Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14470 | A02 | 6763775 | C | T | upstream_gene_variant | MODIFIER | c.-1887C>T| |
S266 |
2 | BAA02g14470 | A02 | 6765332 | G | A | upstream_gene_variant | MODIFIER | c.-330G>A| |
S192 |
3 | BAA02g14470 | A02 | 6766304 | C | T | stop_gained | HIGH | c.643C>T|p.Gln215* |
S216 S241 S265 S39 |
4 | BAA02g14470 | A02 | 6766905 | C | T | missense_variant | MODERATE | c.1244C>T|p.Ser415Phe |
S283 |
5 | BAA02g14470 | A02 | 6767614 | G | A | synonymous_variant | LOW | c.1704G>A|p.Glu568Glu |
S143 |
6 | BAA02g14470 | A02 | 6767693 | G | A | missense_variant | MODERATE | c.1712G>A|p.Gly571Asp |
S238 |
7 | BAA02g14470 | A02 | 6767922 | G | A | missense_variant | MODERATE | c.1840G>A|p.Glu614Lys |
S96 |
8 | BAA02g14470 | A02 | 6769590 | G | A | missense_variant | MODERATE | c.2696G>A|p.Arg899Lys |
S162 |
9 | BAA02g14470 | A02 | 6769801 | C | T | missense_variant | MODERATE | c.2803C>T|p.Leu935Phe |
S15 S3 |
10 | BAA02g14470 | A02 | 6774291 | C | T | downstream_gene_variant | MODIFIER | c.*4261C>T| |
S262 |
11 | BAA02g14470 | A02 | 6774305 | A | T | downstream_gene_variant | MODIFIER | c.*4275A>T| |
S44 |
12 | BAA02g14470 | A02 | 6774351 | C | T | downstream_gene_variant | MODIFIER | c.*4321C>T| |
S44 |
13 | BAA02g14470 | A02 | 6774649 | G | A | downstream_gene_variant | MODIFIER | c.*4619G>A| |
S136 |