Variant #0000604844 (NC_000001.10:g.155205043A>G, NM_000157.3:c.1448T>C (GBA))
| Chromosome |
1 |
| 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.155205043A>G |
| DNA change (hg38) |
g.155235252A>G |
| Published as |
GBA(NM_000157.3):c.1448T>C (p.(Leu483Pro)), GBA(NM_001005741.2):c.1448T>C (p.L483P), GBA(NM_001005741.3):c.1448T>C (p.L483P), GBA1(NM_001005741.3):... |
| ISCN |
- |
| DB-ID |
GBA_000006 See all 93 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) |
0.00131 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-12-04 14:54:23 +01:00 (CET) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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