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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g62260 A09 58844939 C T missense_variant MODERATE c.56C>T|p.Ser19Phe S61
2 BAA09g62260 A09 58845159 G A splice_donor_variant&intron_variant HIGH c.186+1G>A| S167
3 BAA09g62260 A09 58846122 C T missense_variant MODERATE c.511C>T|p.Pro171Ser S174
S27
4 BAA09g62260 A09 58847782 C T synonymous_variant LOW c.1414C>T|p.Leu472Leu S37
5 BAA09g62260 A09 58848256 C T missense_variant MODERATE c.1687C>T|p.Pro563Ser S153
S213
6 BAA09g62260 A09 58850638 G A downstream_gene_variant MODIFIER c.*205G>A| S10
7 BAA09g62260 A09 58851498 G A downstream_gene_variant MODIFIER c.*1065G>A| S90
8 BAA09g62260 A09 58852184 C T downstream_gene_variant MODIFIER c.*1751C>T| S18
9 BAA09g62260 A09 58852969 C T downstream_gene_variant MODIFIER c.*2536C>T| S149
10 BAA09g62260 A09 58853733 G A downstream_gene_variant MODIFIER c.*3300G>A| S172
S217
11 BAA09g62260 A09 58854154 G A downstream_gene_variant MODIFIER c.*3721G>A| S221
12 BAA09g62260 A09 58854660 C T downstream_gene_variant MODIFIER c.*4227C>T| S303
13 BAA09g62260 A09 58855130 C T downstream_gene_variant MODIFIER c.*4697C>T| S124