| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 168051 | BAA02g13510 | A02 | 6226967 | C | T | downstream_gene_variant | MODIFIER | c.*3212G>A| |
S208 S219 |
| 168052 | BAA02g13510 | A02 | 6227075 | C | T | downstream_gene_variant | MODIFIER | c.*3104G>A| |
S138 |
| 168053 | BAA02g13520 | A02 | 6227264 | G | A | upstream_gene_variant | MODIFIER | c.-4964G>A| |
S229 |
| 168054 | BAA02g13510 | A02 | 6230371 | G | A | synonymous_variant | LOW | c.552C>T|p.Ile184Ile |
S169 |
| 168055 | BAA02g13520 | A02 | 6231255 | C | T | upstream_gene_variant | MODIFIER | c.-973C>T| |
S234 |
| 168056 | BAA02g13510 | A02 | 6231786 | G | A | synonymous_variant | LOW | c.30C>T|p.Ser10Ser |
S125 |
| 168057 | BAA02g13520 | A02 | 6232561 | C | T | missense_variant | MODERATE | c.254C>T|p.Pro85Leu |
S6 |
| 168058 | BAA02g13530 | A02 | 6233284 | G | A | synonymous_variant | LOW | c.622C>T|p.Leu208Leu |
S126 |
| 168059 | BAA02g13530 | A02 | 6233767 | C | T | synonymous_variant | LOW | c.447G>A|p.Lys149Lys |
S142 |
| 168060 | BAA02g13530 | A02 | 6233869 | C | T | synonymous_variant | LOW | c.345G>A|p.Gly115Gly |
S255 |
| 168061 | BAA02g13510 | A02 | 6234507 | G | A | upstream_gene_variant | MODIFIER | c.-2692C>T| |
S192 |
| 168062 | BAA02g13510 | A02 | 6234655 | C | T | upstream_gene_variant | MODIFIER | c.-2840G>A| |
S104 S25 |
| 168063 | BAA02g13510 | A02 | 6234871 | C | T | upstream_gene_variant | MODIFIER | c.-3056G>A| |
S135 |
| 168064 | BAA02g13530 | A02 | 6236844 | C | T | upstream_gene_variant | MODIFIER | c.-2631G>A| |
S305 |
| 168065 | BAA02g13530 | A02 | 6237207 | G | A | upstream_gene_variant | MODIFIER | c.-2994C>T| |
S187 |
| 168066 | BAA02g13530 | A02 | 6238910 | G | A | upstream_gene_variant | MODIFIER | c.-4697C>T| |
S36 |
| 168067 | BAA02g13540 | A02 | 6239569 | G | A | upstream_gene_variant | MODIFIER | c.-639G>A| |
S187 |
| 168068 | BAA02g13540 | A02 | 6240261 | C | T | intron_variant | MODIFIER | c.25+29C>T| |
S208 |
| 168069 | BAA02g13540 | A02 | 6240575 | C | T | intron_variant | MODIFIER | c.161+11C>T| |
S245 |
| 168070 | BAA02g13540 | A02 | 6240658 | C | T | missense_variant | MODERATE | c.170C>T|p.Ser57Phe |
S90 |
| 168071 | BAA02g13540 | A02 | 6240917 | C | T | missense_variant | MODERATE | c.311C>T|p.Ser104Phe |
S221 |
| 168072 | BAA02g13540 | A02 | 6241057 | C | T | missense_variant | MODERATE | c.451C>T|p.Pro151Ser |
S292 |
| 168073 | BAA02g13540 | A02 | 6241288 | C | T | downstream_gene_variant | MODIFIER | c.*118C>T| |
S165 |
| 168074 | BAA02g13540 | A02 | 6241522 | C | T | downstream_gene_variant | MODIFIER | c.*352C>T| |
S181 |
| 168075 | BAA02g13540 | A02 | 6241585 | G | A | downstream_gene_variant | MODIFIER | c.*415G>A| |
S134 |