Variant #0000369812 (NC_000016.9:g.1412052T>C, NM_032520.4:c.331T>C (GNPTG))

Chromosome 16
Allele Unknown
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.1412052T>C
DNA change (hg38) g.1362051T>C
Published as -
ISCN -
DB-ID GNPTG_000052
Variant remarks -
Reference Journal: Oussoren 2018
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
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 2018-06-26 15:12:37 +02:00 (CEST)
Date last edited 2018-06-26 15:19:31 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTG NM_032520.4 +/+ 6 c.331T>C r.(?) p.(Trp111Arg)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.