Variant #0000394424 (NC_000012.11:g.102179805_102179806ins[U14569.1:g.1_288], NM_024312.4:c.555_556ins[U14569.1:g.1_288] (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.102179805_102179806ins[U14569.1:g.1_288]
DNA change (hg38) -
Published as Alu insertion mutation
ISCN -
DB-ID GNPTAB_000284
Variant remarks -
Reference Journal: Tappino 2008
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 2018-07-30 15:48:04 +02:00 (CEST)
Date last edited 2024-08-16 12:27:59 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTAB NM_024312.4 +/+ 5 c.555_556ins[U14569.1:g.1_288] r.555_556ins[[U14569.1:g.1_288inv];540_555] p.Glu123*


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