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 BAA05g12030 A05 6087447 G A upstream_gene_variant MODIFIER c.-4782G>A| S66
2 BAA05g12030 A05 6087861 G A upstream_gene_variant MODIFIER c.-4368G>A| S124
3 BAA05g12030 A05 6087882 G A upstream_gene_variant MODIFIER c.-4347G>A| S238
4 BAA05g12030 A05 6088040 C T upstream_gene_variant MODIFIER c.-4189C>T| S174
S27
5 BAA05g12030 A05 6089417 C T upstream_gene_variant MODIFIER c.-2812C>T| S33
6 BAA05g12030 A05 6089520 C T upstream_gene_variant MODIFIER c.-2709C>T| S36
7 BAA05g12030 A05 6089767 C T upstream_gene_variant MODIFIER c.-2462C>T| S28
8 BAA05g12030 A05 6090133 G A upstream_gene_variant MODIFIER c.-2096G>A| S187
9 BAA05g12030 A05 6090700 C T upstream_gene_variant MODIFIER c.-1529C>T| S114
10 BAA05g12030 A05 6090826 G A upstream_gene_variant MODIFIER c.-1403G>A| S245
11 BAA05g12030 A05 6091597 C A upstream_gene_variant MODIFIER c.-632C>A| S138
S219
S265
S66
S96
S97
12 BAA05g12030 A05 6092366 G A synonymous_variant LOW c.48G>A|p.Ser16Ser S107
13 BAA05g12030 A05 6092672 G A missense_variant MODERATE c.127G>A|p.Glu43Lys S161
14 BAA05g12030 A05 6093067 C T intron_variant MODIFIER c.235-97C>T| S113
15 BAA05g12030 A05 6093647 C T missense_variant MODERATE c.508C>T|p.Pro170Ser S229
16 BAA05g12030 A05 6093724 G A splice_region_variant&synonymous_variant LOW c.585G>A|p.Gln195Gln S288
17 BAA05g12030 A05 6094527 G A synonymous_variant LOW c.600G>A|p.Leu200Leu S294
18 BAA05g12030 A05 6095135 G A missense_variant MODERATE c.821G>A|p.Gly274Asp S297
19 BAA05g12030 A05 6096873 G A missense_variant MODERATE c.1552G>A|p.Asp518Asn S6