INDEX ALL INDEX Male INDEX Female INDEX Controls
Allele Count 37 20 17 37
Allele Number 350 202 148 350
Allele Frequency 0.10571 0.09901 0.11486 0.10571
Number of Homozygotes 0 0 0 0

Gene: NCOR1

Region: exonic

Annotation: synonymous_SNV

Consequence: ['c.G222A', 'p.Q74Q']

Average Genotype Quality in variant carriers: 77.59

Average Depth at the site in variant carriers: 62.95

dbSNP ID: rs76375524

ClinVar: chr17-16068362-C-T

UCSC Browser: chr17-16068362-C-T

Browse the variant in INDEX-db genome browser


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 .
Allele Frequency
ExAC ALL 0.4234
ExAC SAS 0.4639
ExAC AFR 0.4214
ExAC AMR 0.4414
ExAC EAS 0.3943
ExAC FIN 0.4466
ExAC NFE 0.4117
ExAC OTH 0.4269
1000 Genomes None