ClinVar for PubMed (Select 25589632) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3773802	NM_001267550.2(TTN):c.62999del (p.Leu21000fs)	TTN, TTN-AS1 (L11935fs +5 more)	Deletion (frameshift variant)	Primary dilated cardiomyopathy	GLikely pathogenic
Select item 3773794	NM_001267550.2(TTN):c.1522del (p.His507_Val508insTer)	TTN	Deletion (nonsense)	Primary dilated cardiomyopathy	GUncertain significance
Select item 3764022	NM_001267550.2(TTN):c.106988C>G (p.Thr35663Ser)	TTN-AS1, TTN (T26598S +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3764002	NM_001267550.2(TTN):c.64352del (p.Leu21451fs)	TTN, TTN-AS1 (L12386fs +5 more)	Deletion (frameshift variant)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3763983	NM_001267550.2(TTN):c.101489T>C (p.Phe33830Ser)	TTN, TTN-AS1 (F24765S +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763982	NM_001267550.2(TTN):c.3523+5G>C	TTN	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763939	NM_001267550.2(TTN):c.102491A>C (p.Gln34164Pro)	TTN, TTN-AS1 (Q25099P +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763887	NM_001267550.2(TTN):c.2612dup (p.Arg872fs)	TTN (R826fs +1 more)	Duplication (frameshift variant)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3763838	NM_001267550.2(TTN):c.101971G>A (p.Val33991Ile)	TTN, TTN-AS1 (V24926I +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763754	NM_001267550.2(TTN):c.101543A>G (p.Lys33848Arg)	TTN, TTN-AS1 (K24783R +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763753	NM_001267550.2(TTN):c.18417G>A (p.Trp6139Ter)	LOC126806430, TTN (W4895* +2 more)	Single nucleotide variant (nonsense +1 more)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3763706	NM_001267550.2(TTN):c.107325_107328delinsAATT (p.Ala35776Ile)	TTN, TTN-AS1 (A26711I +5 more)	Indel (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763696	NM_001267550.2(TTN):c.106919T>G (p.Leu35640Arg)	TTN, TTN-AS1 (L26575R +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763657	NM_001267550.2(TTN):c.74851_74854dup (p.Ser24952delinsLysTer)	TTN, TTN-AS1	Duplication (nonsense)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3763581	NM_001267550.2(TTN):c.101195C>T (p.Thr33732Ile)	TTN-AS1, TTN (T24667I +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763543	NM_001267550.2(TTN):c.18589G>A (p.Glu6197Lys)	LOC126806430, TTN (E6197K +2 more)	Single nucleotide variant (missense variant +1 more)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763490	NM_001267550.2(TTN):c.36281-1G>A	TTN	Single nucleotide variant (intron variant +1 more)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3763449	NM_001267550.2(TTN):c.6322G>T (p.Glu2108Ter)	TTN (E2062* +1 more)	Single nucleotide variant (nonsense)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3763448	NM_001267550.2(TTN):c.28312C>T (p.Arg9438Ter)	TTN (R8194* +2 more)	Single nucleotide variant (nonsense +1 more)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3763447	NM_001267550.2(TTN):c.92525G>A (p.Trp30842Ter)	TTN, TTN-AS1 (W21777* +5 more)	Single nucleotide variant (nonsense)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3763446	NM_001267550.2(TTN):c.97062del (p.Val32355fs)	TTN, TTN-AS1 (V23290fs +5 more)	Deletion (frameshift variant)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3763445	NM_001267550.2(TTN):c.102440G>A (p.Gly34147Asp)	TTN, TTN-AS1 (G25082D +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763421	NM_001267550.2(TTN):c.106795G>T (p.Ala35599Ser)	TTN, TTN-AS1 (A26534S +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763418	NM_001267550.2(TTN):c.40876+2dup	TTN	Duplication (splice donor variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763416	NM_001267550.2(TTN):c.105622G>A (p.Gly35208Arg)	LOC129935183, TTN +1 more (G26143R +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3763314	NM_001267550.2(TTN):c.102580C>A (p.Leu34194Ile)	TTN, TTN-AS1 (L25129I +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3763300	NM_001267550.2(TTN):c.102881C>T (p.Ser34294Leu)	TTN, TTN-AS1 (S25229L +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3763223	NM_001267550.2(TTN):c.104681G>C (p.Arg34894Thr)	TTN, TTN-AS1 (R25829T +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3763217	NM_001267550.2(TTN):c.103504G>T (p.Ala34502Ser)	TTN, TTN-AS1 (A25437S +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3763192	NM_001267550.2(TTN):c.41608G>A (p.Glu13870Lys)	TTN (E11302K +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3763184	NM_001267550.2(TTN):c.91791dup (p.Thr30598fs)	TTN, TTN-AS1 (T21533fs +5 more)	Duplication (frameshift variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3763182	NM_001267550.2(TTN):c.106753G>A (p.Glu35585Lys)	TTN, TTN-AS1 (E26520K +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3763155	NM_001267550.2(TTN):c.105815C>T (p.Thr35272Ile)	LOC129935183, TTN +1 more (T26207I +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3763045	