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


Gene ID

Results: 1 - 35 of 35 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g23420 A09 14836242 G A upstream_gene_variant MODIFIER c.-4689G>A| S84
S93
2 BAA09g23420 A09 14836487 C T upstream_gene_variant MODIFIER c.-4444C>T| S200
3 BAA09g23420 A09 14836871 G A upstream_gene_variant MODIFIER c.-4060G>A| S131
4 BAA09g23420 A09 14838338 G A upstream_gene_variant MODIFIER c.-2593G>A| S1
5 BAA09g23420 A09 14838342 G A upstream_gene_variant MODIFIER c.-2589G>A| S88
6 BAA09g23420 A09 14838352 G A upstream_gene_variant MODIFIER c.-2579G>A| S178
7 BAA09g23420 A09 14840895 C T upstream_gene_variant MODIFIER c.-36C>T| S160
8 BAA09g23420 A09 14840972 G A missense_variant MODERATE c.42G>A|p.Met14Ile S289
9 BAA09g23420 A09 14840994 G A splice_donor_variant&intron_variant HIGH c.63+1G>A| S113
10 BAA09g23420 A09 14841016 C T intron_variant MODIFIER c.63+23C>T| S235
11 BAA09g23420 A09 14841249 G A missense_variant MODERATE c.258G>A|p.Met86Ile S233
12 BAA09g23420 A09 14841266 C T missense_variant MODERATE c.275C>T|p.Ala92Val S28
13 BAA09g23420 A09 14841587 C T missense_variant MODERATE c.497C>T|p.Ser166Phe S164
14 BAA09g23420 A09 14843104 C T missense_variant MODERATE c.671C>T|p.Pro224Leu S259
15 BAA09g23420 A09 14843122 G A missense_variant MODERATE c.689G>A|p.Arg230His S11
16 BAA09g23420 A09 14843158 G A missense_variant MODERATE c.725G>A|p.Gly242Glu S121
17 BAA09g23420 A09 14843299 G A missense_variant MODERATE c.866G>A|p.Arg289Lys S267
18 BAA09g23420 A09 14843553 C T intron_variant MODIFIER c.1098+22C>T| S36
19 BAA09g23420 A09 14844134 C T intron_variant MODIFIER c.1382+123C>T| S92
20 BAA09g23420 A09 14844598 C T intron_variant MODIFIER c.1382+587C>T| S219
21 BAA09g23420 A09 14844920 C T intron_variant MODIFIER c.1382+909C>T| S275
S6
22 BAA09g23420 A09 14845072 G A intron_variant MODIFIER c.1383-1016G>A| S56
23 BAA09g23420 A09 14846326 C T synonymous_variant LOW c.1524C>T|p.Phe508Phe S278
24 BAA09g23420 A09 14847570 C T intron_variant MODIFIER c.1552+1216C>T| S19
25 BAA09g23420 A09 14847572 G A intron_variant MODIFIER c.1552+1218G>A| S176