"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 178150	NM_001267550.2(TTN):c.107961T>C (p.His35987=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1G +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)	TTN-related condition +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)	not provided +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 specified +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 47720	NM_001267550.2(TTN):c.107576T>C (p.Met35859Thr)	TTN, TTN-AS1 (M35859T +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +10 more	GConflicting classifications of pathogenicity
Select item 137821	NM_001267550.2(TTN):c.107397C>T (p.Ser35799=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Early-onset myopathy with fatal cardiomyopathy +8 more	GConflicting classifications of pathogenicity
Select item 178151	NM_001267550.2(TTN):c.107377+14C>T	TTN, TTN-AS1	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1G +6 more	GConflicting classifications of pathogenicity
Select item 47718	NM_001267550.2(TTN):c.107267T>C (p.Val35756Ala)	TTN-AS1, TTN (V35756A +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +6 more	GBenign/Likely benign
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)	Dilated cardiomyopathy 1G +8 more	GConflicting classifications of pathogenicity
Select item 1297536	NM_001267550.2(TTN):c.106858G>A (p.Glu35620Lys)	TTN, TTN-AS1 (E26555K +5 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 47715	NM_001267550.2(TTN):c.106857C>T (p.Asn35619=)	TTN-AS1, TTN	Single nucleotide variant (synonymous variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +8 more	GBenign/Likely benign
Select item 1297550	NM_001267550.2(TTN):c.106828A>G (p.Lys35610Glu)	TTN, TTN-AS1 (K26545E +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +6 more	GUncertain significance
Select item 1284925	NM_001267550.2(TTN):c.106793A>C (p.Gln35598Pro)	TTN, TTN-AS1 (Q26533P +5 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 47712	NM_001267550.2(TTN):c.106787C>T (p.Thr35596Ile)	TTN, TTN-AS1 (T35596I +5 more)	Single nucleotide variant (missense variant)	not specified +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)	Dilated cardiomyopathy 1G +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)	Myopathy, myofibrillar, 9, with early respiratory failure +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)	Dilated cardiomyopathy 1G +9 more	GBenign/Likely benign
Select item 47704	NM_001267550.2(TTN):c.106275G>C (p.Gly35425=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +6 more	GBenign/Likely benign
Select item 202340	NM_001267550.2(TTN):c.105787_105788delinsTT (p.Ala35263Phe)	LOC129935183, TTN +1 more (A26198F +4 more)	Indel (missense variant)	Cardiovascular phenotype +8 more	GBenign/Likely benign
Select item 47700	NM_001267550.2(TTN):c.105782C>T (p.Pro35261Leu)	LOC129935183, TTN +1 more (P35261L +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +6 more	GBenign/Likely benign
Select item 47694	NM_001267550.2(TTN):c.105582C>T (p.Ser35194=)	LOC129935183, TTN +1 more	Single nucleotide variant (synonymous variant)	Myopathy, myofibrillar, 9, with early respiratory failure +6 more	GBenign
Select item 178854	NM_001267550.2(TTN):c.105562A>C (p.Ile35188Leu)	LOC129935184, TTN +1 more (I32620L +5 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 47693	NM_001267550.2(TTN):c.105529G>A (p.Val35177Met)	LOC129935184, TTN +1 more (V35177M +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +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)	Cardiovascular phenotype +8 more	GBenign/Likely benign
Select item 284241	NM_001267550.2(TTN):c.105428del (p.Gly35143fs)	TTN, TTN-AS1 (G33502fs +5 more)	Deletion (frameshift variant)	Dilated cardiomyopathy 1G +2 more	GConflicting classifications of pathogenicity
Select item 47687	NM_001267550.2(TTN):c.105228G>A (p.Ser35076=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +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)	Myopathy, myofibrillar, 9, with early respiratory failure +8 more	GConflicting classifications of pathogenicity
Select item 47684	NM_001267550.2(TTN):c.105180G>C (p.Glu35060Asp)	LOC129935185, TTN +1 more (E35060D +5 more)	Single nucleotide variant (missense variant)	Early-onset myopathy with fatal cardiomyopathy +7 more	GBenign/Likely benign
Select item 47683	NM_001267550.2(TTN):c.105127C>T (p.Arg35043Cys)	TTN, TTN-AS1 (R35043C +5 more)	Single nucleotide variant (missense variant)	Early-onset myopathy with fatal cardiomyopathy +8 more	GConflicting classifications of pathogenicity
Select item 466736	NM_001267550.2(TTN):c.105085T>C (p.Leu35029=)	TTN-AS1, TTN	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +6 more	GBenign/Likely benign
