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 BAA02g40040 A02 33838317 C T upstream_gene_variant MODIFIER c.-3964C>T| S266
2 BAA02g40040 A02 33839304 G A upstream_gene_variant MODIFIER c.-2977G>A| S161
3 BAA02g40040 A02 33839420 G A upstream_gene_variant MODIFIER c.-2861G>A| S45
4 BAA02g40040 A02 33839442 G A upstream_gene_variant MODIFIER c.-2839G>A| S35
5 BAA02g40040 A02 33840164 C T upstream_gene_variant MODIFIER c.-2117C>T| S283
6 BAA02g40040 A02 33840511 G A upstream_gene_variant MODIFIER c.-1770G>A| S136
7 BAA02g40040 A02 33840738 G A upstream_gene_variant MODIFIER c.-1543G>A| S268
8 BAA02g40040 A02 33840760 G A upstream_gene_variant MODIFIER c.-1521G>A| S53
9 BAA02g40040 A02 33840770 C T upstream_gene_variant MODIFIER c.-1511C>T| S242
10 BAA02g40040 A02 33841359 G A upstream_gene_variant MODIFIER c.-922G>A| S176
11 BAA02g40040 A02 33841608 G A upstream_gene_variant MODIFIER c.-673G>A| S148
S210
S30
S31
12 BAA02g40040 A02 33841772 G A upstream_gene_variant MODIFIER c.-509G>A| S251
13 BAA02g40040 A02 33842195 C T upstream_gene_variant MODIFIER c.-86C>T| S241
14 BAA02g40040 A02 33842329 C T missense_variant MODERATE c.49C>T|p.Leu17Phe S179
15 BAA02g40040 A02 33842337 G A synonymous_variant LOW c.57G>A|p.Glu19Glu S38
16 BAA02g40040 A02 33842771 C T synonymous_variant LOW c.417C>T|p.Phe139Phe S13
17 BAA02g40040 A02 33844029 G A downstream_gene_variant MODIFIER c.*34G>A| S150
18 BAA02g40040 A02 33844531 G A downstream_gene_variant MODIFIER c.*536G>A| S204
19 BAA02g40040 A02 33844737 G A downstream_gene_variant MODIFIER c.*742G>A| S278