All variants in the FGF14 gene

Information The variants shown are described using the NM_004115.3 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. - c.-485009A>G r.(?) p.(=) - likely benign g.103054004T>C g.102401654T>C FGF14(NM_175929.2):c.25A>G (p.(Arg9Gly)) - FGF14_000029 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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