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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g21940 A01 10918041 G A splice_acceptor_variant&intron_variant HIGH c.328-1G>A| S287
2 BAA01g21940 A01 10919080 C T missense_variant MODERATE c.823C>T|p.Leu275Phe S38
3 BAA01g21940 A01 10920068 C T missense_variant MODERATE c.1214C>T|p.Pro405Leu S134
4 BAA01g21940 A01 10920411 C T splice_region_variant&intron_variant LOW c.1321-4C>T| S182
5 BAA01g21940 A01 10921901 G A missense_variant MODERATE c.1880G>A|p.Arg627Lys S123
6 BAA01g21940 A01 10923307 G A intron_variant MODIFIER c.2368+75G>A| S244
7 BAA01g21940 A01 10923553 C T missense_variant MODERATE c.2380C>T|p.Pro794Ser S280
8 BAA01g21940 A01 10924516 C T missense_variant MODERATE c.2705C>T|p.Ser902Leu S8
9 BAA01g21940 A01 10925072 C T missense_variant MODERATE c.2897C>T|p.Pro966Leu S256
10 BAA01g21940 A01 10925562 G A missense_variant MODERATE c.3092G>A|p.Gly1031Glu S232
11 BAA01g21940 A01 10925636 A G missense_variant MODERATE c.3166A>G|p.Ile1056Val S232
12 BAA01g21940 A01 10926001 C T synonymous_variant LOW c.3336C>T|p.Ala1112Ala S247
13 BAA01g21940 A01 10926688 G A synonymous_variant LOW c.3846G>A|p.Glu1282Glu S73
14 BAA01g21940 A01 10928713 C T synonymous_variant LOW c.5235C>T|p.Val1745Val S303
15 BAA01g21940 A01 10933133 G A downstream_gene_variant MODIFIER c.*4180G>A| S71
16 BAA01g21940 A01 10933348 G A downstream_gene_variant MODIFIER c.*4395G>A| S271