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 BAA05g23920 A05 28877072 G A upstream_gene_variant MODIFIER c.-3773G>A| S120
2 BAA05g23920 A05 28878004 C T upstream_gene_variant MODIFIER c.-2841C>T| S132
S89
3 BAA05g23920 A05 28878105 G A upstream_gene_variant MODIFIER c.-2740G>A| S40
S49
4 BAA05g23920 A05 28878881 C T upstream_gene_variant MODIFIER c.-1964C>T| S306
S308
5 BAA05g23920 A05 28879175 C T upstream_gene_variant MODIFIER c.-1670C>T| S183
6 BAA05g23920 A05 28879463 G A upstream_gene_variant MODIFIER c.-1382G>A| S210
7 BAA05g23920 A05 28879500 C T upstream_gene_variant MODIFIER c.-1345C>T| S294
8 BAA05g23920 A05 28879934 G A upstream_gene_variant MODIFIER c.-911G>A| S133
9 BAA05g23920 A05 28881238 G A missense_variant MODERATE c.187G>A|p.Val63Met S163
10 BAA05g23920 A05 28881317 G A intron_variant MODIFIER c.255+11G>A| S197
11 BAA05g23920 A05 28882103 G A intron_variant MODIFIER c.409+19G>A| S46
12 BAA05g23920 A05 28882113 C T intron_variant MODIFIER c.409+29C>T| S176
13 BAA05g23920 A05 28882168 G A splice_region_variant&synonymous_variant LOW c.411G>A|p.Glu137Glu S3
14 BAA05g23920 A05 28883555 G A downstream_gene_variant MODIFIER c.*1129G>A| S173
15 BAA05g23920 A05 28883747 G A downstream_gene_variant MODIFIER c.*1321G>A| S163
16 BAA05g23920 A05 28883790 G A downstream_gene_variant MODIFIER c.*1364G>A| S125
17 BAA05g23920 A05 28883796 G A downstream_gene_variant MODIFIER c.*1370G>A| S156
18 BAA05g23920 A05 28884124 C T downstream_gene_variant MODIFIER c.*1698C>T| S180
19 BAA05g23920 A05 28884291 C T downstream_gene_variant MODIFIER c.*1865C>T| S204
20 BAA05g23920 A05 28884377 C T downstream_gene_variant MODIFIER c.*1951C>T| S23
21 BAA05g23920 A05 28884661 C T downstream_gene_variant MODIFIER c.*2235C>T| S148
S30
S31
22 BAA05g23920 A05 28886139 G A downstream_gene_variant MODIFIER c.*3713G>A| S178
23 BAA05g23920 A05 28886504 C T downstream_gene_variant MODIFIER c.*4078C>T| S119