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


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g29690 A01 18760628 C T upstream_gene_variant MODIFIER c.-3978C>T| S115
2 BAA01g29690 A01 18761742 G A upstream_gene_variant MODIFIER c.-2864G>A| S140
S168
S219
S279
S301
3 BAA01g29690 A01 18764470 C T upstream_gene_variant MODIFIER c.-136C>T| S167
4 BAA01g29690 A01 18764549 G A upstream_gene_variant MODIFIER c.-57G>A| S13
S140
S168
S219
S279
5 BAA01g29690 A01 18764827 G A intron_variant MODIFIER c.54-37G>A| S257
6 BAA01g29690 A01 18765504 C T intron_variant MODIFIER c.487-33C>T| S155
S211
7 BAA01g29690 A01 18765618 G A missense_variant MODERATE c.568G>A|p.Gly190Arg S15
S3
8 BAA01g29690 A01 18765885 G A splice_acceptor_variant&intron_variant HIGH c.628-1G>A| S55
9 BAA01g29690 A01 18766386 G A synonymous_variant LOW c.921G>A|p.Lys307Lys S174
S27
10 BAA01g29690 A01 18768846 C T stop_gained HIGH c.2707C>T|p.Gln903* S42
11 BAA01g29690 A01 18768909 C T intron_variant MODIFIER c.2724+46C>T| S143
12 BAA01g29690 A01 18769204 C T stop_gained HIGH c.2887C>T|p.Gln963* S184
13 BAA01g29690 A01 18769237 G A missense_variant MODERATE c.2920G>A|p.Gly974Arg S199
14 BAA01g29690 A01 18769549 C T synonymous_variant LOW c.3141C>T|p.Cys1047Cys S198
15 BAA01g29690 A01 18770501 C T downstream_gene_variant MODIFIER c.*675C>T| S279
16 BAA01g29690 A01 18770777 C T downstream_gene_variant MODIFIER c.*951C>T| S242
17 BAA01g29690 A01 18771766 G A downstream_gene_variant MODIFIER c.*1940G>A| S257
18 BAA01g29690 A01 18772688 C T downstream_gene_variant MODIFIER c.*2862C>T| S50
19 BAA01g29690 A01 18772944 G A downstream_gene_variant MODIFIER c.*3118G>A| S83
20 BAA01g29690 A01 18773619 C T downstream_gene_variant MODIFIER c.*3793C>T| S76
21 BAA01g29690 A01 18773712 G A downstream_gene_variant MODIFIER c.*3886G>A| S257
22 BAA01g29690 A01 18774238 C T downstream_gene_variant MODIFIER c.*4412C>T| S179
23 BAA01g29690 A01 18774366 G A downstream_gene_variant MODIFIER c.*4540G>A| S114
24 BAA01g29690 A01 18774776 G A downstream_gene_variant MODIFIER c.*4950G>A| S223