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Links from Gene

Items: 1 to 100 of 301

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GLikely benign
DMXL1
(I1721L +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(M1071I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(S301C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(T757A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(P2079L +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(Y1487H +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(M1593V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(N886D +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DMXL1
(D1746E +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(S734T)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DMXL1
(T570I)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DMXL1
(S737C)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DMXL1
(I963T +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DMXL1
(L1730F +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(I112T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(R1511L +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(S1620P +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(K1608E +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(L1762F +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(G568S)
Single nucleotide variant
(missense variant +2 more)
not specified
GLikely benign
DMXL1
(H330R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(A326G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(S324T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(T3009I +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(T2917I +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(V2847I +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(N2061S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(T2376I +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(T2032A +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(L2170S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(N1954S +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GLikely benign
DMXL1
(G219R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(L1783P +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(A2100V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(D1770Y +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(D1759N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(S1590Y +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(T1665S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(H1820R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(D1800G +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(S1757I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(R1746C +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
DMXL1
(R1290H +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(R1561Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(R1292Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(H1257R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(P1483T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(D1143E +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(L982I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(T1046I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(K1044E +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(I1251T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
DMXL1
(I1251V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(P884S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(H114R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(N786D +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(S774G +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(L858H +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(S1070C +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(S1050N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(S681F +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DMXL1
(R879C +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DMXL1
(I566V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(V701D)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DMXL1
(N687S)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DMXL1
(T663I)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DMXL1
(M575V)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DMXL1
(C543S)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DMXL1
(H497Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(S495R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(K435T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(Q431H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(E423Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DMXL1
(G388R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
AP3S1, APC
+80 more
Copy number loss
not specified
GPathogenic
DMXL1
(T1969S +3 more)
Single nucleotide variant
(missense variant +1 more)
DMXL1-related disorder
GBenign
DMXL1
Single nucleotide variant
(intron variant)
DMXL1-related disorder
GBenign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GBenign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GBenign
DMXL1
(C1004S +2 more)
Single nucleotide variant
(missense variant +1 more)
DMXL1-related disorder
GBenign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GBenign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GBenign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GLikely benign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GLikely benign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GLikely benign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GLikely benign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GBenign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GLikely benign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GBenign
DMXL1
(A2029T +3 more)
Single nucleotide variant
(missense variant +1 more)
DMXL1-related disorder
GBenign
DMXL1
(M1260V +2 more)
Single nucleotide variant
(missense variant +1 more)
DMXL1-related disorder
GBenign
DMXL1
(S616N +2 more)
Single nucleotide variant
(missense variant +1 more)
DMXL1-related disorder
GBenign
DMXL1
Single nucleotide variant
(intron variant)
DMXL1-related disorder
GLikely benign
DMXL1
(E2307Q +1 more)
Single nucleotide variant
(missense variant +1 more)
DMXL1-related disorder
GLikely benign
DMXL1
(V648I)
Single nucleotide variant
(missense variant +2 more)
DMXL1-related disorder
GBenign
DMXL1
Single nucleotide variant
(synonymous variant +2 more)
DMXL1-related disorder
GBenign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GBenign
DMXL1
Single nucleotide variant
(synonymous variant +1 more)
DMXL1-related disorder
GLikely benign
DMXL1
(Q2202H +3 more)
Single nucleotide variant
(missense variant +1 more)
DMXL1-related disorder
GBenign
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