Variant #0000246213 (NC_000004.11:g.1801542A>G, NC_000004.11(NM_000142.4):c.445+3A>G (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.1801542A>G
DNA change (hg38) g.1799815A>G
Published as FGFR3(NM_000142.4):c.445+3A>G (p.?), FGFR3(NM_001163213.2):c.445+3A>G
ISCN -
DB-ID FGFR3_000028 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) 0.03023 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +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.445+3A>G r.spl? p.?


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