| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 44001 | BAA01g26800 | A01 | 15099026 | C | T | intron_variant | MODIFIER | c.426+140G>A| |
S192 |
| 44002 | BAA01g26800 | A01 | 15102186 | G | A | upstream_gene_variant | MODIFIER | c.-1532C>T| |
S6 |
| 44003 | BAA01g26810 | A01 | 15105445 | C | T | synonymous_variant | LOW | c.693G>A|p.Lys231Lys |
S4 |
| 44004 | BAA01g26810 | A01 | 15105588 | C | T | missense_variant | MODERATE | c.623G>A|p.Gly208Glu |
S256 |
| 44005 | BAA01g26820 | A01 | 15105882 | G | A | upstream_gene_variant | MODIFIER | c.-2592G>A| |
S262 |
| 44006 | BAA01g26820 | A01 | 15106010 | G | A | upstream_gene_variant | MODIFIER | c.-2464G>A| |
S181 |
| 44007 | BAA01g26810 | A01 | 15106319 | C | T | missense_variant&splice_region_variant | MODERATE | c.316G>A|p.Asp106Asn |
S25 |
| 44008 | BAA01g26820 | A01 | 15108581 | C | T | synonymous_variant | LOW | c.108C>T|p.Ile36Ile |
S295 |
| 44009 | BAA01g26820 | A01 | 15109346 | G | A | synonymous_variant | LOW | c.705G>A|p.Gln235Gln |
S70 |
| 44010 | BAA01g26810 | A01 | 15110681 | C | T | upstream_gene_variant | MODIFIER | c.-3889G>A| |
S150 |
| 44011 | BAA01g26810 | A01 | 15110694 | C | T | upstream_gene_variant | MODIFIER | c.-3902G>A| |
S155 S211 |
| 44012 | BAA01g26810 | A01 | 15110901 | G | A | upstream_gene_variant | MODIFIER | c.-4109C>T| |
S76 |
| 44013 | BAA01g26810 | A01 | 15111184 | G | A | upstream_gene_variant | MODIFIER | c.-4392C>T| |
S165 |
| 44014 | BAA01g26830 | A01 | 15111877 | C | T | upstream_gene_variant | MODIFIER | c.-3791C>T| |
S67 |
| 44015 | BAA01g26830 | A01 | 15112631 | G | A | upstream_gene_variant | MODIFIER | c.-3037G>A| |
S174 S27 |
| 44016 | BAA01g26830 | A01 | 15112871 | C | T | upstream_gene_variant | MODIFIER | c.-2797C>T| |
S109 |
| 44017 | BAA01g26830 | A01 | 15113631 | C | T | upstream_gene_variant | MODIFIER | c.-2037C>T| |
S48 |
| 44018 | BAA01g26830 | A01 | 15113995 | G | A | upstream_gene_variant | MODIFIER | c.-1673G>A| |
S86 |
| 44019 | BAA01g26830 | A01 | 15114008 | C | T | upstream_gene_variant | MODIFIER | c.-1660C>T| |
S166 |
| 44020 | BAA01g26830 | A01 | 15114703 | G | A | upstream_gene_variant | MODIFIER | c.-965G>A| |
S276 |
| 44021 | BAA01g26830 | A01 | 15115204 | C | T | upstream_gene_variant | MODIFIER | c.-464C>T| |
S295 |
| 44022 | BAA01g26830 | A01 | 15115851 | G | A | intron_variant | MODIFIER | c.78-83G>A| |
S225 S73 |
| 44023 | BAA01g26830 | A01 | 15116368 | G | A | downstream_gene_variant | MODIFIER | c.*75G>A| |
S236 |
| 44024 | BAA01g26830 | A01 | 15116683 | G | A | downstream_gene_variant | MODIFIER | c.*390G>A| |
S138 |
| 44025 | BAA01g26830 | A01 | 15118458 | C | T | downstream_gene_variant | MODIFIER | c.*2165C>T| |
S69 |