Variant #0000369818 (NC_000016.9:g.1412143_1412167del, NC_000016.9(NM_032520.4):c.409+11_411+35del (GNPTG))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1412143_1412167del
DNA change (hg38) -
Published as c.411+11_411+35del
ISCN -
DB-ID GNPTG_000057
Variant remarks The correction of the mutation was done by email contact with the authors.
Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message.
Reference Journal: Oussoren 2018
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 2018-06-26 15:48:17 +02:00 (CEST)
Date last edited 2019-02-20 19:59:36 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTG NM_032520.4 +/+? 6i c.409+11_411+35del r.(=) p.(=)


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