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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g23690 A04 25615199 C T downstream_gene_variant MODIFIER c.*4852G>A| S162
S178
S234
2 BAA04g23690 A04 25615355 C T downstream_gene_variant MODIFIER c.*4696G>A| S260
3 BAA04g23690 A04 25615391 G A downstream_gene_variant MODIFIER c.*4660C>T| S94
4 BAA04g23690 A04 25615434 G A downstream_gene_variant MODIFIER c.*4617C>T| S281
5 BAA04g23690 A04 25615564 G A downstream_gene_variant MODIFIER c.*4487C>T| S275
6 BAA04g23690 A04 25615665 G A downstream_gene_variant MODIFIER c.*4386C>T| S190
7 BAA04g23690 A04 25619600 C T downstream_gene_variant MODIFIER c.*451G>A| S64
8 BAA04g23690 A04 25620700 G A missense_variant MODERATE c.913C>T|p.Arg305Cys S288
9 BAA04g23690 A04 25621970 C T intron_variant MODIFIER c.428-57G>A| S134
10 BAA04g23690 A04 25621976 C T intron_variant MODIFIER c.428-63G>A| S138
11 BAA04g23690 A04 25623557 C T intron_variant MODIFIER c.427+303G>A| S138
12 BAA04g23690 A04 25623621 C T intron_variant MODIFIER c.427+239G>A| S6
13 BAA04g23690 A04 25623631 G A intron_variant MODIFIER c.427+229C>T| S278
14 BAA04g23690 A04 25624267 G A missense_variant MODERATE c.122C>T|p.Thr41Ile S183
15 BAA04g23690 A04 25624275 C T synonymous_variant LOW c.114G>A|p.Gln38Gln S68
16 BAA04g23690 A04 25625082 C T upstream_gene_variant MODIFIER c.-694G>A| S122
17 BAA04g23690 A04 25625173 C T upstream_gene_variant MODIFIER c.-785G>A| S156
18 BAA04g23690 A04 25625500 C T upstream_gene_variant MODIFIER c.-1112G>A| S293
19 BAA04g23690 A04 25628494 C T upstream_gene_variant MODIFIER c.-4106G>A| S240
20 BAA04g23690 A04 25628798 C T upstream_gene_variant MODIFIER c.-4410G>A| S279