| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 83651 | BAA01g44360 | A01 | 29474809 | C | T | upstream_gene_variant | MODIFIER | c.-2363G>A| |
S219 S72 |
| 83652 | BAA01g44360 | A01 | 29474901 | C | T | upstream_gene_variant | MODIFIER | c.-2455G>A| |
S225 S73 |
| 83653 | BAA01g44360 | A01 | 29475046 | C | T | upstream_gene_variant | MODIFIER | c.-2600G>A| |
S46 |
| 83654 | BAA01g44360 | A01 | 29475173 | C | T | upstream_gene_variant | MODIFIER | c.-2727G>A| |
S40 S49 |
| 83655 | BAA01g44360 | A01 | 29475455 | C | T | upstream_gene_variant | MODIFIER | c.-3009G>A| |
S301 S304 |
| 83656 | BAA01g44360 | A01 | 29475971 | T | C | upstream_gene_variant | MODIFIER | c.-3525A>G| |
S70 |
| 83657 | BAA01g44370 | A01 | 29477914 | G | A | downstream_gene_variant | MODIFIER | c.*1993C>T| |
S252 |
| 83658 | BAA01g44370 | A01 | 29478939 | G | A | downstream_gene_variant | MODIFIER | c.*968C>T| |
S176 |
| 83659 | BAA01g44370 | A01 | 29480945 | C | T | intron_variant | MODIFIER | c.284+74G>A| |
S200 |
| 83660 | BAA01g44370 | A01 | 29481711 | C | T | intron_variant | MODIFIER | c.154+194G>A| |
S15 S156 S3 S34 |
| 83661 | BAA01g44370 | A01 | 29482292 | G | A | upstream_gene_variant | MODIFIER | c.-234C>T| |
S123 |
| 83662 | BAA01g44370 | A01 | 29482556 | G | A | upstream_gene_variant | MODIFIER | c.-498C>T| |
S53 |
| 83663 | BAA01g44370 | A01 | 29484393 | C | T | upstream_gene_variant | MODIFIER | c.-2335G>A| |
S17 |
| 83664 | BAA01g44370 | A01 | 29486104 | G | A | upstream_gene_variant | MODIFIER | c.-4046C>T| |
S268 |
| 83665 | BAA01g44370 | A01 | 29486554 | C | T | upstream_gene_variant | MODIFIER | c.-4496G>A| |
S270 |
| 83666 | BAA01g44370 | A01 | 29486793 | G | A | upstream_gene_variant | MODIFIER | c.-4735C>T| |
S144 |
| 83667 | BAA01g44380 | A01 | 29488640 | G | A | downstream_gene_variant | MODIFIER | c.*2752C>T| |
S284 |
| 83668 | BAA01g44380 | A01 | 29489868 | C | T | downstream_gene_variant | MODIFIER | c.*1524G>A| |
S12 |
| 83669 | BAA01g44380 | A01 | 29491179 | C | T | downstream_gene_variant | MODIFIER | c.*213G>A| |
S18 |
| 83670 | BAA01g44380 | A01 | 29491212 | G | A | downstream_gene_variant | MODIFIER | c.*180C>T| |
S114 |
| 83671 | BAA01g44380 | A01 | 29491407 | C | G | missense_variant | MODERATE | c.801G>C|p.Met267Ile |
S115 |
| 83672 | BAA01g44380 | A01 | 29491459 | G | A | missense_variant | MODERATE | c.749C>T|p.Ala250Val |
S139 |
| 83673 | BAA01g44380 | A01 | 29491464 | G | A | synonymous_variant | LOW | c.744C>T|p.Leu248Leu |
S10 |
| 83674 | BAA01g44380 | A01 | 29491507 | C | T | missense_variant | MODERATE | c.701G>A|p.Gly234Glu |
S256 |
| 83675 | BAA01g44380 | A01 | 29492972 | C | T | upstream_gene_variant | MODIFIER | c.-765G>A| |
S210 S225 |