Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g03060 | A04 | 1842412 | C | T | upstream_gene_variant | MODIFIER | c.-3602C>T| |
S283 |
2 | BAA04g03060 | A04 | 1843096 | C | T | upstream_gene_variant | MODIFIER | c.-2918C>T| |
S144 |
3 | BAA04g03060 | A04 | 1843150 | C | T | upstream_gene_variant | MODIFIER | c.-2864C>T| |
S178 |
4 | BAA04g03060 | A04 | 1843178 | C | T | upstream_gene_variant | MODIFIER | c.-2836C>T| |
S134 |
5 | BAA04g03060 | A04 | 1845299 | C | T | upstream_gene_variant | MODIFIER | c.-715C>T| |
S48 |
6 | BAA04g03060 | A04 | 1845956 | G | A | upstream_gene_variant | MODIFIER | c.-58G>A| |
S13 |
7 | BAA04g03060 | A04 | 1846099 | C | T | missense_variant | MODERATE | c.86C>T|p.Pro29Leu |
S134 |
8 | BAA04g03060 | A04 | 1846231 | C | T | missense_variant | MODERATE | c.218C>T|p.Ser73Phe |
S208 S93 |
9 | BAA04g03060 | A04 | 1846434 | C | T | missense_variant | MODERATE | c.421C>T|p.Arg141Cys |
S115 |
10 | BAA04g03060 | A04 | 1846447 | G | A | missense_variant | MODERATE | c.434G>A|p.Arg145Gln |
S190 |
11 | BAA04g03060 | A04 | 1846624 | G | A | missense_variant | MODERATE | c.611G>A|p.Gly204Glu |
S66 |
12 | BAA04g03060 | A04 | 1846778 | C | T | synonymous_variant | LOW | c.765C>T|p.Ala255Ala |
S157 S163 |
13 | BAA04g03060 | A04 | 1847306 | C | T | downstream_gene_variant | MODIFIER | c.*258C>T| |
S250 |
14 | BAA04g03060 | A04 | 1847840 | C | T | downstream_gene_variant | MODIFIER | c.*792C>T| |
S134 |
15 | BAA04g03060 | A04 | 1848624 | G | A | downstream_gene_variant | MODIFIER | c.*1576G>A| |
S131 |