Variant #0000522087 (NC_000004.11:g.1801511C>T, NM_000142.4:c.417C>T (FGFR3))

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1801511C>T
DNA change (hg38) g.1799784C>T
Published as FGFR3(NM_000142.4):c.417C>T (p.D139=, p.(Asp139=)), FGFR3(NM_001163213.2):c.417C>T (p.D139=)
ISCN -
DB-ID FGFR3_000027 See all 4 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) 0.03981 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGFR3 NM_000142.4 -/. - c.417C>T r.(?) p.(Asp139=)


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