Genomic variant #0000285343

Individual ID 00000001
Chromosome 6
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.163985565_163985568del
Reference -
DB-ID QKI_000041
dbSNP ID rs1165736863
Frequency 0.013
Allele Count 6
Allele Number 476
Combined Depth 2108
Homozygous 0
Heterozygote 6
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
QKI NM_006775.2 ./. - c.934+814_934+817del r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin