Variant #0000280870 (NC_000011.9:g.126139100T>C, NM_017547.3:c.-2T>C (FOXRED1))

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.126139100T>C
DNA change (hg38) g.126269205T>C
Published as FOXRED1(NM_017547.4):c.-2T>C
ISCN -
DB-ID FOXRED1_000003
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) 0.79607 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRPR NM_003139.3 -/. - c.-401A>G r.(?) p.(=)
FOXRED1 NM_017547.3 -/. - c.-2T>C r.(?) p.(=)
FAM118B NM_024556.3 -/. - c.*7072T>C r.(=) p.(=)


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