ClinVar Miner

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

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 45
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HGVS dbSNP gnomAD frequency
NM_001145809.2(MYH14):c.4033G>A (p.Ala1345Thr) rs148054042 0.00104
NM_001145809.2(MYH14):c.615G>A (p.Thr205=) rs199921330 0.00083
NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser) rs199910006 0.00071
NM_001145809.2(MYH14):c.1919G>A (p.Arg640Gln) rs199696801 0.00052
NM_001145809.2(MYH14):c.4705G>T (p.Ala1569Ser) rs145522874 0.00038
NM_001145809.2(MYH14):c.3850C>T (p.Arg1284Trp) rs201515738 0.00037
NM_001145809.2(MYH14):c.1115-4C>T rs142696359 0.00036
NM_001145809.2(MYH14):c.2233-13C>A rs368249273 0.00034
NM_001145809.2(MYH14):c.1427G>A (p.Arg476His) rs375694189 0.00033
NM_001145809.2(MYH14):c.5452C>T (p.Arg1818Cys) rs377096949 0.00029
NM_001145809.2(MYH14):c.5599C>T (p.Arg1867Cys) rs187789045 0.00029
NM_001145809.2(MYH14):c.838G>A (p.Val280Ile) rs202246093 0.00028
NM_001145809.2(MYH14):c.820A>G (p.Ile274Val) rs200424400 0.00027
NM_001145809.2(MYH14):c.4028C>T (p.Ala1343Val) rs374058410 0.00017
NM_001145809.2(MYH14):c.3098C>T (p.Thr1033Met) rs201746408 0.00015
NM_001145809.2(MYH14):c.4827G>A (p.Leu1609=) rs201418071 0.00014
NM_001145809.2(MYH14):c.526G>A (p.Ala176Thr) rs138001307 0.00014
NM_001145809.2(MYH14):c.1229G>A (p.Arg410His) rs374720181 0.00013
NM_001145809.2(MYH14):c.2864G>A (p.Arg955Gln) rs576611342 0.00013
NM_001145809.2(MYH14):c.4740C>T (p.Asp1580=) rs751909208 0.00013
NM_001145809.2(MYH14):c.4752C>T (p.Ser1584=) rs377081835 0.00013
NM_001145809.2(MYH14):c.810C>T (p.Phe270=) rs374146214 0.00013
NM_001145809.2(MYH14):c.3819C>T (p.Ala1273=) rs750779364 0.00012
NM_001145809.2(MYH14):c.4445G>A (p.Arg1482Gln) rs746594902 0.00012
NM_001145809.2(MYH14):c.5876G>A (p.Arg1959Gln) rs200878464 0.00012
NM_001145809.2(MYH14):c.3304C>T (p.Arg1102Trp) rs397516629 0.00011
NM_001145809.2(MYH14):c.4731C>T (p.Ser1577=) rs766728732 0.00011
NM_001145809.2(MYH14):c.1918C>T (p.Arg640Trp) rs376267080 0.00010
NM_001145809.2(MYH14):c.693C>T (p.Pro231=) rs373744231 0.00009
NM_001145809.2(MYH14):c.3778G>A (p.Gly1260Ser) rs200272339 0.00008
NM_001145809.2(MYH14):c.3623C>T (p.Ala1208Val) rs758560911 0.00005
NM_001145809.2(MYH14):c.4220G>A (p.Arg1407His) rs553162373 0.00005
NM_001145809.2(MYH14):c.5105T>C (p.Val1702Ala) rs775130663 0.00004
NM_001145809.2(MYH14):c.543C>T (p.Ala181=) rs746669662 0.00004
NM_001145809.2(MYH14):c.68C>T (p.Ala23Val) rs765789880 0.00004
NM_001145809.2(MYH14):c.3884G>A (p.Arg1295Gln) rs377014092 0.00003
NM_001145809.2(MYH14):c.4903G>A (p.Glu1635Lys) rs140157424 0.00003
NM_001145809.2(MYH14):c.4259C>T (p.Ala1420Val) rs727503225 0.00002
NM_001145809.2(MYH14):c.5566C>T (p.Arg1856Trp) rs539875477 0.00002
NM_001145809.2(MYH14):c.3194G>A (p.Arg1065His) rs769362736 0.00001
NM_001145809.2(MYH14):c.94C>T (p.Arg32Cys) rs549293063 0.00001
NM_001145809.2(MYH14):c.1625T>G (p.Leu542Arg) rs727504564
NM_001145809.2(MYH14):c.2599C>T (p.Arg867Cys) rs753356694
NM_001145809.2(MYH14):c.4539+14G>A rs779431768
NM_001145809.2(MYH14):c.594A>T (p.Gly198=) rs1195002362

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