ClinVar Miner

List of variants in gene combination LOC126806422, TTN reported as likely benign for not specified

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.69740C>T (p.Pro23247Leu) rs115658240 0.00835
NM_001267550.2(TTN):c.69676A>G (p.Ser23226Gly) rs72646885 0.00553
NM_001267550.2(TTN):c.69821G>A (p.Gly23274Asp) rs201043950 0.00110
NM_001267550.2(TTN):c.70250T>C (p.Ile23417Thr) rs201836227 0.00086
NM_001267550.2(TTN):c.70491C>T (p.Thr23497=) rs372382315 0.00031
NM_001267550.2(TTN):c.69864A>G (p.Ile23288Met) rs368867993 0.00026
NM_001267550.2(TTN):c.70056A>G (p.Arg23352=) rs75948012 0.00024
NM_001267550.2(TTN):c.70644C>T (p.Thr23548=) rs148210834 0.00019
NM_001267550.2(TTN):c.70651C>T (p.Leu23551=) rs72646889 0.00011
NM_001267550.2(TTN):c.70131A>G (p.Thr23377=) rs369503828 0.00010
NM_001267550.2(TTN):c.69660A>G (p.Ala23220=) rs371996901 0.00007
NM_001267550.2(TTN):c.70042G>A (p.Ala23348Thr) rs775146212 0.00007
NM_001267550.2(TTN):c.70506G>T (p.Gly23502=) rs181702963 0.00007
NM_001267550.2(TTN):c.69741G>A (p.Pro23247=) rs566393354 0.00006
NM_001267550.2(TTN):c.70305G>A (p.Thr23435=) rs397517684 0.00006
NM_001267550.2(TTN):c.70036C>T (p.Leu23346=) rs397517681 0.00004
NM_001267550.2(TTN):c.69828C>T (p.Val23276=) rs55659506 0.00002
NM_001267550.2(TTN):c.69882C>T (p.Thr23294=) rs376056197 0.00002
NM_001267550.2(TTN):c.69960C>T (p.Asn23320=) rs752969136 0.00002
NM_001267550.2(TTN):c.70260G>A (p.Pro23420=) rs72646887 0.00002
NM_001267550.2(TTN):c.70287C>T (p.Asn23429=) rs757831376 0.00002
NM_001267550.2(TTN):c.69575C>T (p.Thr23192Ile) rs1319888327 0.00001
NM_001267550.2(TTN):c.69639T>C (p.Arg23213=) rs1487392148 0.00001
NM_001267550.2(TTN):c.69822C>T (p.Gly23274=) rs757102551 0.00001
NM_001267550.2(TTN):c.69876A>C (p.Thr23292=) rs1267766480
NM_001267550.2(TTN):c.69888C>G (p.Leu23296=) rs2154172842
NM_001267550.2(TTN):c.69903C>A (p.Phe23301Leu) rs372799151
NM_001267550.2(TTN):c.70086T>C (p.Ile23362=) rs1553614606
NM_001267550.2(TTN):c.70203T>C (p.Ile23401=) rs2154172628
NM_001267550.2(TTN):c.70473A>G (p.Lys23491=) rs397517685
NM_001267550.2(TTN):c.70536G>A (p.Glu23512=) rs1057523375
NM_001267550.2(TTN):c.70538A>G (p.Asn23513Ser) rs1553613561
NM_001267550.2(TTN):c.70623C>A (p.Ile23541=)

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