Variant #0000371877 (NC_000012.11:g.102179792T>A, NM_024312.4:c.569A>T (GNPTAB))

Chromosome 12
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.102179792T>A
DNA change (hg38) g.101786014T>A
Published as -
ISCN -
DB-ID GNPTAB_000087 See all 2 reported entries
Variant remarks Splicing defect or p.Asp190Val
Reference Journal: Kudo 2006
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Renata Voltolini Velho
Database submission license No license selected
Created by Renata Voltolini Velho
Date created 2018-07-09 10:25:58 +02:00 (CEST)
Date last edited 2019-01-15 12:47:24 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTAB NM_024312.4 +/+ 5 c.569A>T r.568_571del p.Asp190Leufs*31


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