| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 152001 | BAA02g00590 | A02 | 321663 | G | A | splice_region_variant&intron_variant | LOW | c.706-8C>T| |
S9 |
| 152002 | BAA02g00590 | A02 | 321907 | C | T | missense_variant | MODERATE | c.532G>A|p.Asp178Asn |
S281 |
| 152003 | BAA02g00590 | A02 | 322901 | C | T | upstream_gene_variant | MODIFIER | c.-463G>A| |
S278 |
| 152004 | BAA02g00590 | A02 | 323085 | C | T | upstream_gene_variant | MODIFIER | c.-647G>A| |
S18 |
| 152005 | BAA02g00590 | A02 | 324833 | C | T | upstream_gene_variant | MODIFIER | c.-2395G>A| |
S38 |
| 152006 | BAA02g00590 | A02 | 326130 | G | A | upstream_gene_variant | MODIFIER | c.-3692C>T| |
S20 |
| 152007 | BAA02g00590 | A02 | 326341 | C | T | upstream_gene_variant | MODIFIER | c.-3903G>A| |
S243 S299 |
| 152008 | BAA02g00620 | A02 | 330368 | G | A | upstream_gene_variant | MODIFIER | c.-3390G>A| |
S52 |
| 152009 | BAA02g00620 | A02 | 330617 | C | T | upstream_gene_variant | MODIFIER | c.-3141C>T| |
S112 |
| 152010 | BAA02g00620 | A02 | 333117 | C | T | upstream_gene_variant | MODIFIER | c.-641C>T| |
S283 |
| 152011 | BAA02g00620 | A02 | 334261 | G | A | synonymous_variant | LOW | c.420G>A|p.Val140Val |
S79 S91 |
| 152012 | BAA02g00620 | A02 | 334872 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.871-1G>A| |
S138 S286 |
| 152013 | BAA02g00640 | A02 | 335762 | C | T | upstream_gene_variant | MODIFIER | c.-2355C>T| |
S257 |
| 152014 | BAA02g00630 | A02 | 337057 | G | A | missense_variant | MODERATE | c.152C>T|p.Ser51Phe |
S176 |
| 152015 | BAA02g00630 | A02 | 337109 | C | T | missense_variant | MODERATE | c.100G>A|p.Glu34Lys |
S135 |
| 152016 | BAA02g00630 | A02 | 337174 | G | A | missense_variant | MODERATE | c.35C>T|p.Ser12Phe |
S302 |
| 152017 | BAA02g00630 | A02 | 337757 | C | T | upstream_gene_variant | MODIFIER | c.-549G>A| |
S38 |
| 152018 | BAA02g00630 | A02 | 337917 | G | A | upstream_gene_variant | MODIFIER | c.-709C>T| |
S168 |
| 152019 | BAA02g00630 | A02 | 338802 | C | T | upstream_gene_variant | MODIFIER | c.-1594G>A| |
S99 |
| 152020 | BAA02g00640 | A02 | 339237 | C | T | missense_variant | MODERATE | c.386C>T|p.Thr129Ile |
S47 |
| 152021 | BAA02g00630 | A02 | 339332 | C | T | upstream_gene_variant | MODIFIER | c.-2124G>A| |
S298 |
| 152022 | BAA02g00630 | A02 | 341399 | G | A | upstream_gene_variant | MODIFIER | c.-4191C>T| |
S110 |
| 152023 | BAA02g00650 | A02 | 342109 | G | A | missense_variant&splice_region_variant | MODERATE | c.619G>A|p.Glu207Lys |
S162 |
| 152024 | BAA02g00640 | A02 | 342523 | C | T | downstream_gene_variant | MODIFIER | c.*2096C>T| |
S47 |
| 152025 | BAA02g00640 | A02 | 342650 | G | A | downstream_gene_variant | MODIFIER | c.*2223G>A| |
S265 |