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
127051 BAA10g15580 A10 15905913 C T upstream_gene_variant MODIFIER c.-895G>A| S2
127052 BAA10g15580 A10 15906438 G A upstream_gene_variant MODIFIER c.-1420C>T| S303
127053 BAA10g15580 A10 15906705 C T upstream_gene_variant MODIFIER c.-1687G>A| S143
127054 BAA10g15580 A10 15906805 A G upstream_gene_variant MODIFIER c.-1787T>C| S192
127055 BAA10g15580 A10 15906837 C A upstream_gene_variant MODIFIER c.-1819G>T| S2
127056 BAA10g15580 A10 15907418 G A upstream_gene_variant MODIFIER c.-2400C>T| S264
127057 BAA10g15580 A10 15907546 C T upstream_gene_variant MODIFIER c.-2528G>A| S173
127058 BAA10g15580 A10 15908722 G A upstream_gene_variant MODIFIER c.-3704C>T| S288
127059 BAA10g15580 A10 15909016 G A upstream_gene_variant MODIFIER c.-3998C>T| S198
127060 BAA10g15590 A10 15910029 G A intron_variant MODIFIER c.722-36C>T| S80
127061 BAA10g15590 A10 15910092 G A synonymous_variant LOW c.708C>T|p.Ala236Ala S233
127062 BAA10g15590 A10 15912557 C T upstream_gene_variant MODIFIER c.-1301G>A| S104
S52
127063 BAA10g15590 A10 15913640 G A upstream_gene_variant MODIFIER c.-2384C>T| S288
127064 BAA10g15590 A10 15913667 G A upstream_gene_variant MODIFIER c.-2411C>T| S270
127065 BAA10g15590 A10 15914276 C T upstream_gene_variant MODIFIER c.-3020G>A| S229
127066 BAA10g15590 A10 15914524 G A upstream_gene_variant MODIFIER c.-3268C>T| S63
127067 BAA10g15590 A10 15914896 G A upstream_gene_variant MODIFIER c.-3640C>T| S9
127068 BAA10g15590 A10 15914980 G A upstream_gene_variant MODIFIER c.-3724C>T| S55
127069 BAA10g15590 A10 15915170 C T upstream_gene_variant MODIFIER c.-3914G>A| S298
127070 BAA10g15600 A10 15915410 G A missense_variant MODERATE c.2363C>T|p.Thr788Ile S217
S248
127071 BAA10g15600 A10 15915623 C T missense_variant MODERATE c.2150G>A|p.Arg717Gln S180
127072 BAA10g15600 A10 15917640 C T intron_variant MODIFIER c.1893-1760G>A| S12
127073 BAA10g15600 A10 15918014 G A intron_variant MODIFIER c.1893-2134C>T| S77
127074 BAA10g15600 A10 15918056 G A intron_variant MODIFIER c.1893-2176C>T| S245
127075 BAA10g15600 A10 15919207 C T intron_variant MODIFIER c.1893-3327G>A| S301
S304