Variant #0000405859 (NC_000016.9:g.1412273_1412274insTAGG, NM_032520.4:c.478_479insTAGG (GNPTG))

Chromosome 16
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1412273_1412274insTAGG
DNA change (hg38) g.1362272_1362273insTAGG
Published as -
ISCN -
DB-ID GNPTG_000086
Variant remarks -
Reference Journal: Khan 2018
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Renata Voltolini Velho
Database submission license No license selected
Created by Renata Voltolini Velho
Date created 2018-09-25 17:17:59 +02:00 (CEST)
Date last edited 2020-03-29 12:37:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTG NM_032520.4 +/+ 7 c.478_479insTAGG r.(?) p.(Ala160Valfs*40)


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