F4IMQ0 · FLX_ARATH

Variants

128820406080100120140160180200220240260280
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_2_12861856_C_T3G>R1000Genomes
tmp_2_12861822_G_A14S>L1000Genomes
tmp_2_12861788_T_A25Q>H1000Genomes
ENSVATH0562911655N>T1000Genomes
tmp_2_12861687_C_A59R>L1000Genomes
tmp_2_12861668_G_C65I>M1000Genomes
tmp_2_12861667_C_T66G>R1000Genomes
ENSVATH0025450486V>A1000Genomes
ENSVATH0025450387K>Q1000Genomes
ENSVATH0562911590A>T1000Genomes
tmp_2_12861556_C_A103A>S1000Genomes
ENSVATH05629114151A>G1000Genomes
ENSVATH01927580163L>S1000Genomes
ENSVATH01927581163L>V1000Genomes
tmp_2_12861341_T_A174K>N1000Genomes
tmp_2_12861149_C_A193E>D1000Genomes
tmp_2_12861147_C_T194R>H1000Genomes
tmp_2_12861140_C_G196M>I1000Genomes
ENSVATH00254502221A>S1000Genomes
tmp_2_12861051_G_A226A>V1000Genomes
tmp_2_12861049_C_T227A>T1000Genomes
ENSVATH01927578233T>N1000Genomes
ENSVATH05629109239A>T1000Genomes
ENSVATH14571855248D>N1000Genomes
tmp_2_12860865_C_A259E>D1000Genomes
ENSVATH01927575268L>V1000Genomes
ENSVATH05629104273Y>N1000Genomes
tmp_2_12860630_G_C282L>V1000Genomes
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