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
39751 BAA01g25350 A01 13731094 G A upstream_gene_variant MODIFIER c.-63G>A| S40
S49
39752 BAA01g25350 A01 13731441 G A splice_region_variant&intron_variant LOW c.159-8G>A| S122
39753 BAA01g25350 A01 13732531 G A missense_variant MODERATE c.1016G>A|p.Gly339Glu S156
39754 BAA01g25350 A01 13733560 C T downstream_gene_variant MODIFIER c.*461C>T| S279
39755 BAA01g25350 A01 13733562 C T downstream_gene_variant MODIFIER c.*463C>T| S104
S52
39756 BAA01g25360 A01 13738018 C T upstream_gene_variant MODIFIER c.-1519C>T| S275
39757 BAA01g25360 A01 13738311 C T upstream_gene_variant MODIFIER c.-1226C>T| S305
39758 BAA01g25360 A01 13738746 C T upstream_gene_variant MODIFIER c.-791C>T| S255
39759 BAA01g25360 A01 13739384 C T upstream_gene_variant MODIFIER c.-153C>T| S176
39760 BAA01g25360 A01 13739428 C T upstream_gene_variant MODIFIER c.-109C>T| S162
39761 BAA01g25360 A01 13739793 C T missense_variant MODERATE c.257C>T|p.Ser86Phe S131
39762 BAA01g25360 A01 13740213 C T missense_variant MODERATE c.521C>T|p.Ser174Leu S18
39763 BAA01g25360 A01 13740618 G A stop_gained HIGH c.926G>A|p.Trp309* S296
39764 BAA01g25360 A01 13741068 C T downstream_gene_variant MODIFIER c.*344C>T| S305
39765 BAA01g25360 A01 13742140 C T downstream_gene_variant MODIFIER c.*1416C>T| S81
S85
39766 BAA01g25360 A01 13742242 G A downstream_gene_variant MODIFIER c.*1518G>A| S197
39767 BAA01g25360 A01 13742744 G A downstream_gene_variant MODIFIER c.*2020G>A| S129
39768 BAA01g25360 A01 13742745 G A downstream_gene_variant MODIFIER c.*2021G>A| S138
39769 BAA01g25360 A01 13743086 G A downstream_gene_variant MODIFIER c.*2362G>A| S252
39770 BAA01g25360 A01 13743099 C T downstream_gene_variant MODIFIER c.*2375C>T| S198
39771 BAA01g25360 A01 13743534 C T downstream_gene_variant MODIFIER c.*2810C>T| S18
39772 BAA01g25360 A01 13743726 C T downstream_gene_variant MODIFIER c.*3002C>T| S213
39773 BAA01g25360 A01 13744070 C T downstream_gene_variant MODIFIER c.*3346C>T| S20
39774 BAA01g25360 A01 13744463 C T downstream_gene_variant MODIFIER c.*3739C>T| S107
39775 BAA01g25360 A01 13744752 G A downstream_gene_variant MODIFIER c.*4028G>A| S186