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


Gene ID

Results: 1 - 29 of 29 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g28170 A09 18529557 C T downstream_gene_variant MODIFIER c.*4726G>A| S216
2 BAA09g28170 A09 18529590 C T downstream_gene_variant MODIFIER c.*4693G>A| S36
3 BAA09g28170 A09 18529669 C T downstream_gene_variant MODIFIER c.*4614G>A| S60
4 BAA09g28170 A09 18529777 G A downstream_gene_variant MODIFIER c.*4506C>T| S97
5 BAA09g28170 A09 18530377 G A downstream_gene_variant MODIFIER c.*3906C>T| S236
6 BAA09g28170 A09 18530390 C T downstream_gene_variant MODIFIER c.*3893G>A| S32
7 BAA09g28170 A09 18532440 C T downstream_gene_variant MODIFIER c.*1843G>A| S183
S198
8 BAA09g28170 A09 18532460 C T downstream_gene_variant MODIFIER c.*1823G>A| S255
9 BAA09g28170 A09 18532479 C T downstream_gene_variant MODIFIER c.*1804G>A| S263
10 BAA09g28170 A09 18532808 T G downstream_gene_variant MODIFIER c.*1475A>C| S54
11 BAA09g28170 A09 18533867 G A downstream_gene_variant MODIFIER c.*416C>T| S236
12 BAA09g28170 A09 18533880 G A downstream_gene_variant MODIFIER c.*403C>T| S79
S91
13 BAA09g28170 A09 18534194 G A downstream_gene_variant MODIFIER c.*89C>T| S262
14 BAA09g28170 A09 18534303 G C missense_variant MODERATE c.688C>G|p.Leu230Val S130
15 BAA09g28170 A09 18534332 G A missense_variant MODERATE c.659C>T|p.Thr220Ile S110
16 BAA09g28170 A09 18534394 G A synonymous_variant LOW c.597C>T|p.Ile199Ile S297
17 BAA09g28170 A09 18534556 A T intron_variant MODIFIER c.488-53T>A| S178
18 BAA09g28170 A09 18534705 G A intron_variant MODIFIER c.488-202C>T| S244
19 BAA09g28170 A09 18534707 G A intron_variant MODIFIER c.488-204C>T| S291
20 BAA09g28170 A09 18535599 C T intron_variant MODIFIER c.488-1096G>A| S305
21 BAA09g28170 A09 18535603 C T intron_variant MODIFIER c.488-1100G>A| S260
22 BAA09g28170 A09 18535653 G A intron_variant MODIFIER c.488-1150C>T| S84
S93
23 BAA09g28170 A09 18535914 G A intron_variant MODIFIER c.487+1312C>T| S170
24 BAA09g28170 A09 18536575 G A intron_variant MODIFIER c.487+651C>T| S132
S137
S215
S89
25 BAA09g28170 A09 18536610 G A intron_variant MODIFIER c.487+616C>T| S280