Variant #0000404766 (NC_000012.11:g.102183715C>T, NC_000012.11(NM_024312.4):c.323+1G>A (GNPTAB))

Chromosome 12
Allele Parent #2
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.102183715C>T
DNA change (hg38) g.101789937C>T
Published as -
ISCN -
DB-ID GNPTAB_000285
Variant remarks -
Reference -
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 2018-08-26 17:44:57 +02:00 (CEST)
Date last edited 2019-01-14 17:14:58 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTAB NM_024312.4 +/+ 3i c.323+1G>A r.204_323del p.Leu69_Arg108del


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