ClinVar Miner

List of variants in gene TTN reported as uncertain significance for Primary familial hypertrophic cardiomyopathy

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Total variants: 17
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HGVS dbSNP
NM_001267550.2(TTN):c.104774A>C (p.Glu34925Ala) rs201218828
NM_001267550.2(TTN):c.105935T>G (p.Leu35312Ter) rs779948923
NM_001267550.2(TTN):c.11311+4663del rs781363456
NM_001267550.2(TTN):c.11312-3964_11312-3963insA rs730880247
NM_001267550.2(TTN):c.12027T>G (p.Tyr4009Ter) rs587782984
NM_001267550.2(TTN):c.2227G>A (p.Ala743Thr) rs370728359
NM_001267550.2(TTN):c.26849A>G (p.Tyr8950Cys) rs199557654
NM_001267550.2(TTN):c.2775+4G>A rs548681281
NM_001267550.2(TTN):c.32731G>A (p.Glu10911Lys) rs199620003
NM_001267550.2(TTN):c.34241_34243AAG[2] (p.Glu11416del) rs397517549
NM_001267550.2(TTN):c.39466C>A (p.Pro13156Thr) rs72650064
NM_001267550.2(TTN):c.46222G>A (p.Ala15408Thr) rs730880239
NM_001267550.2(TTN):c.53519A>G (p.Lys17840Arg) rs730880240
NM_001267550.2(TTN):c.57367A>G (p.Thr19123Ala) rs587782985
NM_001267550.2(TTN):c.57770G>A (p.Arg19257Gln) rs202076328
NM_001267550.2(TTN):c.95415C>A (p.Phe31805Leu) rs587780983
NM_001267550.2(TTN):c.9955G>A (p.Val3319Ile) rs375533809

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