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
177101 BAA02g18680 A02 9572701 G A upstream_gene_variant MODIFIER c.-622C>T| S136
177102 BAA02g18680 A02 9573552 G A upstream_gene_variant MODIFIER c.-1473C>T| S246
177103 BAA02g18680 A02 9573910 C T upstream_gene_variant MODIFIER c.-1831G>A| S242
177104 BAA02g18680 A02 9574422 C T upstream_gene_variant MODIFIER c.-2343G>A| S130
177105 BAA02g18680 A02 9574893 G A upstream_gene_variant MODIFIER c.-2814C>T| S283
177106 BAA02g18680 A02 9575233 G A upstream_gene_variant MODIFIER c.-3154C>T| S143
177107 BAA02g18690 A02 9578681 G A downstream_gene_variant MODIFIER c.*99C>T| S177
177108 BAA02g18690 A02 9579854 G A missense_variant MODERATE c.15248C>T|p.Ala5083Val S159
S243
177109 BAA02g18690 A02 9579936 C T missense_variant MODERATE c.15166G>A|p.Gly5056Arg S183
S198
177110 BAA02g18690 A02 9580184 C T missense_variant MODERATE c.14918G>A|p.Arg4973Lys S242
177111 BAA02g18690 A02 9580217 G A missense_variant MODERATE c.14885C>T|p.Pro4962Leu S293
177112 BAA02g18690 A02 9580851 C T missense_variant MODERATE c.14251G>A|p.Asp4751Asn S308
177113 BAA02g18690 A02 9582646 C T missense_variant MODERATE c.12844G>A|p.Asp4282Asn S94
177114 BAA02g18690 A02 9584200 C T missense_variant MODERATE c.11845G>A|p.Asp3949Asn S124
177115 BAA02g18690 A02 9585323 G A missense_variant MODERATE c.11299C>T|p.Leu3767Phe S36
177116 BAA02g18690 A02 9585561 G A missense_variant MODERATE c.11159C>T|p.Pro3720Leu S265
177117 BAA02g18690 A02 9585861 G A intron_variant MODIFIER c.10987-9C>T| S187
177118 BAA02g18690 A02 9588124 G A intron_variant MODIFIER c.9554-14C>T| S256
177119 BAA02g18690 A02 9588768 C T intron_variant MODIFIER c.9198-24G>A| S18
177120 BAA02g18690 A02 9589628 C T missense_variant MODERATE c.8807G>A|p.Ser2936Asn S71
177121 BAA02g18690 A02 9591057 G A synonymous_variant LOW c.8100C>T|p.Ser2700Ser S202
177122 BAA02g18690 A02 9591270 G A synonymous_variant LOW c.7887C>T|p.Leu2629Leu S205
177123 BAA02g18690 A02 9591680 C T missense_variant MODERATE c.7477G>A|p.Glu2493Lys S216
S241
S265
S39
177124 BAA02g18690 A02 9591696 C T synonymous_variant LOW c.7461G>A|p.Gln2487Gln S255
177125 BAA02g18690 A02 9592307 C T missense_variant MODERATE c.6850G>A|p.Val2284Met S88