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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g18860 A07 24775740 C T synonymous_variant LOW c.3480G>A|p.Glu1160Glu S212
2 BAA07g18860 A07 24775783 C T missense_variant MODERATE c.3437G>A|p.Cys1146Tyr S159
S243
3 BAA07g18860 A07 24776707 G A missense_variant MODERATE c.2513C>T|p.Pro838Leu S298
4 BAA07g18860 A07 24776796 C T stop_gained HIGH c.2424G>A|p.Trp808* S293
5 BAA07g18860 A07 24777050 C T missense_variant MODERATE c.2170G>A|p.Val724Met S305
6 BAA07g18860 A07 24777218 C T missense_variant MODERATE c.2002G>A|p.Gly668Ser S286
7 BAA07g18860 A07 24777929 C T missense_variant MODERATE c.1291G>A|p.Glu431Lys S266
8 BAA07g18860 A07 24778570 C T missense_variant MODERATE c.650G>A|p.Arg217Lys S32
9 BAA07g18860 A07 24778601 C T missense_variant MODERATE c.619G>A|p.Val207Met S173
10 BAA07g18860 A07 24779184 G A synonymous_variant LOW c.36C>T|p.Cys12Cys S278
11 BAA07g18860 A07 24779270 G A upstream_gene_variant MODIFIER c.-51C>T| S43
12 BAA07g18860 A07 24779285 C T upstream_gene_variant MODIFIER c.-66G>A| S63
13 BAA07g18860 A07 24779305 G A upstream_gene_variant MODIFIER c.-86C>T| S278
14 BAA07g18860 A07 24779376 G A upstream_gene_variant MODIFIER c.-157C>T| S151
S236
S257
S263
15 BAA07g18860 A07 24780037 G A upstream_gene_variant MODIFIER c.-818C>T| S107
16 BAA07g18860 A07 24780271 C T upstream_gene_variant MODIFIER c.-1052G>A| S169
17 BAA07g18860 A07 24781294 C T upstream_gene_variant MODIFIER c.-2075G>A| S270
18 BAA07g18860 A07 24781330 G A upstream_gene_variant MODIFIER c.-2111C>T| S295
19 BAA07g18860 A07 24782581 G A upstream_gene_variant MODIFIER c.-3362C>T| S239
20 BAA07g18860 A07 24782822 G A upstream_gene_variant MODIFIER c.-3603C>T| S72
S78
21 BAA07g18860 A07 24783036 G A upstream_gene_variant MODIFIER c.-3817C>T| S48
22 BAA07g18860 A07 24783111 G A upstream_gene_variant MODIFIER c.-3892C>T| S272
23 BAA07g18860 A07 24783180 G A upstream_gene_variant MODIFIER c.-3961C>T| S239