Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49510 | A09 | 52802420 | G | A | missense_variant | MODERATE | c.1208C>T|p.Thr403Ile |
S271 |
2 | BAA09g49510 | A09 | 52803795 | T | C | intron_variant | MODIFIER | c.922-804A>G| |
S197 |
3 | BAA09g49510 | A09 | 52807516 | G | A | missense_variant | MODERATE | c.518C>T|p.Ser173Phe |
S217 S248 |
4 | BAA09g49510 | A09 | 52807549 | G | A | missense_variant | MODERATE | c.485C>T|p.Ala162Val |
S252 |
5 | BAA09g49510 | A09 | 52807719 | G | A | synonymous_variant | LOW | c.315C>T|p.His105His |
S11 |
6 | BAA09g49510 | A09 | 52809228 | A | G | upstream_gene_variant | MODIFIER | c.-445T>C| |
S178 |
7 | BAA09g49510 | A09 | 52810660 | G | A | upstream_gene_variant | MODIFIER | c.-1877C>T| |
S155 S211 |
8 | BAA09g49510 | A09 | 52810701 | C | T | upstream_gene_variant | MODIFIER | c.-1918G>A| |
S118 |
9 | BAA09g49510 | A09 | 52810796 | C | T | upstream_gene_variant | MODIFIER | c.-2013G>A| |
S8 |
10 | BAA09g49510 | A09 | 52811116 | G | A | upstream_gene_variant | MODIFIER | c.-2333C>T| |
S166 |
11 | BAA09g49510 | A09 | 52811223 | G | A | upstream_gene_variant | MODIFIER | c.-2440C>T| |
S116 |
12 | BAA09g49510 | A09 | 52811268 | C | T | upstream_gene_variant | MODIFIER | c.-2485G>A| |
S119 |
13 | BAA09g49510 | A09 | 52812400 | C | A | upstream_gene_variant | MODIFIER | c.-3617G>T| |
S107 S215 S216 S235 S243 S247 S261 S94 S99 |
14 | BAA09g49510 | A09 | 52813361 | G | A | upstream_gene_variant | MODIFIER | c.-4578C>T| |
S132 S137 S215 |