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
89901 BAA10g00100 A10 28897 G A missense_variant MODERATE c.161C>T|p.Ser54Phe S103
89902 BAA10g00090 A10 29812 G A upstream_gene_variant MODIFIER c.-3115C>T| S186
89903 BAA10g00090 A10 29995 C T upstream_gene_variant MODIFIER c.-3298G>A| S273
89904 BAA10g00090 A10 30369 C T upstream_gene_variant MODIFIER c.-3672G>A| S67
89905 BAA10g00090 A10 31103 C T upstream_gene_variant MODIFIER c.-4406G>A| S294
89906 BAA10g00090 A10 31159 G A upstream_gene_variant MODIFIER c.-4462C>T| S255
89907 BAA10g00090 A10 31540 G A upstream_gene_variant MODIFIER c.-4843C>T| S219
S72
89908 BAA10g00090 A10 31621 G A upstream_gene_variant MODIFIER c.-4924C>T| S138
89909 BAA10g00100 A10 31733 C T upstream_gene_variant MODIFIER c.-2676G>A| S132
S137
89910 BAA10g00100 A10 32314 G A upstream_gene_variant MODIFIER c.-3257C>T| S242
89911 BAA10g00100-BAA10g00110 A10 34190 T A intergenic_region MODIFIER n.34190T>A|
89912 BAA10g00100-BAA10g00110 A10 36702 C T intergenic_region MODIFIER n.36702C>T| S73
89913 BAA10g00100-BAA10g00110 A10 36939 G A intergenic_region MODIFIER n.36939G>A| S53
89914 BAA10g00110 A10 37166 G A upstream_gene_variant MODIFIER c.-4882G>A| S50
89915 BAA10g00110 A10 37535 G A upstream_gene_variant MODIFIER c.-4513G>A| S151
89916 BAA10g00110 A10 39770 G A upstream_gene_variant MODIFIER c.-2278G>A| S66
89917 BAA10g00110 A10 40408 G A upstream_gene_variant MODIFIER c.-1640G>A| S278
89918 BAA10g00110 A10 40728 G A upstream_gene_variant MODIFIER c.-1320G>A| S156
89919 BAA10g00110 A10 42013 C T upstream_gene_variant MODIFIER c.-35C>T| S105
S106
89920 BAA10g00110 A10 42609 G A missense_variant MODERATE c.562G>A|p.Glu188Lys S228
89921 BAA10g00130 A10 45049 G A upstream_gene_variant MODIFIER c.-4933G>A| S251
89922 BAA10g00130 A10 45372 C T upstream_gene_variant MODIFIER c.-4610C>T| S281
89923 BAA10g00130 A10 46339 C T upstream_gene_variant MODIFIER c.-3643C>T| S12
89924 BAA10g00120 A10 46743 C T missense_variant MODERATE c.833G>A|p.Arg278Gln S142
89925 BAA10g00120 A10 47465 G A synonymous_variant LOW c.111C>T|p.Ala37Ala S125