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
174551 BAA02g17380 A02 8657093 C T downstream_gene_variant MODIFIER c.*1561C>T| S249
174552 BAA02g17390 A02 8658357 G A upstream_gene_variant MODIFIER c.-4345G>A| S134
174553 BAA02g17390 A02 8658965 G A upstream_gene_variant MODIFIER c.-3737G>A| S200
S261
S303
174554 BAA02g17390 A02 8659234 C T upstream_gene_variant MODIFIER c.-3468C>T| S262
174555 BAA02g17390 A02 8659573 G A upstream_gene_variant MODIFIER c.-3129G>A| S187
174556 BAA02g17390 A02 8664106 C T missense_variant MODERATE c.1333C>T|p.Leu445Phe S66
174557 BAA02g17390 A02 8664505 G A stop_gained HIGH c.1518G>A|p.Trp506* S217
S248
174558 BAA02g17400 A02 8664635 C T upstream_gene_variant MODIFIER c.-477C>T| S94
174559 BAA02g17400 A02 8664948 C T upstream_gene_variant MODIFIER c.-164C>T| S244
174560 BAA02g17400 A02 8665850 G A synonymous_variant LOW c.585G>A|p.Gly195Gly S177
174561 BAA02g17410 A02 8668287 G A missense_variant MODERATE c.305G>A|p.Gly102Glu S116
174562 BAA02g17410 A02 8668376 C T synonymous_variant LOW c.394C>T|p.Leu132Leu S200
174563 BAA02g17390 A02 8668585 C T downstream_gene_variant MODIFIER c.*4008C>T| S18
174564 BAA02g17410 A02 8669730 G A missense_variant MODERATE c.1403G>A|p.Arg468Lys S177
174565 BAA02g17400 A02 8669845 C T downstream_gene_variant MODIFIER c.*3628C>T| S40
S49
174566 BAA02g17410 A02 8671459 C T downstream_gene_variant MODIFIER c.*1254C>T| S255
174567 BAA02g17410 A02 8671665 G A downstream_gene_variant MODIFIER c.*1460G>A| S202
174568 BAA02g17410 A02 8671846 A G downstream_gene_variant MODIFIER c.*1641A>G| S263
174569 BAA02g17410 A02 8671942 G A downstream_gene_variant MODIFIER c.*1737G>A| S95
174570 BAA02g17410 A02 8672079 C T downstream_gene_variant MODIFIER c.*1874C>T| S238
174571 BAA02g17410 A02 8673721 C T downstream_gene_variant MODIFIER c.*3516C>T| S206
S26
174572 BAA02g17420 A02 8674343 C T synonymous_variant LOW c.570G>A|p.Leu190Leu S56
174573 BAA02g17420 A02 8674823 G A synonymous_variant LOW c.90C>T|p.Ser30Ser S107
174574 BAA02g17420 A02 8675164 C T upstream_gene_variant MODIFIER c.-252G>A| S131
174575 BAA02g17420 A02 8675175 G A upstream_gene_variant MODIFIER c.-263C>T| S159
S243