| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 184351 | BAA02g22520 | A02 | 12198488 | C | T | upstream_gene_variant | MODIFIER | c.-1098G>A| |
S78 S83 |
| 184352 | BAA02g22520 | A02 | 12199936 | C | T | upstream_gene_variant | MODIFIER | c.-2546G>A| |
S88 |
| 184353 | BAA02g22520 | A02 | 12200072 | C | T | upstream_gene_variant | MODIFIER | c.-2682G>A| |
S130 |
| 184354 | BAA02g22520 | A02 | 12201010 | G | A | upstream_gene_variant | MODIFIER | c.-3620C>T| |
S210 S225 |
| 184355 | BAA02g22540 | A02 | 12202212 | C | T | missense_variant | MODERATE | c.523G>A|p.Asp175Asn |
S245 |
| 184356 | BAA02g22540 | A02 | 12202425 | C | T | missense_variant | MODERATE | c.310G>A|p.Gly104Ser |
S260 |
| 184357 | BAA02g22550 | A02 | 12209527 | G | A | downstream_gene_variant | MODIFIER | c.*4464C>T| |
S246 |
| 184358 | BAA02g22550 | A02 | 12210003 | C | T | downstream_gene_variant | MODIFIER | c.*3988G>A| |
S289 S290 |
| 184359 | BAA02g22550 | A02 | 12210656 | C | T | downstream_gene_variant | MODIFIER | c.*3335G>A| |
S255 |
| 184360 | BAA02g22550 | A02 | 12210847 | G | A | downstream_gene_variant | MODIFIER | c.*3144C>T| |
S10 |
| 184361 | BAA02g22550 | A02 | 12212536 | G | A | downstream_gene_variant | MODIFIER | c.*1455C>T| |
S206 |
| 184362 | BAA02g22550 | A02 | 12214945 | C | T | synonymous_variant | LOW | c.258G>A|p.Gly86Gly |
S151 |
| 184363 | BAA02g22550 | A02 | 12215063 | C | T | missense_variant | MODERATE | c.140G>A|p.Arg47Lys |
S123 |
| 184364 | BAA02g22550 | A02 | 12217857 | C | T | upstream_gene_variant | MODIFIER | c.-2655G>A| |
S157 S163 |
| 184365 | BAA02g22550 | A02 | 12218171 | C | T | upstream_gene_variant | MODIFIER | c.-2969G>A| |
S139 |
| 184366 | BAA02g22550 | A02 | 12218555 | C | T | upstream_gene_variant | MODIFIER | c.-3353G>A| |
S18 |
| 184367 | BAA02g22550 | A02 | 12218709 | G | A | upstream_gene_variant | MODIFIER | c.-3507C>T| |
S17 |
| 184368 | BAA02g22550 | A02 | 12219228 | G | A | upstream_gene_variant | MODIFIER | c.-4026C>T| |
S202 |
| 184369 | BAA02g22550 | A02 | 12219552 | C | T | upstream_gene_variant | MODIFIER | c.-4350G>A| |
S242 |
| 184370 | BAA02g22550 | A02 | 12219590 | G | A | upstream_gene_variant | MODIFIER | c.-4388C>T| |
S54 |
| 184371 | BAA02g22550 | A02 | 12220007 | C | T | upstream_gene_variant | MODIFIER | c.-4805G>A| |
S5 |
| 184372 | BAA02g22560 | A02 | 12220311 | C | T | upstream_gene_variant | MODIFIER | c.-1649C>T| |
S181 |
| 184373 | BAA02g22560 | A02 | 12220798 | C | T | upstream_gene_variant | MODIFIER | c.-1162C>T| |
S121 |
| 184374 | BAA02g22560 | A02 | 12220964 | G | A | upstream_gene_variant | MODIFIER | c.-996G>A| |
S126 |
| 184375 | BAA02g22560 | A02 | 12222248 | C | T | missense_variant | MODERATE | c.289C>T|p.Pro97Ser |
S203 |