Variant #0000287871 (NC_000011.9:g.126143248C>T, NM_017547.3:c.435C>T (FOXRED1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.126143248C>T
DNA change (hg38) g.126273353C>T
Published as FOXRED1(NM_017547.3):c.435C>T (p.V145=)
ISCN -
DB-ID FOXRED1_000008
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) 0.00106 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 2020-07-01 16:25:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRPR NM_003139.3 -?/. - c.-4549G>A r.(?) p.(=)
FOXRED1 NM_017547.3 -?/. - c.435C>T r.(?) p.(Val145=)
FAM118B NM_024556.3 -?/. - c.*11220C>T r.(=) p.(=)


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