Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39330 | A01 | 26110792 | G | A | upstream_gene_variant | MODIFIER | c.-4394G>A| |
S121 |
2 | BAA01g39330 | A01 | 26110894 | G | A | upstream_gene_variant | MODIFIER | c.-4292G>A| |
S116 |
3 | BAA01g39330 | A01 | 26111285 | G | A | upstream_gene_variant | MODIFIER | c.-3901G>A| |
S163 |
4 | BAA01g39330 | A01 | 26111883 | G | A | upstream_gene_variant | MODIFIER | c.-3303G>A| |
S123 |
5 | BAA01g39330 | A01 | 26112223 | G | A | upstream_gene_variant | MODIFIER | c.-2963G>A| |
S110 |
6 | BAA01g39330 | A01 | 26112855 | G | A | upstream_gene_variant | MODIFIER | c.-2331G>A| |
S51 |
7 | BAA01g39330 | A01 | 26116606 | G | A | missense_variant | MODERATE | c.610G>A|p.Glu204Lys |
S284 |
8 | BAA01g39330 | A01 | 26116689 | C | T | synonymous_variant | LOW | c.693C>T|p.Ser231Ser |
S107 |
9 | BAA01g39330 | A01 | 26116740 | C | T | synonymous_variant | LOW | c.744C>T|p.Ile248Ile |
S213 |
10 | BAA01g39330 | A01 | 26117585 | C | T | missense_variant | MODERATE | c.991C>T|p.Leu331Phe |
S77 S82 |
11 | BAA01g39330 | A01 | 26117730 | G | A | downstream_gene_variant | MODIFIER | c.*11G>A| |
S6 |
12 | BAA01g39330 | A01 | 26118567 | G | A | downstream_gene_variant | MODIFIER | c.*848G>A| |
S95 |
13 | BAA01g39330 | A01 | 26118741 | C | T | downstream_gene_variant | MODIFIER | c.*1022C>T| |
S264 |
14 | BAA01g39330 | A01 | 26119624 | C | T | downstream_gene_variant | MODIFIER | c.*1905C>T| |
S292 |
15 | BAA01g39330 | A01 | 26121727 | G | A | downstream_gene_variant | MODIFIER | c.*4008G>A| |
S189 |