P49599 · P2C57_ARATH

Variants

138850100150200250300350100200300

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_4_13854088_C_T2A>T1000Genomes
ENSVATH0293285114N>T1000Genomes
ENSVATH0293285015T>S1000Genomes
tmp_4_13854043_G_C17R>G1000Genomes
ENSVATH0054184821Y>F1000Genomes
ENSVATH0054184821Y>S1000Genomes
ENSVATH1430376128G>S1000Genomes
tmp_4_13854004_GGCCACC_AGCCACC,G30L>F1000Genomes
ENSVATH0678721759R>S1000Genomes
ENSVATH0293284683V>L1000Genomes
tmp_4_13853821_C_G91V>L1000Genomes
ENSVATH06787213124G>R1000Genomes
tmp_4_13853627_G_C130I>M1000Genomes
ENSVATH00541846167I>F1000Genomes
ENSVATH06787208184V>I1000Genomes
ENSVATH12266299208I>N1000Genomes
tmp_4_13853063_C_T228G>R1000Genomes
tmp_4_13853017_G_T243T>K1000Genomes
ENSVATH02932827246N>D1000Genomes
ENSVATH06787200251K>R1000Genomes
ENSVATH06787200251K>T1000Genomes
ENSVATH02932818309S>N1000Genomes
ENSVATH00541837372T>A1000Genomes
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