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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g15370 A01 7385338 G A downstream_gene_variant MODIFIER c.*4632C>T| S216
2 BAA01g15370 A01 7385624 G A downstream_gene_variant MODIFIER c.*4346C>T| S96
3 BAA01g15370 A01 7386914 C T downstream_gene_variant MODIFIER c.*3056G>A| S223
4 BAA01g15370 A01 7387673 G A downstream_gene_variant MODIFIER c.*2297C>T| S229
5 BAA01g15370 A01 7387962 G A downstream_gene_variant MODIFIER c.*2008C>T| S275
6 BAA01g15370 A01 7387969 C T downstream_gene_variant MODIFIER c.*2001G>A| S16
7 BAA01g15370 A01 7388078 C A downstream_gene_variant MODIFIER c.*1892G>T| S284
8 BAA01g15370 A01 7388821 G A downstream_gene_variant MODIFIER c.*1149C>T| S95
9 BAA01g15370 A01 7388824 C T downstream_gene_variant MODIFIER c.*1146G>A| S134
10 BAA01g15370 A01 7389242 C T downstream_gene_variant MODIFIER c.*728G>A| S4
11 BAA01g15370 A01 7389616 C T downstream_gene_variant MODIFIER c.*354G>A| S260
12 BAA01g15370 A01 7389754 C T downstream_gene_variant MODIFIER c.*216G>A| S265
13 BAA01g15370 A01 7390707 G A missense_variant MODERATE c.521C>T|p.Ser174Phe S294
14 BAA01g15370 A01 7391028 G A intron_variant MODIFIER c.442+141C>T| S229
15 BAA01g15370 A01 7393056 C T upstream_gene_variant MODIFIER c.-1446G>A| S266
16 BAA01g15370 A01 7394898 T A upstream_gene_variant MODIFIER c.-3288A>T| S205