| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 169301 | BAA02g14450 | A02 | 6749224 | G | A | upstream_gene_variant | MODIFIER | c.-4543G>A| |
S282 |
| 169302 | BAA02g14450 | A02 | 6749262 | G | A | upstream_gene_variant | MODIFIER | c.-4505G>A| |
S288 |
| 169303 | BAA02g14450 | A02 | 6749285 | C | T | upstream_gene_variant | MODIFIER | c.-4482C>T| |
S167 |
| 169304 | BAA02g14450 | A02 | 6750959 | G | A | upstream_gene_variant | MODIFIER | c.-2808G>A| |
S251 |
| 169305 | BAA02g14450 | A02 | 6752806 | C | T | upstream_gene_variant | MODIFIER | c.-961C>T| |
S131 |
| 169306 | BAA02g14450 | A02 | 6753183 | G | A | upstream_gene_variant | MODIFIER | c.-584G>A| |
S187 |
| 169307 | BAA02g14450 | A02 | 6753487 | C | T | upstream_gene_variant | MODIFIER | c.-280C>T| |
S206 S26 |
| 169308 | BAA02g14450 | A02 | 6755982 | G | A | missense_variant | MODERATE | c.1486G>A|p.Asp496Asn |
S67 |
| 169309 | BAA02g14450 | A02 | 6756098 | C | T | synonymous_variant | LOW | c.1602C>T|p.Ile534Ile |
S139 |
| 169310 | BAA02g14460 | A02 | 6761364 | G | A | upstream_gene_variant | MODIFIER | c.-364G>A| |
S293 |
| 169311 | BAA02g14460 | A02 | 6761799 | C | T | synonymous_variant | LOW | c.72C>T|p.Leu24Leu |
S51 |
| 169312 | BAA02g14460 | A02 | 6761855 | G | A | missense_variant | MODERATE | c.128G>A|p.Gly43Glu |
S86 |
| 169313 | BAA02g14470 | A02 | 6763775 | C | T | upstream_gene_variant | MODIFIER | c.-1887C>T| |
S266 |
| 169314 | BAA02g14470 | A02 | 6765332 | G | A | upstream_gene_variant | MODIFIER | c.-330G>A| |
S192 |
| 169315 | BAA02g14470 | A02 | 6766304 | C | T | stop_gained | HIGH | c.643C>T|p.Gln215* |
S216 S241 S265 S39 |
| 169316 | BAA02g14470 | A02 | 6766905 | C | T | missense_variant | MODERATE | c.1244C>T|p.Ser415Phe |
S283 |
| 169317 | BAA02g14470 | A02 | 6767614 | G | A | synonymous_variant | LOW | c.1704G>A|p.Glu568Glu |
S143 |
| 169318 | BAA02g14470 | A02 | 6767693 | G | A | missense_variant | MODERATE | c.1712G>A|p.Gly571Asp |
S238 |
| 169319 | BAA02g14470 | A02 | 6767922 | G | A | missense_variant | MODERATE | c.1840G>A|p.Glu614Lys |
S96 |
| 169320 | BAA02g14480 | A02 | 6768223 | G | A | upstream_gene_variant | MODIFIER | c.-3900G>A| |
S295 |
| 169321 | BAA02g14470 | A02 | 6769590 | G | A | missense_variant | MODERATE | c.2696G>A|p.Arg899Lys |
S162 |
| 169322 | BAA02g14470 | A02 | 6769801 | C | T | missense_variant | MODERATE | c.2803C>T|p.Leu935Phe |
S15 S3 |
| 169323 | BAA02g14480 | A02 | 6769913 | C | T | upstream_gene_variant | MODIFIER | c.-2210C>T| |
S152 |
| 169324 | BAA02g14480 | A02 | 6770829 | G | A | upstream_gene_variant | MODIFIER | c.-1294G>A| |
S305 |
| 169325 | BAA02g14480 | A02 | 6770854 | C | T | upstream_gene_variant | MODIFIER | c.-1269C>T| |
S135 |