| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 83601 | BAA01g44330 | A01 | 29457822 | G | A | upstream_gene_variant | MODIFIER | c.-579G>A| |
S284 |
| 83602 | BAA01g44330 | A01 | 29457976 | C | T | upstream_gene_variant | MODIFIER | c.-425C>T| |
S16 |
| 83603 | BAA01g44330 | A01 | 29458288 | C | T | upstream_gene_variant | MODIFIER | c.-113C>T| |
S107 |
| 83604 | BAA01g44340 | A01 | 29458590 | C | T | upstream_gene_variant | MODIFIER | c.-4212C>T| |
S177 |
| 83605 | BAA01g44340 | A01 | 29458596 | C | T | upstream_gene_variant | MODIFIER | c.-4206C>T| |
S19 |
| 83606 | BAA01g44340 | A01 | 29458676 | G | A | upstream_gene_variant | MODIFIER | c.-4126G>A| |
S197 |
| 83607 | BAA01g44330 | A01 | 29458752 | G | A | synonymous_variant | LOW | c.201G>A|p.Glu67Glu |
S245 |
| 83608 | BAA01g44330 | A01 | 29459090 | C | G | stop_gained | HIGH | c.375C>G|p.Tyr125* |
S106 S123 S139 S19 S215 S234 S250 S255 S267 S282 S298 S306 S48 S72 |
| 83609 | BAA01g44330 | A01 | 29459703 | C | T | missense_variant&splice_region_variant | MODERATE | c.635C>T|p.Ala212Val |
S131 |
| 83610 | BAA01g44340 | A01 | 29462191 | C | T | upstream_gene_variant | MODIFIER | c.-611C>T| |
S166 |
| 83611 | BAA01g44340 | A01 | 29463153 | G | A | missense_variant | MODERATE | c.215G>A|p.Gly72Glu |
S110 |
| 83612 | BAA01g44340 | A01 | 29464541 | C | T | synonymous_variant | LOW | c.967C>T|p.Leu323Leu |
S290 |
| 83613 | BAA01g44340 | A01 | 29464718 | G | A | missense_variant | MODERATE | c.1060G>A|p.Gly354Arg |
S211 |
| 83614 | BAA01g44340 | A01 | 29465212 | C | T | synonymous_variant | LOW | c.1281C>T|p.Leu427Leu |
S41 |
| 83615 | BAA01g44350 | A01 | 29465957 | G | A | upstream_gene_variant | MODIFIER | c.-338G>A| |
S43 |
| 83616 | BAA01g44340 | A01 | 29465995 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1642-1G>A| |
S116 |
| 83617 | BAA01g44350 | A01 | 29466185 | C | T | upstream_gene_variant | MODIFIER | c.-110C>T| |
S57 |
| 83618 | BAA01g44350 | A01 | 29466595 | G | A | missense_variant | MODERATE | c.301G>A|p.Glu101Lys |
S276 |
| 83619 | BAA01g44360 | A01 | 29469048 | G | A | missense_variant | MODERATE | c.1672C>T|p.Pro558Ser |
S139 |
| 83620 | BAA01g44360 | A01 | 29469161 | G | A | synonymous_variant | LOW | c.1645C>T|p.Leu549Leu |
S67 |
| 83621 | BAA01g44360 | A01 | 29471453 | C | T | missense_variant | MODERATE | c.308G>A|p.Arg103Lys |
S292 |
| 83622 | BAA01g44350 | A01 | 29471774 | G | A | downstream_gene_variant | MODIFIER | c.*3089G>A| |
S149 |
| 83623 | BAA01g44360 | A01 | 29474012 | G | A | upstream_gene_variant | MODIFIER | c.-1566C>T| |
S122 |
| 83624 | BAA01g44360 | A01 | 29474388 | C | T | upstream_gene_variant | MODIFIER | c.-1942G>A| |
S235 |
| 83625 | BAA01g44360 | A01 | 29474462 | C | T | upstream_gene_variant | MODIFIER | c.-2016G>A| |
S142 |