Genomic variant #0000002256

Individual ID 00000010
Chromosome 13
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.80335808C>T
Reference dbSNP
DB-ID chr13_000002 See all 8 reported entries
Frequency 0.087 Patients_Q37.5_right
Allele Count 4
Allele Number 46
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