ClinVar Miner

List of variants in gene TTN reported as benign for not provided

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Gene type:
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Total variants: 195
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HGVS dbSNP
GRCh37/hg19 2q31.2(chr2:179395958-179522194)x3
NC_000002.12:g.178555347_178555348del
NC_000002.12:g.178582901del
NC_000002.12:g.178604458del
NC_000002.12:g.178617583_178617586del
NC_000002.12:g.178617621_178617624del
NC_000002.12:g.178619018_178619020del
NC_000002.12:g.178654185_178654187del
NC_000002.12:g.178781584dup
NC_000002.12:g.178783236_178783240del
NM_001267550.2(TTN):c.100171+145T>A
NM_001267550.2(TTN):c.1002C>T (p.Thr334=) rs148094198
NM_001267550.2(TTN):c.10104T>G (p.Val3368=) rs142460433
NM_001267550.2(TTN):c.101803A>G (p.Ile33935Val) rs56376197
NM_001267550.2(TTN):c.102103G>A (p.Asp34035Asn) rs144963736
NM_001267550.2(TTN):c.10303+134C>A
NM_001267550.2(TTN):c.10304-162T>C
NM_001267550.2(TTN):c.103147G>C (p.Glu34383Gln) rs148525155
NM_001267550.2(TTN):c.105787_105788delinsTT (p.Ala35263Phe) rs794729250
NM_001267550.2(TTN):c.106476T>C (p.Cys35492=) rs6725673
NM_001267550.2(TTN):c.106580A>T (p.Glu35527Val) rs55725279
NM_001267550.2(TTN):c.107377+216C>T
NM_001267550.2(TTN):c.107576T>C (p.Met35859Thr) rs72629793
NM_001267550.2(TTN):c.107688G>A (p.Pro35896=) rs542575761
NM_001267550.2(TTN):c.11311+284G>A
NM_001267550.2(TTN):c.11312-3515T>A
NM_001267550.2(TTN):c.11370A>G (p.Gln3790=) rs72648918
NM_001267550.2(TTN):c.14093-138C>T
NM_001267550.2(TTN):c.14372-256T>C
NM_001267550.2(TTN):c.14424G>C (p.Val4808=) rs374479775
NM_001267550.2(TTN):c.14870C>G (p.Thr4957Ser) rs72648925
NM_001267550.2(TTN):c.16056T>C (p.Asp5352=) rs376820575
NM_001267550.2(TTN):c.16529A>G (p.Tyr5510Cys) rs72648939
NM_001267550.2(TTN):c.1662+120A>G
NM_001267550.2(TTN):c.1662+317C>T
NM_001267550.2(TTN):c.1663-52A>G
NM_001267550.2(TTN):c.16716A>G (p.Pro5572=) rs367821526
NM_001267550.2(TTN):c.19301G>A (p.Ser6434Asn) rs11888217
NM_001267550.2(TTN):c.1939-89T>C
NM_001267550.2(TTN):c.19714+113T>C
NM_001267550.2(TTN):c.20276-282T>G
NM_001267550.2(TTN):c.2077-86C>T
NM_001267550.2(TTN):c.21019A>T (p.Ile7007Phe) rs114626713
NM_001267550.2(TTN):c.21197A>G (p.Lys7066Arg) rs553548392
NM_001267550.2(TTN):c.21962-23A>G
NM_001267550.2(TTN):c.22080T>C (p.Asp7360=) rs16866473
NM_001267550.2(TTN):c.22384G>C (p.Asp7462His) rs12693166
NM_001267550.2(TTN):c.22529-47dup
NM_001267550.2(TTN):c.23023G>T (p.Asp7675Tyr) rs552951988
NM_001267550.2(TTN):c.23177C>T (p.Ser7726Leu) rs17452588
NM_001267550.2(TTN):c.24431A>C (p.Glu8144Ala) rs16866465
NM_001267550.2(TTN):c.24505+24A>G
NM_001267550.2(TTN):c.24516C>T (p.Thr8172=) rs72648978
NM_001267550.2(TTN):c.24909G>A (p.Lys8303=) rs72648983
NM_001267550.2(TTN):c.2494-271C>T
NM_001267550.2(TTN):c.25008C>T (p.Cys8336=) rs116378128
NM_001267550.2(TTN):c.25063+65T>C
NM_001267550.2(TTN):c.25352-53G>A
NM_001267550.2(TTN):c.25639+182A>T
NM_001267550.2(TTN):c.25640-24G>A
