Variant #0000411423 (NC_000019.9:g.1399895G>A, NM_000156.5:c.224C>T (GAMT))

Chromosome 19
Allele Parent #1
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.1399895G>A
DNA change (hg38) g.1399896G>A
Published as -
ISCN -
DB-ID GAMT_012030 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) 3.0E-5 View details
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 09:49:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GAMT NM_000156.5 +/+ 2 c.224C>T r.(?) p.Ala75Val


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