| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 123051 | BAA10g13120-BAA10g13130 | A10 | 14362879 | C | T | intergenic_region | MODIFIER | n.14362879C>T| |
S51 |
| 123052 | BAA10g13120-BAA10g13130 | A10 | 14365391 | G | A | intergenic_region | MODIFIER | n.14365391G>A| |
S299 |
| 123053 | BAA10g13130 | A10 | 14368688 | C | T | downstream_gene_variant | MODIFIER | c.*4196G>A| |
S117 |
| 123054 | BAA10g13130 | A10 | 14370374 | C | T | downstream_gene_variant | MODIFIER | c.*2510G>A| |
S30 |
| 123055 | BAA10g13130 | A10 | 14370421 | C | T | downstream_gene_variant | MODIFIER | c.*2463G>A| |
S46 |
| 123056 | BAA10g13130 | A10 | 14370522 | G | A | downstream_gene_variant | MODIFIER | c.*2362C>T| |
S53 |
| 123057 | BAA10g13130 | A10 | 14370737 | G | A | downstream_gene_variant | MODIFIER | c.*2147C>T| |
S263 |
| 123058 | BAA10g13130 | A10 | 14371152 | C | T | downstream_gene_variant | MODIFIER | c.*1732G>A| |
S167 |
| 123059 | BAA10g13130 | A10 | 14371735 | C | T | downstream_gene_variant | MODIFIER | c.*1149G>A| |
S38 |
| 123060 | BAA10g13130 | A10 | 14372684 | C | T | downstream_gene_variant | MODIFIER | c.*200G>A| |
S183 |
| 123061 | BAA10g13130 | A10 | 14373247 | C | T | missense_variant | MODERATE | c.3772G>A|p.Asp1258Asn |
S202 |
| 123062 | BAA10g13130 | A10 | 14373300 | G | A | missense_variant | MODERATE | c.3719C>T|p.Ala1240Val |
S159 S243 |
| 123063 | BAA10g13130 | A10 | 14374405 | C | T | synonymous_variant | LOW | c.2973G>A|p.Glu991Glu |
S84 S93 |
| 123064 | BAA10g13130 | A10 | 14374901 | C | T | missense_variant | MODERATE | c.2477G>A|p.Gly826Glu |
S84 S93 |
| 123065 | BAA10g13130 | A10 | 14376564 | G | A | missense_variant | MODERATE | c.965C>T|p.Ser322Phe |
S274 |
| 123066 | BAA10g13130 | A10 | 14377414 | C | T | intron_variant | MODIFIER | c.257-26G>A| |
S146 |
| 123067 | BAA10g13130 | A10 | 14377462 | G | A | intron_variant | MODIFIER | c.256+43C>T| |
S295 |
| 123068 | BAA10g13130 | A10 | 14377617 | G | A | synonymous_variant | LOW | c.144C>T|p.Gly48Gly |
S50 |
| 123069 | BAA10g13130 | A10 | 14377659 | G | A | synonymous_variant | LOW | c.102C>T|p.Pro34Pro |
S74 |
| 123070 | BAA10g13130 | A10 | 14377741 | G | A | missense_variant | MODERATE | c.20C>T|p.Pro7Leu |
S263 S302 |
| 123071 | BAA10g13130 | A10 | 14379895 | G | A | upstream_gene_variant | MODIFIER | c.-2135C>T| |
S72 |
| 123072 | BAA10g13130 | A10 | 14382140 | C | T | upstream_gene_variant | MODIFIER | c.-4380G>A| |
S274 |
| 123073 | BAA10g13130 | A10 | 14382158 | G | A | upstream_gene_variant | MODIFIER | c.-4398C>T| |
S293 |
| 123074 | BAA10g13140 | A10 | 14383783 | G | A | upstream_gene_variant | MODIFIER | c.-3778G>A| |
S192 |
| 123075 | BAA10g13140 | A10 | 14383951 | C | T | upstream_gene_variant | MODIFIER | c.-3610C>T| |
S249 |