| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 130701 | BAA10g18220 | A10 | 17145236 | C | T | upstream_gene_variant | MODIFIER | c.-683G>A| |
S119 |
| 130702 | BAA10g18220 | A10 | 17146960 | G | A | upstream_gene_variant | MODIFIER | c.-2407C>T| |
S136 |
| 130703 | BAA10g18230 | A10 | 17148774 | C | T | missense_variant | MODERATE | c.398C>T|p.Thr133Ile |
S210 |
| 130704 | BAA10g18230 | A10 | 17149111 | C | T | synonymous_variant | LOW | c.648C>T|p.Leu216Leu |
S238 S46 |
| 130705 | BAA10g18230 | A10 | 17149474 | C | T | synonymous_variant | LOW | c.1011C>T|p.His337His |
S108 S183 |
| 130706 | BAA10g18230 | A10 | 17149661 | G | A | missense_variant | MODERATE | c.1198G>A|p.Val400Ile |
S295 |
| 130707 | BAA10g18240 | A10 | 17152609 | C | T | upstream_gene_variant | MODIFIER | c.-1713G>A| |
S125 |
| 130708 | BAA10g18240 | A10 | 17153962 | G | A | upstream_gene_variant | MODIFIER | c.-3066C>T| |
S17 |
| 130709 | BAA10g18240 | A10 | 17154045 | C | T | upstream_gene_variant | MODIFIER | c.-3149G>A| |
S121 |
| 130710 | BAA10g18240 | A10 | 17154094 | G | A | upstream_gene_variant | MODIFIER | c.-3198C>T| |
S236 |
| 130711 | BAA10g18240 | A10 | 17154309 | G | A | upstream_gene_variant | MODIFIER | c.-3413C>T| |
S174 S27 |
| 130712 | BAA10g18260 | A10 | 17156144 | C | T | stop_gained&splice_region_variant | HIGH | c.670C>T|p.Gln224* |
S18 |
| 130713 | BAA10g18260 | A10 | 17156708 | G | A | synonymous_variant | LOW | c.912G>A|p.Lys304Lys |
S208 S219 |
| 130714 | BAA10g18250 | A10 | 17156795 | C | T | upstream_gene_variant | MODIFIER | c.-4355G>A| |
S84 S93 |
| 130715 | BAA10g18260 | A10 | 17157136 | G | A | missense_variant | MODERATE | c.973G>A|p.Glu325Lys |
S278 |
| 130716 | BAA10g18260 | A10 | 17157253 | C | T | missense_variant&splice_region_variant | MODERATE | c.1090C>T|p.Pro364Ser |
S204 |
| 130717 | BAA10g18260 | A10 | 17158471 | G | A | missense_variant | MODERATE | c.2021G>A|p.Gly674Glu |
S273 |
| 130718 | BAA10g18260 | A10 | 17158547 | C | T | synonymous_variant | LOW | c.2097C>T|p.Asn699Asn |
S10 |
| 130719 | BAA10g18260 | A10 | 17158629 | C | T | synonymous_variant | LOW | c.2179C>T|p.Leu727Leu |
S200 |
| 130720 | BAA10g18260 | A10 | 17159352 | C | T | missense_variant | MODERATE | c.2545C>T|p.His849Tyr |
S238 |
| 130721 | BAA10g18270 | A10 | 17161745 | C | T | upstream_gene_variant | MODIFIER | c.-2227C>T| |
S2 |
| 130722 | BAA10g18270 | A10 | 17162926 | C | T | upstream_gene_variant | MODIFIER | c.-1046C>T| |
S150 |
| 130723 | BAA10g18270 | A10 | 17163311 | C | T | upstream_gene_variant | MODIFIER | c.-661C>T| |
S163 |
| 130724 | BAA10g18270 | A10 | 17166503 | C | T | downstream_gene_variant | MODIFIER | c.*1340C>T| |
S91 |
| 130725 | BAA10g18270 | A10 | 17166789 | C | T | downstream_gene_variant | MODIFIER | c.*1626C>T| |
S249 |