{{Rsnum
|rsid=199469705
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TECR
|position=14564841
|Gene_s=TECR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199469705
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=14675653
|CHROM=19
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.14675653C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=610057.0001
|CLNSIG=5
|CLNCUI=C3151462
|CLNDBN=Mental retardation, autosomal recessive 14
|Disease=Mental retardation
|CLNACC=RCV000023795.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151462:614020
|GENEINFO=TECR:9524
|GENE_ID=9524
|GENE_NAME=TECR
}}{{PMID Auto
|PMID=21212097
|Title=Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13.
|OA=1
}}