Variant #0001048202 (NC_000008.10:g.38314948C>T, NM_023110.2:c.17G>A (FGFR1))

Chromosome 8
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.38314948C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID FGFR1_000305
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2151346848
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 2025-09-23 16:05:01 +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.17G>A r.(?) p.(Cys6Tyr)


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