| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 145401 | BAA10g29940 | A10 | 22362877 | G | A | upstream_gene_variant | MODIFIER | c.-3373C>T| |
S130 |
| 145402 | BAA10g29950 | A10 | 22363390 | G | A | stop_gained | HIGH | c.205C>T|p.Gln69* |
S271 |
| 145403 | BAA10g29960 | A10 | 22365720 | G | A | missense_variant | MODERATE | c.178G>A|p.Glu60Lys |
S17 S227 |
| 145404 | BAA10g29950 | A10 | 22366138 | G | A | upstream_gene_variant | MODIFIER | c.-2544C>T| |
S281 S282 |
| 145405 | BAA10g29970 | A10 | 22366793 | C | T | missense_variant | MODERATE | c.751G>A|p.Val251Ile |
S90 |
| 145406 | BAA10g29970 | A10 | 22367033 | C | T | stop_gained | HIGH | c.702G>A|p.Trp234* |
S133 |
| 145407 | BAA10g29950 | A10 | 22367328 | G | A | upstream_gene_variant | MODIFIER | c.-3734C>T| |
S171 |
| 145408 | BAA10g29970 | A10 | 22367354 | G | A | synonymous_variant | LOW | c.573C>T|p.Phe191Phe |
S180 |
| 145409 | BAA10g29970 | A10 | 22368817 | C | T | upstream_gene_variant | MODIFIER | c.-521G>A| |
S157 |
| 145410 | BAA10g29970 | A10 | 22368842 | C | T | upstream_gene_variant | MODIFIER | c.-546G>A| |
S82 S92 |
| 145411 | BAA10g29970 | A10 | 22368937 | G | A | upstream_gene_variant | MODIFIER | c.-641C>T| |
S280 |
| 145412 | BAA10g29970 | A10 | 22369724 | C | T | upstream_gene_variant | MODIFIER | c.-1428G>A| |
S225 |
| 145413 | BAA10g29970 | A10 | 22370178 | G | A | upstream_gene_variant | MODIFIER | c.-1882C>T| |
S100 |
| 145414 | BAA10g29970 | A10 | 22370864 | G | A | upstream_gene_variant | MODIFIER | c.-2568C>T| |
S265 |
| 145415 | BAA10g29980 | A10 | 22371162 | C | T | missense_variant | MODERATE | c.691G>A|p.Asp231Asn |
S37 |
| 145416 | BAA10g29980 | A10 | 22371374 | G | A | missense_variant | MODERATE | c.479C>T|p.Ala160Val |
S126 |
| 145417 | BAA10g29980 | A10 | 22372271 | C | T | missense_variant | MODERATE | c.67G>A|p.Asp23Asn |
S152 |
| 145418 | BAA10g29970 | A10 | 22372460 | C | T | upstream_gene_variant | MODIFIER | c.-4164G>A| |
S185 |
| 145419 | BAA10g29970 | A10 | 22372955 | G | A | upstream_gene_variant | MODIFIER | c.-4659C>T| |
S173 |
| 145420 | BAA10g29990 | A10 | 22373938 | C | T | synonymous_variant | LOW | c.828G>A|p.Arg276Arg |
S206 S26 |
| 145421 | BAA10g29990 | A10 | 22374138 | G | A | missense_variant | MODERATE | c.628C>T|p.Leu210Phe |
S125 |
| 145422 | BAA10g30000 | A10 | 22375815 | C | T | missense_variant | MODERATE | c.1300G>A|p.Val434Ile |
S277 |
| 145423 | BAA10g30000 | A10 | 22376989 | C | T | missense_variant | MODERATE | c.126G>A|p.Met42Ile |
S206 S26 |
| 145424 | BAA10g29990 | A10 | 22378225 | C | T | upstream_gene_variant | MODIFIER | c.-3460G>A| |
S277 |
| 145425 | BAA10g29990 | A10 | 22378474 | C | T | upstream_gene_variant | MODIFIER | c.-3709G>A| |
S42 |