Genomic variant #0000369723

Individual ID 00000003
Chromosome 4
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.145112217_145112218del
Reference -
DB-ID ABCE1_000016
Frequency 0.043
Allele Count 8
Allele Number 184
Depth 993
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCE1 NM_001040876.1 ./.
ABCE1 NM_002940.2 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin