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 BAA05g33010 A05 34911272 G A upstream_gene_variant MODIFIER c.-4671G>A| S161
2 BAA05g33010 A05 34911389 G A upstream_gene_variant MODIFIER c.-4554G>A| S219
S72
3 BAA05g33010 A05 34911706 C T upstream_gene_variant MODIFIER c.-4237C>T| S287
4 BAA05g33010 A05 34912025 A G upstream_gene_variant MODIFIER c.-3918A>G| S256
5 BAA05g33010 A05 34912133 G A upstream_gene_variant MODIFIER c.-3810G>A| S48
6 BAA05g33010 A05 34912844 C T upstream_gene_variant MODIFIER c.-3099C>T| S206
S208
S26
7 BAA05g33010 A05 34913705 C T upstream_gene_variant MODIFIER c.-2238C>T| S42
8 BAA05g33010 A05 34914388 T A upstream_gene_variant MODIFIER c.-1555T>A| S249
S78
9 BAA05g33010 A05 34914517 C T upstream_gene_variant MODIFIER c.-1426C>T| S175
10 BAA05g33010 A05 34915747 G A upstream_gene_variant MODIFIER c.-196G>A| S75
S81
11 BAA05g33010 A05 34916408 G A missense_variant MODERATE c.466G>A|p.Gly156Ser S168
12 BAA05g33010 A05 34916716 C T synonymous_variant LOW c.774C>T|p.Ala258Ala S70
13 BAA05g33010 A05 34916843 G A missense_variant MODERATE c.901G>A|p.Val301Ile S25
14 BAA05g33010 A05 34916870 C T missense_variant MODERATE c.928C>T|p.Pro310Ser S8
15 BAA05g33010 A05 34917006 C T missense_variant MODERATE c.1064C>T|p.Pro355Leu S71
16 BAA05g33010 A05 34917017 C T missense_variant MODERATE c.1075C>T|p.Pro359Ser S289
S290
17 BAA05g33010 A05 34917248 G A missense_variant MODERATE c.1306G>A|p.Asp436Asn S62
18 BAA05g33010 A05 34917354 C T missense_variant MODERATE c.1412C>T|p.Ala471Val S94
19 BAA05g33010 A05 34917376 C T synonymous_variant LOW c.1434C>T|p.Thr478Thr S68
20 BAA05g33010 A05 34917380 C T missense_variant MODERATE c.1438C>T|p.Leu480Phe S294
21 BAA05g33010 A05 34917584 C T missense_variant MODERATE c.1642C>T|p.Pro548Ser S87
22 BAA05g33010 A05 34917688 C T synonymous_variant LOW c.1746C>T|p.Asn582Asn S113
23 BAA05g33010 A05 34918135 G A synonymous_variant LOW c.2193G>A|p.Lys731Lys S150