Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g16480 | A01 | 8006327 | C | T | downstream_gene_variant | MODIFIER | c.*1488G>A| |
S89 |
2 | BAA01g16480 | A01 | 8006716 | G | A | downstream_gene_variant | MODIFIER | c.*1099C>T| |
S105 S106 |
3 | BAA01g16480 | A01 | 8008927 | C | T | missense_variant | MODERATE | c.2233G>A|p.Ala745Thr |
S139 |
4 | BAA01g16480 | A01 | 8008931 | C | T | synonymous_variant | LOW | c.2229G>A|p.Glu743Glu |
S151 S263 |
5 | BAA01g16480 | A01 | 8009614 | G | A | missense_variant | MODERATE | c.1889C>T|p.Ser630Phe |
S116 |
6 | BAA01g16480 | A01 | 8009704 | C | T | missense_variant | MODERATE | c.1799G>A|p.Gly600Glu |
S171 |
7 | BAA01g16480 | A01 | 8010181 | G | A | synonymous_variant | LOW | c.1602C>T|p.Leu534Leu |
S275 |
8 | BAA01g16480 | A01 | 8010911 | C | T | stop_gained | HIGH | c.966G>A|p.Trp322* |
S291 |
9 | BAA01g16480 | A01 | 8010963 | G | A | missense_variant | MODERATE | c.914C>T|p.Ser305Leu |
S165 |
10 | BAA01g16480 | A01 | 8011181 | C | T | synonymous_variant | LOW | c.696G>A|p.Leu232Leu |
S18 |
11 | BAA01g16480 | A01 | 8011255 | G | A | missense_variant | MODERATE | c.622C>T|p.Arg208Cys |
S293 |
12 | BAA01g16480 | A01 | 8011345 | C | T | missense_variant | MODERATE | c.532G>A|p.Asp178Asn |
S50 |
13 | BAA01g16480 | A01 | 8011491 | G | A | missense_variant | MODERATE | c.386C>T|p.Ser129Phe |
S110 |
14 | BAA01g16480 | A01 | 8012095 | C | T | synonymous_variant | LOW | c.189G>A|p.Glu63Glu |
S264 |
15 | BAA01g16480 | A01 | 8012177 | G | A | missense_variant | MODERATE | c.107C>T|p.Ala36Val |
S162 |
16 | BAA01g16480 | A01 | 8012293 | C | T | upstream_gene_variant | MODIFIER | c.-10G>A| |
S284 |
17 | BAA01g16480 | A01 | 8014932 | G | A | upstream_gene_variant | MODIFIER | c.-2649C>T| |
S183 |