Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10440 | A01 | 4773877 | G | A | downstream_gene_variant | MODIFIER | c.*2116C>T| |
S204 |
2 | BAA01g10440 | A01 | 4774063 | C | T | downstream_gene_variant | MODIFIER | c.*1930G>A| |
S125 |
3 | BAA01g10440 | A01 | 4774761 | C | T | downstream_gene_variant | MODIFIER | c.*1232G>A| |
S158 |
4 | BAA01g10440 | A01 | 4774986 | C | T | downstream_gene_variant | MODIFIER | c.*1007G>A| |
S249 |
5 | BAA01g10440 | A01 | 4775452 | G | A | downstream_gene_variant | MODIFIER | c.*541C>T| |
S56 |
6 | BAA01g10440 | A01 | 4775460 | C | T | downstream_gene_variant | MODIFIER | c.*533G>A| |
S45 |
7 | BAA01g10440 | A01 | 4775687 | G | A | downstream_gene_variant | MODIFIER | c.*306C>T| |
S247 |
8 | BAA01g10440 | A01 | 4776384 | C | T | missense_variant | MODERATE | c.1171G>A|p.Gly391Arg |
S170 |
9 | BAA01g10440 | A01 | 4777470 | G | A | intron_variant | MODIFIER | c.439+22C>T| |
S8 |
10 | BAA01g10440 | A01 | 4778473 | G | A | intron_variant | MODIFIER | c.76+29C>T| |
S191 |
11 | BAA01g10440 | A01 | 4779955 | C | T | upstream_gene_variant | MODIFIER | c.-1378G>A| |
S242 |
12 | BAA01g10440 | A01 | 4780725 | C | T | upstream_gene_variant | MODIFIER | c.-2148G>A| |
S296 |
13 | BAA01g10440 | A01 | 4781100 | C | T | upstream_gene_variant | MODIFIER | c.-2523G>A| |
S166 |
14 | BAA01g10440 | A01 | 4781237 | G | A | upstream_gene_variant | MODIFIER | c.-2660C>T| |
S60 |
15 | BAA01g10440 | A01 | 4782335 | G | A | upstream_gene_variant | MODIFIER | c.-3758C>T| |
S263 |
16 | BAA01g10440 | A01 | 4782402 | C | T | upstream_gene_variant | MODIFIER | c.-3825G>A| |
S180 S34 S38 |