Genomic variant #0000795452

Individual ID 00000003
Chromosome 21
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.14291719C>T
Reference dbSNP
DB-ID ABCC13_000017
Frequency 0.042
Allele Count 9
Allele Number 212
Depth 1368
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCC13 NR_003087.1 ./.
ABCC13 NR_003088.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin