ClinVar Miner

List of variants in gene TTN reported as uncertain significance by Erich and Hanna Klessmann Institute for Cardiovascular Research and Development,Heart and Diabetes Center North Rhine-Westphalia

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Total variants: 15
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NM_001267550.2(TTN):c.101774_101776dup (p.Glu33925dup) rs1553497680
NM_001267550.2(TTN):c.102877A>G (p.Lys34293Glu) rs72629783
NM_001267550.2(TTN):c.106403T>A (p.Leu35468His) rs952475900
NM_001267550.2(TTN):c.11887G>A (p.Gly3963Arg) rs1000514079
NM_001267550.2(TTN):c.25570G>A (p.Gly8524Arg) rs371512914
NM_001267550.2(TTN):c.41486G>C (p.Gly13829Ala) rs1114167326
NM_001267550.2(TTN):c.521A>G (p.Tyr174Cys) rs1114167334
NM_001267550.2(TTN):c.54140C>T (p.Ala18047Val) rs373815064
NM_001267550.2(TTN):c.55745C>T (p.Pro18582Leu) rs201194435
NM_001267550.2(TTN):c.68827G>T (p.Ala22943Ser) rs878941853
NM_001267550.2(TTN):c.74305A>G (p.Asn24769Asp) rs372787601
NM_001267550.2(TTN):c.83062C>T (p.Arg27688Cys) rs757441189
NM_001267550.2(TTN):c.86637T>A (p.Asn28879Lys) rs1114167328
NM_001267550.2(TTN):c.92595A>C (p.Leu30865Phe) rs192086736
NM_001267550.2(TTN):c.98759G>A (p.Arg32920Gln) rs752015224

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