ClinVar Miner

List of variants reported as uncertain significance for dilated cardiomyopathy 1A

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 81
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HGVS dbSNP
NM_000116.5(TAZ):c.657C>G (p.Asp219Glu)
NM_000117.3(EMD):c.19C>T (p.Leu7Phe)
NM_000256.3(MYBPC3):c.2956A>G (p.Lys986Glu) rs876657871
NM_000256.3(MYBPC3):c.3224C>G (p.Thr1075Ser) rs150786409
NM_000256.3(MYBPC3):c.478C>T (p.Arg160Trp) rs193068692
NM_000256.3(MYBPC3):c.604A>C (p.Lys202Gln) rs730880623
NM_000257.4(MYH7):c.3676C>G (p.Leu1226Val) rs876661211
NM_000257.4(MYH7):c.4832C>T (p.Ala1611Val) rs757090529
NM_000335.5(SCN5A):c.2819G>A (p.Ser940Asn)
NM_001103.4(ACTN2):c.463G>A (p.Glu155Lys)
NM_001134363.3(RBM20):c.1027C>T (p.His343Tyr) rs112226602
NM_001134363.3(RBM20):c.2588C>G (p.Pro863Arg) rs794729153
NM_001134363.3(RBM20):c.2989G>A (p.Val997Met) rs372370653
NM_001134363.3(RBM20):c.3044C>T (p.Thr1015Ile) rs183770014
NM_001267550.2(TTN):c.96904G>A (p.Val32302Met) rs1339368168
NM_001282625.2(LMNA):c.-206-17C>T
NM_001927.4(DES):c.1123C>T (p.Arg375Trp) rs375218723
NM_001943.5(DSG2):c.2768C>G (p.Pro923Arg)
NM_002471.3(MYH6):c.5278G>A (p.Ala1760Thr) rs146539406
NM_002471.4(MYH6):c.2401A>G (p.Ile801Val) rs75487328
NM_004006.2(DMD):c.3004A>T (p.Thr1002Ser) rs1244241099
NM_004006.2(DMD):c.3419A>T (p.His1140Leu) rs201297190
NM_004415.4(DSP):c.3661A>G (p.Ile1221Val) rs794728120
NM_004415.4(DSP):c.5173C>T (p.Arg1725Trp) rs200336897
NM_004415.4(DSP):c.7850G>A (p.Ser2617Asn)
NM_005159.5(ACTC1):c.455G>A (p.Gly152Asp)
NM_005159.5(ACTC1):c.854T>A (p.Met285Lys)
NM_005572.3(LMNA):c.-210T>C rs886045356
NM_005572.3(LMNA):c.-226C>T rs886045354
NM_007078.3(LDB3):c.1051A>G (p.Thr351Ala) rs138251566
NM_007078.3(LDB3):c.1225C>A (p.Gln409Lys) rs139104492
NM_007078.3(LDB3):c.566C>T (p.Ser189Leu) rs45487699
NM_014391.3(ANKRD1):c.368C>T (p.Thr123Met) rs145387010
NM_020297.3(ABCC9):c.1987C>T (p.Arg663Cys) rs200349671
NM_024422.6(DSC2):c.1281A>C (p.Glu427Asp)
NM_032578.4(MYPN):c.1103G>A (p.Gly368Asp)
NM_032578.4(MYPN):c.2476C>A (p.Pro826Thr)
NM_032578.4(MYPN):c.3763G>A (p.Val1255Met) rs750655311
NM_144573.3(NEXN):c.1271C>T (p.Thr424Ile) rs200442502
NM_144573.4(NEXN):c.1073C>T (p.Pro358Leu)
NM_144573.4(NEXN):c.1695C>G (p.Ile565Met)
NM_144573.4(NEXN):c.460A>G (p.Asn154Asp)
NM_170707.4(LMNA):c.-138T>C rs886045359
NM_170707.4(LMNA):c.-44T>A
NM_170707.4(LMNA):c.1027C>T (p.Arg343Trp) rs749784223
NM_170707.4(LMNA):c.1070A>T (p.Asp357Val) rs1131690785
NM_170707.4(LMNA):c.1123G>A (p.Ala375Thr) rs879254162
NM_170707.4(LMNA):c.1227A>G (p.Thr409=) rs762130433
NM_170707.4(LMNA):c.1243G>A (p.Val415Ile) rs267607606
NM_170707.4(LMNA):c.1324G>A (p.Val442Met) rs368542816
NM_170707.4(LMNA):c.1338T>G (p.Asp446Glu)
NM_170707.4(LMNA):c.1358G>A (p.Arg453Gln) rs267607598
NM_170707.4(LMNA):c.1381-5G>A rs730880133
NM_170707.4(LMNA):c.1445G>T (p.Arg482Leu) rs11575937
NM_170707.4(LMNA):c.1487C>T (p.Thr496Met) rs200466188
NM_170707.4(LMNA):c.1488+14C>T rs377700689
NM_170707.4(LMNA):c.1517A>C (p.His506Pro) rs878855233
NM_170707.4(LMNA):c.1567G>A (p.Gly523Arg) rs201583907
NM_170707.4(LMNA):c.1634G>A (p.Arg545His) rs142191737
NM_170707.4(LMNA):c.1698+57G>A rs557334569
NM_170707.4(LMNA):c.1698+83G>A
NM_170707.4(LMNA):c.1756G>A (p.Val586Met) rs758048062
NM_170707.4(LMNA):c.1930C>T (p.Arg644Cys) rs142000963
NM_170707.4(LMNA):c.193G>C (p.Glu65Gln)
NM_170707.4(LMNA):c.294G>A (p.Glu98=) rs886045363
NM_170707.4(LMNA):c.295C>A (p.Arg99Ser) rs886045364
NM_170707.4(LMNA):c.350A>G (p.Lys117Arg) rs397517901
NM_170707.4(LMNA):c.356+12C>A
NM_170707.4(LMNA):c.357C>T (p.Arg119=) rs41313880
NM_170707.4(LMNA):c.398G>A (p.Arg133Gln) rs60864230
NM_170707.4(LMNA):c.471G>A (p.Thr157=) rs150645079
NM_170707.4(LMNA):c.514-11C>T rs886045365
NM_170707.4(LMNA):c.749C>T (p.Ala250Val) rs397517907
NM_170707.4(LMNA):c.796A>G (p.Thr266Ala)
NM_170707.4(LMNA):c.811-13T>A rs80356809
NM_170707.4(LMNA):c.937-8C>A rs751707982
NM_170707.4(LMNA):c.953C>T (p.Ala318Val) rs1212920276
NM_170707.4(LMNA):c.976T>A (p.Ser326Thr) rs56851164
NM_170707.4(LMNA):c.985C>G (p.Arg329Gly) rs775159300
NM_172244.3(SGCD):c.771A>C (p.Ter257Cys) rs376317697
NM_198056.2(SCN5A):c.1109C>T (p.Thr370Met) rs199473099

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