Variant #0000859089 (NC_000003.11:g.49761081C>G, NM_021971.2:c.79G>C (GMPPB))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.49761081C>G |
| DNA change (hg38) |
- |
| Published as |
GMPPB(NM_013334.3):c.79G>C (p.D27H, p.(Asp27His)), GMPPB(NM_013334.4):c.79G>C (p.D27H) |
| ISCN |
- |
| DB-ID |
GMPPB_000004 See all 19 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) |
0.0007 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2022-05-09 15:51:19 +02:00 (CEST) |
| Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
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