Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g14570 | A08 | 12395096 | C | T | synonymous_variant | LOW | c.2688G>A|p.Val896Val |
S268 |
2 | BAA08g14570 | A08 | 12395256 | G | A | missense_variant | MODERATE | c.2528C>T|p.Ala843Val |
S155 S211 |
3 | BAA08g14570 | A08 | 12395282 | C | T | synonymous_variant | LOW | c.2502G>A|p.Arg834Arg |
S171 |
4 | BAA08g14570 | A08 | 12395379 | C | T | missense_variant | MODERATE | c.2405G>A|p.Gly802Glu |
S206 S26 |
5 | BAA08g14570 | A08 | 12395749 | G | A | synonymous_variant | LOW | c.2187C>T|p.Ile729Ile |
S180 |
6 | BAA08g14570 | A08 | 12396243 | G | A | missense_variant | MODERATE | c.1910C>T|p.Ser637Phe |
S64 |
7 | BAA08g14570 | A08 | 12396359 | C | T | missense_variant&splice_region_variant | MODERATE | c.1873G>A|p.Asp625Asn |
S226 |
8 | BAA08g14570 | A08 | 12396466 | C | T | missense_variant | MODERATE | c.1766G>A|p.Cys589Tyr |
S302 |
9 | BAA08g14570 | A08 | 12397275 | G | A | missense_variant | MODERATE | c.1121C>T|p.Ser374Leu |
S87 |
10 | BAA08g14570 | A08 | 12398187 | G | A | synonymous_variant | LOW | c.604C>T|p.Leu202Leu |
S92 |
11 | BAA08g14570 | A08 | 12399316 | G | A | splice_region_variant&synonymous_variant | LOW | c.60C>T|p.Ile20Ile |
S286 |
12 | BAA08g14570 | A08 | 12402939 | C | T | upstream_gene_variant | MODIFIER | c.-3564G>A| |
S208 S219 |
13 | BAA08g14570 | A08 | 12403953 | C | A | upstream_gene_variant | MODIFIER | c.-4578G>T| |
S243 |