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Links from Gene

Items: 84

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRYZL2P-SEC16B, SEC16B
(P282S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(D250G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(G194E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(S167C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(Q141R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(G996R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(D933G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(E933G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(G91D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(Q896R +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CRYZL2P-SEC16B, SEC16B
(E885A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(H805R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(P785S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R755H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(A702V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CRYZL2P-SEC16B, SEC16B
(Q67H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(C566R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R510W +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(S484N +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
CRYZL2P-SEC16B, SEC16B
(L450F +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(T428M +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(P425L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(D393Y +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(E388K +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(L365P +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R13Q)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
CRYZL2P-SEC16B, SEC16B
(S663R +1 more)
Single nucleotide variant
(missense variant)
EBV-positive nodal T- and NK-cell lymphoma
GLikely benign
CRYZL2P-SEC16B, SEC16B
(T114A)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
CRYZL2P-SEC16B, SEC16B
(K620I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(S920L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(Y649C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(G558R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(I441V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(T945N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(T12I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(E90K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(Y567H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(S232N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(P775T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(V1035L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(Q11H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(A495V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R636L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(Y633H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(E611Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R636C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R375H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(Y126C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(A873T +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CRYZL2P-SEC16B, SEC16B
(M569V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R893Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CRYZL2P-SEC16B, SEC16B
(R619C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(T516K +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(H41Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(V442M +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R618P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R637H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R984Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CRYZL2P-SEC16B, SEC16B
(V813M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(F611L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(L568V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(L3P)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
CRYZL2P-SEC16B, SEC16B
(G128V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(A872S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(D393N +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(G1001V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(P1023T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R28W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(P130S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(C613S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(P780L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(G359E +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(K477R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R1047W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(D336E +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(L560P +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(P198Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CRYZL2P-SEC16B, SEC16B
(R227C)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
CRYZL2P-SEC16B, SEC16B
(N1031S +2 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
CRYZL2P-SEC16B, SEC16B
(G524E +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
CRYZL2P-SEC16B, SEC16B
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CRYZL2P-SEC16B, SEC16B
(A18T)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
SEC16B, CRYZL2P-SEC16B
(Q850H +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
CRYZL2P-SEC16B, SEC16B
(S935L +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
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