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 BAA10g33660 A10 23901028 G A downstream_gene_variant MODIFIER c.*1809C>T| S270
2 BAA10g33660 A10 23902756 G A downstream_gene_variant MODIFIER c.*81C>T| S158
3 BAA10g33660 A10 23903033 G A missense_variant MODERATE c.1325C>T|p.Ser442Leu S59
4 BAA10g33660 A10 23903276 C T missense_variant MODERATE c.1082G>A|p.Arg361Lys S36
5 BAA10g33660 A10 23904075 C T missense_variant MODERATE c.877G>A|p.Glu293Lys S291
6 BAA10g33660 A10 23904160 G A intron_variant MODIFIER c.850-58C>T| S53
7 BAA10g33660 A10 23904308 G A intron_variant MODIFIER c.850-206C>T| S286
8 BAA10g33660 A10 23904708 C T missense_variant MODERATE c.715G>A|p.Gly239Arg S148
S210
S30
S31
9 BAA10g33660 A10 23905419 C T missense_variant MODERATE c.4G>A|p.Ala2Thr S80
10 BAA10g33660 A10 23906153 C T upstream_gene_variant MODIFIER c.-731G>A| S244
11 BAA10g33660 A10 23907383 G A upstream_gene_variant MODIFIER c.-1961C>T| S45
12 BAA10g33660 A10 23907647 G A upstream_gene_variant MODIFIER c.-2225C>T| S17
13 BAA10g33660 A10 23907715 G A upstream_gene_variant MODIFIER c.-2293C>T| S140
S168
S278
S64