Genomic variant #0000721917

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.81133497T>C
Reference dbSNP
DB-ID AATK_000079
Frequency 0.015
Allele Count 3
Allele Number 206
Depth 366
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