Select item 47677	NM_001267550.2(TTN):c.104769A>C (p.Thr34923=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not specified +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)	not specified +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)	Dilated cardiomyopathy 1G +9 more	GConflicting classifications of pathogenicity
Select item 225104	NM_001267550.2(TTN):c.104522G>A (p.Arg34841His)	TTN, TTN-AS1 (R32273H +5 more)	Single nucleotide variant (missense variant)	Myopathy, myofibrillar, 9, with early respiratory failure +8 more	GConflicting classifications of pathogenicity
Select item 203082	NM_001267550.2(TTN):c.104519G>A (p.Arg34840Gln)	TTN, TTN-AS1 (R33199Q +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +4 more	GConflicting classifications of pathogenicity
Select item 641365	NM_001267550.2(TTN):c.104483A>G (p.Glu34828Gly)	TTN, TTN-AS1 (E25888G +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 47670	NM_001267550.2(TTN):c.104377A>C (p.Met34793Leu)	TTN, TTN-AS1 (M34793L +5 more)	Single nucleotide variant (missense variant)	Tibial muscular dystrophy +9 more	GBenign/Likely benign
Select item 47669	NM_001267550.2(TTN):c.104365G>A (p.Glu34789Lys)	TTN, TTN-AS1 (E34789K +5 more)	Single nucleotide variant (missense variant)	not specified +8 more	GConflicting classifications of pathogenicity
Select item 282653	NM_001267550.2(TTN):c.104347C>T (p.Leu34783Phe)	TTN, TTN-AS1 (L32215F +5 more)	Single nucleotide variant (missense variant)	TTN-related condition +10 more	GBenign/Likely benign
Select item 47667	NM_001267550.2(TTN):c.104251G>C (p.Ala34751Pro)	TTN-AS1, TTN (A34751P +5 more)	Single nucleotide variant (missense variant)	Tibial muscular dystrophy +9 more	GConflicting classifications of pathogenicity
Select item 1297682	NM_001267550.2(TTN):c.104245C>T (p.Arg34749Trp)	TTN, TTN-AS1 (R25684W +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +5 more	GUncertain significance
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 47665	NM_001267550.2(TTN):c.103974C>T (p.Ile34658=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not specified +9 more	GConflicting classifications of pathogenicity
Select item 191817	NM_001267550.2(TTN):c.103912C>T (p.Arg34638Cys)	TTN, TTN-AS1 (R32070C +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 191819	NM_001267550.2(TTN):c.103412G>A (p.Arg34471Gln)	TTN-AS1, TTN (R31903Q +5 more)	Single nucleotide variant (missense variant)	TTN-related condition +7 more	GConflicting classifications of pathogenicity
Select item 96326	NM_001267550.2(TTN):c.103365C>T (p.Arg34455=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not provided +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)	Cardiovascular phenotype +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 332697	NM_001267550.2(TTN):c.102984C>T (p.Asp34328=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 1284364	NM_001267550.2(TTN):c.102928G>A (p.Glu34310Lys)	TTN, TTN-AS1 (E25245K +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +6 more	GUncertain significance
Select item 47655	NM_001267550.2(TTN):c.102833G>T (p.Gly34278Val)	TTN-AS1, TTN (G34278V +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +6 more	GBenign/Likely benign
Select item 894176	NM_001267550.2(TTN):c.102790C>T (p.Leu34264Phe)	TTN, TTN-AS1 (L31696F +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +6 more	GConflicting classifications of pathogenicity
Select item 1020927	NM_001267550.2(TTN):c.102782C>A (p.Thr34261Asn)	TTN-AS1, TTN (T25196N +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +3 more	GConflicting classifications of pathogenicity
Select item 167756	NM_001267550.2(TTN):c.102751A>G (p.Met34251Val)	TTN, TTN-AS1 (M31683V +5 more)	Single nucleotide variant (missense variant)	not specified +9 more	GConflicting classifications of pathogenicity
Select item 47654	NM_001267550.2(TTN):c.102737G>A (p.Arg34246His)	TTN, TTN-AS1 (R34246H +5 more)	Single nucleotide variant (missense variant)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 500354	NM_001267550.2(TTN):c.102614G>A (p.Gly34205Asp)	TTN, TTN-AS1 (G31637D +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 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 specified +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, TTN-AS1 (R31523W +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy +11 more	GConflicting classifications of pathogenicity
Select item 47645	NM_001267550.2(TTN):c.102103G>A (p.Asp34035Asn)	TTN-AS1, TTN (D34035N +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +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)	Tibial muscular dystrophy +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)	Autosomal recessive limb-girdle muscular dystrophy type 2J +9 more	GConflicting classifications of pathogenicity
Select item 47642	NM_001267550.2(TTN):c.101803A>G (p.Ile33935Val)	TTN-AS1, TTN (I33935V +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +8 more	GBenign/Likely benign
