ClinVar Miner

Variants in gene MYH14 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 47
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HGVS dbSNP gnomAD frequency
NM_001145809.2(MYH14):c.483G>A (p.Met161Ile) rs34773557 0.01615
NM_001145809.2(MYH14):c.2792G>A (p.Arg931His) rs200351672 0.00460
NM_001145809.2(MYH14):c.826A>G (p.Ile276Val) rs55645295 0.00445
NM_001145809.2(MYH14):c.1330-17T>C rs146235441 0.00346
NM_001145809.2(MYH14):c.4586G>A (p.Arg1529His) rs185232438 0.00309
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys) rs119103280 0.00303
NM_001145809.2(MYH14):c.1034C>G (p.Ser345Cys) rs35315400 0.00249
NM_001145809.2(MYH14):c.5227C>T (p.Leu1743=) rs147447646 0.00218
NM_001145809.2(MYH14):c.3079C>T (p.Leu1027=) rs113152264 0.00210
NM_001145809.2(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363 0.00158
NM_001145809.2(MYH14):c.5127+10G>A rs370928889 0.00153
NM_001145809.2(MYH14):c.5573G>A (p.Arg1858His) rs11882073 0.00137
NM_001145809.2(MYH14):c.4094G>A (p.Ser1365Asn) rs202225655 0.00134
NM_001145809.2(MYH14):c.1944C>T (p.Asp648=) rs189243324 0.00120
NM_001145809.2(MYH14):c.36G>A (p.Lys12=) rs372741317 0.00100
NM_001145809.2(MYH14):c.1275C>T (p.Thr425=) rs149221129 0.00098
NM_001145809.2(MYH14):c.2432C>T (p.Ala811Val) rs201337011 0.00093
NM_001145809.2(MYH14):c.1992G>A (p.Pro664=) rs192745436 0.00086
NM_001145809.2(MYH14):c.5991G>A (p.Thr1997=) rs181567755 0.00084
NM_001145809.2(MYH14):c.615G>A (p.Thr205=) rs199921330 0.00083
NM_001145809.2(MYH14):c.4617T>G (p.Arg1539=) rs375866139 0.00075
NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser) rs199910006 0.00071
NM_001145809.2(MYH14):c.2680C>A (p.Arg894=) rs34805056 0.00062
NM_001145809.2(MYH14):c.5683C>T (p.Arg1895Cys) rs200485394 0.00062
NM_001145809.2(MYH14):c.693+10C>T rs186027440 0.00057
NM_001145809.2(MYH14):c.5778C>T (p.Leu1926=) rs201839634 0.00039
NM_001145809.2(MYH14):c.1224C>T (p.Leu408=) rs145163585 0.00037
NM_001145809.2(MYH14):c.1115-4C>T rs142696359 0.00036
NM_001145809.2(MYH14):c.4753-5A>G rs118097099 0.00036
NM_001145809.2(MYH14):c.2233-13C>A rs368249273 0.00034
NM_001145809.2(MYH14):c.4138-13C>T rs183327883 0.00034
NM_001145809.2(MYH14):c.5960+8C>T rs373176553 0.00034
NM_001145809.2(MYH14):c.3871G>T (p.Val1291Leu) rs202242879 0.00024
NM_001145809.2(MYH14):c.2331C>T (p.Ile777=) rs746261612 0.00014
NM_001145809.2(MYH14):c.5103G>A (p.Ala1701=) rs375599200 0.00012
NM_001145809.2(MYH14):c.5447G>A (p.Arg1816His) rs201923258 0.00009
NM_001145809.2(MYH14):c.2334C>A (p.Leu778=) rs190941610 0.00006
NM_001145809.2(MYH14):c.3172-12T>C rs374486787 0.00006
NM_001145809.2(MYH14):c.3537C>T (p.Ala1179=) rs559356437 0.00005
NM_001145809.2(MYH14):c.5964C>T (p.Arg1988=) rs768413723 0.00005
NM_001145809.2(MYH14):c.4296C>T (p.Ser1432=) rs370811348 0.00004
NM_001145809.2(MYH14):c.1251G>A (p.Thr417=) rs759132835 0.00002
NM_001145809.2(MYH14):c.1205A>G (p.Asn402Ser) rs537153044 0.00001
NM_001145809.2(MYH14):c.4283A>G (p.Gln1428Arg) rs368069617 0.00001
NM_001145809.2(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.2(MYH14):c.5083G>C (p.Gly1695Arg) rs199915414
NM_001145809.2(MYH14):c.660G>T (p.Ser220=) rs201835322

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