Variant #0000608780 (NC_000003.11:g.49759369_49759370insGC, NC_000003.11(NM_021971.2):c.951+28_951+29insGC (GMPPB))
| Chromosome |
3 |
| 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.49759369_49759370insGC |
| DNA change (hg38) |
g.49721936_49721937insGC |
| Published as |
GMPPB(NM_013334.3):c.979_980insGC (p.(Glu327GlyfsTer25)) |
| ISCN |
- |
| DB-ID |
AMIGO3_000035 |
| 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) |
Retrieve |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-12-04 14:54:23 +01:00 (CET) |
| Date last edited |
2022-05-09 15:24:52 +02:00 (CEST) |

Variant on transcripts
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