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 BAA09g12000 A09 6770917 C T upstream_gene_variant MODIFIER c.-3685C>T| S148
S210
2 BAA09g12000 A09 6771002 G A upstream_gene_variant MODIFIER c.-3600G>A| S245
3 BAA09g12000 A09 6771096 C T upstream_gene_variant MODIFIER c.-3506C>T| S42
4 BAA09g12000 A09 6771248 C T upstream_gene_variant MODIFIER c.-3354C>T| S132
S137
S215
5 BAA09g12000 A09 6772170 G A upstream_gene_variant MODIFIER c.-2432G>A| S308
6 BAA09g12000 A09 6772400 G A upstream_gene_variant MODIFIER c.-2202G>A| S207
7 BAA09g12000 A09 6772711 C T upstream_gene_variant MODIFIER c.-1891C>T| S174
8 BAA09g12000 A09 6772994 C T upstream_gene_variant MODIFIER c.-1608C>T| S239
9 BAA09g12000 A09 6773263 G A upstream_gene_variant MODIFIER c.-1339G>A| S8
10 BAA09g12000 A09 6774690 G A missense_variant MODERATE c.89G>A|p.Gly30Glu S60
11 BAA09g12000 A09 6775669 C T intron_variant MODIFIER c.402+515C>T| S6
12 BAA09g12000 A09 6776285 G A intron_variant MODIFIER c.403-826G>A| S110
S240
13 BAA09g12000 A09 6776498 G A intron_variant MODIFIER c.403-613G>A| S289
S290
14 BAA09g12000 A09 6779204 G A missense_variant MODERATE c.1057G>A|p.Val353Ile S45
15 BAA09g12000 A09 6783366 C T downstream_gene_variant MODIFIER c.*2813C>T| S139
16 BAA09g12000 A09 6783494 G A downstream_gene_variant MODIFIER c.*2941G>A| S205