"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "MYH14"[ - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 44065	NM_001145809.2(MYH14):c.33G>C (p.Arg11=)	MYH14	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 329904	NM_001145809.2(MYH14):c.36G>A (p.Lys12=)	MYH14	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 4A +1 more	GBenign/Likely benign
Select item 1412598	NM_001145809.2(MYH14):c.38C>T (p.Ala13Val)	MYH14 (A13V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1308322	NM_001145809.2(MYH14):c.68C>T (p.Ala23Val)	MYH14 (A23V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2880223	NM_001145809.2(MYH14):c.69G>A (p.Ala23=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1376225	NM_001145809.2(MYH14):c.71C>T (p.Ala24Val)	MYH14 (A24V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 44081	NM_001145809.2(MYH14):c.91C>A (p.Pro31Thr)	MYH14 (P31T)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 4A +2 more	GBenign
Select item 2129989	NM_001145809.2(MYH14):c.95G>A (p.Arg32His)	MYH14 (R32H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2158905	NM_001145809.2(MYH14):c.96C>T (p.Arg32=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2903272	NM_001145809.2(MYH14):c.110G>C (p.Gly37Ala)	MYH14 (G37A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2122880	NM_001145809.2(MYH14):c.115G>A (p.Gly39Arg)	MYH14 (G39R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2807469	NM_001145809.2(MYH14):c.157C>T (p.Arg53Trp)	MYH14 (R53W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2091435	NM_001145809.2(MYH14):c.158G>C (p.Arg53Pro)	MYH14 (R53P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1495050	NM_001145809.2(MYH14):c.158G>A (p.Arg53Gln)	MYH14 (R53Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1954388	NM_001145809.2(MYH14):c.161G>A (p.Arg54His)	MYH14 (R54H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2713469	NM_001145809.2(MYH14):c.181G>C (p.Glu61Gln)	MYH14 (E61Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 44052	NM_001145809.2(MYH14):c.192G>T (p.Gly64=)	MYH14	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 2869287	NM_001145809.2(MYH14):c.206C>A (p.Ala69Glu)	MYH14 (A69E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1373751	NM_001145809.2(MYH14):c.230A>C (p.Glu77Ala)	MYH14 (E77A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2871720	NM_001145809.2(MYH14):c.234G>A (p.Ala78=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2726333	NM_001145809.2(MYH14):c.238_243del (p.Val80_Glu81del)	MYH14	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2121815	NM_001145809.2(MYH14):c.260G>C (p.Arg87Thr)	MYH14 (R87T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2900653	NM_001145809.2(MYH14):c.262C>T (p.Arg88Trp)	MYH14 (R88W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 521868	NM_001145809.2(MYH14):c.266T>C (p.Leu89Pro)	MYH14 (L89P)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 2799544	NM_001145809.2(MYH14):c.275C>T (p.Pro92Leu)	MYH14 (P92L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 727036	NM_001145809.2(MYH14):c.276G>A (p.Pro92=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2808727	NM_001145809.2(MYH14):c.285G>C (p.Gln95His)	MYH14 (Q95H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 808623	NM_001145809.2(MYH14):c.293G>A (p.Arg98His)	MYH14 (R98H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1536210	NM_001145809.2(MYH14):c.321C>A (p.Ala107=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 791659	NM_001145809.2(MYH14):c.327C>T (p.Asp109=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2728851	NM_001145809.2(MYH14):c.333C>T (p.Ala111=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 740370	NM_001145809.2(MYH14):c.351C>T (p.Asn117=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2200	NM_001145809.2(MYH14):c.359C>T (p.Ser120Leu)	MYH14 (S120L)	Single nucleotide variant (missense variant)	MYH14-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 2419302	NM_001145809.2(MYH14):c.377G>A (p.Arg126Gln)	MYH14 (R126Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 892760	NM_001145809.2(MYH14):c.393C>T (p.Ser131=)	MYH14	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 178410	NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser)	MYH14 (G132S)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1619860	NM_001145809.2(MYH14):c.405+12C>T	MYH14	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2066040	NM_001145809.2(MYH14):c.405+18G>C	MYH14	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1940034	NM_001145809.2(MYH14):c.406-18C>T	MYH14	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 723857	NM_001145809.2(MYH14):c.408G>A (p.Thr136=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2991437	NM_001145809.2(MYH14):c.441G>A (p.Pro147=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 44071	NM_001145809.2(MYH14):c.474T>C (p.Ile158=)	MYH14	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 4A +2 more	GBenign
Select item 44073	NM_001145809.2(MYH14):c.483G>A (p.Met161Ile)	MYH14 (M161I)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 1698510	NM_001145809.2(MYH14):c.488G>A (p.Arg163Gln)	MYH14 (R163Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1476426	NM_001145809.2(MYH14):c.500G>A (p.Arg167His)	MYH14 (R167H)	Single nucleotide variant (missense variant)	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome +1 more	GUncertain significance
Select item 1904883	NM_001145809.2(MYH14):c.504C>T (p.His168=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2177025	NM_001145809.2(MYH14):c.519C>T (p.His173=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1449461	NM_001145809.2(MYH14):c.520G>A (p.Val174Met)	MYH14 (V174M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2901574	NM_001145809.2(MYH14):c.525C>T (p.Tyr175=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 228878	NM_001145809.2(MYH14):c.526G>A (p.Ala176Thr)	MYH14 (A176T)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 4A +2 more	GConflicting classifications of pathogenicity
