Q9C9L0 · CUL3B_ARATH

Variants

1732100200300400500600700200400600

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
ENSVATH0013400326D>E1000Genomes
ENSVATH1377738274T>I1000Genomes
tmp_1_26204138_G_A77T>I1000Genomes
ENSVATH0013400290A>V1000Genomes
ENSVATH1377738193G>R1000Genomes
tmp_1_26204081_A_G96L>S1000Genomes
ENSVATH13777380100N>D1000Genomes
ENSVATH01509658117L>F1000Genomes
ENSVATH01509656133V>L1000Genomes
ENSVATH01509654139H>Y1000Genomes
ENSVATH13777379148S>L1000Genomes
ENSVATH01509653153T>I1000Genomes
tmp_1_26203895_G_T158T>K1000Genomes
ENSVATH01509651163V>A1000Genomes
ENSVATH05111722179N>I1000Genomes
ENSVATH05111720182K>R1000Genomes
tmp_1_26203758_A_T204S>T1000Genomes
tmp_1_26203748_A_C207F>C1000Genomes
tmp_1_26203736_T_C211E>G1000Genomes
ENSVATH05111717213M>K1000Genomes
ENSVATH05111718213M>L1000Genomes
ENSVATH01509647214E>G1000Genomes
ENSVATH05111716215F>L1000Genomes
tmp_1_26203719_C_T217E>K1000Genomes
ENSVATH05111715219C>Y1000Genomes
ENSVATH05111712240V>L1000Genomes
ENSVATH00134001245A>G1000Genomes
ENSVATH13777378249A>T1000Genomes
ENSVATH01509646253S>N1000Genomes
tmp_1_26203559_A_G270M>T1000Genomes
tmp_1_26203552_A_T272N>K1000Genomes
ENSVATH14456545277N>Y1000Genomes
ENSVATH05111711283K>M1000Genomes
tmp_1_26203505_C_T288G>D1000Genomes
tmp_1_26203484_C_T295R>H1000Genomes
ENSVATH13777376354D>N1000Genomes
tmp_1_26203197_G_C391L>V1000Genomes
ENSVATH05111706405K>N1000Genomes
ENSVATH14456514459S>L1000Genomes
tmp_1_26202952_G_C472H>Q1000Genomes
tmp_1_26202942_G_C476L>V1000Genomes
ENSVATH05111696505P>S1000Genomes
tmp_1_26202720_A_G550F>L1000Genomes
ENSVATH01509642590T>A1000Genomes
tmp_1_26202596_G_A591P>L1000Genomes
tmp_1_26202459_C_A637V>L1000Genomes
ENSVATH14456512669A>S1000Genomes
ENSVATH13777372683H>D1000Genomes
ENSVATH01509640703T>A1000Genomes
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