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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAS13g00150 Scaffold13 4391343 C T upstream_gene_variant MODIFIER c.-4713C>T| S176
2 BAS13g00150 Scaffold13 4391793 C T upstream_gene_variant MODIFIER c.-4263C>T| S272
3 BAS13g00150 Scaffold13 4392448 C T upstream_gene_variant MODIFIER c.-3608C>T| S56
4 BAS13g00150 Scaffold13 4393214 G A upstream_gene_variant MODIFIER c.-2842G>A| S292
5 BAS13g00150 Scaffold13 4393473 C T upstream_gene_variant MODIFIER c.-2583C>T| S127
6 BAS13g00150 Scaffold13 4393670 C T upstream_gene_variant MODIFIER c.-2386C>T| S178
7 BAS13g00150 Scaffold13 4393704 G A upstream_gene_variant MODIFIER c.-2352G>A| S296
8 BAS13g00150 Scaffold13 4394132 G A upstream_gene_variant MODIFIER c.-1924G>A| S16
9 BAS13g00150 Scaffold13 4394475 C T upstream_gene_variant MODIFIER c.-1581C>T| S96
10 BAS13g00150 Scaffold13 4395516 C T upstream_gene_variant MODIFIER c.-540C>T| S71
11 BAS13g00150 Scaffold13 4396082 G A synonymous_variant LOW c.27G>A|p.Gln9Gln S163
12 BAS13g00150 Scaffold13 4396819 G A missense_variant MODERATE c.415G>A|p.Val139Ile S281
13 BAS13g00150 Scaffold13 4397089 G A splice_region_variant&intron_variant LOW c.586-4G>A| S293
14 BAS13g00150 Scaffold13 4397473 C T intron_variant MODIFIER c.834+40C>T| S223
15 BAS13g00150 Scaffold13 4397813 G A synonymous_variant LOW c.1134G>A|p.Arg378Arg S188
16 BAS13g00150 Scaffold13 4400118 C T missense_variant MODERATE c.3134C>T|p.Ser1045Phe S165
17 BAS13g00150 Scaffold13 4400166 C T missense_variant MODERATE c.3182C>T|p.Pro1061Leu S262
18 BAS13g00150 Scaffold13 4401168 G A missense_variant MODERATE c.3892G>A|p.Val1298Ile S8