Genomic variant #0000001889

Individual ID 00000009
Chromosome 1
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.23749386C>T
Reference dbSNP
DB-ID chr1_000002 See all 8 reported entries
Frequency 0.223 Patients_Q37.5_left
Allele Count 25
Allele Number 112
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     
0000000010 DNA TaqMan - 253 Admin