Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g41630 | A01 | 27689055 | G | A | upstream_gene_variant | MODIFIER | c.-2554G>A| |
S306 |
2 | BAA01g41630 | A01 | 27689619 | C | T | upstream_gene_variant | MODIFIER | c.-1990C>T| |
S275 |
3 | BAA01g41630 | A01 | 27691784 | C | T | missense_variant | MODERATE | c.176C>T|p.Pro59Leu |
S301 S304 |
4 | BAA01g41630 | A01 | 27691798 | G | A | missense_variant | MODERATE | c.190G>A|p.Gly64Arg |
S246 |
5 | BAA01g41630 | A01 | 27692678 | C | T | intron_variant | MODIFIER | c.581-95C>T| |
S233 |
6 | BAA01g41630 | A01 | 27692848 | G | A | missense_variant | MODERATE | c.656G>A|p.Cys219Tyr |
S129 |
7 | BAA01g41630 | A01 | 27693520 | G | A | intron_variant | MODIFIER | c.790+187G>A| |
S95 |
8 | BAA01g41630 | A01 | 27694339 | G | A | intron_variant | MODIFIER | c.790+1006G>A| |
S208 S219 |
9 | BAA01g41630 | A01 | 27694760 | G | A | intron_variant | MODIFIER | c.790+1427G>A| |
S265 |
10 | BAA01g41630 | A01 | 27694945 | C | T | intron_variant | MODIFIER | c.790+1612C>T| |
S48 |
11 | BAA01g41630 | A01 | 27694974 | G | A | intron_variant | MODIFIER | c.790+1641G>A| |
S245 |
12 | BAA01g41630 | A01 | 27696575 | C | T | intron_variant | MODIFIER | c.791-2150C>T| |
S275 |
13 | BAA01g41630 | A01 | 27698992 | C | T | missense_variant | MODERATE | c.1058C>T|p.Ser353Phe |
S133 S276 |
14 | BAA01g41630 | A01 | 27699074 | C | T | synonymous_variant | LOW | c.1140C>T|p.Thr380Thr |
S28 |
15 | BAA01g41630 | A01 | 27702790 | C | T | missense_variant | MODERATE | c.1991C>T|p.Thr664Ile |
S129 |