Variant #0001048001 (NC_000008.10:g.38287271G>C, NM_023110.2:c.287C>G (FGFR1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.38287271G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID FGFR1_000304
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2150958177
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-09-16 15:27:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGFR1 NM_023110.2 +?/. - c.287C>G r.(?) p.(Ser96Cys)


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