| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 141401 | BAA10g26410 | A10 | 20960709 | C | T | upstream_gene_variant | MODIFIER | c.-1181C>T| |
S45 |
| 141402 | BAA10g26410 | A10 | 20961962 | C | T | missense_variant | MODERATE | c.73C>T|p.Pro25Ser |
S148 S210 S30 S31 |
| 141403 | BAA10g26420 | A10 | 20965062 | C | T | upstream_gene_variant | MODIFIER | c.-102C>T| |
S140 |
| 141404 | BAA10g26420 | A10 | 20965402 | G | A | missense_variant | MODERATE | c.239G>A|p.Gly80Glu |
S151 |
| 141405 | BAA10g26420 | A10 | 20965511 | C | T | synonymous_variant | LOW | c.348C>T|p.Phe116Phe |
S294 |
| 141406 | BAA10g26410 | A10 | 20966567 | G | A | downstream_gene_variant | MODIFIER | c.*2550G>A| |
S176 |
| 141407 | BAA10g26420 | A10 | 20966774 | C | T | missense_variant | MODERATE | c.1216C>T|p.Leu406Phe |
S295 |
| 141408 | BAA10g26420 | A10 | 20967161 | G | A | missense_variant | MODERATE | c.1529G>A|p.Gly510Glu |
S293 |
| 141409 | BAA10g26440 | A10 | 20967463 | C | T | upstream_gene_variant | MODIFIER | c.-4740C>T| |
S67 |
| 141410 | BAA10g26430 | A10 | 20969234 | C | T | synonymous_variant | LOW | c.528G>A|p.Pro176Pro |
S199 |
| 141411 | BAA10g26430 | A10 | 20969879 | G | A | upstream_gene_variant | MODIFIER | c.-118C>T| |
S176 |
| 141412 | BAA10g26430 | A10 | 20971261 | G | A | upstream_gene_variant | MODIFIER | c.-1500C>T| |
S134 |
| 141413 | BAA10g26430 | A10 | 20973875 | G | A | upstream_gene_variant | MODIFIER | c.-4114C>T| |
S190 |
| 141414 | BAA10g26460 | A10 | 20976382 | C | T | upstream_gene_variant | MODIFIER | c.-1039C>T| |
S296 |
| 141415 | BAA10g26450 | A10 | 20976622 | G | A | missense_variant | MODERATE | c.1387G>A|p.Asp463Asn |
S64 |
| 141416 | BAA10g26460 | A10 | 20977609 | C | T | synonymous_variant | LOW | c.189C>T|p.Gly63Gly |
S243 |
| 141417 | BAA10g26440 | A10 | 20977984 | C | T | downstream_gene_variant | MODIFIER | c.*4230C>T| |
S260 |
| 141418 | BAA10g26460 | A10 | 20978625 | C | T | missense_variant | MODERATE | c.658C>T|p.Leu220Phe |
S286 |
| 141419 | BAA10g26470 | A10 | 20980421 | C | T | missense_variant | MODERATE | c.1028G>A|p.Arg343Lys |
S206 S26 |
| 141420 | BAA10g26470 | A10 | 20980502 | C | T | missense_variant | MODERATE | c.947G>A|p.Arg316His |
S199 |
| 141421 | BAA10g26470 | A10 | 20981466 | G | A | missense_variant | MODERATE | c.236C>T|p.Ser79Leu |
S63 |
| 141422 | BAA10g26470 | A10 | 20981518 | C | T | missense_variant | MODERATE | c.184G>A|p.Glu62Lys |
S168 |
| 141423 | BAA10g26480 | A10 | 20982862 | C | T | synonymous_variant | LOW | c.1053G>A|p.Leu351Leu |
S165 |
| 141424 | BAA10g26480 | A10 | 20984184 | G | A | synonymous_variant | LOW | c.159C>T|p.Leu53Leu |
S240 |
| 141425 | BAA10g26470 | A10 | 20985426 | G | A | upstream_gene_variant | MODIFIER | c.-3725C>T| |
S66 |