MYO18A[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3297736	NM_078471.4(MYO18A):c.*893A>G	MYO18A	Single nucleotide variant (3 prime UTR variant)	not specified	GUncertain significance
Select item 3161832	NM_078471.4(MYO18A):c.*766T>G	MYO18A	Single nucleotide variant (3 prime UTR variant)	not specified	GUncertain significance
Select item 3161804	NM_078471.4(MYO18A):c.*742G>A	MYO18A	Single nucleotide variant (3 prime UTR variant)	not specified	GLikely benign
Select item 768864	NM_078471.4(MYO18A):c.*727G>A	MYO18A	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 2607667	NM_078471.4(MYO18A):c.*712T>G	MYO18A	Single nucleotide variant (3 prime UTR variant)	not specified	GUncertain significance
Select item 785565	NM_078471.4(MYO18A):c.*708A>G	MYO18A	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 3161745	NM_078471.4(MYO18A):c.*683C>T	MYO18A	Single nucleotide variant (3 prime UTR variant)	not specified	GUncertain significance
Select item 2551334	NM_078471.4(MYO18A):c.*671G>A	MYO18A	Single nucleotide variant (3 prime UTR variant)	not specified	GUncertain significance
Select item 3162143	NM_078471.4(MYO18A):c.*663T>A	MYO18A	Single nucleotide variant (3 prime UTR variant)	not specified	GUncertain significance
Select item 2527428	NM_078471.4(MYO18A):c.*643C>T	MYO18A	Single nucleotide variant (3 prime UTR variant)	not specified	GLikely benign
Select item 3161982	NM_078471.4(MYO18A):c.*605C>T	MYO18A	Single nucleotide variant (3 prime UTR variant)	not specified	GUncertain significance
Select item 3162134	NM_078471.4(MYO18A):c.*577T>C	MYO18A	Single nucleotide variant (3 prime UTR variant)	not specified	GUncertain significance
Select item 3047824	NM_078471.4(MYO18A):c.6134_6135del (p.Thr2045fs)	MYO18A (T1572fs +5 more)	Microsatellite (frameshift variant)	MYO18A-related disorder	GLikely benign
Select item 2501804	NM_078471.4(MYO18A):c.6129_6130del (p.Ser2043fs)	MYO18A (S1570fs +5 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2520249	NM_078471.4(MYO18A):c.6101G>A (p.Arg2034Gln)	MYO18A (R1982Q +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326938	NM_078471.4(MYO18A):c.6098C>T (p.Pro2033Leu)	MYO18A (P2033L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777154	NM_078471.4(MYO18A):c.6081C>T (p.Leu2027=)	MYO18A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2647606	NM_078471.4(MYO18A):c.6073G>A (p.Asp2025Asn)	MYO18A (D1552N +5 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3297729	NM_078471.4(MYO18A):c.6070C>T (p.His2024Tyr)	MYO18A (H1551Y +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490086	NM_078471.4(MYO18A):c.6063T>A (p.Asp2021Glu)	MYO18A (D2006E +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219980	NM_078471.4(MYO18A):c.6055C>T (p.Arg2019Trp)	MYO18A (R1967W +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162099	NM_078471.4(MYO18A):c.6032A>T (p.Tyr2011Phe)	MYO18A (Y1538F +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617236	NM_078471.4(MYO18A):c.5929G>A (p.Glu1977Lys)	MYO18A (E1962K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 739030	NM_078471.4(MYO18A):c.5802T>C (p.Ala1934=)	MYO18A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2351051	NM_078471.4(MYO18A):c.5780A>G (p.Lys1927Arg)	MYO18A (K1939R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2647607	NM_078471.4(MYO18A):c.5754G>T (p.Leu1918=)	MYO18A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 769914	NM_078471.4(MYO18A):c.5706C>T (p.His1902=)	MYO18A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 733892	NM_078471.4(MYO18A):c.5691G>A (p.Ala1897=)	MYO18A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 768865	NM_078471.4(MYO18A):c.5685C>T (p.Ala1895=)	MYO18A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2274399	NM_078471.4(MYO18A):c.5473C>T (p.Arg1825Trp)	MYO18A (R1788W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307249	NM_078471.4(MYO18A):c.5440A>G (p.Lys1814Glu)	MYO18A (K1814E +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297737	NM_078471.4(MYO18A):c.5435T>C (p.Val1812Ala)	MYO18A (V1812A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2629676	NM_078471.4(MYO18A):c.5410G>T (p.Val1804Leu)	MYO18A (V1346L +4 more)	Single nucleotide variant (missense variant)	MYO18A-related disorder	GUncertain significance
