| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 169201 | BAA02g14350 | A02 | 6721606 | C | T | upstream_gene_variant | MODIFIER | c.-4281G>A| |
S205 S240 |
| 169202 | BAA02g14360 | A02 | 6723687 | G | A | upstream_gene_variant | MODIFIER | c.-3068C>T| |
S69 |
| 169203 | BAA02g14360 | A02 | 6724739 | G | A | upstream_gene_variant | MODIFIER | c.-4120C>T| |
S203 |
| 169204 | BAA02g14360 | A02 | 6724803 | C | T | upstream_gene_variant | MODIFIER | c.-4184G>A| |
S32 |
| 169205 | BAA02g14380 | A02 | 6725619 | G | A | missense_variant | MODERATE | c.238G>A|p.Glu80Lys |
S148 |
| 169206 | BAA02g14380 | A02 | 6725767 | C | T | missense_variant | MODERATE | c.386C>T|p.Ser129Phe |
S212 |
| 169207 | BAA02g14370 | A02 | 6726081 | G | A | upstream_gene_variant | MODIFIER | c.-2044C>T| |
S279 |
| 169208 | BAA02g14380 | A02 | 6727535 | C | T | synonymous_variant | LOW | c.1038C>T|p.Cys346Cys |
S183 S198 |
| 169209 | BAA02g14380 | A02 | 6727784 | G | A | missense_variant | MODERATE | c.1208G>A|p.Gly403Asp |
S308 |
| 169210 | BAA02g14380 | A02 | 6728460 | G | A | missense_variant | MODERATE | c.1795G>A|p.Asp599Asn |
S190 |
| 169211 | BAA02g14370 | A02 | 6728988 | C | T | upstream_gene_variant | MODIFIER | c.-4951G>A| |
S283 |
| 169212 | BAA02g14390 | A02 | 6729314 | C | T | upstream_gene_variant | MODIFIER | c.-2609C>T| |
S99 |
| 169213 | BAA02g14390 | A02 | 6729355 | G | A | upstream_gene_variant | MODIFIER | c.-2568G>A| |
S47 |
| 169214 | BAA02g14390 | A02 | 6729447 | G | A | upstream_gene_variant | MODIFIER | c.-2476G>A| |
S187 |
| 169215 | BAA02g14390 | A02 | 6729499 | C | T | upstream_gene_variant | MODIFIER | c.-2424C>T| |
S38 |
| 169216 | BAA02g14380 | A02 | 6730194 | G | A | missense_variant | MODERATE | c.2539G>A|p.Glu847Lys |
S67 |
| 169217 | BAA02g14380 | A02 | 6730339 | G | A | missense_variant | MODERATE | c.2582G>A|p.Gly861Glu |
S303 |
| 169218 | BAA02g14380 | A02 | 6730751 | G | A | synonymous_variant | LOW | c.2994G>A|p.Arg998Arg |
S168 |
| 169219 | BAA02g14380 | A02 | 6730856 | C | A | synonymous_variant | LOW | c.3099C>A|p.Ser1033Ser |
S279 |
| 169220 | BAA02g14380 | A02 | 6731199 | C | T | missense_variant | MODERATE | c.3442C>T|p.His1148Tyr |
S130 |
| 169221 | BAA02g14380 | A02 | 6731273 | G | A | synonymous_variant | LOW | c.3516G>A|p.Pro1172Pro |
S153 S213 |
| 169222 | BAA02g14390 | A02 | 6732452 | C | T | missense_variant | MODERATE | c.530C>T|p.Ser177Phe |
S1 S90 |
| 169223 | BAA02g14390 | A02 | 6732517 | G | A | missense_variant | MODERATE | c.595G>A|p.Asp199Asn |
S28 |
| 169224 | BAA02g14390 | A02 | 6732820 | G | A | missense_variant | MODERATE | c.898G>A|p.Gly300Arg |
S159 S243 |
| 169225 | BAA02g14410 | A02 | 6736148 | T | G | upstream_gene_variant | MODIFIER | c.-1808T>G| |
S61 |