| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g12340 | A06 | 6201854 | C | T | upstream_gene_variant | MODIFIER | c.-1138C>T| |
S61 |
| 2 | BAA06g12340 | A06 | 6202126 | C | T | upstream_gene_variant | MODIFIER | c.-866C>T| |
S170 |
| 3 | BAA06g12340 | A06 | 6202453 | G | A | upstream_gene_variant | MODIFIER | c.-539G>A| |
S181 |
| 4 | BAA06g12340 | A06 | 6203177 | C | T | synonymous_variant | LOW | c.186C>T|p.Ile62Ile |
S34 |
| 5 | BAA06g12340 | A06 | 6204904 | G | A | missense_variant | MODERATE | c.1192G>A|p.Asp398Asn |
S63 |
| 6 | BAA06g12340 | A06 | 6205567 | G | A | intron_variant | MODIFIER | c.1257+598G>A| |
S50 |
| 7 | BAA06g12340 | A06 | 6205812 | C | T | intron_variant | MODIFIER | c.1257+843C>T| |
S165 |
| 8 | BAA06g12340 | A06 | 6205842 | C | T | intron_variant | MODIFIER | c.1257+873C>T| |
S111 |
| 9 | BAA06g12340 | A06 | 6206296 | G | A | intron_variant | MODIFIER | c.1258-721G>A| |
S113 |
| 10 | BAA06g12340 | A06 | 6208995 | C | T | missense_variant | MODERATE | c.1841C>T|p.Ser614Phe |
S202 |
| 11 | BAA06g12340 | A06 | 6212035 | C | T | missense_variant | MODERATE | c.2180C>T|p.Ala727Val |
S247 |
| 12 | BAA06g12340 | A06 | 6212149 | G | A | missense_variant | MODERATE | c.2294G>A|p.Arg765His |
S234 |
| 13 | BAA06g12340 | A06 | 6212193 | G | A | missense_variant | MODERATE | c.2338G>A|p.Glu780Lys |
S292 |
| 14 | BAA06g12340 | A06 | 6212605 | C | T | missense_variant | MODERATE | c.2594C>T|p.Ala865Val |
S176 |
| 15 | BAA06g12340 | A06 | 6212608 | G | A | missense_variant | MODERATE | c.2597G>A|p.Arg866Lys |
S125 |
| 16 | BAA06g12340 | A06 | 6212630 | G | A | missense_variant | MODERATE | c.2619G>A|p.Met873Ile |
S146 |
| 17 | BAA06g12340 | A06 | 6215491 | C | T | downstream_gene_variant | MODIFIER | c.*1768C>T| |
S172 S217 |