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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g11140 A08 9991853 C T downstream_gene_variant MODIFIER c.*590G>A| S284
2 BAA08g11140 A08 9993461 G A intron_variant MODIFIER c.2341-19C>T| S107
3 BAA08g11140 A08 9993878 C T synonymous_variant LOW c.2085G>A|p.Thr695Thr S130
4 BAA08g11140 A08 9994903 G A intron_variant MODIFIER c.1745+16C>T| S221
5 BAA08g11140 A08 9996794 C T splice_acceptor_variant&intron_variant HIGH c.855-1G>A| S228
6 BAA08g11140 A08 9997054 C T stop_gained HIGH c.825G>A|p.Trp275* S294
7 BAA08g11140 A08 9997711 G A synonymous_variant LOW c.492C>T|p.Asp164Asp S72
8 BAA08g11140 A08 9997990 C T stop_gained HIGH c.213G>A|p.Trp71* S59
9 BAA08g11140 A08 9998108 C T splice_region_variant&intron_variant LOW c.178+6G>A| S63
10 BAA08g11140 A08 9999101 C T upstream_gene_variant MODIFIER c.-186G>A| S178
11 BAA08g11140 A08 9999131 C T upstream_gene_variant MODIFIER c.-216G>A| S293
12 BAA08g11140 A08 9999277 C T upstream_gene_variant MODIFIER c.-362G>A| S180
13 BAA08g11140 A08 9999316 C T upstream_gene_variant MODIFIER c.-401G>A| S267
14 BAA08g11140 A08 9999446 C T upstream_gene_variant MODIFIER c.-531G>A| S278
15 BAA08g11140 A08 10001061 G A upstream_gene_variant MODIFIER c.-2146C>T| S202
16 BAA08g11140 A08 10002310 G A upstream_gene_variant MODIFIER c.-3395C>T| S65
17 BAA08g11140 A08 10002656 G A upstream_gene_variant MODIFIER c.-3741C>T| S108