Genomic variant #0000799577

Individual ID 00000003
Chromosome 21
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.42216136C>T
Reference dbSNP
DB-ID ABCG1_000009
Frequency 0.01
Allele Count 2
Allele Number 192
Depth 322
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCG1 NM_004915.3 ./.
ABCG1 NM_016818.2 ./.
ABCG1 NM_207174.1 ./.
ABCG1 NM_207627.1 ./.
ABCG1 NM_207628.1 ./.
ABCG1 NM_207629.1 ./.
ABCG1 XM_011529806.1 ./.
ABCG1 XM_011529807.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin