| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 79051 | BAA01g41560 | A01 | 27637257 | C | T | upstream_gene_variant | MODIFIER | c.-49C>T| |
S135 S152 S185 S203 S273 |
| 79052 | BAA01g41560 | A01 | 27643401 | G | A | downstream_gene_variant | MODIFIER | c.*3743G>A| |
S199 |
| 79053 | BAA01g41560 | A01 | 27643479 | C | T | downstream_gene_variant | MODIFIER | c.*3821C>T| |
S290 |
| 79054 | BAA01g41560 | A01 | 27643935 | C | T | downstream_gene_variant | MODIFIER | c.*4277C>T| |
S269 |
| 79055 | BAA01g41560 | A01 | 27644246 | G | A | downstream_gene_variant | MODIFIER | c.*4588G>A| |
S38 |
| 79056 | BAA01g41560 | A01 | 27644342 | G | A | downstream_gene_variant | MODIFIER | c.*4684G>A| |
S202 |
| 79057 | BAA01g41570 | A01 | 27645334 | C | T | upstream_gene_variant | MODIFIER | c.-4321C>T| |
S292 |
| 79058 | BAA01g41570 | A01 | 27645437 | C | T | upstream_gene_variant | MODIFIER | c.-4218C>T| |
S210 S225 |
| 79059 | BAA01g41570 | A01 | 27646521 | C | T | upstream_gene_variant | MODIFIER | c.-3134C>T| |
S274 |
| 79060 | BAA01g41570 | A01 | 27649885 | C | T | synonymous_variant | LOW | c.231C>T|p.Leu77Leu |
S62 |
| 79061 | BAA01g41570 | A01 | 27650196 | C | T | missense_variant | MODERATE | c.542C>T|p.Ala181Val |
S205 |
| 79062 | BAA01g41580 | A01 | 27650953 | C | T | upstream_gene_variant | MODIFIER | c.-4975C>T| |
S142 |
| 79063 | BAA01g41580 | A01 | 27654434 | G | A | upstream_gene_variant | MODIFIER | c.-1494G>A| |
S196 |
| 79064 | BAA01g41580 | A01 | 27654442 | C | T | upstream_gene_variant | MODIFIER | c.-1486C>T| |
S292 |
| 79065 | BAA01g41580 | A01 | 27655151 | C | T | upstream_gene_variant | MODIFIER | c.-777C>T| |
S205 S240 |
| 79066 | BAA01g41580 | A01 | 27655677 | C | T | upstream_gene_variant | MODIFIER | c.-251C>T| |
S261 |
| 79067 | BAA01g41580 | A01 | 27656536 | G | A | synonymous_variant | LOW | c.609G>A|p.Lys203Lys |
S217 S248 |
| 79068 | BAA01g41580 | A01 | 27656859 | C | T | downstream_gene_variant | MODIFIER | c.*227C>T| |
S239 |
| 79069 | BAA01g41590 | A01 | 27657401 | C | T | missense_variant | MODERATE | c.457G>A|p.Asp153Asn |
S39 |
| 79070 | BAA01g41590 | A01 | 27657617 | C | T | missense_variant | MODERATE | c.241G>A|p.Glu81Lys |
S266 |
| 79071 | BAA01g41590 | A01 | 27658536 | G | A | upstream_gene_variant | MODIFIER | c.-679C>T| |
S267 |
| 79072 | BAA01g41590 | A01 | 27658588 | G | A | upstream_gene_variant | MODIFIER | c.-731C>T| |
S140 |
| 79073 | BAA01g41590 | A01 | 27658634 | G | A | upstream_gene_variant | MODIFIER | c.-777C>T| |
S168 |
| 79074 | BAA01g41600 | A01 | 27658983 | C | T | missense_variant | MODERATE | c.488G>A|p.Gly163Glu |
S17 |
| 79075 | BAA01g41590 | A01 | 27659954 | C | T | upstream_gene_variant | MODIFIER | c.-2097G>A| |
S18 |