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


Gene ID

Results: 1 - 33 of 33 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g08190 A10 5843408 A C upstream_gene_variant MODIFIER c.-4798A>C| S126
S144
S181
S188
S202
S227
S230
S61
2 BAA10g08190 A10 5843612 G A upstream_gene_variant MODIFIER c.-4594G>A| S281
3 BAA10g08190 A10 5844072 C T upstream_gene_variant MODIFIER c.-4134C>T| S87
4 BAA10g08190 A10 5844312 C T upstream_gene_variant MODIFIER c.-3894C>T| S269
5 BAA10g08190 A10 5846016 C T upstream_gene_variant MODIFIER c.-2190C>T| S120
6 BAA10g08190 A10 5846090 C T upstream_gene_variant MODIFIER c.-2116C>T| S139
7 BAA10g08190 A10 5846234 G A upstream_gene_variant MODIFIER c.-1972G>A| S1
8 BAA10g08190 A10 5846267 C T upstream_gene_variant MODIFIER c.-1939C>T| S37
9 BAA10g08190 A10 5846559 G A upstream_gene_variant MODIFIER c.-1647G>A| S60
10 BAA10g08190 A10 5846612 G A upstream_gene_variant MODIFIER c.-1594G>A| S187
11 BAA10g08190 A10 5847957 G A upstream_gene_variant MODIFIER c.-249G>A| S15
12 BAA10g08190 A10 5849052 G A intron_variant MODIFIER c.172-45G>A| S127
13 BAA10g08190 A10 5849093 C T splice_region_variant&intron_variant LOW c.172-4C>T| S194
14 BAA10g08190 A10 5849318 C T synonymous_variant LOW c.393C>T|p.Leu131Leu S152
15 BAA10g08190 A10 5849698 G A missense_variant MODERATE c.706G>A|p.Glu236Lys S99
16 BAA10g08190 A10 5850186 G A downstream_gene_variant MODIFIER c.*321G>A| S69
17 BAA10g08190 A10 5850389 C T downstream_gene_variant MODIFIER c.*524C>T| S131
18 BAA10g08190 A10 5850837 C T downstream_gene_variant MODIFIER c.*972C>T| S281
19 BAA10g08190 A10 5851129 C T downstream_gene_variant MODIFIER c.*1264C>T| S296
20 BAA10g08190 A10 5852198 C T downstream_gene_variant MODIFIER c.*2333C>T| S84
S93
21 BAA10g08190 A10 5852408 G A downstream_gene_variant MODIFIER c.*2543G>A| S278
22 BAA10g08190 A10 5852504 G A downstream_gene_variant MODIFIER c.*2639G>A| S140
23 BAA10g08190 A10 5852736 C T downstream_gene_variant MODIFIER c.*2871C>T| S37
24 BAA10g08190 A10 5853315 G A downstream_gene_variant MODIFIER c.*3450G>A| S17
25 BAA10g08190 A10 5853586 C T downstream_gene_variant MODIFIER c.*3721C>T| S199