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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g21590 A02 11602919 C T downstream_gene_variant MODIFIER c.*2529G>A| S293
2 BAA02g21590 A02 11603025 C T downstream_gene_variant MODIFIER c.*2423G>A| S218
3 BAA02g21590 A02 11603052 G A downstream_gene_variant MODIFIER c.*2396C>T| S256
4 BAA02g21590 A02 11603185 C T downstream_gene_variant MODIFIER c.*2263G>A| S88
5 BAA02g21590 A02 11603967 C T downstream_gene_variant MODIFIER c.*1481G>A| S136
6 BAA02g21590 A02 11604122 C T downstream_gene_variant MODIFIER c.*1326G>A| S42
7 BAA02g21590 A02 11604515 C T downstream_gene_variant MODIFIER c.*933G>A| S216
8 BAA02g21590 A02 11605609 C T missense_variant MODERATE c.766G>A|p.Glu256Lys S135
9 BAA02g21590 A02 11605710 C T missense_variant MODERATE c.665G>A|p.Gly222Glu S178
10 BAA02g21590 A02 11605936 C T missense_variant MODERATE c.439G>A|p.Glu147Lys S305
11 BAA02g21590 A02 11606113 C T missense_variant MODERATE c.262G>A|p.Val88Ile S38
12 BAA02g21590 A02 11607445 G A upstream_gene_variant MODIFIER c.-1071C>T| S125
13 BAA02g21590 A02 11607747 G A upstream_gene_variant MODIFIER c.-1373C>T| S136
14 BAA02g21590 A02 11608182 C T upstream_gene_variant MODIFIER c.-1808G>A| S104
S52
15 BAA02g21590 A02 11608640 C T upstream_gene_variant MODIFIER c.-2266G>A| S66
16 BAA02g21590 A02 11608658 C T upstream_gene_variant MODIFIER c.-2284G>A| S105
S106
17 BAA02g21590 A02 11609023 C T upstream_gene_variant MODIFIER c.-2649G>A| S221
18 BAA02g21590 A02 11609155 C T upstream_gene_variant MODIFIER c.-2781G>A| S100
19 BAA02g21590 A02 11609534 C T upstream_gene_variant MODIFIER c.-3160G>A| S302
20 BAA02g21590 A02 11610151 C T upstream_gene_variant MODIFIER c.-3777G>A| S194