ClinVar Miner

List of variants in gene TNNT2 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 86
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HGVS dbSNP
NM_000364.2(TNNT2):c.42-82C>T
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249
NM_000364.3(TNNT2):c.136G>C (p.Ala46Pro) rs397516447
NM_000364.3(TNNT2):c.199+14G>A rs876657590
NM_000364.3(TNNT2):c.294+7G>A rs45490292
NM_000364.3(TNNT2):c.295-14C>T rs747477576
NM_000364.3(TNNT2):c.489+7_489+8insG rs397516467
NM_000364.3(TNNT2):c.68-5_68-3delinsTT rs397516362
NM_000364.3(TNNT2):c.710+13A>C rs563883763
NM_000364.3(TNNT2):c.753G>T (p.Glu251Asp) rs45466197
NM_001001430.1(TNNT2):c.53-11_53-7delCTTCT rs45533739
NM_001001430.2(TNNT2):c.*66G>A rs3729998
NM_001001430.2(TNNT2):c.-15+10G>A rs754752990
NM_001001430.2(TNNT2):c.-15+17G>A rs924166432
NM_001001430.2(TNNT2):c.-15+6G>T rs778890563
NM_001001430.2(TNNT2):c.-3A>G rs752977897
NM_001001430.2(TNNT2):c.-40G>T rs921078883
NM_001001430.2(TNNT2):c.-49C>T rs1050772817
NM_001001430.2(TNNT2):c.-5A>G rs730881093
NM_001001430.2(TNNT2):c.114C>T (p.Thr38=) rs746492909
NM_001001430.2(TNNT2):c.123C>G (p.Thr41=) rs1347127737
NM_001001430.2(TNNT2):c.133+12G>A rs45580032
NM_001001430.2(TNNT2):c.133+12G>T rs45580032
NM_001001430.2(TNNT2):c.133+13T>C rs527486692
NM_001001430.2(TNNT2):c.170-4C>G rs397516448
NM_001001430.2(TNNT2):c.178A>G (p.Met60Val) rs141837529
NM_001001430.2(TNNT2):c.207G>A (p.Ser69=) rs3729845
NM_001001430.2(TNNT2):c.21G>T (p.Val7=) rs777128825
NM_001001430.2(TNNT2):c.225G>A (p.Val75=) rs780115529
NM_001001430.2(TNNT2):c.240C>G (p.Pro80=) rs140245123
NM_001001430.2(TNNT2):c.240C>T (p.Pro80=) rs140245123
NM_001001430.2(TNNT2):c.243T>C (p.Asp81=) rs763782935
NM_001001430.2(TNNT2):c.255G>A (p.Val85=) rs1060503885
NM_001001430.2(TNNT2):c.318C>T (p.Ile106=) rs3729547
NM_001001430.2(TNNT2):c.339G>A (p.Arg113=)
NM_001001430.2(TNNT2):c.33C>T (p.Tyr11=) rs148027842
NM_001001430.2(TNNT2):c.360C>T (p.Leu120=) rs758543857
NM_001001430.2(TNNT2):c.382-4T>G rs757304775
NM_001001430.2(TNNT2):c.382-6_382-4delCCT rs397516462
NM_001001430.2(TNNT2):c.400C>A (p.Arg134=) rs45525839
NM_001001430.2(TNNT2):c.42-20G>A rs45561443
NM_001001430.2(TNNT2):c.42-29C>T rs886038366
NM_001001430.2(TNNT2):c.420C>T (p.Ile140=) rs200604266
NM_001001430.2(TNNT2):c.421C>A (p.Arg141=) rs74315379
NM_001001430.2(TNNT2):c.429G>A (p.Glu143=) rs775274966
NM_001001430.2(TNNT2):c.444G>C (p.Arg148=) rs35914325
NM_001001430.2(TNNT2):c.459+18C>T rs377743847
NM_001001430.2(TNNT2):c.459+9C>A rs1060503884
NM_001001430.2(TNNT2):c.468G>A (p.Arg156=) rs750399630
NM_001001430.2(TNNT2):c.492C>T (p.Asn164=) rs483352833
NM_001001430.2(TNNT2):c.52+17G>A rs776357102
NM_001001430.2(TNNT2):c.52+7G>A rs374443596
NM_001001430.2(TNNT2):c.522G>A (p.Lys174=) rs566113559
NM_001001430.2(TNNT2):c.53-6G>A rs764862951
NM_001001430.2(TNNT2):c.537C>T (p.Ser179=) rs397516474
NM_001001430.2(TNNT2):c.562A>G (p.Ile188Val) rs730881124
NM_001001430.2(TNNT2):c.570+4G>A rs372988386
NM_001001430.2(TNNT2):c.571-6G>A rs760197357
NM_001001430.2(TNNT2):c.579+15C>T rs1057523597
NM_001001430.2(TNNT2):c.580-10C>T rs375547142
NM_001001430.2(TNNT2):c.613C>A (p.Arg205=) rs45586240
NM_001001430.2(TNNT2):c.63T>G (p.Val21=) rs397516477
NM_001001430.2(TNNT2):c.662T>C (p.Ile221Thr) rs45520032
NM_001001430.2(TNNT2):c.68-1590C>T rs751728017
NM_001001430.2(TNNT2):c.68-1596C>T rs727503515
NM_001001430.2(TNNT2):c.68-1602A>G rs370895664
NM_001001430.2(TNNT2):c.68-1627G>A
NM_001001430.2(TNNT2):c.68-81G>A rs45576939
NM_001001430.2(TNNT2):c.690-13C>G
NM_001001430.2(TNNT2):c.690-13_690-11delCTT rs397516480
NM_001001430.2(TNNT2):c.690-4G>T rs201753429
NM_001001430.2(TNNT2):c.690-5T>G rs730881092
NM_001001430.2(TNNT2):c.690-6G>A rs113471285
NM_001001430.2(TNNT2):c.744C>T (p.Phe248=) rs397516481
NM_001001430.2(TNNT2):c.748C>T (p.Leu250=) rs977853063
NM_001001430.2(TNNT2):c.758A>G (p.Lys253Arg) rs3730238
NM_001001430.2(TNNT2):c.780+6C>T rs727504260
NM_001001430.2(TNNT2):c.781-19C>G rs1057522713
NM_001001430.2(TNNT2):c.781-4G>A rs1431082504
NM_001001430.2(TNNT2):c.798C>T (p.Asn266=) rs1553279337
NM_001001430.2(TNNT2):c.807C>T (p.Asn269=) rs376923877
NM_001001430.2(TNNT2):c.822-18G>A rs778928540
NM_001001430.2(TNNT2):c.831C>A (p.Thr277=) rs754211195
NM_001001430.2(TNNT2):c.834C>T (p.Arg278=)
NM_001001430.2(TNNT2):c.84G>A (p.Ala28=) rs200283086
NM_001001430.2(TNNT2):c.852C>T (p.Thr284=) rs45465693

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