"Diagnostic Laboratory, Department of Genetics, University Medical Cen - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 332677	NM_001267550.2(TTN):c.*6C>A	TTN, TTN-AS1	Single nucleotide variant (3 prime UTR variant)	Myopathy, myofibrillar, 9, with early respiratory failure +5 more	GConflicting classifications of pathogenicity
Select item 178150	NM_001267550.2(TTN):c.107961T>C (p.His35987=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Cardiomyopathy +8 more	GConflicting classifications of pathogenicity
Select item 46574	NM_001267550.2(TTN):c.107766T>C (p.Gly35922=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 1007868	NM_001267550.2(TTN):c.107723T>C (p.Ile35908Thr)	TTN, TTN-AS1 (I26843T +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +6 more	GUncertain significance
Select item 47723	NM_001267550.2(TTN):c.107700A>G (p.Glu35900=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not provided +9 more	GBenign/Likely benign
Select item 502239	NM_001267550.2(TTN):c.107593G>A (p.Glu35865Lys)	TTN, TTN-AS1 (E33297K +5 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 137821	NM_001267550.2(TTN):c.107397C>T (p.Ser35799=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Tibial muscular dystrophy +8 more	GConflicting classifications of pathogenicity
Select item 196724	NM_001267550.2(TTN):c.107254C>T (p.Arg35752Cys)	TTN, TTN-AS1 (R35752C +5 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 180004	NM_001267550.2(TTN):c.107082G>A (p.Leu35694=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not specified +7 more	GLikely benign
Select item 47717	NM_001267550.2(TTN):c.106955G>A (p.Arg35652Gln)	TTN, TTN-AS1 (R35652Q +5 more)	Single nucleotide variant (missense variant)	Myopathy, myofibrillar, 9, with early respiratory failure +8 more	GConflicting classifications of pathogenicity
Select item 47715	NM_001267550.2(TTN):c.106857C>T (p.Asn35619=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not specified +8 more	GBenign/Likely benign
Select item 47712	NM_001267550.2(TTN):c.106787C>T (p.Thr35596Ile)	TTN, TTN-AS1 (T35596I +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +8 more	GConflicting classifications of pathogenicity
Select item 47711	NM_001267550.2(TTN):c.106638G>A (p.Arg35546=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +8 more	GBenign/Likely benign
Select item 47710	NM_001267550.2(TTN):c.106619T>C (p.Ile35540Thr)	TTN, TTN-AS1 (I35540T +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +8 more	GBenign/Likely benign
Select item 47706	NM_001267550.2(TTN):c.106476T>C (p.Cys35492=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +9 more	GBenign/Likely benign
Select item 47702	NM_001267550.2(TTN):c.105788C>T (p.Ala35263Val)	LOC129935183, TTN +1 more (A35263V +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +8 more	GBenign/Likely benign
Select item 47701	NM_001267550.2(TTN):c.105787G>T (p.Ala35263Ser)	LOC129935183, TTN +1 more (A35263S +5 more)	Single nucleotide variant (missense variant)	Tibial muscular dystrophy +8 more	GBenign/Likely benign
Select item 47699	NM_001267550.2(TTN):c.105769G>A (p.Glu35257Lys)	LOC129935183, TTN +1 more (E35257K +5 more)	Single nucleotide variant (missense variant)	Myopathy, myofibrillar, 9, with early respiratory failure +7 more	GBenign/Likely benign
Select item 47693	NM_001267550.2(TTN):c.105529G>A (p.Val35177Met)	LOC129935184, TTN +1 more (V35177M +5 more)	Single nucleotide variant (missense variant)	Myopathy, myofibrillar, 9, with early respiratory failure +8 more	GBenign/Likely benign
Select item 47691	NM_001267550.2(TTN):c.105468G>A (p.Pro35156=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1G +8 more	GBenign/Likely benign
