Variant #0000405697 (NC_000012.11:g.102179790C>T, NM_024312.4:c.571G>A (GNPTAB))

Chromosome 12
Allele Both (homozygous)
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.102179790C>T
DNA change (hg38) g.101786012C>T
Published as -
ISCN -
DB-ID GNPTAB_000291
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency Not detected in 100 control chromosomes
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Renata Voltolini Velho
Database submission license No license selected
Created by Renata Voltolini Velho
Date created 2018-09-20 08:39:47 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTAB NM_024312.4 +/+? 5 c.571G>A r.(?) p.(Val191Ile)


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