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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g25960 A06 17775704 C T downstream_gene_variant MODIFIER c.*4834G>A| S182
2 BAA06g25960 A06 17775908 C T downstream_gene_variant MODIFIER c.*4630G>A| S6
3 BAA06g25960 A06 17775928 C T downstream_gene_variant MODIFIER c.*4610G>A| S238
4 BAA06g25960 A06 17775945 G A downstream_gene_variant MODIFIER c.*4593C>T| S38
5 BAA06g25960 A06 17776315 C T downstream_gene_variant MODIFIER c.*4223G>A| S62
6 BAA06g25960 A06 17776782 C T downstream_gene_variant MODIFIER c.*3756G>A| S293
7 BAA06g25960 A06 17777058 C T downstream_gene_variant MODIFIER c.*3480G>A| S164
8 BAA06g25960 A06 17779474 C T downstream_gene_variant MODIFIER c.*1064G>A| S57
9 BAA06g25960 A06 17779648 G A downstream_gene_variant MODIFIER c.*890C>T| S162
10 BAA06g25960 A06 17780820 G A upstream_gene_variant MODIFIER c.-76C>T| S206
S26
11 BAA06g25960 A06 17781266 G A upstream_gene_variant MODIFIER c.-522C>T| S75
S81
12 BAA06g25960 A06 17781282 C T upstream_gene_variant MODIFIER c.-538G>A| S87
13 BAA06g25960 A06 17781587 C T upstream_gene_variant MODIFIER c.-843G>A| S148
S210
S30
S31
14 BAA06g25960 A06 17782590 C T upstream_gene_variant MODIFIER c.-1846G>A| S281
15 BAA06g25960 A06 17782849 G A upstream_gene_variant MODIFIER c.-2105C>T| S226
16 BAA06g25960 A06 17782913 C T upstream_gene_variant MODIFIER c.-2169G>A| S34
17 BAA06g25960 A06 17783152 C T upstream_gene_variant MODIFIER c.-2408G>A| S267
18 BAA06g25960 A06 17783958 C T upstream_gene_variant MODIFIER c.-3214G>A| S6
19 BAA06g25960 A06 17784244 C T upstream_gene_variant MODIFIER c.-3500G>A| S262
20 BAA06g25960 A06 17784345 C T upstream_gene_variant MODIFIER c.-3601G>A| S79
S91
21 BAA06g25960 A06 17784697 G A upstream_gene_variant MODIFIER c.-3953C>T| S237
22 BAA06g25960 A06 17784883 A T upstream_gene_variant MODIFIER c.-4139T>A| S246
23 BAA06g25960 A06 17785472 G A upstream_gene_variant MODIFIER c.-4728C>T| S3