Variant #0000371894 (NC_000012.11:g.102173930C>T, NM_024312.4:c.771G>A (GNPTAB))

Chromosome 12
Allele Maternal (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.102173930C>T
DNA change (hg38) g.101780152C>T
Published as -
ISCN -
DB-ID GNPTAB_000098 See all 2 reported entries
Variant remarks Splicing defect, exon 7 skipped.
Reference Journal: Steet 2005
ClinVar ID -
dbSNP ID -
Origin Germline
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 2018-07-09 15:38:30 +02:00 (CEST)
Date last edited 2019-01-25 14:59:05 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTAB NM_024312.4 +/+ 7 c.771G>A r.637_771del p.Thr213_Leu257del


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