"Illumina Laboratory Services, Illumina"[submitter] AND "MYO15A"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 322100	NM_016239.3(MYO15A):c.-327C>T	LOC105371566, MYO15A	Single nucleotide variant	Nonsyndromic Hearing Loss, Recessive	GUncertain significance
Select item 892286	NM_016239.4(MYO15A):c.-236C>A	LOC105371566, MYO15A	Single nucleotide variant (5 prime UTR variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 322101	NM_016239.4(MYO15A):c.-227G>A	LOC105371566, MYO15A	Single nucleotide variant (5 prime UTR variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 892287	NM_016239.4(MYO15A):c.-224C>T	LOC105371566, MYO15A	Single nucleotide variant (5 prime UTR variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 892288	NM_016239.4(MYO15A):c.-223G>T	LOC105371566, MYO15A	Single nucleotide variant (5 prime UTR variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 322102	NM_016239.4(MYO15A):c.-219-14T>C	MYO15A	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 322103	NM_016239.4(MYO15A):c.-203C>T	MYO15A	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 322104	NM_016239.4(MYO15A):c.-173T>A	MYO15A	Single nucleotide variant (5 prime UTR variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 322105	NM_016239.4(MYO15A):c.-144G>A	MYO15A	Single nucleotide variant (5 prime UTR variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 322106	NM_016239.4(MYO15A):c.-76A>C	MYO15A	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GBenign
Select item 322107	NM_016239.4(MYO15A):c.-33G>C	MYO15A	Single nucleotide variant (5 prime UTR variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 260700	NM_016239.4(MYO15A):c.54G>A (p.Lys18=)	MYO15A	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 888885	NM_016239.4(MYO15A):c.63G>A (p.Pro21=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 506020	NM_016239.4(MYO15A):c.381C>G (p.Leu127=)	MYO15A	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 719301	NM_016239.4(MYO15A):c.393C>G (p.Ser131=)	MYO15A	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 3 +1 more	GConflicting classifications of pathogenicity
Select item 322108	NM_016239.4(MYO15A):c.447G>C (p.Ser149=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 322109	NM_016239.4(MYO15A):c.484C>T (p.Arg162Cys)	MYO15A (R162C)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 890584	NM_016239.4(MYO15A):c.603G>C (p.Glu201Asp)	MYO15A (E201D)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 322110	NM_016239.4(MYO15A):c.642C>T (p.Phe214=)	MYO15A	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 322111	NM_016239.4(MYO15A):c.655T>G (p.Ser219Ala)	MYO15A (S219A)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 322112	NM_016239.4(MYO15A):c.671A>G (p.Tyr224Cys)	MYO15A (Y224C)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 504628	NM_016239.4(MYO15A):c.709G>A (p.Asp237Asn)	MYO15A (D237N)	Single nucleotide variant (missense variant)	MYO15A-related condition +3 more	GConflicting classifications of pathogenicity
Select item 322113	NM_016239.4(MYO15A):c.723C>T (p.Asp241=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 282078	NM_016239.4(MYO15A):c.730G>A (p.Asp244Asn)	MYO15A (D244N)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3 +1 more	GConflicting classifications of pathogenicity
Select item 195311	NM_016239.4(MYO15A):c.823G>C (p.Gly275Arg)	MYO15A (G275R)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 227653	NM_016239.4(MYO15A):c.829C>T (p.His277Tyr)	MYO15A (H277Y)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 891142	NM_016239.4(MYO15A):c.853G>A (p.Asp285Asn)	MYO15A (D285N)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 226791	NM_016239.4(MYO15A):c.876C>T (p.Pro292=)	MYO15A	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 322114	NM_016239.4(MYO15A):c.894C>G (p.Pro298=)	MYO15A	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 3 +1 more	GConflicting classifications of pathogenicity
Select item 322115	NM_016239.4(MYO15A):c.901C>G (p.Pro301Ala)	MYO15A (P301A)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 226792	NM_016239.4(MYO15A):c.915C>T (p.Tyr305=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 892338	NM_016239.4(MYO15A):c.917G>A (p.Gly306Asp)	MYO15A (G306D)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 892339	NM_016239.4(MYO15A):c.1043C>A (p.Pro348Gln)	MYO15A (P348Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity
