| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 141951 | BAA10g26930 | A10 | 21162680 | G | A | synonymous_variant | LOW | c.429C>T|p.Asp143Asp |
S94 |
| 141952 | BAA10g26940 | A10 | 21163343 | C | T | upstream_gene_variant | MODIFIER | c.-1947C>T| |
S40 S49 |
| 141953 | BAA10g26940 | A10 | 21163383 | G | A | upstream_gene_variant | MODIFIER | c.-1907G>A| |
S241 |
| 141954 | BAA10g26930 | A10 | 21163650 | C | T | upstream_gene_variant | MODIFIER | c.-181G>A| |
S277 |
| 141955 | BAA10g26930 | A10 | 21163991 | C | T | upstream_gene_variant | MODIFIER | c.-522G>A| |
S165 |
| 141956 | BAA10g26930 | A10 | 21164653 | C | T | upstream_gene_variant | MODIFIER | c.-1184G>A| |
S36 |
| 141957 | BAA10g26940 | A10 | 21165512 | G | A | missense_variant | MODERATE | c.122G>A|p.Arg41Gln |
S199 |
| 141958 | BAA10g26940 | A10 | 21166338 | G | A | missense_variant | MODERATE | c.566G>A|p.Gly189Glu |
S164 |
| 141959 | BAA10g26930 | A10 | 21166678 | G | A | upstream_gene_variant | MODIFIER | c.-3209C>T| |
S179 |
| 141960 | BAA10g26930 | A10 | 21166818 | C | T | upstream_gene_variant | MODIFIER | c.-3349G>A| |
S244 |
| 141961 | BAA10g26930 | A10 | 21168438 | G | A | upstream_gene_variant | MODIFIER | c.-4969C>T| |
S71 |
| 141962 | BAA10g26940 | A10 | 21168530 | G | A | downstream_gene_variant | MODIFIER | c.*2050G>A| |
S261 |
| 141963 | BAA10g26950 | A10 | 21168757 | G | A | upstream_gene_variant | MODIFIER | c.-34C>T| |
S120 |
| 141964 | BAA10g26950 | A10 | 21169148 | C | T | upstream_gene_variant | MODIFIER | c.-425G>A| |
S182 |
| 141965 | BAA10g26950 | A10 | 21169227 | C | T | upstream_gene_variant | MODIFIER | c.-504G>A| |
S48 |
| 141966 | BAA10g26950 | A10 | 21169393 | C | T | upstream_gene_variant | MODIFIER | c.-670G>A| |
S201 |
| 141967 | BAA10g26950 | A10 | 21169433 | G | A | upstream_gene_variant | MODIFIER | c.-710C>T| |
S289 S290 |
| 141968 | BAA10g26960 | A10 | 21170148 | G | A | missense_variant | MODERATE | c.169C>T|p.Pro57Ser |
S122 |
| 141969 | BAA10g26960 | A10 | 21170157 | C | T | missense_variant | MODERATE | c.160G>A|p.Val54Ile |
S148 S210 S30 S31 |
| 141970 | BAA10g26950 | A10 | 21170781 | C | T | upstream_gene_variant | MODIFIER | c.-2058G>A| |
S135 |
| 141971 | BAA10g26950 | A10 | 21171350 | C | T | upstream_gene_variant | MODIFIER | c.-2627G>A| |
S123 |
| 141972 | BAA10g26950 | A10 | 21171546 | G | A | upstream_gene_variant | MODIFIER | c.-2823C>T| |
S223 |
| 141973 | BAA10g26970 | A10 | 21172781 | G | A | synonymous_variant | LOW | c.2064C>T|p.Leu688Leu |
S167 |
| 141974 | BAA10g26970 | A10 | 21173415 | C | T | missense_variant | MODERATE | c.1430G>A|p.Gly477Glu |
S301 S304 |
| 141975 | BAA10g26970 | A10 | 21174087 | C | T | missense_variant | MODERATE | c.817G>A|p.Gly273Arg |
S246 |