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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g11210 A04 17155485 G A downstream_gene_variant MODIFIER c.*4544C>T| S151
2 BAA04g11210 A04 17155503 G A downstream_gene_variant MODIFIER c.*4526C>T| S198
3 BAA04g11210 A04 17155628 C T downstream_gene_variant MODIFIER c.*4401G>A| S122
4 BAA04g11210 A04 17157879 G A downstream_gene_variant MODIFIER c.*2150C>T| S144
5 BAA04g11210 A04 17157987 G A downstream_gene_variant MODIFIER c.*2042C>T| S87
6 BAA04g11210 A04 17158130 C T downstream_gene_variant MODIFIER c.*1899G>A| S168
7 BAA04g11210 A04 17158374 G A downstream_gene_variant MODIFIER c.*1655C>T| S205
8 BAA04g11210 A04 17158898 G A downstream_gene_variant MODIFIER c.*1131C>T| S266
9 BAA04g11210 A04 17158946 G A downstream_gene_variant MODIFIER c.*1083C>T| S251
10 BAA04g11210 A04 17159003 G A downstream_gene_variant MODIFIER c.*1026C>T| S57
11 BAA04g11210 A04 17159071 G A downstream_gene_variant MODIFIER c.*958C>T| S233
12 BAA04g11210 A04 17159752 C T downstream_gene_variant MODIFIER c.*277G>A| S168
13 BAA04g11210 A04 17160123 G A missense_variant MODERATE c.1448C>T|p.Ser483Leu S208
S219
14 BAA04g11210 A04 17160227 G A synonymous_variant LOW c.1344C>T|p.Thr448Thr S241
15 BAA04g11210 A04 17160535 G A intron_variant MODIFIER c.1090+29C>T| S153
S213
16 BAA04g11210 A04 17160707 G A missense_variant MODERATE c.947C>T|p.Pro316Leu S233
17 BAA04g11210 A04 17166334 A C upstream_gene_variant MODIFIER c.-3932T>G| S12
S166
S200
S222
S304
S54
18 BAA04g11210 A04 17166435 G A upstream_gene_variant MODIFIER c.-4033C>T| S41
19 BAA04g11210 A04 17166900 C T upstream_gene_variant MODIFIER c.-4498G>A| S48
20 BAA04g11210 A04 17167005 G A upstream_gene_variant MODIFIER c.-4603C>T| S305