| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 160401 | BAA02g07600 | A02 | 3274885 | C | T | downstream_gene_variant | MODIFIER | c.*4693C>T| |
S8 |
| 160402 | BAA02g07600 | A02 | 3275162 | G | A | downstream_gene_variant | MODIFIER | c.*4970G>A| |
S176 |
| 160403 | BAA02g07610 | A02 | 3275294 | C | T | downstream_gene_variant | MODIFIER | c.*1518C>T| |
S75 |
| 160404 | BAA02g07630 | A02 | 3277090 | C | T | upstream_gene_variant | MODIFIER | c.-4758C>T| |
S257 |
| 160405 | BAA02g07620 | A02 | 3277444 | C | T | synonymous_variant | LOW | c.36G>A|p.Gln12Gln |
S130 |
| 160406 | BAA02g07620 | A02 | 3279849 | G | A | upstream_gene_variant | MODIFIER | c.-2370C>T| |
S122 |
| 160407 | BAA02g07620 | A02 | 3280667 | C | T | upstream_gene_variant | MODIFIER | c.-3188G>A| |
S33 |
| 160408 | BAA02g07620 | A02 | 3281778 | G | A | upstream_gene_variant | MODIFIER | c.-4299C>T| |
S236 |
| 160409 | BAA02g07620 | A02 | 3281804 | C | T | upstream_gene_variant | MODIFIER | c.-4325G>A| |
S25 |
| 160410 | BAA02g07630 | A02 | 3282290 | C | T | missense_variant | MODERATE | c.443C>T|p.Pro148Leu |
S13 |
| 160411 | BAA02g07620 | A02 | 3282382 | C | T | upstream_gene_variant | MODIFIER | c.-4903G>A| |
S15 S3 |
| 160412 | BAA02g07650 | A02 | 3282663 | G | A | upstream_gene_variant | MODIFIER | c.-4474G>A| |
S64 |
| 160413 | BAA02g07650 | A02 | 3284776 | C | T | upstream_gene_variant | MODIFIER | c.-2361C>T| |
S178 |
| 160414 | BAA02g07640 | A02 | 3285476 | G | A | missense_variant | MODERATE | c.445C>T|p.Pro149Ser |
S109 |
| 160415 | BAA02g07640 | A02 | 3286144 | C | T | upstream_gene_variant | MODIFIER | c.-224G>A| |
S79 S84 |
| 160416 | BAA02g07650 | A02 | 3287325 | G | A | missense_variant&splice_region_variant | MODERATE | c.103G>A|p.Asp35Asn |
S275 |
| 160417 | BAA02g07650 | A02 | 3287589 | G | A | synonymous_variant | LOW | c.207G>A|p.Ala69Ala |
S283 |
| 160418 | BAA02g07660 | A02 | 3288895 | G | A | missense_variant | MODERATE | c.671C>T|p.Ala224Val |
S169 |
| 160419 | BAA02g07640 | A02 | 3289147 | G | A | upstream_gene_variant | MODIFIER | c.-3227C>T| |
S47 |
| 160420 | BAA02g07660 | A02 | 3289222 | C | T | missense_variant | MODERATE | c.574G>A|p.Asp192Asn |
S174 S216 S265 S39 |
| 160421 | BAA02g07660 | A02 | 3289279 | G | A | synonymous_variant | LOW | c.517C>T|p.Leu173Leu |
S113 |
| 160422 | BAA02g07640 | A02 | 3290663 | C | T | upstream_gene_variant | MODIFIER | c.-4743G>A| |
S301 S304 |
| 160423 | BAA02g07660 | A02 | 3291188 | G | A | upstream_gene_variant | MODIFIER | c.-581C>T| |
S291 |
| 160424 | BAA02g07660 | A02 | 3291194 | G | A | upstream_gene_variant | MODIFIER | c.-587C>T| |
S247 |
| 160425 | BAA02g07660 | A02 | 3291286 | G | A | upstream_gene_variant | MODIFIER | c.-679C>T| |
S84 S93 |