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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g61580 A09 58538829 C T upstream_gene_variant MODIFIER c.-4345C>T| S25
S264
2 BAA09g61580 A09 58539184 G A upstream_gene_variant MODIFIER c.-3990G>A| S134
3 BAA09g61580 A09 58539415 G A upstream_gene_variant MODIFIER c.-3759G>A| S200
4 BAA09g61580 A09 58539673 C T upstream_gene_variant MODIFIER c.-3501C>T| S94
5 BAA09g61580 A09 58540749 C T upstream_gene_variant MODIFIER c.-2425C>T| S77
S82
6 BAA09g61580 A09 58542753 C T upstream_gene_variant MODIFIER c.-421C>T| S94
7 BAA09g61580 A09 58542871 C T upstream_gene_variant MODIFIER c.-303C>T| S20
8 BAA09g61580 A09 58542978 C T upstream_gene_variant MODIFIER c.-196C>T| S293
9 BAA09g61580 A09 58544567 G A missense_variant MODERATE c.880G>A|p.Asp294Asn S54
10 BAA09g61580 A09 58545941 G A missense_variant MODERATE c.1633G>A|p.Asp545Asn S221
11 BAA09g61580 A09 58546224 G A missense_variant MODERATE c.1916G>A|p.Gly639Glu S8
12 BAA09g61580 A09 58547039 G A missense_variant MODERATE c.2408G>A|p.Gly803Glu S111
13 BAA09g61580 A09 58547320 C T missense_variant MODERATE c.2600C>T|p.Ala867Val S174
S27
14 BAA09g61580 A09 58547393 C T synonymous_variant LOW c.2673C>T|p.Ile891Ile S249
15 BAA09g61580 A09 58548718 G A downstream_gene_variant MODIFIER c.*286G>A| S193
16 BAA09g61580 A09 58548753 C T downstream_gene_variant MODIFIER c.*321C>T| S293
17 BAA09g61580 A09 58548928 C T downstream_gene_variant MODIFIER c.*496C>T| S136