Variant #0000371889 (NC_000012.11:g.102174070A>C, NC_000012.11(NM_024312.4):c.637-6T>G (GNPTAB))

Chromosome 12
Allele Paternal (confirmed)
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.102174070A>C
DNA change (hg38) g.101780292A>C
Published as -
ISCN -
DB-ID GNPTAB_000093
Variant remarks Affect splicing exon 7, cDNA analysis reveal p.Thr213Phefs*11.
Reference Journal: Yang 2017
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Renata Voltolini Velho
Database submission license No license selected
Created by Renata Voltolini Velho
Date created 2018-07-09 15:27:23 +02:00 (CEST)
Date last edited 2020-07-02 17:53:47 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTAB NM_024312.4 +/+ 6i c.637-6T>G r.(=) p.(Thr213Phefs*11)


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