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
114951 BAA10g09480 A10 11456822 C T downstream_gene_variant MODIFIER c.*3386C>T| S191
114952 BAA10g09510 A10 11475287 G A downstream_gene_variant MODIFIER c.*2399C>T| S274
114953 BAA10g09510 A10 11475533 C T downstream_gene_variant MODIFIER c.*2153G>A| S17
114954 BAA10g09510 A10 11485101 C T upstream_gene_variant MODIFIER c.-4663G>A| S155
114955 BAA10g09530 A10 11486577 G A upstream_gene_variant MODIFIER c.-1573G>A| S18
114956 BAA10g09520 A10 11488881 C T downstream_gene_variant MODIFIER c.*3456C>T| S246
114957 BAA10g09530 A10 11491125 G A downstream_gene_variant MODIFIER c.*2473G>A| S36
114958 BAA10g09530 A10 11491217 G A downstream_gene_variant MODIFIER c.*2565G>A| S290
114959 BAA10g09530 A10 11492920 C T downstream_gene_variant MODIFIER c.*4268C>T| S246
114960 BAA10g09540 A10 11493412 G A upstream_gene_variant MODIFIER c.-351C>T| S264
114961 BAA10g09540 A10 11493641 C T upstream_gene_variant MODIFIER c.-580G>A| S14
114962 BAA10g09540 A10 11494012 C T upstream_gene_variant MODIFIER c.-951G>A| S287
114963 BAA10g09540 A10 11494159 C T upstream_gene_variant MODIFIER c.-1098G>A| S17
114964 BAA10g09540 A10 11494233 C T upstream_gene_variant MODIFIER c.-1172G>A| S170
114965 BAA10g09540 A10 11494419 C T upstream_gene_variant MODIFIER c.-1358G>A| S133
114966 BAA10g09540 A10 11495246 C T upstream_gene_variant MODIFIER c.-2185G>A| S92
114967 BAA10g09540 A10 11498021 C T upstream_gene_variant MODIFIER c.-4960G>A| S23
114968 BAA10g09550 A10 11498940 C T downstream_gene_variant MODIFIER c.*43G>A| S247
114969 BAA10g09550 A10 11499146 G A missense_variant MODERATE c.950C>T|p.Ala317Val S295
114970 BAA10g09550 A10 11500160 C T intron_variant MODIFIER c.395-270G>A| S121
114971 BAA10g09550 A10 11500371 T A intron_variant MODIFIER c.395-481A>T| S225
S73
114972 BAA10g09550 A10 11500786 G A intron_variant MODIFIER c.394+270C>T| S163
114973 BAA10g09550 A10 11501001 G A intron_variant MODIFIER c.394+55C>T| S221
114974 BAA10g09550 A10 11501123 C T synonymous_variant LOW c.327G>A|p.Arg109Arg S166
114975 BAA10g09550 A10 11501798 C T upstream_gene_variant MODIFIER c.-67G>A| S60