| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 67751 | BAA01g35470 | A01 | 23751179 | C | A | downstream_gene_variant | MODIFIER | c.*992C>A| |
S236 |
| 67752 | BAA01g35470 | A01 | 23751655 | C | T | downstream_gene_variant | MODIFIER | c.*1468C>T| |
S264 |
| 67753 | BAA01g35470 | A01 | 23752164 | C | T | downstream_gene_variant | MODIFIER | c.*1977C>T| |
S132 S137 S215 |
| 67754 | BAA01g35470 | A01 | 23752239 | G | A | downstream_gene_variant | MODIFIER | c.*2052G>A| |
S172 |
| 67755 | BAA01g35470 | A01 | 23752397 | G | A | downstream_gene_variant | MODIFIER | c.*2210G>A| |
S209 |
| 67756 | BAA01g35470 | A01 | 23753732 | C | T | downstream_gene_variant | MODIFIER | c.*3545C>T| |
S4 |
| 67757 | BAA01g35490 | A01 | 23754043 | G | A | upstream_gene_variant | MODIFIER | c.-4732G>A| |
S241 |
| 67758 | BAA01g35490 | A01 | 23754112 | C | T | upstream_gene_variant | MODIFIER | c.-4663C>T| |
S161 |
| 67759 | BAA01g35480 | A01 | 23754323 | G | A | synonymous_variant | LOW | c.1240C>T|p.Leu414Leu |
S138 |
| 67760 | BAA01g35490 | A01 | 23755122 | C | T | upstream_gene_variant | MODIFIER | c.-3653C>T| |
S94 |
| 67761 | BAA01g35480 | A01 | 23756341 | C | T | missense_variant | MODERATE | c.22G>A|p.Asp8Asn |
S177 |
| 67762 | BAA01g35480 | A01 | 23756649 | C | T | upstream_gene_variant | MODIFIER | c.-287G>A| |
S238 |
| 67763 | BAA01g35480 | A01 | 23756898 | C | T | upstream_gene_variant | MODIFIER | c.-536G>A| |
S265 |
| 67764 | BAA01g35480 | A01 | 23757229 | C | T | upstream_gene_variant | MODIFIER | c.-867G>A| |
S113 |
| 67765 | BAA01g35480 | A01 | 23759905 | C | T | upstream_gene_variant | MODIFIER | c.-3543G>A| |
S192 |
| 67766 | BAA01g35480 | A01 | 23760552 | G | A | upstream_gene_variant | MODIFIER | c.-4190C>T| |
S172 S217 |
| 67767 | BAA01g35500 | A01 | 23761212 | G | A | missense_variant | MODERATE | c.451G>A|p.Glu151Lys |
S1 S103 S90 |
| 67768 | BAA01g35500 | A01 | 23761265 | T | C | synonymous_variant | LOW | c.504T>C|p.Asp168Asp |
S37 |
| 67769 | BAA01g35500 | A01 | 23761389 | G | A | missense_variant | MODERATE | c.628G>A|p.Val210Met |
S191 |
| 67770 | BAA01g35510 | A01 | 23762575 | G | A | splice_region_variant&intron_variant | LOW | c.835-3C>T| |
S246 |
| 67771 | BAA01g35510 | A01 | 23763161 | C | T | missense_variant | MODERATE | c.655G>A|p.Glu219Lys |
S170 |
| 67772 | BAA01g35510 | A01 | 23763437 | C | T | missense_variant | MODERATE | c.461G>A|p.Gly154Glu |
S28 |
| 67773 | BAA01g35510 | A01 | 23765667 | G | A | upstream_gene_variant | MODIFIER | c.-1213C>T| |
S140 |
| 67774 | BAA01g35510 | A01 | 23766650 | G | A | upstream_gene_variant | MODIFIER | c.-2196C>T| |
S223 |
| 67775 | BAA01g35510 | A01 | 23768455 | C | T | upstream_gene_variant | MODIFIER | c.-4001G>A| |
S69 |