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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g08660 A09 4851711 C T upstream_gene_variant MODIFIER c.-4318C>T| S267
2 BAA09g08660 A09 4851837 G A upstream_gene_variant MODIFIER c.-4192G>A| S188
3 BAA09g08660 A09 4852236 G A upstream_gene_variant MODIFIER c.-3793G>A| S289
S290
4 BAA09g08660 A09 4852995 C T upstream_gene_variant MODIFIER c.-3034C>T| S83
S88
5 BAA09g08660 A09 4855833 G A upstream_gene_variant MODIFIER c.-196G>A| S216
6 BAA09g08660 A09 4855842 G A upstream_gene_variant MODIFIER c.-187G>A| S42
7 BAA09g08660 A09 4856204 A C intron_variant MODIFIER c.67-45A>C| S81
8 BAA09g08660 A09 4857126 G A missense_variant MODERATE c.709G>A|p.Glu237Lys S40
S49
9 BAA09g08660 A09 4857141 C T missense_variant MODERATE c.724C>T|p.Leu242Phe S13
S168
S219
S278
S72
10 BAA09g08660 A09 4859067 G A intron_variant MODIFIER c.907+1476G>A| S64
11 BAA09g08660 A09 4859208 G A intron_variant MODIFIER c.907+1617G>A| S123
12 BAA09g08660 A09 4859364 C T intron_variant MODIFIER c.907+1773C>T| S140
13 BAA09g08660 A09 4859649 G A intron_variant MODIFIER c.907+2058G>A| S233
14 BAA09g08660 A09 4859707 G A intron_variant MODIFIER c.907+2116G>A| S225
S73
15 BAA09g08660 A09 4859755 G A intron_variant MODIFIER c.907+2164G>A| S162
16 BAA09g08660 A09 4860005 C T intron_variant MODIFIER c.907+2414C>T| S134
17 BAA09g08660 A09 4860181 C T intron_variant MODIFIER c.907+2590C>T| S136
18 BAA09g08660 A09 4866598 G A splice_region_variant&intron_variant LOW c.908-4G>A| S202