ClinVar Miner

List of variants in gene combination LOC126806421, TTN reported as likely benign

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Gene type:
ClinVar version:
Total variants: 136
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HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.96158T>C (p.Ile32053Thr) rs62621236 0.08189
NM_001267550.2(TTN):c.96944C>T (p.Thr32315Ile) rs56027402 0.01724
NM_001267550.2(TTN):c.96501T>C (p.Ser32167=) rs139223781 0.00251
NM_001267550.2(TTN):c.96108G>A (p.Val32036=) rs372773283 0.00234
NM_001267550.2(TTN):c.96098G>A (p.Arg32033His) rs200648462 0.00090
NM_001267550.2(TTN):c.96918C>T (p.Ile32306=) rs72648266 0.00064
NM_001267550.2(TTN):c.96234C>T (p.Tyr32078=) rs376532382 0.00018
NM_001267550.2(TTN):c.96252A>G (p.Thr32084=) rs369626133 0.00018
NM_001267550.2(TTN):c.96138A>T (p.Ile32046=) rs368154623 0.00016
NM_001267550.2(TTN):c.96684C>T (p.Tyr32228=) rs368423941 0.00016
NM_001267550.2(TTN):c.96173G>A (p.Arg32058Gln) rs374063064 0.00014
NM_001267550.2(TTN):c.96904+4T>C rs373514079 0.00014
NM_001267550.2(TTN):c.96051A>G (p.Ala32017=) rs367805587 0.00008
NM_001267550.2(TTN):c.96172C>T (p.Arg32058Trp) rs201463708 0.00008
NM_001267550.2(TTN):c.96873T>C (p.Thr32291=) rs368169892 0.00007
NM_001267550.2(TTN):c.96883G>A (p.Val32295Met) rs199532781 0.00007
NM_001267550.2(TTN):c.96637G>A (p.Asp32213Asn) rs764561909 0.00006
NM_001267550.2(TTN):c.96904+13T>G rs779376692 0.00006
NM_001267550.2(TTN):c.96286G>A (p.Ala32096Thr) rs376039623 0.00005
NM_001267550.2(TTN):c.96140C>T (p.Thr32047Met) rs375640847 0.00004
NM_001267550.2(TTN):c.96189C>T (p.Thr32063=) rs544886477 0.00004
NM_001267550.2(TTN):c.96225T>A (p.Val32075=) rs752745266 0.00004
NM_001267550.2(TTN):c.96230G>A (p.Arg32077Gln) rs369835255 0.00004
NM_001267550.2(TTN):c.96389C>T (p.Thr32130Met) rs368998895 0.00004
NM_001267550.2(TTN):c.96390G>A (p.Thr32130=) rs200999706 0.00004
NM_001267550.2(TTN):c.96310+11T>C rs397517764 0.00003
NM_001267550.2(TTN):c.96384T>C (p.Ile32128=) rs757368075 0.00003
NM_001267550.2(TTN):c.96399T>C (p.Gly32133=) rs371827750 0.00003
NM_001267550.2(TTN):c.96525C>T (p.Tyr32175=) rs778126823 0.00003
NM_001267550.2(TTN):c.96708A>G (p.Gly32236=) rs752066259 0.00003
NM_001267550.2(TTN):c.96906G>A (p.Val32302=) rs200276343 0.00003
NM_001267550.2(TTN):c.96921T>C (p.Asp32307=) rs771385738 0.00003
NM_001267550.2(TTN):c.96420C>T (p.Tyr32140=) rs1009407656 0.00002
NM_001267550.2(TTN):c.96060A>G (p.Leu32020=) rs1172164559 0.00001
NM_001267550.2(TTN):c.96112G>A (p.Val32038Ile) rs753330318 0.00001
