Genomic variant #0000664729

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.2289713T>C
Reference dbSNP
DB-ID ABCA3_000041
Frequency 0.16
Allele Count 34
Allele Number 212
Depth 2166
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCA3 NM_001089.2 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin