| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 104251 | BAA10g07930 | A10 | 5022068 | C | T | missense_variant | MODERATE | c.785G>A|p.Ser262Asn |
S175 |
| 104252 | BAA10g07920 | A10 | 5022406 | G | A | downstream_gene_variant | MODIFIER | c.*1048G>A| |
S55 |
| 104253 | BAA10g07920 | A10 | 5022578 | C | T | downstream_gene_variant | MODIFIER | c.*1220C>T| |
S110 |
| 104254 | BAA10g07930 | A10 | 5022639 | G | A | synonymous_variant | LOW | c.531C>T|p.Ile177Ile |
S289 |
| 104255 | BAA10g07930 | A10 | 5022943 | C | T | synonymous_variant | LOW | c.309G>A|p.Gln103Gln |
S34 |
| 104256 | BAA10g07930 | A10 | 5023189 | G | A | synonymous_variant | LOW | c.135C>T|p.Phe45Phe |
S237 |
| 104257 | BAA10g07930 | A10 | 5023336 | G | A | splice_region_variant&intron_variant | LOW | c.50+8C>T| |
S35 |
| 104258 | BAA10g07930 | A10 | 5023880 | C | T | upstream_gene_variant | MODIFIER | c.-487G>A| |
S34 |
| 104259 | BAA10g07930 | A10 | 5024970 | C | T | upstream_gene_variant | MODIFIER | c.-1577G>A| |
S243 S299 |
| 104260 | BAA10g07930 | A10 | 5025222 | C | T | upstream_gene_variant | MODIFIER | c.-1829G>A| |
S114 |
| 104261 | BAA10g07930 | A10 | 5025560 | G | A | upstream_gene_variant | MODIFIER | c.-2167C>T| |
S138 |
| 104262 | BAA10g07930 | A10 | 5026284 | G | A | upstream_gene_variant | MODIFIER | c.-2891C>T| |
S212 |
| 104263 | BAA10g07930 | A10 | 5027771 | C | T | upstream_gene_variant | MODIFIER | c.-4378G>A| |
S177 |
| 104264 | BAA10g07930 | A10 | 5027989 | C | T | upstream_gene_variant | MODIFIER | c.-4596G>A| |
S180 |
| 104265 | BAA10g07930 | A10 | 5028104 | C | T | upstream_gene_variant | MODIFIER | c.-4711G>A| |
S191 |
| 104266 | BAA10g07940 | A10 | 5028402 | C | T | downstream_gene_variant | MODIFIER | c.*1275G>A| |
S166 |
| 104267 | BAA10g07940 | A10 | 5029287 | G | A | downstream_gene_variant | MODIFIER | c.*390C>T| |
S15 |
| 104268 | BAA10g07940 | A10 | 5029918 | C | T | missense_variant | MODERATE | c.491G>A|p.Cys164Tyr |
S176 |
| 104269 | BAA10g07940 | A10 | 5029959 | G | A | synonymous_variant | LOW | c.450C>T|p.Ser150Ser |
S288 |
| 104270 | BAA10g07940 | A10 | 5031135 | G | A | upstream_gene_variant | MODIFIER | c.-44C>T| |
S295 |
| 104271 | BAA10g07940 | A10 | 5031238 | C | T | upstream_gene_variant | MODIFIER | c.-147G>A| |
S133 |
| 104272 | BAA10g07940 | A10 | 5031501 | C | T | upstream_gene_variant | MODIFIER | c.-410G>A| |
S249 |
| 104273 | BAA10g07950 | A10 | 5031627 | C | T | missense_variant | MODERATE | c.1178G>A|p.Gly393Glu |
S256 |
| 104274 | BAA10g07950 | A10 | 5032981 | G | A | synonymous_variant | LOW | c.555C>T|p.Ser185Ser |
S64 |
| 104275 | BAA10g07940 | A10 | 5033338 | G | A | upstream_gene_variant | MODIFIER | c.-2247C>T| |
S236 |