Select item 47640	NM_001267550.2(TTN):c.101697C>T (p.Asp33899=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not specified +8 more	GBenign/Likely benign
Select item 47639	NM_001267550.2(TTN):c.101665G>A (p.Val33889Ile)	TTN, TTN-AS1 (V33889I +5 more)	Single nucleotide variant (missense variant)	Tibial muscular dystrophy +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)	Dilated cardiomyopathy 1G +9 more	GBenign/Likely benign
Select item 202283	NM_001267550.2(TTN):c.101376T>C (p.Tyr33792=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +8 more	GConflicting classifications of pathogenicity
Select item 178159	NM_001267550.2(TTN):c.101281C>T (p.Arg33761Trp)	TTN, TTN-AS1 (R31193W +5 more)	Single nucleotide variant (missense variant)	not specified +9 more	GConflicting classifications of pathogenicity
Select item 47634	NM_001267550.2(TTN):c.101245G>A (p.Val33749Met)	TTN-AS1, TTN (V33749M +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +8 more	GConflicting classifications of pathogenicity
Select item 47633	NM_001267550.2(TTN):c.101212C>T (p.Arg33738Cys)	TTN, TTN-AS1 (R33738C +5 more)	Single nucleotide variant (missense variant)	TTN-related myopathy +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)	Dilated cardiomyopathy 1G +8 more	GBenign/Likely benign
Select item 165660	NM_001267550.2(TTN):c.101055T>C (p.Asp33685=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not provided +5 more	GLikely benign
Select item 191827	NM_001267550.2(TTN):c.100982G>A (p.Arg33661Lys)	TTN, TTN-AS1 (R31093K +5 more)	Single nucleotide variant (missense variant)	TTN-related condition +5 more	GConflicting classifications of pathogenicity
Select item 47628	NM_001267550.2(TTN):c.100459C>T (p.Pro33487Ser)	TTN, TTN-AS1 (P33487S +5 more)	Single nucleotide variant (missense variant)	Early-onset myopathy with fatal cardiomyopathy +7 more	GBenign/Likely benign
Select item 203056	NM_001267550.2(TTN):c.100447G>C (p.Glu33483Gln)	TTN, TTN-AS1 (E31842Q +5 more)	Single nucleotide variant (missense variant)	Abnormality of speech or vocalization +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)	Cardiovascular phenotype +9 more	GConflicting classifications of pathogenicity
Select item 466681	NM_001267550.2(TTN):c.100396C>T (p.Arg33466Cys)	TTN, TTN-AS1 (R33466C +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +2 more	GUncertain significance
Select item 47626	NM_001267550.2(TTN):c.100172-17dup	LOC126806420, TTN +1 more	Duplication (intron variant)	Dilated Cardiomyopathy, Dominant +11 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 47623	NM_001267550.2(TTN):c.100059T>A (p.Ile33353=)	LOC126806420, TTN +1 more	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +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)	Cardiovascular phenotype +8 more	GConflicting classifications of pathogenicity
Select item 332704	NM_001267550.2(TTN):c.99966G>T (p.Trp33322Cys)	LOC126806420, TTN +1 more (W33322C +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +7 more	GConflicting classifications of pathogenicity
Select item 165672	NM_001267550.2(TTN):c.99345T>G (p.Gly33115=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	TTN-related condition +8 more	GBenign/Likely benign
Select item 47616	NM_001267550.2(TTN):c.99340T>C (p.Leu33114=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 178162	NM_001267550.2(TTN):c.99162G>A (p.Lys33054=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	Tibial muscular dystrophy +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)	Cardiovascular phenotype +7 more	GBenign/Likely benign
Select item 47611	NM_001267550.2(TTN):c.99031T>A (p.Ser33011Thr)	TTN, TTN-AS1 (S33011T +5 more)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +8 more	GConflicting classifications of pathogenicity
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, TTN-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 47608	NM_001267550.2(TTN):c.98726T>C (p.Val32909Ala)	TTN, TTN-AS1 (V32909A +5 more)	Single nucleotide variant (missense variant +1 more)	not specified +5 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)	Tibial muscular dystrophy +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 191837	NM_001267550.2(TTN):c.98641C>T (p.Pro32881Ser)	TTN, TTN-AS1 (P30313S +5 more)	Single nucleotide variant (missense variant +1 more)	Myopathy, myofibrillar, 9, with early respiratory failure +8 more	GConflicting classifications of pathogenicity
Select item 47603	NM_001267550.2(TTN):c.98499C>T (p.Leu32833=)	TTN, TTN-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Myopathy, myofibrillar, 9, with early respiratory failure +8 more	GBenign/Likely benign
Select item 47601	NM_001267550.2(TTN):c.98439G>A (p.Val32813=)	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)	not provided +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 specified +10 more	GConflicting classifications of pathogenicity

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