A0A1I9LLF2 · A0A1I9LLF2_ARATH

Variants

162050100150200250300350400450500550600
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_3_5757249_G_C116G>A1000Genomes
tmp_3_5757293_T_G131S>A1000Genomes
ENSVATH02154279159D>E1000Genomes
tmp_3_5757382_A_T160E>D1000Genomes
ENSVATH05846848240M>I1000Genomes
tmp_3_5757900_C_T283P>S1000Genomes
tmp_3_5757903_G_A284A>T1000Genomes
ENSVATH02154285286V>I1000Genomes
ENSVATH13933216292P>L1000Genomes
ENSVATH05846849323P>S1000Genomes
ENSVATH02154286325Q>P1000Genomes
ENSVATH00327998335V>I1000Genomes
ENSVATH05846850343L>P1000Genomes
ENSVATH10729802402R>P1000Genomes
tmp_3_5758264_C_T404S>F1000Genomes
tmp_3_5758333_C_G427T>S1000Genomes
ENSVATH05846853437S>L1000Genomes
tmp_3_5758395_C_A448P>T1000Genomes
tmp_3_5758435_C_T461S>L1000Genomes
ENSVATH05846854463P>R1000Genomes
ENSVATH00328005470Y>F1000Genomes
ENSVATH00328007511S>A1000Genomes
tmp_3_5758644_A_C531N>H1000Genomes
ENSVATH13933218540G>D1000Genomes
ENSVATH05846855546P>T1000Genomes
ENSVATH05846856551V>A1000Genomes
tmp_3_5758710_C_T553H>Y1000Genomes
ENSVATH13933219556V>F1000Genomes
tmp_3_5758728_G_A559D>N1000Genomes
ENSVATH00328008562G>S1000Genomes
tmp_3_5758740_G_A563G>S1000Genomes
ENSVATH13933220574T>M1000Genomes
ENSVATH02154290577A>S1000Genomes
ENSVATH00328009578T>A1000Genomes
ENSVATH10729883602A>G1000Genomes
ENSVATH05846866617N>D1000Genomes
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