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
122101 BAA10g12610 A10 14008218 C T upstream_gene_variant MODIFIER c.-1393G>A| S104
S52
122102 BAA10g12610 A10 14008606 C T upstream_gene_variant MODIFIER c.-1781G>A| S296
122103 BAA10g12610 A10 14008771 C T upstream_gene_variant MODIFIER c.-1946G>A| S305
122104 BAA10g12610 A10 14008862 C T upstream_gene_variant MODIFIER c.-2037G>A| S84
S93
122105 BAA10g12610 A10 14009030 C T upstream_gene_variant MODIFIER c.-2205G>A| S153
S213
122106 BAA10g12610 A10 14009084 G A upstream_gene_variant MODIFIER c.-2259C>T| S39
122107 BAA10g12610 A10 14009702 C T upstream_gene_variant MODIFIER c.-2877G>A| S238
122108 BAA10g12610 A10 14011252 C T upstream_gene_variant MODIFIER c.-4427G>A| S177
122109 BAA10g12610 A10 14011420 C T upstream_gene_variant MODIFIER c.-4595G>A| S16
122110 BAA10g12610 A10 14011820 C T upstream_gene_variant MODIFIER c.-4995G>A| S270
122111 BAA10g12620 A10 14012097 C T downstream_gene_variant MODIFIER c.*1474G>A| S176
122112 BAA10g12620 A10 14012710 C T downstream_gene_variant MODIFIER c.*861G>A| S259
122113 BAA10g12620 A10 14012805 G A downstream_gene_variant MODIFIER c.*766C>T| S28
122114 BAA10g12620 A10 14013344 G A downstream_gene_variant MODIFIER c.*227C>T| S216
122115 BAA10g12620 A10 14013605 G A missense_variant MODERATE c.308C>T|p.Ser103Leu S289
122116 BAA10g12620 A10 14013616 G A synonymous_variant LOW c.297C>T|p.Leu99Leu S148
S210
S30
S31
122117 BAA10g12620 A10 14013717 C T missense_variant MODERATE c.196G>A|p.Gly66Arg S80
122118 BAA10g12620 A10 14014854 C T upstream_gene_variant MODIFIER c.-942G>A| S259
122119 BAA10g12620 A10 14014865 C T upstream_gene_variant MODIFIER c.-953G>A| S249
122120 BAA10g12620 A10 14015684 C T upstream_gene_variant MODIFIER c.-1772G>A| S162
122121 BAA10g12620 A10 14016273 G A upstream_gene_variant MODIFIER c.-2361C>T| S27
122122 BAA10g12620 A10 14016899 G A upstream_gene_variant MODIFIER c.-2987C>T| S1
S157
S163
S90
122123 BAA10g12620 A10 14018788 G A upstream_gene_variant MODIFIER c.-4876C>T| S216
122124 BAA10g12620 A10 14018811 C T upstream_gene_variant MODIFIER c.-4899G>A| S239
122125 BAA10g12630 A10 14018980 C T upstream_gene_variant MODIFIER c.-409G>A| S142