Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14840 | A02 | 7000108 | C | T | missense_variant | MODERATE | c.2174G>A|p.Arg725Lys |
S84 S93 |
2 | BAA02g14840 | A02 | 7000520 | C | T | missense_variant | MODERATE | c.1928G>A|p.Ser643Asn |
S77 S82 |
3 | BAA02g14840 | A02 | 7000752 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1794-1G>A| |
S47 |
4 | BAA02g14840 | A02 | 7001675 | C | T | intron_variant | MODIFIER | c.1312+34G>A| |
S115 |
5 | BAA02g14840 | A02 | 7002169 | C | T | synonymous_variant | LOW | c.1017G>A|p.Arg339Arg |
S208 S219 |
6 | BAA02g14840 | A02 | 7002943 | C | T | missense_variant | MODERATE | c.683G>A|p.Arg228His |
S115 |
7 | BAA02g14840 | A02 | 7003546 | G | A | missense_variant | MODERATE | c.305C>T|p.Ala102Val |
S48 |
8 | BAA02g14840 | A02 | 7004928 | G | A | upstream_gene_variant | MODIFIER | c.-596C>T| |
S13 S168 S279 S64 |
9 | BAA02g14840 | A02 | 7005049 | G | A | upstream_gene_variant | MODIFIER | c.-717C>T| |
S287 |
10 | BAA02g14840 | A02 | 7005080 | G | A | upstream_gene_variant | MODIFIER | c.-748C>T| |
S246 |
11 | BAA02g14840 | A02 | 7005424 | G | A | upstream_gene_variant | MODIFIER | c.-1092C>T| |
S274 |
12 | BAA02g14840 | A02 | 7006644 | G | A | upstream_gene_variant | MODIFIER | c.-2312C>T| |
S52 |
13 | BAA02g14840 | A02 | 7006856 | C | T | upstream_gene_variant | MODIFIER | c.-2524G>A| |
S77 S82 |
14 | BAA02g14840 | A02 | 7007322 | G | A | upstream_gene_variant | MODIFIER | c.-2990C>T| |
S197 |