| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 136351 | BAA10g22020 | A10 | 19132173 | C | T | downstream_gene_variant | MODIFIER | c.*2373C>T| |
S286 |
| 136352 | BAA10g22030 | A10 | 19132253 | G | A | stop_gained&splice_region_variant | HIGH | c.259C>T|p.Gln87* |
S180 |
| 136353 | BAA10g22030 | A10 | 19132382 | G | A | missense_variant | MODERATE | c.130C>T|p.Leu44Phe |
S47 |
| 136354 | BAA10g22030 | A10 | 19133955 | C | T | upstream_gene_variant | MODIFIER | c.-1020G>A| |
S244 |
| 136355 | BAA10g22030 | A10 | 19136528 | C | T | upstream_gene_variant | MODIFIER | c.-3593G>A| |
S5 |
| 136356 | BAA10g22030 | A10 | 19137010 | C | T | upstream_gene_variant | MODIFIER | c.-4075G>A| |
S297 |
| 136357 | BAA10g22040 | A10 | 19138730 | G | A | missense_variant | MODERATE | c.404G>A|p.Gly135Glu |
S223 |
| 136358 | BAA10g22050 | A10 | 19139637 | G | A | upstream_gene_variant | MODIFIER | c.-379G>A| |
S197 |
| 136359 | BAA10g22050 | A10 | 19139999 | C | T | upstream_gene_variant | MODIFIER | c.-17C>T| |
S194 |
| 136360 | BAA10g22040 | A10 | 19140745 | G | A | downstream_gene_variant | MODIFIER | c.*1596G>A| |
S15 |
| 136361 | BAA10g22040 | A10 | 19140932 | A | T | downstream_gene_variant | MODIFIER | c.*1783A>T| |
S152 |
| 136362 | BAA10g22050 | A10 | 19141667 | G | A | synonymous_variant | LOW | c.624G>A|p.Arg208Arg |
S28 |
| 136363 | BAA10g22040 | A10 | 19142101 | C | T | downstream_gene_variant | MODIFIER | c.*2952C>T| |
S25 |
| 136364 | BAA10g22050 | A10 | 19142368 | G | A | synonymous_variant | LOW | c.1074G>A|p.Lys358Lys |
S149 |
| 136365 | BAA10g22040 | A10 | 19143730 | G | A | downstream_gene_variant | MODIFIER | c.*4581G>A| |
S209 |
| 136366 | BAA10g22040 | A10 | 19143939 | C | T | downstream_gene_variant | MODIFIER | c.*4790C>T| |
S183 |
| 136367 | BAA10g22060 | A10 | 19144463 | G | A | upstream_gene_variant | MODIFIER | c.-4500G>A| |
S298 |
| 136368 | BAA10g22060 | A10 | 19145018 | C | T | upstream_gene_variant | MODIFIER | c.-3945C>T| |
S211 |
| 136369 | BAA10g22060 | A10 | 19148087 | G | A | upstream_gene_variant | MODIFIER | c.-876G>A| |
S82 S92 |
| 136370 | BAA10g22060 | A10 | 19148391 | G | T | upstream_gene_variant | MODIFIER | c.-572G>T| |
S104 S108 S12 S134 S146 S169 S176 S184 S192 S196 S238 S257 S279 S301 S68 |
| 136371 | BAA10g22060 | A10 | 19149023 | G | A | intron_variant | MODIFIER | c.30+31G>A| |
S28 |
| 136372 | BAA10g22060 | A10 | 19149188 | G | A | missense_variant | MODERATE | c.146G>A|p.Cys49Tyr |
S36 |
| 136373 | BAA10g22060 | A10 | 19149252 | C | T | synonymous_variant | LOW | c.210C>T|p.Asn70Asn |
S10 |
| 136374 | BAA10g22060 | A10 | 19149594 | G | A | synonymous_variant | LOW | c.552G>A|p.Arg184Arg |
S82 |
| 136375 | BAA10g22060 | A10 | 19149621 | G | A | synonymous_variant | LOW | c.579G>A|p.Arg193Arg |
S168 S219 S72 |