Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g21880 | A04 | 24503316 | C | T | missense_variant | MODERATE | c.2924G>A|p.Gly975Glu |
S271 |
2 | BAA04g21880 | A04 | 24503342 | C | T | synonymous_variant | LOW | c.2898G>A|p.Glu966Glu |
S64 |
3 | BAA04g21880 | A04 | 24503536 | G | A | synonymous_variant | LOW | c.2704C>T|p.Leu902Leu |
S274 |
4 | BAA04g21880 | A04 | 24504204 | G | A | stop_gained | HIGH | c.2107C>T|p.Arg703* |
S298 |
5 | BAA04g21880 | A04 | 24504299 | G | A | missense_variant | MODERATE | c.2012C>T|p.Ala671Val |
S85 |
6 | BAA04g21880 | A04 | 24504555 | G | A | missense_variant | MODERATE | c.1756C>T|p.Leu586Phe |
S206 |
7 | BAA04g21880 | A04 | 24504971 | G | A | missense_variant | MODERATE | c.1340C>T|p.Ser447Phe |
S278 |
8 | BAA04g21880 | A04 | 24505294 | G | A | missense_variant | MODERATE | c.1234C>T|p.Pro412Ser |
S136 |
9 | BAA04g21880 | A04 | 24505945 | C | T | missense_variant | MODERATE | c.583G>A|p.Gly195Arg |
S173 S225 S73 |
10 | BAA04g21880 | A04 | 24506008 | G | A | missense_variant | MODERATE | c.520C>T|p.Pro174Ser |
S59 |
11 | BAA04g21880 | A04 | 24506138 | G | A | intron_variant | MODIFIER | c.451-61C>T| |
S71 |
12 | BAA04g21880 | A04 | 24506514 | A | G | synonymous_variant | LOW | c.333T>C|p.Asp111Asp |
S170 |
13 | BAA04g21880 | A04 | 24507770 | G | A | upstream_gene_variant | MODIFIER | c.-859C>T| |
S192 |
14 | BAA04g21880 | A04 | 24508167 | G | A | upstream_gene_variant | MODIFIER | c.-1256C>T| |
S11 |
15 | BAA04g21880 | A04 | 24508424 | C | T | upstream_gene_variant | MODIFIER | c.-1513G>A| |
S192 |
16 | BAA04g21880 | A04 | 24508841 | C | T | upstream_gene_variant | MODIFIER | c.-1930G>A| |
S42 |
17 | BAA04g21880 | A04 | 24510033 | G | A | upstream_gene_variant | MODIFIER | c.-3122C>T| |
S299 |
18 | BAA04g21880 | A04 | 24510608 | C | T | upstream_gene_variant | MODIFIER | c.-3697G>A| |
S32 |