Genomic variant #0000278759

Individual ID 00000003
Chromosome 2
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.43825008T>C
Reference dbSNP
DB-ID DYNC2LI1_000062
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 3476
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCG5 NM_022436.2 ./.
DYNC2LI1 XM_005264364.3 ./.
DYNC2LI1 XM_005264365.3 ./.
ABCG5 XM_005264480.2 ./.
ABCG5 XM_006712073.2 ./.
ABCG5 XM_006712074.2 ./.
ABCG5 XM_011533024.1 ./.
ABCG5 XM_011533025.1 ./.
ABCG5 XM_011533026.1 ./.
ABCG5 XM_011533027.1 ./.
ABCG5 XM_011533028.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin