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Items: 81

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACAD10, ACADS
+4836 more
Copy number gain
See cases
GPathogenic
AGAP2, AGAP2-AS1
+199 more
Copy number loss
See cases
GPathogenic
AGAP2, AGAP2-AS1
+162 more
Copy number loss
See cases
GPathogenic
LINC02388, LOC100506869
+17 more
Copy number loss
See cases
GUncertain significance
LINC02448, LOC100506869
+24 more
Copy number gain
See cases
GUncertain significance
LRIG3
(H1036R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(Y993C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(S1033W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(P966S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(S924R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(C981S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(T866I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(C860Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(S838R +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
LRIG3
(G829R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(H820del +1 more)
Microsatellite
(inframe_deletion)
not provided
GBenign
LRIG3
(R807G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(P851S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(R775W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(Y771H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(R721H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(V720M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(N779S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(S760I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(N749H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(F685L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(D674N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(L704F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(R641L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(R641W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(N628D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LRIG3
(V664M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(F602L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(E657K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(E623D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(G557R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(A616D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(K518R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(T504A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(V499L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(Q495R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(R493W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(M546I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(S468C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(S509L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(T442M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(C493F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LRIG3
(N368S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(R337Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(R390Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(M318V +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
LOC126861547, LRIG3
(F295L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126861547, LRIG3
(D352V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126861547, LRIG3
(E315K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126861547, LRIG3
(S254N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126861547, LRIG3
(D245V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126861547, LRIG3
(D245N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126861547, LRIG3
(G281A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(E221K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(R118Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(N175S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(L107V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(K142E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(T52I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(N47S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(W75S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130008170, LRIG3
(G40R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(G31D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
(A3S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRIG3
Copy number loss
not specified
GUncertain significance
AGAP2, ARHGAP9
+45 more
Copy number loss
not provided
GLikely pathogenic
SLC16A7, LRIG3
+1 more
Copy number loss
not provided
GUncertain significance
AGAP2, ANKRD52
+105 more
Copy number gain
not provided
GPathogenic
LRIG3
Copy number gain
not provided
GUncertain significance
LRIG3
Copy number loss
not provided
GUncertain significance
SLC15A5, SLC16A7
+1006 more
Copy number gain
See cases
GPathogenic
A2M, A2ML1
+1006 more
Copy number gain
See cases
GPathogenic
LRIG3, SLC16A7
Copy number gain
See cases
GLikely benign
GALNT8, H2AJ
+1007 more
Copy number gain
See cases
GPathogenic
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