Genomic variant #0000669014

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.18592487C>T
Reference dbSNP
DB-ID ABCC6P1_000011
Frequency 0.024
Allele Count 5
Allele Number 212
Depth 1437
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