Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g51080 | A03 | 24791646 | G | A | upstream_gene_variant | MODIFIER | c.-4660G>A| |
S287 |
2 | BAA03g51080 | A03 | 24791970 | G | A | upstream_gene_variant | MODIFIER | c.-4336G>A| |
S169 |
3 | BAA03g51080 | A03 | 24791978 | C | T | upstream_gene_variant | MODIFIER | c.-4328C>T| |
S32 |
4 | BAA03g51080 | A03 | 24793443 | C | T | upstream_gene_variant | MODIFIER | c.-2863C>T| |
S209 |
5 | BAA03g51080 | A03 | 24794095 | G | A | upstream_gene_variant | MODIFIER | c.-2211G>A| |
S247 |
6 | BAA03g51080 | A03 | 24794711 | G | A | upstream_gene_variant | MODIFIER | c.-1595G>A| |
S244 |
7 | BAA03g51080 | A03 | 24794929 | G | A | upstream_gene_variant | MODIFIER | c.-1377G>A| |
S124 |
8 | BAA03g51080 | A03 | 24796339 | C | T | stop_gained | HIGH | c.34C>T|p.Arg12* |
S128 |
9 | BAA03g51080 | A03 | 24796510 | C | T | missense_variant | MODERATE | c.205C>T|p.Pro69Ser |
S9 |
10 | BAA03g51080 | A03 | 24796676 | C | T | missense_variant | MODERATE | c.371C>T|p.Ala124Val |
S32 |
11 | BAA03g51080 | A03 | 24797219 | C | T | intron_variant | MODIFIER | c.529-373C>T| |
S236 |
12 | BAA03g51080 | A03 | 24797404 | C | T | intron_variant | MODIFIER | c.529-188C>T| |
S143 |
13 | BAA03g51080 | A03 | 24797467 | C | T | intron_variant | MODIFIER | c.529-125C>T| |
S293 |
14 | BAA03g51080 | A03 | 24797660 | C | T | synonymous_variant | LOW | c.597C>T|p.Val199Val |
S107 |
15 | BAA03g51080 | A03 | 24797853 | G | A | missense_variant | MODERATE | c.790G>A|p.Glu264Lys |
S191 |
16 | BAA03g51080 | A03 | 24798767 | G | A | intron_variant | MODIFIER | c.820+884G>A| |
S177 |
17 | BAA03g51080 | A03 | 24798798 | C | T | intron_variant | MODIFIER | c.820+915C>T| |
S176 |
18 | BAA03g51080 | A03 | 24798930 | C | T | intron_variant | MODIFIER | c.820+1047C>T| |
S79 S84 |
19 | BAA03g51080 | A03 | 24798990 | C | T | intron_variant | MODIFIER | c.820+1107C>T| |
S149 |
20 | BAA03g51080 | A03 | 24799394 | G | A | intron_variant | MODIFIER | c.821-1309G>A| |
S282 |
21 | BAA03g51080 | A03 | 24799666 | G | A | intron_variant | MODIFIER | c.821-1037G>A| |
S130 |
22 | BAA03g51080 | A03 | 24800255 | G | A | intron_variant | MODIFIER | c.821-448G>A| |
S30 |
23 | BAA03g51080 | A03 | 24800703 | G | A | missense_variant&splice_region_variant | MODERATE | c.821G>A|p.Gly274Asp |
S170 |
24 | BAA03g51080 | A03 | 24800912 | C | T | synonymous_variant | LOW | c.1030C>T|p.Leu344Leu |
S43 |
25 | BAA03g51080 | A03 | 24800967 | C | T | missense_variant | MODERATE | c.1085C>T|p.Ala362Val |
S293 |