Variant #0000909143 (NC_000013.10:g.102813927_102814076GAA[(250-334)], NM_175929.2:c.208+239747_208+239896CTT[(250-334)] (FGF14))
| Chromosome |
13 |
| Allele |
Parent #1 |
| 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.102813927_102814076GAA[(250-334)] |
| DNA change (hg38) |
g.102161577_102161726GAA[(250-334)] |
| Published as |
- |
| ISCN |
- |
| DB-ID |
FGF14_000038 See all 3 reported entries |
| Variant remarks |
allele >250 is pathogenic (dominant) with reduced penetrance |
| Reference |
PubMed: Rafehi 2023, Journal: Rafehi 2023 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-12-22 12:33:06 +01:00 (CET) |
| Date last edited |
N/A |
Variant on transcripts
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