Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g14660 | A01 | 6981219 | G | A | upstream_gene_variant | MODIFIER | c.-4842G>A| |
S186 |
2 | BAA01g14660 | A01 | 6983693 | G | A | upstream_gene_variant | MODIFIER | c.-2368G>A| |
S108 |
3 | BAA01g14660 | A01 | 6983782 | C | T | upstream_gene_variant | MODIFIER | c.-2279C>T| |
S70 |
4 | BAA01g14660 | A01 | 6983854 | G | A | upstream_gene_variant | MODIFIER | c.-2207G>A| |
S139 |
5 | BAA01g14660 | A01 | 6984152 | G | A | upstream_gene_variant | MODIFIER | c.-1909G>A| |
S204 |
6 | BAA01g14660 | A01 | 6984257 | G | A | upstream_gene_variant | MODIFIER | c.-1804G>A| |
S175 |
7 | BAA01g14660 | A01 | 6985064 | T | G | upstream_gene_variant | MODIFIER | c.-997T>G| |
S121 |
8 | BAA01g14660 | A01 | 6985853 | G | A | upstream_gene_variant | MODIFIER | c.-208G>A| |
S202 |
9 | BAA01g14660 | A01 | 6986107 | C | T | missense_variant | MODERATE | c.47C>T|p.Thr16Ile |
S242 |
10 | BAA01g14660 | A01 | 6986824 | C | T | missense_variant | MODERATE | c.764C>T|p.Pro255Leu |
S61 |
11 | BAA01g14660 | A01 | 6986896 | C | T | missense_variant | MODERATE | c.836C>T|p.Pro279Leu |
S153 |
12 | BAA01g14660 | A01 | 6987355 | G | A | downstream_gene_variant | MODIFIER | c.*314G>A| |
S140 |