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 BAA08g25260 A08 18272723 G A downstream_gene_variant MODIFIER c.*3567C>T| S15
S3
2 BAA08g25260 A08 18273044 G A downstream_gene_variant MODIFIER c.*3246C>T| S100
3 BAA08g25260 A08 18273454 C T downstream_gene_variant MODIFIER c.*2836G>A| S261
4 BAA08g25260 A08 18273718 C T downstream_gene_variant MODIFIER c.*2572G>A| S152
5 BAA08g25260 A08 18273937 G A downstream_gene_variant MODIFIER c.*2353C>T| S95
6 BAA08g25260 A08 18274682 C T downstream_gene_variant MODIFIER c.*1608G>A| S19
7 BAA08g25260 A08 18274754 C T downstream_gene_variant MODIFIER c.*1536G>A| S6
8 BAA08g25260 A08 18275237 G A downstream_gene_variant MODIFIER c.*1053C>T| S170
9 BAA08g25260 A08 18275666 C T downstream_gene_variant MODIFIER c.*624G>A| S67
10 BAA08g25260 A08 18275738 G A downstream_gene_variant MODIFIER c.*552C>T| S241
11 BAA08g25260 A08 18276047 C T downstream_gene_variant MODIFIER c.*243G>A| S44
12 BAA08g25260 A08 18276214 C T downstream_gene_variant MODIFIER c.*76G>A| S252
13 BAA08g25260 A08 18276513 G A intron_variant MODIFIER c.1150-50C>T| S151
S263
14 BAA08g25260 A08 18276963 C T intron_variant MODIFIER c.1089+289G>A| S152
S185
15 BAA08g25260 A08 18278410 C T intron_variant MODIFIER c.829-387G>A| S6
16 BAA08g25260 A08 18278907 C T intron_variant MODIFIER c.828+164G>A| S19
17 BAA08g25260 A08 18279178 G A missense_variant MODERATE c.721C>T|p.Pro241Ser S146
18 BAA08g25260 A08 18279944 G A intron_variant MODIFIER c.146+176C>T| S72
19 BAA08g25260 A08 18279962 G A intron_variant MODIFIER c.146+158C>T| S225
20 BAA08g25260 A08 18282845 G A upstream_gene_variant MODIFIER c.-2580C>T| S305
21 BAA08g25260 A08 18283710 C T upstream_gene_variant MODIFIER c.-3445G>A| S192