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
33651 BAA01g22870 A01 11610890 C T synonymous_variant LOW c.318C>T|p.Pro106Pro S230
33652 BAA01g22870 A01 11611031 G A synonymous_variant LOW c.459G>A|p.Val153Val S122
33653 BAA01g22880 A01 11611431 C T upstream_gene_variant MODIFIER c.-2392C>T| S18
33654 BAA01g22880 A01 11612689 C T upstream_gene_variant MODIFIER c.-1134C>T| S19
33655 BAA01g22880 A01 11612764 G A upstream_gene_variant MODIFIER c.-1059G>A| S246
33656 BAA01g22880 A01 11613347 G A upstream_gene_variant MODIFIER c.-476G>A| S226
33657 BAA01g22880 A01 11613424 C T upstream_gene_variant MODIFIER c.-399C>T| S135
33658 BAA01g22880 A01 11613760 C T upstream_gene_variant MODIFIER c.-63C>T| S201
33659 BAA01g22880 A01 11613789 C T upstream_gene_variant MODIFIER c.-34C>T| S148
S30
S31
33660 BAA01g22880 A01 11613830 C T missense_variant MODERATE c.8C>T|p.Ser3Phe S282
33661 BAA01g22880 A01 11614031 G A missense_variant MODERATE c.209G>A|p.Arg70Lys S119
33662 BAA01g22870 A01 11614976 G A downstream_gene_variant MODIFIER c.*2440G>A| S209
33663 BAA01g22870 A01 11615461 G A downstream_gene_variant MODIFIER c.*2925G>A| S28
33664 BAA01g22870 A01 11616903 G A downstream_gene_variant MODIFIER c.*4367G>A| S40
S49
33665 BAA01g22880 A01 11618111 C T missense_variant MODERATE c.1148C>T|p.Thr383Ile S10
33666 BAA01g22880 A01 11618378 G A missense_variant MODERATE c.1415G>A|p.Arg472His S121
33667 BAA01g22880 A01 11618459 C T intron_variant MODIFIER c.1452+44C>T| S99
33668 BAA01g22880 A01 11618658 C T synonymous_variant LOW c.1485C>T|p.Val495Val S104
S52
33669 BAA01g22880 A01 11618788 G A missense_variant MODERATE c.1615G>A|p.Asp539Asn S292
33670 BAA01g22880 A01 11619274 G A intron_variant MODIFIER c.1854-18G>A| S59
33671 BAA01g22880 A01 11619920 C T missense_variant MODERATE c.2482C>T|p.Leu828Phe S179
33672 BAA01g22880 A01 11622063 G A missense_variant MODERATE c.3032G>A|p.Arg1011His S274
33673 BAA01g22880 A01 11622393 C T missense_variant MODERATE c.3362C>T|p.Ala1121Val S272
33674 BAA01g22880 A01 11622897 G A synonymous_variant LOW c.3783G>A|p.Leu1261Leu S280
33675 BAA01g22880 A01 11623010 C T missense_variant MODERATE c.3896C>T|p.Ser1299Phe S289
S290