ClinVar Miner

List of variants in gene combination LOC126806423, TTN reported as likely benign for Cardiovascular phenotype

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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.68079G>A (p.Thr22693=) rs11904444 0.00481
NM_001267550.2(TTN):c.67542T>G (p.Thr22514=) rs72646876 0.00048
NM_001267550.2(TTN):c.67706G>A (p.Arg22569Gln) rs185620750 0.00031
NM_001267550.2(TTN):c.67833C>T (p.Tyr22611=) rs375538420 0.00027
NM_001267550.2(TTN):c.67959T>C (p.Phe22653=) rs72646877 0.00016
NM_001267550.2(TTN):c.67604G>A (p.Ser22535Asn) rs375676529 0.00012
NM_001267550.2(TTN):c.68211G>A (p.Ala22737=) rs536824562 0.00011
NM_001267550.2(TTN):c.68208T>A (p.Val22736=) rs727503575 0.00006
NM_001267550.2(TTN):c.67637-4A>G rs376053678 0.00005
NM_001267550.2(TTN):c.68007G>A (p.Lys22669=) rs755897447 0.00004
NM_001267550.2(TTN):c.67537T>C (p.Leu22513=) rs727504507 0.00003
NM_001267550.2(TTN):c.68154C>T (p.Val22718=) rs755685437 0.00003
NM_001267550.2(TTN):c.67737T>G (p.Ala22579=) rs765975995 0.00002
NM_001267550.2(TTN):c.67809G>A (p.Ala22603=) rs548223512 0.00002
NM_001267550.2(TTN):c.67428C>T (p.His22476=) rs772184456 0.00001
NM_001267550.2(TTN):c.67681T>C (p.Leu22561=) rs397517671 0.00001
NM_001267550.2(TTN):c.67914A>C (p.Ile22638=) rs878934438 0.00001
NM_001267550.2(TTN):c.67923T>C (p.Val22641=) rs759628511 0.00001
NM_001267550.2(TTN):c.67980C>T (p.Ala22660=) rs756764696 0.00001
NM_001267550.2(TTN):c.68040C>T (p.Ile22680=) rs1422070023 0.00001
NM_001267550.2(TTN):c.68142T>C (p.Tyr22714=) rs377007499 0.00001
NM_001267550.2(TTN):c.68160C>T (p.Ala22720=) rs397517673 0.00001
NM_001267550.2(TTN):c.68196G>A (p.Ser22732=) rs397517674 0.00001
NM_001267550.2(TTN):c.68199G>A (p.Glu22733=) rs375672522 0.00001
NM_001267550.2(TTN):c.67541_67542delinsTG (p.Thr22514Met) rs1553622336
NM_001267550.2(TTN):c.67557T>C (p.Tyr22519=)
NM_001267550.2(TTN):c.67575T>A (p.Ala22525=)
NM_001267550.2(TTN):c.67587T>C (p.Asn22529=) rs1057523544
NM_001267550.2(TTN):c.67605C>T (p.Ser22535=) rs750847940
NM_001267550.2(TTN):c.67614T>C (p.Thr22538=) rs1180310461
NM_001267550.2(TTN):c.67653C>T (p.Asp22551=)
NM_001267550.2(TTN):c.67704C>T (p.Phe22568=)
NM_001267550.2(TTN):c.67705C>T (p.Arg22569Trp)
NM_001267550.2(TTN):c.67716C>A (p.Ile22572=) rs754283751
NM_001267550.2(TTN):c.67794T>C (p.Ser22598=) rs960274505
NM_001267550.2(TTN):c.67800G>A (p.Glu22600=)
NM_001267550.2(TTN):c.67818A>G (p.Thr22606=)
NM_001267550.2(TTN):c.67851T>C (p.Asp22617=)
NM_001267550.2(TTN):c.67947A>C (p.Gly22649=)
NM_001267550.2(TTN):c.67971A>G (p.Thr22657=) rs2154175166
NM_001267550.2(TTN):c.68148C>T (p.Phe22716=)
NM_001267550.2(TTN):c.68172T>C (p.Tyr22724=)
NM_001267550.2(TTN):c.68218C>T (p.Pro22740Ser) rs886039082
NM_001267550.2(TTN):c.68232T>C (p.Pro22744=)
NM_001267550.2(TTN):c.68262T>C (p.Asp22754=) rs2047008596
NM_001267550.2(TTN):c.68271C>T (p.His22757=) rs750271244

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