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


Gene ID

Results: 1 - 37 of 37 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g19690 A05 11713589 C T downstream_gene_variant MODIFIER c.*4104G>A| S164
2 BAA05g19690 A05 11714968 C T downstream_gene_variant MODIFIER c.*2725G>A| S59
3 BAA05g19690 A05 11715243 G A downstream_gene_variant MODIFIER c.*2450C>T| S124
4 BAA05g19690 A05 11715273 G A downstream_gene_variant MODIFIER c.*2420C>T| S56
5 BAA05g19690 A05 11715339 C T downstream_gene_variant MODIFIER c.*2354G>A| S206
S26
6 BAA05g19690 A05 11715406 C T downstream_gene_variant MODIFIER c.*2287G>A| S188
7 BAA05g19690 A05 11715527 G A downstream_gene_variant MODIFIER c.*2166C>T| S62
8 BAA05g19690 A05 11716479 C T downstream_gene_variant MODIFIER c.*1214G>A| S13
9 BAA05g19690 A05 11716503 G A downstream_gene_variant MODIFIER c.*1190C>T| S197
10 BAA05g19690 A05 11716527 G A downstream_gene_variant MODIFIER c.*1166C>T| S203
11 BAA05g19690 A05 11716927 C T downstream_gene_variant MODIFIER c.*766G>A| S133
12 BAA05g19690 A05 11717679 G A downstream_gene_variant MODIFIER c.*14C>T| S172
13 BAA05g19690 A05 11717770 C T missense_variant MODERATE c.1384G>A|p.Glu462Lys S92
14 BAA05g19690 A05 11718478 C T intron_variant MODIFIER c.970-70G>A| S175
15 BAA05g19690 A05 11718759 G A intron_variant MODIFIER c.970-351C>T| S297
16 BAA05g19690 A05 11718794 C T intron_variant MODIFIER c.970-386G>A| S273
17 BAA05g19690 A05 11719065 C T intron_variant MODIFIER c.970-657G>A| S255
18 BAA05g19690 A05 11719978 C T intron_variant MODIFIER c.970-1570G>A| S205
19 BAA05g19690 A05 11720888 C T intron_variant MODIFIER c.969+1766G>A| S53
20 BAA05g19690 A05 11721006 G A intron_variant MODIFIER c.969+1648C>T| S125
21 BAA05g19690 A05 11721198 G A intron_variant MODIFIER c.969+1456C>T| S64
22 BAA05g19690 A05 11721638 C T intron_variant MODIFIER c.969+1016G>A| S251
23 BAA05g19690 A05 11721679 C T intron_variant MODIFIER c.969+975G>A| S68
24 BAA05g19690 A05 11723457 C T intron_variant MODIFIER c.508+162G>A| S117
25 BAA05g19690 A05 11723599 C T intron_variant MODIFIER c.508+20G>A| S8