NM_001267550.2(TTN):c.102796A>T (p.Asn34266Tyr)	TTN, TTN-AS1 (N25201Y +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3763041	NM_001267550.2(TTN):c.36281-1G>C	TTN	Single nucleotide variant (intron variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3763024	NM_001267550.2(TTN):c.101825C>T (p.Pro33942Leu)	TTN, TTN-AS1 (P24877L +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3762979	NM_001267550.2(TTN):c.36349dup (p.Val12117fs)	TTN (V12117fs)	Duplication (frameshift variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3762920	NM_001267550.2(TTN):c.103103T>G (p.Leu34368Ter)	TTN, TTN-AS1 (L25303* +5 more)	Single nucleotide variant (nonsense)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3762906	NM_001267550.2(TTN):c.71993G>C (p.Arg23998Pro)	TTN, TTN-AS1 (R14933P +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3762863	NM_001267550.2(TTN):c.36365-1G>C	TTN	Single nucleotide variant (intron variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3762762	NM_001267550.2(TTN):c.107727T>A (p.Asp35909Glu)	TTN, TTN-AS1 (D26844E +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3762749	NM_001267550.2(TTN):c.102223C>G (p.Gln34075Glu)	TTN, TTN-AS1 (Q25010E +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3762704	NM_001267550.2(TTN):c.44490dup (p.Gly14831fs)	TTN (G12263fs +5 more)	Duplication (frameshift variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3762683	NM_001267550.2(TTN):c.35470+2T>A	TTN	Single nucleotide variant (intron variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3762584	NM_001267550.2(TTN):c.26482G>A (p.Glu8828Lys)	TTN (E7584K +2 more)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3762543	NM_001267550.2(TTN):c.102174G>C (p.Arg34058Ser)	TTN, TTN-AS1 (R24993S +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3762514	NM_001267550.2(TTN):c.102097A>G (p.Thr34033Ala)	TTN, TTN-AS1 (T24968A +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3762472	NM_001267550.2(TTN):c.101882G>A (p.Gly33961Asp)	TTN, TTN-AS1 (G24896D +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3762437	NM_001267550.2(TTN):c.106531G>T (p.Ala35511Ser)	TTN, TTN-AS1 (A26446S +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3762291	NM_001267550.2(TTN):c.106040A>G (p.Asn35347Ser)	LOC129935182, TTN +1 more (N26282S +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3762264	NM_001267550.2(TTN):c.36040_36043+4del	TTN	Deletion (intron variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3762225	NM_001267550.2(TTN):c.102304C>T (p.Leu34102Phe)	TTN, TTN-AS1 (L25037F +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3762211	NM_001267550.2(TTN):c.40053_40057+421del	TTN	Deletion (intron variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3762155	NM_001267550.2(TTN):c.105046T>C (p.Cys35016Arg)	TTN, TTN-AS1 (C25951R +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3762044	NM_001267550.2(TTN):c.36097dup (p.Arg12033fs)	TTN (R12033fs)	Duplication (frameshift variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3761949	NM_001267550.2(TTN):c.104210C>T (p.Ala34737Val)	TTN, TTN-AS1 (A25672V +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3761861	NM_001267550.2(TTN):c.105629A>G (p.Gln35210Arg)	LOC129935183, TTN +1 more (Q26145R +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3761841	NM_001267550.2(TTN):c.39953del (p.Pro13318fs)	TTN (P13318fs)	Deletion (frameshift variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3761821	NM_001267550.2(TTN):c.104879G>A (p.Arg34960His)	TTN, TTN-AS1 (R25895H +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3761703	NM_001267550.2(TTN):c.103249G>T (p.Asp34417Tyr)	TTN, TTN-AS1 (D25352Y +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3761642	NM_001267550.2(TTN):c.102297G>C (p.Lys34099Asn)	TTN, TTN-AS1 (K25034N +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3761553	NM_001267550.2(TTN):c.27328+1G>T	TTN	Single nucleotide variant (intron variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3761548	NM_001267550.2(TTN):c.46401del (p.Lys15468fs)	TTN, TTN-AS1 (K12900fs +5 more)	Deletion (non-coding transcript variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3761531	NM_001267550.2(TTN):c.101396C>G (p.Thr33799Ser)	TTN-AS1, TTN (T24734S +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3761498	NM_001267550.2(TTN):c.103964T>G (p.Leu34655Arg)	TTN, TTN-AS1 (L25590R +5 more)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3761452	NM_001267550.2(TTN):c.68329+2T>C	LOC126806423, TTN +1 more	Single nucleotide variant (splice donor variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3761422	NM_001267550.2(TTN):c.36280+1G>C	TTN	Single nucleotide variant (intron variant +1 more)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GLikely pathogenic
Select item 3761368	NM_001267550.2(TTN):c.51436+4A>C	TTN, TTN-AS1	Single nucleotide variant (intron variant)	Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more	GUncertain significance
