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


Gene ID

Results: 1 - 26 of 26 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g33110 A02 28356791 C T upstream_gene_variant MODIFIER c.-4691C>T| S170
2 BAA02g33110 A02 28356871 G A upstream_gene_variant MODIFIER c.-4611G>A| S58
3 BAA02g33110 A02 28356933 G A upstream_gene_variant MODIFIER c.-4549G>A| S280
4 BAA02g33110 A02 28357260 G A upstream_gene_variant MODIFIER c.-4222G>A| S297
5 BAA02g33110 A02 28358722 C A upstream_gene_variant MODIFIER c.-2760C>A| S268
6 BAA02g33110 A02 28359425 C T upstream_gene_variant MODIFIER c.-2057C>T| S177
7 BAA02g33110 A02 28361047 C T upstream_gene_variant MODIFIER c.-435C>T| S112
8 BAA02g33110 A02 28361446 G A upstream_gene_variant MODIFIER c.-36G>A| S13
9 BAA02g33110 A02 28361659 G A missense_variant MODERATE c.178G>A|p.Ala60Thr S217
10 BAA02g33110 A02 28361763 G A synonymous_variant LOW c.282G>A|p.Leu94Leu S59
11 BAA02g33110 A02 28362001 C T missense_variant MODERATE c.520C>T|p.Pro174Ser S274
12 BAA02g33110 A02 28363186 C T intron_variant MODIFIER c.781-66C>T| S144
13 BAA02g33110 A02 28363363 G A missense_variant MODERATE c.892G>A|p.Gly298Arg S223
14 BAA02g33110 A02 28363364 G A missense_variant MODERATE c.893G>A|p.Gly298Glu S207
15 BAA02g33110 A02 28363479 C T synonymous_variant LOW c.1008C>T|p.Tyr336Tyr S206
16 BAA02g33110 A02 28363526 C T missense_variant MODERATE c.1055C>T|p.Ser352Phe S75
S81
17 BAA02g33110 A02 28363772 C T missense_variant MODERATE c.1301C>T|p.Ser434Phe S65
18 BAA02g33110 A02 28363829 G A missense_variant MODERATE c.1358G>A|p.Ser453Asn S35
19 BAA02g33110 A02 28364477 G A downstream_gene_variant MODIFIER c.*425G>A| S47
20 BAA02g33110 A02 28364515 G A downstream_gene_variant MODIFIER c.*463G>A| S7
21 BAA02g33110 A02 28364576 C T downstream_gene_variant MODIFIER c.*524C>T| S262
22 BAA02g33110 A02 28364682 C T downstream_gene_variant MODIFIER c.*630C>T| S175
S177
23 BAA02g33110 A02 28365316 G A downstream_gene_variant MODIFIER c.*1264G>A| S132
S137
S215
S89
24 BAA02g33110 A02 28365831 C T downstream_gene_variant MODIFIER c.*1779C>T| S15
25 BAA02g33110 A02 28365949 C T downstream_gene_variant MODIFIER c.*1897C>T| S138