TMEM181
transmembrane protein 181
Summary
The TMEM181 gene encodes a putative G protein-coupled receptor expressed on the cell surface (Carette et al., 2009 [PubMed 19965467]; Wollscheid et al., 2009 [PubMed 19349973]).[supplied by OMIM, Jan 2010]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1324913255 | 6:158,957,501 | C/T | — | uncertain significance |
| rs189350156 | 6:158,957,542 | C/T | — | uncertain significance |
| rs962979735 | 6:158,957,545 | A/C | — | uncertain significance |
| rs947329926 | 6:158,957,572 | G/T | — | uncertain significance |
| rs1197018497 | 6:158,957,576 | G/T | — | uncertain significance |
| rs757512378 | 6:158,957,607 | T/G | — | uncertain significance |
| rs1249355400 | 6:158,957,689 | T/A | — | likely benign |
| rs774818275 | 6:158,957,750 | C/A | — | uncertain significance |
| rs375585407 | 6:158,957,773 | G/A | — | uncertain significance |
| rs779802741 | 6:158,957,794 | C/T | — | uncertain significance |
| rs758858990 | 6:158,957,857 | A/C | — | uncertain significance |
| rs764697485 | 6:158,957,862 | G/T | — | uncertain significance |
| rs1781127150 | 6:158,957,888 | G/A | — | uncertain significance |
| rs13194719 | 6:158,971,266 | A/T | — | — |
| rs371659971 | 6:158,994,457 | C/T | — | uncertain significance |
| rs752330338 | 6:158,994,463 | T/C | — | uncertain significance |
| rs751065878 | 6:158,994,475 | C/T | — | uncertain significance |
| rs769640826 | 6:158,994,487 | G/A | — | uncertain significance |
| rs751053282 | 6:158,994,520 | T/C | — | uncertain significance |
| rs781100263 | 6:158,994,543 | G/A | — | uncertain significance |
| rs4708796 | 6:159,004,472 | C/T | intron variant | — |
| rs1423836370 | 6:159,005,059 | A/C | — | uncertain significance |
| rs750449294 | 6:159,006,342 | C/A | — | uncertain significance |
| rs370699533 | 6:159,010,705 | A/C | — | uncertain significance |
| rs377172594 | 6:159,010,788 | C/T | — | uncertain significance |
| rs200307986 | 6:159,026,327 | G/A | missense variant | — |
| rs1434033310 | 6:159,029,409 | G/T | — | uncertain significance |
| rs575418364 | 6:159,029,436 | A/G | — | likely benign |
| rs117665206 | 6:159,029,487 | T/C | — | benign |
| rs373615885 | 6:159,029,491 | T/C | — | uncertain significance |
| rs202196627 | 6:159,029,734 | T/C | — | uncertain significance |
| rs748879053 | 6:159,044,604 | A/G | — | uncertain significance |
| rs371313932 | 6:159,044,626 | C/T | — | uncertain significance |
| rs754058548 | 6:159,046,145 | G/A | — | likely benign |
| rs201875244 | 6:159,046,148 | T/G | — | uncertain significance |
| rs771903296 | 6:159,046,202 | C/T | — | uncertain significance |
| rs773138819 | 6:159,046,203 | G/A | — | uncertain significance |
| rs759806891 | 6:159,046,221 | G/A | — | uncertain significance |
| rs372660843 | 6:159,049,444 | G/A | — | uncertain significance |
| rs200662769 | 6:159,050,801 | A/G | — | uncertain significance |
| rs2483304513 | 6:159,052,850 | A/G | — | uncertain significance |
| rs1164556754 | 6:159,052,877 | A/G | — | uncertain significance |
| rs754628447 | 6:159,052,885 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.