Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g25490 | A08 | 18363132 | C | T | upstream_gene_variant | MODIFIER | c.-4027C>T| |
S186 |
2 | BAA08g25490 | A08 | 18364220 | G | A | upstream_gene_variant | MODIFIER | c.-2939G>A| |
S100 |
3 | BAA08g25490 | A08 | 18364255 | C | T | upstream_gene_variant | MODIFIER | c.-2904C>T| |
S166 |
4 | BAA08g25490 | A08 | 18366754 | C | T | upstream_gene_variant | MODIFIER | c.-405C>T| |
S2 |
5 | BAA08g25490 | A08 | 18367024 | G | A | upstream_gene_variant | MODIFIER | c.-135G>A| |
S32 |
6 | BAA08g25490 | A08 | 18367383 | C | T | stop_gained | HIGH | c.10C>T|p.Arg4* |
S2 |
7 | BAA08g25490 | A08 | 18367395 | C | T | missense_variant | MODERATE | c.22C>T|p.Pro8Ser |
S38 |
8 | BAA08g25490 | A08 | 18367463 | G | A | synonymous_variant | LOW | c.90G>A|p.Glu30Glu |
S289 S290 |
9 | BAA08g25490 | A08 | 18368565 | G | A | missense_variant | MODERATE | c.820G>A|p.Ala274Thr |
S264 |
10 | BAA08g25490 | A08 | 18368769 | C | T | missense_variant | MODERATE | c.1024C>T|p.Arg342Cys |
S105 S106 |
11 | BAA08g25490 | A08 | 18369328 | C | T | missense_variant | MODERATE | c.1409C>T|p.Ser470Phe |
S63 |
12 | BAA08g25490 | A08 | 18369711 | C | T | missense_variant | MODERATE | c.1792C>T|p.Leu598Phe |
S181 |
13 | BAA08g25490 | A08 | 18370254 | G | A | missense_variant | MODERATE | c.2335G>A|p.Gly779Arg |
S175 |
14 | BAA08g25490 | A08 | 18370807 | C | T | missense_variant | MODERATE | c.2888C>T|p.Pro963Leu |
S296 |
15 | BAA08g25490 | A08 | 18370921 | C | T | missense_variant | MODERATE | c.3002C>T|p.Ser1001Phe |
S173 |
16 | BAA08g25490 | A08 | 18371825 | C | T | synonymous_variant | LOW | c.3717C>T|p.Asp1239Asp |
S236 |
17 | BAA08g25490 | A08 | 18374381 | C | T | downstream_gene_variant | MODIFIER | c.*2550C>T| |
S166 |