| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 150301 | BAA10g34330 | A10 | 24170518 | C | T | synonymous_variant | LOW | c.1650C>T|p.Asn550Asn |
S92 S93 |
| 150302 | BAA10g34330 | A10 | 24170629 | G | A | synonymous_variant | LOW | c.1761G>A|p.Leu587Leu |
S240 |
| 150303 | BAA10g34330 | A10 | 24170699 | C | T | missense_variant | MODERATE | c.1831C>T|p.Pro611Ser |
S44 |
| 150304 | BAA10g34340 | A10 | 24172232 | G | A | missense_variant | MODERATE | c.1139C>T|p.Ala380Val |
S95 |
| 150305 | BAA10g34340 | A10 | 24172504 | C | T | synonymous_variant | LOW | c.867G>A|p.Ala289Ala |
S105 |
| 150306 | BAA10g34340 | A10 | 24172656 | G | A | missense_variant | MODERATE | c.715C>T|p.Leu239Phe |
S270 |
| 150307 | BAA10g34340 | A10 | 24172835 | G | A | missense_variant | MODERATE | c.536C>T|p.Ala179Val |
S50 |
| 150308 | BAA10g34340 | A10 | 24173027 | G | A | missense_variant | MODERATE | c.344C>T|p.Thr115Ile |
S270 |
| 150309 | BAA10g34340 | A10 | 24174121 | C | T | upstream_gene_variant | MODIFIER | c.-751G>A| |
S302 |
| 150310 | BAA10g34340 | A10 | 24174123 | C | T | upstream_gene_variant | MODIFIER | c.-753G>A| |
S170 |
| 150311 | BAA10g34340 | A10 | 24174579 | C | T | upstream_gene_variant | MODIFIER | c.-1209G>A| |
S12 |
| 150312 | BAA10g34340 | A10 | 24175815 | G | A | upstream_gene_variant | MODIFIER | c.-2445C>T| |
S264 |
| 150313 | BAA10g34340 | A10 | 24176480 | C | T | upstream_gene_variant | MODIFIER | c.-3110G>A| |
S148 S210 S30 S31 |
| 150314 | BAA10g34340 | A10 | 24177166 | C | T | upstream_gene_variant | MODIFIER | c.-3796G>A| |
S192 |
| 150315 | BAA10g34340 | A10 | 24177219 | C | T | upstream_gene_variant | MODIFIER | c.-3849G>A| |
S238 |
| 150316 | BAA10g34340 | A10 | 24177235 | C | T | upstream_gene_variant | MODIFIER | c.-3865G>A| |
S11 |
| 150317 | BAA10g34340 | A10 | 24177504 | G | A | upstream_gene_variant | MODIFIER | c.-4134C>T| |
S57 |
| 150318 | BAA10g34350 | A10 | 24178490 | G | A | missense_variant | MODERATE | c.244G>A|p.Asp82Asn |
S207 |
| 150319 | BAA10g34350 | A10 | 24179950 | C | T | downstream_gene_variant | MODIFIER | c.*286C>T| |
S123 S164 |
| 150320 | BAA10g34350 | A10 | 24181028 | C | T | downstream_gene_variant | MODIFIER | c.*1364C>T| |
S260 |
| 150321 | BAA10g34350 | A10 | 24181313 | C | T | downstream_gene_variant | MODIFIER | c.*1649C>T| |
S23 |
| 150322 | BAA10g34360 | A10 | 24189763 | C | T | downstream_gene_variant | MODIFIER | c.*2443G>A| |
S182 |
| 150323 | BAA10g34360 | A10 | 24189966 | C | T | downstream_gene_variant | MODIFIER | c.*2240G>A| |
S297 |
| 150324 | BAA10g34360 | A10 | 24190251 | C | T | downstream_gene_variant | MODIFIER | c.*1955G>A| |
S87 |
| 150325 | BAA10g34360 | A10 | 24190711 | C | T | downstream_gene_variant | MODIFIER | c.*1495G>A| |
S82 S92 |