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Items: 56

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130001991, SECISBP2
(R7W)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(S17A)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(A18V)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(A40E +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(P11L +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(S46F)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(V54F +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(Y22C +1 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(S36C +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(P43H +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(R47Q +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(Q137H +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(Y80C +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(S105L +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(I183T +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(I132T +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(V136L +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(P156T +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(P151L +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(Q164L +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(P171S +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(L254P +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(P188S +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(N214S +4 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
SECISBP2
(Q233E +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(M322V +4 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(S278F +6 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(T288P +6 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(Y354C +6 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(P387L +6 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
SECISBP2
(V153L +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(A390T +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(K167Q +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(S403P +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(S413P +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(R428H +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
SECISBP2
(R424H +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(M442I +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(T457S +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(K465E +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(D264V +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(E513K +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(T517S +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(K596T +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(E571G +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(A320V +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(R359C +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(R581H +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(R590C +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(R609G +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(L611V +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(K662T +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(A768V +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(Q486R +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
SECISBP2
(L715Q +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SECISBP2
(Q726K +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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