Genomic variant #0000001571

Individual ID 00000007
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 0.098 Patients_Q37.4
Allele Count 10
Allele Number 102
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     
0000000008 DNA TaqMan - 251 Admin