Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04130 | A10 | 2018021 | G | A | downstream_gene_variant | MODIFIER | c.*4159C>T| |
S263 |
2 | BAA10g04130 | A10 | 2019698 | C | T | downstream_gene_variant | MODIFIER | c.*2482G>A| |
S208 S93 |
3 | BAA10g04130 | A10 | 2021080 | G | A | downstream_gene_variant | MODIFIER | c.*1100C>T| |
S157 S163 |
4 | BAA10g04130 | A10 | 2021539 | C | T | downstream_gene_variant | MODIFIER | c.*641G>A| |
S155 |
5 | BAA10g04130 | A10 | 2022315 | C | T | missense_variant | MODERATE | c.3070G>A|p.Gly1024Arg |
S259 |
6 | BAA10g04130 | A10 | 2022801 | G | A | intron_variant | MODIFIER | c.2896-93C>T| |
S286 |
7 | BAA10g04130 | A10 | 2023141 | G | A | intron_variant | MODIFIER | c.2896-433C>T| |
S286 |
8 | BAA10g04130 | A10 | 2024155 | G | A | intron_variant | MODIFIER | c.2896-1447C>T| |
S20 |
9 | BAA10g04130 | A10 | 2024264 | G | A | intron_variant | MODIFIER | c.2896-1556C>T| |
S255 |
10 | BAA10g04130 | A10 | 2026198 | G | A | intron_variant | MODIFIER | c.2895+63C>T| |
S138 |
11 | BAA10g04130 | A10 | 2026980 | C | T | intron_variant | MODIFIER | c.2860+60G>A| |
S190 |
12 | BAA10g04130 | A10 | 2027265 | G | A | stop_gained | HIGH | c.2635C>T|p.Arg879* |
S160 |
13 | BAA10g04130 | A10 | 2027584 | C | T | stop_gained | HIGH | c.2316G>A|p.Trp772* |
S123 |
14 | BAA10g04130 | A10 | 2027683 | C | T | synonymous_variant | LOW | c.2217G>A|p.Leu739Leu |
S270 |
15 | BAA10g04130 | A10 | 2027848 | C | T | synonymous_variant | LOW | c.2052G>A|p.Lys684Lys |
S263 |
16 | BAA10g04130 | A10 | 2027930 | C | T | missense_variant | MODERATE | c.1970G>A|p.Gly657Glu |
S186 |
17 | BAA10g04130 | A10 | 2027952 | G | A | missense_variant | MODERATE | c.1948C>T|p.Leu650Phe |
S178 |
18 | BAA10g04130 | A10 | 2028165 | G | A | missense_variant | MODERATE | c.1735C>T|p.Leu579Phe |
S150 |
19 | BAA10g04130 | A10 | 2028554 | G | A | missense_variant | MODERATE | c.1487C>T|p.Pro496Leu |
S178 |
20 | BAA10g04130 | A10 | 2029184 | C | T | missense_variant | MODERATE | c.857G>A|p.Arg286His |
S308 |
21 | BAA10g04130 | A10 | 2029219 | G | A | synonymous_variant | LOW | c.822C>T|p.His274His |
S36 S58 |
22 | BAA10g04130 | A10 | 2029625 | C | T | missense_variant | MODERATE | c.416G>A|p.Arg139Lys |
S116 |
23 | BAA10g04130 | A10 | 2029803 | C | T | missense_variant | MODERATE | c.238G>A|p.Glu80Lys |
S298 |
24 | BAA10g04130 | A10 | 2029931 | G | A | missense_variant | MODERATE | c.110C>T|p.Pro37Leu |
S107 |
25 | BAA10g04130 | A10 | 2030362 | G | A | upstream_gene_variant | MODIFIER | c.-322C>T| |
S215 |