Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g32610 | A01 | 21538848 | G | A | missense_variant | MODERATE | c.2912C>T|p.Ala971Val |
S6 |
2 | BAA01g32610 | A01 | 21539585 | C | T | missense_variant | MODERATE | c.2320G>A|p.Glu774Lys |
S240 |
3 | BAA01g32610 | A01 | 21540075 | G | A | synonymous_variant | LOW | c.1899C>T|p.Ser633Ser |
S163 |
4 | BAA01g32610 | A01 | 21540094 | G | A | missense_variant | MODERATE | c.1880C>T|p.Ser627Leu |
S138 |
5 | BAA01g32610 | A01 | 21540358 | C | T | missense_variant | MODERATE | c.1616G>A|p.Arg539His |
S179 |
6 | BAA01g32610 | A01 | 21540617 | C | T | missense_variant | MODERATE | c.1357G>A|p.Gly453Arg |
S146 |
7 | BAA01g32610 | A01 | 21540743 | G | A | missense_variant | MODERATE | c.1231C>T|p.His411Tyr |
S296 |
8 | BAA01g32610 | A01 | 21540967 | G | A | missense_variant | MODERATE | c.1007C>T|p.Ser336Leu |
S172 S217 |
9 | BAA01g32610 | A01 | 21541535 | C | T | missense_variant | MODERATE | c.439G>A|p.Gly147Ser |
S210 S225 |
10 | BAA01g32610 | A01 | 21542201 | G | A | synonymous_variant | LOW | c.39C>T|p.Phe13Phe |
S140 |
11 | BAA01g32610 | A01 | 21543452 | G | A | upstream_gene_variant | MODIFIER | c.-1213C>T| |
S115 |
12 | BAA01g32610 | A01 | 21544404 | C | T | upstream_gene_variant | MODIFIER | c.-2165G>A| |
S261 |
13 | BAA01g32610 | A01 | 21544636 | C | T | upstream_gene_variant | MODIFIER | c.-2397G>A| |
S179 |
14 | BAA01g32610 | A01 | 21546268 | G | A | upstream_gene_variant | MODIFIER | c.-4029C>T| |
S34 |
15 | BAA01g32610 | A01 | 21546812 | C | T | upstream_gene_variant | MODIFIER | c.-4573G>A| |
S128 |