Genomic variant #0000721912

Individual ID 00000003
Chromosome 17
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.81132775C>T
Reference dbSNP
DB-ID AATK_000074
Frequency 0.137
Allele Count 29
Allele Number 212
Depth 3983
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
AATK NM_001080395.2 ./.
AATK NM_004920.2 ./.
AATK XM_005257855.2 ./.
AATK XM_006722193.2 ./.
AATK XM_006722194.2 ./.
AATK XM_006722195.1 ./.
AATK XM_006722196.1 ./.
AATK XM_006722197.2 ./.
AATK XM_011525509.1 ./.
AATK XM_011525510.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin