Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00770 | A05 | 438174 | A | G | upstream_gene_variant | MODIFIER | c.-1586A>G| |
S120 |
2 | BAA05g00770 | A05 | 438313 | C | T | upstream_gene_variant | MODIFIER | c.-1447C>T| |
S96 |
3 | BAA05g00770 | A05 | 438794 | G | A | upstream_gene_variant | MODIFIER | c.-966G>A| |
S280 |
4 | BAA05g00770 | A05 | 438895 | G | A | upstream_gene_variant | MODIFIER | c.-865G>A| |
S158 |
5 | BAA05g00770 | A05 | 438905 | G | A | upstream_gene_variant | MODIFIER | c.-855G>A| |
S11 |
6 | BAA05g00770 | A05 | 439077 | C | T | upstream_gene_variant | MODIFIER | c.-683C>T| |
S247 |
7 | BAA05g00770 | A05 | 439272 | C | T | upstream_gene_variant | MODIFIER | c.-488C>T| |
S41 |
8 | BAA05g00770 | A05 | 441450 | C | T | missense_variant | MODERATE | c.1150C>T|p.Pro384Ser |
S136 |
9 | BAA05g00770 | A05 | 442655 | G | A | downstream_gene_variant | MODIFIER | c.*342G>A| |
S45 |
10 | BAA05g00770 | A05 | 442859 | C | T | downstream_gene_variant | MODIFIER | c.*546C>T| |
S120 |
11 | BAA05g00770 | A05 | 442970 | G | A | downstream_gene_variant | MODIFIER | c.*657G>A| |
S62 |
12 | BAA05g00770 | A05 | 443042 | C | T | downstream_gene_variant | MODIFIER | c.*729C>T| |
S10 |
13 | BAA05g00770 | A05 | 444024 | C | T | downstream_gene_variant | MODIFIER | c.*1711C>T| |
S171 |
14 | BAA05g00770 | A05 | 444250 | G | A | downstream_gene_variant | MODIFIER | c.*1937G>A| |
S233 |
15 | BAA05g00770 | A05 | 445624 | C | T | downstream_gene_variant | MODIFIER | c.*3311C>T| |
S37 |