ClinVar Miner

List of variants in gene combination LOC126806423, TTN reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 151
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.68217T>C (p.His22739=) rs10497517 0.09829
NM_001267550.2(TTN):c.67635T>C (p.Val22545=) rs2288570 0.02106
NM_001267550.2(TTN):c.68079G>A (p.Thr22693=) rs11904444 0.00481
NM_001267550.2(TTN):c.67542T>G (p.Thr22514=) rs72646876 0.00048
NM_001267550.2(TTN):c.67706G>A (p.Arg22569Gln) rs185620750 0.00031
NM_001267550.2(TTN):c.67833C>T (p.Tyr22611=) rs375538420 0.00027
NM_001267550.2(TTN):c.68082C>T (p.Cys22694=) rs79406408 0.00024
NM_001267550.2(TTN):c.67959T>C (p.Phe22653=) rs72646877 0.00016
NM_001267550.2(TTN):c.67604G>A (p.Ser22535Asn) rs375676529 0.00012
NM_001267550.2(TTN):c.68161G>A (p.Glu22721Lys) rs374492812 0.00011
NM_001267550.2(TTN):c.68211G>A (p.Ala22737=) rs536824562 0.00011
NM_001267550.2(TTN):c.67445G>A (p.Arg22482Gln) rs200146608 0.00010
NM_001267550.2(TTN):c.68165A>G (p.Asn22722Ser) rs200493270 0.00010
NM_001267550.2(TTN):c.68225-5T>C rs758273663 0.00009
NM_001267550.2(TTN):c.68097G>C (p.Gln22699His) rs727504520 0.00008
NM_001267550.2(TTN):c.67636+11A>G rs185898410 0.00006
NM_001267550.2(TTN):c.68208T>A (p.Val22736=) rs727503575 0.00006
NM_001267550.2(TTN):c.67637-4A>G rs376053678 0.00005
NM_001267550.2(TTN):c.68298C>A (p.Asp22766Glu) rs534340303 0.00005
NM_001267550.2(TTN):c.68007G>A (p.Lys22669=) rs755897447 0.00004
NM_001267550.2(TTN):c.67537T>C (p.Leu22513=) rs727504507 0.00003
NM_001267550.2(TTN):c.67637-6T>C rs759070877 0.00003
NM_001267550.2(TTN):c.68154C>T (p.Val22718=) rs755685437 0.00003
NM_001267550.2(TTN):c.67444C>T (p.Arg22482Trp) rs563233842 0.00002
NM_001267550.2(TTN):c.67731G>A (p.Lys22577=) rs1459363772 0.00002
NM_001267550.2(TTN):c.67737T>G (p.Ala22579=) rs765975995 0.00002
NM_001267550.2(TTN):c.67809G>A (p.Ala22603=) rs548223512 0.00002
NM_001267550.2(TTN):c.67428C>T (p.His22476=) rs772184456 0.00001
NM_001267550.2(TTN):c.67569G>A (p.Val22523=) rs376719475 0.00001
NM_001267550.2(TTN):c.67637-9A>G rs2047164551 0.00001
NM_001267550.2(TTN):c.67681T>C (p.Leu22561=) rs397517671 0.00001
NM_001267550.2(TTN):c.67692A>G (p.Glu22564=) rs780239325 0.00001
NM_001267550.2(TTN):c.67743A>T (p.Ser22581=) rs2047137031 0.00001
NM_001267550.2(TTN):c.67788A>G (p.Arg22596=) rs1326950042 0.00001
NM_001267550.2(TTN):c.67827A>C (p.Ile22609=) rs751153093 0.00001
NM_001267550.2(TTN):c.67834G>A (p.Asp22612Asn) rs757888367 0.00001
NM_001267550.2(TTN):c.67914A>C (p.Ile22638=) rs878934438 0.00001
NM_001267550.2(TTN):c.67923T>C (p.Val22641=) rs759628511 0.00001
NM_001267550.2(TTN):c.67960G>C (p.Asp22654His) rs144295295 0.00001
NM_001267550.2(TTN):c.67980C>T (p.Ala22660=) rs756764696 0.00001
NM_001267550.2(TTN):c.68010T>C (p.Asp22670=) rs767755200 0.00001
