{{Rsnum
|rsid=17028450
|Gene=TMPO
|Chromosome=12
|position=98534325
|Orientation=plus
|GMAF=0.01331
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TMPO
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 98.2 | 1.8 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 93.0 | 7.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 98.2 | 1.8 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 98.1 | 1.9 | 0.0
| GIH | 98.0 | 2.0 | 0.0
| LWK | 97.2 | 2.8 | 0.0
| MEX | 83.9 | 14.3 | 1.8
| MKK | 99.4 | 0.6 | 0.0
| TSI | 97.0 | 3.0 | 0.0
| HapMapRevision=28
}}{{omim
|id=188380
|rsnum=17028450
|variant=0001
}}

{{ClinVar
|rsid=17028450
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=98928103
|CHROM=12
|GMAF=0.0133
|dbSNPBuildID=123
|SSR=0
|SAO=1
|VP=0x050260000000140517110100
|GENEINFO=TMPO:7112
|GENE_NAME=TMPO
|GENE_ID=7112
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.98928103C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=188380.0001
|CLNSIG=5
|CLNCUI=C1861160
|CLNDBN=Dilated cardiomyopathy 1T; AllHighlyPenetrant
|Disease=Dilated cardiomyopathy 1T; AllHighlyPenetrant
|CLNACC=RCV000013544.22; RCV000037751.1
|Tags=PM;S3D;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9867; 0.01331
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1309:C3151039:613740:154; CN169374
|COMMON=1
}}

{{GET Evidence
|gene=TMPO
|aa_change=Arg690Cys
|aa_change_short=R690C
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17028450
|overall_frequency_n=11
|overall_frequency_d=10750
|overall_frequency=0.00102326
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|in_omim=Y
|pph2_score=0.998
|nblosum100=8
|autoscore=4
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}