Variant #0000287384 (NC_000011.9:g.69625412_69625428del, NM_005247.2:c.368_384del (FGF3))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.69625412_69625428del
DNA change (hg38) g.69810644_69810660del
Published as FGF3(NM_005247.3):c.368_384delAGCTGGGCTATAATACG (p.E123Vfs*11)
ISCN -
DB-ID FGF3_000002
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_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 2020-07-01 10:05:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGF3 NM_005247.2 +/. - c.368_384del r.(?) p.(Glu123ValfsTer11)


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