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Items: 78

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130064925, LOC130064926
+1081 more
Copy number gain
See cases
GPathogenic
LOC130064903, LOC130064904
+1093 more
Copy number gain
See cases
GPathogenic
SHANK1
(R2153Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(S2070A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(L2020P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P2013S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(L2003R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(Q1984H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(A1968fs)
Deletion
(frameshift variant)
not provided
GUncertain significance
SHANK1
(S1959F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P1950R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(R1923K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(T1781N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(A1761E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P1754L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(T1753I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P1743S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(G1717R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(S1629I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(E1557K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(S1553L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P1550A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P1543S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(N1497H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
SHANK1
(H1470fs)
Deletion
(frameshift variant)
not provided
GPathogenic
SHANK1
(P1469S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P1453S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(R1384S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(R1379G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(A1363E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P1352R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(G1344R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(A1262E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P1208S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(S1137F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(R1106C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(R1048*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
SHANK1
Duplication
(inframe_insertion)
not provided
GUncertain significance
SHANK1
(P967A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(G960S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P936T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P922L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P899A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(A893V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SHANK1
(R851*)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
SHANK1
(P839T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(E794G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(V766E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(V739M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(R713*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
SHANK1
(V705E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(L702M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P697L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(A683V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
Single nucleotide variant
(intron variant)
not specified
GLikely benign
SHANK1
(R544S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(S520R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
Single nucleotide variant
not provided
GBenign
SHANK1
(R493P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(Q471H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P462R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(A457S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(A456G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(M443V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P414S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(R400*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
SHANK1
(A345V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(L299P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(E298K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P294T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(Y156H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(S53F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(R41Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(Y207D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(A1965D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(T1786A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(P80L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHANK1
(D2048V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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