ClinVar Miner

List of variants in gene TNNT1 reported as likely benign for not provided

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Total variants: 33
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HGVS dbSNP
NM_003283.6(TNNT1):c.-11-250A>G
NM_003283.6(TNNT1):c.102G>A (p.Glu34=) rs766589504
NM_003283.6(TNNT1):c.107-112C>G
NM_003283.6(TNNT1):c.107-282G>T
NM_003283.6(TNNT1):c.129-269G>A
NM_003283.6(TNNT1):c.156G>A (p.Pro52=) rs369149321
NM_003283.6(TNNT1):c.193-218dup
NM_003283.6(TNNT1):c.193-24A>C
NM_003283.6(TNNT1):c.193-42C>G rs73060953
NM_003283.6(TNNT1):c.279A>G (p.Glu93=) rs34313388
NM_003283.6(TNNT1):c.309+79G>A
NM_003283.6(TNNT1):c.310-105T>A
NM_003283.6(TNNT1):c.345C>A (p.Arg115=) rs1599882425
NM_003283.6(TNNT1):c.387+152G>A rs149119868
NM_003283.6(TNNT1):c.387+165T>G
NM_003283.6(TNNT1):c.387+280G>T
NM_003283.6(TNNT1):c.388-296G>A
NM_003283.6(TNNT1):c.486C>T (p.Gly162=) rs746601153
NM_003283.6(TNNT1):c.501+284T>C
NM_003283.6(TNNT1):c.501+71C>T rs115866474
NM_003283.6(TNNT1):c.502-199C>G
NM_003283.6(TNNT1):c.612-216G>A
NM_003283.6(TNNT1):c.612-228A>G rs7259126
NM_003283.6(TNNT1):c.73+10C>G rs1257429782
NM_003283.6(TNNT1):c.750+15C>T rs138664823
NM_003283.6(TNNT1):c.751-5C>T rs192248377
NM_003283.6(TNNT1):c.791+12C>T rs201143291
NM_003283.6(TNNT1):c.791+206T>A
NM_003283.6(TNNT1):c.792-111G>T
NM_003283.6(TNNT1):c.792-214A>C
NM_003283.6(TNNT1):c.792-243C>T
NM_003283.6(TNNT1):c.834G>A (p.Lys278=) rs929705577
Single allele

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