Variant #0000332107 (NC_000008.10:g.38285926T>G, NM_023110.2:c.386A>C (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.38285926T>G
DNA change (hg38) g.38428408T>G
Published as FGFR1(NM_001174063.1):c.386A>C (p.(Asp129Ala)), FGFR1(NM_023110.2):c.386A>C (p.D129A)
ISCN -
DB-ID FGFR1_000024 See all 3 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) 0.00014 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +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.386A>C r.(?) p.(Asp129Ala)


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