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 BAA10g08180 A10 5803070 G A upstream_gene_variant MODIFIER c.-4091G>A| S164
2 BAA10g08180 A10 5804795 G A upstream_gene_variant MODIFIER c.-2366G>A| S17
3 BAA10g08180 A10 5805019 T C upstream_gene_variant MODIFIER c.-2142T>C| S292
4 BAA10g08180 A10 5805220 G A upstream_gene_variant MODIFIER c.-1941G>A| S245
5 BAA10g08180 A10 5805401 G A upstream_gene_variant MODIFIER c.-1760G>A| S53
6 BAA10g08180 A10 5805886 G A upstream_gene_variant MODIFIER c.-1275G>A| S59
7 BAA10g08180 A10 5807089 G A upstream_gene_variant MODIFIER c.-72G>A| S120
8 BAA10g08180 A10 5808309 G A intron_variant MODIFIER c.836+232G>A| S148
S30
S31
9 BAA10g08180 A10 5809544 C T intron_variant MODIFIER c.1433+20C>T| S10
10 BAA10g08180 A10 5809725 C T intron_variant MODIFIER c.1434-9C>T| S259
11 BAA10g08180 A10 5810082 C T intron_variant MODIFIER c.1719-16C>T| S152
S289
12 BAA10g08180 A10 5810713 G A stop_gained HIGH c.2268G>A|p.Trp756* S69
13 BAA10g08180 A10 5811590 C T intron_variant MODIFIER c.2937+28C>T| S200
14 BAA10g08180 A10 5811699 G A missense_variant MODERATE c.2995G>A|p.Ala999Thr S295
15 BAA10g08180 A10 5812762 G A missense_variant MODERATE c.3763G>A|p.Asp1255Asn S293
16 BAA10g08180 A10 5813014 G A intron_variant MODIFIER c.3931-39G>A| S172
S217
17 BAA10g08180 A10 5813071 C T missense_variant MODERATE c.3949C>T|p.Leu1317Phe S162
18 BAA10g08180 A10 5813664 C T missense_variant MODERATE c.4346C>T|p.Pro1449Leu S256