| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 80501 | BAA01g42480 | A01 | 28202698 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1361-1G>A| |
S263 |
| 80502 | BAA01g42470 | A01 | 28203313 | C | T | downstream_gene_variant | MODIFIER | c.*4777C>T| |
S255 |
| 80503 | BAA01g42490 | A01 | 28204162 | G | A | downstream_gene_variant | MODIFIER | c.*4090C>T| |
S295 |
| 80504 | BAA01g42490 | A01 | 28205255 | G | A | downstream_gene_variant | MODIFIER | c.*2997C>T| |
S83 |
| 80505 | BAA01g42480 | A01 | 28205659 | G | A | missense_variant | MODERATE | c.2350G>A|p.Glu784Lys |
S71 |
| 80506 | BAA01g42490 | A01 | 28205926 | G | A | downstream_gene_variant | MODIFIER | c.*2326C>T| |
S180 |
| 80507 | BAA01g42490 | A01 | 28207444 | G | A | downstream_gene_variant | MODIFIER | c.*808C>T| |
S169 |
| 80508 | BAA01g42480 | A01 | 28207448 | C | T | splice_region_variant&intron_variant | LOW | c.3051-6C>T| |
S293 |
| 80509 | BAA01g42480 | A01 | 28207507 | C | T | missense_variant | MODERATE | c.3104C>T|p.Ala1035Val |
S274 |
| 80510 | BAA01g42490 | A01 | 28208962 | G | A | missense_variant | MODERATE | c.1322C>T|p.Thr441Ile |
S95 |
| 80511 | BAA01g42490 | A01 | 28211069 | G | A | missense_variant | MODERATE | c.254C>T|p.Thr85Ile |
S297 |
| 80512 | BAA01g42490 | A01 | 28211124 | C | T | missense_variant | MODERATE | c.199G>A|p.Val67Ile |
S200 |
| 80513 | BAA01g42490 | A01 | 28211290 | G | A | synonymous_variant | LOW | c.33C>T|p.Val11Val |
S190 |
| 80514 | BAA01g42500 | A01 | 28212720 | C | T | missense_variant | MODERATE | c.130G>A|p.Glu44Lys |
S133 |
| 80515 | BAA01g42490 | A01 | 28212982 | C | T | upstream_gene_variant | MODIFIER | c.-1660G>A| |
|
| 80516 | BAA01g42490 | A01 | 28213099 | C | T | upstream_gene_variant | MODIFIER | c.-1777G>A| |
S174 S27 |
| 80517 | BAA01g42490 | A01 | 28213317 | G | A | upstream_gene_variant | MODIFIER | c.-1995C>T| |
S122 |
| 80518 | BAA01g42490 | A01 | 28213968 | G | A | upstream_gene_variant | MODIFIER | c.-2646C>T| |
S234 |
| 80519 | BAA01g42490 | A01 | 28214699 | C | T | upstream_gene_variant | MODIFIER | c.-3377G>A| |
S174 S27 |
| 80520 | BAA01g42490 | A01 | 28214739 | C | T | upstream_gene_variant | MODIFIER | c.-3417G>A| |
S161 |
| 80521 | BAA01g42510 | A01 | 28215614 | C | T | missense_variant | MODERATE | c.184G>A|p.Asp62Asn |
S182 |
| 80522 | BAA01g42490 | A01 | 28215804 | G | A | upstream_gene_variant | MODIFIER | c.-4482C>T| |
S226 |
| 80523 | BAA01g42500 | A01 | 28216599 | C | T | upstream_gene_variant | MODIFIER | c.-3750G>A| |
S249 |
| 80524 | BAA01g42520 | A01 | 28217003 | C | T | missense_variant | MODERATE | c.1048G>A|p.Asp350Asn |
S153 |
| 80525 | BAA01g42500 | A01 | 28217169 | C | T | upstream_gene_variant | MODIFIER | c.-4320G>A| |
S142 |