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 BAA09g20180 A09 12446498 G A upstream_gene_variant MODIFIER c.-4203G>A| S129
2 BAA09g20180 A09 12446542 G A upstream_gene_variant MODIFIER c.-4159G>A| S142
3 BAA09g20180 A09 12447276 C T upstream_gene_variant MODIFIER c.-3425C>T| S263
4 BAA09g20180 A09 12449697 C T upstream_gene_variant MODIFIER c.-1004C>T| S302
5 BAA09g20180 A09 12450685 G A upstream_gene_variant MODIFIER c.-16G>A| S155
6 BAA09g20180 A09 12451299 G A splice_acceptor_variant&intron_variant HIGH c.109-1G>A| S121
7 BAA09g20180 A09 12451328 C T missense_variant MODERATE c.137C>T|p.Pro46Leu S206
S26
8 BAA09g20180 A09 12452221 G A missense_variant MODERATE c.655G>A|p.Gly219Arg S98
9 BAA09g20180 A09 12452587 G A missense_variant MODERATE c.895G>A|p.Asp299Asn S152
10 BAA09g20180 A09 12453823 C T synonymous_variant LOW c.1572C>T|p.Asn524Asn S30
S31
11 BAA09g20180 A09 12454273 C T missense_variant MODERATE c.1838C>T|p.Ser613Phe S288
12 BAA09g20180 A09 12454408 G A intron_variant MODIFIER c.1935+38G>A| S115
13 BAA09g20180 A09 12455319 C T intron_variant MODIFIER c.2490+41C>T| S35
14 BAA09g20180 A09 12455519 G A synonymous_variant LOW c.2538G>A|p.Lys846Lys S291
15 BAA09g20180 A09 12455571 G A missense_variant MODERATE c.2590G>A|p.Glu864Lys S216
16 BAA09g20180 A09 12455964 G A missense_variant MODERATE c.2833G>A|p.Ala945Thr S33
17 BAA09g20180 A09 12457130 C T missense_variant MODERATE c.3569C>T|p.Ala1190Val S200
18 BAA09g20180 A09 12457426 G A synonymous_variant LOW c.3771G>A|p.Lys1257Lys S80
19 BAA09g20180 A09 12457442 C T missense_variant MODERATE c.3787C>T|p.Arg1263Cys S82
S92
20 BAA09g20180 A09 12458489 G A intron_variant MODIFIER c.4266+30G>A| S276
21 BAA09g20180 A09 12459787 G A downstream_gene_variant MODIFIER c.*786G>A| S192
22 BAA09g20180 A09 12459976 C T downstream_gene_variant MODIFIER c.*975C>T| S192
23 BAA09g20180 A09 12461392 G A downstream_gene_variant MODIFIER c.*2391G>A| S155
S211