{{Rsnum
|rsid=34712518
|Gene=TMC6
|Chromosome=17
|position=78124950
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.09596
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TMC6
}}{{Venter SNP
|rsid=34712518
|allele=T
|frequency=
|uid=1103645387113
|type=heterozygous_SNP
|hugo=TMC6
|ensembl gene=ENSG00000141524
|ensembl transcript=ENST00000322914
|sift=TOLERATED
|disease=Defects in TMC6 are a cause of epidermodysplasia verruciformis (EV) (MIM:226400). It is a rare autosomal recessive genodermatosis associated with a high risk of skin carcinoma that results from an abnormal susceptibility to infection by specific human papillomaviruses. Infection leads to persistent wart-like or macular lesions.
}}

{{GET Evidence
|gene=TMC6
|aa_change=Gly191Asp
|aa_change_short=G191D
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs34712518
|overall_frequency_n=968
|overall_frequency_d=10632
|overall_frequency=0.0910459
|n_genomes=11
|n_genomes_annotated=0
|n_haplomes=9
|n_articles=0
|n_articles_annotated=0
|nblosum100=4
|autoscore=0
|webscore=N
}}
{{on chip | HumanOmni1Quad}}