Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g32480 | A01 | 21425117 | C | T | upstream_gene_variant | MODIFIER | c.-4855C>T| |
S20 |
2 | BAA01g32480 | A01 | 21425318 | C | T | upstream_gene_variant | MODIFIER | c.-4654C>T| |
S9 |
3 | BAA01g32480 | A01 | 21425566 | C | T | upstream_gene_variant | MODIFIER | c.-4406C>T| |
S251 |
4 | BAA01g32480 | A01 | 21426011 | C | T | upstream_gene_variant | MODIFIER | c.-3961C>T| |
S136 |
5 | BAA01g32480 | A01 | 21426349 | C | T | upstream_gene_variant | MODIFIER | c.-3623C>T| |
S23 |
6 | BAA01g32480 | A01 | 21428901 | G | A | upstream_gene_variant | MODIFIER | c.-1071G>A| |
S197 |
7 | BAA01g32480 | A01 | 21429147 | C | T | upstream_gene_variant | MODIFIER | c.-825C>T| |
S69 |
8 | BAA01g32480 | A01 | 21431117 | C | T | intron_variant | MODIFIER | c.250-267C>T| |
S239 |
9 | BAA01g32480 | A01 | 21432715 | C | T | missense_variant | MODERATE | c.611C>T|p.Thr204Ile |
S139 |
10 | BAA01g32480 | A01 | 21433307 | G | A | missense_variant | MODERATE | c.980G>A|p.Gly327Asp |
S218 |
11 | BAA01g32480 | A01 | 21435617 | C | T | missense_variant | MODERATE | c.2345C>T|p.Ser782Leu |
S69 |
12 | BAA01g32480 | A01 | 21436249 | C | T | downstream_gene_variant | MODIFIER | c.*622C>T| |
S150 |