Genomic variant #0000369737

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.145127402T>C
Reference dbSNP
DB-ID ABCE1_000004
Frequency 0.274
Allele Count 58
Allele Number 212
Depth 3979
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