Variant #0000411089 (NC_000015.9:g.45658690G>C, NM_001482.2:c.692C>G (GATM))
| Chromosome |
15 |
| Allele |
Parent #1 |
| 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.45658690G>C |
| DNA change (hg38) |
g.45366492G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GATM_009039 See all 3 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) |
0.00011 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) |

Variant on transcripts
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