| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 95651 | BAA10g04190 | A10 | 2106805 | G | A | upstream_gene_variant | MODIFIER | c.-2676G>A| |
S263 |
| 95652 | BAA10g04190 | A10 | 2106863 | G | A | upstream_gene_variant | MODIFIER | c.-2618G>A| |
S16 |
| 95653 | BAA10g04190 | A10 | 2106958 | C | T | upstream_gene_variant | MODIFIER | c.-2523C>T| |
S203 |
| 95654 | BAA10g04190 | A10 | 2108021 | G | A | upstream_gene_variant | MODIFIER | c.-1460G>A| |
S180 |
| 95655 | BAA10g04190 | A10 | 2108074 | C | T | upstream_gene_variant | MODIFIER | c.-1407C>T| |
S281 |
| 95656 | BAA10g04190 | A10 | 2108220 | G | A | upstream_gene_variant | MODIFIER | c.-1261G>A| |
S245 |
| 95657 | BAA10g04190 | A10 | 2108549 | C | T | upstream_gene_variant | MODIFIER | c.-932C>T| |
S252 |
| 95658 | BAA10g04190 | A10 | 2108703 | G | A | upstream_gene_variant | MODIFIER | c.-778G>A| |
S90 |
| 95659 | BAA10g04190 | A10 | 2108832 | C | T | upstream_gene_variant | MODIFIER | c.-649C>T| |
S270 |
| 95660 | BAA10g04190 | A10 | 2108833 | C | T | upstream_gene_variant | MODIFIER | c.-648C>T| |
S136 S186 |
| 95661 | BAA10g04190 | A10 | 2109290 | G | A | upstream_gene_variant | MODIFIER | c.-191G>A| |
S245 |
| 95662 | BAA10g04190 | A10 | 2110147 | C | T | downstream_gene_variant | MODIFIER | c.*511C>T| |
S135 |
| 95663 | BAA10g04190 | A10 | 2110700 | C | T | downstream_gene_variant | MODIFIER | c.*1064C>T| |
S308 |
| 95664 | BAA10g04190 | A10 | 2111258 | T | A | downstream_gene_variant | MODIFIER | c.*1622T>A| |
S108 |
| 95665 | BAA10g04190 | A10 | 2111541 | G | A | downstream_gene_variant | MODIFIER | c.*1905G>A| |
S282 |
| 95666 | BAA10g04200 | A10 | 2111868 | G | A | missense_variant | MODERATE | c.358C>T|p.Arg120Cys |
S145 S196 S209 S245 S246 S27 S277 |
| 95667 | BAA10g04200 | A10 | 2112033 | G | A | missense_variant | MODERATE | c.193C>T|p.Pro65Ser |
S274 |
| 95668 | BAA10g04200 | A10 | 2112143 | G | A | missense_variant | MODERATE | c.83C>T|p.Ser28Leu |
S153 S213 |
| 95669 | BAA10g04200 | A10 | 2112475 | C | T | upstream_gene_variant | MODIFIER | c.-250G>A| |
S131 |
| 95670 | BAA10g04210 | A10 | 2113032 | C | T | synonymous_variant | LOW | c.297G>A|p.Lys99Lys |
S244 |
| 95671 | BAA10g04200 | A10 | 2114832 | G | A | upstream_gene_variant | MODIFIER | c.-2607C>T| |
S208 S219 |
| 95672 | BAA10g04200 | A10 | 2115300 | G | A | upstream_gene_variant | MODIFIER | c.-3075C>T| |
S157 S163 |
| 95673 | BAA10g04200 | A10 | 2116281 | C | T | upstream_gene_variant | MODIFIER | c.-4056G>A| |
S142 |
| 95674 | BAA10g04220 | A10 | 2118788 | C | T | upstream_gene_variant | MODIFIER | c.-4031G>A| |
S162 |
| 95675 | BAA10g04230 | A10 | 2118915 | G | A | missense_variant | MODERATE | c.112G>A|p.Glu38Lys |
S16 |