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
97151 BAA10g05130 A10 2650659 C T upstream_gene_variant MODIFIER c.-724C>T| S54
97152 BAA10g05130 A10 2651235 C T upstream_gene_variant MODIFIER c.-148C>T| S139
97153 BAA10g05130 A10 2651569 G A missense_variant MODERATE c.187G>A|p.Glu63Lys S228
97154 BAA10g05130 A10 2651826 C T synonymous_variant LOW c.444C>T|p.Ile148Ile S123
97155 BAA10g05130 A10 2652298 G A stop_gained HIGH c.519G>A|p.Trp173* S211
S227
97156 BAA10g05130 A10 2653362 C T missense_variant MODERATE c.1162C>T|p.Leu388Phe S232
97157 BAA10g05130 A10 2654375 C A missense_variant MODERATE c.1769C>A|p.Pro590His S306
S308
97158 BAA10g05140 A10 2654430 G A upstream_gene_variant MODIFIER c.-1627G>A| S66
97159 BAA10g05140 A10 2654840 C T upstream_gene_variant MODIFIER c.-1217C>T| S174
S27
97160 BAA10g05140 A10 2654923 G A upstream_gene_variant MODIFIER c.-1134G>A| S280
97161 BAA10g05140 A10 2655677 C T upstream_gene_variant MODIFIER c.-380C>T| S10
97162 BAA10g05130 A10 2656996 G A downstream_gene_variant MODIFIER c.*2237G>A| S284
97163 BAA10g05140 A10 2657110 C T missense_variant MODERATE c.805C>T|p.Pro269Ser S37
97164 BAA10g05140 A10 2657441 G A missense_variant&splice_region_variant MODERATE c.974G>A|p.Arg325Lys S43
97165 BAA10g05140 A10 2657955 G A synonymous_variant LOW c.1227G>A|p.Lys409Lys S129
97166 BAA10g05140 A10 2658313 G A splice_acceptor_variant&intron_variant HIGH c.1435-1G>A| S192
97167 BAA10g05140 A10 2658380 G A missense_variant MODERATE c.1501G>A|p.Gly501Arg S296
97168 BAA10g05140 A10 2660171 C T intron_variant MODIFIER c.1788+1352C>T| S104
S52
97169 BAA10g05140 A10 2660213 C T intron_variant MODIFIER c.1788+1394C>T| S37
97170 BAA10g05140 A10 2662111 C T intron_variant MODIFIER c.1789-376C>T| S206
S26
97171 BAA10g05140 A10 2663004 G A downstream_gene_variant MODIFIER c.*275G>A| S125
97172 BAA10g05140 A10 2663419 C T downstream_gene_variant MODIFIER c.*690C>T| S210
97173 BAA10g05140 A10 2663685 G A downstream_gene_variant MODIFIER c.*956G>A| S95
97174 BAA10g05140 A10 2664110 C T downstream_gene_variant MODIFIER c.*1381C>T| S165
97175 BAA10g05140 A10 2664262 C T downstream_gene_variant MODIFIER c.*1533C>T| S68