Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g02030 | A04 | 1185080 | C | T | upstream_gene_variant | MODIFIER | c.-2664C>T| |
S146 |
2 | BAA04g02030 | A04 | 1186432 | G | A | upstream_gene_variant | MODIFIER | c.-1312G>A| |
S211 S227 |
3 | BAA04g02030 | A04 | 1186789 | C | T | upstream_gene_variant | MODIFIER | c.-955C>T| |
S241 |
4 | BAA04g02030 | A04 | 1186798 | C | T | upstream_gene_variant | MODIFIER | c.-946C>T| |
S46 |
5 | BAA04g02030 | A04 | 1186862 | C | T | upstream_gene_variant | MODIFIER | c.-882C>T| |
S70 |
6 | BAA04g02030 | A04 | 1187336 | C | T | upstream_gene_variant | MODIFIER | c.-408C>T| |
S76 |
7 | BAA04g02030 | A04 | 1187886 | G | A | missense_variant | MODERATE | c.143G>A|p.Gly48Asp |
S112 |
8 | BAA04g02030 | A04 | 1189745 | G | A | missense_variant | MODERATE | c.1208G>A|p.Arg403Lys |
S103 |
9 | BAA04g02030 | A04 | 1189754 | T | C | missense_variant | MODERATE | c.1217T>C|p.Leu406Pro |
S211 S227 |
10 | BAA04g02030 | A04 | 1189871 | C | T | missense_variant | MODERATE | c.1334C>T|p.Ala445Val |
S209 |
11 | BAA04g02030 | A04 | 1192944 | C | T | downstream_gene_variant | MODIFIER | c.*3027C>T| |
S11 |