Select item 1038502	NM_001267550.2(TTN):c.105449G>A (p.Cys35150Tyr)	TTN, TTN-AS1 (C26277Y +5 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 378833	NM_001267550.2(TTN):c.105336G>A (p.Lys35112=)	TTN-AS1, TTN	Single nucleotide variant (synonymous variant)	not specified +3 more	GLikely benign
Select item 1299289	NM_001267550.2(TTN):c.105234del (p.Val35079fs)	TTN, TTN-AS1 (V26014fs +5 more)	Deletion (frameshift variant)	not provided	GLikely pathogenic
Select item 47687	NM_001267550.2(TTN):c.105228G>A (p.Ser35076=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Early-onset myopathy with fatal cardiomyopathy +9 more	GConflicting classifications of pathogenicity
Select item 47685	NM_001267550.2(TTN):c.105183G>A (p.Ala35061=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 203089	NM_001267550.2(TTN):c.105049A>G (p.Thr35017Ala)	TTN, TTN-AS1 (T33376A +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +2 more	GConflicting classifications of pathogenicity
Select item 47677	NM_001267550.2(TTN):c.104769A>C (p.Thr34923=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 47675	NM_001267550.2(TTN):c.104576G>A (p.Arg34859Gln)	TTN, TTN-AS1 (R34859Q +5 more)	Single nucleotide variant (missense variant)	Myopathy, myofibrillar, 9, with early respiratory failure +10 more	GBenign/Likely benign
Select item 47674	NM_001267550.2(TTN):c.104560G>C (p.Val34854Leu)	TTN, TTN-AS1 (V34854L +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +9 more	GConflicting classifications of pathogenicity
Select item 47670	NM_001267550.2(TTN):c.104377A>C (p.Met34793Leu)	TTN, TTN-AS1 (M34793L +5 more)	Single nucleotide variant (missense variant)	not provided +9 more	GBenign/Likely benign
Select item 1146430	NM_001267550.2(TTN):c.104082A>G (p.Ser34694=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely benign
Select item 332695	NM_001267550.2(TTN):c.103992C>G (p.Leu34664=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 47665	NM_001267550.2(TTN):c.103974C>T (p.Ile34658=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Myopathy, myofibrillar, 9, with early respiratory failure +9 more	GConflicting classifications of pathogenicity
Select item 191817	NM_001267550.2(TTN):c.103912C>T (p.Arg34638Cys)	TTN-AS1, TTN (R32070C +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 179636	NM_001267550.2(TTN):c.103730A>G (p.Gln34577Arg)	TTN, TTN-AS1 (Q32009R +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +8 more	GUncertain significance
Select item 96326	NM_001267550.2(TTN):c.103365C>T (p.Arg34455=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not specified +7 more	GBenign/Likely benign
Select item 47659	NM_001267550.2(TTN):c.103363C>T (p.Arg34455Cys)	TTN, TTN-AS1 (R34455C +5 more)	Single nucleotide variant (missense variant)	Early-onset myopathy with fatal cardiomyopathy +8 more	GConflicting classifications of pathogenicity
Select item 130690	NM_001267550.2(TTN):c.103147G>C (p.Glu34383Gln)	TTN, TTN-AS1 (E34383Q +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy +5 more	GConflicting classifications of pathogenicity
Select item 287619	NM_001267550.2(TTN):c.103053C>T (p.Thr34351=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 332697	NM_001267550.2(TTN):c.102984C>T (p.Asp34328=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Tibial muscular dystrophy +6 more	GConflicting classifications of pathogenicity
Select item 47656	NM_001267550.2(TTN):c.102877A>G (p.Lys34293Glu)	TTN, TTN-AS1 (K34293E +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +7 more	GConflicting classifications of pathogenicity
