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
101201 BAA10g07140 A10 3972573 G A upstream_gene_variant MODIFIER c.-3510C>T| S89
101202 BAA10g07140 A10 3973088 C T upstream_gene_variant MODIFIER c.-4025G>A| S108
101203 BAA10g07140 A10 3973684 G A upstream_gene_variant MODIFIER c.-4621C>T| S136
101204 BAA10g07150 A10 3974299 C T downstream_gene_variant MODIFIER c.*628C>T| S246
101205 BAA10g07150 A10 3974892 G A downstream_gene_variant MODIFIER c.*1221G>A| S107
101206 BAA10g07160 A10 3978851 G A upstream_gene_variant MODIFIER c.-3891G>A| S13
101207 BAA10g07160 A10 3983222 C T intron_variant MODIFIER c.300+181C>T| S286
101208 BAA10g07160 A10 3985561 G A missense_variant MODERATE c.846G>A|p.Met282Ile S290
101209 BAA10g07160 A10 3986444 G A intron_variant MODIFIER c.1106+623G>A| S284
101210 BAA10g07160 A10 3986466 G A intron_variant MODIFIER c.1106+645G>A| S128
101211 BAA10g07160 A10 3987324 C T intron_variant MODIFIER c.1221+76C>T| S142
101212 BAA10g07160 A10 3987417 G A intron_variant MODIFIER c.1222-42G>A| S236
101213 BAA10g07160 A10 3987919 C T intron_variant MODIFIER c.1624+58C>T| S135
101214 BAA10g07160 A10 3988512 G A intron_variant MODIFIER c.1624+651G>A| S245
101215 BAA10g07160 A10 3988536 G A intron_variant MODIFIER c.1624+675G>A| S262
101216 BAA10g07160 A10 3988575 C T intron_variant MODIFIER c.1624+714C>T| S19
101217 BAA10g07160 A10 3988798 G A intron_variant MODIFIER c.1625-831G>A| S55
101218 BAA10g07160 A10 3989591 C T intron_variant MODIFIER c.1625-38C>T| S246
101219 BAA10g07160 A10 3990612 G A missense_variant MODERATE c.2245G>A|p.Gly749Arg S202
101220 BAA10g07160 A10 3991026 G A missense_variant MODERATE c.2572G>A|p.Val858Met S236
101221 BAA10g07160 A10 3991472 C T intron_variant MODIFIER c.2695+323C>T| S199
101222 BAA10g07160 A10 3991843 C T intron_variant MODIFIER c.2696-496C>T| S243
S299
101223 BAA10g07160 A10 3992172 G A intron_variant MODIFIER c.2696-167G>A| S208
S219
101224 BAA10g07160 A10 3993312 C G downstream_gene_variant MODIFIER c.*500C>G| S109
101225 BAA10g07160 A10 3993575 C T downstream_gene_variant MODIFIER c.*763C>T| S199