Variant #0000371859 (NC_000012.11:g.102183816_102190540dup, NM_024312.4:c.118_223dup (GNPTAB))

Chromosome 12
Allele Unknown
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.102183816_102190540dup
DNA change (hg38) g.101790038_101796762dup
Published as Duplication ex 2
ISCN -
DB-ID GNPTAB_000075
Variant remarks -
Reference Journal: Otomo 2009
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
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 09:33:26 +02:00 (CEST)
Date last edited 2019-01-14 17:09:09 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTAB NM_024312.4 +/+ 2 c.118_223dup r.118_203dup p.(Leu69Trpfs*43)


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