Select item 47652	NM_001267550.2(TTN):c.102595A>G (p.Ile34199Val)	TTN, TTN-AS1 (I34199V +5 more)	Single nucleotide variant (missense variant)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 191822	NM_001267550.2(TTN):c.102275G>A (p.Arg34092His)	TTN, TTN-AS1 (R31524H +5 more)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 178157	NM_001267550.2(TTN):c.102271C>T (p.Arg34091Trp)	TTN-AS1, TTN (R31523W +5 more)	Single nucleotide variant (missense variant)	Primary dilated cardiomyopathy +11 more	GConflicting classifications of pathogenicity
Select item 47645	NM_001267550.2(TTN):c.102103G>A (p.Asp34035Asn)	TTN, TTN-AS1 (D34035N +5 more)	Single nucleotide variant (missense variant)	not specified +9 more	GConflicting classifications of pathogenicity
Select item 178158	NM_001267550.2(TTN):c.101925A>G (p.Leu33975=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1G +8 more	GConflicting classifications of pathogenicity
Select item 47643	NM_001267550.2(TTN):c.101891G>A (p.Arg33964His)	TTN, TTN-AS1 (R33964H +5 more)	Single nucleotide variant (missense variant)	not provided +9 more	GConflicting classifications of pathogenicity
Select item 47642	NM_001267550.2(TTN):c.101803A>G (p.Ile33935Val)	TTN, TTN-AS1 (I33935V +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +8 more	GBenign/Likely benign
Select item 675868	NM_001267550.2(TTN):c.101728G>A (p.Glu33910Lys)	TTN, TTN-AS1 (E31342K +5 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 47639	NM_001267550.2(TTN):c.101665G>A (p.Val33889Ile)	TTN, TTN-AS1 (V33889I +5 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +10 more	GConflicting classifications of pathogenicity
Select item 47638	NM_001267550.2(TTN):c.101406C>G (p.Val33802=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Early-onset myopathy with fatal cardiomyopathy +9 more	GBenign/Likely benign
Select item 915607	NM_001267550.2(TTN):c.101282G>A (p.Arg33761Gln)	TTN, TTN-AS1 (R24888Q +5 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 47633	NM_001267550.2(TTN):c.101212C>T (p.Arg33738Cys)	TTN, TTN-AS1 (R33738C +5 more)	Single nucleotide variant (missense variant)	not specified +10 more	GConflicting classifications of pathogenicity
Select item 47632	NM_001267550.2(TTN):c.101064T>C (p.Asp33688=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not specified +8 more	GBenign/Likely benign
Select item 413180	NM_001267550.2(TTN):c.100766-9dup	TTN, TTN-AS1	Duplication (intron variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GBenign
Select item 203056	NM_001267550.2(TTN):c.100447G>C (p.Glu33483Gln)	TTN-AS1, TTN (E31842Q +5 more)	Single nucleotide variant (missense variant)	Tibial muscular dystrophy +15 more	GConflicting classifications of pathogenicity
Select item 165664	NM_001267550.2(TTN):c.100400T>G (p.Val33467Gly)	TTN, TTN-AS1 (V30899G +5 more)	Single nucleotide variant (missense variant)	not provided +9 more	GConflicting classifications of pathogenicity
Select item 1174908	NM_001267550.2(TTN):c.100139T>A (p.Val33380Glu)	LOC126806420, TTN +1 more (V24315E +5 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 47624	NM_001267550.2(TTN):c.100094G>A (p.Arg33365Gln)	LOC126806420, TTN +1 more (R33365Q +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +7 more	GBenign/Likely benign
Select item 47623	NM_001267550.2(TTN):c.100059T>A (p.Ile33353=)	LOC126806420, TTN +1 more	Single nucleotide variant (synonymous variant)	not provided +8 more	GBenign/Likely benign
Select item 47622	NM_001267550.2(TTN):c.99991T>C (p.Cys33331Arg)	LOC126806420, TTN +1 more (C33331R +5 more)	Single nucleotide variant (missense variant)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 47620	NM_001267550.2(TTN):c.99830G>A (p.Gly33277Glu)	LOC126806420, TTN +1 more (G33277E +5 more)	Single nucleotide variant (missense variant +1 more)	Dilated Cardiomyopathy, Dominant +10 more	GConflicting classifications of pathogenicity
