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


Gene ID

Results: 1 - 28 of 28 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g08260 A10 6026206 G A upstream_gene_variant MODIFIER c.-4019G>A| S295
2 BAA10g08260 A10 6026229 C T upstream_gene_variant MODIFIER c.-3996C>T| S166
3 BAA10g08260 A10 6026408 C T upstream_gene_variant MODIFIER c.-3817C>T| S266
4 BAA10g08260 A10 6026480 G A upstream_gene_variant MODIFIER c.-3745G>A| S69
5 BAA10g08260 A10 6026682 G A upstream_gene_variant MODIFIER c.-3543G>A| S226
6 BAA10g08260 A10 6026761 G A upstream_gene_variant MODIFIER c.-3464G>A| S290
7 BAA10g08260 A10 6026885 A C upstream_gene_variant MODIFIER c.-3340A>C| S2
8 BAA10g08260 A10 6027771 G A upstream_gene_variant MODIFIER c.-2454G>A| S92
9 BAA10g08260 A10 6028695 G A upstream_gene_variant MODIFIER c.-1530G>A| S306
S308
10 BAA10g08260 A10 6029307 C T upstream_gene_variant MODIFIER c.-918C>T| S263
11 BAA10g08260 A10 6030603 G A missense_variant MODERATE c.379G>A|p.Glu127Lys S120
12 BAA10g08260 A10 6031131 G A missense_variant MODERATE c.811G>A|p.Val271Ile S140
13 BAA10g08260 A10 6031696 C T missense_variant MODERATE c.1139C>T|p.Ser380Leu S286
14 BAA10g08260 A10 6032180 C T synonymous_variant LOW c.1467C>T|p.Arg489Arg S237
15 BAA10g08260 A10 6032362 G A stop_gained HIGH c.1572G>A|p.Trp524* S184
16 BAA10g08260 A10 6032460 A G intron_variant MODIFIER c.1602+68A>G| S32
17 BAA10g08260 A10 6033977 G A downstream_gene_variant MODIFIER c.*734G>A| S296
18 BAA10g08260 A10 6034140 G A downstream_gene_variant MODIFIER c.*897G>A| S83
19 BAA10g08260 A10 6034472 G A downstream_gene_variant MODIFIER c.*1229G>A| S293
20 BAA10g08260 A10 6034883 C T downstream_gene_variant MODIFIER c.*1640C>T| S23
21 BAA10g08260 A10 6035321 C T downstream_gene_variant MODIFIER c.*2078C>T| S114
22 BAA10g08260 A10 6035450 C T downstream_gene_variant MODIFIER c.*2207C>T| S161
23 BAA10g08260 A10 6036130 C T downstream_gene_variant MODIFIER c.*2887C>T| S103
24 BAA10g08260 A10 6036385 C T downstream_gene_variant MODIFIER c.*3142C>T| S58
25 BAA10g08260 A10 6036394 C T downstream_gene_variant MODIFIER c.*3151C>T| S176