ClinVar Miner

List of variants in gene TNNT1 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_003283.6(TNNT1):c.*110T>C
NM_003283.6(TNNT1):c.*129C>G
NM_003283.6(TNNT1):c.-12+15G>A rs539247551
NM_003283.6(TNNT1):c.279A>G (p.Glu93=) rs34313388
NM_003283.6(TNNT1):c.310-14T>C rs115663668
NM_003283.6(TNNT1):c.34G>C (p.Glu12Gln) rs748000993
NM_003283.6(TNNT1):c.355G>A (p.Glu119Lys) rs752992299
NM_003283.6(TNNT1):c.366C>T (p.Arg122=)
NM_003283.6(TNNT1):c.47-6C>G rs375682055
NM_003283.6(TNNT1):c.487G>A (p.Gly163Ser)
NM_003283.6(TNNT1):c.535C>T (p.Arg179Trp) rs757227738
NM_003283.6(TNNT1):c.580G>A (p.Asp194Asn) rs141774400
NM_003283.6(TNNT1):c.611+12G>A rs376456377
NM_003283.6(TNNT1):c.611+12G>T rs376456377
NM_003283.6(TNNT1):c.73+15T>G rs759885491
NM_003283.6(TNNT1):c.73G>A (p.Ala25Thr)
NM_003283.6(TNNT1):c.750+15C>T rs138664823
NM_003283.6(TNNT1):c.751-5C>T rs192248377
NM_003283.6(TNNT1):c.757G>A (p.Val253Met) rs572119503
NM_003283.6(TNNT1):c.791+12C>T rs201143291

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