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
91051 BAA10g01080 A10 538109 C T downstream_gene_variant MODIFIER c.*1315G>A| S123
91052 BAA10g01080 A10 539359 G A downstream_gene_variant MODIFIER c.*65C>T| S9
91053 BAA10g01080 A10 540586 G A stop_gained HIGH c.307C>T|p.Arg103* S105
S106
91054 BAA10g01080 A10 541594 G A upstream_gene_variant MODIFIER c.-587C>T| S268
91055 BAA10g01080 A10 541970 G A upstream_gene_variant MODIFIER c.-963C>T| S251
91056 BAA10g01080 A10 543269 G A upstream_gene_variant MODIFIER c.-2262C>T| S82
S92
91057 BAA10g01080 A10 543442 G A upstream_gene_variant MODIFIER c.-2435C>T| S81
S85
91058 BAA10g01080 A10 543620 C T upstream_gene_variant MODIFIER c.-2613G>A| S225
S73
91059 BAA10g01080 A10 543642 C T upstream_gene_variant MODIFIER c.-2635G>A| S104
S52
91060 BAA10g01080 A10 543773 G A upstream_gene_variant MODIFIER c.-2766C>T| S13
91061 BAA10g01080 A10 544250 G A upstream_gene_variant MODIFIER c.-3243C>T| S171
91062 BAA10g01080 A10 544290 C T upstream_gene_variant MODIFIER c.-3283G>A| S87
91063 BAA10g01080 A10 545029 C T upstream_gene_variant MODIFIER c.-4022G>A| S119
91064 BAA10g01080 A10 545307 G A upstream_gene_variant MODIFIER c.-4300C>T| S242
91065 BAA10g01090 A10 546052 G A downstream_gene_variant MODIFIER c.*3425C>T| S263
91066 BAA10g01090 A10 546409 C T downstream_gene_variant MODIFIER c.*3068G>A| S287
91067 BAA10g01100 A10 547204 G A upstream_gene_variant MODIFIER c.-4952G>A| S219
S72
91068 BAA10g01100 A10 547364 G A upstream_gene_variant MODIFIER c.-4792G>A| S136
91069 BAA10g01100 A10 549025 G A upstream_gene_variant MODIFIER c.-3131G>A| S189
91070 BAA10g01100 A10 549091 G A upstream_gene_variant MODIFIER c.-3065G>A| S197
91071 BAA10g01100 A10 549152 C T upstream_gene_variant MODIFIER c.-3004C>T| S249
91072 BAA10g01100 A10 549938 G A upstream_gene_variant MODIFIER c.-2218G>A| S127
91073 BAA10g01090 A10 550127 C T missense_variant MODERATE c.736G>A|p.Asp246Asn S259
91074 BAA10g01090 A10 550360 G A missense_variant MODERATE c.571C>T|p.His191Tyr S228
91075 BAA10g01090 A10 551210 G A upstream_gene_variant MODIFIER c.-107C>T| S241