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
168001 BAA02g13490 A02 6211033 G A missense_variant MODERATE c.317C>T|p.Ser106Phe S12
168002 BAA02g13490 A02 6211187 C T missense_variant MODERATE c.163G>A|p.Asp55Asn S221
168003 BAA02g13490 A02 6212968 G A upstream_gene_variant MODIFIER c.-1619C>T| S279
168004 BAA02g13490 A02 6213257 G A upstream_gene_variant MODIFIER c.-1908C>T| S225
S50
S73
168005 BAA02g13490 A02 6213701 C T upstream_gene_variant MODIFIER c.-2352G>A| S180
168006 BAA02g13490 A02 6215079 G A upstream_gene_variant MODIFIER c.-3730C>T| S92
168007 BAA02g13490 A02 6216152 C T upstream_gene_variant MODIFIER c.-4803G>A| S116
168008 BAA02g13490 A02 6216229 G A upstream_gene_variant MODIFIER c.-4880C>T| S294
168009 BAA02g13500 A02 6217722 G A intron_variant MODIFIER c.16-5681G>A| S136
168010 BAA02g13500 A02 6217754 C T intron_variant MODIFIER c.16-5649C>T| S44
168011 BAA02g13500 A02 6218477 G A intron_variant MODIFIER c.16-4926G>A| S246
168012 BAA02g13500 A02 6220167 G A intron_variant MODIFIER c.16-3236G>A| S265
168013 BAA02g13500 A02 6220318 G A intron_variant MODIFIER c.16-3085G>A| S76
168014 BAA02g13500 A02 6220872 G A intron_variant MODIFIER c.16-2531G>A| S223
168015 BAA02g13500 A02 6220947 G A intron_variant MODIFIER c.16-2456G>A| S295
168016 BAA02g13500 A02 6221227 G A intron_variant MODIFIER c.16-2176G>A| S235
168017 BAA02g13500 A02 6221471 G A intron_variant MODIFIER c.16-1932G>A| S245
168018 BAA02g13500 A02 6221513 G A intron_variant MODIFIER c.16-1890G>A| S223
168019 BAA02g13500 A02 6223312 G A intron_variant MODIFIER c.16-91G>A| S308
168020 BAA02g13500 A02 6224207 G A intron_variant MODIFIER c.306+98G>A| S176
168021 BAA02g13500 A02 6224664 G A intron_variant MODIFIER c.306+555G>A| S166
168022 BAA02g13500 A02 6224948 C T intron_variant MODIFIER c.306+839C>T| S219
S72
168023 BAA02g13510 A02 6225724 G A downstream_gene_variant MODIFIER c.*4455C>T| S116
S118
S296
S54
168024 BAA02g13510 A02 6225965 G A downstream_gene_variant MODIFIER c.*4214C>T| S264
168025 BAA02g13510 A02 6226965 C T downstream_gene_variant MODIFIER c.*3214G>A| S5