Genomic variant #0000000979

Individual ID 00000004
Chromosome 11
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.76185528G>A
Reference dbSNP
DB-ID chr11_000001 See all 9 reported entries
Frequency 1.000 Patients_Q37.2
Allele Count 4
Allele Number 4
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000005 DNA TaqMan - 174 Admin