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


Gene ID

Results: 1 - 35 of 35 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g08030 A10 5191132 G A upstream_gene_variant MODIFIER c.-4556G>A| S217
S248
2 BAA10g08030 A10 5191320 C T upstream_gene_variant MODIFIER c.-4368C>T| S177
3 BAA10g08030 A10 5191654 C T upstream_gene_variant MODIFIER c.-4034C>T| S70
4 BAA10g08030 A10 5191754 G A upstream_gene_variant MODIFIER c.-3934G>A| S115
5 BAA10g08030 A10 5191829 C T upstream_gene_variant MODIFIER c.-3859C>T| S116
6 BAA10g08030 A10 5191903 C T upstream_gene_variant MODIFIER c.-3785C>T| S122
7 BAA10g08030 A10 5193032 C T upstream_gene_variant MODIFIER c.-2656C>T| S1
S161
S228
S244
S290
S90
8 BAA10g08030 A10 5193782 G A upstream_gene_variant MODIFIER c.-1906G>A| S283
9 BAA10g08030 A10 5193976 G A upstream_gene_variant MODIFIER c.-1712G>A| S4
10 BAA10g08030 A10 5194971 G A upstream_gene_variant MODIFIER c.-717G>A| S176
11 BAA10g08030 A10 5195043 C T upstream_gene_variant MODIFIER c.-645C>T| S193
12 BAA10g08030 A10 5195181 G A upstream_gene_variant MODIFIER c.-507G>A| S7
13 BAA10g08030 A10 5195535 G A upstream_gene_variant MODIFIER c.-153G>A| S48
14 BAA10g08030 A10 5197355 C T intron_variant MODIFIER c.1032+119C>T| S282
15 BAA10g08030 A10 5197999 C T intron_variant MODIFIER c.1158+27C>T| S51
16 BAA10g08030 A10 5198144 C T intron_variant MODIFIER c.1158+172C>T| S142
17 BAA10g08030 A10 5198148 G A intron_variant MODIFIER c.1158+176G>A| S50
S51
18 BAA10g08030 A10 5198452 G A intron_variant MODIFIER c.1158+480G>A| S212
19 BAA10g08030 A10 5198621 G A intron_variant MODIFIER c.1159-642G>A| S234
20 BAA10g08030 A10 5199037 G A intron_variant MODIFIER c.1159-226G>A| S69
21 BAA10g08030 A10 5199290 G A missense_variant MODERATE c.1186G>A|p.Ala396Thr S245
22 BAA10g08030 A10 5199339 C A missense_variant MODERATE c.1235C>A|p.Thr412Lys S185
23 BAA10g08030 A10 5199486 G A synonymous_variant LOW c.1290G>A|p.Lys430Lys S192
24 BAA10g08030 A10 5199573 G A stop_gained HIGH c.1377G>A|p.Trp459* S18
25 BAA10g08030 A10 5199657 C T downstream_gene_variant MODIFIER c.*3C>T| S84
S93