Genomic variant #0000000052

Individual ID 00000001
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.792448G>A
Reference -
DB-ID chr1_000026
dbSNP ID rs140050759
Frequency 0.003876
Allele Count 2
Allele Number 516
Combined Depth 9456
Homozygous 0
Heterozygote 2
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin