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
8151 BAA01g06490 A01 2914993 C T upstream_gene_variant MODIFIER c.-2582G>A| S81
S85
8152 BAA01g06490 A01 2915627 C T upstream_gene_variant MODIFIER c.-3216G>A| S144
8153 BAA01g06490 A01 2915992 G A upstream_gene_variant MODIFIER c.-3581C>T| S169
8154 BAA01g06490 A01 2916054 C T upstream_gene_variant MODIFIER c.-3643G>A| S18
8155 BAA01g06490 A01 2916199 G A upstream_gene_variant MODIFIER c.-3788C>T| S153
8156 BAA01g06490 A01 2916371 C T upstream_gene_variant MODIFIER c.-3960G>A| S233
8157 BAA01g06490 A01 2916482 G A upstream_gene_variant MODIFIER c.-4071C>T| S187
8158 BAA01g06490 A01 2916540 G A upstream_gene_variant MODIFIER c.-4129C>T| S23
8159 BAA01g06490 A01 2917079 C T upstream_gene_variant MODIFIER c.-4668G>A| S42
8160 BAA01g06520 A01 2917941 C T upstream_gene_variant MODIFIER c.-315C>T| S117
8161 BAA01g06520 A01 2918477 C T synonymous_variant LOW c.222C>T|p.Leu74Leu S182
8162 BAA01g06520 A01 2918890 G A downstream_gene_variant MODIFIER c.*242G>A| S124
8163 BAA01g06530 A01 2919958 G A synonymous_variant LOW c.633C>T|p.Ile211Ile S207
8164 BAA01g06530 A01 2920027 C T synonymous_variant LOW c.564G>A|p.Gly188Gly S79
8165 BAA01g06530 A01 2920041 G A missense_variant MODERATE c.550C>T|p.Leu184Phe S10
8166 BAA01g06530 A01 2920073 C T missense_variant MODERATE c.518G>A|p.Ser173Asn S70
8167 BAA01g06530 A01 2920406 C T missense_variant MODERATE c.185G>A|p.Gly62Asp S76
8168 BAA01g06530 A01 2924107 G A upstream_gene_variant MODIFIER c.-3517C>T| S33
8169 BAA01g06540 A01 2926041 G A synonymous_variant LOW c.1815C>T|p.Asp605Asp S186
8170 BAA01g06540 A01 2926249 G A missense_variant MODERATE c.1607C>T|p.Thr536Ile S286
8171 BAA01g06540 A01 2926927 G A missense_variant MODERATE c.929C>T|p.Thr310Met S180
8172 BAA01g06540 A01 2927697 C T synonymous_variant LOW c.159G>A|p.Gln53Gln S185
8173 BAA01g06550 A01 2928579 C T synonymous_variant LOW c.477G>A|p.Leu159Leu S68
8174 BAA01g06550 A01 2928883 G A splice_region_variant&intron_variant LOW c.176-3C>T| S294
8175 BAA01g06540 A01 2928992 G A upstream_gene_variant MODIFIER c.-1137C>T| S34