Variant #0000255444 (NC_000013.10:g.102379135A>G, NM_175929.2:c.449T>C (FGF14))
| Chromosome |
13 |
| 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.102379135A>G |
| DNA change (hg38) |
g.101726785A>G |
| Published as |
FGF14(NM_175929.2):c.449T>C (p.F150S) |
| ISCN |
- |
| DB-ID |
FGF14_000017 See all 15 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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