Select item 1387722	NM_001145809.2(MYH14):c.527C>T (p.Ala176Val)	MYH14 (A176V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 329906	NM_001145809.2(MYH14):c.535G>A (p.Glu179Lys)	MYH14 (E179K)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 4A +1 more	GUncertain significance
Select item 3007079	NM_001145809.2(MYH14):c.541G>T (p.Ala181Ser)	MYH14 (A181S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1162846	NM_001145809.2(MYH14):c.548G>A (p.Arg183Gln)	MYH14 (R183Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 893565	NM_001145809.2(MYH14):c.560A>G (p.Gln187Arg)	MYH14 (Q187R)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1651981	NM_001145809.2(MYH14):c.563-17C>A	MYH14	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 3002086	NM_001145809.2(MYH14):c.563-6del	MYH14	Deletion (intron variant)	not provided	GBenign
Select item 178411	NM_001145809.2(MYH14):c.565C>T (p.Arg189Cys)	MYH14 (R189C)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 1418104	NM_001145809.2(MYH14):c.566G>A (p.Arg189His)	MYH14 (R189H)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2068366	NM_001145809.2(MYH14):c.591-3C>T	MYH14	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1304393	NM_001145809.2(MYH14):c.594A>T (p.Gly198=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 1351059	NM_001145809.2(MYH14):c.614C>T (p.Thr205Met)	MYH14 (T205M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 499477	NM_001145809.2(MYH14):c.615G>A (p.Thr205=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 1943476	NM_001145809.2(MYH14):c.645C>T (p.Leu215=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1913873	NM_001145809.2(MYH14):c.646G>A (p.Ala216Thr)	MYH14 (A216T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1534703	NM_001145809.2(MYH14):c.651C>T (p.His217=)	MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 44079	NM_001145809.2(MYH14):c.657G>A (p.Ala219=)	MYH14	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 4A +3 more	GBenign
Select item 2040889	NM_001145809.2(MYH14):c.659C>T (p.Ser220Leu)	MYH14 (S220L)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 4A +2 more	GUncertain significance
Select item 504945	NM_001145809.2(MYH14):c.660G>A (p.Ser220=)	MYH14	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 164165	NM_001145809.2(MYH14):c.660G>T (p.Ser220=)	MYH14	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 505603	NM_001145809.2(MYH14):c.693C>T (p.Pro231=)	MYH14	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 726155	NM_001145809.2(MYH14):c.693+10C>T	MYH14	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 164166	NM_001145809.2(MYH14):c.693+12C>T	MYH14	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1919835	NM_001145809.2(MYH14):c.693+13G>A	MYH14	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2174491	NM_001145809.2(MYH14):c.718-6C>T	MYH14	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2080256	NM_001145809.2(MYH14):c.718-4G>A	MYH14	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3009314	NM_001145809.2(MYH14):c.723G>C (p.Glu241Asp)	MYH14 (E233D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2186275	NM_001145809.2(MYH14):c.727G>C (p.Glu243Gln)	MYH14 (E235Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 44080	NM_001145809.2(MYH14):c.810C>T (p.Phe270=)	MYH14	Single nucleotide variant (synonymous variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2707418	NM_001145809.2(MYH14):c.810+14_810+38del	MYH14	Deletion (intron variant)	not provided	GBenign
Select item 2704327	NM_001145809.2(MYH14):c.810+14G>T	MYH14	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 178412	NM_001145809.2(MYH14):c.820A>G (p.Ile274Val)	MYH14 (I274V +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 178413	NM_001145809.2(MYH14):c.826A>G (p.Ile276Val)	MYH14 (I276V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 546265	NM_001145809.2(MYH14):c.838G>A (p.Val280Ile)	MYH14 (V272I +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 4A +1 more	GConflicting classifications of pathogenicity
Select item 637025	NM_001145809.2(MYH14):c.851T>C (p.Ile284Thr)	MYH14 (I284T +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 4A +1 more	GUncertain significance
Select item 2794015	NM_001145809.2(MYH14):c.876C>T (p.Tyr292=)	LOC121852992, MYH14	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1961763	NM_001145809.2(MYH14):c.901C>T (p.Arg301Cys)	LOC121852992, MYH14 (R301C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 893859	NM_001145809.2(MYH14):c.909C>T (p.Ala303=)	LOC121852992, MYH14	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3011757	NM_001145809.2(MYH14):c.912G>A (p.Lys304=)	LOC121852992, MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3013595	NM_001145809.2(MYH14):c.918G>A (p.Glu306=)	LOC121852992, MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3004449	NM_001145809.2(MYH14):c.945G>A (p.Leu315=)	LOC121852992, MYH14	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2720312	NM_001145809.2(MYH14):c.950G>C (p.Gly317Ala)	LOC121852992, MYH14 (G309A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2975665	NM_001145809.2(MYH14):c.967C>T (p.Leu323Phe)	LOC121852992, MYH14 (L315F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2739272	NM_001145809.2(MYH14):c.973+8C>G	LOC121852992, MYH14	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1959112	NM_001145809.2(MYH14):c.973+16T>C	LOC121852992, MYH14	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2024208	NM_001145809.2(MYH14):c.974-7C>T	MYH14	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 227583	NM_001145809.2(MYH14):c.975C>T (p.Ala325=)	MYH14	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1985677	NM_001145809.2(MYH14):c.976G>A (p.Asp326Asn)	MYH14 (D318N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1073575	NM_001145809.2(MYH14):c.979del (p.Leu327fs)	MYH14 (L319fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 1907026	NM_001145809.2(MYH14):c.988G>A (p.Glu330Lys)	MYH14 (E322K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

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