Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40290 | A02 | 34007666 | C | T | upstream_gene_variant | MODIFIER | c.-4756C>T| |
S13 |
2 | BAA02g40290 | A02 | 34009183 | G | A | upstream_gene_variant | MODIFIER | c.-3239G>A| |
S103 |
3 | BAA02g40290 | A02 | 34010903 | C | T | upstream_gene_variant | MODIFIER | c.-1519C>T| |
S92 |
4 | BAA02g40290 | A02 | 34010981 | C | T | upstream_gene_variant | MODIFIER | c.-1441C>T| |
S133 |
5 | BAA02g40290 | A02 | 34012262 | C | T | upstream_gene_variant | MODIFIER | c.-160C>T| |
S157 S163 |
6 | BAA02g40290 | A02 | 34012707 | C | T | missense_variant | MODERATE | c.169C>T|p.Pro57Ser |
S46 |
7 | BAA02g40290 | A02 | 34012908 | G | A | missense_variant | MODERATE | c.281G>A|p.Gly94Glu |
S225 S73 |
8 | BAA02g40290 | A02 | 34013341 | G | A | missense_variant | MODERATE | c.472G>A|p.Gly158Ser |
S103 |
9 | BAA02g40290 | A02 | 34013450 | C | T | missense_variant | MODERATE | c.517C>T|p.Pro173Ser |
S66 |
10 | BAA02g40290 | A02 | 34014929 | C | T | missense_variant | MODERATE | c.1355C>T|p.Ala452Val |
S39 |
11 | BAA02g40290 | A02 | 34015045 | G | A | missense_variant | MODERATE | c.1471G>A|p.Asp491Asn |
S126 |
12 | BAA02g40290 | A02 | 34015123 | G | A | missense_variant&splice_region_variant | MODERATE | c.1549G>A|p.Glu517Lys |
S70 |
13 | BAA02g40290 | A02 | 34015222 | G | A | missense_variant | MODERATE | c.1567G>A|p.Glu523Lys |
S132 S137 S138 S215 S288 S89 |
14 | BAA02g40290 | A02 | 34015332 | C | T | synonymous_variant | LOW | c.1677C>T|p.Pro559Pro |
S42 |
15 | BAA02g40290 | A02 | 34016024 | C | T | downstream_gene_variant | MODIFIER | c.*241C>T| |
S202 |
16 | BAA02g40290 | A02 | 34017302 | G | A | downstream_gene_variant | MODIFIER | c.*1519G>A| |
S238 |