Variant #0001039549 (NC_000013.10:g.102480248T>C, NC_000013.10(NM_175929.2):c.423+40827A>G (FGF14))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.102480248T>C
DNA change (hg38) -
Published as FGF14(NM_001321937.2):c.448A>G (p.(Thr150Ala))
ISCN -
DB-ID FGF14_000102
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 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FGF14 NM_004115.3 ?/. - c.408+40827A>G - r.(=) p.(=)
FGF14 NM_175929.2 ?/. - c.423+40827A>G - r.(=) p.(=)


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