|
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 |
Region: exonic
Annotation: synonymous_SNV
Consequence: ['c.A687G', 'p.T229T']
Average Genotype Quality in variant carriers: 134.00
Average Depth at the site in variant carriers: 82.00
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 |
None |
ExAC SAS |
None |
ExAC AFR |
None |
ExAC AMR |
None |
ExAC EAS |
None |
ExAC FIN |
None |
ExAC NFE |
None |
ExAC OTH |
None |
1000 Genomes |
None |