Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g11370 | A09 | 6384726 | G | A | missense_variant | MODERATE | c.1058C>T|p.Pro353Leu |
S42 |
2 | BAA09g11370 | A09 | 6385327 | C | T | splice_donor_variant&intron_variant | HIGH | c.786+1G>A| |
S153 |
3 | BAA09g11370 | A09 | 6385342 | C | T | missense_variant | MODERATE | c.772G>A|p.Val258Ile |
S212 |
4 | BAA09g11370 | A09 | 6385596 | G | A | stop_gained | HIGH | c.607C>T|p.Gln203* |
S64 |
5 | BAA09g11370 | A09 | 6385624 | G | A | synonymous_variant | LOW | c.579C>T|p.Ile193Ile |
S32 |
6 | BAA09g11370 | A09 | 6385888 | C | T | splice_region_variant&intron_variant | LOW | c.319-4G>A| |
S132 S137 S215 |
7 | BAA09g11370 | A09 | 6386261 | C | T | missense_variant | MODERATE | c.166G>A|p.Ala56Thr |
S28 |
8 | BAA09g11370 | A09 | 6386285 | G | A | missense_variant | MODERATE | c.142C>T|p.Pro48Ser |
S45 |
9 | BAA09g11370 | A09 | 6387971 | C | T | upstream_gene_variant | MODIFIER | c.-1545G>A| |
S19 |
10 | BAA09g11370 | A09 | 6387983 | G | A | upstream_gene_variant | MODIFIER | c.-1557C>T| |
S245 |
11 | BAA09g11370 | A09 | 6388613 | G | A | upstream_gene_variant | MODIFIER | c.-2187C>T| |
S146 |
12 | BAA09g11370 | A09 | 6388825 | C | T | upstream_gene_variant | MODIFIER | c.-2399G>A| |
S84 S93 |
13 | BAA09g11370 | A09 | 6389212 | C | T | upstream_gene_variant | MODIFIER | c.-2786G>A| |
S264 |