Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g22910 | A03 | 10441723 | C | T | upstream_gene_variant | MODIFIER | c.-1742C>T| |
S34 |
2 | BAA03g22910 | A03 | 10441784 | G | A | upstream_gene_variant | MODIFIER | c.-1681G>A| |
S33 |
3 | BAA03g22910 | A03 | 10441831 | G | A | upstream_gene_variant | MODIFIER | c.-1634G>A| |
S123 |
4 | BAA03g22910 | A03 | 10442757 | G | A | upstream_gene_variant | MODIFIER | c.-708G>A| |
S195 |
5 | BAA03g22910 | A03 | 10442904 | G | C | upstream_gene_variant | MODIFIER | c.-561G>C| |
S177 |
6 | BAA03g22910 | A03 | 10443318 | C | T | upstream_gene_variant | MODIFIER | c.-147C>T| |
S164 |
7 | BAA03g22910 | A03 | 10443810 | G | A | missense_variant | MODERATE | c.278G>A|p.Arg93Lys |
S63 |
8 | BAA03g22910 | A03 | 10445160 | G | A | missense_variant | MODERATE | c.1189G>A|p.Glu397Lys |
S105 |
9 | BAA03g22910 | A03 | 10447090 | C | T | intron_variant | MODIFIER | c.1801-10C>T| |
S87 |
10 | BAA03g22910 | A03 | 10448062 | G | T | missense_variant | MODERATE | c.2273G>T|p.Gly758Val |
S26 |
11 | BAA03g22910 | A03 | 10448063 | A | T | synonymous_variant | LOW | c.2274A>T|p.Gly758Gly |
S26 |
12 | BAA03g22910 | A03 | 10449067 | G | A | intron_variant | MODIFIER | c.2580+141G>A| |
S10 |
13 | BAA03g22910 | A03 | 10449996 | G | A | missense_variant | MODERATE | c.2803G>A|p.Asp935Asn |
S63 |
14 | BAA03g22910 | A03 | 10452839 | G | A | missense_variant | MODERATE | c.3742G>A|p.Glu1248Lys |
S5 |
15 | BAA03g22910 | A03 | 10454282 | G | A | synonymous_variant | LOW | c.4554G>A|p.Ala1518Ala |
S172 S217 |
16 | BAA03g22910 | A03 | 10456161 | G | A | downstream_gene_variant | MODIFIER | c.*1402G>A| |
S168 |
17 | BAA03g22910 | A03 | 10456458 | C | T | downstream_gene_variant | MODIFIER | c.*1699C>T| |
S266 |
18 | BAA03g22910 | A03 | 10456648 | C | T | downstream_gene_variant | MODIFIER | c.*1889C>T| |
S136 |