 9 , 75%
# Effects by functional class
Type , Count , Percent
Missense_Silent_ratio, 0
# Count by effects
Type , Count , Percent
3_prime_UTR_variant , 2 , 16.666667%
conservative_inframe_deletion , 1 , 8.333333%
disruptive_inframe_deletion , 1 , 8.333333%
disruptive_inframe_insertion , 1 , 8.333333%
downstream_gene_variant , 4 , 33.333333%
intron_variant , 1 , 8.333333%
upstream_gene_variant , 2 , 16.666667%
# Count by genomic region
Type , Count , Percent
DOWNSTREAM , 4 , 33.333333%
EXON , 3 , 25%
INTRON , 1 , 8.333333%
UPSTREAM , 2 , 16.666667%
UTR_3_PRIME , 2 , 16.666667%
# Quality
# InDel lengths
Values , 0,1,2
Count , 1,4,1
# Base changes
base , A , C , G , T
A , 0 , 0 , 0 , 0
C , 0 , 0 , 0 , 0
G , 0 , 0 , 0 , 0
T , 0 , 0 , 0 , 0
# Ts/Tv summary
Transitions , 0
Transversions , 0
Ts_Tv_ratio , 0
# Ts/Tv : All variants
No results available (empty input?)
# Ts/Tv : Known variants
No results available (empty input?)
# Allele frequency
# Allele frequency : All variants
Values , 0
Count , 6
# Allele Count
Values , 0
Count , 6
# Hom/Het table
Sample_names , NORMAL, TUMOR
Reference , 0, 0
Het , 0, 0
Hom , 0, 0
Missing , 6, 6
# Codon change table
codons , - , CAC , CAT , CCG , CTA , GCC , GCG , GCT , GGG
- , 0 , 0 , 1 , 0 , 0 , 0 , 0 , 0 , 0
CAC , 0 , 0 , 0 , 0 , 0 , 0 , 0 , 0 , 0
CAT , 0 , 1 , 0 , 0 , 0 , 0 , 0 , 0 , 0
CCG , 1 , 0 , 0 , 0 , 0 , 0 , 0 , 0 , 0
CTA , 1 , 0 , 0 , 0 , 0 , 0 , 0 , 0 , 0
GCC , 2 , 0 , 0 , 0 , 0 , 0 , 1 , 0 , 0
GCG , 2 , 0 , 0 , 0 , 0 , 0 , 0 , 0 , 0
GCT , 1 , 0 , 0 , 0 , 0 , 0 , 0 , 0 , 0
GGG , 2 , 0 , 0 , 0 , 0 , 0 , 0 , 0 , 0
# Amino acid change table
aa , - , A , G , H , L , P
- , 0 , 0 , 0 , 1 , 0 , 0
A , 5 , 1 , 0 , 0 , 0 , 0
G , 2 , 0 , 0 , 0 , 0 , 0
H , 0 , 0 , 0 , 1 , 0 , 0
L , 1 , 0 , 0 , 0 , 0 , 0
P , 1 , 0 , 0 , 0 , 0 , 0
# Chromosome change table
21, Position,0,1000000,2000000,3000000,4000000,5000000,6000000,7000000,8000000,9000000,10000000,11000000,12000000,13000000,14000000,15000000,16000000,17000000,18000000,19000000,20000000,21000000,22000000,23000000,24000000,25000000,26000000,27000000,28000000,29000000,30000000,31000000,32000000,33000000,34000000,35000000,36000000,37000000,38000000,39000000,40000000,41000000,42000000,43000000,44000000,45000000,46000000
21,Count,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,1,3,0,0,0,0,0,0,0,0,0,1,0,1
139 rows