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Items: 75

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SEL1L3
(P1093L +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SEL1L3
(Q1086P +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(T1103A +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SEL1L3
(T1066I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(V1044M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(H1059R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(W1054C +2 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
SEL1L3
(R1051Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(T1013I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(F854L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(E842K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(E852A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(V842A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(L721V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(Y838F +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(Y838H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(Y619F +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(A686T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(G549W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(R694Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(T504A +2 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
SEL1L3
(Y619H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(T612I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(N587H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(T527M +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SEL1L3
(H517R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(A388G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(E497Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
Single nucleotide variant
(synonymous variant)
not provided
GBenign
SEL1L3
(P370L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(F358S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(F476L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(F344S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(R342S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(R451H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(R333C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
Single nucleotide variant
(intron variant)
not provided
GLikely benign
SEL1L3
(Q472K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(G468R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(I422L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(E418G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(E437A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(P393T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(R389L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(R389H +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SEL1L3
(Y420C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(S405N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(I402T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(G221E +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(G211R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(F323L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(G165S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(N314I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(N150S +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SEL1L3
(R236Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SEL1L3
(F232L +2 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
SEL1L3
(R198W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(N78K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(G74V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(M226T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
Single nucleotide variant
(synonymous variant)
not provided
GBenign
SEL1L3
(A199T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(H43Y +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(I172T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(A17S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEL1L3
(Q107R +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
SEL1L3
(V96I +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
SEL1L3
(R59G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SEL1L3
(T87A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SEL1L3
(E75G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SEL1L3
(P37T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SEL1L3
(T67M +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SEL1L3
(T29A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SEL1L3
Copy number gain
not provided
GUncertain significance
SEL1L3
Copy number loss
not provided
GUncertain significance
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Format
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