Variant #0001025958 (NC_000011.9:g.2182108C>T, NM_000207.2:c.94G>A (INS))
| Chromosome |
11 |
| 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.2182108C>T |
| DNA change (hg38) |
- |
| Published as |
INS(NM_000207.2):c.94G>A (p.(Gly32Ser)) |
| ISCN |
- |
| DB-ID |
INS_000012 See all 4 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) |
Retrieve |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2025-02-07 18:57:27 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
|