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Items: 1 to 100 of 101

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KIF16B
(F1249L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A1279T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(D1219N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A1207fs +1 more)
Deletion
(frameshift variant)
Muscular atrophy
GUncertain significance
KIF16B
(N1200S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A1240S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R1220H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(F1204C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KIF16B
(E1203K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A1149S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(Y1191C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KIF16B
(I1135V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(I1133V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KIF16B
(R1171H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A1382V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(I1732T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
KIF16B
(V1277M +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(N1271K)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
KIF16B
(S1699P +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(L1231F +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(M1227T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(D1666E +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(Q1221R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(T1203I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(V1635F +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(C1624R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(R1110C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KIF16B
(D1110G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(S1087N +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
KIF16B
(R1078H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R1066S +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KIF16B
(S1100N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(D1082N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(I1078T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(L1053R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R1033T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(M1027I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(G1026C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(H1022R)
Single nucleotide variant
(missense variant)
not provided
GBenign
KIF16B
(R1021K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A1010D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R1018W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(K1000R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(M960I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(L931I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(K896E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(E887D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(E871D +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
KIF16B
(H868R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(C877F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(K865R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(E862D)
Single nucleotide variant
(missense variant)
Intellectual disability
GUncertain significance
KIF16B
(I860V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(Q855R)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
KIF16B
(L836P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(E816K)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
KIF16B
(D823V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R781H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R780L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(E777K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(L746Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(E756D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(D738Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(Q706H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(V705I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R715H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R672C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R660H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R641S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(E638D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R614H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(N585T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KIF16B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KIF16B
(L543F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A532T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(V530M)
Single nucleotide variant
(missense variant)
Malignant tumor of prostate
GUncertain significance
KIF16B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
KIF16B
(T511I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(E501D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(L496P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(D461G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(E405K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A388T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(N369S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(I364V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(S347N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(V285I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(G266R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(S238T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A213T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(K165R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KIF16B
(R157H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
KIF16B
(R132Q)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
KIF16B
(R132W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(L129P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(C97S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(V87M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(G83S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(L82V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
Display optionsSort by LocationDownload
Format
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