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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g17130 A04 21364910 C T upstream_gene_variant MODIFIER c.-4935C>T| S296
2 BAA04g17130 A04 21365137 G A upstream_gene_variant MODIFIER c.-4708G>A| S251
3 BAA04g17130 A04 21370129 C T synonymous_variant LOW c.285C>T|p.Leu95Leu S210
4 BAA04g17130 A04 21371646 C T intron_variant MODIFIER c.291+1511C>T| S296
5 BAA04g17130 A04 21372827 C T intron_variant MODIFIER c.292-2595C>T| S242
6 BAA04g17130 A04 21372885 G A intron_variant MODIFIER c.292-2537G>A| S234
7 BAA04g17130 A04 21372917 G A intron_variant MODIFIER c.292-2505G>A| S161
8 BAA04g17130 A04 21374181 C T intron_variant MODIFIER c.292-1241C>T| S1
S90
9 BAA04g17130 A04 21374276 G A intron_variant MODIFIER c.292-1146G>A| S36
10 BAA04g17130 A04 21374334 C T intron_variant MODIFIER c.292-1088C>T| S243
S299
11 BAA04g17130 A04 21375789 G A splice_region_variant&intron_variant LOW c.486-8G>A| S213
12 BAA04g17130 A04 21376163 C T missense_variant MODERATE c.662C>T|p.Ala221Val S217
13 BAA04g17130 A04 21376733 C T downstream_gene_variant MODIFIER c.*506C>T| S43
14 BAA04g17130 A04 21378646 C T downstream_gene_variant MODIFIER c.*2419C>T| S84
S93
15 BAA04g17130 A04 21379951 G A downstream_gene_variant MODIFIER c.*3724G>A| S125
16 BAA04g17130 A04 21380036 G A downstream_gene_variant MODIFIER c.*3809G>A| S284
17 BAA04g17130 A04 21380560 G A downstream_gene_variant MODIFIER c.*4333G>A| S32
18 BAA04g17130 A04 21380831 G A downstream_gene_variant MODIFIER c.*4604G>A| S218
19 BAA04g17130 A04 21381133 G A downstream_gene_variant MODIFIER c.*4906G>A| S170