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
2651 BAA01g02140 A01 983093 C T upstream_gene_variant MODIFIER c.-1602G>A| S2
2652 BAA01g02140 A01 983426 G A upstream_gene_variant MODIFIER c.-1935C>T| S17
2653 BAA01g02140 A01 985351 G A upstream_gene_variant MODIFIER c.-3860C>T| S202
2654 BAA01g02140 A01 986176 C T upstream_gene_variant MODIFIER c.-4685G>A| S205
2655 BAA01g02150 A01 987575 G A upstream_gene_variant MODIFIER c.-4881G>A| S84
2656 BAA01g02150 A01 987584 C A upstream_gene_variant MODIFIER c.-4872C>A|
2657 BAA01g02150 A01 988704 C T upstream_gene_variant MODIFIER c.-3752C>T| S208
S219
2658 BAA01g02150 A01 988760 G A upstream_gene_variant MODIFIER c.-3696G>A| S159
S243
2659 BAA01g02150 A01 989853 C T upstream_gene_variant MODIFIER c.-2603C>T| S179
2660 BAA01g02150 A01 989979 T G upstream_gene_variant MODIFIER c.-2477T>G| S113
2661 BAA01g02150 A01 991751 C T upstream_gene_variant MODIFIER c.-705C>T| S66
2662 BAA01g02150 A01 991830 G A upstream_gene_variant MODIFIER c.-626G>A| S12
2663 BAA01g02150 A01 992555 G A missense_variant MODERATE c.100G>A|p.Asp34Asn S67
2664 BAA01g02150 A01 994047 G A synonymous_variant LOW c.1026G>A|p.Glu342Glu S116
2665 BAA01g02160 A01 995551 C T upstream_gene_variant MODIFIER c.-3821C>T| S59
2666 BAA01g02160 A01 995950 G A upstream_gene_variant MODIFIER c.-3422G>A| S172
S217
2667 BAA01g02160 A01 996482 C T upstream_gene_variant MODIFIER c.-2890C>T| S1
S90
2668 BAA01g02160 A01 997511 C T upstream_gene_variant MODIFIER c.-1861C>T| S302
2669 BAA01g02160 A01 997545 C T upstream_gene_variant MODIFIER c.-1827C>T| S240
2670 BAA01g02160 A01 998587 G A upstream_gene_variant MODIFIER c.-785G>A| S221
2671 BAA01g02160 A01 1003073 G A downstream_gene_variant MODIFIER c.*107G>A| S98
2672 BAA01g02160 A01 1003314 C T downstream_gene_variant MODIFIER c.*348C>T| S233
2673 BAA01g02160 A01 1003441 C T downstream_gene_variant MODIFIER c.*475C>T| S62
2674 BAA01g02170 A01 1004191 C T missense_variant MODERATE c.689G>A|p.Gly230Asp S139
2675 BAA01g02170 A01 1004643 G A missense_variant MODERATE c.344C>T|p.Ala115Val S9