Variant #0000411082 (NC_000015.9:g.45660402C>T, GATM(NM_001482.2):c.541G>A)
Chromosome |
15 |
Allele |
Parent #2 |
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.45660402C>T |
DNA change (hg38) |
g.45368204C>T |
Published as |
- |
ISCN |
- |
DB-ID |
GATM_009046 See all 3 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) |
0 View details |
Owner |
Rahma MANI |
Database submission license |
No license selected |
Created by |
Gajja Salomons |

Variant on transcripts
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