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 BAA09g31510 A09 39459583 C T downstream_gene_variant MODIFIER c.*3863G>A| S19
S259
2 BAA09g31510 A09 39460423 C T downstream_gene_variant MODIFIER c.*3023G>A| S261
S274
3 BAA09g31510 A09 39460592 G A downstream_gene_variant MODIFIER c.*2854C>T| S45
4 BAA09g31510 A09 39460623 G A downstream_gene_variant MODIFIER c.*2823C>T| S246
5 BAA09g31510 A09 39461923 C T downstream_gene_variant MODIFIER c.*1523G>A| S77
S82
6 BAA09g31510 A09 39462382 C T downstream_gene_variant MODIFIER c.*1064G>A| S193
7 BAA09g31510 A09 39462487 C T downstream_gene_variant MODIFIER c.*959G>A| S279
8 BAA09g31510 A09 39462573 G A downstream_gene_variant MODIFIER c.*873C>T| S249
9 BAA09g31510 A09 39462636 A T downstream_gene_variant MODIFIER c.*810T>A| S25
10 BAA09g31510 A09 39462640 G A downstream_gene_variant MODIFIER c.*806C>T| S48
11 BAA09g31510 A09 39465314 C T missense_variant MODERATE c.2486G>A|p.Arg829Lys S121
12 BAA09g31510 A09 39465345 C T missense_variant MODERATE c.2455G>A|p.Glu819Lys S251
13 BAA09g31510 A09 39469938 C T missense_variant&splice_region_variant MODERATE c.670G>A|p.Ala224Thr S183
S198
14 BAA09g31510 A09 39471480 G A intron_variant MODIFIER c.437-1309C>T| S51
S92
15 BAA09g31510 A09 39474493 G A missense_variant MODERATE c.31C>T|p.Pro11Ser S107
16 BAA09g31510 A09 39476308 C T upstream_gene_variant MODIFIER c.-1785G>A| S296
17 BAA09g31510 A09 39476393 G A upstream_gene_variant MODIFIER c.-1870C>T| S262
18 BAA09g31510 A09 39476972 C T upstream_gene_variant MODIFIER c.-2449G>A| S247
19 BAA09g31510 A09 39477497 C T upstream_gene_variant MODIFIER c.-2974G>A| S251
20 BAA09g31510 A09 39477529 G A upstream_gene_variant MODIFIER c.-3006C>T| S67
21 BAA09g31510 A09 39477634 G A upstream_gene_variant MODIFIER c.-3111C>T| S165
22 BAA09g31510 A09 39477970 G C upstream_gene_variant MODIFIER c.-3447C>G| S276
23 BAA09g31510 A09 39477992 G A upstream_gene_variant MODIFIER c.-3469C>T| S166