Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g55940 | A09 | 55824647 | C | T | upstream_gene_variant | MODIFIER | c.-4212C>T| |
S20 |
2 | BAA09g55940 | A09 | 55825722 | A | T | upstream_gene_variant | MODIFIER | c.-3137A>T| |
S127 S261 |
3 | BAA09g55940 | A09 | 55825852 | C | T | upstream_gene_variant | MODIFIER | c.-3007C>T| |
S229 |
4 | BAA09g55940 | A09 | 55827750 | G | A | upstream_gene_variant | MODIFIER | c.-1109G>A| |
S297 |
5 | BAA09g55940 | A09 | 55827759 | C | T | upstream_gene_variant | MODIFIER | c.-1100C>T| |
S305 |
6 | BAA09g55940 | A09 | 55828381 | G | A | upstream_gene_variant | MODIFIER | c.-478G>A| |
S209 |
7 | BAA09g55940 | A09 | 55828735 | C | T | upstream_gene_variant | MODIFIER | c.-124C>T| |
S33 |
8 | BAA09g55940 | A09 | 55829004 | C | T | missense_variant | MODERATE | c.146C>T|p.Pro49Leu |
S279 |
9 | BAA09g55940 | A09 | 55829401 | G | A | missense_variant | MODERATE | c.466G>A|p.Asp156Asn |
S262 |
10 | BAA09g55940 | A09 | 55830973 | G | A | intron_variant | MODIFIER | c.678+161G>A| |
S13 |
11 | BAA09g55940 | A09 | 55831305 | G | A | missense_variant | MODERATE | c.824G>A|p.Cys275Tyr |
S113 |
12 | BAA09g55940 | A09 | 55833466 | G | A | downstream_gene_variant | MODIFIER | c.*1968G>A| |
S274 |
13 | BAA09g55940 | A09 | 55835400 | C | T | downstream_gene_variant | MODIFIER | c.*3902C>T| |
S305 |