Variant #0000411425 (NC_000019.9:g.1399845T>C, NM_000156.5:c.274A>G (GAMT))
| Chromosome |
19 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1399845T>C |
| DNA change (hg38) |
g.1399846T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GAMT_012025 See all 3 reported entries |
| Variant remarks |
overexpression in primary GAMT deficient fibroblasts does not restore GAMT activity |
| Reference |
Mahmutoglu et al, in preparation |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Gajja Salomons |
| Database submission license |
No license selected |
| Created by |
Gajja Salomons |
| Date created |
2016-01-05 14:33:53 +01:00 (CET) |
| Date last edited |
2020-07-15 09:48:54 +02:00 (CEST) |

Variant on transcripts
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