| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 92101 | BAA10g01940 | A10 | 926818 | G | A | upstream_gene_variant | MODIFIER | c.-1063C>T| |
S81 S85 |
| 92102 | BAA10g01940 | A10 | 928323 | G | A | upstream_gene_variant | MODIFIER | c.-2568C>T| |
S279 |
| 92103 | BAA10g01940 | A10 | 928901 | C | T | upstream_gene_variant | MODIFIER | c.-3146G>A| |
S206 S26 |
| 92104 | BAA10g01940 | A10 | 929674 | G | A | upstream_gene_variant | MODIFIER | c.-3919C>T| |
S133 |
| 92105 | BAA10g01940 | A10 | 929750 | C | T | upstream_gene_variant | MODIFIER | c.-3995G>A| |
S166 |
| 92106 | BAA10g01940 | A10 | 929766 | G | A | upstream_gene_variant | MODIFIER | c.-4011C>T| |
S69 |
| 92107 | BAA10g01950 | A10 | 930475 | G | T | missense_variant | MODERATE | c.2420C>A|p.Ser807Tyr |
S1 S107 S251 S258 S264 S37 S47 S48 S97 |
| 92108 | BAA10g01950 | A10 | 930663 | C | T | synonymous_variant | LOW | c.2232G>A|p.Pro744Pro |
S206 S26 |
| 92109 | BAA10g01950 | A10 | 930695 | C | T | missense_variant | MODERATE | c.2200G>A|p.Val734Met |
S87 |
| 92110 | BAA10g01950 | A10 | 930777 | G | A | synonymous_variant | LOW | c.2118C>T|p.Phe706Phe |
S192 |
| 92111 | BAA10g01950 | A10 | 930828 | C | T | synonymous_variant | LOW | c.2067G>A|p.Thr689Thr |
S263 |
| 92112 | BAA10g01950 | A10 | 931759 | G | A | missense_variant | MODERATE | c.1235C>T|p.Ala412Val |
S33 |
| 92113 | BAA10g01950 | A10 | 932026 | G | A | missense_variant | MODERATE | c.968C>T|p.Thr323Ile |
S107 |
| 92114 | BAA10g01960 | A10 | 932101 | G | A | upstream_gene_variant | MODIFIER | c.-4893G>A| |
S38 |
| 92115 | BAA10g01950 | A10 | 932725 | G | A | missense_variant | MODERATE | c.610C>T|p.Pro204Ser |
S118 |
| 92116 | BAA10g01960 | A10 | 932883 | C | T | upstream_gene_variant | MODIFIER | c.-4111C>T| |
S116 |
| 92117 | BAA10g01960 | A10 | 932966 | C | T | upstream_gene_variant | MODIFIER | c.-4028C>T| |
S10 |
| 92118 | BAA10g01960 | A10 | 933495 | G | A | upstream_gene_variant | MODIFIER | c.-3499G>A| |
S234 |
| 92119 | BAA10g01960 | A10 | 933525 | G | A | upstream_gene_variant | MODIFIER | c.-3469G>A| |
S283 |
| 92120 | BAA10g01960 | A10 | 933556 | C | T | upstream_gene_variant | MODIFIER | c.-3438C>T| |
S74 |
| 92121 | BAA10g01950 | A10 | 935091 | C | T | upstream_gene_variant | MODIFIER | c.-1067G>A| |
S182 |
| 92122 | BAA10g01960 | A10 | 939672 | C | T | missense_variant&splice_region_variant | MODERATE | c.242C>T|p.Ala81Val |
S95 |
| 92123 | BAA10g01970 | A10 | 939796 | G | T | upstream_gene_variant | MODIFIER | c.-3519G>T| |
S158 S160 |
| 92124 | BAA10g01970 | A10 | 939845 | G | A | upstream_gene_variant | MODIFIER | c.-3470G>A| |
S198 |
| 92125 | BAA10g01960 | A10 | 939952 | C | T | missense_variant | MODERATE | c.392C>T|p.Ala131Val |
S74 |