Variant #0000369825 (NC_000016.9:g.1412294dup, NM_032520.4:c.499dup (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.1412294dup
DNA change (hg38) g.1362293dup
Published as -
ISCN -
DB-ID GNPTG_000026 See all 5 reported entries
Variant remarks -
Reference Journal: Raas-Rothschild 2000
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
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 16:24:15 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTG NM_032520.4 +/+ 7 c.499dup r.(?) p.(Leu167Profs*32)


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