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Links from Gene

Items: 74

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TASOR
(P941R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TASOR
(Q959K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(E1200D +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(A89S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(R1184W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(R1143Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(V239I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(L155P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(V1033A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(T1021A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(N1408S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(N911I +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(I1294T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(S1331P +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(F1282L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(Y1278H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(C1260R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(I1116T +3 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
TASOR
(S1098N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(E1035K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(E626K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(T552S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(Q975L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TASOR
(D930N +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TASOR
(R899H +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
TASOR
(D885G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(V833A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(P432H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(P424L +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
TASOR
(S392P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(A384V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(F376L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(I744F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(I348V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
TASOR
(P347R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(I664M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(R259Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(F236C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(Q234K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(N549D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(A547T +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
TASOR
(Y71C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(R43S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(V393F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
TASOR
(N365S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CCDC66, TASOR
(N916T +11 more)
Single nucleotide variant
(3 prime UTR variant +2 more)
not specified
GUncertain significance
ABHD14A, ABHD14B
+86 more
Copy number loss
not specified
GPathogenic
CCDC66, ERC2
+1 more
Copy number gain
not provided
GUncertain significance
APPL1, ARHGEF3
+8 more
Copy number loss
not provided
GUncertain significance
TASOR
(V983I +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(I1032V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(A1459V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(C434F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(K1258Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(T364A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(E1054D +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(E738G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(E954K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(I369F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(H1119Y +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CCDC66, TASOR
(A903V +11 more)
Single nucleotide variant
(3 prime UTR variant +2 more)
not specified
GUncertain significance
TASOR
(P1060L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TASOR
(M1121T +3 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CCDC66, TASOR
(E643K +11 more)
Single nucleotide variant
(3 prime UTR variant +2 more)
not specified
GUncertain significance
TASOR
(Q975K)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
TASOR
Single nucleotide variant
(synonymous variant)
not provided
GBenign
CCDC66, TASOR
(S579fs +11 more)
Microsatellite
(3 prime UTR variant +2 more)
not provided
GLikely benign
TASOR
(E33K)
Single nucleotide variant
(missense variant)
Ependymoma
GUncertain significance
ARHGEF3, IL17RD
+2 more
Copy number gain
See cases
GUncertain significance
HHLA2, HIGD1A
+1054 more
Copy number gain
See cases
GPathogenic
A4GNT, AADAC
+1054 more
Copy number gain
See cases
GPathogenic
ABHD6, ACOX2
+66 more
Copy number loss
See cases
GPathogenic
ACTR8, ARHGEF3
+53 more
Copy number loss
See cases
GUncertain significance
ABHD6, ACOX2
+218 more
Copy number loss
See cases
GPathogenic
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