Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
5251 | BAA01g04290 | A01 | 1927183 | G | A | upstream_gene_variant | MODIFIER | c.-2136C>T| |
S262 |
5252 | BAA01g04290 | A01 | 1928251 | C | T | upstream_gene_variant | MODIFIER | c.-3204G>A| |
S158 |
5253 | BAA01g04300 | A01 | 1929760 | C | T | missense_variant | MODERATE | c.346G>A|p.Glu116Lys |
S18 |
5254 | BAA01g04300 | A01 | 1931978 | C | T | upstream_gene_variant | MODIFIER | c.-1873G>A| |
S118 |
5255 | BAA01g04300 | A01 | 1933140 | C | T | upstream_gene_variant | MODIFIER | c.-3035G>A| |
S51 |
5256 | BAA01g04310 | A01 | 1933389 | G | A | missense_variant | MODERATE | c.323C>T|p.Ser108Leu |
S123 |
5257 | BAA01g04300 | A01 | 1934046 | G | A | upstream_gene_variant | MODIFIER | c.-3941C>T| |
S15 S3 |
5258 | BAA01g04300 | A01 | 1934231 | G | A | upstream_gene_variant | MODIFIER | c.-4126C>T| |
S286 |
5259 | BAA01g04320 | A01 | 1934488 | G | A | missense_variant | MODERATE | c.232G>A|p.Glu78Lys |
S188 |
5260 | BAA01g04320 | A01 | 1934590 | G | A | missense_variant | MODERATE | c.334G>A|p.Glu112Lys |
S293 |
5261 | BAA01g04320 | A01 | 1934673 | G | A | synonymous_variant | LOW | c.417G>A|p.Gln139Gln |
S105 S106 |
5262 | BAA01g04320 | A01 | 1934730 | C | T | synonymous_variant | LOW | c.474C>T|p.Leu158Leu |
S36 |
5263 | BAA01g04320 | A01 | 1934930 | C | T | missense_variant | MODERATE | c.674C>T|p.Ser225Phe |
S92 |
5264 | BAA01g04320 | A01 | 1935252 | G | A | synonymous_variant | LOW | c.996G>A|p.Pro332Pro |
S5 |
5265 | BAA01g04320 | A01 | 1935485 | G | A | missense_variant | MODERATE | c.1229G>A|p.Arg410His |
S259 |
5266 | BAA01g04320 | A01 | 1935648 | G | A | synonymous_variant | LOW | c.1392G>A|p.Lys464Lys |
S14 |
5267 | BAA01g04320 | A01 | 1936012 | G | A | missense_variant | MODERATE | c.1756G>A|p.Val586Ile |
S142 |
5268 | BAA01g04320 | A01 | 1938232 | G | A | missense_variant | MODERATE | c.3976G>A|p.Glu1326Lys |
S263 |
5269 | BAA01g04330 | A01 | 1939392 | C | T | missense_variant | MODERATE | c.1139G>A|p.Gly380Glu |
S223 |
5270 | BAA01g04330 | A01 | 1939483 | A | T | missense_variant | MODERATE | c.1048T>A|p.Phe350Ile |
S288 |
5271 | BAA01g04330 | A01 | 1939851 | C | T | stop_gained | HIGH | c.941G>A|p.Trp314* |
S20 |
5272 | BAA01g04330 | A01 | 1941053 | G | A | synonymous_variant | LOW | c.312C>T|p.Ile104Ile |
S219 |
5273 | BAA01g04330 | A01 | 1943522 | C | T | upstream_gene_variant | MODIFIER | c.-1901G>A| |
S19 |
5274 | BAA01g04330 | A01 | 1945131 | G | A | upstream_gene_variant | MODIFIER | c.-3510C>T| |
S202 |
5275 | BAA01g04330 | A01 | 1946376 | G | A | upstream_gene_variant | MODIFIER | c.-4755C>T| |
S157 S163 |