NM_001267550.2(TTN):c.96311-4T>C rs1553518208 0.00001
NM_001267550.2(TTN):c.96315T>G (p.Thr32105=) rs727503540 0.00001
NM_001267550.2(TTN):c.96336G>T (p.Val32112=) rs964067201 0.00001
NM_001267550.2(TTN):c.96615G>A (p.Val32205=) rs763674509 0.00001
NM_001267550.2(TTN):c.96654T>C (p.Thr32218=) rs774339567 0.00001
NM_001267550.2(TTN):c.96717C>T (p.Leu32239=) rs1317384618 0.00001
NM_001267550.2(TTN):c.96824T>C (p.Phe32275Ser) rs1559119971 0.00001
NM_001267550.2(TTN):c.96834G>A (p.Arg32278=) rs558927011 0.00001
NM_001267550.2(TTN):c.96837A>C (p.Ala32279=) rs1232489828 0.00001
NM_001267550.2(TTN):c.96904+8C>T rs528358945 0.00001
NM_001267550.2(TTN):c.96949C>G (p.His32317Asp) rs779019939 0.00001
NM_001267550.2(TTN):c.96042T>G (p.Leu32014=) rs2154144025
NM_001267550.2(TTN):c.96048T>C (p.Leu32016=)
NM_001267550.2(TTN):c.96069T>G (p.Thr32023=)
NM_001267550.2(TTN):c.96075C>T (p.Thr32025=)
NM_001267550.2(TTN):c.96084T>C (p.Ala32028=) rs1553518744
NM_001267550.2(TTN):c.96090C>T (p.Ala32030=) rs1575420522
NM_001267550.2(TTN):c.96096G>A (p.Leu32032=) rs1197841768
NM_001267550.2(TTN):c.96117T>C (p.Ser32039=)
NM_001267550.2(TTN):c.96141G>A (p.Thr32047=) rs752553035
NM_001267550.2(TTN):c.96153G>A (p.Gln32051=)
NM_001267550.2(TTN):c.96180T>C (p.Ile32060=) rs572401798
NM_001267550.2(TTN):c.96189C>G (p.Thr32063=) rs544886477
NM_001267550.2(TTN):c.96228T>C (p.Asn32076=)
NM_001267550.2(TTN):c.96229C>A (p.Arg32077=) rs751316145
NM_001267550.2(TTN):c.96235G>A (p.Asp32079Asn) rs200540781
NM_001267550.2(TTN):c.96252A>T (p.Thr32084=) rs369626133
NM_001267550.2(TTN):c.96270A>G (p.Gln32090=) rs2154143870
NM_001267550.2(TTN):c.96294C>T (p.Val32098=)
NM_001267550.2(TTN):c.96297T>C (p.Leu32099=)
NM_001267550.2(TTN):c.96310+20T>C
NM_001267550.2(TTN):c.96311-16_96311-15del
NM_001267550.2(TTN):c.96311-20T>A
NM_001267550.2(TTN):c.96311-20T>G
NM_001267550.2(TTN):c.96311-9G>A rs2154143671
NM_001267550.2(TTN):c.96336G>A (p.Val32112=)
NM_001267550.2(TTN):c.96411C>G (p.Val32137=) rs1329249610
NM_001267550.2(TTN):c.96414C>T (p.Asn32138=) rs933403975
NM_001267550.2(TTN):c.96417T>C (p.Asn32139=)
NM_001267550.2(TTN):c.96421A>G (p.Ile32141Val) rs794729249
NM_001267550.2(TTN):c.96423C>T (p.Ile32141=) rs1356358644
NM_001267550.2(TTN):c.96442G>A (p.Ala32148Thr)
NM_001267550.2(TTN):c.96453A>G (p.Ala32151=)
NM_001267550.2(TTN):c.96468T>G (p.Thr32156=) rs2154143561
NM_001267550.2(TTN):c.96507T>C (p.Leu32169=)
NM_001267550.2(TTN):c.96519C>T (p.Thr32173=)
NM_001267550.2(TTN):c.96534A>G (p.Arg32178=)
NM_001267550.2(TTN):c.96537G>A (p.Val32179=) rs2154143503
NM_001267550.2(TTN):c.96538C>T (p.Leu32180=)
