Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g21780 | A04 | 24456493 | C | T | upstream_gene_variant | MODIFIER | c.-4182C>T| |
S242 |
2 | BAA04g21780 | A04 | 24456916 | C | T | upstream_gene_variant | MODIFIER | c.-3759C>T| |
S242 |
3 | BAA04g21780 | A04 | 24456975 | C | A | upstream_gene_variant | MODIFIER | c.-3700C>A| |
S11 S122 S125 S186 S197 S199 S217 S227 S249 S255 S267 S282 S298 S299 S55 S74 S79 |
4 | BAA04g21780 | A04 | 24457273 | C | T | upstream_gene_variant | MODIFIER | c.-3402C>T| |
S238 |
5 | BAA04g21780 | A04 | 24457814 | G | A | upstream_gene_variant | MODIFIER | c.-2861G>A| |
S18 |
6 | BAA04g21780 | A04 | 24457998 | T | G | upstream_gene_variant | MODIFIER | c.-2677T>G| |
S252 |
7 | BAA04g21780 | A04 | 24459848 | G | A | upstream_gene_variant | MODIFIER | c.-827G>A| |
S88 |
8 | BAA04g21780 | A04 | 24460840 | C | T | missense_variant | MODERATE | c.166C>T|p.Leu56Phe |
S267 |
9 | BAA04g21780 | A04 | 24460844 | C | T | missense_variant | MODERATE | c.170C>T|p.Pro57Leu |
S189 |
10 | BAA04g21780 | A04 | 24461177 | C | T | missense_variant | MODERATE | c.503C>T|p.Ala168Val |
S200 |
11 | BAA04g21780 | A04 | 24461438 | G | A | missense_variant | MODERATE | c.764G>A|p.Arg255Lys |
S218 |
12 | BAA04g21780 | A04 | 24461725 | C | T | missense_variant | MODERATE | c.1051C>T|p.Pro351Ser |
S267 |
13 | BAA04g21780 | A04 | 24461818 | G | A | missense_variant | MODERATE | c.1144G>A|p.Val382Met |
S144 |
14 | BAA04g21780 | A04 | 24466706 | G | A | downstream_gene_variant | MODIFIER | c.*4688G>A| |
S11 |