| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 30001 | BAA01g21070-BAA01g21080 | A01 | 10384209 | C | T | intergenic_region | MODIFIER | n.10384209C>T| |
S247 |
| 30002 | BAA01g21070-BAA01g21080 | A01 | 10384382 | C | T | intergenic_region | MODIFIER | n.10384382C>T| |
S305 |
| 30003 | BAA01g21070-BAA01g21080 | A01 | 10385954 | G | A | intergenic_region | MODIFIER | n.10385954G>A| |
S8 |
| 30004 | BAA01g21080 | A01 | 10386721 | C | T | upstream_gene_variant | MODIFIER | c.-4756C>T| |
S133 |
| 30005 | BAA01g21080 | A01 | 10387387 | G | A | upstream_gene_variant | MODIFIER | c.-4090G>A| |
S288 |
| 30006 | BAA01g21080 | A01 | 10387543 | C | T | upstream_gene_variant | MODIFIER | c.-3934C>T| |
S267 |
| 30007 | BAA01g21080 | A01 | 10387945 | C | T | upstream_gene_variant | MODIFIER | c.-3532C>T| |
S177 |
| 30008 | BAA01g21080 | A01 | 10387969 | C | T | upstream_gene_variant | MODIFIER | c.-3508C>T| |
S69 |
| 30009 | BAA01g21080 | A01 | 10388325 | G | A | upstream_gene_variant | MODIFIER | c.-3152G>A| |
S32 |
| 30010 | BAA01g21080 | A01 | 10388628 | C | T | upstream_gene_variant | MODIFIER | c.-2849C>T| |
S104 |
| 30011 | BAA01g21080 | A01 | 10388988 | C | T | upstream_gene_variant | MODIFIER | c.-2489C>T| |
S202 |
| 30012 | BAA01g21080 | A01 | 10392939 | G | A | missense_variant | MODERATE | c.644G>A|p.Gly215Asp |
S268 |
| 30013 | BAA01g21080 | A01 | 10394086 | G | A | missense_variant | MODERATE | c.1102G>A|p.Asp368Asn |
S245 |
| 30014 | BAA01g21080 | A01 | 10394212 | G | A | missense_variant | MODERATE | c.1228G>A|p.Asp410Asn |
S204 |
| 30015 | BAA01g21080 | A01 | 10395634 | G | A | downstream_gene_variant | MODIFIER | c.*1222G>A| |
S302 |
| 30016 | BAA01g21080 | A01 | 10396010 | C | T | downstream_gene_variant | MODIFIER | c.*1598C>T| |
S239 |
| 30017 | BAA01g21080 | A01 | 10398840 | G | A | downstream_gene_variant | MODIFIER | c.*4428G>A| |
S209 |
| 30018 | BAA01g21090 | A01 | 10399647 | C | T | missense_variant | MODERATE | c.857G>A|p.Gly286Glu |
S20 S89 |
| 30019 | BAA01g21090 | A01 | 10400324 | T | A | missense_variant | MODERATE | c.470A>T|p.Asn157Ile |
S38 |
| 30020 | BAA01g21090 | A01 | 10400373 | C | T | missense_variant | MODERATE | c.421G>A|p.Gly141Arg |
S242 |
| 30021 | BAA01g21090 | A01 | 10400380 | G | A | synonymous_variant | LOW | c.414C>T|p.Ala138Ala |
S302 |
| 30022 | BAA01g21090 | A01 | 10400627 | G | A | missense_variant | MODERATE | c.242C>T|p.Ser81Phe |
S2 |
| 30023 | BAA01g21090 | A01 | 10402157 | C | T | upstream_gene_variant | MODIFIER | c.-1289G>A| |
S150 S201 |
| 30024 | BAA01g21090 | A01 | 10402495 | G | A | upstream_gene_variant | MODIFIER | c.-1627C>T| |
S224 |
| 30025 | BAA01g21090 | A01 | 10402649 | C | T | upstream_gene_variant | MODIFIER | c.-1781G>A| |
S134 |