NM_001267550.2(TTN):c.25640-82A>G
NM_001267550.2(TTN):c.25922-102T>G
NM_001267550.2(TTN):c.25922-77T>G
NM_001267550.2(TTN):c.26201-66C>T
NM_001267550.2(TTN):c.26408A>G (p.Asn8803Ser) rs12693164
NM_001267550.2(TTN):c.26483-35T>C
NM_001267550.2(TTN):c.26761+146G>T
NM_001267550.2(TTN):c.27886+270G>A
NM_001267550.2(TTN):c.27886+75T>A
NM_001267550.2(TTN):c.2842-33C>T
NM_001267550.2(TTN):c.28463-132T>C
NM_001267550.2(TTN):c.28970C>T (p.Ser9657Leu) rs200049911
NM_001267550.2(TTN):c.29041+145T>C
NM_001267550.2(TTN):c.29041+281C>G
NM_001267550.2(TTN):c.29042-261G>A
NM_001267550.2(TTN):c.29128G>A (p.Val9710Ile) rs72649002
NM_001267550.2(TTN):c.29421-30T>A
NM_001267550.2(TTN):c.30223+192G>A
NM_001267550.2(TTN):c.30224-244A>G
NM_001267550.2(TTN):c.30274C>T (p.His10092Tyr) rs72650011
NM_001267550.2(TTN):c.30512-19dup rs397517532
NM_001267550.2(TTN):c.30682+288dup
NM_001267550.2(TTN):c.30755-245A>G
NM_001267550.2(TTN):c.30952G>A (p.Glu10318Lys) rs73038324
NM_001267550.2(TTN):c.31594+54A>T
NM_001267550.2(TTN):c.31678+40A>G
NM_001267550.2(TTN):c.32012-54C>T
NM_001267550.2(TTN):c.32049A>G (p.Lys10683=) rs375408527
NM_001267550.2(TTN):c.32807-10T>A rs138192315
NM_001267550.2(TTN):c.32887+78T>C
NM_001267550.2(TTN):c.33094+131C>T
NM_001267550.2(TTN):c.33580+52G>T
NM_001267550.2(TTN):c.33743-148C>T
NM_001267550.2(TTN):c.33834G>A (p.Glu11278=) rs35112591
NM_001267550.2(TTN):c.33910+82T>C
NM_001267550.2(TTN):c.34291+115C>T
NM_001267550.2(TTN):c.34538-123A>G
NM_001267550.2(TTN):c.34538-63G>T
NM_001267550.2(TTN):c.3523+117G>T
NM_001267550.2(TTN):c.3523+271G>A
NM_001267550.2(TTN):c.35797+107C>T
NM_001267550.2(TTN):c.36281-164G>A
NM_001267550.2(TTN):c.36299A>T (p.Glu12100Val) rs73973133
NM_001267550.2(TTN):c.36318A>G (p.Lys12106=) rs2115557
NM_001267550.2(TTN):c.36508G>A (p.Glu12170Lys) rs2163008
NM_001267550.2(TTN):c.36532+19A>G
NM_001267550.2(TTN):c.36655T>G (p.Leu12219Val) rs12994774
NM_001267550.2(TTN):c.36855G>A (p.Pro12285=) rs535294541
NM_001267550.2(TTN):c.37432C>T (p.Pro12478Ser) rs200992277
NM_001267550.2(TTN):c.37543+64C>T
NM_001267550.2(TTN):c.37955-29C>T
NM_001267550.2(TTN):c.38311A>G (p.Lys12771Glu) rs551811137
NM_001267550.2(TTN):c.38323C>T (p.Leu12775Phe) rs186232617
NM_001267550.2(TTN):c.38336T>C (p.Val12779Ala) rs2099130
NM_001267550.2(TTN):c.38708-29T>C
NM_001267550.2(TTN):c.39625+196T>C
NM_001267550.2(TTN):c.39896-75A>G
NM_001267550.2(TTN):c.39973+73C>T
NM_001267550.2(TTN):c.40057+52T>A
NM_001267550.2(TTN):c.40250C>T (p.Pro13417Leu) rs537578226
NM_001267550.2(TTN):c.40409-157C>T
NM_001267550.2(TTN):c.40478-297T>C
NM_001267550.2(TTN):c.40877-243T>C
NM_001267550.2(TTN):c.42415+55T>C
NM_001267550.2(TTN):c.44549-268T>C
NM_001267550.2(TTN):c.44784T>C (p.Asp14928=) rs186105748
NM_001267550.2(TTN):c.44816-189A>C
NM_001267550.2(TTN):c.44913+259T>A
NM_001267550.2(TTN):c.45174C>T (p.Gly15058=) rs372609980
NM_001267550.2(TTN):c.45328G>A (p.Asp15110Asn) rs17354992
NM_001267550.2(TTN):c.45349+23T>A
NM_001267550.2(TTN):c.45349+26_45349+35del
