| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 117001 | BAA10g10490-BAA10g10500 | A10 | 12240918 | C | T | intergenic_region | MODIFIER | n.12240918C>T| |
S206 S26 |
| 117002 | BAA10g10490-BAA10g10500 | A10 | 12241373 | C | T | intergenic_region | MODIFIER | n.12241373C>T| |
S175 S177 |
| 117003 | BAA10g10490-BAA10g10500 | A10 | 12241470 | G | A | intergenic_region | MODIFIER | n.12241470G>A| |
S105 S106 |
| 117004 | BAA10g10490-BAA10g10500 | A10 | 12242106 | C | T | intergenic_region | MODIFIER | n.12242106C>T| |
S278 |
| 117005 | BAA10g10490-BAA10g10500 | A10 | 12242199 | G | A | intergenic_region | MODIFIER | n.12242199G>A| |
S172 S217 |
| 117006 | BAA10g10490-BAA10g10500 | A10 | 12242518 | C | T | intergenic_region | MODIFIER | n.12242518C>T| |
S270 |
| 117007 | BAA10g10490-BAA10g10500 | A10 | 12243233 | G | A | intergenic_region | MODIFIER | n.12243233G>A| |
S289 |
| 117008 | BAA10g10490-BAA10g10500 | A10 | 12243426 | C | T | intergenic_region | MODIFIER | n.12243426C>T| |
S76 |
| 117009 | BAA10g10490-BAA10g10500 | A10 | 12243703 | G | A | intergenic_region | MODIFIER | n.12243703G>A| |
S172 S217 |
| 117010 | BAA10g10490-BAA10g10500 | A10 | 12243729 | G | A | intergenic_region | MODIFIER | n.12243729G>A| |
S112 |
| 117011 | BAA10g10490-BAA10g10500 | A10 | 12243851 | C | T | intergenic_region | MODIFIER | n.12243851C>T| |
S206 S26 |
| 117012 | BAA10g10500 | A10 | 12253536 | C | T | upstream_gene_variant | MODIFIER | c.-777C>T| |
S235 |
| 117013 | BAA10g10500 | A10 | 12253868 | C | T | upstream_gene_variant | MODIFIER | c.-445C>T| |
S161 |
| 117014 | BAA10g10500 | A10 | 12254462 | G | A | stop_gained | HIGH | c.150G>A|p.Trp50* |
S16 |
| 117015 | BAA10g10500 | A10 | 12254887 | C | T | missense_variant | MODERATE | c.575C>T|p.Ser192Phe |
S92 |
| 117016 | BAA10g10500 | A10 | 12255118 | C | T | missense_variant | MODERATE | c.806C>T|p.Ala269Val |
S282 |
| 117017 | BAA10g10510 | A10 | 12256280 | C | T | synonymous_variant | LOW | c.225C>T|p.Phe75Phe |
S280 |
| 117018 | BAA10g10510 | A10 | 12256283 | G | A | synonymous_variant | LOW | c.228G>A|p.Arg76Arg |
S1 S90 |
| 117019 | BAA10g10510 | A10 | 12256652 | G | A | stop_gained | HIGH | c.597G>A|p.Trp199* |
S158 |
| 117020 | BAA10g10510 | A10 | 12256842 | C | T | missense_variant | MODERATE | c.787C>T|p.Pro263Ser |
S270 |
| 117021 | BAA10g10510 | A10 | 12257133 | G | A | missense_variant | MODERATE | c.1078G>A|p.Asp360Asn |
S296 |
| 117022 | BAA10g10520 | A10 | 12258485 | C | T | upstream_gene_variant | MODIFIER | c.-2124C>T| |
S126 |
| 117023 | BAA10g10520 | A10 | 12261204 | G | A | missense_variant | MODERATE | c.596G>A|p.Gly199Glu |
S262 |
| 117024 | BAA10g10530 | A10 | 12262253 | G | A | synonymous_variant | LOW | c.888C>T|p.Val296Val |
S306 S308 |
| 117025 | BAA10g10530 | A10 | 12262503 | G | A | missense_variant | MODERATE | c.638C>T|p.Ser213Phe |
S85 |