Variant #0000920467 (NC_000008.10:g.119941159_119941161del, NM_002546.3:c.408_410del (TNFRSF11B))

Chromosome 8
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.119941159_119941161del
DNA change (hg38) -
Published as -
ISCN -
DB-ID TNFRSF11B_000008
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-03-02 16:17:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF11B NM_002546.3 -/. - c.408_410del r.(?) p.(Glu137del)


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