Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g17200 | A04 | 21423332 | G | A | downstream_gene_variant | MODIFIER | c.*4174C>T| |
S223 |
2 | BAA04g17200 | A04 | 21423707 | C | T | downstream_gene_variant | MODIFIER | c.*3799G>A| |
S305 |
3 | BAA04g17200 | A04 | 21424910 | G | A | downstream_gene_variant | MODIFIER | c.*2596C>T| |
S251 |
4 | BAA04g17200 | A04 | 21425746 | G | A | downstream_gene_variant | MODIFIER | c.*1760C>T| |
S175 |
5 | BAA04g17200 | A04 | 21425996 | G | A | downstream_gene_variant | MODIFIER | c.*1510C>T| |
S57 |
6 | BAA04g17200 | A04 | 21427305 | G | A | downstream_gene_variant | MODIFIER | c.*201C>T| |
S140 |
7 | BAA04g17200 | A04 | 21427515 | C | T | synonymous_variant | LOW | c.2184G>A|p.Arg728Arg |
S264 |
8 | BAA04g17200 | A04 | 21427792 | C | T | intron_variant | MODIFIER | c.2083-176G>A| |
S216 |
9 | BAA04g17200 | A04 | 21428352 | G | A | synonymous_variant | LOW | c.1716C>T|p.Asp572Asp |
S128 |
10 | BAA04g17200 | A04 | 21428631 | G | A | intron_variant | MODIFIER | c.1549-11C>T| |
S126 |
11 | BAA04g17200 | A04 | 21430769 | C | T | stop_gained | HIGH | c.534G>A|p.Trp178* |
S270 |
12 | BAA04g17200 | A04 | 21431990 | G | A | synonymous_variant | LOW | c.312C>T|p.Leu104Leu |
S219 |
13 | BAA04g17200 | A04 | 21432216 | G | A | missense_variant | MODERATE | c.166C>T|p.His56Tyr |
S144 |
14 | BAA04g17200 | A04 | 21432838 | G | A | upstream_gene_variant | MODIFIER | c.-457C>T| |
S56 |
15 | BAA04g17200 | A04 | 21433000 | C | T | upstream_gene_variant | MODIFIER | c.-619G>A| |
S2 |
16 | BAA04g17200 | A04 | 21435663 | G | A | upstream_gene_variant | MODIFIER | c.-3282C>T| |
S85 |