| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 146751 | BAA10g31170 | A10 | 22838439 | G | A | upstream_gene_variant | MODIFIER | c.-4885C>T| |
S256 |
| 146752 | BAA10g31180 | A10 | 22838685 | G | A | upstream_gene_variant | MODIFIER | c.-1985C>T| |
S261 |
| 146753 | BAA10g31190 | A10 | 22840019 | C | T | synonymous_variant | LOW | c.1821G>A|p.Leu607Leu |
S140 |
| 146754 | BAA10g31180 | A10 | 22840347 | G | A | upstream_gene_variant | MODIFIER | c.-3647C>T| |
S279 |
| 146755 | BAA10g31190 | A10 | 22841018 | G | A | missense_variant | MODERATE | c.1300C>T|p.Leu434Phe |
S100 |
| 146756 | BAA10g31210 | A10 | 22842674 | G | A | upstream_gene_variant | MODIFIER | c.-4355G>A| |
S212 |
| 146757 | BAA10g31190 | A10 | 22842977 | C | T | missense_variant | MODERATE | c.248G>A|p.Arg83His |
S256 |
| 146758 | BAA10g31190 | A10 | 22843912 | G | A | upstream_gene_variant | MODIFIER | c.-531C>T| |
S263 |
| 146759 | BAA10g31200 | A10 | 22844265 | C | T | missense_variant | MODERATE | c.571G>A|p.Val191Ile |
S152 |
| 146760 | BAA10g31200 | A10 | 22844717 | C | T | missense_variant&splice_region_variant | MODERATE | c.370G>A|p.Glu124Lys |
S11 |
| 146761 | BAA10g31190 | A10 | 22845137 | C | T | upstream_gene_variant | MODIFIER | c.-1756G>A| |
S292 |
| 146762 | BAA10g31190 | A10 | 22845949 | G | A | upstream_gene_variant | MODIFIER | c.-2568C>T| |
S219 S72 |
| 146763 | BAA10g31190 | A10 | 22846438 | C | T | upstream_gene_variant | MODIFIER | c.-3057G>A| |
S177 |
| 146764 | BAA10g31210 | A10 | 22847195 | C | T | missense_variant | MODERATE | c.167C>T|p.Pro56Leu |
S11 |
| 146765 | BAA10g31190 | A10 | 22848022 | C | T | upstream_gene_variant | MODIFIER | c.-4641G>A| |
S16 |
| 146766 | BAA10g31190 | A10 | 22848327 | G | A | upstream_gene_variant | MODIFIER | c.-4946C>T| |
S43 |
| 146767 | BAA10g31220 | A10 | 22849943 | C | T | synonymous_variant | LOW | c.486C>T|p.Gly162Gly |
S295 |
| 146768 | BAA10g31220 | A10 | 22850013 | G | A | missense_variant | MODERATE | c.556G>A|p.Asp186Asn |
S230 |
| 146769 | BAA10g31220 | A10 | 22850066 | G | A | stop_gained | HIGH | c.609G>A|p.Trp203* |
S79 S84 |
| 146770 | BAA10g31220 | A10 | 22850091 | G | A | missense_variant | MODERATE | c.634G>A|p.Asp212Asn |
S265 |
| 146771 | BAA10g31200 | A10 | 22850517 | C | T | upstream_gene_variant | MODIFIER | c.-4989G>A| |
S190 |
| 146772 | BAA10g31230 | A10 | 22851875 | C | T | upstream_gene_variant | MODIFIER | c.-231C>T| |
S168 |
| 146773 | BAA10g31220 | A10 | 22854155 | G | A | downstream_gene_variant | MODIFIER | c.*3984G>A| |
S1 S90 |
| 146774 | BAA10g31220 | A10 | 22854358 | C | T | downstream_gene_variant | MODIFIER | c.*4187C>T| |
S160 |
| 146775 | BAA10g31230 | A10 | 22855299 | C | T | downstream_gene_variant | MODIFIER | c.*1514C>T| |
S103 |