ClinVar Miner

List of variants in gene MYH14 reported by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Total variants: 37
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HGVS dbSNP
NM_001145809.2(MYH14):c.1006C>T (p.Arg336Trp) rs371272700
NM_001145809.2(MYH14):c.1115-4C>T rs142696359
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys) rs119103280
NM_001145809.2(MYH14):c.1436C>A (p.Ala479Asp) rs886044300
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.24G>T (p.Val8=)
NM_001145809.2(MYH14):c.2763A>G (p.Lys921=) rs191788683
NM_001145809.2(MYH14):c.2792G>A (p.Arg931His) rs200351672
NM_001145809.2(MYH14):c.2841C>T (p.Arg947=) rs138987081
NM_001145809.2(MYH14):c.3079C>T (p.Leu1027=) rs113152264
NM_001145809.2(MYH14):c.3363G>C (p.Glu1121Asp) rs374915603
NM_001145809.2(MYH14):c.33G>C (p.Arg11=) rs8106196
NM_001145809.2(MYH14):c.3401A>G (p.Gln1134Arg)
NM_001145809.2(MYH14):c.3468-3C>T rs78192108
NM_001145809.2(MYH14):c.3642G>A (p.Glu1214=) rs886044561
NM_001145809.2(MYH14):c.3663C>T (p.Asn1221=) rs78573213
NM_001145809.2(MYH14):c.3680+9C>T rs76579307
NM_001145809.2(MYH14):c.3749C>A (p.Ala1250Glu) rs11669191
NM_001145809.2(MYH14):c.3884G>A (p.Arg1295Gln) rs377014092
NM_001145809.2(MYH14):c.3940C>T (p.Arg1314Cys) rs776550700
NM_001145809.2(MYH14):c.4445G>A (p.Arg1482Gln) rs746594902
NM_001145809.2(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363
NM_001145809.2(MYH14):c.4740C>T (p.Asp1580=) rs751909208
NM_001145809.2(MYH14):c.4808G>A (p.Arg1603Gln) rs886043615
NM_001145809.2(MYH14):c.483G>A (p.Met161Ile) rs34773557
NM_001145809.2(MYH14):c.487C>T (p.Arg163Trp) rs373470153
NM_001145809.2(MYH14):c.5215C>A (p.Arg1739Ser) rs761663501
NM_001145809.2(MYH14):c.5401G>A (p.Glu1801Lys)
NM_001145809.2(MYH14):c.5452C>T (p.Arg1818Cys) rs377096949
NM_001145809.2(MYH14):c.5573G>A (p.Arg1858His) rs11882073
NM_001145809.2(MYH14):c.615G>A (p.Thr205=) rs199921330
NM_001145809.2(MYH14):c.660G>T (p.Ser220=) rs201835322
NM_001145809.2(MYH14):c.731G>A (p.Arg244Gln) rs767108206
NM_001145809.2(MYH14):c.752C>A (p.Pro251His) rs779215539
NM_001145809.2(MYH14):c.820A>G (p.Ile274Val) rs200424400

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