Variant #0000000032 (NC_000020.10:g.3899388A>G, PANK2(NM_153638.2):c.1607A>G)

Individual ID 00000044
Chromosome 20
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.3899388A>G
Reference -
DB-ID PANK2_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     
PANK2 NM_153638.2 +/+ - c.1607A>G r.(?) p.(Tyr536Cys) Likely Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000044 DNA SEQ-NG PANK2 1 variome.ir