{{Rsnum
|rsid=11090865
|Gene=TRMU
|Chromosome=22
|position=46335792
|Orientation=plus
|GMAF=0.1088
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=TRMU
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 67.7 | 30.8 | 1.5
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 69.8 | 23.8 | 6.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 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
}}{{omim
|id=610230
|rsnum=11090865
|variant=0001
}}

{{ClinVar
|rsid=11090865
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=46731689
|CHROM=22
|GMAF=0.1085
|dbSNPBuildID=120
|SSR=0
|SAO=1
|VP=0x050360000000170517110100
|GENEINFO=TRMU:55687
|GENE_NAME=TRMU
|GENE_ID=55687
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.46731689G>T
|CLNORIGIN=0
|CLNSIG=5
|Tags=PM;S3D;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.8912; 0.1088
|CLNACC=RCV000001353.1
|CLNDBN=Deafness, mitochondrial, modifier of
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=610230.0001
|COMMON=1
|Disease=Deafness
}}

{{GET Evidence
|gene=TRMU
|aa_change=Ala10Ser
|aa_change_short=A10S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11090865
|overall_frequency_n=1368
|overall_frequency_d=10156
|overall_frequency=0.134699
|n_genomes=5
|n_genomes_annotated=0
|n_haplomes=5
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.78
|genetests_testable=Y
|nblosum100=-1
|autoscore=2
|n_web_uneval=10
}}

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