Variant #0000287380 (NC_000013.10:g.102568873G>A, NC_000013.10(NM_175929.2):c.209-41227C>T (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.102568873G>A
DNA change (hg38) g.101916523G>A
Published as FGF14(NM_004115.3):c.123C>T (p.N41=)
ISCN -
DB-ID FGF14_000021 See all 3 reported entries
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) 0.00034 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FGF14 NM_004115.3 -?/. - c.123C>T - r.(?) p.(Asn41=)
FGF14 NM_175929.2 -?/. - c.209-41227C>T - r.(=) p.(=)


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