Genomic variant #0000369735

Individual ID 00000003
Chromosome 4
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.145124986T>C
Reference dbSNP
DB-ID ABCE1_000002
Frequency 0.947
Allele Count 161
Allele Number 170
Depth 489
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCE1 NM_001040876.1 ./.
ABCE1 NM_002940.2 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin