Variant #0000997118 (NC_000008.10:g.22874837G>A, NM_003842.4:c.*5347C>T (TNFRSF10B))

Chromosome 8
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.22874837G>A
DNA change (hg38) -
Published as RHOBTB2(NM_015178.2):c.2039G>A (p.(Arg680Gln))
ISCN -
DB-ID RHOBTB2_000041
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Predict-BioInf     
RHOBTB2 NM_001160036.1 ?/. - c.2105G>A r.(?) p.(Arg702Gln) -
TNFRSF10B NM_003842.4 ?/. - c.*5347C>T r.(=) p.(=) -


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