List of variants in gene TTN reported as likely benign by Genetics and Genomics Program, Sidra Medicine

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: 42

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.69130C>T (p.Pro23044Ser)	rs55980498	0.00372
NM_133379.5(TTN):c.16160G>A (p.Cys5387Tyr)	rs72648913	0.00258
NM_001267550.2(TTN):c.98294C>G (p.Ala32765Gly)	rs72648273	0.00253
NM_001267550.2(TTN):c.9077A>T (p.Asn3026Ile)	rs11900987	0.00205
NM_001267550.2(TTN):c.35264A>C (p.Lys11755Thr)	rs189966800	0.00172
NM_001267550.2(TTN):c.68458G>C (p.Ala22820Pro)	rs72646880	0.00151
NM_001267550.2(TTN):c.79612A>G (p.Thr26538Ala)	rs150682764	0.00100
NM_001267550.2(TTN):c.87412C>A (p.Pro29138Thr)	rs72648227	0.00073
NM_133379.5(TTN):c.16613G>A (p.Arg5538His)	rs145932311	0.00071
NM_001267550.2(TTN):c.89386G>A (p.Val29796Met)	rs72648237	0.00066
NM_001267550.2(TTN):c.107576T>C (p.Met35859Thr)	rs72629793	0.00063
NM_001267550.2(TTN):c.88733G>A (p.Arg29578His)	rs374147064	0.00030
NM_001267550.2(TTN):c.65729T>C (p.Ile21910Thr)	rs146941600	0.00028
NM_001267550.2(TTN):c.65534C>T (p.Pro21845Leu)	rs201662134	0.00026
NM_001267550.2(TTN):c.38975A>T (p.Lys12992Ile)	rs746094582	0.00019
NM_001267550.2(TTN):c.9338G>A (p.Arg3113His)	rs141258018	0.00019
NM_001267550.2(TTN):c.54148C>T (p.Arg18050Cys)	rs55734111	0.00017
NM_001267550.2(TTN):c.102877A>G (p.Lys34293Glu)	rs72629783	0.00016
NM_001267550.2(TTN):c.92699A>G (p.Asn30900Ser)	rs186234393	0.00015
NM_001267550.2(TTN):c.107696T>C (p.Ile35899Thr)	rs372276487	0.00006
NM_001267550.2(TTN):c.75034C>T (p.Arg25012Trp)	rs368914555	0.00006
NM_001267550.2(TTN):c.56686G>A (p.Val18896Met)	rs370629962	0.00004
NM_001267550.2(TTN):c.26765G>A (p.Arg8922Gln)	rs397517520	0.00002
NM_001267550.2(TTN):c.62995T>G (p.Phe20999Val)	rs568886353	0.00002
NM_001267550.2(TTN):c.80858C>T (p.Thr26953Met)	rs377506142	0.00002
NM_001267550.2(TTN):c.103540G>A (p.Val34514Ile)	rs769311670	0.00001
NM_001267550.2(TTN):c.104347C>T (p.Leu34783Phe)	rs539735520	0.00001
NM_001267550.2(TTN):c.41282G>A (p.Arg13761His)	rs781139091	0.00001
NM_001267550.2(TTN):c.71881G>A (p.Val23961Ile)	rs397517690	0.00001
NM_001267550.2(TTN):c.74527A>G (p.Asn24843Asp)	rs373527654	0.00001
NM_001267550.2(TTN):c.81809T>C (p.Ile27270Thr)	rs368527797	0.00001
NM_001267550.2(TTN):c.25616G>T (p.Cys8539Phe)	rs550882549
NM_001267550.2(TTN):c.37502C>T (p.Pro12501Leu)	rs1236045684
NM_001267550.2(TTN):c.39020A>C (p.Lys13007Thr)	rs532069408
NM_001267550.2(TTN):c.40133C>T (p.Pro13378Leu)	rs2062187429
NM_001267550.2(TTN):c.63571C>A (p.Pro21191Thr)	rs2049345864
NM_001267550.2(TTN):c.74468C>G (p.Ala24823Gly)	rs368071644
NM_001267550.2(TTN):c.75296C>A (p.Ala25099Glu)	rs1707934758
NM_001267550.2(TTN):c.78068T>C (p.Ile26023Thr)	rs572384303
NM_001267550.2(TTN):c.81036G>T (p.Lys27012Asn)	rs550999055
NM_001267550.2(TTN):c.97760G>C (p.Arg32587Pro)	rs55704830
NM_133379.5(TTN):c.11684T>C (p.Ile3895Thr)	rs2085229392

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