Variant #0000666242 (NC_000008.10:g.38287347C>T, NM_023110.2:c.211G>A (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.38287347C>T
DNA change (hg38) g.38429829C>T
Published as -
ISCN -
DB-ID FGFR1_000257
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 04:52:06 +02:00 (CEST)
Date last edited 2020-05-24 10:34:17 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGFR1 NM_023110.2 +/. - c.211G>A r.(211g>a) p.(Val71Met)



Screenings

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