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
99301 BAA10g06490 A10 3354164 A G upstream_gene_variant MODIFIER c.-2275A>G| S174
99302 BAA10g06490 A10 3356146 G A upstream_gene_variant MODIFIER c.-293G>A| S180
99303 BAA10g06500 A10 3357731 T C upstream_gene_variant MODIFIER c.-4493T>C| S75
S81
99304 BAA10g06490 A10 3357781 G A missense_variant MODERATE c.871G>A|p.Glu291Lys S4
99305 BAA10g06490 A10 3358553 G A synonymous_variant LOW c.1275G>A|p.Arg425Arg S172
S217
99306 BAA10g06500 A10 3359422 G A upstream_gene_variant MODIFIER c.-2802G>A| S255
99307 BAA10g06500 A10 3360744 A T upstream_gene_variant MODIFIER c.-1480A>T| S227
S258
S75
99308 BAA10g06490 A10 3363772 C T downstream_gene_variant MODIFIER c.*5000C>T| S70
99309 BAA10g06500 A10 3364317 C T downstream_gene_variant MODIFIER c.*1239C>T| S97
99310 BAA10g06500 A10 3364488 G A downstream_gene_variant MODIFIER c.*1410G>A| S39
99311 BAA10g06500 A10 3365423 G A downstream_gene_variant MODIFIER c.*2345G>A| S13
99312 BAA10g06500 A10 3365838 C T downstream_gene_variant MODIFIER c.*2760C>T| S115
99313 BAA10g06500 A10 3366171 C T downstream_gene_variant MODIFIER c.*3093C>T| S2
99314 BAA10g06510 A10 3368868 C T intron_variant MODIFIER c.2101+2204G>A| S25
99315 BAA10g06510 A10 3370366 C T intron_variant MODIFIER c.2101+706G>A| S298
99316 BAA10g06510 A10 3370397 C T intron_variant MODIFIER c.2101+675G>A| S170
S171
99317 BAA10g06510 A10 3370994 C T intron_variant MODIFIER c.2101+78G>A| S305
99318 BAA10g06510 A10 3371038 C T intron_variant MODIFIER c.2101+34G>A| S270
99319 BAA10g06510 A10 3371101 G A missense_variant MODERATE c.2072C>T|p.Ser691Leu S277
99320 BAA10g06510 A10 3371125 T C missense_variant MODERATE c.2048A>G|p.Asp683Gly S246
99321 BAA10g06510 A10 3371546 G A stop_gained HIGH c.1627C>T|p.Arg543* S290
99322 BAA10g06510 A10 3371766 G A synonymous_variant LOW c.1407C>T|p.Ala469Ala S278
99323 BAA10g06510 A10 3371860 G A missense_variant MODERATE c.1313C>T|p.Ala438Val S65
99324 BAA10g06510 A10 3371959 C T missense_variant MODERATE c.1214G>A|p.Gly405Asp S166
99325 BAA10g06510 A10 3372461 C T synonymous_variant LOW c.795G>A|p.Ala265Ala S87