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


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g01750 A08 1277306 C T upstream_gene_variant MODIFIER c.-3059C>T| S143
2 BAA08g01750 A08 1277530 C T upstream_gene_variant MODIFIER c.-2835C>T| S138
3 BAA08g01750 A08 1277569 C T upstream_gene_variant MODIFIER c.-2796C>T| S162
4 BAA08g01750 A08 1278153 G A upstream_gene_variant MODIFIER c.-2212G>A| S259
5 BAA08g01750 A08 1278370 G A upstream_gene_variant MODIFIER c.-1995G>A| S278
6 BAA08g01750 A08 1278486 G A upstream_gene_variant MODIFIER c.-1879G>A| S282
7 BAA08g01750 A08 1278778 C T upstream_gene_variant MODIFIER c.-1587C>T| S289
8 BAA08g01750 A08 1279356 C T upstream_gene_variant MODIFIER c.-1009C>T| S251
9 BAA08g01750 A08 1279519 G A upstream_gene_variant MODIFIER c.-846G>A| S15
S3
10 BAA08g01750 A08 1279561 G A upstream_gene_variant MODIFIER c.-804G>A| S39
11 BAA08g01750 A08 1279696 G A upstream_gene_variant MODIFIER c.-669G>A| S192
12 BAA08g01750 A08 1281511 C T intron_variant MODIFIER c.375+598C>T| S170
13 BAA08g01750 A08 1282106 G A intron_variant MODIFIER c.376-798G>A| S298
14 BAA08g01750 A08 1282610 G A intron_variant MODIFIER c.376-294G>A| S95
15 BAA08g01750 A08 1282874 G A intron_variant MODIFIER c.376-30G>A| S62
16 BAA08g01750 A08 1282998 C T missense_variant MODERATE c.470C>T|p.Ser157Phe S73
S91
17 BAA08g01750 A08 1283255 G A missense_variant MODERATE c.727G>A|p.Asp243Asn S124
18 BAA08g01750 A08 1283631 C T missense_variant MODERATE c.1103C>T|p.Thr368Ile S162
19 BAA08g01750 A08 1285013 C T downstream_gene_variant MODIFIER c.*221C>T| S294
20 BAA08g01750 A08 1286595 G A downstream_gene_variant MODIFIER c.*1803G>A| S19
21 BAA08g01750 A08 1286602 C T downstream_gene_variant MODIFIER c.*1810C>T| S80
22 BAA08g01750 A08 1287206 G A downstream_gene_variant MODIFIER c.*2414G>A| S273
23 BAA08g01750 A08 1288248 C T downstream_gene_variant MODIFIER c.*3456C>T| S296
24 BAA08g01750 A08 1289524 C T downstream_gene_variant MODIFIER c.*4732C>T| S272