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: 10
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HGVS dbSNP
NM_001145809.2(MYH14):c.1115-4C>T rs142696359
NM_001145809.2(MYH14):c.1427G>A (p.Arg476His)
NM_001145809.2(MYH14):c.1918C>T (p.Arg640Trp) rs376267080
NM_001145809.2(MYH14):c.1919G>A (p.Arg640Gln) rs199696801
NM_001145809.2(MYH14):c.3778G>A (p.Gly1260Ser) rs200272339
NM_001145809.2(MYH14):c.3819C>T (p.Ala1273=) rs750779364
NM_001145809.2(MYH14):c.4033G>A (p.Ala1345Thr) rs148054042
NM_001145809.2(MYH14):c.4705G>T (p.Ala1569Ser) rs145522874
NM_001145809.2(MYH14):c.4740C>T (p.Asp1580=) rs751909208
NM_001145809.2(MYH14):c.820A>G (p.Ile274Val) rs200424400

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