Variant: chr20-31369126-C-G

INDEX-db frequencies

INDEX ALL INDEX Male INDEX Female INDEX Controls
Allele Count 1 1 0 1
Allele Number 350 202 148 350
Allele Frequency 0.00286 0.00495 0.00000 0.00286
Number of Homozygotes 0 0 0 0

Gene: DNMT3B

Region: intronic

Annotation: None

Consequence: None

Average Genotype Quality in variant carriers: 69.00

Average Depth at the site in variant carriers: 41.00

dbSNP ID: rs190353959

ClinVar: chr20-31369126-C-G

UCSC Browser: chr20-31369126-C-G

Browse the variant in INDEX-db genome browser


In silico functional predictions

Score Prediction
SIFT None None
Polyphen2 HDIV None None
Polyphen2 HVAR None None
Mutation Taster None None
Mutation Assessor None None
LRT None None
FATHMM None None
CADD Phred None .
CADD Raw None .

Exome Aggregation Consortium frequencies

Allele Frequency
ExAC ALL 0.0072
ExAC SAS 0.0057
ExAC AFR 0.0012
ExAC AMR 0.0026
ExAC EAS 0
ExAC FIN 0.0130
ExAC NFE 0.0086
ExAC OTH 0.0103
1000 Genomes 0.00259585