Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g22820 | A08 | 17068640 | G | A | synonymous_variant | LOW | c.2406C>T|p.Cys802Cys |
S229 |
2 | BAA08g22820 | A08 | 17069035 | C | T | missense_variant | MODERATE | c.2193G>A|p.Met731Ile |
S168 |
3 | BAA08g22820 | A08 | 17069337 | C | T | synonymous_variant | LOW | c.1974G>A|p.Lys658Lys |
S132 S137 S89 |
4 | BAA08g22820 | A08 | 17070864 | C | T | missense_variant | MODERATE | c.1102G>A|p.Glu368Lys |
S303 |
5 | BAA08g22820 | A08 | 17070908 | G | A | missense_variant | MODERATE | c.1058C>T|p.Pro353Leu |
S109 |
6 | BAA08g22820 | A08 | 17071634 | G | A | missense_variant | MODERATE | c.602C>T|p.Ala201Val |
S46 |
7 | BAA08g22820 | A08 | 17071973 | G | A | synonymous_variant | LOW | c.343C>T|p.Leu115Leu |
S36 |
8 | BAA08g22820 | A08 | 17071981 | G | A | missense_variant | MODERATE | c.335C>T|p.Ala112Val |
S211 S227 |
9 | BAA08g22820 | A08 | 17072375 | G | A | missense_variant | MODERATE | c.158C>T|p.Thr53Ile |
S76 |
10 | BAA08g22820 | A08 | 17072848 | G | A | upstream_gene_variant | MODIFIER | c.-316C>T| |
S221 |
11 | BAA08g22820 | A08 | 17074631 | G | A | upstream_gene_variant | MODIFIER | c.-2099C>T| |
S281 |
12 | BAA08g22820 | A08 | 17074649 | C | T | upstream_gene_variant | MODIFIER | c.-2117G>A| |
S293 |
13 | BAA08g22820 | A08 | 17075566 | C | T | upstream_gene_variant | MODIFIER | c.-3034G>A| |
S172 |