Q8LEC0 · RLPHL_ARATH

Variants

131120406080100120140160180200220240260280300
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
ENSVATH1057448117G>V1000Genomes
ENSVATH1057448218N>H1000Genomes
ENSVATH0580089235N>I1000Genomes
ENSVATH0212722468E>D1000Genomes
tmp_3_3062198_A_G70H>R1000Genomes
ENSVATH0031429474T>A1000Genomes
tmp_3_3062212_C_T75H>Y1000Genomes
tmp_3_3062276_C_T96P>L1000Genomes
tmp_3_3062282_A_T98D>V1000Genomes
ENSVATH1057448499G>W1000Genomes
tmp_3_3062322_A_C111K>N1000Genomes
tmp_3_3062343_G_A118W>*1000Genomes
ENSVATH05800897120K>R1000Genomes
tmp_3_3062371_C_A128H>N1000Genomes
ENSVATH00314295130Q>K1000Genomes
tmp_3_3062384_G_A132R>K1000Genomes
ENSVATH00314296157D>N1000Genomes
tmp_3_3062483_A_T165Y>F1000Genomes
ENSVATH02127225168P>T1000Genomes
tmp_3_3062498_G_A170G>E1000Genomes
ENSVATH05800919173D>E1000Genomes
ENSVATH13890562179P>T1000Genomes
tmp_3_3062836_T_C189M>T1000Genomes
ENSVATH00314298193H>L1000Genomes
ENSVATH00314298193H>R1000Genomes
ENSVATH05800920194K>E1000Genomes
ENSVATH05800921194K>T1000Genomes
ENSVATH10574567201E>K1000Genomes
ENSVATH10574568203E>G1000Genomes
ENSVATH05800923204E>D1000Genomes
ENSVATH05800924207T>K1000Genomes
ENSVATH10574569213A>G1000Genomes
ENSVATH10574569213A>V1000Genomes
tmp_3_3063070_G_A217G>D1000Genomes
ENSVATH05800927221K>E1000Genomes
ENSVATH05800928225E>K1000Genomes
ENSVATH10574570246G>R1000Genomes
ENSVATH10574574260K>R1000Genomes
tmp_3_3063345_G_T276G>C1000Genomes
tmp_3_3063356_G_T279L>F1000Genomes
ENSVATH05800937282D>N1000Genomes
tmp_3_3063381_A_G288T>A1000Genomes
ENSVATH05800939290T>K1000Genomes
ENSVATH05800940291P>H1000Genomes
ENSVATH00314301306T>I1000Genomes
ENSVATH10574617308N>K1000Genomes
ENSVATH05800941310S>F1000Genomes
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