Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15980 | A01 | 7783502 | G | A | intron_variant | MODIFIER | c.394+63G>A| |
S293 |
2 | BAA01g15980 | A01 | 7784683 | C | T | synonymous_variant | LOW | c.1170C>T|p.Ile390Ile |
S8 |
3 | BAA01g15980 | A01 | 7784881 | C | T | synonymous_variant | LOW | c.1368C>T|p.Leu456Leu |
S296 |
4 | BAA01g15980 | A01 | 7784955 | C | T | missense_variant | MODERATE | c.1442C>T|p.Ser481Phe |
S221 |
5 | BAA01g15980 | A01 | 7785031 | G | A | missense_variant | MODERATE | c.1518G>A|p.Met506Ile |
S95 |
6 | BAA01g15980 | A01 | 7785910 | C | T | downstream_gene_variant | MODIFIER | c.*369C>T| |
S151 S157 S166 S167 S262 S263 |
7 | BAA01g15980 | A01 | 7786203 | G | A | downstream_gene_variant | MODIFIER | c.*662G>A| |
S165 |
8 | BAA01g15980 | A01 | 7786831 | C | T | downstream_gene_variant | MODIFIER | c.*1290C>T| |
S41 |
9 | BAA01g15980 | A01 | 7786966 | G | A | downstream_gene_variant | MODIFIER | c.*1425G>A| |
S298 |
10 | BAA01g15980 | A01 | 7787545 | C | T | downstream_gene_variant | MODIFIER | c.*2004C>T| |
S265 |
11 | BAA01g15980 | A01 | 7788603 | G | A | downstream_gene_variant | MODIFIER | c.*3062G>A| |
S115 |
12 | BAA01g15980 | A01 | 7788664 | G | A | downstream_gene_variant | MODIFIER | c.*3123G>A| |
S197 |
13 | BAA01g15980 | A01 | 7788837 | G | A | downstream_gene_variant | MODIFIER | c.*3296G>A| |
S149 |
14 | BAA01g15980 | A01 | 7789200 | G | A | downstream_gene_variant | MODIFIER | c.*3659G>A| |
S217 |
15 | BAA01g15980 | A01 | 7789425 | C | T | downstream_gene_variant | MODIFIER | c.*3884C>T| |
S250 |
16 | BAA01g15980 | A01 | 7789764 | C | T | downstream_gene_variant | MODIFIER | c.*4223C>T| |
S148 S30 S31 |