Variant #0000000056 (NC_000003.11:g.100962953G>C, IMPG2(NM_016247.3):c.2222C>G)

Individual ID 00000076
Chromosome 3
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.100962953G>C
Reference -
DB-ID IMPG2_000004
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.2222C>G r.(?) p.(Ala741Gly) VUS



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000076 DNA SEQ-NG IMPG2 1 variome.ir