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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g16770 A09 9856957 G A downstream_gene_variant MODIFIER c.*4271C>T| S202
2 BAA09g16770 A09 9857075 G A downstream_gene_variant MODIFIER c.*4153C>T| S126
3 BAA09g16770 A09 9857119 G A downstream_gene_variant MODIFIER c.*4109C>T| S198
4 BAA09g16770 A09 9857421 C T downstream_gene_variant MODIFIER c.*3807G>A| S303
5 BAA09g16770 A09 9857427 C T downstream_gene_variant MODIFIER c.*3801G>A| S255
6 BAA09g16770 A09 9857906 G A downstream_gene_variant MODIFIER c.*3322C>T| S88
7 BAA09g16770 A09 9857955 C T downstream_gene_variant MODIFIER c.*3273G>A| S17
S218
8 BAA09g16770 A09 9858451 G A downstream_gene_variant MODIFIER c.*2777C>T| S45
9 BAA09g16770 A09 9858615 G A downstream_gene_variant MODIFIER c.*2613C>T| S167
S34
10 BAA09g16770 A09 9859420 G A downstream_gene_variant MODIFIER c.*1808C>T| S219
S72
11 BAA09g16770 A09 9859527 C T downstream_gene_variant MODIFIER c.*1701G>A| S148
12 BAA09g16770 A09 9860365 C T downstream_gene_variant MODIFIER c.*863G>A| S132
S137
S215
13 BAA09g16770 A09 9860777 C T downstream_gene_variant MODIFIER c.*451G>A| S204
14 BAA09g16770 A09 9861423 C T synonymous_variant LOW c.768G>A|p.Pro256Pro S297
15 BAA09g16770 A09 9861461 C T missense_variant MODERATE c.730G>A|p.Glu244Lys S203
16 BAA09g16770 A09 9861692 G A intron_variant MODIFIER c.675+81C>T| S180
17 BAA09g16770 A09 9861854 G A synonymous_variant LOW c.594C>T|p.Leu198Leu S121
18 BAA09g16770 A09 9862276 G A intron_variant MODIFIER c.341+143C>T| S142
19 BAA09g16770 A09 9862458 G A missense_variant MODERATE c.302C>T|p.Ser101Phe S191
20 BAA09g16770 A09 9864510 C T upstream_gene_variant MODIFIER c.-1655G>A| S204
21 BAA09g16770 A09 9864643 C T upstream_gene_variant MODIFIER c.-1788G>A| S96
22 BAA09g16770 A09 9866287 C T upstream_gene_variant MODIFIER c.-3432G>A| S306
S308