| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 121951 | BAA10g12550 | A10 | 13953637 | C | T | stop_gained | HIGH | c.1054C>T|p.Arg352* |
S119 |
| 121952 | BAA10g12550 | A10 | 13953788 | G | A | missense_variant | MODERATE | c.1205G>A|p.Gly402Glu |
S161 |
| 121953 | BAA10g12560 | A10 | 13954383 | G | A | upstream_gene_variant | MODIFIER | c.-3291G>A| |
S292 |
| 121954 | BAA10g12560 | A10 | 13954548 | C | T | upstream_gene_variant | MODIFIER | c.-3126C>T| |
S275 |
| 121955 | BAA10g12560 | A10 | 13954791 | G | A | upstream_gene_variant | MODIFIER | c.-2883G>A| |
S139 |
| 121956 | BAA10g12560 | A10 | 13955774 | G | A | upstream_gene_variant | MODIFIER | c.-1900G>A| |
S120 |
| 121957 | BAA10g12560 | A10 | 13956020 | G | A | upstream_gene_variant | MODIFIER | c.-1654G>A| |
S1 S90 |
| 121958 | BAA10g12560 | A10 | 13956440 | C | T | upstream_gene_variant | MODIFIER | c.-1234C>T| |
S247 |
| 121959 | BAA10g12560 | A10 | 13957522 | G | A | upstream_gene_variant | MODIFIER | c.-152G>A| |
S59 |
| 121960 | BAA10g12560 | A10 | 13958057 | G | A | synonymous_variant | LOW | c.384G>A|p.Leu128Leu |
S302 |
| 121961 | BAA10g12550 | A10 | 13958622 | C | T | downstream_gene_variant | MODIFIER | c.*4626C>T| |
S11 |
| 121962 | BAA10g12560 | A10 | 13959358 | G | A | downstream_gene_variant | MODIFIER | c.*869G>A| |
S18 |
| 121963 | BAA10g12560 | A10 | 13959951 | C | T | downstream_gene_variant | MODIFIER | c.*1462C>T| |
S80 |
| 121964 | BAA10g12560 | A10 | 13960058 | G | A | downstream_gene_variant | MODIFIER | c.*1569G>A| |
S250 |
| 121965 | BAA10g12560 | A10 | 13961294 | G | A | downstream_gene_variant | MODIFIER | c.*2805G>A| |
S258 |
| 121966 | BAA10g12560 | A10 | 13961465 | G | A | downstream_gene_variant | MODIFIER | c.*2976G>A| |
S186 |
| 121967 | BAA10g12560 | A10 | 13961627 | C | T | downstream_gene_variant | MODIFIER | c.*3138C>T| |
S235 |
| 121968 | BAA10g12560 | A10 | 13961738 | T | C | downstream_gene_variant | MODIFIER | c.*3249T>C| |
S168 |
| 121969 | BAA10g12570 | A10 | 13962764 | C | T | missense_variant | MODERATE | c.1510G>A|p.Glu504Lys |
S164 |
| 121970 | BAA10g12570 | A10 | 13963585 | C | T | missense_variant | MODERATE | c.781G>A|p.Glu261Lys |
S308 |
| 121971 | BAA10g12570 | A10 | 13966386 | C | T | upstream_gene_variant | MODIFIER | c.-1698G>A| |
S168 |
| 121972 | BAA10g12570 | A10 | 13966534 | C | T | upstream_gene_variant | MODIFIER | c.-1846G>A| |
S203 |
| 121973 | BAA10g12570 | A10 | 13967617 | C | T | upstream_gene_variant | MODIFIER | c.-2929G>A| |
S246 |
| 121974 | BAA10g12570 | A10 | 13967629 | C | T | upstream_gene_variant | MODIFIER | c.-2941G>A| |
S177 |
| 121975 | BAA10g12570 | A10 | 13967765 | G | A | upstream_gene_variant | MODIFIER | c.-3077C>T| |
S15 |