Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g03200 | A08 | 2225313 | C | T | missense_variant | MODERATE | c.185C>T|p.Ser62Phe |
S66 |
2 | BAA08g03200 | A08 | 2225518 | G | A | synonymous_variant | LOW | c.390G>A|p.Lys130Lys |
S262 |
3 | BAA08g03200 | A08 | 2225545 | G | A | synonymous_variant | LOW | c.417G>A|p.Glu139Glu |
S100 |
4 | BAA08g03200 | A08 | 2225714 | G | A | missense_variant | MODERATE | c.514G>A|p.Asp172Asn |
S75 S81 |
5 | BAA08g03200 | A08 | 2226141 | G | A | synonymous_variant | LOW | c.786G>A|p.Glu262Glu |
S286 |
6 | BAA08g03200 | A08 | 2229934 | C | T | intron_variant | MODIFIER | c.1611+155C>T| |
S295 |
7 | BAA08g03200 | A08 | 2230495 | T | C | missense_variant | MODERATE | c.1829T>C|p.Leu610Ser |
S292 |
8 | BAA08g03200 | A08 | 2231480 | C | T | missense_variant | MODERATE | c.2366C>T|p.Ala789Val |
S189 |
9 | BAA08g03200 | A08 | 2232740 | C | T | downstream_gene_variant | MODIFIER | c.*191C>T| |
S12 |
10 | BAA08g03200 | A08 | 2233076 | C | T | downstream_gene_variant | MODIFIER | c.*527C>T| |
S243 S299 |
11 | BAA08g03200 | A08 | 2234312 | G | A | downstream_gene_variant | MODIFIER | c.*1763G>A| |
S65 |
12 | BAA08g03200 | A08 | 2234770 | G | A | downstream_gene_variant | MODIFIER | c.*2221G>A| |
S68 |
13 | BAA08g03200 | A08 | 2235001 | G | A | downstream_gene_variant | MODIFIER | c.*2452G>A| |
S192 |
14 | BAA08g03200 | A08 | 2236008 | G | A | downstream_gene_variant | MODIFIER | c.*3459G>A| |
S139 |
15 | BAA08g03200 | A08 | 2236709 | G | A | downstream_gene_variant | MODIFIER | c.*4160G>A| |
S174 |
16 | BAA08g03200 | A08 | 2237292 | G | A | downstream_gene_variant | MODIFIER | c.*4743G>A| |
S16 |
17 | BAA08g03200 | A08 | 2237416 | C | T | downstream_gene_variant | MODIFIER | c.*4867C>T| |
S104 S52 |