| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 60451 | BAA01g32240 | A01 | 21159316 | G | A | intron_variant | MODIFIER | c.736+39C>T| |
S197 |
| 60452 | BAA01g32240 | A01 | 21160096 | C | T | missense_variant | MODERATE | c.248G>A|p.Gly83Glu |
S167 |
| 60453 | BAA01g32240 | A01 | 21160566 | G | A | synonymous_variant | LOW | c.129C>T|p.Leu43Leu |
S296 |
| 60454 | BAA01g32240 | A01 | 21161946 | C | T | upstream_gene_variant | MODIFIER | c.-1252G>A| |
S155 S211 |
| 60455 | BAA01g32240 | A01 | 21162794 | C | T | upstream_gene_variant | MODIFIER | c.-2100G>A| |
S73 |
| 60456 | BAA01g32240 | A01 | 21162883 | C | T | upstream_gene_variant | MODIFIER | c.-2189G>A| |
S54 |
| 60457 | BAA01g32240 | A01 | 21163859 | G | A | upstream_gene_variant | MODIFIER | c.-3165C>T| |
S291 |
| 60458 | BAA01g32240 | A01 | 21164069 | G | A | upstream_gene_variant | MODIFIER | c.-3375C>T| |
S2 |
| 60459 | BAA01g32240 | A01 | 21164162 | C | T | upstream_gene_variant | MODIFIER | c.-3468G>A| |
S205 |
| 60460 | BAA01g32240 | A01 | 21164573 | G | T | upstream_gene_variant | MODIFIER | c.-3879C>A| |
S58 |
| 60461 | BAA01g32240 | A01 | 21164765 | G | A | upstream_gene_variant | MODIFIER | c.-4071C>T| |
S287 |
| 60462 | BAA01g32240 | A01 | 21164877 | C | T | upstream_gene_variant | MODIFIER | c.-4183G>A| |
S20 |
| 60463 | BAA01g32240 | A01 | 21165423 | G | A | upstream_gene_variant | MODIFIER | c.-4729C>T| |
S274 |
| 60464 | BAA01g32250 | A01 | 21166414 | C | T | missense_variant | MODERATE | c.2776G>A|p.Asp926Asn |
S132 S137 S215 S89 |
| 60465 | BAA01g32250 | A01 | 21166476 | C | T | missense_variant | MODERATE | c.2714G>A|p.Arg905Lys |
S19 |
| 60466 | BAA01g32250 | A01 | 21168434 | G | A | intron_variant | MODIFIER | c.1963+34C>T| |
S308 |
| 60467 | BAA01g32250 | A01 | 21169599 | C | T | missense_variant | MODERATE | c.1519G>A|p.Glu507Lys |
S186 |
| 60468 | BAA01g32250 | A01 | 21169662 | G | A | missense_variant | MODERATE | c.1456C>T|p.Pro486Ser |
S97 |
| 60469 | BAA01g32250 | A01 | 21170190 | G | A | intron_variant | MODIFIER | c.1395+98C>T| |
S280 |
| 60470 | BAA01g32250 | A01 | 21170206 | C | T | intron_variant | MODIFIER | c.1395+82G>A| |
S23 |
| 60471 | BAA01g32250 | A01 | 21170369 | C | T | synonymous_variant | LOW | c.1314G>A|p.Gln438Gln |
S182 |
| 60472 | BAA01g32250 | A01 | 21170429 | C | T | synonymous_variant | LOW | c.1254G>A|p.Lys418Lys |
S167 |
| 60473 | BAA01g32250 | A01 | 21171738 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.602-1G>A| |
S107 |
| 60474 | BAA01g32250 | A01 | 21172728 | C | T | missense_variant | MODERATE | c.151G>A|p.Ala51Thr |
S128 |
| 60475 | BAA01g32250 | A01 | 21172799 | G | A | missense_variant | MODERATE | c.80C>T|p.Thr27Ile |
S268 |