Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41660 | A09 | 48326545 | C | T | splice_region_variant&stop_retained_variant | LOW | c.2964G>A|p.Ter988Ter |
S183 S198 |
2 | BAA09g41660 | A09 | 48326901 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.2701-1G>A| |
S272 |
3 | BAA09g41660 | A09 | 48327052 | C | T | missense_variant | MODERATE | c.2660G>A|p.Arg887Lys |
S186 |
4 | BAA09g41660 | A09 | 48330434 | C | T | synonymous_variant | LOW | c.1089G>A|p.Arg363Arg |
S279 |
5 | BAA09g41660 | A09 | 48331193 | C | T | synonymous_variant | LOW | c.432G>A|p.Ser144Ser |
S192 |
6 | BAA09g41660 | A09 | 48332397 | C | T | upstream_gene_variant | MODIFIER | c.-773G>A| |
S32 |
7 | BAA09g41660 | A09 | 48332965 | C | T | upstream_gene_variant | MODIFIER | c.-1341G>A| |
S255 |
8 | BAA09g41660 | A09 | 48333095 | C | T | upstream_gene_variant | MODIFIER | c.-1471G>A| |
S18 |
9 | BAA09g41660 | A09 | 48333281 | C | T | upstream_gene_variant | MODIFIER | c.-1657G>A| |
S297 |
10 | BAA09g41660 | A09 | 48333313 | C | T | upstream_gene_variant | MODIFIER | c.-1689G>A| |
S296 |
11 | BAA09g41660 | A09 | 48333336 | G | A | upstream_gene_variant | MODIFIER | c.-1712C>T| |
S42 |