Variant #0000719839 (NC_000004.11:g.1803571C>G, NM_000142.4:c.749C>G (FGFR3))

Chromosome 4
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.1803571C>G
DNA change (hg38) -
Published as FGFR3(NM_000142.4):c.749C>G (p.P250R), FGFR3(NM_000142.5):c.749C>G (p.P250R), FGFR3(NM_001163213.2):c.749C>G (p.P250R)
ISCN -
DB-ID FGFR3_000003 See all 6 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 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +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.749C>G r.(?) p.(Pro250Arg)


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