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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g02110 A10 987530 C T upstream_gene_variant MODIFIER c.-3882C>T| S72
2 BAA10g02110 A10 988236 G A upstream_gene_variant MODIFIER c.-3176G>A| S124
3 BAA10g02110 A10 988359 G A upstream_gene_variant MODIFIER c.-3053G>A| S290
4 BAA10g02110 A10 989032 G A upstream_gene_variant MODIFIER c.-2380G>A| S164
5 BAA10g02110 A10 989576 C T upstream_gene_variant MODIFIER c.-1836C>T| S195
6 BAA10g02110 A10 991219 G A upstream_gene_variant MODIFIER c.-193G>A| S296
7 BAA10g02110 A10 991411 G A upstream_gene_variant MODIFIER c.-1G>A| S156
8 BAA10g02110 A10 991567 C T synonymous_variant LOW c.156C>T|p.Ser52Ser S224
9 BAA10g02110 A10 992177 G A missense_variant MODERATE c.412G>A|p.Val138Ile S62
10 BAA10g02110 A10 992641 G A missense_variant MODERATE c.670G>A|p.Glu224Lys S292
11 BAA10g02110 A10 992664 C T synonymous_variant LOW c.693C>T|p.Thr231Thr S11
12 BAA10g02110 A10 992802 G A synonymous_variant LOW c.831G>A|p.Gln277Gln S242
13 BAA10g02110 A10 994225 C T missense_variant MODERATE c.1937C>T|p.Pro646Leu S143
14 BAA10g02110 A10 994914 G A synonymous_variant LOW c.2358G>A|p.Lys786Lys S215
15 BAA10g02110 A10 995387 G A missense_variant MODERATE c.2725G>A|p.Glu909Lys S45
16 BAA10g02110 A10 995658 C T downstream_gene_variant MODIFIER c.*116C>T| S165