Variant #0000411085 (NC_000015.9:g.45660335T>G, GATM(NM_001482.2):c.608A>C)

Chromosome 15
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.45660335T>G
DNA change (hg38) g.45368137T>G
Published as -
ISCN -
DB-ID GATM_009009 See all 13 reported entries
Variant remarks overexpression studies showed 0% AGAT activity
Reference PubMed: DesRoches 2016
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Rahma MANI
Database submission license No license selected
Created by Gajja Salomons
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GATM NM_001482.2 +/+? 4 c.608A>C r.(?) p.Tyr203Ser