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
124851 BAA10g14240 A10 15043567 C T upstream_gene_variant MODIFIER c.-1755C>T| S206
124852 BAA10g14240 A10 15045697 C T stop_gained HIGH c.376C>T|p.Gln126* S45
124853 BAA10g14240 A10 15045873 G A synonymous_variant LOW c.552G>A|p.Pro184Pro S67
124854 BAA10g14240 A10 15046595 C T missense_variant MODERATE c.1193C>T|p.Ala398Val S210
124855 BAA10g14250 A10 15047311 G A upstream_gene_variant MODIFIER c.-1240G>A| S198
124856 BAA10g14250 A10 15047550 C T upstream_gene_variant MODIFIER c.-1001C>T| S152
124857 BAA10g14250 A10 15048184 G A upstream_gene_variant MODIFIER c.-367G>A| S139
124858 BAA10g14240 A10 15049217 C T downstream_gene_variant MODIFIER c.*1936C>T| S46
124859 BAA10g14240 A10 15049704 C T downstream_gene_variant MODIFIER c.*2423C>T| S78
S83
124860 BAA10g14240 A10 15050455 C T downstream_gene_variant MODIFIER c.*3174C>T| S246
124861 BAA10g14260 A10 15055158 G A downstream_gene_variant MODIFIER c.*4176C>T| S138
124862 BAA10g14260 A10 15056034 C T downstream_gene_variant MODIFIER c.*3300G>A| S84
S93
124863 BAA10g14270 A10 15058750 G A upstream_gene_variant MODIFIER c.-4344G>A| S172
S217
124864 BAA10g14270 A10 15058880 C T upstream_gene_variant MODIFIER c.-4214C>T| S185
124865 BAA10g14270 A10 15058887 C T upstream_gene_variant MODIFIER c.-4207C>T| S283
124866 BAA10g14270 A10 15059133 G A upstream_gene_variant MODIFIER c.-3961G>A| S207
124867 BAA10g14270 A10 15059138 G A upstream_gene_variant MODIFIER c.-3956G>A| S205
124868 BAA10g14270 A10 15059888 G A upstream_gene_variant MODIFIER c.-3206G>A| S276
124869 BAA10g14270 A10 15059952 G A upstream_gene_variant MODIFIER c.-3142G>A| S43
124870 BAA10g14260 A10 15061950 G A upstream_gene_variant MODIFIER c.-1648C>T| S17
124871 BAA10g14260 A10 15061959 G A upstream_gene_variant MODIFIER c.-1657C>T| S178
124872 BAA10g14270 A10 15063159 C T synonymous_variant LOW c.66C>T|p.Phe22Phe S20
124873 BAA10g14270 A10 15063532 C T splice_region_variant&intron_variant LOW c.264+6C>T| S33
124874 BAA10g14270 A10 15063824 C T missense_variant MODERATE c.484C>T|p.Arg162Trp S99
124875 BAA10g14270 A10 15064369 G A missense_variant MODERATE c.760G>A|p.Ala254Thr S221