Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g25590 | A07 | 28260215 | G | A | synonymous_variant | LOW | c.2940C>T|p.Val980Val |
S259 |
2 | BAA07g25590 | A07 | 28260585 | G | A | missense_variant | MODERATE | c.2657C>T|p.Ala886Val |
S251 |
3 | BAA07g25590 | A07 | 28261607 | G | A | missense_variant | MODERATE | c.2060C>T|p.Ser687Phe |
S15 S3 |
4 | BAA07g25590 | A07 | 28263031 | C | T | missense_variant | MODERATE | c.1205G>A|p.Ser402Asn |
S114 |
5 | BAA07g25590 | A07 | 28263354 | G | A | synonymous_variant | LOW | c.981C>T|p.Phe327Phe |
S105 S106 |
6 | BAA07g25590 | A07 | 28263703 | G | A | missense_variant | MODERATE | c.823C>T|p.Pro275Ser |
S180 |
7 | BAA07g25590 | A07 | 28263897 | C | T | splice_region_variant&intron_variant | LOW | c.711+4G>A| |
S207 |
8 | BAA07g25590 | A07 | 28263920 | G | A | missense_variant | MODERATE | c.692C>T|p.Pro231Leu |
S294 |
9 | BAA07g25590 | A07 | 28264253 | C | T | synonymous_variant | LOW | c.444G>A|p.Lys148Lys |
S37 |
10 | BAA07g25590 | A07 | 28264389 | C | T | intron_variant | MODIFIER | c.374+13G>A| |
S190 |
11 | BAA07g25590 | A07 | 28267179 | C | T | upstream_gene_variant | MODIFIER | c.-2233G>A| |
S176 |
12 | BAA07g25590 | A07 | 28267191 | G | A | upstream_gene_variant | MODIFIER | c.-2245C>T| |
S296 |
13 | BAA07g25590 | A07 | 28267393 | G | A | upstream_gene_variant | MODIFIER | c.-2447C>T| |
S225 S73 |
14 | BAA07g25590 | A07 | 28268070 | G | A | upstream_gene_variant | MODIFIER | c.-3124C>T| |
S9 |