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Links from Gene

Items: 1 to 100 of 588

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ERBB4
(K1202R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
ERBB4-related disorder
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
ERBB4-related disorder
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant +1 more)
ERBB4-related disorder
GLikely benign
ERBB4
(R72Q)
Single nucleotide variant
(missense variant)
ERBB4-related disorder
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
ERBB4-related disorder
GLikely benign
ERBB4
Single nucleotide variant
(intron variant)
ERBB4-related disorder
GLikely benign
ERBB4
(P3L)
Single nucleotide variant
(missense variant)
ERBB4-related disorder
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
ERBB4-related disorder
GLikely benign
ERBB4
(D1087Y +1 more)
Single nucleotide variant
(missense variant)
ERBB4-related disorder
GUncertain significance
ERBB4
(H856R)
Single nucleotide variant
(missense variant)
ERBB4-related disorder
GUncertain significance
ERBB4
(D1115N +1 more)
Single nucleotide variant
(missense variant)
ERBB4-related disorder
GUncertain significance
ERBB4
(S1001I)
Single nucleotide variant
(missense variant)
ERBB4-related disorder
GUncertain significance
ERBB4
(G573D)
Single nucleotide variant
(missense variant)
ERBB4-related disorder
GUncertain significance
ERBB4
(A773T)
Single nucleotide variant
(missense variant)
ERBB4-related disorder
GUncertain significance
ERBB4
(F1221Y +1 more)
Single nucleotide variant
(missense variant)
ERBB4-related disorder
GUncertain significance
ERBB4
(P1240A +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ERBB4
(R72W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ERBB4
(P943A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ERBB4
(T1199I +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ERBB4
(G936A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ERBB4
(A888P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ERBB4
(A769G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ERBB4
(V723I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ERBB4
(L521V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ERBB4
(T791A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ABI2, ACADL
+95 more
Copy number loss
not specified
GPathogenic
ERBB4
Copy number gain
not specified
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
ERBB4-related disorder
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
ERBB4-related disorder
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
ERBB4-related disorder
GLikely benign
ERBB4
(E276G)
Single nucleotide variant
(missense variant)
ERBB4-related disorder
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
ERBB4-related disorder
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
ERBB4-related disorder
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
ERBB4-related disorder
GLikely benign
ERBB4
Deletion
(intron variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
(F478fs)
Microsatellite
(frameshift variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ERBB4
(D1009G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
(Y1081C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
(G571A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
(S1086N +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
(G319R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
(I353V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
(R524C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
(L661V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
(Y222C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ERBB4
(V391I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Insertion
(intron variant)
not provided
GLikely benign
ERBB4
(R525C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
(L1145M +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
(S1046N)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ERBB4
(I1041T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ERBB4
(R1139Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
(R232Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GBenign
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
(L644S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
(M562T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
(T703K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ERBB4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
ERBB4
(E810K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
(R114Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
(T1098P +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
(K873T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
(L567F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ERBB4
(R81Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
(P1281L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ERBB4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
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