Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g20420 | A07 | 25659616 | C | T | missense_variant | MODERATE | c.545C>T|p.Ser182Phe |
S247 |
2 | BAA07g20420 | A07 | 25660815 | C | T | intron_variant | MODIFIER | c.1378-26C>T| |
S148 S210 S30 |
3 | BAA07g20420 | A07 | 25661276 | G | A | missense_variant&splice_region_variant | MODERATE | c.1708G>A|p.Ala570Thr |
S133 |
4 | BAA07g20420 | A07 | 25661817 | C | T | synonymous_variant | LOW | c.2073C>T|p.Asp691Asp |
S247 |
5 | BAA07g20420 | A07 | 25662581 | C | T | missense_variant | MODERATE | c.2425C>T|p.Leu809Phe |
S9 |
6 | BAA07g20420 | A07 | 25664207 | C | T | splice_region_variant&intron_variant | LOW | c.3234+8C>T| |
S37 |
7 | BAA07g20420 | A07 | 25665126 | C | T | missense_variant | MODERATE | c.3740C>T|p.Ser1247Phe |
S200 |
8 | BAA07g20420 | A07 | 25667575 | C | T | missense_variant | MODERATE | c.5036C>T|p.Ala1679Val |
S35 |
9 | BAA07g20420 | A07 | 25669239 | G | A | missense_variant | MODERATE | c.5677G>A|p.Glu1893Lys |
S292 |
10 | BAA07g20420 | A07 | 25671351 | C | T | missense_variant | MODERATE | c.6986C>T|p.Pro2329Leu |
S148 S30 |