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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g19410 A02 10065316 C T upstream_gene_variant MODIFIER c.-4162C>T| S138
2 BAA02g19410 A02 10065363 C T upstream_gene_variant MODIFIER c.-4115C>T| S216
S241
S265
S39
3 BAA02g19410 A02 10065704 C T upstream_gene_variant MODIFIER c.-3774C>T| S124
4 BAA02g19410 A02 10065762 C T upstream_gene_variant MODIFIER c.-3716C>T| S277
5 BAA02g19410 A02 10066357 G A upstream_gene_variant MODIFIER c.-3121G>A| S111
6 BAA02g19410 A02 10066572 G A upstream_gene_variant MODIFIER c.-2906G>A| S251
7 BAA02g19410 A02 10066823 G A upstream_gene_variant MODIFIER c.-2655G>A| S148
S30
S31
8 BAA02g19410 A02 10067207 C A upstream_gene_variant MODIFIER c.-2271C>A| S121
9 BAA02g19410 A02 10067567 G A upstream_gene_variant MODIFIER c.-1911G>A| S136
10 BAA02g19410 A02 10068032 C T upstream_gene_variant MODIFIER c.-1446C>T| S302
11 BAA02g19410 A02 10068300 C T upstream_gene_variant MODIFIER c.-1178C>T| S212
12 BAA02g19410 A02 10070473 G A missense_variant MODERATE c.739G>A|p.Glu247Lys S217
S248
13 BAA02g19410 A02 10070547 G A synonymous_variant LOW c.813G>A|p.Glu271Glu S247
14 BAA02g19410 A02 10070714 C T missense_variant MODERATE c.980C>T|p.Ala327Val S32
15 BAA02g19410 A02 10071086 C T missense_variant MODERATE c.1352C>T|p.Pro451Leu S139