Genomic variant #0000369733

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.145123373C>A
Reference dbSNP
DB-ID ABCE1_000026
Frequency 0.009434
Allele Count 2
Allele Number 212
Depth 3072
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