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


Gene ID

Results: 1 - 27 of 27 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g18830 A02 9689714 C T downstream_gene_variant MODIFIER c.*4728G>A| S174
2 BAA02g18830 A02 9689802 C T downstream_gene_variant MODIFIER c.*4640G>A| S281
3 BAA02g18830 A02 9690194 C T downstream_gene_variant MODIFIER c.*4248G>A| S270
4 BAA02g18830 A02 9690565 G A downstream_gene_variant MODIFIER c.*3877C>T| S172
S217
5 BAA02g18830 A02 9691604 C T downstream_gene_variant MODIFIER c.*2838G>A| S276
6 BAA02g18830 A02 9691655 C T downstream_gene_variant MODIFIER c.*2787G>A| S167
7 BAA02g18830 A02 9691663 C T downstream_gene_variant MODIFIER c.*2779G>A| S194
8 BAA02g18830 A02 9692253 C T downstream_gene_variant MODIFIER c.*2189G>A| S264
9 BAA02g18830 A02 9692267 G A downstream_gene_variant MODIFIER c.*2175C>T| S288
10 BAA02g18830 A02 9692384 C T downstream_gene_variant MODIFIER c.*2058G>A| S79
11 BAA02g18830 A02 9693487 C T downstream_gene_variant MODIFIER c.*955G>A| S138
12 BAA02g18830 A02 9694163 G A downstream_gene_variant MODIFIER c.*279C>T| S291
13 BAA02g18830 A02 9694295 G A downstream_gene_variant MODIFIER c.*147C>T| S169
14 BAA02g18830 A02 9695200 C T splice_region_variant&intron_variant LOW c.1776-4G>A| S218
15 BAA02g18830 A02 9695282 C T intron_variant MODIFIER c.1776-86G>A| S177
16 BAA02g18830 A02 9695975 C T synonymous_variant LOW c.1506G>A|p.Thr502Thr S209
17 BAA02g18830 A02 9696322 G A missense_variant MODERATE c.1159C>T|p.Leu387Phe S166
18 BAA02g18830 A02 9696338 G A synonymous_variant LOW c.1143C>T|p.Leu381Leu S173
19 BAA02g18830 A02 9696494 G A synonymous_variant LOW c.987C>T|p.Gly329Gly S72
S78
20 BAA02g18830 A02 9696917 G A synonymous_variant LOW c.564C>T|p.Asn188Asn S33
21 BAA02g18830 A02 9698420 C T upstream_gene_variant MODIFIER c.-597G>A| S152
22 BAA02g18830 A02 9698645 G A upstream_gene_variant MODIFIER c.-822C>T| S148
S210
S30
S31
23 BAA02g18830 A02 9699248 G A upstream_gene_variant MODIFIER c.-1425C>T| S228
24 BAA02g18830 A02 9699415 C T upstream_gene_variant MODIFIER c.-1592G>A| S302
25 BAA02g18830 A02 9700837 C T upstream_gene_variant MODIFIER c.-3014G>A| S181