Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g27160 | A07 | 29007068 | G | A | synonymous_variant | LOW | c.3198C>T|p.Ala1066Ala |
S50 |
2 | BAA07g27160 | A07 | 29007120 | G | A | missense_variant | MODERATE | c.3146C>T|p.Ser1049Phe |
S139 |
3 | BAA07g27160 | A07 | 29007174 | G | A | missense_variant | MODERATE | c.3092C>T|p.Pro1031Leu |
S158 |
4 | BAA07g27160 | A07 | 29007208 | G | A | missense_variant | MODERATE | c.3058C>T|p.Arg1020Cys |
S130 |
5 | BAA07g27160 | A07 | 29007268 | C | T | splice_region_variant&intron_variant | LOW | c.3004-6G>A| |
S233 |
6 | BAA07g27160 | A07 | 29007767 | C | T | synonymous_variant | LOW | c.2670G>A|p.Lys890Lys |
S168 |
7 | BAA07g27160 | A07 | 29009970 | C | T | missense_variant | MODERATE | c.1636G>A|p.Glu546Lys |
S270 |
8 | BAA07g27160 | A07 | 29011597 | C | T | missense_variant | MODERATE | c.969G>A|p.Met323Ile |
S274 |
9 | BAA07g27160 | A07 | 29012078 | G | A | missense_variant | MODERATE | c.644C>T|p.Pro215Leu |
S187 |
10 | BAA07g27160 | A07 | 29012865 | C | T | synonymous_variant | LOW | c.231G>A|p.Thr77Thr |
S177 |
11 | BAA07g27160 | A07 | 29014299 | G | A | upstream_gene_variant | MODIFIER | c.-1204C>T| |
S70 |
12 | BAA07g27160 | A07 | 29016879 | C | T | upstream_gene_variant | MODIFIER | c.-3784G>A| |
S230 |