ClinVar Miner

List of variants in gene combination LOC126806421, TTN reported by Eurofins Ntd Llc (ga)

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Gene type:
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Total variants: 35
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HGVS dbSNP gnomAD frequency
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.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.96637G>A (p.Asp32213Asn) rs764561909 0.00006
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.96644C>G (p.Thr32215Ser) rs975713554 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.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.96159T>G (p.Ile32053Met) rs906167122 0.00001
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.96260C>G (p.Ala32087Gly) rs1559126910
NM_001267550.2(TTN):c.96316_96447del (p.Pro32106_Met32149del) rs1575413743
NM_001267550.2(TTN):c.96447G>A (p.Met32149Ile) rs886042242
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.96877A>C (p.Thr32293Pro) rs200555813
NM_001267550.2(TTN):c.96904+8C>A rs528358945

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