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


Gene ID

Results: 1 - 34 of 34 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g40960 A02 34368768 C T downstream_gene_variant MODIFIER c.*4771G>A| S138
2 BAA02g40960 A02 34369332 C T downstream_gene_variant MODIFIER c.*4207G>A| S167
3 BAA02g40960 A02 34369422 G A downstream_gene_variant MODIFIER c.*4117C>T| S132
S137
S215
S89
4 BAA02g40960 A02 34370584 G A downstream_gene_variant MODIFIER c.*2955C>T| S209
5 BAA02g40960 A02 34370598 C T downstream_gene_variant MODIFIER c.*2941G>A| S130
6 BAA02g40960 A02 34370656 G A downstream_gene_variant MODIFIER c.*2883C>T| S207
7 BAA02g40960 A02 34370697 G A downstream_gene_variant MODIFIER c.*2842C>T| S160
8 BAA02g40960 A02 34371860 G A downstream_gene_variant MODIFIER c.*1679C>T| S245
9 BAA02g40960 A02 34372021 C T downstream_gene_variant MODIFIER c.*1518G>A| S179
10 BAA02g40960 A02 34372414 C T downstream_gene_variant MODIFIER c.*1125G>A| S295
11 BAA02g40960 A02 34372673 G A downstream_gene_variant MODIFIER c.*866C>T| S113
12 BAA02g40960 A02 34372866 G A downstream_gene_variant MODIFIER c.*673C>T| S4
13 BAA02g40960 A02 34373585 G A missense_variant MODERATE c.2399C>T|p.Ala800Val S159
S243
14 BAA02g40960 A02 34373621 C T missense_variant MODERATE c.2363G>A|p.Ser788Asn S180
15 BAA02g40960 A02 34374003 C T missense_variant MODERATE c.1981G>A|p.Glu661Lys S120
16 BAA02g40960 A02 34374051 T A stop_gained HIGH c.1933A>T|p.Lys645* S249
17 BAA02g40960 A02 34374088 G A synonymous_variant LOW c.1896C>T|p.Phe632Phe S96
18 BAA02g40960 A02 34374262 C T splice_region_variant&synonymous_variant LOW c.1800G>A|p.Ser600Ser S100
19 BAA02g40960 A02 34374841 C T synonymous_variant LOW c.1302G>A|p.Thr434Thr S6
20 BAA02g40960 A02 34374907 C T synonymous_variant LOW c.1236G>A|p.Gln412Gln S19
21 BAA02g40960 A02 34375230 C T missense_variant MODERATE c.983G>A|p.Gly328Glu S64
22 BAA02g40960 A02 34375938 G A intron_variant MODIFIER c.913-638C>T| S136
23 BAA02g40960 A02 34379495 G A missense_variant MODERATE c.428C>T|p.Thr143Ile S13
24 BAA02g40960 A02 34379625 G A missense_variant MODERATE c.298C>T|p.Arg100Trp S270
25 BAA02g40960 A02 34379831 C T missense_variant MODERATE c.92G>A|p.Cys31Tyr S161