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


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g22460 A03 10224941 G A missense_variant MODERATE c.3815C>T|p.Ala1272Val S202
2 BAA03g22460 A03 10225079 G A missense_variant MODERATE c.3677C>T|p.Ser1226Phe S288
3 BAA03g22460 A03 10225116 G A synonymous_variant LOW c.3640C>T|p.Leu1214Leu
4 BAA03g22460 A03 10225471 G A synonymous_variant LOW c.3285C>T|p.Arg1095Arg S289
S290
5 BAA03g22460 A03 10225769 G A missense_variant MODERATE c.2987C>T|p.Ser996Phe S180
6 BAA03g22460 A03 10226215 G A intron_variant MODIFIER c.2789-248C>T| S206
S26
7 BAA03g22460 A03 10226692 G A synonymous_variant LOW c.2709C>T|p.Thr903Thr S225
S73
8 BAA03g22460 A03 10226961 G A missense_variant MODERATE c.2440C>T|p.Leu814Phe S271
9 BAA03g22460 A03 10227713 C T missense_variant MODERATE c.1688G>A|p.Arg563Lys S125
10 BAA03g22460 A03 10227736 C T synonymous_variant LOW c.1665G>A|p.Arg555Arg S164
11 BAA03g22460 A03 10227795 C T missense_variant MODERATE c.1606G>A|p.Glu536Lys S28
12 BAA03g22460 A03 10227975 C T intron_variant MODIFIER c.1514-88G>A| S132
S137
13 BAA03g22460 A03 10228100 G A intron_variant MODIFIER c.1513+32C>T| S282
14 BAA03g22460 A03 10228856 T A synonymous_variant LOW c.789A>T|p.Leu263Leu S269
15 BAA03g22460 A03 10229542 G A missense_variant MODERATE c.103C>T|p.Pro35Ser S267
16 BAA03g22460 A03 10229611 G A missense_variant MODERATE c.34C>T|p.Pro12Ser S261
17 BAA03g22460 A03 10230162 C T upstream_gene_variant MODIFIER c.-518G>A| S66
18 BAA03g22460 A03 10231757 G A upstream_gene_variant MODIFIER c.-2113C>T| S182
19 BAA03g22460 A03 10232043 C G upstream_gene_variant MODIFIER c.-2399G>C| S132
S137
20 BAA03g22460 A03 10234563 C T upstream_gene_variant MODIFIER c.-4919G>A| S295
21 BAA03g22460 A03 10234575 C T upstream_gene_variant MODIFIER c.-4931G>A| S255