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 BAA01g31790 A01 20790501 C G synonymous_variant LOW c.1848G>C|p.Val616Val S179
2 BAA01g31790 A01 20792308 C T missense_variant MODERATE c.1310G>A|p.Arg437His S126
3 BAA01g31790 A01 20792548 C T missense_variant MODERATE c.1159G>A|p.Glu387Lys S162
4 BAA01g31790 A01 20793438 C T missense_variant MODERATE c.553G>A|p.Glu185Lys S81
S85
5 BAA01g31790 A01 20793460 C T synonymous_variant LOW c.531G>A|p.Lys177Lys S192
6 BAA01g31790 A01 20793505 C T synonymous_variant LOW c.486G>A|p.Leu162Leu S206
S26
7 BAA01g31790 A01 20793585 G A missense_variant MODERATE c.406C>T|p.Leu136Phe S207
8 BAA01g31790 A01 20793687 C T missense_variant MODERATE c.304G>A|p.Glu102Lys S162
9 BAA01g31790 A01 20795622 G A intron_variant MODIFIER c.44-474C>T| S283
10 BAA01g31790 A01 20797029 C T intron_variant MODIFIER c.44-1881G>A| S210
11 BAA01g31790 A01 20798137 G A intron_variant MODIFIER c.43+2618C>T| S72
12 BAA01g31790 A01 20798417 G A intron_variant MODIFIER c.43+2338C>T| S123
13 BAA01g31790 A01 20798795 G A intron_variant MODIFIER c.43+1960C>T| S115
14 BAA01g31790 A01 20799132 G A intron_variant MODIFIER c.43+1623C>T| S265
15 BAA01g31790 A01 20799962 G A intron_variant MODIFIER c.43+793C>T| S302
16 BAA01g31790 A01 20800991 C T upstream_gene_variant MODIFIER c.-194G>A| S56
17 BAA01g31790 A01 20801073 C T upstream_gene_variant MODIFIER c.-276G>A| S294
18 BAA01g31790 A01 20802797 G A upstream_gene_variant MODIFIER c.-2000C>T| S70
19 BAA01g31790 A01 20802922 C T upstream_gene_variant MODIFIER c.-2125G>A| S64
20 BAA01g31790 A01 20803757 C T upstream_gene_variant MODIFIER c.-2960G>A| S125
21 BAA01g31790 A01 20803760 C T upstream_gene_variant MODIFIER c.-2963G>A| S295
22 BAA01g31790 A01 20804978 C T upstream_gene_variant MODIFIER c.-4181G>A| S167
23 BAA01g31790 A01 20805102 C T upstream_gene_variant MODIFIER c.-4305G>A| S68
24 BAA01g31790 A01 20805681 C T upstream_gene_variant MODIFIER c.-4884G>A| S98