Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19380 | A09 | 11794871 | C | T | downstream_gene_variant | MODIFIER | c.*2475G>A| |
S134 |
2 | BAA09g19380 | A09 | 11794955 | G | A | downstream_gene_variant | MODIFIER | c.*2391C>T| |
S274 |
3 | BAA09g19380 | A09 | 11795655 | G | A | downstream_gene_variant | MODIFIER | c.*1691C>T| |
S79 S91 |
4 | BAA09g19380 | A09 | 11795831 | G | A | downstream_gene_variant | MODIFIER | c.*1515C>T| |
S34 |
5 | BAA09g19380 | A09 | 11796382 | G | A | downstream_gene_variant | MODIFIER | c.*964C>T| |
S240 |
6 | BAA09g19380 | A09 | 11796982 | G | A | downstream_gene_variant | MODIFIER | c.*364C>T| |
S75 S81 |
7 | BAA09g19380 | A09 | 11797069 | G | A | downstream_gene_variant | MODIFIER | c.*277C>T| |
S201 |
8 | BAA09g19380 | A09 | 11797456 | G | A | missense_variant | MODERATE | c.976C>T|p.Leu326Phe |
S201 |
9 | BAA09g19380 | A09 | 11797647 | G | A | missense_variant | MODERATE | c.785C>T|p.Thr262Ile |
S203 |
10 | BAA09g19380 | A09 | 11798029 | C | T | missense_variant | MODERATE | c.403G>A|p.Gly135Arg |
S37 |
11 | BAA09g19380 | A09 | 11798035 | G | A | synonymous_variant | LOW | c.397C>T|p.Leu133Leu |
S182 |
12 | BAA09g19380 | A09 | 11798050 | C | T | missense_variant | MODERATE | c.382G>A|p.Glu128Lys |
S63 |
13 | BAA09g19380 | A09 | 11799834 | G | A | upstream_gene_variant | MODIFIER | c.-1403C>T| |
S267 |
14 | BAA09g19380 | A09 | 11800121 | G | A | upstream_gene_variant | MODIFIER | c.-1690C>T| |
S59 |
15 | BAA09g19380 | A09 | 11801397 | G | A | upstream_gene_variant | MODIFIER | c.-2966C>T| |
S23 |
16 | BAA09g19380 | A09 | 11801612 | C | T | upstream_gene_variant | MODIFIER | c.-3181G>A| |
S302 |
17 | BAA09g19380 | A09 | 11802618 | C | T | upstream_gene_variant | MODIFIER | c.-4187G>A| |
S6 |