F4IFQ0 · F4IFQ0_ARATH

Variants

110011002003004005006007008009001,000
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
ENSVATH1455933516I>T1000Genomes
ENSVATH1342879323S>A1000Genomes
ENSVATH0190645835Q>E1000Genomes
ENSVATH0025090443A>T1000Genomes
ENSVATH0790039368V>G1000Genomes
ENSVATH01906467161S>T1000Genomes
ENSVATH13428825168T>I1000Genomes
tmp_2_11630953_C_T176P>S1000Genomes
tmp_2_11631172_C_A212Q>K1000Genomes
tmp_2_11631173_A_T212Q>L1000Genomes
ENSVATH05604119224G>S1000Genomes
tmp_2_11632747_C_A391A>E1000Genomes
ENSVATH14559340457T>M1000Genomes
tmp_2_11633357_C_T479S>L1000Genomes
ENSVATH00250913512I>T1000Genomes
tmp_2_11633548_C_G515T>R1000Genomes
tmp_2_11633550_A_G516S>G1000Genomes
tmp_2_11633552_C_G516S>R1000Genomes
ENSVATH05604133551L>V1000Genomes
ENSVATH13428830556R>H1000Genomes
ENSVATH00250916574D>E1000Genomes
ENSVATH13428831583P>S1000Genomes
tmp_2_11633755_C_G584A>G1000Genomes
tmp_2_11633757_G_T585G>W1000Genomes
ENSVATH14559344647P>S1000Genomes
tmp_2_11634457_G_A684R>H1000Genomes
tmp_2_11635082_A_G815I>V1000Genomes
ENSVATH05604148967H>R1000Genomes
tmp_2_11636151_C_T992P>L1000Genomes
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