Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g41100 | A01 | 27342842 | C | T | upstream_gene_variant | MODIFIER | c.-4880C>T| |
S183 S198 |
2 | BAA01g41100 | A01 | 27342913 | C | T | upstream_gene_variant | MODIFIER | c.-4809C>T| |
S54 |
3 | BAA01g41100 | A01 | 27343383 | G | A | upstream_gene_variant | MODIFIER | c.-4339G>A| |
S243 |
4 | BAA01g41100 | A01 | 27344109 | G | A | upstream_gene_variant | MODIFIER | c.-3613G>A| |
S299 |
5 | BAA01g41100 | A01 | 27344509 | C | T | upstream_gene_variant | MODIFIER | c.-3213C>T| |
S275 |
6 | BAA01g41100 | A01 | 27344835 | C | T | upstream_gene_variant | MODIFIER | c.-2887C>T| |
S4 |
7 | BAA01g41100 | A01 | 27346691 | G | A | upstream_gene_variant | MODIFIER | c.-1031G>A| |
S268 |
8 | BAA01g41100 | A01 | 27347184 | C | T | upstream_gene_variant | MODIFIER | c.-538C>T| |
S48 |
9 | BAA01g41100 | A01 | 27347928 | C | T | synonymous_variant | LOW | c.207C>T|p.Ile69Ile |
S200 |
10 | BAA01g41100 | A01 | 27347947 | G | A | missense_variant | MODERATE | c.226G>A|p.Asp76Asn |
S238 |
11 | BAA01g41100 | A01 | 27348024 | G | A | synonymous_variant | LOW | c.303G>A|p.Glu101Glu |
S139 |
12 | BAA01g41100 | A01 | 27348284 | G | A | missense_variant | MODERATE | c.563G>A|p.Arg188Gln |
S77 S82 |
13 | BAA01g41100 | A01 | 27349253 | G | A | downstream_gene_variant | MODIFIER | c.*950G>A| |
S217 S248 |
14 | BAA01g41100 | A01 | 27351508 | T | C | downstream_gene_variant | MODIFIER | c.*3205T>C| |
S286 |
15 | BAA01g41100 | A01 | 27351875 | G | A | downstream_gene_variant | MODIFIER | c.*3572G>A| |
S86 |
16 | BAA01g41100 | A01 | 27352574 | C | T | downstream_gene_variant | MODIFIER | c.*4271C>T| |
S206 S26 |
17 | BAA01g41100 | A01 | 27353033 | G | A | downstream_gene_variant | MODIFIER | c.*4730G>A| |
S123 |