TRIM49

tripartite motif containing 49

Summary

The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. This gene has been found to be preferentially expressed in testis. Related pseudogenes and gene duplicates have also been identified on chromosome 11. [provided by RefSeq, Aug 2010]

Known Variants30 total

rsidPosition (GRCh37)AllelesClassClinVar
rs213001711:89,502,376C/T——
rs249623036811:89,531,353G/C—uncertain significance
rs75857923911:89,531,401G/T—uncertain significance
rs75609558211:89,531,434C/T—uncertain significance
rs116864212411:89,531,498T/C—uncertain significance
rs18678369611:89,531,512C/T—uncertain significance
rs74774393411:89,531,545A/G—uncertain significance
rs15102651111:89,531,572C/T—uncertain significance
rs77466365011:89,531,653G/T—uncertain significance
rs76080972311:89,531,669C/G—uncertain significance
rs77130960311:89,531,763A/C—uncertain significance
rs74995280811:89,531,779T/C—uncertain significance
rs142288416911:89,532,886C/T—uncertain significance
rs134048216011:89,532,905C/T—uncertain significance
rs76154268711:89,532,910A/G—uncertain significance
rs76716519311:89,532,928G/C—uncertain significance
rs135143498711:89,532,950G/C—uncertain significance
rs75014554211:89,532,960G/C—uncertain significance
rs120183110311:89,534,895T/C—uncertain significance
rs131254285711:89,534,905C/T—uncertain significance
rs132027867111:89,534,906G/C—likely benign
rs77762983511:89,537,245C/A—uncertain significance
rs194976300711:89,537,247A/C—uncertain significance
rs76953873911:89,537,259G/A—likely benign
rs77688444311:89,537,358C/G—uncertain significance
rs249624236111:89,537,363A/G—uncertain significance
rs75717053011:89,537,411A/C—uncertain significance
rs117081957011:89,537,543T/C—uncertain significance
rs129295102211:89,537,631A/G—uncertain significance
rs37260513111:89,538,685T/A——

Gene information from NCBI Gene. Variant classifications from ClinVar.