Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
251 | BAA01g00170 | A01 | 90884 | G | A | missense_variant | MODERATE | c.982C>T|p.Pro328Ser |
S209 |
252 | BAA01g00170 | A01 | 91164 | G | A | synonymous_variant | LOW | c.702C>T|p.Pro234Pro |
S262 |
253 | BAA01g00170 | A01 | 91360 | G | A | missense_variant | MODERATE | c.506C>T|p.Pro169Leu |
S288 |
254 | BAA01g00170 | A01 | 91588 | C | T | missense_variant | MODERATE | c.278G>A|p.Gly93Glu |
S155 S211 |
255 | BAA01g00170 | A01 | 91831 | G | A | missense_variant | MODERATE | c.137C>T|p.Pro46Leu |
S209 |
256 | BAA01g00170 | A01 | 93921 | G | A | upstream_gene_variant | MODIFIER | c.-1954C>T| |
S259 |
257 | BAA01g00170 | A01 | 94565 | C | T | upstream_gene_variant | MODIFIER | c.-2598G>A| |
S265 |
258 | BAA01g00170 | A01 | 94738 | C | T | upstream_gene_variant | MODIFIER | c.-2771G>A| |
S150 |
259 | BAA01g00170 | A01 | 94757 | G | A | upstream_gene_variant | MODIFIER | c.-2790C>T| |
S263 |
260 | BAA01g00170 | A01 | 95890 | G | A | upstream_gene_variant | MODIFIER | c.-3923C>T| |
S105 S106 |
261 | BAA01g00170 | A01 | 96518 | C | T | upstream_gene_variant | MODIFIER | c.-4551G>A| |
S218 |
262 | BAA01g00190 | A01 | 99950 | C | T | synonymous_variant | LOW | c.312C>T|p.Ile104Ile |
S278 |
263 | BAA01g00200 | A01 | 100370 | G | A | upstream_gene_variant | MODIFIER | c.-3485G>A| |
S241 |
264 | BAA01g00200 | A01 | 100427 | A | T | upstream_gene_variant | MODIFIER | c.-3428A>T| |
S234 |
265 | BAA01g00200 | A01 | 102347 | C | T | upstream_gene_variant | MODIFIER | c.-1508C>T| |
S299 |
266 | BAA01g00200 | A01 | 102812 | G | A | upstream_gene_variant | MODIFIER | c.-1043G>A| |
S70 |
267 | BAA01g00200 | A01 | 104435 | A | T | missense_variant | MODERATE | c.581A>T|p.Glu194Val |
S217 |
268 | BAA01g00200 | A01 | 105287 | G | A | missense_variant | MODERATE | c.1433G>A|p.Ser478Asn |
S63 |
269 | BAA01g00210 | A01 | 105977 | G | A | missense_variant | MODERATE | c.1786C>T|p.Pro596Ser |
S197 |
270 | BAA01g00200 | A01 | 106313 | G | A | downstream_gene_variant | MODIFIER | c.*830G>A| |
S9 |
271 | BAA01g00210 | A01 | 107222 | G | A | missense_variant | MODERATE | c.898C>T|p.Leu300Phe |
S162 |
272 | BAA01g00210 | A01 | 107964 | C | T | synonymous_variant | LOW | c.495G>A|p.Arg165Arg |
S138 |
273 | BAA01g00210 | A01 | 107975 | C | T | missense_variant | MODERATE | c.484G>A|p.Glu162Lys |
S38 |
274 | BAA01g00210 | A01 | 109018 | G | A | upstream_gene_variant | MODIFIER | c.-378C>T| |
S209 |
275 | BAA01g00210 | A01 | 109414 | G | A | upstream_gene_variant | MODIFIER | c.-774C>T| |
S259 |