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
2951 BAA01g02400 A01 1095766 C T upstream_gene_variant MODIFIER c.-41G>A| S46
2952 BAA01g02400 A01 1096758 C T upstream_gene_variant MODIFIER c.-1033G>A| S119
2953 BAA01g02400 A01 1098226 C T upstream_gene_variant MODIFIER c.-2501G>A| S284
2954 BAA01g02400 A01 1098388 G A upstream_gene_variant MODIFIER c.-2663C>T| S13
2955 BAA01g02400 A01 1098636 G A upstream_gene_variant MODIFIER c.-2911C>T| S116
2956 BAA01g02400 A01 1099503 G A upstream_gene_variant MODIFIER c.-3778C>T| S292
2957 BAA01g02410 A01 1102528 C T upstream_gene_variant MODIFIER c.-3081G>A| S117
2958 BAA01g02420 A01 1106782 G A upstream_gene_variant MODIFIER c.-252G>A| S174
2959 BAA01g02420 A01 1107318 C T synonymous_variant LOW c.210C>T|p.Tyr70Tyr S54
2960 BAA01g02420 A01 1107543 C T missense_variant MODERATE c.259C>T|p.Leu87Phe S246
2961 BAA01g02430 A01 1110735 C T upstream_gene_variant MODIFIER c.-1164C>T| S270
2962 BAA01g02430 A01 1111289 C T upstream_gene_variant MODIFIER c.-610C>T| S133
2963 BAA01g02420 A01 1112005 C T downstream_gene_variant MODIFIER c.*2446C>T| S75
2964 BAA01g02430 A01 1112953 C T missense_variant MODERATE c.821C>T|p.Ala274Val S57
2965 BAA01g02420 A01 1113656 C T downstream_gene_variant MODIFIER c.*4097C>T| S193
2966 BAA01g02440 A01 1113989 G A upstream_gene_variant MODIFIER c.-4898G>A| S10
2967 BAA01g02440 A01 1114759 G A upstream_gene_variant MODIFIER c.-4128G>A| S298
2968 BAA01g02440 A01 1114858 T C upstream_gene_variant MODIFIER c.-4029T>C| S188
2969 BAA01g02440 A01 1115154 G A upstream_gene_variant MODIFIER c.-3733G>A| S283
2970 BAA01g02440 A01 1116589 C T upstream_gene_variant MODIFIER c.-2298C>T| S182
2971 BAA01g02440 A01 1116758 C T upstream_gene_variant MODIFIER c.-2129C>T| S269
2972 BAA01g02440 A01 1117084 C T upstream_gene_variant MODIFIER c.-1803C>T| S44
2973 BAA01g02440 A01 1117179 C T upstream_gene_variant MODIFIER c.-1708C>T| S111
2974 BAA01g02440 A01 1117491 G A upstream_gene_variant MODIFIER c.-1396G>A| S10
2975 BAA01g02440 A01 1117699 C T upstream_gene_variant MODIFIER c.-1188C>T| S35