ClinVar Miner

List of variants in gene combination LOC126806421, TTN reported as uncertain significance for not provided

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Total variants: 68
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HGVS dbSNP gnomAD frequency
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.96928A>C (p.Thr32310Pro) rs542208825 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.96172C>T (p.Arg32058Trp) rs201463708 0.00008
NM_001267550.2(TTN):c.96883G>A (p.Val32295Met) rs199532781 0.00007
NM_001267550.2(TTN):c.96424G>A (p.Val32142Ile) rs779663332 0.00006
NM_001267550.2(TTN):c.96526T>A (p.Tyr32176Asn) rs377291343 0.00006
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.96434G>A (p.Arg32145His) rs759948951 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.96921T>C (p.Asp32307=) rs771385738 0.00003
NM_001267550.2(TTN):c.96934C>T (p.Pro32312Ser) rs1024823449 0.00003
NM_001267550.2(TTN):c.96433C>T (p.Arg32145Cys) rs878907981 0.00002
NM_001267550.2(TTN):c.96475T>C (p.Cys32159Arg) rs1375895455 0.00002
NM_001267550.2(TTN):c.96604G>T (p.Val32202Leu) rs755717335 0.00002
NM_001267550.2(TTN):c.96745T>C (p.Trp32249Arg) rs370515456 0.00002
NM_001267550.2(TTN):c.96054T>G (p.Asp32018Glu) rs773714477 0.00001
NM_001267550.2(TTN):c.96057T>A (p.Asp32019Glu) rs786205366 0.00001
NM_001267550.2(TTN):c.96159T>G (p.Ile32053Met) rs906167122 0.00001
NM_001267550.2(TTN):c.96428A>G (p.Glu32143Gly) rs904892183 0.00001
NM_001267550.2(TTN):c.96535G>A (p.Val32179Met) rs727505082 0.00001
NM_001267550.2(TTN):c.96551T>C (p.Ile32184Thr) rs952755219 0.00001
NM_001267550.2(TTN):c.96566A>T (p.Glu32189Val) rs1002475776 0.00001
NM_001267550.2(TTN):c.96685G>A (p.Asp32229Asn) rs770101398 0.00001
NM_001267550.2(TTN):c.96698G>A (p.Arg32233Gln) rs755082341 0.00001
NM_001267550.2(TTN):c.96872C>T (p.Thr32291Ile) rs780461366 0.00001
NM_001267550.2(TTN):c.96049G>A (p.Ala32017Thr)
NM_001267550.2(TTN):c.96082G>A (p.Ala32028Thr)
NM_001267550.2(TTN):c.96125C>T (p.Pro32042Leu)
NM_001267550.2(TTN):c.96212T>G (p.Ile32071Arg) rs755545981
NM_001267550.2(TTN):c.96229C>T (p.Arg32077Trp) rs751316145
NM_001267550.2(TTN):c.96235G>A (p.Asp32079Asn) rs200540781
NM_001267550.2(TTN):c.96235G>C (p.Asp32079His) rs200540781
NM_001267550.2(TTN):c.96259G>A (p.Ala32087Thr)
NM_001267550.2(TTN):c.96260C>G (p.Ala32087Gly) rs1559126910
NM_001267550.2(TTN):c.96316_96447del (p.Pro32106_Met32149del) rs1575413743
NM_001267550.2(TTN):c.96356G>A (p.Arg32119Lys)
NM_001267550.2(TTN):c.96378G>C (p.Trp32126Cys) rs794729542
NM_001267550.2(TTN):c.96413A>T (p.Asn32138Ile)
NM_001267550.2(TTN):c.96440C>T (p.Ala32147Val)
NM_001267550.2(TTN):c.96447G>A (p.Met32149Ile) rs886042242
NM_001267550.2(TTN):c.96503G>A (p.Gly32168Glu)
NM_001267550.2(TTN):c.96522G>C (p.Met32174Ile)
NM_001267550.2(TTN):c.96574G>A (p.Glu32192Lys)
NM_001267550.2(TTN):c.96599C>T (p.Ser32200Leu)
NM_001267550.2(TTN):c.96655G>A (p.Val32219Ile) rs398124460
NM_001267550.2(TTN):c.96655G>T (p.Val32219Phe) rs398124460
NM_001267550.2(TTN):c.96707G>A (p.Gly32236Glu) rs1559121031
NM_001267550.2(TTN):c.96723C>G (p.Ala32241=) rs1223885458
NM_001267550.2(TTN):c.96725G>A (p.Cys32242Tyr)
NM_001267550.2(TTN):c.96803A>G (p.Asn32268Ser)
NM_001267550.2(TTN):c.96830T>A (p.Ile32277Lys)
NM_001267550.2(TTN):c.96854T>C (p.Val32285Ala)
NM_001267550.2(TTN):c.96868G>A (p.Glu32290Lys) rs1060500512
NM_001267550.2(TTN):c.96877A>C (p.Thr32293Pro) rs200555813
NM_001267550.2(TTN):c.96904+8C>A rs528358945
NM_001267550.2(TTN):c.96919G>A (p.Asp32307Asn)
NM_001267550.2(TTN):c.96929C>T (p.Thr32310Ile)
NM_001267550.2(TTN):c.96947T>C (p.Ile32316Thr)

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