Variant #0001038319 (NC_000011.9:g.126143336G>A, NM_017547.3:c.523G>A (FOXRED1))

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.126143336G>A
DNA change (hg38) -
Published as FOXRED1(NM_017547.4):c.523G>A (p.(Val175Met))
ISCN -
DB-ID FAM118B_000009
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRPR NM_003139.3 ?/. - c.-4637C>T r.(?) p.(=)
FOXRED1 NM_017547.3 ?/. - c.523G>A r.(?) p.(Val175Met)
FAM118B NM_024556.3 ?/. - c.*11308G>A r.(=) p.(=)


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