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


Gene ID

Results: 1 - 32 of 32 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g23850 A05 28652018 G A downstream_gene_variant MODIFIER c.*4013C>T| S67
2 BAA05g23850 A05 28652250 C T downstream_gene_variant MODIFIER c.*3781G>A| S81
S85
3 BAA05g23850 A05 28652413 C T downstream_gene_variant MODIFIER c.*3618G>A| S237
4 BAA05g23850 A05 28653095 C T downstream_gene_variant MODIFIER c.*2936G>A| S206
S26
5 BAA05g23850 A05 28653751 C T downstream_gene_variant MODIFIER c.*2280G>A| S165
6 BAA05g23850 A05 28653849 G A downstream_gene_variant MODIFIER c.*2182C>T| S138
7 BAA05g23850 A05 28654044 C T downstream_gene_variant MODIFIER c.*1987G>A| S182
8 BAA05g23850 A05 28654256 G A downstream_gene_variant MODIFIER c.*1775C>T| S12
9 BAA05g23850 A05 28654652 G A downstream_gene_variant MODIFIER c.*1379C>T| S293
10 BAA05g23850 A05 28655270 C A downstream_gene_variant MODIFIER c.*761G>T| S43
11 BAA05g23850 A05 28656552 G A stop_gained HIGH c.2425C>T|p.Gln809* S210
S225
12 BAA05g23850 A05 28657411 C T intron_variant MODIFIER c.1649-83G>A| S189
13 BAA05g23850 A05 28657647 C T intron_variant MODIFIER c.1649-319G>A| S246
14 BAA05g23850 A05 28657737 G A intron_variant MODIFIER c.1649-409C>T| S144
15 BAA05g23850 A05 28658161 C T intron_variant MODIFIER c.1648+629G>A| S89
16 BAA05g23850 A05 28658646 G A intron_variant MODIFIER c.1648+144C>T| S45
17 BAA05g23850 A05 28659424 G A intron_variant MODIFIER c.1520-506C>T| S269
18 BAA05g23850 A05 28659766 C T intron_variant MODIFIER c.1519+397G>A| S292
19 BAA05g23850 A05 28659874 G A intron_variant MODIFIER c.1519+289C>T| S46
20 BAA05g23850 A05 28660489 G A missense_variant MODERATE c.1193C>T|p.Ala398Val S278
21 BAA05g23850 A05 28660511 C T missense_variant MODERATE c.1171G>A|p.Glu391Lys S111
S18
22 BAA05g23850 A05 28660823 C T missense_variant MODERATE c.859G>A|p.Glu287Lys S305
23 BAA05g23850 A05 28660857 G A synonymous_variant LOW c.825C>T|p.Ala275Ala S276
24 BAA05g23850 A05 28661651 C T missense_variant MODERATE c.31G>A|p.Gly11Arg S262
25 BAA05g23850 A05 28662084 C T upstream_gene_variant MODIFIER c.-403G>A| S157