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
9151 BAA01g07370 A01 3263376 C T intron_variant MODIFIER c.976+117C>T| S20
9152 BAA01g07370 A01 3263544 C T intron_variant MODIFIER c.976+285C>T| S296
9153 BAA01g07370 A01 3264442 C T downstream_gene_variant MODIFIER c.*353C>T| S250
9154 BAA01g07370 A01 3265141 G A downstream_gene_variant MODIFIER c.*1052G>A| S17
9155 BAA01g07380 A01 3270063 G A upstream_gene_variant MODIFIER c.-1241G>A| S122
9156 BAA01g07380 A01 3270105 C T upstream_gene_variant MODIFIER c.-1199C>T| S38
9157 BAA01g07380 A01 3271330 C T synonymous_variant LOW c.27C>T|p.Leu9Leu S136
9158 BAA01g07380 A01 3271977 C T synonymous_variant LOW c.408C>T|p.Leu136Leu S166
9159 BAA01g07390 A01 3273402 G A upstream_gene_variant MODIFIER c.-2532G>A| S237
9160 BAA01g07390 A01 3273607 A T upstream_gene_variant MODIFIER c.-2327A>T| S105
S106
9161 BAA01g07390 A01 3273629 C T upstream_gene_variant MODIFIER c.-2305C>T| S18
9162 BAA01g07390 A01 3274539 C T upstream_gene_variant MODIFIER c.-1395C>T| S164
S260
9163 BAA01g07390 A01 3275234 C T upstream_gene_variant MODIFIER c.-700C>T| S62
9164 BAA01g07390 A01 3276117 C T stop_gained HIGH c.184C>T|p.Gln62* S247
9165 BAA01g07390 A01 3276249 G A missense_variant MODERATE c.316G>A|p.Glu106Lys S191
9166 BAA01g07390 A01 3276283 C T missense_variant MODERATE c.350C>T|p.Thr117Ile S303
9167 BAA01g07400 A01 3277351 C T upstream_gene_variant MODIFIER c.-581C>T| S150
9168 BAA01g07380 A01 3278208 G A downstream_gene_variant MODIFIER c.*4815G>A| S208
9169 BAA01g07380 A01 3278212 C T downstream_gene_variant MODIFIER c.*4819C>T| S218
9170 BAA01g07400 A01 3278474 G A missense_variant MODERATE c.415G>A|p.Asp139Asn S86
9171 BAA01g07400 A01 3279326 C T splice_region_variant&intron_variant LOW c.1070+6C>T| S287
9172 BAA01g07390 A01 3279403 G A downstream_gene_variant MODIFIER c.*2117G>A| S149
9173 BAA01g07430 A01 3279817 G A upstream_gene_variant MODIFIER c.-4848G>A| S169
9174 BAA01g07430 A01 3280850 G A upstream_gene_variant MODIFIER c.-3815G>A| S142
9175 BAA01g07420 A01 3281823 C T missense_variant MODERATE c.322G>A|p.Gly108Arg S42