Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1251 | BAA01g00980 | A01 | 426266 | G | A | splice_region_variant&intron_variant | LOW | c.782+5G>A| |
S260 |
1252 | BAA01g00990 | A01 | 428101 | G | A | upstream_gene_variant | MODIFIER | c.-905G>A| |
S234 S294 |
1253 | BAA01g00990 | A01 | 429170 | G | A | synonymous_variant | LOW | c.165G>A|p.Gln55Gln |
S264 |
1254 | BAA01g00980 | A01 | 429375 | G | A | downstream_gene_variant | MODIFIER | c.*2046G>A| |
S295 |
1255 | BAA01g00990 | A01 | 429703 | C | T | missense_variant | MODERATE | c.494C>T|p.Thr165Ile |
S11 |
1256 | BAA01g00990 | A01 | 429704 | C | T | synonymous_variant | LOW | c.495C>T|p.Thr165Thr |
S203 |
1257 | BAA01g00990 | A01 | 429738 | G | A | missense_variant | MODERATE | c.529G>A|p.Glu177Lys |
S280 |
1258 | BAA01g01000 | A01 | 431892 | C | T | upstream_gene_variant | MODIFIER | c.-830G>A| |
S1 S90 |
1259 | BAA01g01000 | A01 | 432816 | G | A | upstream_gene_variant | MODIFIER | c.-1754C>T| |
S96 |
1260 | BAA01g01000 | A01 | 433011 | C | T | upstream_gene_variant | MODIFIER | c.-1949G>A| |
S179 |
1261 | BAA01g01000 | A01 | 433503 | C | T | upstream_gene_variant | MODIFIER | c.-2441G>A| |
S266 |
1262 | BAA01g01000 | A01 | 433666 | G | A | upstream_gene_variant | MODIFIER | c.-2604C>T| |
S251 |
1263 | BAA01g01000 | A01 | 434425 | C | T | upstream_gene_variant | MODIFIER | c.-3363G>A| |
S233 |
1264 | BAA01g01010 | A01 | 435970 | G | A | missense_variant | MODERATE | c.1282C>T|p.Leu428Phe |
S306 S308 |
1265 | BAA01g01010 | A01 | 436453 | C | T | missense_variant | MODERATE | c.941G>A|p.Gly314Glu |
S18 |
1266 | BAA01g01010 | A01 | 436796 | G | A | synonymous_variant | LOW | c.735C>T|p.His245His |
S180 |
1267 | BAA01g01020 | A01 | 436924 | G | A | downstream_gene_variant | MODIFIER | c.*1801C>T| |
S165 |
1268 | BAA01g01010 | A01 | 438694 | C | T | upstream_gene_variant | MODIFIER | c.-628G>A| |
S94 |
1269 | BAA01g01020 | A01 | 439274 | G | A | synonymous_variant | LOW | c.720C>T|p.Ile240Ile |
S142 |
1270 | BAA01g01020 | A01 | 440064 | C | T | missense_variant | MODERATE | c.328G>A|p.Gly110Arg |
S208 |
1271 | BAA01g01010 | A01 | 440490 | G | A | upstream_gene_variant | MODIFIER | c.-2424C>T| |
S298 |
1272 | BAA01g01020 | A01 | 440824 | G | A | synonymous_variant | LOW | c.183C>T|p.Ile61Ile |
S263 |
1273 | BAA01g01010 | A01 | 441586 | C | T | upstream_gene_variant | MODIFIER | c.-3520G>A| |
S262 |
1274 | BAA01g01010 | A01 | 441783 | C | T | upstream_gene_variant | MODIFIER | c.-3717G>A| |
S135 |
1275 | BAA01g01010 | A01 | 442554 | G | A | upstream_gene_variant | MODIFIER | c.-4488C>T| |
S146 |