NM_001267550.2(TTN):c.46696+294G>A
NM_001267550.2(TTN):c.47271T>C (p.Asp15757=) rs76081119
NM_001267550.2(TTN):c.47955A>G (p.Pro15985=) rs192953152
NM_001267550.2(TTN):c.48639-46C>T
NM_001267550.2(TTN):c.48953T>C (p.Ile16318Thr) rs72677243
NM_001267550.2(TTN):c.49172G>A (p.Arg16391Gln) rs200944827
NM_001267550.2(TTN):c.52917T>C (p.Asp17639=) rs73036398
NM_001267550.2(TTN):c.53882-25G>T
NM_001267550.2(TTN):c.54381+49T>C
NM_001267550.2(TTN):c.54812-5A>G rs375343798
NM_001267550.2(TTN):c.57544+123T>C
NM_001267550.2(TTN):c.57544+306G>A
NM_001267550.2(TTN):c.57848-286G>A
NM_001267550.2(TTN):c.58612A>G (p.Thr19538Ala) rs200017524
NM_001267550.2(TTN):c.59835C>T (p.Asn19945=) rs72646842
NM_001267550.2(TTN):c.60490G>C (p.Val20164Leu) rs72646843
NM_001267550.2(TTN):c.65275+92C>T
NM_001267550.2(TTN):c.67542T>G (p.Thr22514=) rs72646876
NM_001267550.2(TTN):c.68079G>A (p.Thr22693=) rs11904444
NM_001267550.2(TTN):c.68329+121A>C
NM_001267550.2(TTN):c.69145A>G (p.Ile23049Val) rs72646881
NM_001267550.2(TTN):c.69821G>A (p.Gly23274Asp) rs201043950
NM_001267550.2(TTN):c.70131A>G (p.Thr23377=) rs369503828
NM_001267550.2(TTN):c.70305G>A (p.Thr23435=) rs397517684
NM_001267550.2(TTN):c.7174G>A (p.Gly2392Ser) rs4894048
NM_001267550.2(TTN):c.7545C>T (p.Tyr2515=) rs2291306
NM_001267550.2(TTN):c.77073T>C (p.Asp25691=) rs375398118
NM_001267550.2(TTN):c.77205G>A (p.Val25735=) rs55857909
NM_001267550.2(TTN):c.7856-59A>T
NM_001267550.2(TTN):c.8116+88A>G
NM_001267550.2(TTN):c.81558T>C (p.Asn27186=) rs56181243
NM_001267550.2(TTN):c.82489G>A (p.Gly27497Arg) rs201158906
NM_001267550.2(TTN):c.82798G>A (p.Ala27600Thr) rs11896637
NM_001267550.2(TTN):c.83133G>A (p.Lys27711=) rs369223412
NM_001267550.2(TTN):c.86821+156T>C
NM_001267550.2(TTN):c.87808G>A (p.Val29270Ile) rs141624266
NM_001267550.2(TTN):c.88009+22G>T
NM_001267550.2(TTN):c.88297G>A (p.Asp29433Asn) rs189202799
NM_001267550.2(TTN):c.88306+281G>A
NM_001267550.2(TTN):c.88476C>G (p.Thr29492=) rs190406444
NM_001267550.2(TTN):c.8919C>G (p.Ser2973=) rs4894045
NM_001267550.2(TTN):c.90968G>A (p.Arg30323Lys) rs11887722
NM_001267550.2(TTN):c.91+47_91+51del
NM_001267550.2(TTN):c.914+164T>C
NM_001267550.2(TTN):c.91573A>G (p.Ile30525Val) rs72648244
NM_001267550.2(TTN):c.9163+123G>A
NM_001267550.2(TTN):c.9163+213A>G
NM_001267550.2(TTN):c.9164-208T>C
NM_001267550.2(TTN):c.91853-37G>T
NM_001267550.2(TTN):c.91884A>T (p.Arg30628Ser) rs144922355
NM_001267550.2(TTN):c.92-22G>A
NM_001267550.2(TTN):c.92537T>C (p.Val30846Ala) rs77968867
NM_001267550.2(TTN):c.93901G>A (p.Val31301Ile) rs67665715
NM_001267550.2(TTN):c.94523-33T>C
NM_001267550.2(TTN):c.9461A>G (p.Lys3154Arg) rs4893853
NM_001267550.2(TTN):c.9472-23T>G
NM_001267550.2(TTN):c.9472-26del
NM_001267550.2(TTN):c.95035G>A (p.Asp31679Asn) rs116567963
NM_001267550.2(TTN):c.95723-142T>C
NM_001267550.2(TTN):c.97492+263T>C
NM_001267550.2(TTN):c.97795+202T>C
NM_001267550.2(TTN):c.98595A>G (p.Glu32865=) rs55977045
NM_133379.5(TTN):c.1537-4G>A rs56006378

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