ClinVar Miner

List of variants reported as likely benign for dilated cardiomyopathy 1D by Genome-Nilou Lab

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_001276345.2(TNNT2):c.237G>A (p.Ser79=) rs3729845 0.08311
NM_001276345.2(TNNT2):c.788A>G (p.Lys263Arg) rs3730238 0.05965
NM_001276345.2(TNNT2):c.474G>C (p.Arg158=) rs35914325 0.00788
NM_001276345.2(TNNT2):c.852-19C>T rs759855940 0.00011
NM_001276345.2(TNNT2):c.852-23A>G rs371692788 0.00010
NM_001276345.2(TNNT2):c.774C>T (p.Phe258=) rs397516481 0.00009
NM_001276345.2(TNNT2):c.430C>A (p.Arg144=) rs45525839 0.00006
NM_001276345.2(TNNT2):c.489+18C>T rs377743847 0.00006
NM_001276345.2(TNNT2):c.90C>T (p.Asp30=) rs727503515 0.00006
NM_001276345.2(TNNT2):c.567C>T (p.Ser189=) rs397516474 0.00005
NM_001276345.2(TNNT2):c.864C>T (p.Arg288=) rs45503195 0.00005
NM_001276345.2(TNNT2):c.720-13C>G rs377714587 0.00004
NM_001276345.2(TNNT2):c.882C>T (p.Thr294=) rs45465693 0.00004
NM_001276345.2(TNNT2):c.435C>T (p.Ala145=) rs375675827 0.00003
NM_001276345.2(TNNT2):c.552G>A (p.Lys184=) rs566113559 0.00003
NM_001276345.2(TNNT2):c.601-6G>A rs760197357 0.00003
NM_001276345.2(TNNT2):c.96C>T (p.Asp32=) rs751728017 0.00003
NM_001276345.2(TNNT2):c.282A>G (p.Arg94=) rs397516453 0.00002
NM_001276345.2(TNNT2):c.135G>A (p.Glu45=) rs756174289 0.00001
NM_001276345.2(TNNT2):c.144C>T (p.Thr48=) rs746492909 0.00001
NM_001276345.2(TNNT2):c.153C>G (p.Thr51=) rs1347127737 0.00001
NM_001276345.2(TNNT2):c.163+13T>C rs527486692 0.00001
NM_001276345.2(TNNT2):c.164-11G>A rs1410150306 0.00001
NM_001276345.2(TNNT2):c.192G>A (p.Glu64=) rs1180516886 0.00001
NM_001276345.2(TNNT2):c.21G>T (p.Val7=) rs777128825 0.00001
NM_001276345.2(TNNT2):c.255G>A (p.Val85=) rs780115529 0.00001
NM_001276345.2(TNNT2):c.390C>T (p.Leu130=) rs758543857 0.00001
NM_001276345.2(TNNT2):c.412-14C>A rs745721749 0.00001
NM_001276345.2(TNNT2):c.450C>T (p.Ile150=) rs200604266 0.00001
NM_001276345.2(TNNT2):c.459G>A (p.Glu153=) rs775274966 0.00001
NM_001276345.2(TNNT2):c.522C>T (p.Asn174=) rs483352833 0.00001
NM_001276345.2(TNNT2):c.720-14C>A rs761998371 0.00001
NM_001276345.2(TNNT2):c.778C>T (p.Leu260=) rs977853063 0.00001
NM_001276345.2(TNNT2):c.852-18G>A rs778928540 0.00001
NM_001276345.2(TNNT2):c.861C>A (p.Thr287=) rs754211195 0.00001
NC_000001.11:g.201369848_201369850delinsAA rs397516362
NM_001276345.2(TNNT2):c.-5A>G rs730881093
NM_001276345.2(TNNT2):c.163+12G>T rs45580032
NM_001276345.2(TNNT2):c.200-6C>T rs1659750096
NM_001276345.2(TNNT2):c.207A>G (p.Pro69=) rs531954320
NM_001276345.2(TNNT2):c.216G>A (p.Glu72=) rs2102273980
NM_001276345.2(TNNT2):c.228G>A (p.Lys76=) rs727504869
NM_001276345.2(TNNT2):c.234-10T>C rs1342160801
NM_001276345.2(TNNT2):c.237G>T (p.Ser79=) rs3729845
NM_001276345.2(TNNT2):c.255G>T (p.Val85=) rs780115529
NM_001276345.2(TNNT2):c.321G>A (p.Lys107=) rs397516459
NM_001276345.2(TNNT2):c.342G>A (p.Ala114=) rs918054429
NM_001276345.2(TNNT2):c.357C>T (p.His119=)
NM_001276345.2(TNNT2):c.41+6dup rs1479180367
NM_001276345.2(TNNT2):c.42-6T>C rs1660720268
NM_001276345.2(TNNT2):c.441G>A (p.Gln147=) rs1044313920
NM_001276345.2(TNNT2):c.444G>A (p.Gln148=) rs2102253556
NM_001276345.2(TNNT2):c.451C>A (p.Arg151=) rs74315379
NM_001276345.2(TNNT2):c.453G>C (p.Arg151=) rs786204406
NM_001276345.2(TNNT2):c.570C>T (p.Asn190=) rs764636823
NM_001276345.2(TNNT2):c.719+13A>C rs563883763
NM_001276345.2(TNNT2):c.720-10G>A rs2102229886
NM_001276345.2(TNNT2):c.720-6G>T rs113471285
NM_001276345.2(TNNT2):c.834C>T (p.Ile278=) rs1278830616
NM_001276345.2(TNNT2):c.885G>A (p.Gly295=) rs2102212901
NM_001276345.2(TNNT2):c.897G>A (p.Ter299=) rs1311267989

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