Genomic variant #0000649955

Individual ID 00000003
Chromosome 15
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.67254963C>A
Reference dbSNP
DB-ID AAGAB_000016
Frequency 0.222
Allele Count 47
Allele Number 212
Depth 7652
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
IQCH NM_001031715.2 ./.
AAGAB NM_001271885.1 ./.
AAGAB NM_001271886.1 ./.
IQCH NM_001284347.1 ./.
IQCH NM_001284348.1 ./.
IQCH NM_001284349.1 ./.
IQCH NM_022784.2 ./.
AAGAB NM_024666.4 ./.
AAGAB XM_005254664.2 ./.
AAGAB XM_006720683.2 ./.
IQCH XM_011521907.1 ./.
IQCH XM_011521908.1 ./.
IQCH XM_011521909.1 ./.
IQCH XM_011521910.1 ./.
IQCH XM_011521911.1 ./.
IQCH XM_011521912.1 ./.
IQCH XM_011521913.1 ./.
IQCH XM_011521915.1 ./.
IQCH XM_011521918.1 ./.
IQCH XM_011521920.1 ./.
IQCH XM_011521921.1 ./.
IQCH XM_011521922.1 ./.
IQCH XM_011521923.1 ./.
AAGAB XM_011522020.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin