Genomic variant #0000002394

Individual ID 00000011
Chromosome 1
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.75128190G>A
Reference dbSNP
DB-ID chr1_000008 See all 9 reported entries
Frequency 0.431 Patients_Q37
Allele Count 25
Allele Number 58
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     
0000000012 DNA TaqMan - 249 Admin