Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g64850 | A09 | 60005782 | G | A | downstream_gene_variant | MODIFIER | c.*4542C>T| |
S47 |
2 | BAA09g64850 | A09 | 60010441 | G | A | synonymous_variant | LOW | c.4083C>T|p.Leu1361Leu |
S19 |
3 | BAA09g64850 | A09 | 60010864 | G | A | synonymous_variant | LOW | c.3852C>T|p.Thr1284Thr |
S255 |
4 | BAA09g64850 | A09 | 60011540 | C | T | intron_variant | MODIFIER | c.3513+29G>A| |
S272 |
5 | BAA09g64850 | A09 | 60011542 | C | T | intron_variant | MODIFIER | c.3513+27G>A| |
S219 |
6 | BAA09g64850 | A09 | 60011893 | G | A | intron_variant | MODIFIER | c.3402+89C>T| |
S205 |
7 | BAA09g64850 | A09 | 60012125 | G | A | intron_variant | MODIFIER | c.3277-18C>T| |
S32 |
8 | BAA09g64850 | A09 | 60013684 | G | A | intron_variant | MODIFIER | c.2457+33C>T| |
S178 |
9 | BAA09g64850 | A09 | 60014264 | C | T | missense_variant | MODERATE | c.2176G>A|p.Asp726Asn |
S239 |
10 | BAA09g64850 | A09 | 60014391 | C | T | intron_variant | MODIFIER | c.2118+65G>A| |
S296 |
11 | BAA09g64850 | A09 | 60014399 | C | T | intron_variant | MODIFIER | c.2118+57G>A| |
S292 |
12 | BAA09g64850 | A09 | 60015215 | C | T | missense_variant&splice_region_variant | MODERATE | c.1679G>A|p.Arg560Lys |
S208 S219 |
13 | BAA09g64850 | A09 | 60016089 | G | A | missense_variant | MODERATE | c.1303C>T|p.Leu435Phe |
S178 |
14 | BAA09g64850 | A09 | 60016597 | G | A | missense_variant | MODERATE | c.1006C>T|p.Arg336Trp |
S161 |
15 | BAA09g64850 | A09 | 60017598 | C | T | synonymous_variant | LOW | c.495G>A|p.Glu165Glu |
S52 |
16 | BAA09g64850 | A09 | 60019330 | G | A | upstream_gene_variant | MODIFIER | c.-647C>T| |
S86 |
17 | BAA09g64850 | A09 | 60023159 | C | T | upstream_gene_variant | MODIFIER | c.-4476G>A| |
S192 |
18 | BAA09g64850 | A09 | 60023525 | G | A | upstream_gene_variant | MODIFIER | c.-4842C>T| |
S265 |