Variant #0000861795 (NC_000010.10:g.103534948_103534965dup, NM_033163.3:c.86_103dup (FGF8))
| Chromosome |
10 |
| 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.103534948_103534965dup |
| DNA change (hg38) |
- |
| Published as |
FGF8(NM_001206389.1):c.-123-321_-123-304dup (p.(=)), FGF8(NM_033163.3):c.86_103dupGCCCTGCGCTGGGCAGGG (p.G29_R34dup), FGF8(NM_033163.4):c.86_103dupG... |
| ISCN |
- |
| DB-ID |
FGF8_000005 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 |
2022-05-09 15:51:19 +02:00 (CEST) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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