Q5XF51 · 3MMP_ARATH

Variants

138450100150200250300350100200300

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_1_8537276_T_G4I>L1000Genomes
tmp_1_8537266_A_G7F>S1000Genomes
ENSVATH0109775215A>T1000Genomes
ENSVATH0109775115A>V1000Genomes
ENSVATH1395878228S>A1000Genomes
tmp_1_8537203_G_A28S>L1000Genomes
ENSVATH1194909232P>L1000Genomes
ENSVATH0004175733Q>E1000Genomes
ENSVATH0109775053H>N1000Genomes
ENSVATH0463479154A>G1000Genomes
ENSVATH0109774863M>K1000Genomes
ENSVATH0109774775T>P1000Genomes
ENSVATH0463479091L>F1000Genomes
ENSVATH1194908996E>K1000Genomes
tmp_1_8536995_C_T97M>I1000Genomes
ENSVATH04634789106V>I1000Genomes
ENSVATH00041751120I>V1000Genomes
tmp_1_8536898_T_C130N>D1000Genomes
tmp_1_8536895_C_G131G>R1000Genomes
tmp_1_8536875_G_C137S>R1000Genomes
tmp_1_8536868_T_C140K>E1000Genomes
ENSVATH01097742140K>R1000Genomes
ENSVATH09374305151Q>*1000Genomes
ENSVATH09374304151Q>P1000Genomes
tmp_1_8536822_G_T155A>D1000Genomes
tmp_1_8536820_C_T156V>I1000Genomes
ENSVATH01097739159Y>F1000Genomes
tmp_1_8536808_A_T160S>T1000Genomes
tmp_1_8536766_C_T174D>N1000Genomes
tmp_1_8536753_G_C178A>G1000Genomes
ENSVATH11949087181P>S1000Genomes
ENSVATH00041745184A>T1000Genomes
ENSVATH11949086191S>N1000Genomes
tmp_1_8536707_G_C193F>L1000Genomes
ENSVATH01097737198T>A1000Genomes
ENSVATH04634788199R>C1000Genomes
ENSVATH00041743201E>A1000Genomes
ENSVATH11949085208F>S1000Genomes
ENSVATH00041742213R>K1000Genomes
ENSVATH04634787214F>V1000Genomes
ENSVATH01097735244A>T1000Genomes
ENSVATH11948963262V>I1000Genomes
ENSVATH13958780263S>A1000Genomes
tmp_1_8536418_G_T290L>I1000Genomes
tmp_1_8536385_A_C301S>A1000Genomes
ENSVATH13958779309T>M1000Genomes
tmp_1_8536280_C_T336G>S1000Genomes
tmp_1_8536267_G_A340P>L1000Genomes
ENSVATH11948961354A>P1000Genomes
tmp_1_8536208_C_T360G>S1000Genomes
ENSVATH13958777368L>V1000Genomes
ENSVATH01097734376I>L1000Genomes
tmp_1_8536148_A_G380F>L1000Genomes
tmp_1_8536130_TCTACA_T384V>D1000Genomes
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