| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 22051 | BAA01g15980 | A01 | 7787545 | C | T | downstream_gene_variant | MODIFIER | c.*2004C>T| |
S265 |
| 22052 | BAA01g15980 | A01 | 7788603 | G | A | downstream_gene_variant | MODIFIER | c.*3062G>A| |
S115 |
| 22053 | BAA01g15980 | A01 | 7788664 | G | A | downstream_gene_variant | MODIFIER | c.*3123G>A| |
S197 |
| 22054 | BAA01g15980 | A01 | 7788837 | G | A | downstream_gene_variant | MODIFIER | c.*3296G>A| |
S149 |
| 22055 | BAA01g15980 | A01 | 7789200 | G | A | downstream_gene_variant | MODIFIER | c.*3659G>A| |
S217 |
| 22056 | BAA01g15980 | A01 | 7789425 | C | T | downstream_gene_variant | MODIFIER | c.*3884C>T| |
S250 |
| 22057 | BAA01g15980 | A01 | 7789764 | C | T | downstream_gene_variant | MODIFIER | c.*4223C>T| |
S148 S30 S31 |
| 22058 | BAA01g15990 | A01 | 7794096 | G | A | upstream_gene_variant | MODIFIER | c.-834G>A| |
S72 S78 |
| 22059 | BAA01g15990 | A01 | 7794102 | C | T | upstream_gene_variant | MODIFIER | c.-828C>T| |
S296 |
| 22060 | BAA01g15990 | A01 | 7794437 | G | A | upstream_gene_variant | MODIFIER | c.-493G>A| |
S139 |
| 22061 | BAA01g15990 | A01 | 7794510 | G | A | upstream_gene_variant | MODIFIER | c.-420G>A| |
S263 |
| 22062 | BAA01g15990 | A01 | 7796570 | G | A | downstream_gene_variant | MODIFIER | c.*1012G>A| |
S162 |
| 22063 | BAA01g15990 | A01 | 7797060 | G | A | downstream_gene_variant | MODIFIER | c.*1502G>A| |
S181 |
| 22064 | BAA01g15990 | A01 | 7797396 | C | T | downstream_gene_variant | MODIFIER | c.*1838C>T| |
S215 |
| 22065 | BAA01g16000 | A01 | 7801982 | G | A | upstream_gene_variant | MODIFIER | c.-1273C>T| |
S236 |
| 22066 | BAA01g16010 | A01 | 7806917 | C | T | missense_variant | MODERATE | c.983G>A|p.Gly328Glu |
S221 |
| 22067 | BAA01g16010 | A01 | 7807066 | G | A | missense_variant&splice_region_variant | MODERATE | c.959C>T|p.Pro320Leu |
S149 |
| 22068 | BAA01g16010 | A01 | 7807305 | C | T | synonymous_variant | LOW | c.720G>A|p.Ser240Ser |
S135 |
| 22069 | BAA01g16010 | A01 | 7807488 | G | A | intron_variant | MODIFIER | c.632-95C>T| |
S116 |
| 22070 | BAA01g16010 | A01 | 7807673 | C | T | missense_variant | MODERATE | c.595G>A|p.Asp199Asn |
S294 |
| 22071 | BAA01g16010 | A01 | 7807779 | C | T | synonymous_variant | LOW | c.489G>A|p.Glu163Glu |
S16 S182 |
| 22072 | BAA01g16010 | A01 | 7808017 | C | T | intron_variant | MODIFIER | c.264-13G>A| |
S113 |
| 22073 | BAA01g16010 | A01 | 7808764 | A | G | upstream_gene_variant | MODIFIER | c.-29T>C| |
S168 |
| 22074 | BAA01g16010 | A01 | 7809222 | C | T | upstream_gene_variant | MODIFIER | c.-487G>A| |
S295 |
| 22075 | BAA01g16010 | A01 | 7809824 | C | T | upstream_gene_variant | MODIFIER | c.-1089G>A| |
S179 |