Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g40090 | A07 | 35722017 | G | A | synonymous_variant | LOW | c.1692C>T|p.Cys564Cys |
S297 |
2 | BAA07g40090 | A07 | 35722133 | C | T | missense_variant | MODERATE | c.1576G>A|p.Gly526Ser |
S92 |
3 | BAA07g40090 | A07 | 35724492 | C | T | stop_gained&splice_region_variant | HIGH | c.1439G>A|p.Trp480* |
S2 |
4 | BAA07g40090 | A07 | 35724811 | G | A | missense_variant | MODERATE | c.1120C>T|p.Leu374Phe |
S69 |
5 | BAA07g40090 | A07 | 35724847 | C | T | missense_variant | MODERATE | c.1084G>A|p.Glu362Lys |
S88 |
6 | BAA07g40090 | A07 | 35724850 | C | T | missense_variant | MODERATE | c.1081G>A|p.Glu361Lys |
S233 |
7 | BAA07g40090 | A07 | 35725642 | C | T | missense_variant | MODERATE | c.721G>A|p.Glu241Lys |
S161 |
8 | BAA07g40090 | A07 | 35728169 | G | A | synonymous_variant | LOW | c.577C>T|p.Leu193Leu |
S234 |
9 | BAA07g40090 | A07 | 35728182 | G | A | synonymous_variant | LOW | c.564C>T|p.Val188Val |
S226 |
10 | BAA07g40090 | A07 | 35729014 | G | A | missense_variant | MODERATE | c.503C>T|p.Thr168Ile |
S255 |
11 | BAA07g40090 | A07 | 35729063 | C | T | missense_variant | MODERATE | c.454G>A|p.Ala152Thr |
S98 |
12 | BAA07g40090 | A07 | 35729074 | G | A | missense_variant | MODERATE | c.443C>T|p.Pro148Leu |
S166 |
13 | BAA07g40090 | A07 | 35729252 | C | T | missense_variant | MODERATE | c.265G>A|p.Asp89Asn |
S47 |
14 | BAA07g40090 | A07 | 35729708 | T | A | upstream_gene_variant | MODIFIER | c.-192A>T| |
S79 S91 |
15 | BAA07g40090 | A07 | 35731386 | G | A | upstream_gene_variant | MODIFIER | c.-1870C>T| |
S64 |
16 | BAA07g40090 | A07 | 35731581 | C | T | upstream_gene_variant | MODIFIER | c.-2065G>A| |
S86 |
17 | BAA07g40090 | A07 | 35731985 | C | T | upstream_gene_variant | MODIFIER | c.-2469G>A| |
S132 S137 S215 S89 |
18 | BAA07g40090 | A07 | 35732694 | C | T | upstream_gene_variant | MODIFIER | c.-3178G>A| |
S292 |