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


Gene ID

Results: 1 - 27 of 27 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g02930 A04 1727890 C T upstream_gene_variant MODIFIER c.-4472C>T| S72
S78
2 BAA04g02930 A04 1728283 G A upstream_gene_variant MODIFIER c.-4079G>A| S280
3 BAA04g02930 A04 1729595 C T upstream_gene_variant MODIFIER c.-2767C>T| S178
S234
4 BAA04g02930 A04 1729637 C T upstream_gene_variant MODIFIER c.-2725C>T| S283
5 BAA04g02930 A04 1730139 G A upstream_gene_variant MODIFIER c.-2223G>A| S162
6 BAA04g02930 A04 1730676 C T upstream_gene_variant MODIFIER c.-1686C>T| S246
7 BAA04g02930 A04 1736387 G A intron_variant MODIFIER c.263-168G>A| S219
S72
8 BAA04g02930 A04 1736499 C T intron_variant MODIFIER c.263-56C>T| S18
9 BAA04g02930 A04 1737318 C T intron_variant MODIFIER c.321+705C>T| S63
10 BAA04g02930 A04 1737451 C T intron_variant MODIFIER c.322-572C>T| S230
11 BAA04g02930 A04 1738362 C T missense_variant MODERATE c.583C>T|p.Pro195Ser S153
12 BAA04g02930 A04 1739743 C T intron_variant MODIFIER c.1074+707C>T| S172
S217
13 BAA04g02930 A04 1739852 G A intron_variant MODIFIER c.1075-792G>A| S56
14 BAA04g02930 A04 1739987 A G intron_variant MODIFIER c.1075-657A>G| S260
15 BAA04g02930 A04 1740614 C T intron_variant MODIFIER c.1075-30C>T| S45
16 BAA04g02930 A04 1741187 C T intron_variant MODIFIER c.1215+261C>T| S295
17 BAA04g02930 A04 1741544 C T intron_variant MODIFIER c.1216-87C>T| S129
18 BAA04g02930 A04 1743301 G A downstream_gene_variant MODIFIER c.*1419G>A| S123
19 BAA04g02930 A04 1743346 C T downstream_gene_variant MODIFIER c.*1464C>T| S158
20 BAA04g02930 A04 1743524 C T downstream_gene_variant MODIFIER c.*1642C>T| S8
21 BAA04g02930 A04 1743692 A T downstream_gene_variant MODIFIER c.*1810A>T| S5
22 BAA04g02930 A04 1744027 C T downstream_gene_variant MODIFIER c.*2145C>T| S33
23 BAA04g02930 A04 1745083 G A downstream_gene_variant MODIFIER c.*3201G>A| S167
24 BAA04g02930 A04 1745264 C T downstream_gene_variant MODIFIER c.*3382C>T| S293
25 BAA04g02930 A04 1745655 C T downstream_gene_variant MODIFIER c.*3773C>T| S9