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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g58100 A09 56999776 C T upstream_gene_variant MODIFIER c.-4567C>T| S299
2 BAA09g58100 A09 57000427 G A upstream_gene_variant MODIFIER c.-3916G>A| S144
3 BAA09g58100 A09 57001945 G A upstream_gene_variant MODIFIER c.-2398G>A| S10
4 BAA09g58100 A09 57004578 G A missense_variant MODERATE c.149G>A|p.Cys50Tyr S42
5 BAA09g58100 A09 57004938 C T synonymous_variant LOW c.333C>T|p.Ala111Ala S219
S72
6 BAA09g58100 A09 57005310 A C missense_variant MODERATE c.522A>C|p.Lys174Asn S113
S120
S122
S55
S65
7 BAA09g58100 A09 57005578 C T synonymous_variant LOW c.651C>T|p.Pro217Pro S208
S93
8 BAA09g58100 A09 57005583 C T missense_variant MODERATE c.656C>T|p.Pro219Leu S208
S219
9 BAA09g58100 A09 57005591 G A missense_variant MODERATE c.664G>A|p.Glu222Lys S216
10 BAA09g58100 A09 57007423 G A synonymous_variant LOW c.1257G>A|p.Pro419Pro S144
11 BAA09g58100 A09 57007586 G A missense_variant MODERATE c.1420G>A|p.Asp474Asn S74
12 BAA09g58100 A09 57008430 C T synonymous_variant LOW c.1974C>T|p.Phe658Phe S156
13 BAA09g58100 A09 57008677 C T missense_variant MODERATE c.2141C>T|p.Thr714Met S83
S88
14 BAA09g58100 A09 57008882 C T synonymous_variant LOW c.2256C>T|p.Pro752Pro S204
15 BAA09g58100 A09 57009503 G A synonymous_variant LOW c.2877G>A|p.Gln959Gln S11
16 BAA09g58100 A09 57010829 G A downstream_gene_variant MODIFIER c.*1284G>A| S132
S137
S215
S89
17 BAA09g58100 A09 57011078 G A downstream_gene_variant MODIFIER c.*1533G>A| S288
18 BAA09g58100 A09 57011504 C T downstream_gene_variant MODIFIER c.*1959C>T| S136
19 BAA09g58100 A09 57013434 C T downstream_gene_variant MODIFIER c.*3889C>T| S292