Variant #0000909142 (NC_000013.10:g.102813927_102814076GAA[(335_?)], NM_175929.2:c.208+239747_208+239896CTT[(335_?)] (FGF14))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.102813927_102814076GAA[(335_?)]
DNA change (hg38) g.102161577_102161726GAA[(335_?)]
Published as -
ISCN -
DB-ID FGF14_000038 See all 3 reported entries
Variant remarks allele >335 fully penetrant
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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-12-22 12:28:57 +01:00 (CET)
Date last edited N/A




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FGF14 NM_004115.3 +/. _1 - - r.? p.?
FGF14 NM_175929.2 +/. 1i c.208+239747_208+239896CTT[(335_?)] GAA[>335] r.? p.?


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