| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 66701 | BAA01g34930 | A01 | 23350544 | T | A | upstream_gene_variant | MODIFIER | c.-4222T>A| |
S166 |
| 66702 | BAA01g34930 | A01 | 23351278 | C | T | upstream_gene_variant | MODIFIER | c.-3488C>T| |
S130 |
| 66703 | BAA01g34930 | A01 | 23351643 | C | T | upstream_gene_variant | MODIFIER | c.-3123C>T| |
S18 |
| 66704 | BAA01g34930 | A01 | 23351876 | G | A | upstream_gene_variant | MODIFIER | c.-2890G>A| |
S62 |
| 66705 | BAA01g34930 | A01 | 23352035 | C | T | upstream_gene_variant | MODIFIER | c.-2731C>T| |
S206 S26 |
| 66706 | BAA01g34930 | A01 | 23352665 | C | T | upstream_gene_variant | MODIFIER | c.-2101C>T| |
S11 |
| 66707 | BAA01g34930 | A01 | 23353124 | C | T | upstream_gene_variant | MODIFIER | c.-1642C>T| |
S204 |
| 66708 | BAA01g34920 | A01 | 23353928 | C | T | upstream_gene_variant | MODIFIER | c.-111G>A| |
S133 |
| 66709 | BAA01g34920 | A01 | 23354319 | C | T | upstream_gene_variant | MODIFIER | c.-502G>A| |
S183 S198 |
| 66710 | BAA01g34920 | A01 | 23354369 | C | T | upstream_gene_variant | MODIFIER | c.-552G>A| |
S108 S203 |
| 66711 | BAA01g34920 | A01 | 23354542 | C | T | upstream_gene_variant | MODIFIER | c.-725G>A| |
S50 |
| 66712 | BAA01g34930 | A01 | 23354947 | G | A | missense_variant | MODERATE | c.182G>A|p.Arg61Lys |
S76 |
| 66713 | BAA01g34930 | A01 | 23355092 | G | A | synonymous_variant | LOW | c.327G>A|p.Lys109Lys |
S135 |
| 66714 | BAA01g34930 | A01 | 23355318 | C | T | synonymous_variant | LOW | c.553C>T|p.Leu185Leu |
S48 |
| 66715 | BAA01g34930 | A01 | 23355374 | C | T | synonymous_variant | LOW | c.609C>T|p.Val203Val |
S50 |
| 66716 | BAA01g34930 | A01 | 23355840 | C | T | missense_variant | MODERATE | c.1075C>T|p.Leu359Phe |
S193 |
| 66717 | BAA01g34930 | A01 | 23355929 | C | T | synonymous_variant | LOW | c.1164C>T|p.Val388Val |
S272 |
| 66718 | BAA01g34930 | A01 | 23356246 | G | A | missense_variant | MODERATE | c.1400G>A|p.Arg467Gln |
S38 |
| 66719 | BAA01g34920 | A01 | 23356528 | G | A | upstream_gene_variant | MODIFIER | c.-2711C>T| |
S278 |
| 66720 | BAA01g34920 | A01 | 23357192 | C | T | upstream_gene_variant | MODIFIER | c.-3375G>A| |
S303 |
| 66721 | BAA01g34920 | A01 | 23357222 | C | T | upstream_gene_variant | MODIFIER | c.-3405G>A| |
S216 |
| 66722 | BAA01g34920 | A01 | 23358156 | C | T | upstream_gene_variant | MODIFIER | c.-4339G>A| |
S179 |
| 66723 | BAA01g34920 | A01 | 23358231 | G | A | upstream_gene_variant | MODIFIER | c.-4414C>T| |
S79 S91 |
| 66724 | BAA01g34920 | A01 | 23358666 | C | T | upstream_gene_variant | MODIFIER | c.-4849G>A| |
S215 |
| 66725 | BAA01g34940 | A01 | 23359397 | G | A | splice_region_variant&intron_variant | LOW | c.309+5G>A| |
S95 |