ClinVar Miner

List of variants in gene combination LOC126806421, TTN reported by GeneDx

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Total variants: 54
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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.96286G>A (p.Ala32096Thr) rs376039623 0.00005
NM_001267550.2(TTN):c.96140C>T (p.Thr32047Met) rs375640847 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.96310+11T>C rs397517764 0.00003
NM_001267550.2(TTN):c.96525C>T (p.Tyr32175=) rs778126823 0.00003
NM_001267550.2(TTN):c.96644C>G (p.Thr32215Ser) rs975713554 0.00003
NM_001267550.2(TTN):c.96708A>G (p.Gly32236=) rs752066259 0.00003
NM_001267550.2(TTN):c.96796T>C (p.Ser32266Pro) rs933521240 0.00003
NM_001267550.2(TTN):c.96433C>T (p.Arg32145Cys) rs878907981 0.00002
NM_001267550.2(TTN):c.96604G>T (p.Val32202Leu) rs755717335 0.00002
NM_001267550.2(TTN):c.96112G>A (p.Val32038Ile) rs753330318 0.00001
NM_001267550.2(TTN):c.96299T>C (p.Val32100Ala) rs794729541 0.00001
NM_001267550.2(TTN):c.96685G>A (p.Asp32229Asn) rs770101398 0.00001
NM_001267550.2(TTN):c.96824T>C (p.Phe32275Ser) rs1559119971 0.00001
NM_001267550.2(TTN):c.96949C>G (p.His32317Asp) rs779019939 0.00001
NM_001267550.2(TTN):c.96180T>C (p.Ile32060=) rs572401798
NM_001267550.2(TTN):c.96212T>G (p.Ile32071Arg) rs755545981
NM_001267550.2(TTN):c.96235G>A (p.Asp32079Asn) rs200540781
NM_001267550.2(TTN):c.96310+2T>G rs794729303
NM_001267550.2(TTN):c.96311-1G>A
NM_001267550.2(TTN):c.96378G>C (p.Trp32126Cys) rs794729542
NM_001267550.2(TTN):c.96421A>G (p.Ile32141Val) rs794729249
NM_001267550.2(TTN):c.96549T>C (p.Asn32183=) rs1057522601
NM_001267550.2(TTN):c.96628G>T (p.Glu32210Ter)
NM_001267550.2(TTN):c.96669G>A (p.Trp32223Ter) rs2154143423
NM_001267550.2(TTN):c.96680_96684del (p.Leu32227fs)
NM_001267550.2(TTN):c.96697C>T (p.Arg32233Ter) rs781171206
NM_001267550.2(TTN):c.96725G>A (p.Cys32242Tyr)
NM_001267550.2(TTN):c.96838C>T (p.Gln32280Ter)
NM_001267550.2(TTN):c.96849del (p.Gly32284fs) rs2154143293
NM_001267550.2(TTN):c.96879A>G (p.Thr32293=) rs373707659
NM_001267550.2(TTN):c.96892C>G (p.Gln32298Glu) rs201108270
NM_001267550.2(TTN):c.96904+18dup rs58609542
NM_001267550.2(TTN):c.96904+34T>A rs780737619
NM_001267550.2(TTN):c.96929C>T (p.Thr32310Ile)

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