Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41740 | A09 | 48358734 | C | T | missense_variant | MODERATE | c.3373G>A|p.Ala1125Thr |
S279 |
2 | BAA09g41740 | A09 | 48359200 | G | A | stop_gained | HIGH | c.3082C>T|p.Gln1028* |
S231 |
3 | BAA09g41740 | A09 | 48359202 | G | A | missense_variant | MODERATE | c.3080C>T|p.Pro1027Leu |
S193 |
4 | BAA09g41740 | A09 | 48359357 | C | T | synonymous_variant | LOW | c.2925G>A|p.Lys975Lys |
S60 |
5 | BAA09g41740 | A09 | 48360666 | C | T | missense_variant | MODERATE | c.1819G>A|p.Glu607Lys |
S272 |
6 | BAA09g41740 | A09 | 48361543 | G | A | missense_variant | MODERATE | c.1036C>T|p.Leu346Phe |
S45 |
7 | BAA09g41740 | A09 | 48361730 | C | T | splice_donor_variant&intron_variant | HIGH | c.920+1G>A| |
S182 |
8 | BAA09g41740 | A09 | 48362131 | G | A | intron_variant | MODIFIER | c.627-33C>T| |
S15 S3 |
9 | BAA09g41740 | A09 | 48362678 | C | T | intron_variant | MODIFIER | c.221-17G>A| |
S18 |
10 | BAA09g41740 | A09 | 48363174 | C | T | upstream_gene_variant | MODIFIER | c.-46G>A| |
S40 S49 |
11 | BAA09g41740 | A09 | 48363539 | C | T | upstream_gene_variant | MODIFIER | c.-411G>A| |
S56 |
12 | BAA09g41740 | A09 | 48363789 | C | T | upstream_gene_variant | MODIFIER | c.-661G>A| |
S293 |
13 | BAA09g41740 | A09 | 48364945 | G | A | upstream_gene_variant | MODIFIER | c.-1817C>T| |
S236 |
14 | BAA09g41740 | A09 | 48365129 | C | T | upstream_gene_variant | MODIFIER | c.-2001G>A| |
S63 |
15 | BAA09g41740 | A09 | 48366964 | G | A | upstream_gene_variant | MODIFIER | c.-3836C>T| |
S86 |
16 | BAA09g41740 | A09 | 48367679 | G | A | upstream_gene_variant | MODIFIER | c.-4551C>T| |
S268 |
17 | BAA09g41740 | A09 | 48367862 | G | A | upstream_gene_variant | MODIFIER | c.-4734C>T| |
S194 |
18 | BAA09g41740 | A09 | 48368121 | C | G | upstream_gene_variant | MODIFIER | c.-4993G>C| |
S18 |