ClinVar Miner

List of variants in gene MYH14 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Total variants: 74
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HGVS dbSNP
NM_001145809.1(MYH14):c.5227C>T (p.Leu1743=) rs147447646
NM_024729.3(MYH14):c.*142C>G rs770209944
NM_024729.3(MYH14):c.*144C>T rs773312540
NM_024729.3(MYH14):c.*243G>A rs561898739
NM_024729.3(MYH14):c.*337C>T rs753307318
NM_024729.3(MYH14):c.*400T>C rs886054596
NM_024729.3(MYH14):c.*400_*403delTCTC rs376379600
NM_024729.3(MYH14):c.*402_*403dupTC rs376379600
NM_024729.3(MYH14):c.*474A>G rs886054597
NM_024729.3(MYH14):c.*531C>T rs886054598
NM_024729.3(MYH14):c.*64G>A rs779130953
NM_024729.3(MYH14):c.*667G>A rs886054599
NM_024729.3(MYH14):c.*81A>G rs772326631
NM_024729.3(MYH14):c.-3-6C>T rs886054586
NM_024729.3(MYH14):c.-37C>T rs549250648
NM_024729.3(MYH14):c.-4+8C>A rs778355560
NM_024729.3(MYH14):c.1002G>A (p.Pro334=) rs368124508
NM_024729.3(MYH14):c.1090+13C>G rs11666328
NM_024729.3(MYH14):c.1271G>A (p.Arg424Gln) rs751011647
NM_024729.3(MYH14):c.1395C>T (p.Arg465=) rs371946306
NM_024729.3(MYH14):c.1755G>A (p.Pro585=) rs557237074
NM_024729.3(MYH14):c.1776C>T (p.Ala592=) rs745625855
NM_024729.3(MYH14):c.1945C>G (p.Gln649Glu) rs370124751
NM_024729.3(MYH14):c.1963G>A (p.Asp655Asn) rs539256005
NM_024729.3(MYH14):c.1966G>A (p.Gly656Ser) rs778416774
NM_024729.3(MYH14):c.2003G>A (p.Arg668Gln) rs766802012
NM_024729.3(MYH14):c.2110-13C>A rs368249273
NM_024729.3(MYH14):c.2148T>C (p.Leu716=) rs371266692
NM_024729.3(MYH14):c.2156A>G (p.Asn719Ser) rs886054589
NM_024729.3(MYH14):c.2211C>A (p.Leu737=) rs190941610
NM_024729.3(MYH14):c.2309C>T (p.Ala770Val) rs201337011
NM_024729.3(MYH14):c.2364G>A (p.Arg788=) rs746813925
NM_024729.3(MYH14):c.2625C>T (p.Ala875=) rs886054590
NM_024729.3(MYH14):c.2741G>A (p.Arg914Gln) rs576611342
NM_024729.3(MYH14):c.2818G>A (p.Val940Met) rs886054591
NM_024729.3(MYH14):c.2975C>T (p.Thr992Met) rs201746408
NM_024729.3(MYH14):c.3018C>T (p.Leu1006=) rs886054592
NM_024729.3(MYH14):c.3049-12T>C rs374486787
NM_024729.3(MYH14):c.3084C>G (p.Phe1028Leu) rs886054593
NM_024729.3(MYH14):c.3136C>T (p.Arg1046Trp) rs368372273
NM_024729.3(MYH14):c.3304C>T (p.Leu1102=) rs770366755
NM_024729.3(MYH14):c.3470A>T (p.Gln1157Leu) rs755161446
NM_024729.3(MYH14):c.3581C>T (p.Thr1194Met) rs200988515
NM_024729.3(MYH14):c.3655G>A (p.Gly1219Ser) rs200272339
NM_024729.3(MYH14):c.3696C>T (p.Ala1232=) rs750779364
NM_024729.3(MYH14):c.36G>A (p.Lys12=) rs372741317
NM_024729.3(MYH14):c.3702+2T>G
NM_024729.3(MYH14):c.3727C>T (p.Arg1243Trp) rs201515738
NM_024729.3(MYH14):c.3748G>T (p.Val1250Leu) rs202242879
NM_024729.3(MYH14):c.3790C>T (p.Arg1264Cys) rs755704452
NM_024729.3(MYH14):c.3822G>A (p.Leu1274=) rs769999356
NM_024729.3(MYH14):c.4097G>A (p.Arg1366His) rs553162373
NM_024729.3(MYH14):c.4173C>T (p.Ser1391=) rs370811348
NM_024729.3(MYH14):c.440C>T (p.Pro147Leu) rs886054587
NM_024729.3(MYH14):c.4416+10C>T rs561531825
NM_024729.3(MYH14):c.4487G>A (p.Arg1496Gln) rs752388019
NM_024729.3(MYH14):c.4558G>A (p.Glu1520Lys) rs761025607
NM_024729.3(MYH14):c.4570C>A (p.Arg1524=) rs769989306
NM_024729.3(MYH14):c.4608C>T (p.Ser1536=) rs766728732
NM_024729.3(MYH14):c.4650C>T (p.Ala1550=) rs746906367
NM_024729.3(MYH14):c.4918G>A (p.Glu1640Lys) rs556548077
NM_024729.3(MYH14):c.5004+12C>T rs373755483
NM_024729.3(MYH14):c.526G>A (p.Ala176Thr) rs138001307
NM_024729.3(MYH14):c.5324G>A (p.Arg1775His) rs201923258
NM_024729.3(MYH14):c.535G>A (p.Glu179Lys) rs886054588
NM_024729.3(MYH14):c.543C>T (p.Ala181=) rs746669662
NM_024729.3(MYH14):c.5476C>T (p.Arg1826Cys) rs187789045
NM_024729.3(MYH14):c.565C>T (p.Arg189Cys) rs200818171
NM_024729.3(MYH14):c.5679C>A (p.Asn1893Lys) rs745991888
NM_024729.3(MYH14):c.5735G>A (p.Arg1912Gln) rs754203387
NM_024729.3(MYH14):c.5838-10C>T rs776693090
NM_024729.3(MYH14):c.5867C>T (p.Thr1956Met) rs201986144
NM_024729.3(MYH14):c.5C>T (p.Ala2Val) rs750407725
NM_024729.3(MYH14):c.842T>C (p.Ile281Thr) rs777836668

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