Select item 203048	NM_001267550.2(TTN):c.99478G>A (p.Val33160Ile)	TTN, TTN-AS1 (V31519I +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 165672	NM_001267550.2(TTN):c.99345T>G (p.Gly33115=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Cardiomyopathy +8 more	GBenign/Likely benign
Select item 178162	NM_001267550.2(TTN):c.99162G>A (p.Lys33054=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +8 more	GConflicting classifications of pathogenicity
Select item 47613	NM_001267550.2(TTN):c.99111T>C (p.Tyr33037=)	TTN, TTN-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Tibial muscular dystrophy +7 more	GBenign/Likely benign
Select item 1175010	NM_001267550.2(TTN):c.98990-1G>T	TTN, TTN-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GPathogenic/Likely pathogenic
Select item 137817	NM_001267550.2(TTN):c.98892C>T (p.Pro32964=)	TTN-AS1, TTN	Single nucleotide variant (non-coding transcript variant +1 more)	Myopathy, myofibrillar, 9, with early respiratory failure +8 more	GConflicting classifications of pathogenicity
Select item 165678	NM_001267550.2(TTN):c.98866A>G (p.Met32956Val)	TTN-AS1, TTN (M30388V +5 more)	Single nucleotide variant (missense variant +1 more)	TTN-related disorder +9 more	GConflicting classifications of pathogenicity
Select item 196641	NM_001267550.2(TTN):c.98781T>C (p.Ser32927=)	TTN, TTN-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Dilated cardiomyopathy 1G +2 more	GConflicting classifications of pathogenicity
Select item 47607	NM_001267550.2(TTN):c.98721C>A (p.Leu32907=)	TTN, TTN-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +7 more	GBenign/Likely benign
Select item 47605	NM_001267550.2(TTN):c.98683+7G>C	TTN, TTN-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +6 more	GConflicting classifications of pathogenicity
Select item 47604	NM_001267550.2(TTN):c.98595A>G (p.Glu32865=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant +1 more)	not specified +8 more	GBenign/Likely benign
Select item 47603	NM_001267550.2(TTN):c.98499C>T (p.Leu32833=)	TTN, TTN-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Dilated cardiomyopathy 1G +8 more	GBenign/Likely benign
Select item 47600	NM_001267550.2(TTN):c.98390A>G (p.Asn32797Ser)	TTN, TTN-AS1 (N32797S +5 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Dilated cardiomyopathy 1G +9 more	GConflicting classifications of pathogenicity
Select item 47598	NM_001267550.2(TTN):c.98294C>G (p.Ala32765Gly)	TTN, TTN-AS1 (A32765G +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +10 more	GConflicting classifications of pathogenicity
Select item 47596	NM_001267550.2(TTN):c.98242C>T (p.Arg32748Cys)	TTN, TTN-AS1 (R32748C +5 more)	Single nucleotide variant (missense variant +1 more)	not specified +9 more	GConflicting classifications of pathogenicity
Select item 894036	NM_001267550.2(TTN):c.97592T>A (p.Val32531Glu)	TTN, TTN-AS1 (V23658E +5 more)	Single nucleotide variant (missense variant)	Early-onset myopathy with fatal cardiomyopathy +4 more	GUncertain significance
Select item 192140	NM_001267550.2(TTN):c.97538G>A (p.Arg32513His)	TTN, TTN-AS1 (R29945H +5 more)	Single nucleotide variant (missense variant)	Tibial muscular dystrophy +8 more	GConflicting classifications of pathogenicity
Select item 519191	NM_001267550.2(TTN):c.97417C>T (p.Arg32473Cys)	TTN, TTN-AS1 (R23408C +5 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Dilated cardiomyopathy 1G +3 more	GUncertain significance