Select item 423766	NM_016239.4(MYO15A):c.1111C>A (p.Pro371Thr)	MYO15A (P371T)	Single nucleotide variant (missense variant)	Nonsyndromic genetic hearing loss	GLikely benign FDA Recognized database
Select item 500061	NM_016239.4(MYO15A):c.1137del (p.Tyr380fs)	MYO15A (Y380fs)	Deletion (frameshift variant)	Nonsyndromic genetic hearing loss	GLikely pathogenic FDA Recognized database
Select item 226776	NM_016239.4(MYO15A):c.1158C>T (p.Gly386=)	MYO15A	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 322116	NM_016239.4(MYO15A):c.1162G>A (p.Gly388Arg)	MYO15A (G388R)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 892340	NM_016239.4(MYO15A):c.1259C>T (p.Ser420Leu)	MYO15A (S420L)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 226777	NM_016239.4(MYO15A):c.1385G>A (p.Gly462Asp)	MYO15A (G462D)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3 +3 more	GBenign/Likely benign
Select item 227634	NM_016239.4(MYO15A):c.1387A>G (p.Met463Val)	MYO15A (M463V)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3 +3 more	GConflicting classifications of pathogenicity
Select item 322117	NM_016239.4(MYO15A):c.1418T>G (p.Leu473Arg)	MYO15A (L473R)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 322118	NM_016239.4(MYO15A):c.1450C>G (p.Gln484Glu)	MYO15A (Q484E)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 195313	NM_016239.4(MYO15A):c.1454T>C (p.Val485Ala)	MYO15A (V485A)	Single nucleotide variant (missense variant)	not specified +13 more	GConflicting classifications of pathogenicity
Select item 888947	NM_016239.4(MYO15A):c.1589C>T (p.Pro530Leu)	MYO15A (P530L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 322119	NM_016239.4(MYO15A):c.1602C>T (p.Phe534=)	MYO15A	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 888948	NM_016239.4(MYO15A):c.1613G>A (p.Arg538His)	MYO15A (R538H)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity
Select item 322120	NM_016239.4(MYO15A):c.1634C>T (p.Ala545Val)	MYO15A (A545V)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 888949	NM_016239.4(MYO15A):c.1688G>T (p.Arg563Leu)	MYO15A (R563L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 195315	NM_016239.4(MYO15A):c.1783G>A (p.Ala595Thr)	MYO15A (A595T)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 322121	NM_016239.4(MYO15A):c.1791G>A (p.Ala597=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 226778	NM_016239.4(MYO15A):c.1899A>G (p.Pro633=)	MYO15A	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 889627	NM_016239.4(MYO15A):c.1903G>C (p.Ala635Pro)	MYO15A (A635P)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 322122	NM_016239.4(MYO15A):c.2019G>T (p.Gly673=)	MYO15A	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 322123	NM_016239.4(MYO15A):c.2020C>T (p.Pro674Ser)	MYO15A (P674S)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 227636	NM_016239.4(MYO15A):c.2028C>A (p.Pro676=)	MYO15A	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 891197	NM_016239.4(MYO15A):c.2045C>T (p.Pro682Leu)	MYO15A (P682L)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 891198	NM_016239.4(MYO15A):c.2070G>C (p.Pro690=)	MYO15A	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 3 +1 more	GConflicting classifications of pathogenicity
Select item 891199	NM_016239.4(MYO15A):c.2116G>A (p.Ala706Thr)	MYO15A (A706T)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 226779	NM_016239.4(MYO15A):c.2152T>G (p.Trp718Gly)	MYO15A (W718G)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 392812	NM_016239.4(MYO15A):c.2194C>T (p.Pro732Ser)	MYO15A (P732S)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3 +2 more	GConflicting classifications of pathogenicity
Select item 891200	NM_016239.4(MYO15A):c.2200G>A (p.Asp734Asn)	MYO15A (D734N)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 322124	NM_016239.4(MYO15A):c.2259G>T (p.Ala753=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 322125	NM_016239.4(MYO15A):c.2287C>T (p.Arg763Trp)	MYO15A (R763W)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 632270	NM_016239.4(MYO15A):c.2384dup (p.Ser796fs)	MYO15A (S796fs)	Duplication (frameshift variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 195312	NM_016239.4(MYO15A):c.2418C>T (p.Phe806=)	MYO15A	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 226781	NM_016239.4(MYO15A):c.2462A>C (p.Gln821Pro)	MYO15A (Q821P)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 227637	NM_016239.4(MYO15A):c.2562C>T (p.Cys854=)	MYO15A	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 3 +3 more	GConflicting classifications of pathogenicity
