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 BAA05g07630 A05 3763727 C T upstream_gene_variant MODIFIER c.-3107C>T| S228
2 BAA05g07630 A05 3764174 G A upstream_gene_variant MODIFIER c.-2660G>A| S1
S90
3 BAA05g07630 A05 3764469 C T upstream_gene_variant MODIFIER c.-2365C>T| S291
4 BAA05g07630 A05 3765285 G A upstream_gene_variant MODIFIER c.-1549G>A| S149
5 BAA05g07630 A05 3766206 C T upstream_gene_variant MODIFIER c.-628C>T| S228
6 BAA05g07630 A05 3766637 G A upstream_gene_variant MODIFIER c.-197G>A| S212
7 BAA05g07630 A05 3768741 G A missense_variant MODERATE c.568G>A|p.Ala190Thr S64
8 BAA05g07630 A05 3768836 A T intron_variant MODIFIER c.648+15A>T| S200
9 BAA05g07630 A05 3769131 G A intron_variant MODIFIER c.648+310G>A| S178
10 BAA05g07630 A05 3769625 G A intron_variant MODIFIER c.648+804G>A| S155
11 BAA05g07630 A05 3770433 C T intron_variant MODIFIER c.648+1612C>T| S28
12 BAA05g07630 A05 3770488 G A intron_variant MODIFIER c.648+1667G>A| S238
13 BAA05g07630 A05 3771065 G A intron_variant MODIFIER c.648+2244G>A| S23
14 BAA05g07630 A05 3771563 C T intron_variant MODIFIER c.648+2742C>T| S295
15 BAA05g07630 A05 3772777 G A intron_variant MODIFIER c.648+3956G>A| S165
16 BAA05g07630 A05 3775446 C T intron_variant MODIFIER c.649-1820C>T| S108
17 BAA05g07630 A05 3778555 C T missense_variant MODERATE c.1211C>T|p.Pro404Leu S161
18 BAA05g07630 A05 3779629 A T downstream_gene_variant MODIFIER c.*842A>T| S298
19 BAA05g07630 A05 3781764 C T downstream_gene_variant MODIFIER c.*2977C>T| S28