Variant #0001030031 (NC_000004.11:g.1801218G>A, NM_000142.4:c.347G>A (FGFR3))

Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.1801218G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID FGFR3_000282 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs569221269
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 5.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-03-24 16:01:01 +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.347G>A r.(?) p.(Arg116His)


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