Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g54780 | A09 | 55245941 | G | A | missense_variant | MODERATE | c.58G>A|p.Gly20Arg |
S72 |
2 | BAA09g54780 | A09 | 55245982 | C | T | synonymous_variant | LOW | c.99C>T|p.Ser33Ser |
S278 |
3 | BAA09g54780 | A09 | 55246065 | G | A | missense_variant | MODERATE | c.182G>A|p.Gly61Asp |
S65 |
4 | BAA09g54780 | A09 | 55246130 | G | A | missense_variant | MODERATE | c.247G>A|p.Asp83Asn |
S10 |
5 | BAA09g54780 | A09 | 55246425 | G | A | missense_variant | MODERATE | c.542G>A|p.Gly181Glu |
S130 |
6 | BAA09g54780 | A09 | 55247530 | G | A | missense_variant | MODERATE | c.1486G>A|p.Val496Ile |
S144 |
7 | BAA09g54780 | A09 | 55248431 | C | T | intron_variant | MODIFIER | c.1886+284C>T| |
S136 |
8 | BAA09g54780 | A09 | 55248435 | G | A | intron_variant | MODIFIER | c.1886+288G>A| |
S107 |
9 | BAA09g54780 | A09 | 55248563 | C | T | intron_variant | MODIFIER | c.1887-358C>T| |
S302 |
10 | BAA09g54780 | A09 | 55249284 | G | A | intron_variant | MODIFIER | c.2156+94G>A| |
S42 |
11 | BAA09g54780 | A09 | 55251758 | C | T | missense_variant | MODERATE | c.2323C>T|p.Pro775Ser |
S153 |
12 | BAA09g54780 | A09 | 55251789 | G | A | missense_variant | MODERATE | c.2354G>A|p.Arg785Gln |
S58 |
13 | BAA09g54780 | A09 | 55252961 | C | T | missense_variant | MODERATE | c.3085C>T|p.Pro1029Ser |
S146 |
14 | BAA09g54780 | A09 | 55252974 | G | A | stop_gained | HIGH | c.3098G>A|p.Trp1033* |
S167 |
15 | BAA09g54780 | A09 | 55253035 | G | A | synonymous_variant | LOW | c.3159G>A|p.Gln1053Gln |
S288 |
16 | BAA09g54780 | A09 | 55253513 | G | A | missense_variant | MODERATE | c.3637G>A|p.Val1213Met |
S86 |