Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g12280 | A06 | 6154522 | G | A | missense_variant | MODERATE | c.3535C>T|p.Leu1179Phe |
S62 |
2 | BAA06g12280 | A06 | 6155291 | C | T | missense_variant | MODERATE | c.3061G>A|p.Ala1021Thr |
S286 |
3 | BAA06g12280 | A06 | 6155601 | C | T | synonymous_variant | LOW | c.2751G>A|p.Arg917Arg |
S189 |
4 | BAA06g12280 | A06 | 6155704 | G | A | missense_variant | MODERATE | c.2648C>T|p.Ala883Val |
S35 |
5 | BAA06g12280 | A06 | 6158050 | G | A | synonymous_variant | LOW | c.2268C>T|p.Tyr756Tyr |
S219 S72 |
6 | BAA06g12280 | A06 | 6158807 | C | T | synonymous_variant | LOW | c.1584G>A|p.Gly528Gly |
S95 |
7 | BAA06g12280 | A06 | 6158954 | G | T | missense_variant | MODERATE | c.1490C>A|p.Ser497Tyr |
|
8 | BAA06g12280 | A06 | 6159011 | C | T | missense_variant | MODERATE | c.1433G>A|p.Arg478Lys |
S179 |
9 | BAA06g12280 | A06 | 6159050 | C | T | missense_variant | MODERATE | c.1394G>A|p.Gly465Glu |
S208 S93 |
10 | BAA06g12280 | A06 | 6159641 | C | T | missense_variant | MODERATE | c.803G>A|p.Arg268Lys |
S123 |
11 | BAA06g12280 | A06 | 6159673 | G | A | synonymous_variant | LOW | c.771C>T|p.Cys257Cys |
S45 |
12 | BAA06g12280 | A06 | 6159682 | C | T | synonymous_variant | LOW | c.762G>A|p.Gln254Gln |
S28 |
13 | BAA06g12280 | A06 | 6159971 | C | T | missense_variant | MODERATE | c.473G>A|p.Cys158Tyr |
S256 |
14 | BAA06g12280 | A06 | 6160296 | C | T | missense_variant | MODERATE | c.148G>A|p.Glu50Lys |
S78 |
15 | BAA06g12280 | A06 | 6160468 | C | T | missense_variant | MODERATE | c.68G>A|p.Ser23Asn |
S67 |
16 | BAA06g12280 | A06 | 6163461 | C | T | upstream_gene_variant | MODIFIER | c.-2816G>A| |
S264 |
17 | BAA06g12280 | A06 | 6163569 | A | C | upstream_gene_variant | MODIFIER | c.-2924T>G| |
S276 S54 S63 |
18 | BAA06g12280 | A06 | 6164461 | C | T | upstream_gene_variant | MODIFIER | c.-3816G>A| |
S37 |