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Items: 1 to 100 of 203

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLT3, MYO18A
Translocation
Atypical chronic myeloid leukemia, BCR-ABL1 negative
GLikely pathogenic
DHRS13, ERAL1
+39 more
Copy number gain
See cases
GUncertain significance
ABHD15, ADAP2
+202 more
Copy number loss
See cases
GPathogenic
LOC125177445, MYO18A
Copy number gain
See cases
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
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
LOC125177445, MYO18A
(R1434K +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC125177445, MYO18A
(E1901K +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC125177445, MYO18A
(R1844W +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC125177445, MYO18A
(A1827V +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC125177445, MYO18A
(A1406T +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC125177445, MYO18A
(E1869V +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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
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