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Items: 35

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRM6, ZNF454
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
GRM6, LOC100130798
+1 more
(R719Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ZNF454, GRM6
+1 more
(I700F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GRM6, ZNF454
(L698V)
Single nucleotide variant
(missense variant)
not specified
+1 more
GLikely benign
GRM6, ZNF454
(S685W)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
GRM6, ZNF454
(R674H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GRM6, ZNF454
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
GRM6, ZNF454
Single nucleotide variant
(synonymous variant)
GRM6-related condition
+2 more
GBenign/Likely benign
GRM6, ZNF454
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
GRM6, ZNF454
Single nucleotide variant
(synonymous variant)
GRM6-related condition
+3 more
GBenign/Likely benign
GRM6, ZNF454
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
GRM6, ZNF454
(R578C)
Single nucleotide variant
(missense variant)
GRM6-related condition
+2 more
GBenign/Likely benign
GRM6, LOC100130798
+1 more
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
ZNF454, GRM6
(D551E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GRM6, ZNF454
(R547C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ZNF454, GRM6
(P524L)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
GRM6, ZNF454
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
ZNF454, GRM6
+1 more
(Q488*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
GRM6, ZNF454
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
GRM6, ZNF454
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
ZNF454, GRM6
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
GRM6, LOC100130798
+1 more
(R449C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GRM6, ZNF454
(T436I)
Indel
(missense variant)
not specified
+1 more
GBenign
GRM6, ZNF454
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
GRM6, ZNF454
(T436I)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
GRM6, ZNF454
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
GRM6, ZNF454
(I405T)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
GRM6, ZNF454
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
GRM6
(G338R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GRM6
(V243F)
Single nucleotide variant
(missense variant)
GRM6-related condition
+3 more
GBenign/Likely benign
GRM6
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
GRM6
(F189L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GRM6
Single nucleotide variant
(intron variant)
not provided
GConflicting classifications of pathogenicity
GRM6
(Q59P)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
GRM6
(A7T)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
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