Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g67560 | A09 | 61161563 | C | T | synonymous_variant | LOW | c.3369G>A|p.Ser1123Ser |
S209 |
2 | BAA09g67560 | A09 | 61161574 | C | T | missense_variant | MODERATE | c.3358G>A|p.Glu1120Lys |
S114 |
3 | BAA09g67560 | A09 | 61161696 | C | T | splice_region_variant&intron_variant | LOW | c.3242-6G>A| |
S219 |
4 | BAA09g67560 | A09 | 61161907 | C | T | missense_variant | MODERATE | c.3126G>A|p.Met1042Ile |
S35 |
5 | BAA09g67560 | A09 | 61162717 | C | T | missense_variant&splice_region_variant | MODERATE | c.2738G>A|p.Arg913Lys |
S303 |
6 | BAA09g67560 | A09 | 61162738 | C | T | missense_variant | MODERATE | c.2717G>A|p.Cys906Tyr |
S87 |
7 | BAA09g67560 | A09 | 61163846 | G | A | missense_variant | MODERATE | c.1934C>T|p.Ala645Val |
S124 |
8 | BAA09g67560 | A09 | 61164345 | C | T | missense_variant | MODERATE | c.1435G>A|p.Glu479Lys |
S279 |
9 | BAA09g67560 | A09 | 61164515 | C | T | missense_variant | MODERATE | c.1265G>A|p.Gly422Glu |
S100 |
10 | BAA09g67560 | A09 | 61165426 | C | T | synonymous_variant | LOW | c.354G>A|p.Arg118Arg |
S51 |
11 | BAA09g67560 | A09 | 61165534 | G | A | splice_region_variant&intron_variant | LOW | c.330+3C>T| |
S37 |
12 | BAA09g67560 | A09 | 61166141 | G | A | missense_variant | MODERATE | c.8C>T|p.Pro3Leu |
S158 |
13 | BAA09g67560 | A09 | 61166270 | G | A | upstream_gene_variant | MODIFIER | c.-122C>T| |
S244 |
14 | BAA09g67560 | A09 | 61167252 | G | A | upstream_gene_variant | MODIFIER | c.-1104C>T| |
S13 |
15 | BAA09g67560 | A09 | 61168082 | G | A | upstream_gene_variant | MODIFIER | c.-1934C>T| |
S231 |