| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 120951 | BAA10g12130 | A10 | 13615080 | G | A | upstream_gene_variant | MODIFIER | c.-350G>A| |
S158 |
| 120952 | BAA10g12130 | A10 | 13615570 | C | T | synonymous_variant | LOW | c.141C>T|p.Ile47Ile |
S162 |
| 120953 | BAA10g12130 | A10 | 13615596 | C | T | missense_variant | MODERATE | c.167C>T|p.Ser56Phe |
S156 |
| 120954 | BAA10g12140 | A10 | 13616499 | C | T | downstream_gene_variant | MODIFIER | c.*3779G>A| |
S259 S42 |
| 120955 | BAA10g12140 | A10 | 13617281 | C | T | downstream_gene_variant | MODIFIER | c.*2997G>A| |
S242 |
| 120956 | BAA10g12140 | A10 | 13617391 | C | T | downstream_gene_variant | MODIFIER | c.*2887G>A| |
S282 |
| 120957 | BAA10g12130 | A10 | 13618263 | G | A | missense_variant | MODERATE | c.869G>A|p.Gly290Glu |
S50 |
| 120958 | BAA10g12130 | A10 | 13618681 | G | A | downstream_gene_variant | MODIFIER | c.*192G>A| |
S280 |
| 120959 | BAA10g12130 | A10 | 13619165 | C | T | downstream_gene_variant | MODIFIER | c.*676C>T| |
S149 |
| 120960 | BAA10g12150 | A10 | 13620026 | C | T | upstream_gene_variant | MODIFIER | c.-4146C>T| |
S144 |
| 120961 | BAA10g12140 | A10 | 13620535 | T | G | missense_variant | MODERATE | c.1093A>C|p.Ile365Leu |
S109 S111 S158 S17 S180 S23 S248 S25 S262 S28 S291 |
| 120962 | BAA10g12140 | A10 | 13620667 | C | T | missense_variant | MODERATE | c.961G>A|p.Gly321Arg |
S70 |
| 120963 | BAA10g12140 | A10 | 13620757 | C | T | missense_variant | MODERATE | c.871G>A|p.Asp291Asn |
S149 |
| 120964 | BAA10g12150 | A10 | 13621017 | C | T | upstream_gene_variant | MODIFIER | c.-3155C>T| |
S164 |
| 120965 | BAA10g12140 | A10 | 13621910 | G | A | missense_variant | MODERATE | c.202C>T|p.Pro68Ser |
S138 |
| 120966 | BAA10g12140 | A10 | 13622520 | G | A | upstream_gene_variant | MODIFIER | c.-409C>T| |
S290 |
| 120967 | BAA10g12150 | A10 | 13625320 | G | A | missense_variant | MODERATE | c.1051G>A|p.Ala351Thr |
S276 |
| 120968 | BAA10g12150 | A10 | 13625615 | C | T | missense_variant | MODERATE | c.1346C>T|p.Ala449Val |
S122 |
| 120969 | BAA10g12140 | A10 | 13625818 | C | T | upstream_gene_variant | MODIFIER | c.-3707G>A| |
S270 |
| 120970 | BAA10g12140 | A10 | 13625822 | C | T | upstream_gene_variant | MODIFIER | c.-3711G>A| |
S8 |
| 120971 | BAA10g12140 | A10 | 13626017 | C | T | upstream_gene_variant | MODIFIER | c.-3906G>A| |
S140 |
| 120972 | BAA10g12140 | A10 | 13626828 | G | A | upstream_gene_variant | MODIFIER | c.-4717C>T| |
S32 |
| 120973 | BAA10g12140 | A10 | 13627081 | C | T | upstream_gene_variant | MODIFIER | c.-4970G>A| |
S25 |
| 120974 | BAA10g12150 | A10 | 13627909 | G | A | downstream_gene_variant | MODIFIER | c.*2140G>A| |
S178 |
| 120975 | BAA10g12150 | A10 | 13628224 | C | T | downstream_gene_variant | MODIFIER | c.*2455C>T| |
S197 |