Variant #0000369820 (NC_000016.9:g.1412240del, NM_032520.4:c.445del (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.1412240del
DNA change (hg38) g.1362239del
Published as -
ISCN -
DB-ID GNPTG_000059 See all 2 reported entries
Variant remarks -
Reference Journal: Raas-Rothschild 2004
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 16:07:43 +02:00 (CEST)
Date last edited 2019-02-17 21:01:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTG NM_032520.4 +/+ 7 c.445del r.445del p.Ala149Profs*13


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