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
133451 BAA10g19920 A10 18118273 C T upstream_gene_variant MODIFIER c.-19C>T| S149
133452 BAA10g19930 A10 18118452 C T upstream_gene_variant MODIFIER c.-3945C>T| S47
133453 BAA10g19920 A10 18118712 G A synonymous_variant LOW c.129G>A|p.Lys43Lys S273
133454 BAA10g19920 A10 18118953 C T stop_gained HIGH c.292C>T|p.Gln98* S225
133455 BAA10g19930 A10 18120271 C T upstream_gene_variant MODIFIER c.-2126C>T| S243
133456 BAA10g19930 A10 18121413 C T upstream_gene_variant MODIFIER c.-984C>T| S146
133457 BAA10g19930 A10 18122286 C T upstream_gene_variant MODIFIER c.-111C>T| S277
133458 BAA10g19920 A10 18123562 G A downstream_gene_variant MODIFIER c.*3303G>A| S120
133459 BAA10g19930 A10 18123818 G A missense_variant MODERATE c.740G>A|p.Arg247Gln S112
133460 BAA10g19920 A10 18123921 C T downstream_gene_variant MODIFIER c.*3662C>T| S172
S202
133461 BAA10g19940 A10 18125804 C T downstream_gene_variant MODIFIER c.*4994G>A| S259
133462 BAA10g19930 A10 18126390 C T missense_variant MODERATE c.1880C>T|p.Ser627Phe S72
S78
133463 BAA10g19930 A10 18127773 G A missense_variant MODERATE c.2293G>A|p.Ala765Thr S139
133464 BAA10g19930 A10 18128365 C T downstream_gene_variant MODIFIER c.*256C>T| S266
133465 BAA10g19930 A10 18128619 C T downstream_gene_variant MODIFIER c.*510C>T| S308
133466 BAA10g19930 A10 18130032 G A downstream_gene_variant MODIFIER c.*1923G>A| S184
133467 BAA10g19930 A10 18130105 G A downstream_gene_variant MODIFIER c.*1996G>A| S158
133468 BAA10g19940 A10 18132487 G A upstream_gene_variant MODIFIER c.-463C>T| S131
133469 BAA10g19940 A10 18132585 G A upstream_gene_variant MODIFIER c.-561C>T| S43
133470 BAA10g19940 A10 18133713 G A upstream_gene_variant MODIFIER c.-1689C>T| S4
133471 BAA10g19940 A10 18133903 C T upstream_gene_variant MODIFIER c.-1879G>A| S170
133472 BAA10g19940 A10 18134766 G A upstream_gene_variant MODIFIER c.-2742C>T| S62
133473 BAA10g19940 A10 18134988 G A upstream_gene_variant MODIFIER c.-2964C>T| S65
133474 BAA10g19940 A10 18135234 G A upstream_gene_variant MODIFIER c.-3210C>T| S105
S106
133475 BAA10g19950 A10 18136016 C T missense_variant MODERATE c.164C>T|p.Pro55Leu S56