Select item 892398	NM_016239.4(MYO15A):c.2612C>T (p.Thr871Met)	MYO15A (T871M)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 322126	NM_016239.4(MYO15A):c.2670C>T (p.Pro890=)	MYO15A	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 286669	NM_016239.4(MYO15A):c.2680C>T (p.Pro894Ser)	MYO15A (P894S)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 287434	NM_016239.4(MYO15A):c.2790C>T (p.Asp930=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 889003	NM_016239.4(MYO15A):c.2805C>T (p.Pro935=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 322127	NM_016239.4(MYO15A):c.2855G>A (p.Gly952Asp)	MYO15A (G952D)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 889004	NM_016239.4(MYO15A):c.2920C>T (p.Pro974Ser)	MYO15A (P974S)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 742012	NM_016239.4(MYO15A):c.2926C>T (p.Leu976Phe)	MYO15A (L976F)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 889005	NM_016239.4(MYO15A):c.2978A>C (p.His993Pro)	MYO15A (H993P)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 322128	NM_016239.4(MYO15A):c.3012A>G (p.Ser1004=)	MYO15A	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 3 +2 more	GConflicting classifications of pathogenicity
Select item 287435	NM_016239.4(MYO15A):c.3023C>G (p.Thr1008Ser)	MYO15A (T1008S)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3 +2 more	GConflicting classifications of pathogenicity
Select item 889698	NM_016239.4(MYO15A):c.3133A>C (p.Thr1045Pro)	MYO15A (T1045P)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 322129	NM_016239.4(MYO15A):c.3140C>A (p.Pro1047His)	MYO15A (P1047H)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 226783	NM_016239.4(MYO15A):c.3140C>G (p.Pro1047Arg)	MYO15A (P1047R)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 512848	NM_016239.4(MYO15A):c.3201G>A (p.Ala1067=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 667134	NM_016239.4(MYO15A):c.3203G>T (p.Cys1068Phe)	MYO15A (C1068F)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 889699	NM_016239.4(MYO15A):c.3275C>T (p.Ala1092Val)	MYO15A (A1092V)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 889700	NM_016239.4(MYO15A):c.3320G>A (p.Arg1107His)	MYO15A (R1107H)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 226784	NM_016239.4(MYO15A):c.3413A>G (p.Gln1138Arg)	MYO15A (Q1138R)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 322130	NM_016239.4(MYO15A):c.3591G>A (p.Pro1197=)	MYO15A	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 3 +3 more	GConflicting classifications of pathogenicity
Select item 228949	NM_016239.4(MYO15A):c.3622C>T (p.Arg1208Cys)	MYO15A (R1208C)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 322131	NM_016239.4(MYO15A):c.3623G>A (p.Arg1208His)	MYO15A (R1208H)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3 +1 more	GUncertain significance
Select item 179931	NM_016239.4(MYO15A):c.3640C>A (p.Arg1214=)	MYO15A	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 493208	NM_016239.4(MYO15A):c.3647G>A (p.Arg1216His)	MYO15A (R1216H)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 322132	NM_016239.4(MYO15A):c.3652C>G (p.Gln1218Glu)	MYO15A (Q1218E)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 164513	NM_016239.4(MYO15A):c.3658G>A (p.Gly1220Arg)	MYO15A (G1220R)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 227639	NM_016239.4(MYO15A):c.3659G>A (p.Gly1220Glu)	MYO15A (G1220E)	Single nucleotide variant (missense variant)	MYO15A-related condition +3 more	GConflicting classifications of pathogenicity
Select item 892443	NM_016239.4(MYO15A):c.3679A>G (p.Met1227Val)	MYO15A (M1227V)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GUncertain significance
Select item 164514	NM_016239.4(MYO15A):c.3756C>T (p.Tyr1252=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 322133	NM_016239.4(MYO15A):c.3757-13G>A	MYO15A	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 178440	NM_016239.4(MYO15A):c.3774C>T (p.Ile1258=)	MYO15A	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 892444	NM_016239.4(MYO15A):c.3807A>G (p.Gly1269=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 449525	NM_016239.4(MYO15A):c.3844C>T (p.Arg1282Trp)	MYO15A (R1282W)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3 +1 more	GUncertain significance

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