Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g06100 | A08 | 4824665 | G | A | missense_variant | MODERATE | c.1154C>T|p.Ser385Phe |
S10 |
2 | BAA08g06100 | A08 | 4824745 | T | A | missense_variant | MODERATE | c.1074A>T|p.Gln358His |
S108 |
3 | BAA08g06100 | A08 | 4824746 | T | A | missense_variant | MODERATE | c.1073A>T|p.Gln358Leu |
S108 |
4 | BAA08g06100 | A08 | 4824784 | G | C | synonymous_variant | LOW | c.1035C>G|p.Val345Val |
S108 |
5 | BAA08g06100 | A08 | 4824787 | G | A | synonymous_variant | LOW | c.1032C>T|p.Ile344Ile |
S108 |
6 | BAA08g06100 | A08 | 4824820 | A | G | synonymous_variant | LOW | c.999T>C|p.Val333Val |
S108 S257 S91 |
7 | BAA08g06100 | A08 | 4824924 | G | A | synonymous_variant | LOW | c.895C>T|p.Leu299Leu |
S265 |
8 | BAA08g06100 | A08 | 4825583 | C | T | synonymous_variant | LOW | c.480G>A|p.Thr160Thr |
S74 |
9 | BAA08g06100 | A08 | 4825639 | C | T | missense_variant | MODERATE | c.424G>A|p.Asp142Asn |
S142 |
10 | BAA08g06100 | A08 | 4825701 | G | A | missense_variant | MODERATE | c.362C>T|p.Thr121Met |
S107 S144 |
11 | BAA08g06100 | A08 | 4825822 | C | T | missense_variant | MODERATE | c.241G>A|p.Val81Ile |
S135 |
12 | BAA08g06100 | A08 | 4825888 | C | T | missense_variant | MODERATE | c.175G>A|p.Gly59Arg |
S46 |
13 | BAA08g06100 | A08 | 4825973 | C | T | synonymous_variant | LOW | c.90G>A|p.Glu30Glu |
S2 |
14 | BAA08g06100 | A08 | 4829398 | C | T | upstream_gene_variant | MODIFIER | c.-3336G>A| |
S271 |
15 | BAA08g06100 | A08 | 4829615 | C | A | upstream_gene_variant | MODIFIER | c.-3553G>T| |
S168 |
16 | BAA08g06100 | A08 | 4829693 | G | A | upstream_gene_variant | MODIFIER | c.-3631C>T| |
S124 |
17 | BAA08g06100 | A08 | 4829732 | C | T | upstream_gene_variant | MODIFIER | c.-3670G>A| |
S155 S211 |