Variant #0000337936 (NC_000008.10:g.38285620G>C, NC_000008.10(NM_023110.2):c.449-9C>G (FGFR1))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38285620G>C
DNA change (hg38) g.38428102G>C
Published as FGFR1(NM_001174064.1):c.425-9C>G, FGFR1(NM_001174064.2):c.425-9C>G, FGFR1(NM_023110.2):c.449-9C>G
ISCN -
DB-ID FGFR1_000050 See all 4 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) 0.00087 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.449-9C>G r.(=) p.(=)


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