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
44601 BAA01g27000 A01 15306145 G A synonymous_variant LOW c.867G>A|p.Val289Val S217
S248
44602 BAA01g27000 A01 15307460 G A downstream_gene_variant MODIFIER c.*1225G>A| S262
44603 BAA01g27000 A01 15308090 C T downstream_gene_variant MODIFIER c.*1855C>T| S289
S290
44604 BAA01g27000 A01 15308253 G A downstream_gene_variant MODIFIER c.*2018G>A| S249
44605 BAA01g27000 A01 15308402 G A downstream_gene_variant MODIFIER c.*2167G>A| S172
S217
44606 BAA01g27000 A01 15308547 G A downstream_gene_variant MODIFIER c.*2312G>A| S236
44607 BAA01g27000 A01 15309461 G A downstream_gene_variant MODIFIER c.*3226G>A| S59
44608 BAA01g27000 A01 15310439 G A downstream_gene_variant MODIFIER c.*4204G>A| S110
44609 BAA01g27000 A01 15310511 C T downstream_gene_variant MODIFIER c.*4276C>T| S231
44610 BAA01g27000 A01 15310981 C T downstream_gene_variant MODIFIER c.*4746C>T| S38
44611 BAA01g27000 A01 15311013 G A downstream_gene_variant MODIFIER c.*4778G>A| S245
44612 BAA01g27010 A01 15311261 C T downstream_gene_variant MODIFIER c.*2658G>A| S7
44613 BAA01g27010 A01 15312552 G A downstream_gene_variant MODIFIER c.*1367C>T| S172
S217
44614 BAA01g27010 A01 15312589 G A downstream_gene_variant MODIFIER c.*1330C>T| S191
44615 BAA01g27010 A01 15312687 C A downstream_gene_variant MODIFIER c.*1232G>T| S213
44616 BAA01g27010 A01 15312918 C T downstream_gene_variant MODIFIER c.*1001G>A| S128
44617 BAA01g27010 A01 15313146 C T downstream_gene_variant MODIFIER c.*773G>A| S96
44618 BAA01g27010 A01 15313549 C T downstream_gene_variant MODIFIER c.*370G>A| S113
44619 BAA01g27010 A01 15313800 C T downstream_gene_variant MODIFIER c.*119G>A| S66
44620 BAA01g27010 A01 15314331 C T intron_variant MODIFIER c.3571-29G>A| S41
44621 BAA01g27010 A01 15315075 G A missense_variant MODERATE c.3058C>T|p.Leu1020Phe S292
44622 BAA01g27010 A01 15315162 C T intron_variant MODIFIER c.3008-37G>A| S182
44623 BAA01g27010 A01 15315453 G A intron_variant MODIFIER c.2959-36C>T| S308
44624 BAA01g27010 A01 15315955 G A intron_variant MODIFIER c.2959-538C>T| S105
S106
44625 BAA01g27010 A01 15316040 G A intron_variant MODIFIER c.2959-623C>T| S207