{{Rsnum
|rsid=1129424
|Gene=TNFRSF10B
|Chromosome=8
|position=23068800
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|GMAF=0.2567
|Gene_s=POU3F4,TNFRSF10B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 11.3 | 27.4 | 61.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=1129424
|allele=A
|frequency=
|uid=1103652271861
|type=homozygous_SNP
|hugo=TNFRSF10B
|ensembl gene=ENSG00000120889
|ensembl transcript=ENST00000381063
|sift=TOLERATED
|disease=Defects in TNFRSF10B may be a cause of squamous cell carcinoma of the head and neck (HNSCC) (MIM:275355).
}}

{{GET Evidence
|gene=TNFRSF10B
|aa_change=Pro32Leu
|aa_change_short=P32L
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1129424
|overall_frequency_n=6995
|overall_frequency_d=10710
|overall_frequency=0.653128
|n_genomes=49
|n_genomes_annotated=0
|n_haplomes=77
|n_articles=0
|n_articles_annotated=0
|nblosum100=7
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}