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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g13690 A05 7171935 C T upstream_gene_variant MODIFIER c.-303C>T| S117
2 BAA05g13690 A05 7175195 A G intron_variant MODIFIER c.472-721A>G| S70
3 BAA05g13690 A05 7177601 C T intron_variant MODIFIER c.737+1211C>T| S287
4 BAA05g13690 A05 7178138 G A intron_variant MODIFIER c.738-1224G>A| S192
S25
5 BAA05g13690 A05 7179636 G A intron_variant MODIFIER c.962+50G>A| S139
6 BAA05g13690 A05 7180055 C T intron_variant MODIFIER c.1146+51C>T| S142
7 BAA05g13690 A05 7180182 G A intron_variant MODIFIER c.1146+178G>A| S34
8 BAA05g13690 A05 7180956 C T intron_variant MODIFIER c.1146+952C>T| S36
9 BAA05g13690 A05 7181008 G T intron_variant MODIFIER c.1146+1004G>T| S298
10 BAA05g13690 A05 7181214 C T intron_variant MODIFIER c.1146+1210C>T| S211
S227
11 BAA05g13690 A05 7181227 C T intron_variant MODIFIER c.1146+1223C>T| S98
12 BAA05g13690 A05 7181952 C T intron_variant MODIFIER c.1147-918C>T| S281
13 BAA05g13690 A05 7182252 G A intron_variant MODIFIER c.1147-618G>A| S218
14 BAA05g13690 A05 7182267 C T intron_variant MODIFIER c.1147-603C>T| S280
15 BAA05g13690 A05 7183407 C T stop_gained HIGH c.1450C>T|p.Gln484* S103
16 BAA05g13690 A05 7183641 T A downstream_gene_variant MODIFIER c.*7T>A| S28
17 BAA05g13690 A05 7183708 G A downstream_gene_variant MODIFIER c.*74G>A| S279
18 BAA05g13690 A05 7184219 C T downstream_gene_variant MODIFIER c.*585C>T| S292
19 BAA05g13690 A05 7185180 G A downstream_gene_variant MODIFIER c.*1546G>A| S263
20 BAA05g13690 A05 7185216 G A downstream_gene_variant MODIFIER c.*1582G>A| S272
21 BAA05g13690 A05 7185811 C T downstream_gene_variant MODIFIER c.*2177C>T| S36
22 BAA05g13690 A05 7187250 G A downstream_gene_variant MODIFIER c.*3616G>A| S296