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 BAA09g43060 A09 49262739 C T downstream_gene_variant MODIFIER c.*1533G>A| S6
2 BAA09g43060 A09 49264413 G A synonymous_variant LOW c.5523C>T|p.Asn1841Asn S165
3 BAA09g43060 A09 49264448 G A stop_gained HIGH c.5488C>T|p.Gln1830* S46
4 BAA09g43060 A09 49264937 G A missense_variant MODERATE c.5081C>T|p.Ser1694Phe S159
S187
S188
S243
S276
S299
5 BAA09g43060 A09 49265795 G A missense_variant MODERATE c.4297C>T|p.Pro1433Ser S79
S91
6 BAA09g43060 A09 49266038 G A missense_variant MODERATE c.4153C>T|p.Pro1385Ser S142
7 BAA09g43060 A09 49266122 C T missense_variant MODERATE c.4069G>A|p.Ala1357Thr S40
S49
8 BAA09g43060 A09 49267354 C T synonymous_variant LOW c.3570G>A|p.Val1190Val S206
S26
9 BAA09g43060 A09 49267484 C T missense_variant MODERATE c.3440G>A|p.Arg1147Lys S140
10 BAA09g43060 A09 49267627 C T synonymous_variant LOW c.3297G>A|p.Lys1099Lys S36
11 BAA09g43060 A09 49268150 G A missense_variant MODERATE c.2774C>T|p.Ser925Phe S42
12 BAA09g43060 A09 49268627 C T missense_variant MODERATE c.2297G>A|p.Gly766Glu S18
13 BAA09g43060 A09 49268734 G A synonymous_variant LOW c.2190C>T|p.Arg730Arg S86
14 BAA09g43060 A09 49268853 G A missense_variant MODERATE c.2071C>T|p.Pro691Ser S233
15 BAA09g43060 A09 49268956 C T synonymous_variant LOW c.1968G>A|p.Pro656Pro S256
16 BAA09g43060 A09 49269603 C T missense_variant MODERATE c.1321G>A|p.Glu441Lys S94
17 BAA09g43060 A09 49269629 C T missense_variant MODERATE c.1295G>A|p.Arg432Lys S36
18 BAA09g43060 A09 49269682 C T synonymous_variant LOW c.1242G>A|p.Leu414Leu S168
19 BAA09g43060 A09 49269954 C T missense_variant MODERATE c.970G>A|p.Asp324Asn S251
20 BAA09g43060 A09 49270628 C T missense_variant MODERATE c.296G>A|p.Gly99Asp S119
21 BAA09g43060 A09 49270707 C T missense_variant MODERATE c.217G>A|p.Gly73Ser S213
22 BAA09g43060 A09 49271246 G A upstream_gene_variant MODIFIER c.-323C>T| S162
23 BAA09g43060 A09 49271458 G A upstream_gene_variant MODIFIER c.-535C>T| S202
24 BAA09g43060 A09 49272177 C T upstream_gene_variant MODIFIER c.-1254G>A| S302