MYO15A[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1261079	NM_016239.4(MYO15A):c.-219-289G>A	MYO15A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 322102	NM_016239.4(MYO15A):c.-219-14T>C	MYO15A	Single nucleotide variant (intron variant)	Autosomal recessive nonsyndromic hearing loss 3 +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)	Autosomal recessive nonsyndromic hearing loss 3 +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 2715192	NM_016239.4(MYO15A):c.5C>G (p.Ala2Gly)	MYO15A (A2G)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1975915	NM_016239.4(MYO15A):c.9G>A (p.Lys3=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3006514	NM_016239.4(MYO15A):c.21G>A (p.Glu7=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1365295	NM_016239.4(MYO15A):c.23A>T (p.Glu8Val)	MYO15A (E8V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2955657	NM_016239.4(MYO15A):c.28_31del (p.Lys10fs)	MYO15A (K10fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2261772	NM_016239.4(MYO15A):c.25A>C (p.Lys9Gln)	MYO15A (K9Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1706211	NM_016239.4(MYO15A):c.25A>G (p.Lys9Glu)	MYO15A (K9E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 593188	NM_016239.4(MYO15A):c.32_40del (p.Ala11_Lys13del)	MYO15A	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 3012837	NM_016239.4(MYO15A):c.27G>A (p.Lys9=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1704060	NM_016239.4(MYO15A):c.32C>A (p.Ala11Asp)	MYO15A (A11D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3012593	NM_016239.4(MYO15A):c.33C>T (p.Ala11=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2767057	NM_016239.4(MYO15A):c.33C>G (p.Ala11=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3007723	NM_016239.4(MYO15A):c.51G>C (p.Gly17=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2735995	NM_016239.4(MYO15A):c.51G>T (p.Gly17=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 2995054	NM_016239.4(MYO15A):c.69G>A (p.Pro23=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2834769	NM_016239.4(MYO15A):c.69G>T (p.Pro23=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2270856	NM_016239.4(MYO15A):c.77C>T (p.Pro26Leu)	MYO15A (P26L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2859711	NM_016239.4(MYO15A):c.84G>T (p.Arg28=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2982401	NM_016239.4(MYO15A):c.90G>A (p.Leu30=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2985195	NM_016239.4(MYO15A):c.92del (p.Lys31fs)	MYO15A (K31fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2843539	NM_016239.4(MYO15A):c.93G>A (p.Lys31=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3297683	NM_016239.4(MYO15A):c.98C>T (p.Thr33Met)	MYO15A (T33M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2894576	NM_016239.4(MYO15A):c.99G>A (p.Thr33=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1490617	NM_016239.4(MYO15A):c.104G>C (p.Arg35Pro)	MYO15A (R35P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2857777	NM_016239.4(MYO15A):c.108G>C (p.Leu36=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1398612	NM_016239.4(MYO15A):c.112A>C (p.Met38Leu)	MYO15A (M38L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1655373	NM_016239.4(MYO15A):c.117C>A (p.Gly39=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2962328	NM_016239.4(MYO15A):c.121del (p.Arg41fs)	MYO15A (R41fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2827200	NM_016239.4(MYO15A):c.120C>T (p.Phe40=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2848697	NM_016239.4(MYO15A):c.123C>T (p.Arg41=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3401273	NM_016239.4(MYO15A):c.140T>C (p.Ile47Thr)	MYO15A (I47T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2999015	NM_016239.4(MYO15A):c.141C>A (p.Ile47=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 739105	NM_016239.4(MYO15A):c.150G>A (p.Lys50=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2662599	NM_016239.4(MYO15A):c.151G>A (p.Gly51Ser)	MYO15A (G51S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1707870	NM_016239.4(MYO15A):c.160C>T (p.Arg54Cys)	MYO15A (R54C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 741197	NM_016239.4(MYO15A):c.165C>T (p.Ser55=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2808842	NM_016239.4(MYO15A):c.170C>A (p.Ser57Ter)	MYO15A (S57*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2744226	NM_016239.4(MYO15A):c.172del (p.Ala58fs)	MYO15A (A58fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 1482149	NM_016239.4(MYO15A):c.175T>A (p.Phe59Ile)	MYO15A (F59I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2175682	NM_016239.4(MYO15A):c.185G>A (p.Gly62Asp)	MYO15A (G62D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2715368	NM_016239.4(MYO15A):c.186C>A (p.Gly62=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2843156	NM_016239.4(MYO15A):c.195C>T (p.Thr65=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2833198	NM_016239.4(MYO15A):c.202dup (p.Gln68fs)	MYO15A (Q68fs)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 1301914	NM_016239.4(MYO15A):c.201_202del (p.Gln68fs)	MYO15A (Q68fs)	Deletion (frameshift variant)	Autosomal recessive nonsyndromic hearing loss 3	GPathogenic
Select item 2970513	NM_016239.4(MYO15A):c.204G>A (p.Gln68=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1185647	NM_016239.4(MYO15A):c.212del (p.Lys71fs)	MYO15A (K71fs)	Deletion (frameshift variant)	Autosomal recessive nonsyndromic hearing loss 3	GPathogenic
