Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
39101 BAA01g25140 A01 13492798 C T stop_gained HIGH c.433C>T|p.Gln145* S171
39102 BAA01g25140 A01 13492996 G A missense_variant MODERATE c.631G>A|p.Gly211Arg S207
S234
39103 BAA01g25140 A01 13493021 C T missense_variant MODERATE c.656C>T|p.Pro219Leu S148
S210
39104 BAA01g25130 A01 13493884 C T upstream_gene_variant MODIFIER c.-2817G>A| S140
39105 BAA01g25130 A01 13493936 G A upstream_gene_variant MODIFIER c.-2869C>T| S28
39106 BAA01g25150 A01 13496329 G A synonymous_variant LOW c.273G>A|p.Gly91Gly S284
39107 BAA01g25150 A01 13496563 C T synonymous_variant LOW c.507C>T|p.Leu169Leu S204
39108 BAA01g25140 A01 13497340 C T downstream_gene_variant MODIFIER c.*4135C>T| S107
39109 BAA01g25140 A01 13497922 G A downstream_gene_variant MODIFIER c.*4717G>A| S7
39110 BAA01g25140 A01 13497954 G A downstream_gene_variant MODIFIER c.*4749G>A| S191
39111 BAA01g25140 A01 13498101 C T downstream_gene_variant MODIFIER c.*4896C>T| S47
39112 BAA01g25150 A01 13498737 G A downstream_gene_variant MODIFIER c.*1748G>A| S245
39113 BAA01g25150 A01 13499158 C T downstream_gene_variant MODIFIER c.*2169C>T| S36
39114 BAA01g25150 A01 13499511 G A downstream_gene_variant MODIFIER c.*2522G>A| S58
39115 BAA01g25150 A01 13499557 C T downstream_gene_variant MODIFIER c.*2568C>T| S284
39116 BAA01g25150 A01 13499586 G A downstream_gene_variant MODIFIER c.*2597G>A| S183
39117 BAA01g25150 A01 13500601 C T downstream_gene_variant MODIFIER c.*3612C>T| S302
39118 BAA01g25150 A01 13500937 G A downstream_gene_variant MODIFIER c.*3948G>A| S45
39119 BAA01g25150 A01 13501682 G A downstream_gene_variant MODIFIER c.*4693G>A| S32
39120 BAA01g25160 A01 13502202 C T missense_variant MODERATE c.1103G>A|p.Gly368Glu S261
39121 BAA01g25160 A01 13502237 G A synonymous_variant LOW c.1068C>T|p.Phe356Phe S239
39122 BAA01g25160 A01 13502402 G A splice_region_variant&intron_variant LOW c.1014+8C>T| S84
S93
39123 BAA01g25160 A01 13502409 C T splice_donor_variant&intron_variant HIGH c.1014+1G>A| S255
39124 BAA01g25160 A01 13502514 G A intron_variant MODIFIER c.919-9C>T| S232
39125 BAA01g25160 A01 13503245 G A missense_variant MODERATE c.509C>T|p.Ser170Phe S279