Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g38600 | A07 | 35003858 | G | A | missense_variant | MODERATE | c.4142C>T|p.Pro1381Leu |
S167 |
2 | BAA07g38600 | A07 | 35004249 | G | A | stop_gained | HIGH | c.3751C>T|p.Gln1251* |
S69 |
3 | BAA07g38600 | A07 | 35004269 | C | T | missense_variant | MODERATE | c.3731G>A|p.Gly1244Asp |
S224 |
4 | BAA07g38600 | A07 | 35004381 | G | A | missense_variant | MODERATE | c.3619C>T|p.Leu1207Phe |
S12 |
5 | BAA07g38600 | A07 | 35004578 | C | T | missense_variant | MODERATE | c.3422G>A|p.Ser1141Asn |
S59 |
6 | BAA07g38600 | A07 | 35004891 | C | T | missense_variant | MODERATE | c.3184G>A|p.Val1062Ile |
S127 |
7 | BAA07g38600 | A07 | 35005093 | G | A | synonymous_variant | LOW | c.2982C>T|p.Ala994Ala |
S51 |
8 | BAA07g38600 | A07 | 35005440 | G | A | missense_variant | MODERATE | c.2635C>T|p.Leu879Phe |
S294 |
9 | BAA07g38600 | A07 | 35005614 | G | A | synonymous_variant | LOW | c.2461C>T|p.Leu821Leu |
S33 |
10 | BAA07g38600 | A07 | 35006454 | C | T | missense_variant | MODERATE | c.1621G>A|p.Gly541Arg |
S189 |
11 | BAA07g38600 | A07 | 35006456 | C | T | missense_variant | MODERATE | c.1619G>A|p.Gly540Glu |
S292 |
12 | BAA07g38600 | A07 | 35006749 | C | T | stop_gained | HIGH | c.1326G>A|p.Trp442* |
S168 |
13 | BAA07g38600 | A07 | 35007020 | C | T | missense_variant | MODERATE | c.1055G>A|p.Ser352Asn |
S274 |
14 | BAA07g38600 | A07 | 35007488 | C | T | missense_variant | MODERATE | c.667G>A|p.Val223Ile |
S277 |
15 | BAA07g38600 | A07 | 35007552 | C | T | synonymous_variant | LOW | c.603G>A|p.Arg201Arg |
S281 |
16 | BAA07g38600 | A07 | 35009031 | C | T | upstream_gene_variant | MODIFIER | c.-625G>A| |
S224 |
17 | BAA07g38600 | A07 | 35009164 | C | T | upstream_gene_variant | MODIFIER | c.-758G>A| |
S81 |
18 | BAA07g38600 | A07 | 35009833 | G | A | upstream_gene_variant | MODIFIER | c.-1427C>T| |
S178 |
19 | BAA07g38600 | A07 | 35010011 | G | A | upstream_gene_variant | MODIFIER | c.-1605C>T| |
S295 |
20 | BAA07g38600 | A07 | 35010358 | C | T | upstream_gene_variant | MODIFIER | c.-1952G>A| |
S179 |
21 | BAA07g38600 | A07 | 35012420 | C | T | upstream_gene_variant | MODIFIER | c.-4014G>A| |
S252 S266 |
22 | BAA07g38600 | A07 | 35013253 | G | A | upstream_gene_variant | MODIFIER | c.-4847C>T| |
S273 |