Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04920 | A02 | 2143551 | C | T | missense_variant | MODERATE | c.5722G>A|p.Val1908Met |
S108 |
2 | BAA02g04920 | A02 | 2145181 | C | T | missense_variant | MODERATE | c.4637G>A|p.Gly1546Glu |
S249 |
3 | BAA02g04920 | A02 | 2145186 | C | T | synonymous_variant | LOW | c.4632G>A|p.Leu1544Leu |
S112 |
4 | BAA02g04920 | A02 | 2146414 | C | T | splice_donor_variant&intron_variant | HIGH | c.3912+1G>A| |
S250 |
5 | BAA02g04920 | A02 | 2146690 | C | T | missense_variant | MODERATE | c.3721G>A|p.Gly1241Ser |
S207 |
6 | BAA02g04920 | A02 | 2147534 | G | A | missense_variant | MODERATE | c.3200C>T|p.Ser1067Phe |
S268 |
7 | BAA02g04920 | A02 | 2148155 | C | T | missense_variant | MODERATE | c.2821G>A|p.Val941Met |
S202 |
8 | BAA02g04920 | A02 | 2148453 | G | A | synonymous_variant | LOW | c.2634C>T|p.Asn878Asn |
S122 |
9 | BAA02g04920 | A02 | 2149273 | G | A | missense_variant | MODERATE | c.2177C>T|p.Ala726Val |
S264 |
10 | BAA02g04920 | A02 | 2149690 | C | T | splice_donor_variant&intron_variant | HIGH | c.1997+1G>A| |
S6 |
11 | BAA02g04920 | A02 | 2150116 | G | A | synonymous_variant | LOW | c.1657C>T|p.Leu553Leu |
S155 S211 |
12 | BAA02g04920 | A02 | 2150266 | C | T | missense_variant | MODERATE | c.1585G>A|p.Ala529Thr |
S112 |
13 | BAA02g04920 | A02 | 2151140 | G | A | synonymous_variant | LOW | c.1081C>T|p.Leu361Leu |
S126 |
14 | BAA02g04920 | A02 | 2153101 | C | T | missense_variant | MODERATE | c.14G>A|p.Arg5Lys |
S306 S308 |
15 | BAA02g04920 | A02 | 2153556 | G | A | upstream_gene_variant | MODIFIER | c.-442C>T| |
S162 |