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Items: 38

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GPR84-AS1, ITGA5
(R1028C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(G1014D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(R948W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(Q935R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(F917C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(P912L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(R894Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(Q891R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
ITGA5, GPR84-AS1
(S887F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(T865M)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(V803A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ITGA5, GPR84-AS1
(R783W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(V723M)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(E700K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(Q640E)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(K638E)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(V618L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(D613Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(I589M)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ITGA5, GPR84-AS1
(Q567E)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(E545G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ITGA5, GPR84-AS1
(T500N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ITGA5, GPR84-AS1
(F455I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(N408D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ITGA5, GPR84-AS1
(D341G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ITGA5, GPR84-AS1
(A332T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(T299I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ITGA5, GPR84-AS1
(D284V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(L178V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(R163C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(C108F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(G70V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(R38S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ITGA5, GPR84-AS1
(P37R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(V13L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(P9A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GPR84-AS1, ITGA5
(E7G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
ITGA5, GPR84-AS1
(R4L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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