ClinVar Miner

List of variants in gene TNNI3 studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 85
Download table as spreadsheet
HGVS dbSNP
NM_000363.5(TNNI3):c.105C>A (p.Ala35=) rs397516339
NM_000363.5(TNNI3):c.108+21G>A rs3729837
NM_000363.5(TNNI3):c.109-15A>G rs779144176
NM_000363.5(TNNI3):c.109-17C>A rs139150276
NM_000363.5(TNNI3):c.109-20G>C rs1555864156
NM_000363.5(TNNI3):c.12-7del rs370714315
NM_000363.5(TNNI3):c.127G>T (p.Ala43Ser) rs727505023
NM_000363.5(TNNI3):c.132G>C (p.Ser44=) rs727504941
NM_000363.5(TNNI3):c.139T>C (p.Leu47=) rs587780967
NM_000363.5(TNNI3):c.150+13G>T rs73617692
NM_000363.5(TNNI3):c.151-6C>G rs377258542
NM_000363.5(TNNI3):c.167T>C (p.Ile56Thr) rs545441942
NM_000363.5(TNNI3):c.168T>G (p.Ile56Met) rs727503509
NM_000363.5(TNNI3):c.198G>A (p.Glu66=) rs3729710
NM_000363.5(TNNI3):c.204del (p.Arg69fs) rs727504872
NM_000363.5(TNNI3):c.225T>G (p.Ala75=) rs1555864028
NM_000363.5(TNNI3):c.233C>T (p.Thr78Ile) rs786205288
NM_000363.5(TNNI3):c.235C>T (p.Arg79Cys) rs3729712
NM_000363.5(TNNI3):c.236G>T (p.Arg79Leu) rs397516342
NM_000363.5(TNNI3):c.24+19G>A rs368708903
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser) rs77615401
NM_000363.5(TNNI3):c.246G>T (p.Pro82=) rs397516343
NM_000363.5(TNNI3):c.25-4C>T rs202086705
NM_000363.5(TNNI3):c.258C>T (p.Ala86=) rs727503508
NM_000363.5(TNNI3):c.258del (p.Leu88fs) rs727503507
NM_000363.5(TNNI3):c.264G>A (p.Leu88=) rs772928416
NM_000363.5(TNNI3):c.273G>A (p.Ala91=) rs75491697
NM_000363.5(TNNI3):c.282+16_282+17delinsTT rs1555864004
NM_000363.5(TNNI3):c.282+6G>C rs1210217999
NM_000363.5(TNNI3):c.288G>C (p.Leu96Phe)
NM_000363.5(TNNI3):c.298C>T (p.Leu100Phe) rs773216333
NM_000363.5(TNNI3):c.302A>G (p.His101Arg) rs730881087
NM_000363.5(TNNI3):c.303C>T (p.His101=) rs199539066
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr) rs374618872
NM_000363.5(TNNI3):c.307C>T (p.Arg103Cys) rs397516344
NM_000363.5(TNNI3):c.308G>A (p.Arg103His) rs371000425
NM_000363.5(TNNI3):c.309T>C (p.Arg103=) rs749136271
NM_000363.5(TNNI3):c.336C>T (p.Tyr112=) rs559450042
NM_000363.5(TNNI3):c.34C>T (p.Pro12Ser)
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn) rs184709702
NM_000363.5(TNNI3):c.363C>T (p.Asn121=) rs371490136
NM_000363.5(TNNI3):c.368C>T (p.Thr123Met) rs397516345
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln) rs727503506
NM_000363.5(TNNI3):c.372+20C>T rs529338677
NM_000363.5(TNNI3):c.372+7C>T rs367809676
NM_000363.5(TNNI3):c.373-15C>G rs192630178
NM_000363.5(TNNI3):c.373-15C>T rs192630178
NM_000363.5(TNNI3):c.373-16C>T rs373508654
NM_000363.5(TNNI3):c.373-17C>T
NM_000363.5(TNNI3):c.373-4C>G rs2288530
NM_000363.5(TNNI3):c.384G>A (p.Leu128=) rs373130533
NM_000363.5(TNNI3):c.39C>G (p.Arg13=) rs397516346
NM_000363.5(TNNI3):c.401A>G (p.Asp134Gly) rs727503505
NM_000363.5(TNNI3):c.417T>C (p.Phe139=) rs1371643118
NM_000363.5(TNNI3):c.428C>A (p.Thr143Asn) rs397516348
NM_000363.5(TNNI3):c.432G>T (p.Leu144=) rs776615304
NM_000363.5(TNNI3):c.462G>A (p.Met154Ile) rs397516350
NM_000363.5(TNNI3):c.471G>A (p.Ala157=) rs747756509
NM_000363.5(TNNI3):c.474G>C (p.Leu158=) rs749880457
NM_000363.5(TNNI3):c.488C>T (p.Ala163Val) rs727504367
NM_000363.5(TNNI3):c.508C>G (p.Arg170Gly) rs727503504
NM_000363.5(TNNI3):c.525G>C (p.Gln175His) rs727503502
NM_000363.5(TNNI3):c.526G>A (p.Val176Met) rs727503501
NM_000363.5(TNNI3):c.538del (p.Asp180fs) rs876658023
NM_000363.5(TNNI3):c.539A>G (p.Asp180Gly) rs1060499912
NM_000363.5(TNNI3):c.550-10C>T rs201240150
NM_000363.5(TNNI3):c.550-12G>A
NM_000363.5(TNNI3):c.559G>A (p.Glu187Lys) rs727505069
NM_000363.5(TNNI3):c.562G>A (p.Val188Met) rs193922409
NM_000363.5(TNNI3):c.579G>C (p.Lys193Asn) rs397516358
NM_000363.5(TNNI3):c.583A>C (p.Ile195Leu) rs876658024
NM_000363.5(TNNI3):c.586G>T (p.Asp196Tyr) rs104894727
NM_000363.5(TNNI3):c.592C>G (p.Leu198Val) rs727504285
NM_000363.5(TNNI3):c.5C>T (p.Ala2Val) rs397516359
NM_000363.5(TNNI3):c.609C>T (p.Gly203=) rs587780968
NM_000363.5(TNNI3):c.610C>T (p.Arg204Cys) rs727504243
NM_000363.5(TNNI3):c.613A>C (p.Lys205Gln) rs727505331
NM_000363.5(TNNI3):c.622T>A (p.Phe208Ile) rs876658025
NM_000363.5(TNNI3):c.624T>G (p.Phe208Leu) rs876658026
NM_000363.5(TNNI3):c.625G>A (p.Glu209Lys) rs727504268
NM_000363.5(TNNI3):c.632G>T (p.Ter211Leu) rs730881084
NM_000363.5(TNNI3):c.65G>A (p.Arg22His) rs397516360
NM_000363.5(TNNI3):c.6G>A (p.Ala2=) rs397516361
NM_000363.5(TNNI3):c.79C>G (p.Arg27Gly) rs1555864366
NM_000363.5(TNNI3):c.85T>G (p.Tyr29Asp) rs727503510

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.