ClinVar Miner

List of variants in gene TNNT2 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_000364.4(TNNT2):c.-1C>A rs776936911
NM_000364.4(TNNT2):c.-22G>C rs886045829
NM_000364.4(TNNT2):c.-22G>T rs886045829
NM_000364.4(TNNT2):c.233+6T>C rs397516449
NM_000364.4(TNNT2):c.270C>G (p.Pro90=) rs140245123
NM_000364.4(TNNT2):c.52+7G>A rs374443596
NM_000364.4(TNNT2):c.544G>T (p.Ala182Ser) rs730881097
NM_000364.4(TNNT2):c.601-380C>T rs397516475
NM_000364.4(TNNT2):c.682A>G (p.Ile228Val) rs886045828
NM_000364.4(TNNT2):c.683T>C (p.Ile228Thr) rs45520032
NM_000364.4(TNNT2):c.711-5T>G rs730881092
NM_000364.4(TNNT2):c.711-9C>A rs763204242
NM_000364.4(TNNT2):c.753G>T (p.Glu251Asp) rs45466197

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