Select item 3761302	NM_001267550.2(TTN):c.101708G>T (p.Arg33903Leu)	TTN, TTN-AS1 (R24838L +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3761279	NM_001267550.2(TTN):c.105952A>G (p.Thr35318Ala)	LOC129935183, TTN +1 more (T26253A +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3761208	NM_001267550.2(TTN):c.34637del (p.Pro11546fs)	TTN (P10245fs +2 more)	Deletion (frameshift variant +1 more)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3761195	NM_001267550.2(TTN):c.669G>A (p.Lys223=)	TTN	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3761171	NM_001267550.2(TTN):c.104171A>G (p.Lys34724Arg)	TTN, TTN-AS1 (K25659R +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3761137	NM_001267550.2(TTN):c.103654A>G (p.Thr34552Ala)	TTN, TTN-AS1 (T25487A +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3761117	NM_001267550.2(TTN):c.11311+1G>A	TTN	Single nucleotide variant (splice donor variant)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3761070	NM_001267550.2(TTN):c.104173G>A (p.Asp34725Asn)	TTN, TTN-AS1 (D25660N +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3760870	NM_001267550.2(TTN):c.103238A>G (p.His34413Arg)	TTN, TTN-AS1 (H25348R +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3760857	NM_001267550.2(TTN):c.105665G>A (p.Arg35222Lys)	LOC129935183, TTN +1 more (R26157K +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3760854	NM_001267550.2(TTN):c.102683G>A (p.Gly34228Asp)	TTN, TTN-AS1 (G25163D +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3760845	NM_001267550.2(TTN):c.35537del (p.Glu11846fs)	TTN (E11846fs)	Deletion (frameshift variant +1 more)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3760840	NM_001267550.2(TTN):c.107658A>C (p.Lys35886Asn)	TTN, TTN-AS1 (K26821N +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3760768	NM_001267550.2(TTN):c.36048del (p.Glu12017fs)	TTN (E12017fs)	Deletion (frameshift variant +1 more)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3760721	NM_001267550.2(TTN):c.103530T>A (p.Tyr34510Ter)	TTN, TTN-AS1 (Y25445* +5 more)	Single nucleotide variant (nonsense)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3760646	NM_001267550.2(TTN):c.56962G>A (p.Ala18988Thr)	TTN, TTN-AS1 (A10048T +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3760623	NM_001267550.2(TTN):c.102131T>C (p.Ile34044Thr)	TTN, TTN-AS1 (I24979T +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3760513	NM_001267550.2(TTN):c.3100+1_3100+3dup	TTN	Duplication (splice donor variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3760443	NM_001267550.2(TTN):c.69662del (p.Gly23221fs)	TTN-AS1, LOC126806422 +1 more (G14348fs +5 more)	Deletion (frameshift variant)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3760437	NM_001267550.2(TTN):c.56459dup (p.Tyr18820Ter)	TTN, TTN-AS1 (Y16252* +5 more)	Duplication (nonsense)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3760436	NM_001267550.2(TTN):c.65615del (p.Leu21872fs)	TTN, TTN-AS1 (L12807fs +5 more)	Deletion (frameshift variant)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3760426	NM_001267550.2(TTN):c.61720C>T (p.Gln20574Ter)	TTN, TTN-AS1 (Q11509* +5 more)	Single nucleotide variant (nonsense)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3760425	NM_001267550.2(TTN):c.44311A>T (p.Lys14771Ter)	TTN (K12203* +5 more)	Single nucleotide variant (nonsense)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3760418	NM_001267550.2(TTN):c.105100G>C (p.Gly35034Arg)	TTN, TTN-AS1 (G25969R +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3760410	NM_001267550.2(TTN):c.8380+5G>A	TTN	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3760395	NM_001267550.2(TTN):c.105719G>T (p.Arg35240Leu)	LOC129935183, TTN +1 more (R26175L +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3760383	NM_001267550.2(TTN):c.80780del (p.Asn26927fs)	TTN, TTN-AS1 (N17862fs +5 more)	Deletion (frameshift variant)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3760330	NM_001267550.2(TTN):c.72926del (p.Ser24309fs)	TTN, TTN-AS1 (S15244fs +5 more)	Deletion (frameshift variant)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3760299	NM_001267550.2(TTN):c.107053A>G (p.Ile35685Val)	TTN, TTN-AS1 (I26620V +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +1 more	GUncertain significance
Select item 3760295	NM_001267550.2(TTN):c.46245del (p.Arg15416fs)	TTN (R12848fs +5 more)	Deletion (frameshift variant)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3760288	NM_001267550.2(TTN):c.101309del (p.Leu33770fs)	TTN, TTN-AS1 (L24705fs +5 more)	Deletion (frameshift variant)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic
Select item 3760285	NM_001267550.2(TTN):c.45937del (p.Thr15313fs)	TTN (T12745fs +5 more)	Deletion (frameshift variant)	Dilated cardiomyopathy 1G +1 more	GLikely pathogenic

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