Select item 506304	NM_001267550.2(TTN):c.97192+6G>A	LOC129935186, TTN +1 more	Single nucleotide variant (intron variant)	Early-onset myopathy with fatal cardiomyopathy +6 more	GConflicting classifications of pathogenicity
Select item 47577	NM_001267550.2(TTN):c.96998G>A (p.Arg32333His)	TTN, TTN-AS1 (R32333H +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy +9 more	GBenign/Likely benign
Select item 47575	NM_001267550.2(TTN):c.96960T>C (p.Ala32320=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not specified +7 more	GBenign/Likely benign
Select item 47574	NM_001267550.2(TTN):c.96944C>T (p.Thr32315Ile)	LOC126806421, TTN +1 more (T32315I +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +8 more	GBenign/Likely benign
Select item 47573	NM_001267550.2(TTN):c.96918C>T (p.Ile32306=)	LOC126806421, TTN +1 more	Single nucleotide variant (synonymous variant)	Tibial muscular dystrophy +8 more	GConflicting classifications of pathogenicity
Select item 96318	NM_001267550.2(TTN):c.96501T>C (p.Ser32167=)	LOC126806421, TTN +1 more	Single nucleotide variant (synonymous variant)	not specified +8 more	GConflicting classifications of pathogenicity
Select item 1284608	NM_001267550.2(TTN):c.96475T>C (p.Cys32159Arg)	LOC126806421, TTN +1 more (C23094R +5 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 698916	NM_001267550.2(TTN):c.96390G>A (p.Thr32130=)	LOC126806421, TTN +1 more	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 165704	NM_001267550.2(TTN):c.96180T>C (p.Ile32060=)	LOC126806421, TTN +1 more	Single nucleotide variant (synonymous variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +7 more	GBenign/Likely benign
Select item 47563	NM_001267550.2(TTN):c.96108G>A (p.Val32036=)	LOC126806421, TTN +1 more	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1G +8 more	GBenign/Likely benign
Select item 1137606	NM_001267550.2(TTN):c.95877G>A (p.Val31959=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely benign
Select item 47561	NM_001267550.2(TTN):c.95653G>A (p.Ala31885Thr)	TTN, TTN-AS1 (A31885T +5 more)	Single nucleotide variant (missense variant)	Myopathy, myofibrillar, 9, with early respiratory failure +10 more	GConflicting classifications of pathogenicity
Select item 467677	NM_001267550.2(TTN):c.95562G>C (p.Trp31854Cys)	TTN, TTN-AS1 (W31854C +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +2 more	GUncertain significance
Select item 47559	NM_001267550.2(TTN):c.95555T>C (p.Leu31852Pro)	TTN, TTN-AS1 (L31852P +5 more)	Single nucleotide variant (missense variant)	Early-onset myopathy with fatal cardiomyopathy +8 more	GBenign/Likely benign
Select item 47558	NM_001267550.2(TTN):c.95553C>T (p.Ser31851=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1G +8 more	GBenign/Likely benign
Select item 47555	NM_001267550.2(TTN):c.95297C>T (p.Ser31766Phe)	TTN, TTN-AS1 (S31766F +5 more)	Single nucleotide variant (missense variant)	Primary dilated cardiomyopathy +9 more	GConflicting classifications of pathogenicity
Select item 47554	NM_001267550.2(TTN):c.95259C>T (p.Leu31753=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Tibial muscular dystrophy +8 more	GBenign/Likely benign
Select item 47553	NM_001267550.2(TTN):c.95244C>T (p.Arg31748=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not specified +7 more	GConflicting classifications of pathogenicity
Select item 47550	NM_001267550.2(TTN):c.95148C>T (p.Thr31716=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Myopathy, myofibrillar, 9, with early respiratory failure +8 more	GBenign/Likely benign
Select item 404930	NM_001267550.2(TTN):c.94880T>C (p.Ile31627Thr)	TTN, TTN-AS1 (I31627T +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +2 more	GUncertain significance

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