C0LGE4 · Y1124_ARATH

Variants

1882100200300400500600700800
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_1_4247715_C_A5H>N1000Genomes
tmp_1_4247718_C_A6L>I1000Genomes
ENSVATH1106204113F>L1000Genomes
ENSVATH1106204222D>N1000Genomes
ENSVATH0456498323S>F1000Genomes
ENSVATH0001988538S>C1000Genomes
ENSVATH0456498443N>S1000Genomes
tmp_1_4247856_G_A52G>S1000Genomes
tmp_1_4247996_G_C98L>F1000Genomes
tmp_1_4248019_A_T106N>I1000Genomes
tmp_1_4248024_C_G108P>A1000Genomes
tmp_1_4248087_G_T129G>C1000Genomes
tmp_1_4248121_G_T140S>I1000Genomes
tmp_1_4248128_G_T142R>S1000Genomes
ENSVATH11062043143F>L1000Genomes
tmp_1_4248156_A_T152T>S1000Genomes
ENSVATH04564988179S>A1000Genomes
tmp_1_4248269_C_A189N>K1000Genomes
ENSVATH00019886206P>L1000Genomes
ENSVATH11062044208I>F1000Genomes
tmp_1_4248361_G_A220R>K1000Genomes
tmp_1_4248447_C_G249H>D1000Genomes
tmp_1_4248466_C_T255A>V1000Genomes
tmp_1_4248487_T_C262I>T1000Genomes
tmp_1_4248592_C_G297T>S1000Genomes
ENSVATH00019887329G>V1000Genomes
ENSVATH11062115357F>Y1000Genomes
ENSVATH04564993413R>Q1000Genomes
tmp_1_4249111_C_T439S>L1000Genomes
tmp_1_4249123_C_T443P>L1000Genomes
ENSVATH04564994449G>R1000Genomes
ENSVATH04564994449G>W1000Genomes
ENSVATH11062118455T>M1000Genomes
ENSVATH11062118455T>R1000Genomes
tmp_1_4249161_C_T456H>Y1000Genomes
ENSVATH01041610491D>Y1000Genomes
tmp_1_4249287_A_G498N>D1000Genomes
ENSVATH01041611510D>N1000Genomes
ENSVATH11062119520I>V1000Genomes
ENSVATH04564996543R>M1000Genomes
tmp_1_4249495_T_G567I>R1000Genomes
ENSVATH13885855610A>T1000Genomes
ENSVATH00019888616V>I1000Genomes
ENSVATH11062122683I>F1000Genomes
ENSVATH00019889748L>I1000Genomes
ENSVATH11062124756D>G1000Genomes
ENSVATH04565002777Q>H1000Genomes
tmp_1_4250140_C_T782A>V1000Genomes
ENSVATH04565003817R>T1000Genomes
tmp_1_4250248_A_G818D>G1000Genomes
ENSVATH04565005856T>M1000Genomes
ENSVATH01041613861L>R1000Genomes
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