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Items: 54

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TLE2
(R722K +2 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
TLE2
(V701I)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
TLE2
(S712L +2 more)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GUncertain significance
TLE2
(S583N +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
TLE2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
TLE2
(S550N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(P540L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(R538C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(R500H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(M582V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(C444S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(E420A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(R538L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(A411V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(I407V +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TLE2
(T493M +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(V483M +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(R446W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(V310I +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(S298F +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(G414V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(S407F +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(R266H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(S224P +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(G194R +3 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
TLE2
(S303C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(P299T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(P295S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(R267Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(P247H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TLE2
(S196L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(A188V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(S183P +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(V191M +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(A167V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(T165M +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(R141H +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(T139S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(P135L +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(P135A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(P149T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(A134V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(P129Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(R122C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(V107I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(R83H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(V81G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(E24Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
(G69R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TLE2
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
TLE2
(A37D +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(K31E +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TLE2
(G14S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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