Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g16830 | A04 | 21115767 | C | T | missense_variant&splice_region_variant | MODERATE | c.2254G>A|p.Asp752Asn |
S80 |
2 | BAA04g16830 | A04 | 21118774 | C | T | missense_variant | MODERATE | c.1786G>A|p.Val596Ile |
S262 |
3 | BAA04g16830 | A04 | 21120004 | C | T | missense_variant | MODERATE | c.556G>A|p.Val186Ile |
S95 |
4 | BAA04g16830 | A04 | 21120015 | G | A | missense_variant | MODERATE | c.545C>T|p.Thr182Ile |
S259 |
5 | BAA04g16830 | A04 | 21120256 | C | T | missense_variant | MODERATE | c.304G>A|p.Glu102Lys |
S20 |
6 | BAA04g16830 | A04 | 21120449 | C | T | synonymous_variant | LOW | c.111G>A|p.Lys37Lys |
S226 |
7 | BAA04g16830 | A04 | 21120508 | G | A | missense_variant | MODERATE | c.52C>T|p.Pro18Ser |
S236 |
8 | BAA04g16830 | A04 | 21120849 | G | A | upstream_gene_variant | MODIFIER | c.-290C>T| |
S40 S49 |
9 | BAA04g16830 | A04 | 21120970 | C | T | upstream_gene_variant | MODIFIER | c.-411G>A| |
S260 |
10 | BAA04g16830 | A04 | 21121494 | G | A | upstream_gene_variant | MODIFIER | c.-935C>T| |
S108 |
11 | BAA04g16830 | A04 | 21122628 | C | T | upstream_gene_variant | MODIFIER | c.-2069G>A| |
S178 |
12 | BAA04g16830 | A04 | 21122654 | T | A | upstream_gene_variant | MODIFIER | c.-2095A>T| |
S201 |
13 | BAA04g16830 | A04 | 21122867 | G | A | upstream_gene_variant | MODIFIER | c.-2308C>T| |
S71 |