Variant #0000458925 (NC_000016.9:g.1412098G>A, NM_032520.4:c.377G>A (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.1412098G>A
DNA change (hg38) g.1362097G>A
Published as -
ISCN -
DB-ID GNPTG_000087
Variant remarks -
Reference Journal: Gheldof 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 2019-02-17 20:50:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTG NM_032520.4 +/+? 6 c.377G>A r.(?) p.(Gly126Asp)


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