Variant #0000411090 (NC_000015.9:g.45658681T>C, GATM(NM_001482.2):c.701A>G)

Chromosome 15
Allele Parent #2
Affects function (as reported) Does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.45658681T>C
DNA change (hg38) g.45366483T>C
Published as -
ISCN -
DB-ID GATM_009040 See all 4 reported entries
Variant remarks overexpression studies showed 82% 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) 0.00021 View details
Owner Rahma MANI
Database submission license No license selected
Created by Gajja Salomons
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GATM NM_001482.2 -/-? 5 c.701A>G r.(?) p.Asp234Gly