| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 115051 | BAA10g09580 | A10 | 11516129 | C | T | upstream_gene_variant | MODIFIER | c.-794G>A| |
S180 |
| 115052 | BAA10g09580 | A10 | 11516136 | C | T | upstream_gene_variant | MODIFIER | c.-801G>A| |
S272 |
| 115053 | BAA10g09580 | A10 | 11516182 | C | T | upstream_gene_variant | MODIFIER | c.-847G>A| |
S271 |
| 115054 | BAA10g09580 | A10 | 11516212 | C | T | upstream_gene_variant | MODIFIER | c.-877G>A| |
S177 |
| 115055 | BAA10g09580 | A10 | 11516232 | C | T | upstream_gene_variant | MODIFIER | c.-897G>A| |
S23 |
| 115056 | BAA10g09580 | A10 | 11516436 | C | T | upstream_gene_variant | MODIFIER | c.-1101G>A| |
S87 |
| 115057 | BAA10g09580-BAA10g09590 | A10 | 11522921 | A | G | intergenic_region | MODIFIER | n.11522921A>G| |
S62 |
| 115058 | BAA10g09590 | A10 | 11526559 | C | T | downstream_gene_variant | MODIFIER | c.*4093G>A| |
S155 S211 |
| 115059 | BAA10g09590 | A10 | 11527052 | C | T | downstream_gene_variant | MODIFIER | c.*3600G>A| |
S143 |
| 115060 | BAA10g09590 | A10 | 11527170 | C | T | downstream_gene_variant | MODIFIER | c.*3482G>A| |
S204 |
| 115061 | BAA10g09590 | A10 | 11527210 | C | T | downstream_gene_variant | MODIFIER | c.*3442G>A| |
S259 |
| 115062 | BAA10g09590 | A10 | 11527231 | G | A | downstream_gene_variant | MODIFIER | c.*3421C>T| |
S138 S288 |
| 115063 | BAA10g09590 | A10 | 11527531 | C | T | downstream_gene_variant | MODIFIER | c.*3121G>A| |
S224 |
| 115064 | BAA10g09590 | A10 | 11530027 | C | T | downstream_gene_variant | MODIFIER | c.*625G>A| |
S150 |
| 115065 | BAA10g09590 | A10 | 11530352 | T | C | downstream_gene_variant | MODIFIER | c.*300A>G| |
S111 |
| 115066 | BAA10g09590 | A10 | 11530573 | A | T | downstream_gene_variant | MODIFIER | c.*79T>A| |
S134 |
| 115067 | BAA10g09590 | A10 | 11530822 | C | T | missense_variant | MODERATE | c.910G>A|p.Val304Met |
S91 |
| 115068 | BAA10g09590 | A10 | 11530969 | C | T | missense_variant | MODERATE | c.763G>A|p.Glu255Lys |
S249 |
| 115069 | BAA10g09590 | A10 | 11531386 | G | A | missense_variant | MODERATE | c.553C>T|p.Pro185Ser |
S292 |
| 115070 | BAA10g09590 | A10 | 11531573 | C | T | intron_variant | MODIFIER | c.383-17G>A| |
S287 |
| 115071 | BAA10g09590 | A10 | 11531718 | G | A | intron_variant | MODIFIER | c.383-162C>T| |
S221 |
| 115072 | BAA10g09600 | A10 | 11531945 | G | A | upstream_gene_variant | MODIFIER | c.-4847G>A| |
S278 |
| 115073 | BAA10g09600 | A10 | 11532151 | G | A | upstream_gene_variant | MODIFIER | c.-4641G>A| |
S62 |
| 115074 | BAA10g09600 | A10 | 11532375 | C | T | upstream_gene_variant | MODIFIER | c.-4417C>T| |
S235 |
| 115075 | BAA10g09600 | A10 | 11532452 | G | A | upstream_gene_variant | MODIFIER | c.-4340G>A| |
S234 |