Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45070 | A02 | 37010140 | G | A | splice_region_variant&synonymous_variant | LOW | c.1431C>T|p.Val477Val |
S237 |
2 | BAA02g45070 | A02 | 37010515 | C | T | missense_variant | MODERATE | c.1253G>A|p.Cys418Tyr |
S158 |
3 | BAA02g45070 | A02 | 37010575 | G | A | missense_variant | MODERATE | c.1193C>T|p.Ala398Val |
S134 |
4 | BAA02g45070 | A02 | 37011927 | A | G | missense_variant | MODERATE | c.548T>C|p.Ile183Thr |
S3 |
5 | BAA02g45070 | A02 | 37012151 | G | A | intron_variant | MODIFIER | c.511-187C>T| |
S229 |
6 | BAA02g45070 | A02 | 37013358 | G | A | intron_variant | MODIFIER | c.510+44C>T| |
S13 |
7 | BAA02g45070 | A02 | 37013555 | G | A | intron_variant | MODIFIER | c.390-33C>T| |
S143 |
8 | BAA02g45070 | A02 | 37013694 | C | T | missense_variant | MODERATE | c.325G>A|p.Glu109Lys |
S130 |
9 | BAA02g45070 | A02 | 37014394 | G | A | intron_variant | MODIFIER | c.198-481C>T| |
S261 |
10 | BAA02g45070 | A02 | 37014403 | G | A | intron_variant | MODIFIER | c.198-490C>T| |
S16 |
11 | BAA02g45070 | A02 | 37014558 | C | T | intron_variant | MODIFIER | c.197+363G>A| |
S123 |
12 | BAA02g45070 | A02 | 37014878 | C | T | intron_variant | MODIFIER | c.197+43G>A| |
S119 |
13 | BAA02g45070 | A02 | 37015671 | G | A | upstream_gene_variant | MODIFIER | c.-474C>T| |
S267 |
14 | BAA02g45070 | A02 | 37015849 | T | C | upstream_gene_variant | MODIFIER | c.-652A>G| |
S183 S198 |
15 | BAA02g45070 | A02 | 37017533 | G | A | upstream_gene_variant | MODIFIER | c.-2336C>T| |
S111 |
16 | BAA02g45070 | A02 | 37017572 | G | A | upstream_gene_variant | MODIFIER | c.-2375C>T| |
S146 |
17 | BAA02g45070 | A02 | 37017705 | C | T | upstream_gene_variant | MODIFIER | c.-2508G>A| |
S64 |
18 | BAA02g45070 | A02 | 37019342 | G | A | upstream_gene_variant | MODIFIER | c.-4145C>T| |
S166 |