Genomic variant #0000209059

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.17697G>C
Reference dbSNP
DB-ID WASH7P_000034
Frequency 0.03
Allele Count 5
Allele Number 164
Depth 237
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
WASH7P NR_024540.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin