Variant #0000545654 (NC_000011.9:g.71906793T>C, NC_000011.9(NM_016725.2):c.493+2T>C (FOLR1))

Chromosome 11
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.71906793T>C
DNA change (hg38) g.72195749T>C
Published as FOLR1(NM_016724.2):c.493+2T>C, FOLR1(NM_016724.3):c.493+2T>C, FOLR1(NM_016725.3):c.493+2T>C
ISCN -
DB-ID FOLR1_000007 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) 0.00336 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2026-01-20 18:57:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FOLR1 NM_016725.2 ?/. - c.493+2T>C r.spl? p.?


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