Variant #0000371900 (NC_000012.11:g.102164817dup, NM_024312.4:c.890dup (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.102164817dup
DNA change (hg38) g.101771039dup
Published as -
ISCN -
DB-ID GNPTAB_000104
Variant remarks -
Reference Journal: Wang et al. 2018
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 16:23:31 +02:00 (CEST)
Date last edited 2018-08-01 09:14:55 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTAB NM_024312.4 +/+ 8 c.890dup r.(?) p.(Ser298Lysfs*16)


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