Select item 517275	NM_016239.4(MYO15A):c.215G>A (p.Arg72His)	MYO15A (R72H)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 2969966	NM_016239.4(MYO15A):c.216C>T (p.Arg72=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2316249	NM_016239.4(MYO15A):c.218A>G (p.Lys73Arg)	MYO15A (K73R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2762332	NM_016239.4(MYO15A):c.232dup (p.Thr78fs)	MYO15A (T78fs)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 2091159	NM_016239.4(MYO15A):c.233C>A (p.Thr78Asn)	MYO15A (T78N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2757659	NM_016239.4(MYO15A):c.234C>A (p.Thr78=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2830757	NM_016239.4(MYO15A):c.240C>G (p.Leu80=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2889366	NM_016239.4(MYO15A):c.243G>A (p.Lys81=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2885535	NM_016239.4(MYO15A):c.249G>A (p.Thr83=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 727010	NM_016239.4(MYO15A):c.250T>A (p.Ser84Thr)	MYO15A (S84T)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3160940	NM_016239.4(MYO15A):c.253A>G (p.Lys85Glu)	MYO15A (K85E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 626215	NM_016239.4(MYO15A):c.263C>T (p.Thr88Met)	MYO15A (T88M)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 3	GLikely pathogenic
Select item 227638	NM_016239.4(MYO15A):c.264G>A (p.Thr88=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2746164	NM_016239.4(MYO15A):c.265C>T (p.Gln89Ter)	MYO15A (Q89*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1064959	NM_016239.4(MYO15A):c.266A>C (p.Gln89Pro)	MYO15A (Q89P)	Single nucleotide variant (missense variant)	Hearing impairment	GUncertain significance
Select item 228945	NM_016239.4(MYO15A):c.269T>C (p.Met90Thr)	MYO15A (M90T)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 2736459	NM_016239.4(MYO15A):c.284dup (p.Lys96fs)	MYO15A (K96fs)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 3011123	NM_016239.4(MYO15A):c.289del (p.Arg97fs)	MYO15A (R97fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 3391587	NM_016239.4(MYO15A):c.298_321del (p.Lys100_Met107del)	MYO15A	Deletion	not provided	GUncertain significance
Select item 2822811	NM_016239.4(MYO15A):c.300G>A (p.Lys100=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1912171	NM_016239.4(MYO15A):c.311C>T (p.Pro104Leu)	MYO15A (P104L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2994524	NM_016239.4(MYO15A):c.315C>T (p.Ser105=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2965186	NM_016239.4(MYO15A):c.315C>G (p.Ser105=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 618238	NM_016239.4(MYO15A):c.328C>T (p.Arg110Cys)	MYO15A (R110C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2770251	NM_016239.4(MYO15A):c.330C>A (p.Arg110=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2754828	NM_016239.4(MYO15A):c.343_367dup (p.Arg123fs)	MYO15A (R123fs)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 2393180	NM_016239.4(MYO15A):c.340C>T (p.Arg114Cys)	MYO15A (R114C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1454505	NM_016239.4(MYO15A):c.343dup (p.Arg115fs)	MYO15A (R115fs)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 2683913	NM_016239.4(MYO15A):c.343del (p.Arg115fs)	MYO15A (R115fs)	Deletion (frameshift variant)	Autosomal recessive nonsyndromic hearing loss 3	GPathogenic
Select item 800766	NM_016239.4(MYO15A):c.346_376del (p.Gly116fs)	MYO15A (G116fs)	Deletion (frameshift variant)	Autosomal recessive nonsyndromic hearing loss 3	GLikely pathogenic
Select item 2779825	NM_016239.4(MYO15A):c.345T>C (p.Arg115=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2804304	NM_016239.4(MYO15A):c.349_364del (p.Tyr117fs)	MYO15A (Y117fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 228948	NM_016239.4(MYO15A):c.349_357del (p.Tyr117_Arg119del)	MYO15A	Deletion	Autosomal recessive nonsyndromic hearing loss 3 +1 more	GUncertain significance
Select item 1379512	NM_016239.4(MYO15A):c.350_363del (p.Tyr117fs)	MYO15A (Y117fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 3075914	NM_016239.4(MYO15A):c.352G>A (p.Gly118Ser)	MYO15A (G118S)	Single nucleotide variant (missense variant)	Rare genetic deafness	GUncertain significance
Select item 1505553	NM_016239.4(MYO15A):c.352_360del (p.Gly118_Leu120del)	MYO15A	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2407003	NM_016239.4(MYO15A):c.359T>G (p.Leu120Arg)	MYO15A (L120R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3401250	NM_016239.4(MYO15A):c.362G>A (p.Arg121Gln)	MYO15A (R121Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2860919	NM_016239.4(MYO15A):c.370_371del (p.Ala124fs)	MYO15A (A124fs)	Microsatellite (frameshift variant)	not provided	GPathogenic
Select item 2696174	NM_016239.4(MYO15A):c.369C>A (p.Arg123=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 666866	NM_016239.4(MYO15A):c.370G>A (p.Ala124Thr)	MYO15A (A124T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2858239	NM_016239.4(MYO15A):c.372C>A (p.Ala124=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 242390	NM_016239.4(MYO15A):c.373_374del (p.Arg125fs)	MYO15A (R125fs)	Deletion (frameshift variant)	Autosomal recessive nonsyndromic hearing loss 3	GPathogenic
Select item 2647539	NM_016239.4(MYO15A):c.374G>A (p.Arg125Gln)	MYO15A (R125Q)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2730739	NM_016239.4(MYO15A):c.375G>A (p.Arg125=)	MYO15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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