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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g01690 A03 760915 G A upstream_gene_variant MODIFIER c.-4402G>A| S148
S31
2 BAA03g01690 A03 765493 C T synonymous_variant LOW c.99C>T|p.Ser33Ser S159
S187
S188
S243
S298
3 BAA03g01690 A03 766052 C T splice_region_variant&intron_variant LOW c.381+6C>T| S221
4 BAA03g01690 A03 767588 G A missense_variant MODERATE c.1118G>A|p.Arg373Lys S251
5 BAA03g01690 A03 767779 G A missense_variant MODERATE c.1211G>A|p.Gly404Glu S6
6 BAA03g01690 A03 768035 C T intron_variant MODIFIER c.1404+63C>T| S142
7 BAA03g01690 A03 768126 G A intron_variant MODIFIER c.1404+154G>A| S217
S248
8 BAA03g01690 A03 769121 G A intron_variant MODIFIER c.1597+398G>A| S149
9 BAA03g01690 A03 769319 G A intron_variant MODIFIER c.1597+596G>A| S115
10 BAA03g01690 A03 769999 C T intron_variant MODIFIER c.1597+1276C>T| S60
11 BAA03g01690 A03 770173 G A intron_variant MODIFIER c.1597+1450G>A| S168
12 BAA03g01690 A03 770376 A G intron_variant MODIFIER c.1597+1653A>G| S258
13 BAA03g01690 A03 770504 C T intron_variant MODIFIER c.1597+1781C>T| S221
14 BAA03g01690 A03 771375 C T intron_variant MODIFIER c.1598-2566C>T| S221
15 BAA03g01690 A03 773541 G A intron_variant MODIFIER c.1598-400G>A| S97
16 BAA03g01690 A03 773595 G A intron_variant MODIFIER c.1598-346G>A| S6
17 BAA03g01690 A03 775750 C T synonymous_variant LOW c.2196C>T|p.Leu732Leu S25
18 BAA03g01690 A03 776397 G A missense_variant MODERATE c.2584G>A|p.Gly862Arg S208
S93