| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 70001 | BAA01g36660 | A01 | 24520726 | C | T | upstream_gene_variant | MODIFIER | c.-553G>A| |
S62 |
| 70002 | BAA01g36660 | A01 | 24521936 | G | A | upstream_gene_variant | MODIFIER | c.-1763C>T| |
S276 S298 S299 |
| 70003 | BAA01g36660 | A01 | 24522727 | G | A | upstream_gene_variant | MODIFIER | c.-2554C>T| |
S267 |
| 70004 | BAA01g36660 | A01 | 24523125 | G | A | upstream_gene_variant | MODIFIER | c.-2952C>T| |
S42 |
| 70005 | BAA01g36660 | A01 | 24523714 | C | T | upstream_gene_variant | MODIFIER | c.-3541G>A| |
S88 |
| 70006 | BAA01g36680 | A01 | 24525451 | T | G | upstream_gene_variant | MODIFIER | c.-2967A>C| |
S155 S211 |
| 70007 | BAA01g36690 | A01 | 24526354 | C | T | missense_variant | MODERATE | c.640G>A|p.Glu214Lys |
S272 |
| 70008 | BAA01g36690 | A01 | 24526416 | G | A | missense_variant | MODERATE | c.578C>T|p.Thr193Ile |
S1 S90 |
| 70009 | BAA01g36680 | A01 | 24526470 | G | A | upstream_gene_variant | MODIFIER | c.-3986C>T| |
S38 |
| 70010 | BAA01g36690 | A01 | 24527023 | G | A | splice_region_variant&synonymous_variant | LOW | c.417C>T|p.Ile139Ile |
S84 S93 |
| 70011 | BAA01g36690 | A01 | 24527899 | C | T | upstream_gene_variant | MODIFIER | c.-68G>A| |
S150 |
| 70012 | BAA01g36690 | A01 | 24528104 | C | T | upstream_gene_variant | MODIFIER | c.-273G>A| |
S37 |
| 70013 | BAA01g36690 | A01 | 24531679 | C | T | upstream_gene_variant | MODIFIER | c.-3848G>A| |
S282 |
| 70014 | BAA01g36690 | A01 | 24532263 | G | A | upstream_gene_variant | MODIFIER | c.-4432C>T| |
S157 S163 |
| 70015 | BAA01g36710 | A01 | 24532828 | G | A | missense_variant | MODERATE | c.1265C>T|p.Pro422Leu |
S33 |
| 70016 | BAA01g36710 | A01 | 24533470 | C | T | missense_variant | MODERATE | c.698G>A|p.Gly233Glu |
S255 |
| 70017 | BAA01g36710 | A01 | 24533602 | C | T | missense_variant | MODERATE | c.566G>A|p.Gly189Glu |
S167 |
| 70018 | BAA01g36710 | A01 | 24533930 | C | T | missense_variant | MODERATE | c.238G>A|p.Asp80Asn |
S177 |
| 70019 | BAA01g36710 | A01 | 24534033 | G | A | splice_region_variant&intron_variant | LOW | c.204+7C>T| |
S189 |
| 70020 | BAA01g36710 | A01 | 24534178 | G | A | synonymous_variant | LOW | c.66C>T|p.Ile22Ile |
S259 |
| 70021 | BAA01g36700 | A01 | 24534669 | C | T | upstream_gene_variant | MODIFIER | c.-3050G>A| |
S131 |
| 70022 | BAA01g36700 | A01 | 24535047 | C | T | upstream_gene_variant | MODIFIER | c.-3428G>A| |
S131 |
| 70023 | BAA01g36710 | A01 | 24537972 | C | T | upstream_gene_variant | MODIFIER | c.-3729G>A| |
S107 |
| 70024 | BAA01g36710 | A01 | 24538059 | C | T | upstream_gene_variant | MODIFIER | c.-3816G>A| |
S14 |
| 70025 | BAA01g36720 | A01 | 24538290 | C | T | synonymous_variant | LOW | c.111C>T|p.Asp37Asp |
S170 |