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
2101 BAA01g01700 A01 758071 C T downstream_gene_variant MODIFIER c.*1533G>A| S38
2102 BAA01g01700 A01 759749 G A missense_variant MODERATE c.1619C>T|p.Ala540Val S209
2103 BAA01g01700 A01 759776 C T missense_variant MODERATE c.1592G>A|p.Gly531Asp S18
2104 BAA01g01700 A01 760459 C T synonymous_variant LOW c.909G>A|p.Lys303Lys S208
S219
2105 BAA01g01700 A01 761267 C T intron_variant MODIFIER c.312-97G>A| S152
2106 BAA01g01700 A01 761433 G A missense_variant MODERATE c.265C>T|p.Arg89Cys S303
2107 BAA01g01700 A01 762783 G A upstream_gene_variant MODIFIER c.-1086C>T| S73
S91
2108 BAA01g01700 A01 765611 G A upstream_gene_variant MODIFIER c.-3914C>T| S177
2109 BAA01g01710 A01 767589 C T upstream_gene_variant MODIFIER c.-2189C>T| S71
2110 BAA01g01710 A01 768977 G A upstream_gene_variant MODIFIER c.-801G>A| S32
2111 BAA01g01710 A01 769045 C T upstream_gene_variant MODIFIER c.-733C>T| S223
2112 BAA01g01710 A01 770018 G A missense_variant MODERATE c.241G>A|p.Val81Met S60
2113 BAA01g01710 A01 770176 C T synonymous_variant LOW c.399C>T|p.Arg133Arg S164
2114 BAA01g01710 A01 770864 G A synonymous_variant LOW c.717G>A|p.Thr239Thr S308
2115 BAA01g01720 A01 771083 G A upstream_gene_variant MODIFIER c.-2045G>A| S89
2116 BAA01g01710 A01 771523 G A missense_variant MODERATE c.1261G>A|p.Glu421Lys S262
2117 BAA01g01710 A01 771767 C T missense_variant MODERATE c.1505C>T|p.Ser502Phe S170
S176
2118 BAA01g01720 A01 771981 C T upstream_gene_variant MODIFIER c.-1147C>T| S130
2119 BAA01g01720 A01 772069 C T upstream_gene_variant MODIFIER c.-1059C>T| S38
2120 BAA01g01720 A01 773177 C T missense_variant MODERATE c.50C>T|p.Ser17Phe S164
2121 BAA01g01720 A01 773283 C T synonymous_variant LOW c.156C>T|p.Leu52Leu S170
2122 BAA01g01720 A01 773331 C T synonymous_variant LOW c.204C>T|p.Ile68Ile S302
2123 BAA01g01720 A01 773463 C T synonymous_variant LOW c.336C>T|p.Tyr112Tyr S50
2124 BAA01g01730 A01 774029 G A upstream_gene_variant MODIFIER c.-4309G>A| S201
2125 BAA01g01730 A01 774738 G A upstream_gene_variant MODIFIER c.-3600G>A| S133