Genomic variant #0000669001

Individual ID 00000003
Chromosome 16
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.18574799C>T
Reference -
DB-ID ABCC6P1_000016
Frequency 0.009709
Allele Count 2
Allele Number 206
Depth 0
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCC6P1 NR_003569.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin