ClinVar Miner

List of variants in gene combination LOC126806421, TTN studied for Cardiomyopathy

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Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.96944C>T (p.Thr32315Ile) rs56027402 0.01724
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.96173G>A (p.Arg32058Gln) rs374063064 0.00014
NM_001267550.2(TTN):c.96424G>A (p.Val32142Ile) rs779663332 0.00006
NM_001267550.2(TTN):c.96180T>C (p.Ile32060=) rs572401798
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.96266dup (p.Asn32089fs) rs1695802877
NM_001267550.2(TTN):c.96289A>G (p.Thr32097Ala) rs1559126718
NM_001267550.2(TTN):c.96414C>T (p.Asn32138=) rs933403975
NM_001267550.2(TTN):c.96593T>C (p.Leu32198Pro) rs2154143465
NM_001267550.2(TTN):c.96812A>G (p.Glu32271Gly) rs1559120065
NM_001267550.2(TTN):c.96919G>A (p.Asp32307Asn)

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