TRANK1

tetratricopeptide repeat and ankyrin repeat containing 1

Known Variants209 total

rsidPosition (GRCh37)AllelesClassClinVar
rs47893:36,869,439T/C3 prime UTR variant
rs5537903583:36,869,786C/Guncertain significance
rs7513615223:36,869,795G/Cuncertain significance
rs24706435303:36,871,061T/Clikely benign
rs7759389843:36,871,102T/Guncertain significance
rs3747720213:36,871,116G/Cuncertain significance
rs20786690633:36,871,127T/Guncertain significance
rs76526373:36,871,507T/A
rs37323863:36,871,993C/Tintron variant
rs37323853:36,872,193C/Aintron variant
rs1996593213:36,872,541C/Auncertain significance
rs7779449623:36,872,547C/Tuncertain significance
rs2675997773:36,872,619C/Tuncertain significance
rs7759238323:36,872,629G/Cuncertain significance
rs1807432593:36,872,741C/Tuncertain significance
rs7602471113:36,872,819C/Guncertain significance
rs7551593463:36,872,879A/Guncertain significance
rs7796273773:36,872,912C/Tuncertain significance
rs12242023393:36,872,916G/Tuncertain significance
rs12626550693:36,872,917T/Cuncertain significance
rs13353834623:36,873,042G/Cuncertain significance
rs7757102413:36,873,060G/Auncertain significance
rs7607277613:36,873,073C/Guncertain significance
rs2001323973:36,873,092C/Tconflicting classifications of pathogenicity
rs7513675333:36,873,093G/Auncertain significance
rs24706549573:36,873,099T/Clikely benign
rs3680522993:36,873,197G/Cuncertain significance
rs13350658753:36,873,213C/Auncertain significance
rs3690975563:36,873,224C/Tuncertain significance
rs3692663353:36,873,293G/Auncertain significance
rs2006103773:36,873,314C/Tuncertain significance
rs12391543103:36,873,392C/Tuncertain significance
rs2019358363:36,873,494G/Cuncertain significance
rs3685439093:36,873,505C/Glikely benign
rs7563257443:36,873,506C/Tuncertain significance
rs24706580903:36,873,552G/Tuncertain significance
rs24706585363:36,873,603A/Guncertain significance
rs2000522413:36,873,657T/Guncertain significance
rs7704949613:36,873,713G/Tuncertain significance
rs24706593713:36,873,719G/Auncertain significance
rs7812423703:36,873,772C/Tuncertain significance
rs3735491093:36,873,819C/Tuncertain significance
rs7621405573:36,873,851C/Tuncertain significance
rs7654721243:36,873,852G/Auncertain significance
rs12447538733:36,873,877C/Tuncertain significance
rs7580642243:36,873,945C/Tuncertain significance
rs24706611333:36,873,952C/Guncertain significance
rs3684405303:36,874,043G/Auncertain significance
rs7713833913:36,874,112C/Guncertain significance
rs5782435193:36,874,113G/Auncertain significance
rs3759885143:36,874,116C/Auncertain significance
rs14570132773:36,874,139T/Auncertain significance
rs5334429313:36,874,172C/Tuncertain significance
rs3747154063:36,874,173G/Auncertain significance
rs1483629473:36,874,285G/Clikely benign
rs2019074313:36,874,292A/Guncertain significance
rs7751693973:36,874,310T/Cuncertain significance
rs7803105253:36,874,377C/Tuncertain significance
rs14242428763:36,874,403G/Auncertain significance
rs7603109453:36,874,431G/Auncertain significance
rs7683969053:36,874,491A/Cuncertain significance
rs24706649163:36,874,574G/Tuncertain significance
rs1999343863:36,874,599T/Cuncertain significance
rs20787204283:36,874,616G/Tassociation
rs15594142153:36,874,814C/Auncertain significance
rs7525194373:36,874,910G/Auncertain significance
rs1508601593:36,874,972G/Alikely benign
rs7618771423:36,874,985G/Auncertain significance
rs3698645283:36,875,001G/Cuncertain significance
rs7474206743:36,875,070T/Cuncertain significance
rs5699943043:36,875,085G/Auncertain significance
rs7580642823:36,875,124C/Tuncertain significance
rs3725891063:36,875,237C/Tuncertain significance
rs3680417563:36,875,267A/Tuncertain significance
rs2011386683:36,875,279G/Auncertain significance
rs2020627343:36,875,292T/Cuncertain significance
rs24706700833:36,875,331C/Auncertain significance
rs3734086453:36,876,350C/Tuncertain significance
rs2005624883:36,876,362A/Guncertain significance
rs3743489963:36,876,367C/Tuncertain significance
rs5692185593:36,876,370C/Tuncertain significance
rs24706873543:36,879,937T/Cuncertain significance
rs11857276983:36,880,141T/Cuncertain significance
rs24707038443:36,884,150G/Auncertain significance
rs13277430103:36,887,805C/Auncertain significance
rs3712982873:36,887,886C/Tuncertain significance
rs3736435513:36,888,722C/Tuncertain significance
rs7612500513:36,888,795A/Tuncertain significance
rs7751172113:36,893,220G/Auncertain significance
rs24707416083:36,893,296C/Guncertain significance
rs3752387953:36,893,323C/Tuncertain significance
rs11663223483:36,893,675T/Cuncertain significance
rs3699108773:36,893,683C/Tuncertain significance
rs3730395673:36,893,686A/Guncertain significance
rs3773080063:36,893,710C/Tuncertain significance
rs3696765123:36,893,718C/Tlikely benign
rs3775746083:36,893,770C/Tuncertain significance
rs5662295163:36,893,771G/Auncertain significance
rs13172046343:36,893,821G/Auncertain significance
rs1853339733:36,893,827T/Cuncertain significance

Showing 100 of 209 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.