| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 69601 | BAA01g36420 | A01 | 24401967 | G | A | synonymous_variant | LOW | c.114G>A|p.Lys38Lys |
S188 |
| 69602 | BAA01g36420 | A01 | 24402375 | G | A | synonymous_variant | LOW | c.522G>A|p.Gly174Gly |
S61 |
| 69603 | BAA01g36420 | A01 | 24404587 | C | T | synonymous_variant | LOW | c.2734C>T|p.Leu912Leu |
S284 |
| 69604 | BAA01g36410 | A01 | 24404967 | C | T | downstream_gene_variant | MODIFIER | c.*4218C>T| |
S233 |
| 69605 | BAA01g36430 | A01 | 24405721 | G | A | upstream_gene_variant | MODIFIER | c.-90C>T| |
S159 S243 |
| 69606 | BAA01g36430 | A01 | 24406104 | C | T | upstream_gene_variant | MODIFIER | c.-473G>A| |
S228 |
| 69607 | BAA01g36430 | A01 | 24407899 | C | T | upstream_gene_variant | MODIFIER | c.-2268G>A| |
S250 |
| 69608 | BAA01g36430 | A01 | 24408580 | C | T | upstream_gene_variant | MODIFIER | c.-2949G>A| |
S26 |
| 69609 | BAA01g36440 | A01 | 24412113 | C | T | missense_variant | MODERATE | c.824C>T|p.Ser275Phe |
S82 S92 |
| 69610 | BAA01g36450 | A01 | 24413750 | G | A | missense_variant | MODERATE | c.2045C>T|p.Ala682Val |
S185 |
| 69611 | BAA01g36450 | A01 | 24414013 | C | T | missense_variant | MODERATE | c.1879G>A|p.Val627Ile |
S136 |
| 69612 | BAA01g36460 | A01 | 24414643 | G | A | upstream_gene_variant | MODIFIER | c.-2523G>A| |
S135 |
| 69613 | BAA01g36450 | A01 | 24415672 | C | T | missense_variant | MODERATE | c.865G>A|p.Val289Met |
S192 |
| 69614 | BAA01g36450 | A01 | 24416094 | C | T | missense_variant | MODERATE | c.748G>A|p.Glu250Lys |
S303 |
| 69615 | BAA01g36450 | A01 | 24416199 | C | T | missense_variant | MODERATE | c.643G>A|p.Glu215Lys |
S234 |
| 69616 | BAA01g36450 | A01 | 24416290 | C | T | synonymous_variant | LOW | c.552G>A|p.Lys184Lys |
S75 S81 |
| 69617 | BAA01g36450 | A01 | 24417025 | C | T | upstream_gene_variant | MODIFIER | c.-184G>A| |
S266 |
| 69618 | BAA01g36450 | A01 | 24417545 | C | T | upstream_gene_variant | MODIFIER | c.-704G>A| |
S213 |
| 69619 | BAA01g36460 | A01 | 24418671 | C | T | missense_variant | MODERATE | c.608C>T|p.Ser203Leu |
S273 |
| 69620 | BAA01g36460 | A01 | 24418837 | C | T | missense_variant | MODERATE | c.686C>T|p.Ala229Val |
S298 |
| 69621 | BAA01g36450 | A01 | 24420440 | C | T | upstream_gene_variant | MODIFIER | c.-3599G>A| |
S4 |
| 69622 | BAA01g36470 | A01 | 24420743 | C | T | missense_variant | MODERATE | c.275C>T|p.Ser92Phe |
S113 |
| 69623 | BAA01g36470 | A01 | 24420931 | G | A | missense_variant | MODERATE | c.463G>A|p.Gly155Arg |
S298 |
| 69624 | BAA01g36470 | A01 | 24421059 | C | T | synonymous_variant | LOW | c.591C>T|p.Asn197Asn |
S32 |
| 69625 | BAA01g36460 | A01 | 24422283 | C | T | downstream_gene_variant | MODIFIER | c.*3019C>T| |
S142 |