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
150101 BAA10g34140 A10 24095235 C T missense_variant MODERATE c.1348C>T|p.His450Tyr S105
150102 BAA10g34140 A10 24095990 G A synonymous_variant LOW c.2103G>A|p.Glu701Glu S125
150103 BAA10g34140 A10 24096025 G A missense_variant MODERATE c.2138G>A|p.Cys713Tyr S17
150104 BAA10g34150 A10 24096459 C T upstream_gene_variant MODIFIER c.-1807C>T| S187
150105 BAA10g34150 A10 24096915 G A upstream_gene_variant MODIFIER c.-1351G>A| S212
150106 BAA10g34150 A10 24097142 G A upstream_gene_variant MODIFIER c.-1124G>A| S240
150107 BAA10g34150 A10 24097567 G A upstream_gene_variant MODIFIER c.-699G>A| S106
150108 BAA10g34150 A10 24097576 G A upstream_gene_variant MODIFIER c.-690G>A| S244
150109 BAA10g34150 A10 24098467 G A missense_variant MODERATE c.202G>A|p.Asp68Asn S250
150110 BAA10g34140 A10 24099567 G A downstream_gene_variant MODIFIER c.*3424G>A| S132
S137
S138
S215
S89
150111 BAA10g34140 A10 24099819 C T downstream_gene_variant MODIFIER c.*3676C>T| S142
150112 BAA10g34140 A10 24099890 C A downstream_gene_variant MODIFIER c.*3747C>A| S67
150113 BAA10g34160 A10 24100716 G A splice_region_variant&intron_variant LOW c.894+8C>T| S158
150114 BAA10g34160 A10 24102038 G A upstream_gene_variant MODIFIER c.-254C>T| S127
150115 BAA10g34160 A10 24103957 C T upstream_gene_variant MODIFIER c.-2173G>A| S286
S305
150116 BAA10g34160 A10 24104317 C G upstream_gene_variant MODIFIER c.-2533G>C| S140
S168
S278
S64
150117 BAA10g34170 A10 24109019 C T upstream_gene_variant MODIFIER c.-678G>A| S275
150118 BAA10g34170 A10 24109655 C T upstream_gene_variant MODIFIER c.-1314G>A| S97
150119 BAA10g34180 A10 24110060 G A missense_variant MODERATE c.593C>T|p.Pro198Leu S158
150120 BAA10g34180 A10 24110644 C T missense_variant&splice_region_variant MODERATE c.472G>A|p.Val158Met S28
150121 BAA10g34180 A10 24111018 C T missense_variant MODERATE c.275G>A|p.Cys92Tyr S218
150122 BAA10g34170 A10 24111165 C T upstream_gene_variant MODIFIER c.-2824G>A| S58
150123 BAA10g34190 A10 24111784 C T missense_variant MODERATE c.518G>A|p.Gly173Asp S260
150124 BAA10g34190 A10 24112199 C T missense_variant MODERATE c.103G>A|p.Ala35Thr S232
150125 BAA10g34170 A10 24112751 C T upstream_gene_variant MODIFIER c.-4410G>A| S256