Variant #0000287834 (NC_000011.9:g.71906438C>T, NM_016725.2:c.292C>T (FOLR1))

Chromosome 11
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.71906438C>T
DNA change (hg38) g.72195394C>T
Published as FOLR1(NM_016724.2):c.292C>T (p.R98W), FOLR1(NM_016724.3):c.292C>T (p.R98W), FOLR1(NM_016725.3):c.292C>T (p.R98W)
ISCN -
DB-ID FOLR1_000005 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) 0.00338 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FOLR1 NM_016725.2 -/. - c.292C>T r.(?) p.(Arg98Trp)


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