Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
2301 | BAA01g01830 | A01 | 854197 | G | A | upstream_gene_variant | MODIFIER | c.-3011G>A| |
S201 |
2302 | BAA01g01830 | A01 | 854505 | C | T | upstream_gene_variant | MODIFIER | c.-2703C>T| |
S278 S282 |
2303 | BAA01g01830 | A01 | 854715 | G | A | upstream_gene_variant | MODIFIER | c.-2493G>A| |
S169 |
2304 | BAA01g01830 | A01 | 854758 | G | A | upstream_gene_variant | MODIFIER | c.-2450G>A| |
S275 |
2305 | BAA01g01830 | A01 | 855757 | G | A | upstream_gene_variant | MODIFIER | c.-1451G>A| |
S86 |
2306 | BAA01g01830 | A01 | 858882 | G | A | missense_variant | MODERATE | c.1007G>A|p.Gly336Glu |
S112 |
2307 | BAA01g01830 | A01 | 858929 | G | A | downstream_gene_variant | MODIFIER | c.*13G>A| |
S136 |
2308 | BAA01g01830 | A01 | 860089 | C | T | downstream_gene_variant | MODIFIER | c.*1173C>T| |
S188 |
2309 | BAA01g01830 | A01 | 862127 | C | T | downstream_gene_variant | MODIFIER | c.*3211C>T| |
S8 |
2310 | BAA01g01840 | A01 | 862970 | C | T | missense_variant | MODERATE | c.968G>A|p.Arg323Lys |
S252 |
2311 | BAA01g01840 | A01 | 863791 | C | T | synonymous_variant | LOW | c.147G>A|p.Glu49Glu |
S128 |
2312 | BAA01g01840 | A01 | 865808 | C | T | upstream_gene_variant | MODIFIER | c.-1871G>A| |
S266 |
2313 | BAA01g01840 | A01 | 866279 | C | T | upstream_gene_variant | MODIFIER | c.-2342G>A| |
S150 |
2314 | BAA01g01840 | A01 | 866764 | C | T | upstream_gene_variant | MODIFIER | c.-2827G>A| |
S19 |
2315 | BAA01g01850 | A01 | 867803 | G | A | missense_variant | MODERATE | c.2329C>T|p.Pro777Ser |
S32 |
2316 | BAA01g01850 | A01 | 867822 | C | T | synonymous_variant | LOW | c.2310G>A|p.Arg770Arg |
S189 |
2317 | BAA01g01850 | A01 | 867873 | G | A | synonymous_variant | LOW | c.2259C>T|p.Phe753Phe |
S201 |
2318 | BAA01g01850 | A01 | 868405 | C | T | missense_variant | MODERATE | c.1907G>A|p.Gly636Glu |
S19 |
2319 | BAA01g01850 | A01 | 869050 | C | T | missense_variant&splice_region_variant | MODERATE | c.1645G>A|p.Ala549Thr |
S18 |
2320 | BAA01g01850 | A01 | 869735 | G | A | missense_variant | MODERATE | c.1187C>T|p.Ser396Phe |
S116 |
2321 | BAA01g01850 | A01 | 869761 | G | A | synonymous_variant | LOW | c.1161C>T|p.Cys387Cys |
S6 |
2322 | BAA01g01850 | A01 | 869906 | C | T | missense_variant | MODERATE | c.1016G>A|p.Cys339Tyr |
S19 |
2323 | BAA01g01850 | A01 | 869991 | G | A | missense_variant | MODERATE | c.931C>T|p.Pro311Ser |
S239 |
2324 | BAA01g01850 | A01 | 870197 | C | T | missense_variant | MODERATE | c.818G>A|p.Ser273Asn |
S44 |
2325 | BAA01g01850 | A01 | 871075 | G | A | upstream_gene_variant | MODIFIER | c.-61C>T| |
S288 |