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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g28570 A05 32429601 C T downstream_gene_variant MODIFIER c.*4966G>A| S94
2 BAA05g28570 A05 32429983 G A downstream_gene_variant MODIFIER c.*4584C>T| S34
3 BAA05g28570 A05 32430102 C T downstream_gene_variant MODIFIER c.*4465G>A| S292
4 BAA05g28570 A05 32431488 G A downstream_gene_variant MODIFIER c.*3079C>T| S243
S299
5 BAA05g28570 A05 32431885 C T downstream_gene_variant MODIFIER c.*2682G>A| S182
6 BAA05g28570 A05 32432524 G A downstream_gene_variant MODIFIER c.*2043C>T| S257
7 BAA05g28570 A05 32432971 C T downstream_gene_variant MODIFIER c.*1596G>A| S81
8 BAA05g28570 A05 32433242 C T downstream_gene_variant MODIFIER c.*1325G>A| S242
9 BAA05g28570 A05 32434601 C T missense_variant MODERATE c.1313G>A|p.Gly438Glu S59
10 BAA05g28570 A05 32434853 C T synonymous_variant LOW c.1149G>A|p.Gln383Gln S113
11 BAA05g28570 A05 32435071 G A missense_variant MODERATE c.931C>T|p.Pro311Ser S19
S222
12 BAA05g28570 A05 32435454 G A missense_variant MODERATE c.548C>T|p.Ser183Leu S136
13 BAA05g28570 A05 32435496 G A missense_variant MODERATE c.506C>T|p.Ala169Val S77
S82
14 BAA05g28570 A05 32435696 G A synonymous_variant LOW c.384C>T|p.Val128Val S134
15 BAA05g28570 A05 32435856 C T missense_variant MODERATE c.224G>A|p.Arg75Lys S71
16 BAA05g28570 A05 32436393 C T upstream_gene_variant MODIFIER c.-314G>A| S58
17 BAA05g28570 A05 32436525 C T upstream_gene_variant MODIFIER c.-446G>A| S181
18 BAA05g28570 A05 32436679 C T upstream_gene_variant MODIFIER c.-600G>A| S206
S26
19 BAA05g28570 A05 32436692 C T upstream_gene_variant MODIFIER c.-613G>A| S19
20 BAA05g28570 A05 32437229 C T upstream_gene_variant MODIFIER c.-1150G>A| S73
S74
S91
21 BAA05g28570 A05 32437501 C T upstream_gene_variant MODIFIER c.-1422G>A| S221
22 BAA05g28570 A05 32439470 G A upstream_gene_variant MODIFIER c.-3391C>T| S257
23 BAA05g28570 A05 32439741 A T upstream_gene_variant MODIFIER c.-3662T>A| S8