Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g48450 | A09 | 52254445 | C | T | downstream_gene_variant | MODIFIER | c.*3905G>A| |
S17 S67 |
2 | BAA09g48450 | A09 | 52254522 | C | T | downstream_gene_variant | MODIFIER | c.*3828G>A| |
S272 |
3 | BAA09g48450 | A09 | 52255752 | C | T | downstream_gene_variant | MODIFIER | c.*2598G>A| |
S139 S201 |
4 | BAA09g48450 | A09 | 52255762 | C | T | downstream_gene_variant | MODIFIER | c.*2588G>A| |
S132 S137 S215 |
5 | BAA09g48450 | A09 | 52255794 | G | A | downstream_gene_variant | MODIFIER | c.*2556C>T| |
S305 |
6 | BAA09g48450 | A09 | 52256184 | C | T | downstream_gene_variant | MODIFIER | c.*2166G>A| |
S261 |
7 | BAA09g48450 | A09 | 52256237 | G | A | downstream_gene_variant | MODIFIER | c.*2113C>T| |
S180 |
8 | BAA09g48450 | A09 | 52256634 | G | A | downstream_gene_variant | MODIFIER | c.*1716C>T| |
S243 |
9 | BAA09g48450 | A09 | 52257172 | C | T | downstream_gene_variant | MODIFIER | c.*1178G>A| |
S183 |
10 | BAA09g48450 | A09 | 52258332 | C | T | downstream_gene_variant | MODIFIER | c.*18G>A| |
S117 |
11 | BAA09g48450 | A09 | 52258862 | C | T | missense_variant | MODERATE | c.736G>A|p.Asp246Asn |
S18 |
12 | BAA09g48450 | A09 | 52258885 | C | T | missense_variant | MODERATE | c.713G>A|p.Gly238Asp |
S50 |
13 | BAA09g48450 | A09 | 52259131 | C | T | missense_variant | MODERATE | c.467G>A|p.Arg156His |
S208 S219 |
14 | BAA09g48450 | A09 | 52259224 | C | T | missense_variant | MODERATE | c.374G>A|p.Arg125His |
S13 |
15 | BAA09g48450 | A09 | 52259357 | G | A | missense_variant | MODERATE | c.241C>T|p.Leu81Phe |
S171 |