Variant #0001024907 (NC_000004.11:g.1801487G>A, NM_000142.4:c.393G>A (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.1801487G>A
DNA change (hg38) -
Published as FGFR3(NM_000142.4):c.393G>A (p.S131=, p.(Ser131=)), FGFR3(NM_001163213.2):c.393G>A (p.S131=)
ISCN -
DB-ID FGFR3_000026 See all 5 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) 0.00283 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 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGFR3 NM_000142.4 -/. - c.393G>A r.(?) p.(Ser131=)


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