List of variants in gene combination LOC126806422, TTN reported as uncertain significance for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 72

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.69821G>A (p.Gly23274Asp)	rs201043950	0.00110
NM_001267550.2(TTN):c.69904G>A (p.Val23302Ile)	rs190421400	0.00036
NM_001267550.2(TTN):c.70491C>T (p.Thr23497=)	rs372382315	0.00031
NM_001267550.2(TTN):c.70097T>C (p.Val23366Ala)	rs372782502	0.00030
NM_001267550.2(TTN):c.69864A>G (p.Ile23288Met)	rs368867993	0.00026
NM_001267550.2(TTN):c.69984G>A (p.Ala23328=)	rs56052239	0.00026
NM_001267550.2(TTN):c.70492G>A (p.Gly23498Ser)	rs370771532	0.00026
NM_001267550.2(TTN):c.70056A>G (p.Arg23352=)	rs75948012	0.00024
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.69638G>A (p.Arg23213His)	rs374883884	0.00009
NM_001267550.2(TTN):c.70163G>A (p.Arg23388Gln)	rs55853138	0.00008
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.70172T>C (p.Ile23391Thr)	rs375202101	0.00007
NM_001267550.2(TTN):c.70645G>A (p.Val23549Ile)	rs755669336	0.00006
NM_001267550.2(TTN):c.70102A>G (p.Ile23368Val)	rs367914610	0.00005
NM_001267550.2(TTN):c.70288G>A (p.Val23430Ile)	rs549709481	0.00004
NM_001267550.2(TTN):c.70328G>A (p.Arg23443Gln)	rs762529671	0.00004
NM_001267550.2(TTN):c.70424G>A (p.Arg23475His)	rs370257707	0.00004
NM_001267550.2(TTN):c.70570A>G (p.Thr23524Ala)	rs369526268	0.00004
NM_001267550.2(TTN):c.69749C>T (p.Thr23250Ile)	rs771327436	0.00003
NM_001267550.2(TTN):c.70044C>T (p.Ala23348=)	rs771534964	0.00003
NM_001267550.2(TTN):c.70047G>C (p.Glu23349Asp)	rs774136558	0.00003
NM_001267550.2(TTN):c.70260G>A (p.Pro23420=)	rs72646887	0.00002
NM_001267550.2(TTN):c.70396C>T (p.Arg23466Cys)	rs749744742	0.00002
NM_001267550.2(TTN):c.70435C>T (p.Arg23479Trp)	rs760509116	0.00002
NM_001267550.2(TTN):c.70485A>T (p.Lys23495Asn)	rs1482776876	0.00002
NM_001267550.2(TTN):c.69639T>C (p.Arg23213=)	rs1487392148	0.00001
NM_001267550.2(TTN):c.69725G>A (p.Gly23242Glu)	rs1292885710	0.00001
NM_001267550.2(TTN):c.69815T>G (p.Ile23272Ser)	rs758398301	0.00001
NM_001267550.2(TTN):c.69957C>G (p.Ile23319Met)	rs540840413	0.00001
NM_001267550.2(TTN):c.69959A>G (p.Asn23320Ser)	rs756468956	0.00001
NM_001267550.2(TTN):c.70166C>G (p.Ala23389Gly)	rs1194442496	0.00001
NM_001267550.2(TTN):c.70181C>T (p.Thr23394Met)	rs397517683	0.00001
NM_001267550.2(TTN):c.70231G>A (p.Gly23411Ser)	rs767075037	0.00001
NM_001267550.2(TTN):c.70436G>A (p.Arg23479Gln)	rs140127488	0.00001
NM_001267550.2(TTN):c.70562C>G (p.Thr23521Arg)	rs775589244	0.00001
NM_001267550.2(TTN):c.69568A>G (p.Ile23190Val)	rs762698812
NM_001267550.2(TTN):c.69631G>A (p.Glu23211Lys)
NM_001267550.2(TTN):c.69650A>C (p.Glu23217Ala)	rs72646884
NM_001267550.2(TTN):c.69742C>T (p.His23248Tyr)
NM_001267550.2(TTN):c.69806G>A (p.Gly23269Glu)
NM_001267550.2(TTN):c.69808C>T (p.Leu23270Phe)
NM_001267550.2(TTN):c.69829G>A (p.Val23277Met)
NM_001267550.2(TTN):c.69845T>C (p.Val23282Ala)	rs886042580
NM_001267550.2(TTN):c.69857C>A (p.Ala23286Asp)	rs1465961266
NM_001267550.2(TTN):c.69876A>C (p.Thr23292=)	rs1267766480
NM_001267550.2(TTN):c.69903C>A (p.Phe23301Leu)	rs372799151
NM_001267550.2(TTN):c.69903C>T (p.Phe23301=)	rs372799151
NM_001267550.2(TTN):c.69916C>A (p.Leu23306Ile)
NM_001267550.2(TTN):c.69937A>G (p.Asn23313Asp)
NM_001267550.2(TTN):c.69937_69939del (p.Asn23313del)	rs1459956579
NM_001267550.2(TTN):c.69961G>C (p.Asp23321His)
NM_001267550.2(TTN):c.69983C>T (p.Ala23328Val)
NM_001267550.2(TTN):c.70026T>C (p.Pro23342=)	rs878983731
NM_001267550.2(TTN):c.70067T>C (p.Val23356Ala)
NM_001267550.2(TTN):c.70091T>C (p.Ile23364Thr)
NM_001267550.2(TTN):c.70105A>G (p.Lys23369Glu)	rs1277463353
NM_001267550.2(TTN):c.70112G>A (p.Arg23371His)
NM_001267550.2(TTN):c.70137C>A (p.Thr23379=)	rs770349910
NM_001267550.2(TTN):c.70179T>G (p.Asn23393Lys)	rs1040909022
NM_001267550.2(TTN):c.70244T>C (p.Met23415Thr)
NM_001267550.2(TTN):c.70301A>C (p.Asp23434Ala)	rs1011201907
NM_001267550.2(TTN):c.70304C>A (p.Thr23435Lys)
NM_001267550.2(TTN):c.70371C>A (p.Asp23457Glu)
NM_001267550.2(TTN):c.70409A>G (p.Tyr23470Cys)	rs750891099
NM_001267550.2(TTN):c.70423C>T (p.Arg23475Cys)
NM_001267550.2(TTN):c.70526T>C (p.Val23509Ala)
NM_001267550.2(TTN):c.70552G>T (p.Gly23518Cys)	rs2154172371
NM_001267550.2(TTN):c.70615C>G (p.Leu23539Val)
NM_001267550.2(TTN):c.70640G>C (p.Ser23547Thr)	rs1553613338

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