Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g20920 | A06 | 11207907 | G | A | downstream_gene_variant | MODIFIER | c.*1249C>T| |
S234 |
2 | BAA06g20920 | A06 | 11209771 | G | A | missense_variant | MODERATE | c.3169C>T|p.Pro1057Ser |
S63 |
3 | BAA06g20920 | A06 | 11210143 | C | T | missense_variant | MODERATE | c.2968G>A|p.Glu990Lys |
S180 |
4 | BAA06g20920 | A06 | 11212127 | T | C | missense_variant | MODERATE | c.2033A>G|p.Asp678Gly |
S171 |
5 | BAA06g20920 | A06 | 11212822 | C | T | synonymous_variant | LOW | c.1899G>A|p.Val633Val |
S229 |
6 | BAA06g20920 | A06 | 11213149 | C | T | missense_variant | MODERATE | c.1795G>A|p.Gly599Ser |
S65 |
7 | BAA06g20920 | A06 | 11213337 | G | A | synonymous_variant | LOW | c.1684C>T|p.Leu562Leu |
S153 |
8 | BAA06g20920 | A06 | 11213861 | G | A | synonymous_variant | LOW | c.1299C>T|p.Ser433Ser |
S44 |
9 | BAA06g20920 | A06 | 11214437 | G | A | missense_variant | MODERATE | c.893C>T|p.Thr298Ile |
S246 |
10 | BAA06g20920 | A06 | 11214885 | G | A | missense_variant | MODERATE | c.445C>T|p.Arg149Cys |
S226 |
11 | BAA06g20920 | A06 | 11215695 | G | A | missense_variant | MODERATE | c.73C>T|p.Pro25Ser |
S265 |
12 | BAA06g20920 | A06 | 11215958 | C | T | upstream_gene_variant | MODIFIER | c.-191G>A| |
S191 |
13 | BAA06g20920 | A06 | 11216113 | G | A | upstream_gene_variant | MODIFIER | c.-346C>T| |
S273 |
14 | BAA06g20920 | A06 | 11216899 | G | A | upstream_gene_variant | MODIFIER | c.-1132C>T| |
S69 |
15 | BAA06g20920 | A06 | 11217365 | G | A | upstream_gene_variant | MODIFIER | c.-1598C>T| |
S48 |
16 | BAA06g20920 | A06 | 11219492 | C | T | upstream_gene_variant | MODIFIER | c.-3725G>A| |
S80 |