| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 151201 | BAA02g00030 | A02 | 27083 | C | T | intron_variant | MODIFIER | c.2815-1379C>T| |
S211 |
| 151202 | BAA02g00030 | A02 | 27367 | C | T | intron_variant | MODIFIER | c.2815-1095C>T| |
S250 |
| 151203 | BAA02g00030 | A02 | 27473 | G | A | intron_variant | MODIFIER | c.2815-989G>A| |
S122 |
| 151204 | BAA02g00030 | A02 | 27563 | C | T | intron_variant | MODIFIER | c.2815-899C>T| |
S123 |
| 151205 | BAA02g00030 | A02 | 28009 | G | A | intron_variant | MODIFIER | c.2815-453G>A| |
S259 |
| 151206 | BAA02g00030 | A02 | 28871 | C | T | synonymous_variant | LOW | c.3117C>T|p.Tyr1039Tyr |
S262 |
| 151207 | BAA02g00030 | A02 | 29234 | G | A | synonymous_variant | LOW | c.3480G>A|p.Glu1160Glu |
S162 |
| 151208 | BAA02g00030 | A02 | 29289 | G | A | missense_variant | MODERATE | c.3535G>A|p.Ala1179Thr |
S59 |
| 151209 | BAA02g00030 | A02 | 29483 | C | T | synonymous_variant | LOW | c.3729C>T|p.Asp1243Asp |
S298 |
| 151210 | BAA02g00040 | A02 | 29891 | G | A | upstream_gene_variant | MODIFIER | c.-3133G>A| |
|
| 151211 | BAA02g00030 | A02 | 31138 | C | T | synonymous_variant | LOW | c.4587C>T|p.Ile1529Ile |
S306 S308 |
| 151212 | BAA02g00040 | A02 | 31455 | C | T | upstream_gene_variant | MODIFIER | c.-1569C>T| |
S200 |
| 151213 | BAA02g00040 | A02 | 31703 | C | T | upstream_gene_variant | MODIFIER | c.-1321C>T| |
S174 |
| 151214 | BAA02g00040 | A02 | 31947 | C | T | upstream_gene_variant | MODIFIER | c.-1077C>T| |
S196 |
| 151215 | BAA02g00040 | A02 | 32144 | G | A | upstream_gene_variant | MODIFIER | c.-880G>A| |
S17 |
| 151216 | BAA02g00040 | A02 | 32233 | C | T | upstream_gene_variant | MODIFIER | c.-791C>T| |
S115 |
| 151217 | BAA02g00040 | A02 | 33664 | G | A | missense_variant | MODERATE | c.641G>A|p.Gly214Glu |
S33 |
| 151218 | BAA02g00040 | A02 | 33716 | G | A | synonymous_variant | LOW | c.693G>A|p.Gly231Gly |
S118 |
| 151219 | BAA02g00040 | A02 | 34814 | G | A | missense_variant | MODERATE | c.1711G>A|p.Ala571Thr |
S259 |
| 151220 | BAA02g00040 | A02 | 34994 | G | A | missense_variant | MODERATE | c.1891G>A|p.Gly631Arg |
S189 |
| 151221 | BAA02g00040 | A02 | 35186 | G | A | missense_variant | MODERATE | c.2083G>A|p.Gly695Ser |
S48 |
| 151222 | BAA02g00030 | A02 | 35898 | C | T | downstream_gene_variant | MODIFIER | c.*4550C>T| |
S207 |
| 151223 | BAA02g00040 | A02 | 36520 | C | T | downstream_gene_variant | MODIFIER | c.*636C>T| |
S167 |
| 151224 | BAA02g00040 | A02 | 37384 | C | T | downstream_gene_variant | MODIFIER | c.*1500C>T| |
S108 |
| 151225 | BAA02g00040 | A02 | 37741 | G | A | downstream_gene_variant | MODIFIER | c.*1857G>A| |
S237 |