ClinVar Miner

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

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 24
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HGVS dbSNP
NM_001145809.2(MYH14):c.1034C>G (p.Ser345Cys) rs35315400
NM_001145809.2(MYH14):c.1115-4C>T rs142696359
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys) rs119103280
NM_001145809.2(MYH14):c.1205A>G (p.Asn402Ser) rs537153044
NM_001145809.2(MYH14):c.1275C>T (p.Thr425=) rs149221129
NM_001145809.2(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.2(MYH14):c.1944C>T (p.Asp648=) rs189243324
NM_001145809.2(MYH14):c.2432C>T (p.Ala811Val) rs201337011
NM_001145809.2(MYH14):c.2680C>A (p.Arg894=) rs34805056
NM_001145809.2(MYH14):c.3079C>T (p.Leu1027=) rs113152264
NM_001145809.2(MYH14):c.3537C>T (p.Ala1179=) rs559356437
NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser) rs199910006
NM_001145809.2(MYH14):c.4586G>A (p.Arg1529His) rs185232438
NM_001145809.2(MYH14):c.4617T>G (p.Arg1539=) rs375866139
NM_001145809.2(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363
NM_001145809.2(MYH14):c.5083G>C (p.Gly1695Arg) rs199915414
NM_001145809.2(MYH14):c.5127+10G>A rs370928889
NM_001145809.2(MYH14):c.5227C>T (p.Leu1743=) rs147447646
NM_001145809.2(MYH14):c.5573G>A (p.Arg1858His) rs11882073
NM_001145809.2(MYH14):c.5683C>T (p.Arg1895Cys) rs200485394
NM_001145809.2(MYH14):c.5778C>T (p.Leu1926=) rs201839634
NM_001145809.2(MYH14):c.5960+8C>T rs373176553
NM_001145809.2(MYH14):c.5964C>T (p.Arg1988=) rs768413723
NM_001145809.2(MYH14):c.826A>G (p.Ile276Val) rs55645295

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