| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 131051 | BAA10g18490 | A10 | 17275919 | G | A | downstream_gene_variant | MODIFIER | c.*3095C>T| |
S239 |
| 131052 | BAA10g18490 | A10 | 17276335 | G | A | downstream_gene_variant | MODIFIER | c.*2679C>T| |
S66 |
| 131053 | BAA10g18490 | A10 | 17276497 | G | A | downstream_gene_variant | MODIFIER | c.*2517C>T| |
S67 |
| 131054 | BAA10g18490 | A10 | 17276595 | C | T | downstream_gene_variant | MODIFIER | c.*2419G>A| |
S81 |
| 131055 | BAA10g18490 | A10 | 17277032 | C | T | downstream_gene_variant | MODIFIER | c.*1982G>A| |
S95 |
| 131056 | BAA10g18490 | A10 | 17277323 | G | A | downstream_gene_variant | MODIFIER | c.*1691C>T| |
S36 |
| 131057 | BAA10g18490 | A10 | 17277797 | C | T | downstream_gene_variant | MODIFIER | c.*1217G>A| |
S238 |
| 131058 | BAA10g18490 | A10 | 17277967 | G | A | downstream_gene_variant | MODIFIER | c.*1047C>T| |
S265 |
| 131059 | BAA10g18490 | A10 | 17278123 | C | T | downstream_gene_variant | MODIFIER | c.*891G>A| |
S259 |
| 131060 | BAA10g18490 | A10 | 17279142 | G | A | missense_variant | MODERATE | c.295C>T|p.Arg99Cys |
S293 |
| 131061 | BAA10g18490 | A10 | 17279228 | G | A | missense_variant | MODERATE | c.209C>T|p.Ser70Leu |
S74 |
| 131062 | BAA10g18490 | A10 | 17279347 | G | A | synonymous_variant | LOW | c.90C>T|p.Leu30Leu |
S74 |
| 131063 | BAA10g18490 | A10 | 17279441 | G | A | upstream_gene_variant | MODIFIER | c.-5C>T| |
S197 |
| 131064 | BAA10g18490 | A10 | 17279820 | C | T | upstream_gene_variant | MODIFIER | c.-384G>A| |
S44 |
| 131065 | BAA10g18490 | A10 | 17281045 | C | T | upstream_gene_variant | MODIFIER | c.-1609G>A| |
S170 |
| 131066 | BAA10g18490 | A10 | 17281827 | C | T | upstream_gene_variant | MODIFIER | c.-2391G>A| |
S287 |
| 131067 | BAA10g18490 | A10 | 17281955 | G | A | upstream_gene_variant | MODIFIER | c.-2519C>T| |
S120 |
| 131068 | BAA10g18500 | A10 | 17282576 | G | A | synonymous_variant | LOW | c.396C>T|p.Leu132Leu |
S134 |
| 131069 | BAA10g18500 | A10 | 17283036 | G | A | missense_variant | MODERATE | c.253C>T|p.Leu85Phe |
S241 |
| 131070 | BAA10g18490 | A10 | 17283419 | C | T | upstream_gene_variant | MODIFIER | c.-3983G>A| |
S260 |
| 131071 | BAA10g18490 | A10 | 17283443 | C | T | upstream_gene_variant | MODIFIER | c.-4007G>A| |
S281 |
| 131072 | BAA10g18500 | A10 | 17283764 | G | A | missense_variant | MODERATE | c.38C>T|p.Pro13Leu |
S209 |
| 131073 | BAA10g18490 | A10 | 17283889 | G | A | upstream_gene_variant | MODIFIER | c.-4453C>T| |
S250 |
| 131074 | BAA10g18490 | A10 | 17284246 | C | T | upstream_gene_variant | MODIFIER | c.-4810G>A| |
S251 |
| 131075 | BAA10g18490 | A10 | 17284303 | C | T | upstream_gene_variant | MODIFIER | c.-4867G>A| |
S11 |