Variant #0000000050 (NC_000003.11:g.100951806C>T, IMPG2(NM_016247.3):c.3052G>A)

Individual ID 00000069
Chromosome 3
Allele Both (homozygous)
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.100951806C>T
Reference -
DB-ID IMPG2_000003
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.3052G>A r.(?) p.(Ala1018Thr) VUS LP



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000069 DNA SEQ-NG IMPG2 1 variome.ir