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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g10800 A04 16885997 G A upstream_gene_variant MODIFIER c.-4814G>A| S262
2 BAA04g10800 A04 16886140 T A upstream_gene_variant MODIFIER c.-4671T>A| S70
3 BAA04g10800 A04 16889161 G A upstream_gene_variant MODIFIER c.-1650G>A| S240
4 BAA04g10800 A04 16889195 G A upstream_gene_variant MODIFIER c.-1616G>A| S170
5 BAA04g10800 A04 16889226 C T upstream_gene_variant MODIFIER c.-1585C>T| S1
6 BAA04g10800 A04 16889789 G A upstream_gene_variant MODIFIER c.-1022G>A| S97
7 BAA04g10800 A04 16889891 C T upstream_gene_variant MODIFIER c.-920C>T| S295
8 BAA04g10800 A04 16889912 G A upstream_gene_variant MODIFIER c.-899G>A| S160
9 BAA04g10800 A04 16890047 C T upstream_gene_variant MODIFIER c.-764C>T| S80
10 BAA04g10800 A04 16890753 C T upstream_gene_variant MODIFIER c.-58C>T| S197
11 BAA04g10800 A04 16890813 G A start_lost HIGH c.3G>A|p.Met1? S273
12 BAA04g10800 A04 16890844 G A missense_variant MODERATE c.34G>A|p.Glu12Lys S75
S81
13 BAA04g10800 A04 16891859 C T intron_variant MODIFIER c.556-9C>T| S159
S299
14 BAA04g10800 A04 16892036 G A splice_acceptor_variant&intron_variant HIGH c.618-1G>A| S206
S26
15 BAA04g10800 A04 16893663 G A downstream_gene_variant MODIFIER c.*1392G>A| S217
16 BAA04g10800 A04 16893891 C T downstream_gene_variant MODIFIER c.*1620C>T| S7
17 BAA04g10800 A04 16894865 C T downstream_gene_variant MODIFIER c.*2594C>T| S247
18 BAA04g10800 A04 16894886 C T downstream_gene_variant MODIFIER c.*2615C>T| S240
19 BAA04g10800 A04 16895836 C T downstream_gene_variant MODIFIER c.*3565C>T| S146
20 BAA04g10800 A04 16895951 G A downstream_gene_variant MODIFIER c.*3680G>A| S171
21 BAA04g10800 A04 16896584 C T downstream_gene_variant MODIFIER c.*4313C>T| S10
22 BAA04g10800 A04 16896802 C T downstream_gene_variant MODIFIER c.*4531C>T| S148
S210