Select item 2408105	NM_078471.4(MYO18A):c.5398C>G (p.Leu1800Val)	MYO18A (L1800V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376964	NM_078471.4(MYO18A):c.5341G>A (p.Ala1781Thr)	MYO18A (A1793T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478068	NM_078471.4(MYO18A):c.5330A>G (p.Asn1777Ser)	MYO18A (N1319S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536757	NM_078471.4(MYO18A):c.5315A>G (p.Asp1772Gly)	MYO18A (D1314G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297731	NM_078471.4(MYO18A):c.5312G>A (p.Arg1771Gln)	MYO18A (R1313Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330449	NM_078471.4(MYO18A):c.5284C>T (p.His1762Tyr)	MYO18A (H1304Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162060	NM_078471.4(MYO18A):c.5281A>C (p.Lys1761Gln)	MYO18A (K1303Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 806003	NM_078471.4(MYO18A):c.5240G>A (p.Arg1747Gln)	MYO18A (R1289Q +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3162053	NM_078471.4(MYO18A):c.5225A>G (p.Asn1742Ser)	MYO18A (N1754S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243476	NM_078471.4(MYO18A):c.5216G>A (p.Arg1739His)	MYO18A (R1739H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3046335	NM_078471.4(MYO18A):c.5207G>A (p.Arg1736His)	MYO18A (R1278H +4 more)	Single nucleotide variant (missense variant)	MYO18A-related disorder	GLikely benign
Select item 808246	NM_078471.4(MYO18A):c.5107G>A (p.Val1703Met)	MYO18A (V1703M +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2351122	NM_078471.4(MYO18A):c.5099C>T (p.Ala1700Val)	MYO18A (A1242V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162048	NM_078471.4(MYO18A):c.5048G>A (p.Arg1683Gln)	MYO18A (R1225Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366215	NM_078471.4(MYO18A):c.5042G>A (p.Ser1681Asn)	MYO18A (S1700N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375308	NM_078471.4(MYO18A):c.4963C>T (p.Arg1655Trp)	MYO18A (R1197W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162045	NM_078471.4(MYO18A):c.4943T>G (p.Phe1648Cys)	MYO18A (F1648C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162041	NM_078471.4(MYO18A):c.4901G>A (p.Gly1634Asp)	MYO18A (G1176D +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 808247	NM_078471.4(MYO18A):c.4829A>C (p.Gln1610Pro)	MYO18A (Q1152P +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3064056	NM_078471.4(MYO18A):c.4778G>A (p.Arg1593Gln)	MYO18A (R1135Q +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	Gnot provided
Select item 2311565	NM_078471.4(MYO18A):c.4441C>T (p.Arg1481Trp)	MYO18A (R1493W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454894	NM_078471.4(MYO18A):c.4427G>A (p.Arg1476Gln)	MYO18A (R1018Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297739	NM_078471.4(MYO18A):c.4420G>A (p.Ala1474Thr)	MYO18A (A1016T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340920	NM_078471.4(MYO18A):c.4388T>G (p.Phe1463Cys)	MYO18A (F1475C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162034	NM_078471.4(MYO18A):c.4342G>A (p.Gly1448Ser)	MYO18A (G1448S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317317	NM_078471.4(MYO18A):c.4226G>A (p.Arg1409Gln)	MYO18A (R1421Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333695	NM_078471.4(MYO18A):c.4152C>A (p.Phe1384Leu)	MYO18A (F1384L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 774930	NM_078471.4(MYO18A):c.4115G>A (p.Arg1372Gln)	MYO18A (R1372Q +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2399923	NM_078471.4(MYO18A):c.4114C>T (p.Arg1372Trp)	MYO18A (R1372W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599058	NM_078471.4(MYO18A):c.4061G>A (p.Arg1354Gln)	MYO18A (R1354Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398005	NM_078471.4(MYO18A):c.4060C>T (p.Arg1354Trp)	MYO18A (R1373W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606577	NM_078471.4(MYO18A):c.4054C>T (p.Leu1352Phe)	MYO18A (L1364F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389438	NM_078471.4(MYO18A):c.4051C>T (p.Arg1351Cys)	MYO18A (R1351C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228518	NM_078471.4(MYO18A):c.4034T>C (p.Met1345Thr)	MYO18A (M1345T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 780420	NM_078471.4(MYO18A):c.4017G>A (p.Gln1339=)	MYO18A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 774348	NM_078471.4(MYO18A):c.3981G>A (p.Lys1327=)	MYO18A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3162004	NM_078471.4(MYO18A):c.3940G>A (p.Ala1314Thr)	MYO18A (A1326T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2647608	NM_078471.4(MYO18A):c.3939C>T (p.Asp1313=)	MYO18A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2471826	NM_078471.4(MYO18A):c.3922G>A (p.Ala1308Thr)	MYO18A (A1308T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291480	NM_078471.4(MYO18A):c.3904C>T (p.Arg1302Cys)	MYO18A (R1321C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398078	NM_078471.4(MYO18A):c.3815A>C (p.Lys1272Thr)	MYO18A (K1284T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537537	NM_078471.4(MYO18A):c.3800G>A (p.Arg1267Gln)	MYO18A (R1267Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 790718	NM_078471.4(MYO18A):c.3770G>A (p.Arg1257Gln)	MYO18A (R1257Q +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2237423	NM_078471.4(MYO18A):c.3704C>T (p.Pro1235Leu)	MYO18A (P777L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244584	NM_078471.4(MYO18A):c.3687A>T (p.Lys1229Asn)	MYO18A (K1241N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297733	NM_078471.4(MYO18A):c.3624C>G (p.Phe1208Leu)	MYO18A (F1220L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558616	NM_078471.4(MYO18A):c.3561A>C (p.Gln1187His)	MYO18A (Q1206H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326176	NM_078471.4(MYO18A):c.3546G>T (p.Glu1182Asp)	MYO18A (E1182D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 786313	NM_078471.4(MYO18A):c.3535C>T (p.Arg1179Trp)	MYO18A (R1179W +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3161968	NM_078471.4(MYO18A):c.3517C>T (p.Arg1173Trp)	MYO18A (R1173W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370304	NM_078471.4(MYO18A):c.3424G>T (p.Val1142Leu)	MYO18A (V1142L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161963	NM_078471.4(MYO18A):c.3400A>G (p.Lys1134Glu)	MYO18A (K1146E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213174	NM_078471.4(MYO18A):c.3343C>T (p.His1115Tyr)	MYO18A (H1127Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781273	NM_078471.4(MYO18A):c.3331+8C>A	MYO18A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2497725	NM_078471.4(MYO18A):c.3325C>T (p.Arg1109Cys)	MYO18A (R1109C +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2312995	NM_078471.4(MYO18A):c.3292G>A (p.Gly1098Ser)	MYO18A (G1098S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263997	NM_078471.4(MYO18A):c.3266T>A (p.Val1089Glu)	MYO18A (V1101E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513551	NM_078471.4(MYO18A):c.3265G>A (p.Val1089Met)	MYO18A (V631M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3350774	NM_078471.4(MYO18A):c.3228G>A (p.Ser1076=)	MYO18A	Single nucleotide variant (synonymous variant)	MYO18A-related disorder	GLikely benign
Select item 2409587	NM_078471.4(MYO18A):c.3223C>A (p.Pro1075Thr)	MYO18A (P1075T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345160	NM_078471.4(MYO18A):c.3194G>A (p.Arg1065Gln)	MYO18A (R607Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495452	NM_078471.4(MYO18A):c.3191G>A (p.Arg1064His)	MYO18A (R1064H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323934	NM_078471.4(MYO18A):c.3190C>T (p.Arg1064Cys)	MYO18A (R606C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250312	NM_078471.4(MYO18A):c.3181G>A (p.Ala1061Thr)	MYO18A (A603T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161931	NM_078471.4(MYO18A):c.3175C>T (p.Arg1059Cys)	MYO18A (R601C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623882	NM_078471.4(MYO18A):c.3122T>C (p.Leu1041Pro)	MYO18A (L1053P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618009	NM_078471.4(MYO18A):c.3026T>A (p.Phe1009Tyr)	MYO18A (F1009Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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