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
100451 BAA10g06970 A10 3745605 C T downstream_gene_variant MODIFIER c.*4531G>A| S259
100452 BAA10g06970 A10 3745899 C T downstream_gene_variant MODIFIER c.*4237G>A| S44
100453 BAA10g06970 A10 3746059 C T downstream_gene_variant MODIFIER c.*4077G>A| S35
100454 BAA10g06970 A10 3746642 G A downstream_gene_variant MODIFIER c.*3494C>T| S215
100455 BAA10g06970 A10 3746979 G A downstream_gene_variant MODIFIER c.*3157C>T| S64
100456 BAA10g06970 A10 3747089 G A downstream_gene_variant MODIFIER c.*3047C>T| S291
100457 BAA10g06970 A10 3747280 G A downstream_gene_variant MODIFIER c.*2856C>T| S13
100458 BAA10g06970 A10 3747381 C T downstream_gene_variant MODIFIER c.*2755G>A| S10
100459 BAA10g06970 A10 3747808 C T downstream_gene_variant MODIFIER c.*2328G>A| S249
100460 BAA10g06970 A10 3748421 G A downstream_gene_variant MODIFIER c.*1715C>T| S240
100461 BAA10g06970 A10 3749040 C T downstream_gene_variant MODIFIER c.*1096G>A| S159
S187
S243
S298
S299
100462 BAA10g06970 A10 3749624 C T downstream_gene_variant MODIFIER c.*512G>A| S15
S156
S2
S3
S34
100463 BAA10g06970 A10 3750590 G A intron_variant MODIFIER c.295-21C>T| S105
S106
100464 BAA10g06970 A10 3750695 G A missense_variant MODERATE c.256C>T|p.Pro86Ser S138
100465 BAA10g06970 A10 3750868 G A intron_variant MODIFIER c.136-53C>T| S46
100466 BAA10g06970 A10 3751599 G A missense_variant MODERATE c.116C>T|p.Pro39Leu S230
100467 BAA10g06970 A10 3752052 C T upstream_gene_variant MODIFIER c.-338G>A| S37
100468 BAA10g06970 A10 3752641 G A upstream_gene_variant MODIFIER c.-927C>T| S293
100469 BAA10g06970 A10 3752711 G A upstream_gene_variant MODIFIER c.-997C>T| S136
100470 BAA10g06970 A10 3753312 G A upstream_gene_variant MODIFIER c.-1598C>T| S251
100471 BAA10g06970 A10 3753759 C T upstream_gene_variant MODIFIER c.-2045G>A| S170
100472 BAA10g06970 A10 3754060 C T upstream_gene_variant MODIFIER c.-2346G>A| S117
100473 BAA10g06970 A10 3754266 T A upstream_gene_variant MODIFIER c.-2552A>T| S121
100474 BAA10g06970 A10 3754997 G A upstream_gene_variant MODIFIER c.-3283C>T| S18
100475 BAA10g06970 A10 3755343 C T upstream_gene_variant MODIFIER c.-3629G>A| S225
S73