NM_001267550.2(TTN):c.68040C>T (p.Ile22680=) rs1422070023 0.00001
NM_001267550.2(TTN):c.68052G>A (p.Arg22684=) rs770247697 0.00001
NM_001267550.2(TTN):c.68067C>T (p.Asn22689=) rs777832243 0.00001
NM_001267550.2(TTN):c.68083G>A (p.Ala22695Thr) rs767279296 0.00001
NM_001267550.2(TTN):c.68142T>C (p.Tyr22714=) rs377007499 0.00001
NM_001267550.2(TTN):c.68160C>T (p.Ala22720=) rs397517673 0.00001
NM_001267550.2(TTN):c.68181G>A (p.Gly22727=) rs2047051742 0.00001
NM_001267550.2(TTN):c.68195C>T (p.Ser22732Leu) rs727505352 0.00001
NM_001267550.2(TTN):c.68196G>A (p.Ser22732=) rs397517674 0.00001
NM_001267550.2(TTN):c.68199G>A (p.Glu22733=) rs375672522 0.00001
NM_001267550.2(TTN):c.68224+20A>G rs753714710 0.00001
NM_001267550.2(TTN):c.68225-9T>A rs780964424 0.00001
NM_001267550.2(TTN):c.68304G>A (p.Lys22768=) rs776267206 0.00001
NM_001267550.2(TTN):c.67434T>C (p.Asp22478=)
NM_001267550.2(TTN):c.67446G>A (p.Arg22482=) rs2154175758
NM_001267550.2(TTN):c.67458T>C (p.Tyr22486=)
NM_001267550.2(TTN):c.67485T>C (p.Asn22495=) rs2154175738
NM_001267550.2(TTN):c.67488G>A (p.Lys22496=) rs2154175733
NM_001267550.2(TTN):c.67495C>A (p.Arg22499=)
NM_001267550.2(TTN):c.67512A>G (p.Leu22504=)
NM_001267550.2(TTN):c.67524C>T (p.Tyr22508=) rs2154175717
NM_001267550.2(TTN):c.67534G>T (p.Asp22512Tyr) rs786205540
NM_001267550.2(TTN):c.67541_67542delinsTG (p.Thr22514Met) rs1553622336
NM_001267550.2(TTN):c.67548G>A (p.Gly22516=) rs1437157451
NM_001267550.2(TTN):c.67557T>C (p.Tyr22519=)
NM_001267550.2(TTN):c.67569G>C (p.Val22523=)
NM_001267550.2(TTN):c.67571G>A (p.Ser22524Asn) rs397517670
NM_001267550.2(TTN):c.67575T>A (p.Ala22525=)
NM_001267550.2(TTN):c.67575T>G (p.Ala22525=) rs755060136
NM_001267550.2(TTN):c.67587T>C (p.Asn22529=) rs1057523544
NM_001267550.2(TTN):c.67596A>G (p.Gly22532=)
NM_001267550.2(TTN):c.67605C>T (p.Ser22535=) rs750847940
NM_001267550.2(TTN):c.67614T>C (p.Thr22538=) rs1180310461
NM_001267550.2(TTN):c.67620G>A (p.Val22540=)
NM_001267550.2(TTN):c.67636+12T>C
NM_001267550.2(TTN):c.67636+12T>G
NM_001267550.2(TTN):c.67636+13G>A
NM_001267550.2(TTN):c.67636+17A>C
NM_001267550.2(TTN):c.67636+18C>T
NM_001267550.2(TTN):c.67636+19A>G
NM_001267550.2(TTN):c.67636G>A (p.Val22546Met) rs794729244
NM_001267550.2(TTN):c.67637-14C>G
NM_001267550.2(TTN):c.67637-19del
NM_001267550.2(TTN):c.67637-20T>C
NM_001267550.2(TTN):c.67637-8T>C
NM_001267550.2(TTN):c.67653C>T (p.Asp22551=)
NM_001267550.2(TTN):c.67662T>C (p.Gly22554=)
NM_001267550.2(TTN):c.67665A>G (p.Leu22555=)
NM_001267550.2(TTN):c.67704C>T (p.Phe22568=)
NM_001267550.2(TTN):c.67705C>T (p.Arg22569Trp)
NM_001267550.2(TTN):c.67707G>C (p.Arg22569=)
NM_001267550.2(TTN):c.67716C>A (p.Ile22572=) rs754283751
NM_001267550.2(TTN):c.67716C>G (p.Ile22572Met) rs754283751
NM_001267550.2(TTN):c.67716C>T (p.Ile22572=) rs754283751
