Genomic variant #0000668871

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.16198014G>C
Reference dbSNP
DB-ID ABCC6_000017
Frequency 0.587
Allele Count 108
Allele Number 184
Depth 1616
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCC6 NM_001171.5 ./.
ABCC6 XM_011522479.1 ./.
ABCC6 XM_011522480.1 ./.
ABCC6 XM_011522481.1 ./.
ABCC6 XM_011522482.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin