Variant #0000612113 (NC_000009.11:g.35740293C>G, NM_006368.4:c.*3570C>G (CREB3))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.35740293C>G |
| DNA change (hg38) |
g.35740296C>G |
| Published as |
GBA2(NM_001330660.2):c.1196G>C (p.R399P), GBA2(NM_020944.2):c.1196G>C (p.R399P, p.(Arg399Pro)) |
| ISCN |
- |
| DB-ID |
GBA2_000008 See all 3 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) |
0.0013 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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