Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g05890 A09 3328216 G A upstream_gene_variant MODIFIER c.-4203G>A| S20
2 BAA09g05890 A09 3328922 C T upstream_gene_variant MODIFIER c.-3497C>T| S186
3 BAA09g05890 A09 3329228 C T upstream_gene_variant MODIFIER c.-3191C>T| S204
4 BAA09g05890 A09 3329501 G A upstream_gene_variant MODIFIER c.-2918G>A| S159
S299
5 BAA09g05890 A09 3329509 T A upstream_gene_variant MODIFIER c.-2910T>A| S103
6 BAA09g05890 A09 3330115 T A upstream_gene_variant MODIFIER c.-2304T>A| S287
7 BAA09g05890 A09 3332014 G A upstream_gene_variant MODIFIER c.-405G>A| S225
S73
8 BAA09g05890 A09 3332283 G A upstream_gene_variant MODIFIER c.-136G>A| S200
9 BAA09g05890 A09 3332313 C T upstream_gene_variant MODIFIER c.-106C>T| S288
10 BAA09g05890 A09 3332341 C T upstream_gene_variant MODIFIER c.-78C>T| S43
11 BAA09g05890 A09 3333166 G A missense_variant MODERATE c.153G>A|p.Met51Ile S259
12 BAA09g05890 A09 3333192 C T missense_variant MODERATE c.179C>T|p.Pro60Leu S230
13 BAA09g05890 A09 3334402 G A missense_variant MODERATE c.628G>A|p.Ala210Thr S6
14 BAA09g05890 A09 3334410 C T synonymous_variant LOW c.636C>T|p.Val212Val S173
15 BAA09g05890 A09 3335319 C T synonymous_variant LOW c.1149C>T|p.Ser383Ser S204
16 BAA09g05890 A09 3335553 G A synonymous_variant LOW c.1383G>A|p.Ser461Ser S306
S308