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


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g54190 A03 26717943 C T upstream_gene_variant MODIFIER c.-3299C>T| S157
2 BAA03g54190 A03 26718387 C T upstream_gene_variant MODIFIER c.-2855C>T| S237
3 BAA03g54190 A03 26718404 G A upstream_gene_variant MODIFIER c.-2838G>A| S160
4 BAA03g54190 A03 26718565 G A upstream_gene_variant MODIFIER c.-2677G>A|
5 BAA03g54190 A03 26718673 C T upstream_gene_variant MODIFIER c.-2569C>T| S209
6 BAA03g54190 A03 26718919 G A upstream_gene_variant MODIFIER c.-2323G>A| S302
7 BAA03g54190 A03 26718995 C T upstream_gene_variant MODIFIER c.-2247C>T| S301
S304
8 BAA03g54190 A03 26719033 C T upstream_gene_variant MODIFIER c.-2209C>T| S200
9 BAA03g54190 A03 26719253 C T upstream_gene_variant MODIFIER c.-1989C>T| S9
10 BAA03g54190 A03 26719486 C T upstream_gene_variant MODIFIER c.-1756C>T| S78
11 BAA03g54190 A03 26721052 C T upstream_gene_variant MODIFIER c.-190C>T| S276
S298
12 BAA03g54190 A03 26721522 G A intron_variant MODIFIER c.182+99G>A| S133
13 BAA03g54190 A03 26722178 G A splice_acceptor_variant&intron_variant HIGH c.298-1G>A| S63
14 BAA03g54190 A03 26722929 C T intron_variant MODIFIER c.394+654C>T| S244
15 BAA03g54190 A03 26723384 G C intron_variant MODIFIER c.394+1109G>C| S123
S270
16 BAA03g54190 A03 26732285 C T downstream_gene_variant MODIFIER c.*331C>T| S99
17 BAA03g54190 A03 26732526 C T downstream_gene_variant MODIFIER c.*572C>T| S2
18 BAA03g54190 A03 26732565 G A downstream_gene_variant MODIFIER c.*611G>A| S48
19 BAA03g54190 A03 26732619 G A downstream_gene_variant MODIFIER c.*665G>A| S175
20 BAA03g54190 A03 26735363 G A downstream_gene_variant MODIFIER c.*3409G>A| S191
21 BAA03g54190 A03 26736647 C T downstream_gene_variant MODIFIER c.*4693C>T| S283