Genomic variant #0000209025

Individual ID 00000003
Chromosome 1
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.13649G>C
Reference -
DB-ID DDX11L1_000008
Frequency 0.127
Allele Count 26
Allele Number 204
Depth 994
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
DDX11L1 NR_046018.2 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin