Genomic variant #0000668866

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.16187064T>C
Reference dbSNP
DB-ID ABCC6_000012
Frequency 0.95
Allele Count 76
Allele Number 80
Depth 0
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