Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g22770 | A09 | 14324659 | C | T | missense_variant | MODERATE | c.2782G>A|p.Gly928Arg |
S148 S210 |
2 | BAA09g22770 | A09 | 14324890 | C | T | splice_region_variant&synonymous_variant | LOW | c.2652G>A|p.Leu884Leu |
S153 |
3 | BAA09g22770 | A09 | 14326304 | G | A | missense_variant | MODERATE | c.1604C>T|p.Ala535Val |
S95 |
4 | BAA09g22770 | A09 | 14326477 | G | A | synonymous_variant | LOW | c.1431C>T|p.Asp477Asp |
S42 |
5 | BAA09g22770 | A09 | 14326587 | G | A | synonymous_variant | LOW | c.1321C>T|p.Leu441Leu |
S169 |
6 | BAA09g22770 | A09 | 14328289 | C | T | upstream_gene_variant | MODIFIER | c.-382G>A| |
S118 |
7 | BAA09g22770 | A09 | 14328575 | G | A | upstream_gene_variant | MODIFIER | c.-668C>T| |
S23 |
8 | BAA09g22770 | A09 | 14328576 | G | A | upstream_gene_variant | MODIFIER | c.-669C>T| |
S37 |
9 | BAA09g22770 | A09 | 14328718 | C | T | upstream_gene_variant | MODIFIER | c.-811G>A| |
S18 |
10 | BAA09g22770 | A09 | 14330866 | C | T | upstream_gene_variant | MODIFIER | c.-2959G>A| |
S63 |
11 | BAA09g22770 | A09 | 14331530 | C | T | upstream_gene_variant | MODIFIER | c.-3623G>A| |
S62 |
12 | BAA09g22770 | A09 | 14331662 | C | T | upstream_gene_variant | MODIFIER | c.-3755G>A| |
S231 |