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


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g43030 A02 35743071 C T missense_variant MODERATE c.3137G>A|p.Arg1046Lys S237
2 BAA02g43030 A02 35743423 G A missense_variant MODERATE c.2870C>T|p.Ala957Val S134
3 BAA02g43030 A02 35744124 C T intron_variant MODIFIER c.2457+49G>A| S216
4 BAA02g43030 A02 35744225 C T missense_variant MODERATE c.2405G>A|p.Arg802Lys S261
5 BAA02g43030 A02 35744227 G A synonymous_variant LOW c.2403C>T|p.Cys801Cys S23
S295
6 BAA02g43030 A02 35744434 C T missense_variant MODERATE c.2303G>A|p.Arg768Lys S273
7 BAA02g43030 A02 35744509 G A missense_variant MODERATE c.2228C>T|p.Pro743Leu S152
8 BAA02g43030 A02 35745752 C T intron_variant MODIFIER c.1540+19G>A| S40
S49
9 BAA02g43030 A02 35745912 G A splice_region_variant&intron_variant LOW c.1500+6C>T| S23
10 BAA02g43030 A02 35747753 C T intron_variant MODIFIER c.766-192G>A| S120
11 BAA02g43030 A02 35748094 C T intron_variant MODIFIER c.766-533G>A| S18
12 BAA02g43030 A02 35748785 G T missense_variant MODERATE c.626C>A|p.Ser209Tyr S70
13 BAA02g43030 A02 35749675 C T missense_variant MODERATE c.283G>A|p.Ala95Thr S64
14 BAA02g43030 A02 35750448 G C upstream_gene_variant MODIFIER c.-97C>G| S250
15 BAA02g43030 A02 35750467 G A upstream_gene_variant MODIFIER c.-116C>T| S111
16 BAA02g43030 A02 35750472 G A upstream_gene_variant MODIFIER c.-121C>T| S245
17 BAA02g43030 A02 35751130 G A upstream_gene_variant MODIFIER c.-779C>T| S136
S186
18 BAA02g43030 A02 35751149 C T upstream_gene_variant MODIFIER c.-798G>A| S221
19 BAA02g43030 A02 35751955 C T upstream_gene_variant MODIFIER c.-1604G>A| S47
20 BAA02g43030 A02 35752174 G A upstream_gene_variant MODIFIER c.-1823C>T| S51
21 BAA02g43030 A02 35752702 C T upstream_gene_variant MODIFIER c.-2351G>A| S130