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
73801 BAA01g38720 A01 25832401 C T upstream_gene_variant MODIFIER c.-3242G>A| S54
73802 BAA01g38730 A01 25834046 C T synonymous_variant LOW c.126G>A|p.Leu42Leu S62
73803 BAA01g38730 A01 25834062 G A missense_variant MODERATE c.110C>T|p.Pro37Leu S158
73804 BAA01g38730 A01 25834283 C T upstream_gene_variant MODIFIER c.-112G>A| S221
73805 BAA01g38740 A01 25835408 C T stop_gained HIGH c.127C>T|p.Gln43* S305
73806 BAA01g38730 A01 25835926 C T upstream_gene_variant MODIFIER c.-1755G>A| S289
S290
73807 BAA01g38730 A01 25837206 G A upstream_gene_variant MODIFIER c.-3035C>T| S36
73808 BAA01g38740 A01 25837283 G A missense_variant MODERATE c.1024G>A|p.Glu342Lys S87
73809 BAA01g38760 A01 25839399 C T upstream_gene_variant MODIFIER c.-4455C>T| S63
73810 BAA01g38760 A01 25840205 G A upstream_gene_variant MODIFIER c.-3649G>A| S76
73811 BAA01g38760 A01 25840620 G A upstream_gene_variant MODIFIER c.-3234G>A| S197
73812 BAA01g38760 A01 25841486 C T upstream_gene_variant MODIFIER c.-2368C>T| S165
73813 BAA01g38750 A01 25841784 G A missense_variant MODERATE c.503C>T|p.Thr168Ile S13
73814 BAA01g38760 A01 25842744 G A upstream_gene_variant MODIFIER c.-1110G>A| S265
73815 BAA01g38760 A01 25844023 C T missense_variant MODERATE c.170C>T|p.Ser57Phe S237
73816 BAA01g38750 A01 25844703 C T upstream_gene_variant MODIFIER c.-1149G>A| S284
73817 BAA01g38760 A01 25844847 C T missense_variant MODERATE c.368C>T|p.Ser123Phe S228
73818 BAA01g38750 A01 25845260 C T upstream_gene_variant MODIFIER c.-1706G>A| S233
73819 BAA01g38770 A01 25847430 C T missense_variant MODERATE c.517G>A|p.Ala173Thr S272
73820 BAA01g38770 A01 25847649 C T missense_variant MODERATE c.298G>A|p.Glu100Lys S104
S52
73821 BAA01g38770 A01 25847954 C T missense_variant MODERATE c.73G>A|p.Gly25Ser S263
73822 BAA01g38750 A01 25848068 C T upstream_gene_variant MODIFIER c.-4514G>A| S156
73823 BAA01g38750 A01 25848173 C T upstream_gene_variant MODIFIER c.-4619G>A| S115
73824 BAA01g38770 A01 25848325 G A splice_region_variant&intron_variant LOW c.51+8C>T| S152
73825 BAA01g38770 A01 25848355 G A missense_variant MODERATE c.29C>T|p.Ala10Val S296