Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g01930 | A05 | 1050114 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.483-1G>A| |
S271 |
2 | BAA05g01930 | A05 | 1050801 | C | T | intron_variant | MODIFIER | c.377+46G>A| |
S292 |
3 | BAA05g01930 | A05 | 1051045 | G | A | missense_variant | MODERATE | c.179C>T|p.Ala60Val |
S9 |
4 | BAA05g01930 | A05 | 1051238 | G | A | upstream_gene_variant | MODIFIER | c.-15C>T| |
S218 |
5 | BAA05g01930 | A05 | 1052220 | G | A | upstream_gene_variant | MODIFIER | c.-997C>T| |
S167 |
6 | BAA05g01930 | A05 | 1052369 | C | T | upstream_gene_variant | MODIFIER | c.-1146G>A| |
S276 |
7 | BAA05g01930 | A05 | 1053694 | C | T | upstream_gene_variant | MODIFIER | c.-2471G>A| |
S303 |
8 | BAA05g01930 | A05 | 1053758 | G | A | upstream_gene_variant | MODIFIER | c.-2535C>T| |
S165 |
9 | BAA05g01930 | A05 | 1053921 | C | T | upstream_gene_variant | MODIFIER | c.-2698G>A| |
S168 |
10 | BAA05g01930 | A05 | 1054003 | G | A | upstream_gene_variant | MODIFIER | c.-2780C>T| |
S11 |
11 | BAA05g01930 | A05 | 1054505 | G | A | upstream_gene_variant | MODIFIER | c.-3282C>T| |
S148 S210 |
12 | BAA05g01930 | A05 | 1054602 | G | A | upstream_gene_variant | MODIFIER | c.-3379C>T| |
S104 S52 |
13 | BAA05g01930 | A05 | 1055100 | G | A | upstream_gene_variant | MODIFIER | c.-3877C>T| |
S174 S216 S27 S39 |