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
101901 BAA10g07340 A10 4206144 G A synonymous_variant LOW c.1126C>T|p.Leu376Leu S18
101902 BAA10g07340 A10 4207277 G A intron_variant MODIFIER c.1014-1021C>T| S129
101903 BAA10g07340 A10 4208379 G A intron_variant MODIFIER c.1014-2123C>T| S125
101904 BAA10g07340 A10 4210557 C T intron_variant MODIFIER c.1013+3888G>A| S35
101905 BAA10g07340 A10 4211177 G A intron_variant MODIFIER c.1013+3268C>T| S57
101906 BAA10g07340 A10 4213866 G A intron_variant MODIFIER c.1013+579C>T| S295
101907 BAA10g07340 A10 4213987 C T intron_variant MODIFIER c.1013+458G>A| S199
101908 BAA10g07340 A10 4214495 G A synonymous_variant LOW c.963C>T|p.Leu321Leu S13
S140
S219
S278
S64
S72
101909 BAA10g07340 A10 4214533 C T missense_variant MODERATE c.925G>A|p.Glu309Lys S132
S137
S215
101910 BAA10g07340 A10 4215139 T C missense_variant MODERATE c.613A>G|p.Thr205Ala S53
101911 BAA10g07340 A10 4215345 G A missense_variant MODERATE c.479C>T|p.Pro160Leu S36
101912 BAA10g07340 A10 4216086 G A missense_variant MODERATE c.49C>T|p.Pro17Ser S286
101913 BAA10g07340 A10 4216919 C T upstream_gene_variant MODIFIER c.-785G>A| S205
101914 BAA10g07340 A10 4217451 C T upstream_gene_variant MODIFIER c.-1317G>A| S177
101915 BAA10g07340 A10 4217895 G A upstream_gene_variant MODIFIER c.-1761C>T| S33
101916 BAA10g07340 A10 4217991 C T upstream_gene_variant MODIFIER c.-1857G>A| S51
101917 BAA10g07340 A10 4218225 C A upstream_gene_variant MODIFIER c.-2091G>T| S104
101918 BAA10g07340 A10 4218449 C T upstream_gene_variant MODIFIER c.-2315G>A| S98
101919 BAA10g07340 A10 4218795 C T upstream_gene_variant MODIFIER c.-2661G>A| S123
101920 BAA10g07340 A10 4220953 G A upstream_gene_variant MODIFIER c.-4819C>T| S43
101921 BAA10g07340 A10 4221037 C T upstream_gene_variant MODIFIER c.-4903G>A| S281
101922 BAA10g07340 A10 4221079 C T upstream_gene_variant MODIFIER c.-4945G>A| S177
101923 BAA10g07350 A10 4221159 C T upstream_gene_variant MODIFIER c.-250C>T| S8
101924 BAA10g07350 A10 4221390 C T upstream_gene_variant MODIFIER c.-19C>T| S185
101925 BAA10g07350 A10 4222611 G A missense_variant MODERATE c.527G>A|p.Arg176His S255