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


Gene ID

Results: 1 - 35 of 35 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g27770 A01 16765113 G A upstream_gene_variant MODIFIER c.-4863G>A| S172
2 BAA01g27770 A01 16765249 G A upstream_gene_variant MODIFIER c.-4727G>A| S284
3 BAA01g27770 A01 16765585 G A upstream_gene_variant MODIFIER c.-4391G>A| S187
4 BAA01g27770 A01 16765680 C T upstream_gene_variant MODIFIER c.-4296C>T| S42
5 BAA01g27770 A01 16766708 C T upstream_gene_variant MODIFIER c.-3268C>T| S185
6 BAA01g27770 A01 16766806 C T upstream_gene_variant MODIFIER c.-3170C>T| S134
7 BAA01g27770 A01 16766816 G A upstream_gene_variant MODIFIER c.-3160G>A| S199
8 BAA01g27770 A01 16766832 C T upstream_gene_variant MODIFIER c.-3144C>T| S148
S30
S31
9 BAA01g27770 A01 16767230 G A upstream_gene_variant MODIFIER c.-2746G>A| S74
10 BAA01g27770 A01 16767236 C T upstream_gene_variant MODIFIER c.-2740C>T| S139
11 BAA01g27770 A01 16767276 G A upstream_gene_variant MODIFIER c.-2700G>A| S292
12 BAA01g27770 A01 16769691 G A upstream_gene_variant MODIFIER c.-285G>A| S181
13 BAA01g27770 A01 16769702 C T upstream_gene_variant MODIFIER c.-274C>T| S286
14 BAA01g27770 A01 16770208 G A missense_variant MODERATE c.145G>A|p.Val49Met S138
15 BAA01g27770 A01 16770276 C T synonymous_variant LOW c.213C>T|p.Cys71Cys S46
16 BAA01g27770 A01 16770370 C T missense_variant MODERATE c.307C>T|p.Leu103Phe S282
17 BAA01g27770 A01 16770426 C T synonymous_variant LOW c.363C>T|p.Tyr121Tyr S282
18 BAA01g27770 A01 16770777 A T missense_variant MODERATE c.714A>T|p.Glu238Asp S159
S243
19 BAA01g27770 A01 16771132 G A missense_variant MODERATE c.910G>A|p.Val304Ile S32
20 BAA01g27770 A01 16771638 C T missense_variant MODERATE c.1352C>T|p.Thr451Ile S242
21 BAA01g27770 A01 16771879 C T missense_variant MODERATE c.1478C>T|p.Ser493Phe S303
22 BAA01g27770 A01 16771889 C T synonymous_variant LOW c.1488C>T|p.His496His S69
23 BAA01g27770 A01 16771948 A G missense_variant MODERATE c.1547A>G|p.Asn516Ser S257
24 BAA01g27770 A01 16772240 C T missense_variant MODERATE c.1724C>T|p.Ser575Phe S48
25 BAA01g27770 A01 16772293 C T missense_variant MODERATE c.1777C>T|p.His593Tyr S10