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
104551 BAA10g08010 A10 5122646 C T downstream_gene_variant MODIFIER c.*1083G>A| S195
104552 BAA10g08010 A10 5123153 C T downstream_gene_variant MODIFIER c.*576G>A| S202
104553 BAA10g08010 A10 5123754 G A missense_variant MODERATE c.1745C>T|p.Ala582Val S1
S90
104554 BAA10g08010 A10 5123820 G A missense_variant MODERATE c.1679C>T|p.Pro560Leu S296
104555 BAA10g08010 A10 5124230 G A synonymous_variant LOW c.1269C>T|p.Ser423Ser S262
104556 BAA10g08010 A10 5125839 C T missense_variant MODERATE c.428G>A|p.Gly143Asp S40
S49
104557 BAA10g08010 A10 5126935 C T upstream_gene_variant MODIFIER c.-315G>A| S104
S52
104558 BAA10g08010 A10 5128325 C T upstream_gene_variant MODIFIER c.-1705G>A| S287
104559 BAA10g08010 A10 5128328 C T upstream_gene_variant MODIFIER c.-1708G>A| S270
104560 BAA10g08010 A10 5129072 C T upstream_gene_variant MODIFIER c.-2452G>A| S10
104561 BAA10g08010 A10 5129330 G A upstream_gene_variant MODIFIER c.-2710C>T| S125
104562 BAA10g08010 A10 5129500 C T upstream_gene_variant MODIFIER c.-2880G>A| S84
S93
104563 BAA10g08010 A10 5129575 C T upstream_gene_variant MODIFIER c.-2955G>A| S244
104564 BAA10g08010 A10 5130639 G A upstream_gene_variant MODIFIER c.-4019C>T| S274
104565 BAA10g08010 A10 5130753 C T upstream_gene_variant MODIFIER c.-4133G>A| S171
104566 BAA10g08010 A10 5131021 C T upstream_gene_variant MODIFIER c.-4401G>A| S183
104567 BAA10g08020 A10 5131682 C T upstream_gene_variant MODIFIER c.-880C>T| S126
S47
104568 BAA10g08020 A10 5132036 C T upstream_gene_variant MODIFIER c.-526C>T| S247
104569 BAA10g08020 A10 5133347 C T intron_variant MODIFIER c.570+59C>T| S210
S225
104570 BAA10g08020 A10 5133627 G A intron_variant MODIFIER c.682+39G>A| S53
104571 BAA10g08020 A10 5135354 C T intron_variant MODIFIER c.1464+32C>T| S202
104572 BAA10g08020 A10 5136628 C T downstream_gene_variant MODIFIER c.*467C>T| S276
S38
104573 BAA10g08020 A10 5136771 G A downstream_gene_variant MODIFIER c.*610G>A| S176
104574 BAA10g08020 A10 5136965 G A downstream_gene_variant MODIFIER c.*804G>A| S35
104575 BAA10g08020 A10 5137073 C T downstream_gene_variant MODIFIER c.*912C>T| S203