Variant #0000378643 (NC_000012.11:g.102163960G>A, NM_024312.4:c.1123C>T (GNPTAB))

Chromosome 12
Allele Both (homozygous)
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.102163960G>A
DNA change (hg38) g.101770182G>A
Published as -
ISCN -
DB-ID GNPTAB_000005 See all 5 reported entries
Variant remarks -
Reference Journal: Tappino 2009
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner Renata Voltolini Velho
Database submission license No license selected
Created by Renata Voltolini Velho
Date created 2018-07-16 13:16:35 +02:00 (CEST)
Date last edited 2019-01-25 16:24:16 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTAB NM_024312.4 +/+ 10 c.1123C>T r.1123c>u p.Arg375*


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