| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 90151 | BAA10g00240 | A10 | 116893 | C | T | upstream_gene_variant | MODIFIER | c.-4505G>A| |
S173 |
| 90152 | BAA10g00240 | A10 | 117122 | C | T | upstream_gene_variant | MODIFIER | c.-4734G>A| |
S55 |
| 90153 | BAA10g00250 | A10 | 117768 | C | T | upstream_gene_variant | MODIFIER | c.-1172C>T| |
S185 |
| 90154 | BAA10g00250 | A10 | 118361 | C | T | upstream_gene_variant | MODIFIER | c.-579C>T| |
S35 |
| 90155 | BAA10g00250 | A10 | 118584 | C | T | upstream_gene_variant | MODIFIER | c.-356C>T| |
S293 |
| 90156 | BAA10g00250 | A10 | 119015 | C | T | missense_variant | MODERATE | c.76C>T|p.Pro26Ser |
S287 |
| 90157 | BAA10g00250 | A10 | 119668 | G | A | synonymous_variant | LOW | c.501G>A|p.Thr167Thr |
S194 |
| 90158 | BAA10g00250 | A10 | 120089 | C | T | missense_variant | MODERATE | c.773C>T|p.Ser258Phe |
S134 |
| 90159 | BAA10g00250 | A10 | 120244 | C | T | synonymous_variant | LOW | c.862C>T|p.Leu288Leu |
S201 |
| 90160 | BAA10g00250 | A10 | 120483 | C | T | missense_variant | MODERATE | c.1007C>T|p.Thr336Ile |
S11 |
| 90161 | BAA10g00270 | A10 | 120749 | C | T | upstream_gene_variant | MODIFIER | c.-2481C>T| |
S132 S137 S89 |
| 90162 | BAA10g00260 | A10 | 121674 | C | T | missense_variant | MODERATE | c.58G>A|p.Glu20Lys |
S44 |
| 90163 | BAA10g00260 | A10 | 122989 | G | A | upstream_gene_variant | MODIFIER | c.-1170C>T| |
S290 |
| 90164 | BAA10g00260 | A10 | 123105 | G | A | upstream_gene_variant | MODIFIER | c.-1286C>T| |
S15 |
| 90165 | BAA10g00270 | A10 | 123989 | A | T | missense_variant | MODERATE | c.515A>T|p.Glu172Val |
S11 |
| 90166 | BAA10g00260 | A10 | 125064 | G | A | upstream_gene_variant | MODIFIER | c.-3245C>T| |
S5 |
| 90167 | BAA10g00260 | A10 | 126146 | C | T | upstream_gene_variant | MODIFIER | c.-4327G>A| |
S6 |
| 90168 | BAA10g00280 | A10 | 128053 | G | A | upstream_gene_variant | MODIFIER | c.-110C>T| |
S160 S293 |
| 90169 | BAA10g00280 | A10 | 128061 | G | A | upstream_gene_variant | MODIFIER | c.-118C>T| |
S18 |
| 90170 | BAA10g00290 | A10 | 130115 | G | A | missense_variant&splice_region_variant | MODERATE | c.772C>T|p.Leu258Phe |
S218 |
| 90171 | BAA10g00280 | A10 | 130566 | G | A | upstream_gene_variant | MODIFIER | c.-2623C>T| |
S18 |
| 90172 | BAA10g00290 | A10 | 131343 | C | T | missense_variant | MODERATE | c.217G>A|p.Glu73Lys |
S171 |
| 90173 | BAA10g00290 | A10 | 133538 | G | A | upstream_gene_variant | MODIFIER | c.-1723C>T| |
S290 |
| 90174 | BAA10g00290 | A10 | 133961 | C | T | upstream_gene_variant | MODIFIER | c.-2146G>A| |
S235 |
| 90175 | BAA10g00290 | A10 | 134230 | G | A | upstream_gene_variant | MODIFIER | c.-2415C>T| |
S80 |