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F4IN32 · MCC06_ARATH

Variants

129920406080100120140160180200220240260280100200300

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_2_17679227_C_A7Q>H1000Genomes
tmp_2_17679217_T_A11T>S1000Genomes
tmp_2_17679181_G_A23P>S1000Genomes
ENSVATH0570375324I>M1000Genomes
ENSVATH0198094836C>W1000Genomes
tmp_2_17679141_C_T36C>Y1000Genomes
tmp_2_17678986_T_C45D>G1000Genomes
ENSVATH1460887849D>N1000Genomes
ENSVATH0570374658G>A1000Genomes
ENSVATH1460887659N>K1000Genomes
tmp_2_17678935_G_A62S>L1000Genomes
ENSVATH0570374565P>H1000Genomes
ENSVATH1361875070R>Q1000Genomes
tmp_2_17678896_A_C75F>C1000Genomes
ENSVATH0570374480Q>*1000Genomes
tmp_2_17678864_G_T86H>N1000Genomes
ENSVATH0198094294L>F1000Genomes
ENSVATH0791617896G>C1000Genomes
ENSVATH1361874898E>K1000Genomes
ENSVATH05703739102W>*1000Genomes
tmp_2_17678683_A_G108L>S1000Genomes
tmp_2_17678633_A_T125F>I1000Genomes
tmp_2_17678627_C_A127E>*1000Genomes
ENSVATH05703737130I>M1000Genomes
ENSVATH13618747145D>E1000Genomes
ENSVATH14608863151G>R1000Genomes
ENSVATH14608862164P>L1000Genomes
tmp_2_17678401_C_T173A>T1000Genomes
tmp_2_17678378_G_T180S>R1000Genomes
tmp_2_17678367_T_C184K>R1000Genomes
ENSVATH05703732196K>M1000Genomes
tmp_2_17678321_G_T199N>K1000Genomes
ENSVATH05703731203E>K1000Genomes
tmp_2_17678293_C_T209E>K1000Genomes
ENSVATH00271228215S>G1000Genomes
ENSVATH05703730221M>L1000Genomes
ENSVATH00271226224G>S1000Genomes
ENSVATH05703729226R>K1000Genomes
ENSVATH05703728228K>E1000Genomes
ENSVATH13618745235D>G1000Genomes
ENSVATH05703727251R>G1000Genomes
ENSVATH13618734252V>L1000Genomes
ENSVATH05703726254E>G1000Genomes
ENSVATH05703725261N>I1000Genomes
tmp_2_17678120_G_C266D>E1000Genomes
ENSVATH05703724266D>Y1000Genomes
ENSVATH00271223291W>R1000Genomes
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