Variant #0000666241 (NC_000008.10:g.38287269C>G, NM_023110.2:c.289G>C (FGFR1))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.38287269C>G
DNA change (hg38) g.38429751C>G
Published as -
ISCN -
DB-ID FGFR1_000258
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Daoqi Wang
Database submission license No license selected
Created by Daoqi Wang
Date created 2020-05-23 04:49:48 +02:00 (CEST)
Date last edited 2020-05-24 10:34:59 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGFR1 NM_023110.2 +/. - c.289G>C r.(289g>c) p.(Gly97Arg)



Screenings

Stop! No screenings found!


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.