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Links from Gene

Items: 1 to 100 of 123

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KIF16B
(R132Q)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
KIF16B
(R132W)
Single nucleotide variant
(missense variant)
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
(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
(T1203I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(A1149S +1 more)
Single nucleotide variant
(missense variant)
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
(R1171H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(I1078T)
Single nucleotide variant
(missense variant +1 more)
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
(C97S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(G83S)
Single nucleotide variant
(missense variant)
not specified
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
(L746Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R641S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(L496P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BANF2, BFSP1
+49 more
Deletion
Hyperinsulinemic hypoglycemia, familial, 1
GPathogenic
KIF16B
(R1066S +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SEC23B, SEL1L2
+164 more
Copy number gain
not provided
GPathogenic
KIF16B
(E638D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(S238T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(H868R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(E405K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R614H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R157H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(K896E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(I860V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM33, ADISSP
+731 more
Copy number gain
Renal agenesis
GPathogenic
KIF16B
(F1249L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(I1135V +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
(R672C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(D1666E +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(L543F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(Q706H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(T511I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(V705I +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
(A532T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A1010D +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
(R780L +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
(G1026C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(E501D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(C877F +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
(Q1221R +1 more)
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
(R715H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(T81A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A388T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(L82V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R1220H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(S347N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R1033T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(G266R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R1078H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(L1053R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(L129P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(N369S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(M960I +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
(D1110G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(V87M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A213T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(A1240S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(E1203K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(L836P +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
(I364V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(V285I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(D461G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(R1021K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KIF16B
(S1100N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(S1699P +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KIF16B
(N1200S +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
(A1279T +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
(E887D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BANF2, BFSP1
+28 more
Copy number gain
not provided
GUncertain significance
KIF16B
(I1133V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KIF16B
(A1207fs +1 more)
Deletion
(frameshift variant)
Muscular atrophy
GUncertain significance
KIF16B
(N585T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KIF16B
(Q855R)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
KIF16B
(E862D)
Single nucleotide variant
(missense variant)
Intellectual disability
GUncertain significance
KIF16B
(K165R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KIF16B
(E816K)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
KIF16B
(R1110C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KIF16B
(N1271K)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
MACROD2, SNRPB2
+2 more
Copy number loss
not provided
GUncertain significance
KIF16B, SLC24A3
+49 more
Copy number loss
not provided
GPathogenic
ABHD12, ACSS1
+177 more
Copy number gain
not provided
GPathogenic
KIF16B
(F1204C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
Display optionsSort by RelevanceDownload
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