Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g31500 | A01 | 20480431 | G | A | intron_variant | MODIFIER | c.2344+696C>T| |
S205 S292 S64 |
2 | BAA01g31500 | A01 | 20480512 | C | T | intron_variant | MODIFIER | c.2344+615G>A| |
S12 S152 |
3 | BAA01g31500 | A01 | 20480598 | C | T | intron_variant | MODIFIER | c.2344+529G>A| |
S43 |
4 | BAA01g31500 | A01 | 20481138 | C | T | missense_variant | MODERATE | c.2333G>A|p.Gly778Glu |
S28 |
5 | BAA01g31500 | A01 | 20481368 | A | G | synonymous_variant | LOW | c.2103T>C|p.Arg701Arg |
S37 |
6 | BAA01g31500 | A01 | 20481413 | G | A | synonymous_variant | LOW | c.2058C>T|p.Leu686Leu |
S43 |
7 | BAA01g31500 | A01 | 20481457 | C | T | missense_variant | MODERATE | c.2014G>A|p.Glu672Lys |
S295 |
8 | BAA01g31500 | A01 | 20482161 | G | A | synonymous_variant | LOW | c.1392C>T|p.Ala464Ala |
S299 |
9 | BAA01g31500 | A01 | 20482283 | C | T | missense_variant | MODERATE | c.1270G>A|p.Gly424Arg |
S152 |
10 | BAA01g31500 | A01 | 20482368 | G | A | synonymous_variant | LOW | c.1185C>T|p.Arg395Arg |
S287 |
11 | BAA01g31500 | A01 | 20482384 | G | A | missense_variant | MODERATE | c.1169C>T|p.Thr390Ile |
S35 |
12 | BAA01g31500 | A01 | 20482650 | C | T | synonymous_variant | LOW | c.903G>A|p.Arg301Arg |
S146 |
13 | BAA01g31500 | A01 | 20482799 | G | A | missense_variant | MODERATE | c.754C>T|p.Pro252Ser |
S238 |
14 | BAA01g31500 | A01 | 20482908 | G | A | synonymous_variant | LOW | c.645C>T|p.Ile215Ile |
S297 |
15 | BAA01g31500 | A01 | 20483839 | C | T | intron_variant | MODIFIER | c.571+850G>A| |
S166 |
16 | BAA01g31500 | A01 | 20483988 | C | T | intron_variant | MODIFIER | c.571+701G>A| |
S65 |
17 | BAA01g31500 | A01 | 20484824 | G | A | intron_variant | MODIFIER | c.502-66C>T| |
S153 |
18 | BAA01g31500 | A01 | 20485359 | C | T | intron_variant | MODIFIER | c.501+557G>A| |
S132 S137 S215 S89 |
19 | BAA01g31500 | A01 | 20485549 | G | A | intron_variant | MODIFIER | c.501+367C>T| |
S13 |
20 | BAA01g31500 | A01 | 20485684 | G | A | intron_variant | MODIFIER | c.501+232C>T| |
S96 |
21 | BAA01g31500 | A01 | 20486487 | C | T | intron_variant | MODIFIER | c.408-478G>A| |
S251 |
22 | BAA01g31500 | A01 | 20487441 | C | T | intron_variant | MODIFIER | c.407+215G>A| |
S164 |
23 | BAA01g31500 | A01 | 20487683 | C | T | missense_variant | MODERATE | c.380G>A|p.Gly127Glu |
S156 |
24 | BAA01g31500 | A01 | 20488418 | G | A | intron_variant | MODIFIER | c.259-283C>T| |
S43 |
25 | BAA01g31500 | A01 | 20488481 | G | A | intron_variant | MODIFIER | c.259-346C>T| |
S95 |