Variant #0000658505 (NC_000019.9:g.1399792C>T, NM_000156.5:c.327G>A (GAMT))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1399792C>T |
| DNA change (hg38) |
g.1399793C>T |
| Published as |
GAMT(NM_138924.2):c.327G>A (p.K109=), GAMT(NM_138924.3):c.327G>A (p.K109=) |
| ISCN |
- |
| DB-ID |
GAMT_012004 See all 67 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00019 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2020-07-15 09:48:38 +02:00 (CEST) |

Variant on transcripts
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