ClinVar Miner

List of variants in gene TNNT1 reported as likely benign

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Total variants: 65
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HGVS dbSNP
NM_003283.6(TNNT1):c.*12C>T rs547467795
NM_003283.6(TNNT1):c.-11-250A>G
NM_003283.6(TNNT1):c.-12+15G>A rs539247551
NM_003283.6(TNNT1):c.102G>A (p.Glu34=) rs766589504
NM_003283.6(TNNT1):c.106+7G>A rs990953458
NM_003283.6(TNNT1):c.107-112C>G
NM_003283.6(TNNT1):c.107-282G>T
NM_003283.6(TNNT1):c.128+17T>G rs201135309
NM_003283.6(TNNT1):c.129-269G>A
NM_003283.6(TNNT1):c.129-9T>G rs67795913
NM_003283.6(TNNT1):c.134C>T (p.Pro45Leu) rs201722303
NM_003283.6(TNNT1):c.144T>A (p.Pro48=) rs141999523
NM_003283.6(TNNT1):c.156G>A (p.Pro52=) rs369149321
NM_003283.6(TNNT1):c.183T>G (p.Val61=)
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.219A>G (p.Lys73=)
NM_003283.6(TNNT1):c.24A>G (p.Glu8=) rs1314161035
NM_003283.6(TNNT1):c.279A>G (p.Glu93=) rs34313388
NM_003283.6(TNNT1):c.294C>T (p.Ala98=) rs373544170
NM_003283.6(TNNT1):c.295T>C (p.Leu99=)
NM_003283.6(TNNT1):c.309+79G>A
NM_003283.6(TNNT1):c.309+8G>C
NM_003283.6(TNNT1):c.310-105T>A
NM_003283.6(TNNT1):c.310-4C>A rs1322730617
NM_003283.6(TNNT1):c.32+8C>T rs371750770
NM_003283.6(TNNT1):c.33-4G>A
NM_003283.6(TNNT1):c.345C>A (p.Arg115=) rs1599882425
NM_003283.6(TNNT1):c.366C>T (p.Arg122=)
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.46G>C (p.Glu16Gln) rs533504444
NM_003283.6(TNNT1):c.47-6C>G rs375682055
NM_003283.6(TNNT1):c.486C>T (p.Gly162=) rs746601153
NM_003283.6(TNNT1):c.501+18_501+19del rs1555856952
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.561C>T (p.Ser187=) rs534454139
NM_003283.6(TNNT1):c.585T>C (p.Ile195=)
NM_003283.6(TNNT1):c.611+10G>A
NM_003283.6(TNNT1):c.611+12G>A rs376456377
NM_003283.6(TNNT1):c.612-216G>A
NM_003283.6(TNNT1):c.612-228A>G rs7259126
NM_003283.6(TNNT1):c.612-4C>T
NM_003283.6(TNNT1):c.617G>A (p.Arg206Gln)
NM_003283.6(TNNT1):c.714C>T (p.Phe238=)
NM_003283.6(TNNT1):c.73+10C>G rs1257429782
NM_003283.6(TNNT1):c.73+39dup rs772892687
NM_003283.6(TNNT1):c.74-5C>T
NM_003283.6(TNNT1):c.750+15C>T rs138664823
NM_003283.6(TNNT1):c.751-5C>T rs192248377
NM_003283.6(TNNT1):c.756C>T (p.Asn252=)
NM_003283.6(TNNT1):c.78C>G (p.Pro26=)
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
NM_003283.6(TNNT1):c.87G>A (p.Pro29=) rs930840597
Single allele

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