Genomic variant #0000002187

Individual ID 00000010
Chromosome 4
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.123394883A>G
Reference dbSNP
DB-ID chr4_000001 See all 10 reported entries
Frequency 0.795 Patients_Q37.5_right
Allele Count 35
Allele Number 44
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     
0000000011 DNA TaqMan - 250 Admin