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


Gene ID

Results: 1 - 26 of 26 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g37950 A09 46003332 C T upstream_gene_variant MODIFIER c.-4657C>T| S109
2 BAA09g37950 A09 46005836 G A upstream_gene_variant MODIFIER c.-2153G>A| S271
3 BAA09g37950 A09 46006844 C T upstream_gene_variant MODIFIER c.-1145C>T| S63
4 BAA09g37950 A09 46007192 G A upstream_gene_variant MODIFIER c.-797G>A| S62
5 BAA09g37950 A09 46007685 C T upstream_gene_variant MODIFIER c.-304C>T| S19
6 BAA09g37950 A09 46008521 C T missense_variant MODERATE c.454C>T|p.Pro152Ser S82
S92
7 BAA09g37950 A09 46009346 C T intron_variant MODIFIER c.997-82C>T| S302
8 BAA09g37950 A09 46010375 C T intron_variant MODIFIER c.1768+176C>T| S171
9 BAA09g37950 A09 46010672 C T synonymous_variant LOW c.1795C>T|p.Leu599Leu S54
10 BAA09g37950 A09 46011066 C T intron_variant MODIFIER c.1928+36C>T| S260
11 BAA09g37950 A09 46011531 C T intron_variant MODIFIER c.2104-34C>T| S43
12 BAA09g37950 A09 46011962 C T synonymous_variant LOW c.2361C>T|p.Asp787Asp S50
13 BAA09g37950 A09 46012242 G A missense_variant MODERATE c.2584G>A|p.Ala862Thr S12
S222
14 BAA09g37950 A09 46012336 C T missense_variant MODERATE c.2678C>T|p.Pro893Leu S242
15 BAA09g37950 A09 46012373 C T downstream_gene_variant MODIFIER c.*12C>T| S279
16 BAA09g37950 A09 46012902 G A downstream_gene_variant MODIFIER c.*541G>A| S266
17 BAA09g37950 A09 46013487 G A downstream_gene_variant MODIFIER c.*1126G>A| S262
18 BAA09g37950 A09 46013640 C T downstream_gene_variant MODIFIER c.*1279C>T| S297
19 BAA09g37950 A09 46013689 G A downstream_gene_variant MODIFIER c.*1328G>A| S53
20 BAA09g37950 A09 46013958 G A downstream_gene_variant MODIFIER c.*1597G>A| S48
21 BAA09g37950 A09 46014113 C T downstream_gene_variant MODIFIER c.*1752C>T| S18
22 BAA09g37950 A09 46014477 C T downstream_gene_variant MODIFIER c.*2116C>T| S293
23 BAA09g37950 A09 46015544 G A downstream_gene_variant MODIFIER c.*3183G>A| S148
S210
24 BAA09g37950 A09 46015886 C A downstream_gene_variant MODIFIER c.*3525C>A| S239
S33
25 BAA09g37950 A09 46016124 C T downstream_gene_variant MODIFIER c.*3763C>T| S259