Variant #0000371892 (NC_000012.11:g.102173950_102173951insT, NM_024312.4:c.750_751insA (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.102173950_102173951insT
DNA change (hg38) g.101780172_101780173insT
Published as -
ISCN -
DB-ID GNPTAB_000096
Variant remarks -
Reference Journal: Cathey 2010
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 15:33:36 +02:00 (CEST)
Date last edited 2018-07-31 16:16:12 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTAB NM_024312.4 +/+ 7 c.750_751insA r.(?) p.(Leu251Thrfs*4)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.