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Items: 89

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SORCS1
(Q1141*)
Single nucleotide variant
(nonsense +2 more)
Alzheimer disease 6
GLikely pathogenic
SORCS1
(P1127L)
Single nucleotide variant
(missense variant +2 more)
Malignant tumor of prostate
GUncertain significance
SORCS1
(F1122L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(V1118I)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
SORCS1
(T1063M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(H1062R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(E1054A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(K1047Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(Q1040R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(L1037P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(A1023T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(A971T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(T946A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(I941M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(G939R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(V912M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
SORCS1
(S879N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(R866H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(V858I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(S849T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
SORCS1
(R830Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(L819V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(H815R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
SORCS1
(R798W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(P789Q)
Single nucleotide variant
(missense variant)
not provided
GBenign
SORCS1
(V781I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(Y769H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(M708V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(R672W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(S621N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(R608Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(T603A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(M600V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
SORCS1
(H517R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(T509K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(T509M)
Single nucleotide variant
(missense variant)
not provided
GBenign
SORCS1
(R502H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
SORCS1
(G460V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(A451T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(I440T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(D434G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
SORCS1
(A398E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(R387G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
SORCS1
(H376Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(Q374R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(P368A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(N352K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(A336S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(D330E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
SORCS1
Single nucleotide variant
(intron variant)
not provided
GBenign
SORCS1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
SORCS1
(E250A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(T238A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(T228N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(S186T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(H183R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(G169A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(T163A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(M155I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(G141V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(V101F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(T68M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(G60R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(R54M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(P41L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(P39S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(A28S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(A12V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
(S10Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SORCS1
Copy number loss
not provided
GUncertain significance
SORCS1
Copy number loss
not specified
GUncertain significance
SORCS1
Copy number gain
not specified
GUncertain significance
SORCS1
Copy number loss
not provided
GUncertain significance
SORCS1
Copy number gain
not provided
GUncertain significance
SORCS1
Copy number gain
not provided
GUncertain significance
SORCS1
Copy number gain
not provided
GUncertain significance
SORCS1
Copy number gain
not provided
GUncertain significance
SORCS1
Copy number loss
See cases
GLikely benign
SORCS1
Copy number gain
See cases
GUncertain significance
SORCS1
Copy number gain
See cases
GUncertain significance
SORCS1
Copy number gain
VATER association
GLikely benign
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