Variant #0000411421 (NC_000019.9:g.1399917C>A, NM_000156.5:c.202G>T (GAMT))

Chromosome 19
Allele Parent #2
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.1399917C>A
DNA change (hg38) g.1399918C>A
Published as -
ISCN -
DB-ID GAMT_012040 See all 5 reported entries
Variant remarks overexpression in primary GAMT deficient fibroblasts does not restore GAMT activity
Reference Mahmutoglu et al, in preparation
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Gajja Salomons
Database submission license No license selected
Created by Gajja Salomons
Date created 2016-01-05 14:33:53 +01:00 (CET)
Date last edited 2020-07-15 09:49:03 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GAMT NM_000156.5 +/+ 2 c.202G>T r.(?) p.Gly68Cys


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.