Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g18010 | A07 | 24132464 | C | T | upstream_gene_variant | MODIFIER | c.-590C>T| |
S8 |
2 | BAA07g18010 | A07 | 24132643 | C | T | upstream_gene_variant | MODIFIER | c.-411C>T| |
S232 |
3 | BAA07g18010 | A07 | 24133377 | G | A | synonymous_variant | LOW | c.324G>A|p.Arg108Arg |
S1 S161 S228 S289 S290 |
4 | BAA07g18010 | A07 | 24133477 | G | A | missense_variant | MODERATE | c.424G>A|p.Ala142Thr |
S244 |
5 | BAA07g18010 | A07 | 24133478 | C | T | missense_variant | MODERATE | c.425C>T|p.Ala142Val |
S260 |
6 | BAA07g18010 | A07 | 24133636 | G | A | synonymous_variant | LOW | c.507G>A|p.Leu169Leu |
S135 |
7 | BAA07g18010 | A07 | 24133950 | C | T | synonymous_variant | LOW | c.753C>T|p.His251His |
S272 |
8 | BAA07g18010 | A07 | 24134463 | C | T | intron_variant | MODIFIER | c.1152+35C>T| |
S15 S156 S3 S4 S6 |
9 | BAA07g18010 | A07 | 24135215 | C | T | missense_variant | MODERATE | c.1592C>T|p.Ser531Leu |
S88 |
10 | BAA07g18010 | A07 | 24136607 | G | A | downstream_gene_variant | MODIFIER | c.*587G>A| |
S7 |
11 | BAA07g18010 | A07 | 24138076 | G | A | downstream_gene_variant | MODIFIER | c.*2056G>A| |
S244 |
12 | BAA07g18010 | A07 | 24140819 | C | T | downstream_gene_variant | MODIFIER | c.*4799C>T| |
S289 |