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Items: 31

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXG1
Microsatellite
(inframe_insertion)
FOXG1 disorder
GBenign
FOXG1
Deletion
(inframe_deletion)
FOXG1 disorder
GBenign
FOXG1
Deletion
(inframe_deletion)
FOXG1 disorder
GBenign
FOXG1
(P69Q)
Single nucleotide variant
(missense variant)
FOXG1-related condition
+4 more
GBenign/Likely benign
FOXG1
Microsatellite
(inframe_insertion)
FOXG1 disorder
GBenign
FOXG1
(Q73P)
Single nucleotide variant
(missense variant)
FOXG1 disorder
GBenign
FOXG1
Microsatellite
(inframe_insertion)
FOXG1 disorder
GLikely benign
FOXG1
(P84R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
FOXG1
(Q86K)
Single nucleotide variant
(missense variant)
FOXG1 disorder
GLikely benign
FOXG1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
FOXG1
(P109L)
Single nucleotide variant
(missense variant)
FOXG1 disorder
GLikely benign
FOXG1
Duplication
(inframe_insertion)
not specified
+1 more
GConflicting classifications of pathogenicity
FOXG1
Single nucleotide variant
(synonymous variant)
FOXG1 disorder
GBenign
FOXG1
(E154fs)
Duplication
(frameshift variant)
FOXG1 disorder
GPathogenic
FOXG1
Single nucleotide variant
(synonymous variant)
FOXG1 disorder
GBenign
FOXG1
(K157N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FOXG1
(K157N)
Single nucleotide variant
(missense variant)
FOXG1 disorder
GLikely benign
FOXG1
Single nucleotide variant
(synonymous variant)
FOXG1 disorder
GBenign
FOXG1
(G168A)
Single nucleotide variant
(missense variant)
FOXG1 disorder
GBenign
FOXG1
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GConflicting classifications of pathogenicity
FOXG1
(Y217fs)
Deletion
(frameshift variant)
not provided
GPathogenic
FOXG1
(G224S)
Single nucleotide variant
(missense variant)
FOXG1 disorder
GLikely pathogenic
FOXG1
(R230L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FOXG1
(S349A)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FOXG1
Single nucleotide variant
(synonymous variant)
FOXG1 disorder
GBenign
FOXG1
Single nucleotide variant
(synonymous variant)
FOXG1 disorder
GLikely benign
FOXG1
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GBenign
FOXG1
Single nucleotide variant
(synonymous variant)
FOXG1 disorder
GBenign
FOXG1
Single nucleotide variant
(3 prime UTR variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
FOXG1
Single nucleotide variant
(3 prime UTR variant)
not specified
+1 more
GUncertain significance
FOXG1
Single nucleotide variant
(3 prime UTR variant)
not specified
GBenign
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