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


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g16880 A09 10000127 G A upstream_gene_variant MODIFIER c.-4641G>A| S301
2 BAA09g16880 A09 10002043 C T upstream_gene_variant MODIFIER c.-2725C>T| S241
3 BAA09g16880 A09 10002046 T C upstream_gene_variant MODIFIER c.-2722T>C| S89
4 BAA09g16880 A09 10002108 C T upstream_gene_variant MODIFIER c.-2660C>T| S84
S93
5 BAA09g16880 A09 10002832 C T upstream_gene_variant MODIFIER c.-1936C>T| S11
6 BAA09g16880 A09 10002951 G A upstream_gene_variant MODIFIER c.-1817G>A| S62
7 BAA09g16880 A09 10002969 C T upstream_gene_variant MODIFIER c.-1799C>T| S54
8 BAA09g16880 A09 10003038 C T upstream_gene_variant MODIFIER c.-1730C>T| S174
S27
9 BAA09g16880 A09 10003488 G A upstream_gene_variant MODIFIER c.-1280G>A| S20
10 BAA09g16880 A09 10003751 C T upstream_gene_variant MODIFIER c.-1017C>T| S30
S31
11 BAA09g16880 A09 10004131 G A upstream_gene_variant MODIFIER c.-637G>A| S110
12 BAA09g16880 A09 10004379 C T upstream_gene_variant MODIFIER c.-389C>T| S125
13 BAA09g16880 A09 10007247 G A synonymous_variant LOW c.1968G>A|p.Lys656Lys S185
14 BAA09g16880 A09 10007371 C T missense_variant MODERATE c.2092C>T|p.Pro698Ser S83
S88
15 BAA09g16880 A09 10007673 C T missense_variant MODERATE c.2321C>T|p.Ala774Val S158
16 BAA09g16880 A09 10009003 C T intron_variant MODIFIER c.2787+601C>T| S187
17 BAA09g16880 A09 10009713 G A intron_variant MODIFIER c.2787+1311G>A| S280
18 BAA09g16880 A09 10009731 G A intron_variant MODIFIER c.2787+1329G>A| S88
19 BAA09g16880 A09 10009763 C T intron_variant MODIFIER c.2787+1361C>T| S23
20 BAA09g16880 A09 10010757 G A intron_variant MODIFIER c.2787+2355G>A| S247
21 BAA09g16880 A09 10011323 G A intron_variant MODIFIER c.2788-1897G>A| S105
S106
22 BAA09g16880 A09 10011468 C T intron_variant MODIFIER c.2788-1752C>T| S5
23 BAA09g16880 A09 10012868 G A intron_variant MODIFIER c.2788-352G>A| S221
24 BAA09g16880 A09 10016583 G A downstream_gene_variant MODIFIER c.*3301G>A| S271
25 BAA09g16880 A09 10017244 T C downstream_gene_variant MODIFIER c.*3962T>C|