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


Gene ID

Results: 1 - 31 of 31 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g13350 A05 6910932 C T downstream_gene_variant MODIFIER c.*4733G>A| S30
S31
2 BAA05g13350 A05 6911854 C T downstream_gene_variant MODIFIER c.*3811G>A| S273
3 BAA05g13350 A05 6912371 C T downstream_gene_variant MODIFIER c.*3294G>A| S130
4 BAA05g13350 A05 6912456 G A downstream_gene_variant MODIFIER c.*3209C>T| S173
S225
5 BAA05g13350 A05 6912993 C T downstream_gene_variant MODIFIER c.*2672G>A| S12
6 BAA05g13350 A05 6913699 G A downstream_gene_variant MODIFIER c.*1966C>T| S241
7 BAA05g13350 A05 6914826 C T downstream_gene_variant MODIFIER c.*839G>A| S26
8 BAA05g13350 A05 6915066 C T downstream_gene_variant MODIFIER c.*599G>A| S103
9 BAA05g13350 A05 6915188 T A downstream_gene_variant MODIFIER c.*477A>T| S250
10 BAA05g13350 A05 6915292 G A downstream_gene_variant MODIFIER c.*373C>T| S109
11 BAA05g13350 A05 6915299 G A downstream_gene_variant MODIFIER c.*366C>T| S121
12 BAA05g13350 A05 6915782 A T missense_variant MODERATE c.4602T>A|p.Phe1534Leu S134
13 BAA05g13350 A05 6916204 C T missense_variant MODERATE c.4180G>A|p.Gly1394Ser S20
14 BAA05g13350 A05 6916902 G A missense_variant MODERATE c.3482C>T|p.Ala1161Val S79
15 BAA05g13350 A05 6917191 C T missense_variant MODERATE c.3193G>A|p.Asp1065Asn S140
16 BAA05g13350 A05 6917467 C T missense_variant MODERATE c.2917G>A|p.Gly973Ser S153
S213
17 BAA05g13350 A05 6917574 C T missense_variant MODERATE c.2810G>A|p.Gly937Glu S67
18 BAA05g13350 A05 6917777 C T synonymous_variant LOW c.2607G>A|p.Leu869Leu S105
S106
19 BAA05g13350 A05 6918246 C T intron_variant MODIFIER c.2553+113G>A| S103
20 BAA05g13350 A05 6918347 G A intron_variant MODIFIER c.2553+12C>T|
21 BAA05g13350 A05 6919640 G A missense_variant MODERATE c.1445C>T|p.Pro482Leu S109
22 BAA05g13350 A05 6920549 G A missense_variant MODERATE c.623C>T|p.Thr208Ile S156
23 BAA05g13350 A05 6920727 C T missense_variant MODERATE c.445G>A|p.Asp149Asn S247
24 BAA05g13350 A05 6920929 A G synonymous_variant LOW c.243T>C|p.Thr81Thr S198
25 BAA05g13350 A05 6921550 C T upstream_gene_variant MODIFIER c.-379G>A| S53