{{Rsnum
|rsid=2853493
|Gene=MT-ND4
|Chromosome=MT
|position=11467
|Orientation=plus
|GMAF=0.1001
|Gene_s=MT-ND4
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|Summary=A11467G, defines MT-haplogroup U
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 75.4 | 0.0 | 24.6
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| 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
}}
More commonly known as A11467G, or 11467. One of 3 Mitochondrial mutations that together define Mitochondrial Haplogroup U, and its descendants.
This is a synonymous change that still codes for the exact same amino acid, so it probably has no biological effect.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}