Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g23080 | A06 | 12999847 | C | A | upstream_gene_variant | MODIFIER | c.-4125C>A| |
S38 |
2 | BAA06g23080 | A06 | 13001200 | G | A | upstream_gene_variant | MODIFIER | c.-2772G>A| |
S8 |
3 | BAA06g23080 | A06 | 13001434 | G | A | upstream_gene_variant | MODIFIER | c.-2538G>A| |
S197 |
4 | BAA06g23080 | A06 | 13001662 | C | T | upstream_gene_variant | MODIFIER | c.-2310C>T| |
S207 |
5 | BAA06g23080 | A06 | 13002309 | G | A | upstream_gene_variant | MODIFIER | c.-1663G>A| |
S160 |
6 | BAA06g23080 | A06 | 13002784 | C | T | upstream_gene_variant | MODIFIER | c.-1188C>T| |
S291 |
7 | BAA06g23080 | A06 | 13003503 | G | A | upstream_gene_variant | MODIFIER | c.-469G>A| |
S104 |
8 | BAA06g23080 | A06 | 13003632 | G | A | upstream_gene_variant | MODIFIER | c.-340G>A| |
S197 |
9 | BAA06g23080 | A06 | 13004080 | C | T | intron_variant | MODIFIER | c.17+92C>T| |
S176 |
10 | BAA06g23080 | A06 | 13004929 | G | A | missense_variant | MODERATE | c.586G>A|p.Asp196Asn |
S53 |
11 | BAA06g23080 | A06 | 13011888 | C | T | downstream_gene_variant | MODIFIER | c.*4501C>T| |
S172 S217 |
12 | BAA06g23080 | A06 | 13011906 | C | T | downstream_gene_variant | MODIFIER | c.*4519C>T| |
S40 S49 |