Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37900 | A02 | 32413332 | G | A | missense_variant | MODERATE | c.148G>A|p.Glu50Lys |
S228 |
2 | BAA02g37900 | A02 | 32413869 | C | T | intron_variant | MODIFIER | c.160-439C>T| |
S128 |
3 | BAA02g37900 | A02 | 32413967 | C | T | intron_variant | MODIFIER | c.160-341C>T| |
S183 S198 |
4 | BAA02g37900 | A02 | 32414113 | G | A | intron_variant | MODIFIER | c.160-195G>A| |
S127 |
5 | BAA02g37900 | A02 | 32414153 | G | A | intron_variant | MODIFIER | c.160-155G>A| |
S175 |
6 | BAA02g37900 | A02 | 32414535 | C | T | synonymous_variant | LOW | c.387C>T|p.Ile129Ile |
S226 |
7 | BAA02g37900 | A02 | 32414734 | C | T | missense_variant | MODERATE | c.521C>T|p.Thr174Ile |
S77 |
8 | BAA02g37900 | A02 | 32414967 | G | A | missense_variant | MODERATE | c.754G>A|p.Glu252Lys |
S229 |
9 | BAA02g37900 | A02 | 32415085 | G | A | downstream_gene_variant | MODIFIER | c.*53G>A| |
S136 |
10 | BAA02g37900 | A02 | 32415136 | C | T | downstream_gene_variant | MODIFIER | c.*104C>T| |
S308 |
11 | BAA02g37900 | A02 | 32415812 | C | T | downstream_gene_variant | MODIFIER | c.*780C>T| |
S242 |
12 | BAA02g37900 | A02 | 32416364 | G | A | downstream_gene_variant | MODIFIER | c.*1332G>A| |
S94 |
13 | BAA02g37900 | A02 | 32416502 | C | T | downstream_gene_variant | MODIFIER | c.*1470C>T| |
S183 S198 |
14 | BAA02g37900 | A02 | 32416782 | G | A | downstream_gene_variant | MODIFIER | c.*1750G>A| |
S302 |
15 | BAA02g37900 | A02 | 32419646 | G | A | downstream_gene_variant | MODIFIER | c.*4614G>A| |
S4 |
16 | BAA02g37900 | A02 | 32419678 | C | T | downstream_gene_variant | MODIFIER | c.*4646C>T| |
S157 S163 |