Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g65380 | A09 | 60264163 | C | T | synonymous_variant | LOW | c.3963G>A|p.Lys1321Lys |
S5 |
2 | BAA09g65380 | A09 | 60265608 | C | T | missense_variant | MODERATE | c.2936G>A|p.Arg979Lys |
S153 S166 S167 S236 S262 |
3 | BAA09g65380 | A09 | 60265719 | C | T | missense_variant | MODERATE | c.2825G>A|p.Ser942Asn |
S35 |
4 | BAA09g65380 | A09 | 60266551 | G | A | synonymous_variant | LOW | c.2386C>T|p.Leu796Leu |
S271 |
5 | BAA09g65380 | A09 | 60266667 | C | T | missense_variant | MODERATE | c.2270G>A|p.Arg757Lys |
S66 |
6 | BAA09g65380 | A09 | 60267081 | C | T | missense_variant | MODERATE | c.2005G>A|p.Val669Ile |
S153 |
7 | BAA09g65380 | A09 | 60268945 | G | A | intron_variant | MODIFIER | c.1269+606C>T| |
S234 |
8 | BAA09g65380 | A09 | 60269131 | C | T | intron_variant | MODIFIER | c.1269+420G>A| |
S56 |
9 | BAA09g65380 | A09 | 60272296 | C | T | synonymous_variant | LOW | c.90G>A|p.Gly30Gly |
S33 |
10 | BAA09g65380 | A09 | 60274029 | G | A | upstream_gene_variant | MODIFIER | c.-1644C>T| |
S73 S91 |
11 | BAA09g65380 | A09 | 60275328 | G | A | upstream_gene_variant | MODIFIER | c.-2943C>T| |
S233 |
12 | BAA09g65380 | A09 | 60275960 | C | T | upstream_gene_variant | MODIFIER | c.-3575G>A| |
S225 |