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Items: 52

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DGKH, LOC130009645
(H8Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DGKH, LOC130009645
(G20A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DGKH, LOC130009645
(E46D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DGKH
(R62Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DGKH
(R85P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DGKH
(R85L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DGKH
(S19Y +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(V20A +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(Y26N +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(Q30H +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(T86A +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(T229I +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(D317G +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(C84Y +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(R215H +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(P125A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(A506T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(V274I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(V387I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(T393M +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(E310K +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(P440A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(P369S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(A382T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(P642A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(E527K +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(D425V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(G427S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(R439Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(R473K +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(T616M +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(I510V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(V525I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(M643V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
DGKH
(P931L +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(A849T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(C1007R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(L1065R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(H1106N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(P868T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(T898I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGKH
(E1154D +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(D1161H +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(L1163F +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(N1164S +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(R1038S +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(R1174C +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(L1183F +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(H1048Y +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DGKH
(D1192V +2 more)
Single nucleotide variant
(synonymous variant +2 more)
not specified
GUncertain significance
DGKH
(P1196L +2 more)
Single nucleotide variant
(synonymous variant +2 more)
not specified
GUncertain significance
DGKH
(V1084M +2 more)
Single nucleotide variant
(3 prime UTR variant +2 more)
not specified
GUncertain significance
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