Variant #0000542914 (NC_000011.9:g.126134973G>C, NM_017547.3:c.-4129G>C (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.126134973G>C
DNA change (hg38) g.126265078G>C
Published as SRPRA(NM_001177842.1):c.1322C>G (p.T441S)
ISCN -
DB-ID FAM118B_000002
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_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 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRPR NM_003139.3 ?/. - c.1406C>G r.(?) p.(Thr469Ser)
FOXRED1 NM_017547.3 ?/. - c.-4129G>C r.(?) p.(=)
FAM118B NM_024556.3 ?/. - c.*2945G>C r.(=) p.(=)


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