{{Rsnum
|rsid = 34585297
|geno1 = (G;G)
|geno2 = (G;T)
|geno3 = (T;T)
|Gene = TRIM24
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|Chromosome=7
|position=138584825
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TRIM24
}}{{Venter SNP
|rsid=34585297
|allele=T
|frequency=
|uid=1103652718176
|type=heterozygous_SNP
|hugo=TRIM24
|ensembl gene=ENSG00000122779
|ensembl transcript=ENST00000343526
|sift=AFFECT FUNCTION
|disease=A chromosomal aberration involving TIF1 is a cause of thyroid papillary carcinoma (PACT) (MIM:188550). Translocation t(7;10)(q32;q11) with RET. The translocation generates the TIF1/RET (PTC6) oncogene.
}}

{{GET Evidence
|gene=TRIM24
|aa_change=Arg975Ser
|aa_change_short=R975S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs34585297
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=1
|webscore=N
}}

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