Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38310 | A09 | 46243127 | C | T | missense_variant | MODERATE | c.2995G>A|p.Glu999Lys |
S267 |
2 | BAA09g38310 | A09 | 46243235 | G | A | stop_gained | HIGH | c.2887C>T|p.Gln963* |
S47 |
3 | BAA09g38310 | A09 | 46243412 | C | T | splice_donor_variant&intron_variant | HIGH | c.2789+1G>A| |
S237 |
4 | BAA09g38310 | A09 | 46243577 | C | T | synonymous_variant | LOW | c.2625G>A|p.Ser875Ser |
S260 |
5 | BAA09g38310 | A09 | 46243783 | C | T | missense_variant | MODERATE | c.2419G>A|p.Ala807Thr |
S153 |
6 | BAA09g38310 | A09 | 46246144 | C | T | missense_variant | MODERATE | c.1780G>A|p.Asp594Asn |
S50 |
7 | BAA09g38310 | A09 | 46246832 | C | T | missense_variant | MODERATE | c.1169G>A|p.Arg390Lys |
S118 |
8 | BAA09g38310 | A09 | 46247371 | C | T | synonymous_variant | LOW | c.630G>A|p.Gln210Gln |
S183 S198 |
9 | BAA09g38310 | A09 | 46247462 | C | T | missense_variant | MODERATE | c.539G>A|p.Arg180Lys |
|
10 | BAA09g38310 | A09 | 46247559 | C | T | missense_variant | MODERATE | c.442G>A|p.Ala148Thr |
S242 |
11 | BAA09g38310 | A09 | 46247688 | G | A | synonymous_variant | LOW | c.313C>T|p.Leu105Leu |
S175 S177 |
12 | BAA09g38310 | A09 | 46247919 | G | A | missense_variant | MODERATE | c.82C>T|p.Pro28Ser |
S105 S106 |
13 | BAA09g38310 | A09 | 46248367 | C | T | upstream_gene_variant | MODIFIER | c.-367G>A| |
S168 |
14 | BAA09g38310 | A09 | 46248959 | G | A | upstream_gene_variant | MODIFIER | c.-959C>T| |
S249 |
15 | BAA09g38310 | A09 | 46250560 | C | T | upstream_gene_variant | MODIFIER | c.-2560G>A| |
S195 |
16 | BAA09g38310 | A09 | 46250955 | G | A | upstream_gene_variant | MODIFIER | c.-2955C>T| |
S46 |
17 | BAA09g38310 | A09 | 46251421 | G | A | upstream_gene_variant | MODIFIER | c.-3421C>T| |
S107 |
18 | BAA09g38310 | A09 | 46252752 | C | T | upstream_gene_variant | MODIFIER | c.-4752G>A| |
S193 S28 |
19 | BAA09g38310 | A09 | 46252845 | C | T | upstream_gene_variant | MODIFIER | c.-4845G>A| |
S36 |