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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g26090 A02 14453630 G A downstream_gene_variant MODIFIER c.*921C>T| S156
2 BAA02g26090 A02 14453752 G A downstream_gene_variant MODIFIER c.*799C>T| S146
S212
S259
S69
3 BAA02g26090 A02 14456800 G A synonymous_variant LOW c.3064C>T|p.Leu1022Leu S13
4 BAA02g26090 A02 14457716 G A intron_variant MODIFIER c.2730+16C>T| S232
5 BAA02g26090 A02 14457955 G A missense_variant MODERATE c.2585C>T|p.Ser862Leu S148
S30
S31
6 BAA02g26090 A02 14458285 C T intron_variant MODIFIER c.2481+123G>A| S161
7 BAA02g26090 A02 14458433 C T missense_variant MODERATE c.2456G>A|p.Gly819Asp S179
8 BAA02g26090 A02 14460379 G A missense_variant MODERATE c.1867C>T|p.Leu623Phe S208
9 BAA02g26090 A02 14460756 G A synonymous_variant LOW c.1779C>T|p.Ala593Ala S187
10 BAA02g26090 A02 14461147 G A missense_variant MODERATE c.1564C>T|p.Leu522Phe S240
11 BAA02g26090 A02 14461710 C T missense_variant MODERATE c.1175G>A|p.Arg392Lys S255
12 BAA02g26090 A02 14463313 C T missense_variant MODERATE c.191G>A|p.Arg64Lys S112
13 BAA02g26090 A02 14463851 G A upstream_gene_variant MODIFIER c.-82C>T| S25
14 BAA02g26090 A02 14464713 C T upstream_gene_variant MODIFIER c.-944G>A| S211
15 BAA02g26090 A02 14464784 C T upstream_gene_variant MODIFIER c.-1015G>A| S183
S198
16 BAA02g26090 A02 14464821 C T upstream_gene_variant MODIFIER c.-1052G>A| S121
17 BAA02g26090 A02 14464858 C T upstream_gene_variant MODIFIER c.-1089G>A| S18
18 BAA02g26090 A02 14466689 G A upstream_gene_variant MODIFIER c.-2920C>T| S129
19 BAA02g26090 A02 14466829 C T upstream_gene_variant MODIFIER c.-3060G>A| S79
S84
20 BAA02g26090 A02 14466910 C T upstream_gene_variant MODIFIER c.-3141G>A| S167
21 BAA02g26090 A02 14466919 A T upstream_gene_variant MODIFIER c.-3150T>A| S271
22 BAA02g26090 A02 14466955 G A upstream_gene_variant MODIFIER c.-3186C>T| S72
S78
23 BAA02g26090 A02 14468242 G A upstream_gene_variant MODIFIER c.-4473C>T| S128