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Links from Gene

Items: 40

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GCK
(E321* +2 more)
Single nucleotide variant
(nonsense +1 more)
not provided
GLikely pathogenic
GCK
(D246E +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
GCK
(I210T +2 more)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
GCK
(R185Q +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
Deletion
(genic upstream transcript variant)
not provided
GUncertain significance
GCK
(M114V +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(A10T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(S75Y +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(M56K +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(T25fs +4 more)
Duplication
(frameshift variant +1 more)
not provided
GPathogenic
GCK
Single nucleotide variant
(splice donor variant)
Maturity-onset diabetes of the young type 2
GPathogenic
GCK
(H316P +2 more)
Single nucleotide variant
(missense variant +1 more)
Maturity-onset diabetes of the young type 2
GUncertain significance
GCK
(N230I +2 more)
Single nucleotide variant
(missense variant)
Type 2 diabetes mellitus
+3 more
GUncertain significance
GCK
(D4fs)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
GCK
Single nucleotide variant
not provided
GUncertain significance
GCK
(T25A +5 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(E236V +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(G27D +5 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(K34N +5 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(D28Y +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(D77E +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(D204E +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(C128F +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(E235V +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(F315V +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
GCK
(E92A +2 more)
Single nucleotide variant
(missense variant)
Type 2 diabetes mellitus
+2 more
GUncertain significance
GCK
(R7fs)
Deletion
(frameshift variant)
not provided
GPathogenic
GCK
(A113fs +2 more)
Duplication
(frameshift variant)
not provided
GLikely pathogenic
GCK
Single nucleotide variant
(synonymous variant +1 more)
not provided
GUncertain significance
GCK
Duplication
(inframe_insertion)
not provided
GUncertain significance
GCK
(L76P +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(A383P +5 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(L323R +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
GCK
(D273E +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(W256S +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GCK
(V303L +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
GCK
(M57I +2 more)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
GCK
Duplication
Maturity-onset diabetes of the young type 2
GLikely pathogenic
GCK
Single nucleotide variant
Maturity-onset diabetes of the young type 2
GLikely pathogenic
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