Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g28290 | A08 | 19706193 | G | A | synonymous_variant | LOW | c.510G>A|p.Val170Val |
S238 S30 S31 |
2 | BAA08g28290 | A08 | 19707071 | C | T | synonymous_variant | LOW | c.1299C>T|p.Cys433Cys |
S156 |
3 | BAA08g28290 | A08 | 19709018 | G | A | stop_gained | HIGH | c.2247G>A|p.Trp749* |
S129 |
4 | BAA08g28290 | A08 | 19710451 | C | T | missense_variant | MODERATE | c.2867C>T|p.Ser956Phe |
S205 |
5 | BAA08g28290 | A08 | 19710526 | C | T | missense_variant | MODERATE | c.2942C>T|p.Ser981Leu |
S268 |
6 | BAA08g28290 | A08 | 19710691 | G | A | missense_variant | MODERATE | c.3107G>A|p.Ser1036Asn |
S11 |
7 | BAA08g28290 | A08 | 19710998 | G | T | synonymous_variant | LOW | c.3414G>T|p.Ala1138Ala |
S173 |
8 | BAA08g28290 | A08 | 19711217 | C | T | synonymous_variant | LOW | c.3633C>T|p.Ser1211Ser |
S162 |
9 | BAA08g28290 | A08 | 19711299 | G | A | missense_variant | MODERATE | c.3715G>A|p.Val1239Ile |
S225 |