Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21230 | A01 | 10512418 | C | T | downstream_gene_variant | MODIFIER | c.*649G>A| |
S179 |
2 | BAA01g21230 | A01 | 10513446 | G | A | intron_variant | MODIFIER | c.1366-80C>T| |
S37 |
3 | BAA01g21230 | A01 | 10513765 | G | A | synonymous_variant | LOW | c.1320C>T|p.Ser440Ser |
S45 |
4 | BAA01g21230 | A01 | 10515986 | C | T | missense_variant | MODERATE | c.359G>A|p.Arg120Lys |
S215 |
5 | BAA01g21230 | A01 | 10517828 | C | T | upstream_gene_variant | MODIFIER | c.-1295G>A| |
S44 |
6 | BAA01g21230 | A01 | 10517872 | G | A | upstream_gene_variant | MODIFIER | c.-1339C>T| |
S224 |
7 | BAA01g21230 | A01 | 10518726 | G | A | upstream_gene_variant | MODIFIER | c.-2193C>T| |
S302 |
8 | BAA01g21230 | A01 | 10519472 | C | T | upstream_gene_variant | MODIFIER | c.-2939G>A| |
S85 |
9 | BAA01g21230 | A01 | 10519687 | C | T | upstream_gene_variant | MODIFIER | c.-3154G>A| |
S176 |
10 | BAA01g21230 | A01 | 10519906 | C | T | upstream_gene_variant | MODIFIER | c.-3373G>A| |
S69 |
11 | BAA01g21230 | A01 | 10520099 | G | A | upstream_gene_variant | MODIFIER | c.-3566C>T| |
S237 |
12 | BAA01g21230 | A01 | 10520343 | G | C | upstream_gene_variant | MODIFIER | c.-3810C>G| |
S116 S148 S157 S163 S249 S295 S296 S30 S31 S43 S54 |
13 | BAA01g21230 | A01 | 10520507 | G | A | upstream_gene_variant | MODIFIER | c.-3974C>T| |
S188 |
14 | BAA01g21230 | A01 | 10520769 | C | T | upstream_gene_variant | MODIFIER | c.-4236G>A| |
S112 |
15 | BAA01g21230 | A01 | 10521193 | C | T | upstream_gene_variant | MODIFIER | c.-4660G>A| |
S79 S84 |
16 | BAA01g21230 | A01 | 10521388 | G | A | upstream_gene_variant | MODIFIER | c.-4855C>T| |
S262 |
17 | BAA01g21230 | A01 | 10521420 | G | A | upstream_gene_variant | MODIFIER | c.-4887C>T| |
S193 |