NM_001267550.2(TTN):c.96540G>C (p.Leu32180=) rs754837315
NM_001267550.2(TTN):c.96549T>C (p.Asn32183=) rs1057522601
NM_001267550.2(TTN):c.96555T>C (p.Tyr32185=) rs1575412584
NM_001267550.2(TTN):c.96570T>C (p.Pro32190=) rs1223460802
NM_001267550.2(TTN):c.96585T>C (p.Asp32195=)
NM_001267550.2(TTN):c.96588A>G (p.Ala32196=)
NM_001267550.2(TTN):c.96591A>T (p.Val32197=)
NM_001267550.2(TTN):c.96610T>C (p.Leu32204=) rs1419384451
NM_001267550.2(TTN):c.96618T>C (p.Pro32206=) rs1553517635
NM_001267550.2(TTN):c.96621A>G (p.Ala32207=)
NM_001267550.2(TTN):c.96636C>T (p.Val32212=)
NM_001267550.2(TTN):c.96681C>G (p.Leu32227=)
NM_001267550.2(TTN):c.96708A>C (p.Gly32236=)
NM_001267550.2(TTN):c.96708A>T (p.Gly32236=) rs752066259
NM_001267550.2(TTN):c.96711T>C (p.Tyr32237=)
NM_001267550.2(TTN):c.96720G>A (p.Glu32240=)
NM_001267550.2(TTN):c.96723C>G (p.Ala32241=) rs1223885458
NM_001267550.2(TTN):c.96735C>T (p.Gly32245=)
NM_001267550.2(TTN):c.96738A>T (p.Thr32246=)
NM_001267550.2(TTN):c.96756T>C (p.Val32252=) rs752935152
NM_001267550.2(TTN):c.96762C>G (p.Thr32254=)
NM_001267550.2(TTN):c.96774A>G (p.Thr32258=)
NM_001267550.2(TTN):c.96789T>A (p.Thr32263=)
NM_001267550.2(TTN):c.96789T>C (p.Thr32263=)
NM_001267550.2(TTN):c.96798C>A (p.Ser32266=)
NM_001267550.2(TTN):c.96804T>C (p.Asn32268=)
NM_001267550.2(TTN):c.96816A>G (p.Gln32272=) rs2154143321
NM_001267550.2(TTN):c.96819C>T (p.Tyr32273=)
NM_001267550.2(TTN):c.96837A>T (p.Ala32279=) rs1232489828
NM_001267550.2(TTN):c.96840A>G (p.Gln32280=) rs776900012
NM_001267550.2(TTN):c.96843T>C (p.Asn32281=)
NM_001267550.2(TTN):c.96852T>C (p.Gly32284=)
NM_001267550.2(TTN):c.96858A>G (p.Ser32286=) rs1035330963
NM_001267550.2(TTN):c.96873T>A (p.Thr32291=)
NM_001267550.2(TTN):c.96879A>C (p.Thr32293=) rs373707659
NM_001267550.2(TTN):c.96879A>G (p.Thr32293=) rs373707659
NM_001267550.2(TTN):c.96882C>T (p.Ala32294=)
NM_001267550.2(TTN):c.96892C>G (p.Gln32298Glu) rs201108270
NM_001267550.2(TTN):c.96897C>T (p.Asp32299=)
NM_001267550.2(TTN):c.96904+10A>G
NM_001267550.2(TTN):c.96904+13T>C
NM_001267550.2(TTN):c.96904+17C>A
NM_001267550.2(TTN):c.96904+18dup rs58609542
NM_001267550.2(TTN):c.96904+34T>A rs780737619
NM_001267550.2(TTN):c.96904+8C>A rs528358945
NM_001267550.2(TTN):c.96904+9C>A rs1375732060
NM_001267550.2(TTN):c.96905-11C>A
NM_001267550.2(TTN):c.96905-20G>A
NM_001267550.2(TTN):c.96907T>C (p.Leu32303=)
NM_001267550.2(TTN):c.96915A>C (p.Thr32305=) rs1418791443
NM_001267550.2(TTN):c.96919G>A (p.Asp32307Asn)
NM_001267550.2(TTN):c.96951T>C (p.His32317=)

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