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
61551 BAA01g32620 A01 21548940 C T intron_variant MODIFIER c.847-17G>A| S167
61552 BAA01g32620 A01 21549678 G A synonymous_variant LOW c.510C>T|p.Phe170Phe S138
61553 BAA01g32620 A01 21549725 C T missense_variant MODERATE c.463G>A|p.Glu155Lys S130
61554 BAA01g32630 A01 21550499 G A downstream_gene_variant MODIFIER c.*3997C>T| S149
61555 BAA01g32620 A01 21552228 G A upstream_gene_variant MODIFIER c.-1636C>T| S176
61556 BAA01g32620 A01 21552560 C T upstream_gene_variant MODIFIER c.-1968G>A| S231
61557 BAA01g32620 A01 21552767 C T upstream_gene_variant MODIFIER c.-2175G>A| S273
61558 BAA01g32620 A01 21554012 G A upstream_gene_variant MODIFIER c.-3420C>T| S123
61559 BAA01g32620 A01 21554058 C T upstream_gene_variant MODIFIER c.-3466G>A| S112
61560 BAA01g32620 A01 21554430 C T upstream_gene_variant MODIFIER c.-3838G>A| S128
61561 BAA01g32630 A01 21554791 G A missense_variant MODERATE c.1031C>T|p.Ser344Leu S262
61562 BAA01g32620 A01 21555281 G A upstream_gene_variant MODIFIER c.-4689C>T| S292
61563 BAA01g32620 A01 21555316 C T upstream_gene_variant MODIFIER c.-4724G>A| S233
61564 BAA01g32630 A01 21557429 C T synonymous_variant LOW c.588G>A|p.Leu196Leu S203
61565 BAA01g32630 A01 21558006 C T missense_variant MODERATE c.200G>A|p.Arg67Lys S64
61566 BAA01g32630 A01 21560122 C T upstream_gene_variant MODIFIER c.-1736G>A| S136
61567 BAA01g32630 A01 21560412 G A upstream_gene_variant MODIFIER c.-2026C>T| S84
61568 BAA01g32630 A01 21560761 G A upstream_gene_variant MODIFIER c.-2375C>T| S109
61569 BAA01g32630 A01 21560851 G A upstream_gene_variant MODIFIER c.-2465C>T| S105
S106
61570 BAA01g32630 A01 21562106 C T upstream_gene_variant MODIFIER c.-3720G>A| S136
61571 BAA01g32630-BAA01g32640 A01 21563411 C T intergenic_region MODIFIER n.21563411C>T| S77
S82
61572 BAA01g32630-BAA01g32640 A01 21563641 G A intergenic_region MODIFIER n.21563641G>A| S181
61573 BAA01g32630-BAA01g32640 A01 21564313 C T intergenic_region MODIFIER n.21564313C>T| S266
61574 BAA01g32630-BAA01g32640 A01 21565774 C T intergenic_region MODIFIER n.21565774C>T| S18
61575 BAA01g32630-BAA01g32640 A01 21565780 C T intergenic_region MODIFIER n.21565780C>T| S266