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Items: 1 to 100 of 183

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYO18A
Single nucleotide variant
(3 prime UTR variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(3 prime UTR variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(3 prime UTR variant)
not specified
GLikely benign
MYO18A
Single nucleotide variant
(3 prime UTR variant)
not provided
GBenign
MYO18A
Single nucleotide variant
(3 prime UTR variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(3 prime UTR variant)
not provided
GBenign
MYO18A
Single nucleotide variant
(3 prime UTR variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(3 prime UTR variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(3 prime UTR variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(3 prime UTR variant)
not specified
GLikely benign
MYO18A
Single nucleotide variant
(3 prime UTR variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(3 prime UTR variant)
not specified
GUncertain significance
MYO18A
(T1572fs +5 more)
Microsatellite
(frameshift variant)
MYO18A-related disorder
GLikely benign
MYO18A
(S1570fs +5 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
MYO18A
(R1982Q +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(P2033L +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MYO18A
(D1552N +5 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
MYO18A
(H1551Y +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(D2006E +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1967W +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(Y1538F +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(E1962K +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(synonymous variant)
not provided
GBenign
MYO18A
(K1939R +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MYO18A
Single nucleotide variant
(synonymous variant)
not provided
GBenign
MYO18A
Single nucleotide variant
(synonymous variant)
not provided
GBenign
MYO18A
Single nucleotide variant
(synonymous variant)
not provided
GBenign
MYO18A
(R1788W +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(K1814E +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(V1812A +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(V1346L +4 more)
Single nucleotide variant
(missense variant)
MYO18A-related disorder
GUncertain significance
MYO18A
(L1800V +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(A1793T +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(N1319S +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(D1314G +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1313Q +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(H1304Y +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(K1303Q +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1289Q +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO18A
(N1754S +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1739H +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1278H +4 more)
Single nucleotide variant
(missense variant)
MYO18A-related disorder
GLikely benign
MYO18A
(V1703M +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO18A
(A1242V +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1225Q +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(S1700N +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1197W +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(F1648C +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(G1176D +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(Q1152P +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO18A
(R1135Q +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
Gnot provided
MYO18A
(R1493W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1018Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(A1016T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(F1475C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(G1448S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1421Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(F1384L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1372Q +3 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
MYO18A
(R1372W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1354Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1373W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(L1364F +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1351C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(M1345T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(synonymous variant)
not provided
GBenign
MYO18A
Single nucleotide variant
(synonymous variant)
not provided
GBenign
MYO18A
(A1326T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MYO18A
(A1308T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1321C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(K1284T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1267Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1257Q +3 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
MYO18A
(P777L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(K1241N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(F1220L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(Q1206H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(E1182D +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1179W +3 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
MYO18A
(R1173W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(V1142L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(K1146E +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(H1127Y +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(intron variant)
not provided
GBenign
MYO18A
(R1109C +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO18A
(G1098S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(V1101E +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(V631M +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
Single nucleotide variant
(synonymous variant)
MYO18A-related disorder
GLikely benign
MYO18A
(P1075T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R607Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R1064H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R606C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(A603T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(R601C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(L1053P +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYO18A
(F1009Y +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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