NM_001267550.2(TTN):c.67740A>G (p.Pro22580=)
NM_001267550.2(TTN):c.67743A>G (p.Ser22581=)
NM_001267550.2(TTN):c.67761G>C (p.Gly22587=)
NM_001267550.2(TTN):c.67782C>T (p.Asp22594=) rs1575865334
NM_001267550.2(TTN):c.67794T>C (p.Ser22598=) rs960274505
NM_001267550.2(TTN):c.67800G>A (p.Glu22600=)
NM_001267550.2(TTN):c.67818A>G (p.Thr22606=)
NM_001267550.2(TTN):c.67836T>C (p.Asp22612=) rs1375493430
NM_001267550.2(TTN):c.67839C>T (p.Cys22613=) rs2154175290
NM_001267550.2(TTN):c.67845A>G (p.Lys22615=) rs1575864065
NM_001267550.2(TTN):c.67851T>C (p.Asp22617=)
NM_001267550.2(TTN):c.67854T>C (p.Ala22618=)
NM_001267550.2(TTN):c.67866A>C (p.Thr22622=) rs1559485882
NM_001267550.2(TTN):c.67881T>C (p.Asn22627=)
NM_001267550.2(TTN):c.67887T>G (p.Ala22629=) rs2154175252
NM_001267550.2(TTN):c.67890C>G (p.Gly22630=)
NM_001267550.2(TTN):c.67905T>G (p.Thr22635=) rs2154175245
NM_001267550.2(TTN):c.67932T>A (p.Pro22644=) rs2154175212
NM_001267550.2(TTN):c.67947A>C (p.Gly22649=)
NM_001267550.2(TTN):c.67962T>C (p.Asp22654=) rs779729130
NM_001267550.2(TTN):c.67965A>G (p.Glu22655=) rs2154175172
NM_001267550.2(TTN):c.67971A>G (p.Thr22657=) rs2154175166
NM_001267550.2(TTN):c.67977A>G (p.Glu22659=)
NM_001267550.2(TTN):c.67980C>G (p.Ala22660=) rs756764696
NM_001267550.2(TTN):c.67984A>T (p.Thr22662Ser) rs1484148632
NM_001267550.2(TTN):c.68034C>T (p.Asn22678=) rs1553620816
NM_001267550.2(TTN):c.68043A>G (p.Leu22681=)
NM_001267550.2(TTN):c.68061G>C (p.Val22687=)
NM_001267550.2(TTN):c.68091T>C (p.Ala22697=)
NM_001267550.2(TTN):c.68140T>C (p.Tyr22714His) rs1575858946
NM_001267550.2(TTN):c.68148C>T (p.Phe22716=)
NM_001267550.2(TTN):c.68163A>G (p.Glu22721=)
NM_001267550.2(TTN):c.68169A>G (p.Lys22723=)
NM_001267550.2(TTN):c.68172T>C (p.Tyr22724=)
NM_001267550.2(TTN):c.68218C>T (p.Pro22740Ser) rs886039082
NM_001267550.2(TTN):c.68220A>G (p.Pro22740=)
NM_001267550.2(TTN):c.68224+12A>G
NM_001267550.2(TTN):c.68224+19G>A
NM_001267550.2(TTN):c.68224+7G>A
NM_001267550.2(TTN):c.68225-10T>C rs1378546349
NM_001267550.2(TTN):c.68225-12A>G
NM_001267550.2(TTN):c.68225-15T>C
NM_001267550.2(TTN):c.68225-18T>C rs1416277306
NM_001267550.2(TTN):c.68225-6T>A
NM_001267550.2(TTN):c.68225-8T>C
NM_001267550.2(TTN):c.68229G>C (p.Val22743=)
NM_001267550.2(TTN):c.68229G>T (p.Val22743=)
NM_001267550.2(TTN):c.68232T>C (p.Pro22744=)
NM_001267550.2(TTN):c.68235T>C (p.Asp22745=) rs757244505
NM_001267550.2(TTN):c.68262T>C (p.Asp22754=) rs2047008596
NM_001267550.2(TTN):c.68266A>C (p.Arg22756=) rs2154174824
NM_001267550.2(TTN):c.68271C>T (p.His22757=) rs750271244
NM_001267550.2(TTN):c.68310T>C (p.Thr22770=)
NM_001267550.2(TTN):c.68329+11T>A
NM_001267550.2(TTN):c.68329+12G>C
NM_001267550.2(TTN):c.68329+8G>T rs1026061408

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.