Variant #0000411081 (NC_000015.9:g.45661601G>A, NM_001482.2:c.407C>T (GATM))

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.45661601G>A
DNA change (hg38) g.45369403G>A
Published as -
ISCN -
DB-ID GATM_009037 See all 4 reported entries
Variant remarks overexpression studies showed 100% 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) 0.00037 View details
Owner Rahma MANI
Database submission license No license selected
Created by Gajja Salomons
Date created 2016-08-30 16:36:34 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GATM NM_001482.2 -/-? 3 c.407C>T r.(?) p.Thr136Met


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