Variant #0000000030 (NC_000003.11:g.100964681_100964702del, IMPG2(NM_016247.3):c.1487_1508del)

Individual ID 00000039
Chromosome 3
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.100964681_100964702del
Reference -
DB-ID IMPG2_000001
Average frequency (gnomAD v.2.1.1) Retrieve
Owner variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by variome.ir
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
IMPG2 NM_016247.3 +/+ - c.1487_1508del r.(?) p.(Thr496Argfs*10) Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000040 DNA SEQ-NG IMPG2 1 variome.ir