Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g25630 | A05 | 30410888 | G | A | upstream_gene_variant | MODIFIER | c.-4798G>A| |
S221 |
2 | BAA05g25630 | A05 | 30412872 | C | T | upstream_gene_variant | MODIFIER | c.-2814C>T| |
S94 |
3 | BAA05g25630 | A05 | 30414542 | G | A | upstream_gene_variant | MODIFIER | c.-1144G>A| |
S184 |
4 | BAA05g25630 | A05 | 30415544 | C | T | upstream_gene_variant | MODIFIER | c.-142C>T| |
S140 |
5 | BAA05g25630 | A05 | 30415790 | G | A | synonymous_variant | LOW | c.105G>A|p.Val35Val |
S166 |
6 | BAA05g25630 | A05 | 30416506 | C | T | intron_variant | MODIFIER | c.405-271C>T| |
S195 |
7 | BAA05g25630 | A05 | 30416514 | G | A | intron_variant | MODIFIER | c.405-263G>A| |
S158 |
8 | BAA05g25630 | A05 | 30416840 | C | T | synonymous_variant | LOW | c.468C>T|p.Asp156Asp |
S216 |
9 | BAA05g25630 | A05 | 30417876 | G | A | stop_gained | HIGH | c.1086G>A|p.Trp362* |
S296 |
10 | BAA05g25630 | A05 | 30418198 | C | T | missense_variant | MODERATE | c.1408C>T|p.Leu470Phe |
S148 S30 S31 |
11 | BAA05g25630 | A05 | 30418255 | G | A | missense_variant | MODERATE | c.1465G>A|p.Glu489Lys |
S252 |
12 | BAA05g25630 | A05 | 30418767 | C | T | intron_variant | MODIFIER | c.1601-41C>T| |
S305 |
13 | BAA05g25630 | A05 | 30420084 | G | A | downstream_gene_variant | MODIFIER | c.*1179G>A| |
S124 |
14 | BAA05g25630 | A05 | 30420386 | C | T | downstream_gene_variant | MODIFIER | c.*1481C>T| |
S37 |
15 | BAA05g25630 | A05 | 30420924 | C | T | downstream_gene_variant | MODIFIER | c.*2019C>T| |
S119 |
16 | BAA05g25630 | A05 | 30423099 | G | T | downstream_gene_variant | MODIFIER | c.*4194G>T| |
S131 |
17 | BAA05g25630 | A05 | 30423349 | C | T | downstream_gene_variant | MODIFIER | c.*4444C>T| |
S37 |