Variant #0001039550 (NC_000013.10:g.103018992del, NC_000013.10(NM_175929.2):c.208+34852del (FGF14))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.103018992del
DNA change (hg38) -
Published as FGF14(NM_001321946.2):c.-228-6del
ISCN -
DB-ID FGF14_000103
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.-449974del - r.(?) p.(=)
FGF14 NM_175929.2 -?/. - c.208+34852del - r.(=) p.(=)
FGF14-IT1 NR_036486.1 -?/. - n.241-6del - r.(?) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.