Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g23170 | A10 | 19610881 | G | A | synonymous_variant | LOW | c.2940C>T|p.Val980Val |
S286 |
2 | BAA10g23170 | A10 | 19612363 | G | A | splice_region_variant&intron_variant | LOW | c.2178-4C>T| |
S172 S217 |
3 | BAA10g23170 | A10 | 19614080 | C | T | synonymous_variant | LOW | c.1494G>A|p.Leu498Leu |
S121 |
4 | BAA10g23170 | A10 | 19614784 | C | T | missense_variant | MODERATE | c.1195G>A|p.Val399Ile |
S206 S26 |
5 | BAA10g23170 | A10 | 19614927 | G | A | intron_variant | MODIFIER | c.1173+12C>T| |
S130 |
6 | BAA10g23170 | A10 | 19615268 | C | T | missense_variant | MODERATE | c.977G>A|p.Arg326Gln |
S206 S26 |
7 | BAA10g23170 | A10 | 19616912 | G | A | missense_variant | MODERATE | c.253C>T|p.Leu85Phe |
S271 |
8 | BAA10g23170 | A10 | 19617773 | G | A | upstream_gene_variant | MODIFIER | c.-4C>T| |
S279 |
9 | BAA10g23170 | A10 | 19617818 | G | A | upstream_gene_variant | MODIFIER | c.-49C>T| |
S166 |
10 | BAA10g23170 | A10 | 19620182 | C | T | upstream_gene_variant | MODIFIER | c.-2413G>A| |
S10 |
11 | BAA10g23170 | A10 | 19621059 | G | A | upstream_gene_variant | MODIFIER | c.-3290C>T| |
S167 |