| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 127801 | BAA10g16190 | A10 | 16133458 | G | A | synonymous_variant | LOW | c.507C>T|p.Val169Val |
S178 |
| 127802 | BAA10g16190 | A10 | 16134034 | C | T | missense_variant | MODERATE | c.167G>A|p.Arg56Lys |
S272 |
| 127803 | BAA10g16180 | A10 | 16134796 | G | A | upstream_gene_variant | MODIFIER | c.-4123C>T| |
S63 |
| 127804 | BAA10g16180 | A10 | 16134900 | C | T | upstream_gene_variant | MODIFIER | c.-4227G>A| |
S180 |
| 127805 | BAA10g16180 | A10 | 16135070 | G | A | upstream_gene_variant | MODIFIER | c.-4397C>T| |
S59 |
| 127806 | BAA10g16180 | A10 | 16135342 | C | T | upstream_gene_variant | MODIFIER | c.-4669G>A| |
S276 |
| 127807 | BAA10g16190 | A10 | 16136183 | C | T | upstream_gene_variant | MODIFIER | c.-1983G>A| |
S123 |
| 127808 | BAA10g16190 | A10 | 16136451 | C | G | upstream_gene_variant | MODIFIER | c.-2251G>C| |
S5 |
| 127809 | BAA10g16190 | A10 | 16138087 | C | T | upstream_gene_variant | MODIFIER | c.-3887G>A| |
S284 |
| 127810 | BAA10g16200 | A10 | 16138600 | C | T | stop_gained | HIGH | c.907C>T|p.Gln303* |
S297 |
| 127811 | BAA10g16190 | A10 | 16138861 | T | A | upstream_gene_variant | MODIFIER | c.-4661A>T| |
S262 |
| 127812 | BAA10g16200 | A10 | 16139688 | C | T | downstream_gene_variant | MODIFIER | c.*939C>T| |
S298 |
| 127813 | BAA10g16200 | A10 | 16139821 | C | T | downstream_gene_variant | MODIFIER | c.*1072C>T| |
S73 |
| 127814 | BAA10g16200 | A10 | 16140175 | G | A | downstream_gene_variant | MODIFIER | c.*1426G>A| |
S292 |
| 127815 | BAA10g16200 | A10 | 16141460 | G | A | downstream_gene_variant | MODIFIER | c.*2711G>A| |
S279 |
| 127816 | BAA10g16200 | A10 | 16141484 | A | T | downstream_gene_variant | MODIFIER | c.*2735A>T| |
S57 |
| 127817 | BAA10g16210 | A10 | 16143892 | C | T | downstream_gene_variant | MODIFIER | c.*1056G>A| |
S236 |
| 127818 | BAA10g16210 | A10 | 16143926 | G | A | downstream_gene_variant | MODIFIER | c.*1022C>T| |
S105 S106 |
| 127819 | BAA10g16230 | A10 | 16144541 | G | A | upstream_gene_variant | MODIFIER | c.-4954G>A| |
S178 |
| 127820 | BAA10g16230 | A10 | 16144665 | C | T | upstream_gene_variant | MODIFIER | c.-4830C>T| |
S296 |
| 127821 | BAA10g16210 | A10 | 16144994 | C | T | missense_variant | MODERATE | c.1235G>A|p.Gly412Glu |
S302 |
| 127822 | BAA10g16230 | A10 | 16145322 | G | A | upstream_gene_variant | MODIFIER | c.-4173G>A| |
S53 |
| 127823 | BAA10g16210 | A10 | 16146197 | C | T | missense_variant | MODERATE | c.716G>A|p.Gly239Asp |
S5 |
| 127824 | BAA10g16210 | A10 | 16146761 | G | A | synonymous_variant | LOW | c.261C>T|p.Gly87Gly |
S239 |
| 127825 | BAA10g16210 | A10 | 16147026 | C | T | missense_variant | MODERATE | c.131G>A|p.Arg44His |
S260 |