ClinVar Miner

List of variants in gene TTN studied for Familial hypertrophic cardiomyopathy 9

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Total variants: 17
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NM_001267550.2(TTN):c.103360del (p.Glu34454fs) rs760768093
NM_001267550.2(TTN):c.104261C>T (p.Ala34754Val) rs727505020
NM_001267550.2(TTN):c.11311+1080del rs58651353
NM_001267550.2(TTN):c.2219G>T (p.Arg740Leu) rs28933405
NM_001267550.2(TTN):c.2447T>C (p.Phe816Ser)
NM_001267550.2(TTN):c.44281C>T (p.Pro14761Ser) rs192766485
NM_001267550.2(TTN):c.48426T>A (p.Tyr16142Ter) rs1576476485
NM_001267550.2(TTN):c.49621G>T (p.Glu16541Ter)
NM_001267550.2(TTN):c.52702A>G (p.Ile17568Val) rs377571654
NM_001267550.2(TTN):c.54796G>T (p.Ala18266Ser) rs199837769
NM_001267550.2(TTN):c.55154A>G (p.Gln18385Arg)
NM_001267550.2(TTN):c.61009G>T (p.Glu20337Ter)
NM_001267550.2(TTN):c.65629G>T (p.Ala21877Ser) rs72646866
NM_001267550.2(TTN):c.68641C>T (p.Arg22881Ter) rs1213930919
NM_001267550.2(TTN):c.72088A>T (p.Lys24030Ter)
NM_001267550.2(TTN):c.96904+4T>C rs373514079

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