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Links from Gene

Items: 89

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PAK1
(N319K +5 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
PAK1
(I24N)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
PAK1
(V107M +3 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GUncertain significance
PAK1
(K146N +3 more)
Single nucleotide variant
(missense variant +2 more)
See cases
GUncertain significance
PAK1
(G311fs +6 more)
Deletion
(frameshift variant +2 more)
PAK1-related disorder
GUncertain significance
PAK1
(M143V +2 more)
Single nucleotide variant
(missense variant +2 more)
PAK1-related disorder
GUncertain significance
PAK1
Single nucleotide variant
(synonymous variant +2 more)
PAK1-related disorder
GLikely benign
PAK1
(G88S)
Single nucleotide variant
(missense variant +3 more)
PAK1-related disorder
GLikely pathogenic
PAK1
Single nucleotide variant
(synonymous variant +3 more)
PAK1-related disorder
GBenign
PAK1
Single nucleotide variant
(synonymous variant +2 more)
PAK1-related disorder
GLikely benign
PAK1
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
PAK1
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
PAK1
(A123V +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
PAK1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
PAK1
Microsatellite
(inframe_insertion +1 more)
PAK1-related disorder
+1 more
GLikely benign
PAK1
Single nucleotide variant
(synonymous variant +2 more)
not provided
+1 more
GLikely benign
PAK1
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
PAK1
Single nucleotide variant
(synonymous variant +1 more)
PAK1-related disorder
+1 more
GLikely benign
PAK1
(L423M +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
PAK1
(I438V +2 more)
Single nucleotide variant
(missense variant +3 more)
not provided
GUncertain significance
PAK1
(V87F)
Single nucleotide variant
(missense variant +3 more)
Neurodevelopmental disorder
GUncertain significance
PAK1
(R418W +7 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GLikely pathogenic
PAK1
(N231S +5 more)
Single nucleotide variant
(missense variant +2 more)
Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia
GUncertain significance
PAK1
(R160* +3 more)
Single nucleotide variant
(nonsense +3 more)
not provided
GUncertain significance
PAK1
(P15S)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
PAK1
(A356T +7 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
PAK1
(P85S +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
PAK1
(T84R)
Single nucleotide variant
(missense variant +3 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
PAK1
(R273C +6 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
PAK1
(I378V +6 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
PAK1
(I214S +5 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
PAK1
(Q144E +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GLikely benign
PAK1
(E176Q +4 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
PAK1
(P364S +7 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
PAK1
(P88L +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GLikely benign
PAK1
(L372Q +7 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
PAK1
(G27S)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GUncertain significance
PAK1
(K225N +5 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GUncertain significance
PAK1
(K422* +2 more)
Single nucleotide variant
(nonsense +1 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GUncertain significance
PAK1
Single nucleotide variant
(intron variant)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GUncertain significance
PAK1
Single nucleotide variant
(intron variant)
Inborn genetic diseases
GUncertain significance
PAK1
(G181C +4 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
PAK1
(N130T +3 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
PAK1
(N129K +3 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
PAK1
Single nucleotide variant
(intron variant)
Inborn genetic diseases
GLikely benign
PAK1
(L498F +2 more)
Single nucleotide variant
(missense variant +3 more)
Inborn genetic diseases
GUncertain significance
PAK1
(R224T +5 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
PAK1
(E328fs +5 more)
Deletion
(frameshift variant +2 more)
not provided
GUncertain significance
PAK1
Microsatellite
(intron variant)
Schizophrenia
GUncertain significance
PAK1
(S133L +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
PAK1
(R105C +2 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
GRIA4, GRIK4
+956 more
Copy number gain
MISSED ABORTION
GPathogenic
PAK1
(Y376H +6 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
PAK1
(E336G +6 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
PAK1
(Y142H +2 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
PAK1
(R117W +3 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
PAK1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
PAK1
(R53Q)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
PAK1
(S122P +3 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GUncertain significance
PAK1
(L429F +11 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GUncertain significance
PAK1
Single nucleotide variant
(intron variant)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GBenign
PAK1
(S110T +2 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
PAK1
(P121S +2 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
+1 more
GPathogenic/Likely pathogenic
PAK1
(S133P +2 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
PAK1
Single nucleotide variant
(intron variant)
PAK1-related disorder
+2 more
GBenign
PAK1
(V127M +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GConflicting classifications of pathogenicity
PAK1
(E129fs +2 more)
Deletion
(frameshift variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GUncertain significance
PAK1
(Y131N +2 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GPathogenic
ACER3, ACP2
+904 more
Deletion
Intellectual disability
GPathogenic
PAK1
(M143T +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GLikely pathogenic
PAK1
(G311R +6 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
PAK1
(L372R +7 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
PAK1
(R174W +4 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual disability
+1 more
GUncertain significance
PAK1
(R397G +6 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GUncertain significance
PAK1
(P128L +2 more)
Single nucleotide variant
(missense variant +2 more)
PAK1-related neurodevelopmental disorders
+2 more
GPathogenic
PAK1
(R112H +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
PAK1
(M143K +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GLikely pathogenic
PAK1
(I393T +6 more)
Single nucleotide variant
(missense variant +2 more)
See cases
+2 more
GPathogenic/Likely pathogenic
PAK1
Single nucleotide variant
(synonymous variant +2 more)
not provided
+1 more
GBenign
PAK1
Single nucleotide variant
(synonymous variant +2 more)
not provided
+1 more
GBenign
PAK1
(Y429C +7 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
PAK1
(Y131C +2 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual developmental disorder with macrocephaly, seizures, and speech delay
GLikely pathogenic
AAMDC, AASDHPPT
+261 more
Copy number gain
not provided
GPathogenic
PAK1, AQP11
+5 more
Copy number gain
not provided
GUncertain significance
ACP2, CREBZF
+1289 more
Copy number gain
See cases
GPathogenic
GALNT18, MPZL3
+1289 more
Copy number gain
See cases
GPathogenic
CAPN5, GDPD4
+2 more
Copy number loss
See cases
GUncertain significance
AAMDC, ACER3
+474 more
Copy number loss
See cases
GPathogenic
AAMDC, ACER3
+355 more
Copy number loss
See cases
GPathogenic
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