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
156801 BAA02g04730 A02 2052641 G A upstream_gene_variant MODIFIER c.-901C>T| S76
156802 BAA02g04740 A02 2052980 G A missense_variant MODERATE c.1651C>T|p.Pro551Ser S166
156803 BAA02g04730 A02 2053686 C T upstream_gene_variant MODIFIER c.-1946G>A| S288
156804 BAA02g04740 A02 2053719 C T missense_variant MODERATE c.1298G>A|p.Arg433His S288
156805 BAA02g04740 A02 2053996 C T missense_variant MODERATE c.1155G>A|p.Met385Ile S79
S84
156806 BAA02g04740 A02 2054899 G A missense_variant MODERATE c.790C>T|p.Leu264Phe S134
156807 BAA02g04740 A02 2055420 G A synonymous_variant LOW c.426C>T|p.Asn142Asn S105
S106
156808 BAA02g04740 A02 2055446 C T missense_variant MODERATE c.400G>A|p.Val134Ile S278
156809 BAA02g04730 A02 2055776 G A upstream_gene_variant MODIFIER c.-4036C>T| S259
156810 BAA02g04730 A02 2055912 G A upstream_gene_variant MODIFIER c.-4172C>T| S43
156811 BAA02g04740 A02 2056366 C T missense_variant MODERATE c.83G>A|p.Ser28Asn S87
156812 BAA02g04740 A02 2056386 C T synonymous_variant LOW c.63G>A|p.Glu21Glu S179
156813 BAA02g04740 A02 2056851 C T upstream_gene_variant MODIFIER c.-403G>A| S121
156814 BAA02g04740 A02 2057003 G A upstream_gene_variant MODIFIER c.-555C>T| S276
156815 BAA02g04740 A02 2057251 G A upstream_gene_variant MODIFIER c.-803C>T| S96
156816 BAA02g04740 A02 2057660 C T upstream_gene_variant MODIFIER c.-1212G>A| S278
156817 BAA02g04740 A02 2057695 C T upstream_gene_variant MODIFIER c.-1247G>A| S250
156818 BAA02g04740 A02 2057722 G A upstream_gene_variant MODIFIER c.-1274C>T| S259
156819 BAA02g04740 A02 2060092 G A upstream_gene_variant MODIFIER c.-3644C>T| S153
S213
156820 BAA02g04740 A02 2060346 G A upstream_gene_variant MODIFIER c.-3898C>T| S146
156821 BAA02g04750 A02 2061522 C T missense_variant MODERATE c.956G>A|p.Gly319Glu S272
156822 BAA02g04750 A02 2061907 C T intron_variant MODIFIER c.829+122G>A| S138
156823 BAA02g04750 A02 2062329 C T missense_variant MODERATE c.529G>A|p.Ala177Thr S301
S304
156824 BAA02g04750 A02 2063075 C T upstream_gene_variant MODIFIER c.-218G>A| S240
156825 BAA02g04750 A02 2063096 G A upstream_gene_variant MODIFIER c.-239C>T| S259