Variant #0000534746 (NC_000008.10:g.38282064A>G, NM_023110.2:c.899T>C (FGFR1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38282064A>G
DNA change (hg38) g.38424546A>G
Published as FGFR1(NM_001174064.1):c.875T>C (p.I292T), FGFR1(NM_023110.3):c.899T>C (p.(Ile300Thr))
ISCN -
DB-ID FGFR1_000005 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) 0.0003 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGFR1 NM_023110.2 -?/. - c.899T>C r.(?) p.(Ile300Thr)


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