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 BAA09g26220 A09 16993369 G A missense_variant MODERATE c.5300C>T|p.Ser1767Phe S170
2 BAA09g26220 A09 16993418 C T missense_variant MODERATE c.5251G>A|p.Ala1751Thr S134
3 BAA09g26220 A09 16993497 C T synonymous_variant LOW c.5172G>A|p.Leu1724Leu S32
4 BAA09g26220 A09 16993538 C T missense_variant MODERATE c.5131G>A|p.Val1711Met S221
5 BAA09g26220 A09 16993786 G A missense_variant MODERATE c.4883C>T|p.Ala1628Val S298
6 BAA09g26220 A09 16994830 C T missense_variant MODERATE c.3839G>A|p.Arg1280Lys S256
7 BAA09g26220 A09 16994970 G A synonymous_variant LOW c.3699C>T|p.Asn1233Asn S236
8 BAA09g26220 A09 16995814 C T missense_variant MODERATE c.2855G>A|p.Arg952His S96
9 BAA09g26220 A09 16996028 G A missense_variant MODERATE c.2641C>T|p.Leu881Phe S97
10 BAA09g26220 A09 16996070 G A missense_variant MODERATE c.2599C>T|p.Pro867Ser S289
11 BAA09g26220 A09 16996197 C G missense_variant MODERATE c.2472G>C|p.Leu824Phe
12 BAA09g26220 A09 16996225 C T missense_variant MODERATE c.2444G>A|p.Ser815Asn S156
13 BAA09g26220 A09 16996403 C T missense_variant MODERATE c.2266G>A|p.Val756Met S159
S243
S299
14 BAA09g26220 A09 16996620 G A synonymous_variant LOW c.2049C>T|p.Leu683Leu S201
15 BAA09g26220 A09 16998127 G A missense_variant MODERATE c.635C>T|p.Ser212Phe S124
16 BAA09g26220 A09 16998570 G A synonymous_variant LOW c.192C>T|p.Arg64Arg S138
17 BAA09g26220 A09 16998730 G A missense_variant MODERATE c.32C>T|p.Thr11Ile S84
S93
18 BAA09g26220 A09 16998899 G A upstream_gene_variant MODIFIER c.-138C>T| S34
19 BAA09g26220 A09 16998937 C T upstream_gene_variant MODIFIER c.-176G>A| S111
20 BAA09g26220 A09 16998947 A C upstream_gene_variant MODIFIER c.-186T>G| S26
21 BAA09g26220 A09 16999029 G A upstream_gene_variant MODIFIER c.-268C>T| S287
22 BAA09g26220 A09 16999903 G A upstream_gene_variant MODIFIER c.-1142C>T| S182
23 BAA09g26220 A09 17001379 C T upstream_gene_variant MODIFIER c.-2618G>A| S23
24 BAA09g26220 A09 17001934 G A upstream_gene_variant MODIFIER c.-3173C>T| S185