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 BAA02g20330 A02 10757614 C T downstream_gene_variant MODIFIER c.*1268G>A| S299
2 BAA02g20330 A02 10759633 C T splice_region_variant&synonymous_variant LOW c.513G>A|p.Glu171Glu S182
3 BAA02g20330 A02 10760489 C T synonymous_variant LOW c.195G>A|p.Lys65Lys S234
4 BAA02g20330 A02 10760639 C T intron_variant MODIFIER c.186-141G>A| S233
5 BAA02g20330 A02 10762133 G A upstream_gene_variant MODIFIER c.-208C>T| S43
6 BAA02g20330 A02 10762239 G A upstream_gene_variant MODIFIER c.-314C>T| S45
7 BAA02g20330 A02 10762807 C T upstream_gene_variant MODIFIER c.-882G>A| S202
8 BAA02g20330 A02 10762952 C T upstream_gene_variant MODIFIER c.-1027G>A| S270
9 BAA02g20330 A02 10763136 G A upstream_gene_variant MODIFIER c.-1211C>T| S298
10 BAA02g20330 A02 10763553 G A upstream_gene_variant MODIFIER c.-1628C>T| S303
11 BAA02g20330 A02 10763558 G A upstream_gene_variant MODIFIER c.-1633C>T| S175
12 BAA02g20330 A02 10763564 G A upstream_gene_variant MODIFIER c.-1639C>T| S136
13 BAA02g20330 A02 10763648 G A upstream_gene_variant MODIFIER c.-1723C>T| S133
14 BAA02g20330 A02 10763954 G A upstream_gene_variant MODIFIER c.-2029C>T| S173
15 BAA02g20330 A02 10764179 G A upstream_gene_variant MODIFIER c.-2254C>T| S48
16 BAA02g20330 A02 10764642 G A upstream_gene_variant MODIFIER c.-2717C>T| S110
17 BAA02g20330 A02 10764675 C T upstream_gene_variant MODIFIER c.-2750G>A| S171
18 BAA02g20330 A02 10764742 G A upstream_gene_variant MODIFIER c.-2817C>T| S86
19 BAA02g20330 A02 10765014 C T upstream_gene_variant MODIFIER c.-3089G>A| S276
20 BAA02g20330 A02 10765067 G A upstream_gene_variant MODIFIER c.-3142C>T| S263
21 BAA02g20330 A02 10765178 G A upstream_gene_variant MODIFIER c.-3253C>T| S273
S288
S294
22 BAA02g20330 A02 10765637 G A upstream_gene_variant MODIFIER c.-3712C>T| S109
23 BAA02g20330 A02 10765943 G A upstream_gene_variant MODIFIER c.-4018C>T| S136