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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g61690 A03 31199796 C T missense_variant MODERATE c.2092G>A|p.Asp698Asn S129
2 BAA03g61690 A03 31199883 G A synonymous_variant LOW c.2005C>T|p.Leu669Leu S124
3 BAA03g61690 A03 31200532 C T intron_variant MODIFIER c.1709-353G>A| S120
4 BAA03g61690 A03 31202238 C T intron_variant MODIFIER c.1708+900G>A| S16
5 BAA03g61690 A03 31203706 C T synonymous_variant LOW c.1140G>A|p.Lys380Lys S232
6 BAA03g61690 A03 31203861 G A missense_variant MODERATE c.985C>T|p.Leu329Phe S56
7 BAA03g61690 A03 31204815 C T intron_variant MODIFIER c.495-464G>A| S205
8 BAA03g61690 A03 31204898 C T intron_variant MODIFIER c.495-547G>A| S251
9 BAA03g61690 A03 31204927 C T intron_variant MODIFIER c.495-576G>A| S93
10 BAA03g61690 A03 31205064 C T intron_variant MODIFIER c.495-713G>A| S142
11 BAA03g61690 A03 31205566 C T intron_variant MODIFIER c.494+586G>A| S209
12 BAA03g61690 A03 31205741 C T intron_variant MODIFIER c.494+411G>A| S134
13 BAA03g61690 A03 31205916 G A intron_variant MODIFIER c.494+236C>T| S164
14 BAA03g61690 A03 31205967 C T intron_variant MODIFIER c.494+185G>A| S202
15 BAA03g61690 A03 31206222 C T missense_variant MODERATE c.424G>A|p.Asp142Asn S143
16 BAA03g61690 A03 31206433 C T synonymous_variant LOW c.213G>A|p.Glu71Glu S30
S31
17 BAA03g61690 A03 31206528 C T missense_variant MODERATE c.118G>A|p.Glu40Lys S12
S34
18 BAA03g61690 A03 31207424 G A upstream_gene_variant MODIFIER c.-779C>T| S124
19 BAA03g61690 A03 31208517 C T upstream_gene_variant MODIFIER c.-1872G>A| S8
20 BAA03g61690 A03 31209699 C T upstream_gene_variant MODIFIER c.-3054G>A| S174
21 BAA03g61690 A03 31210426 G A upstream_gene_variant MODIFIER c.-3781C>T| S122
22 BAA03g61690 A03 31210807 G A upstream_gene_variant MODIFIER c.-4162C>T| S202
23 BAA03g61690 A03 31211473 C T upstream_gene_variant MODIFIER c.-4828G>A| S85