Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38070 | A09 | 46100078 | G | A | downstream_gene_variant | MODIFIER | c.*3322C>T| |
S109 |
2 | BAA09g38070 | A09 | 46100284 | C | T | downstream_gene_variant | MODIFIER | c.*3116G>A| |
S66 |
3 | BAA09g38070 | A09 | 46100418 | C | T | downstream_gene_variant | MODIFIER | c.*2982G>A| |
S156 |
4 | BAA09g38070 | A09 | 46103706 | C | T | synonymous_variant | LOW | c.3126G>A|p.Glu1042Glu |
S242 |
5 | BAA09g38070 | A09 | 46104269 | C | T | missense_variant | MODERATE | c.2648G>A|p.Gly883Glu |
S245 |
6 | BAA09g38070 | A09 | 46105173 | G | A | missense_variant | MODERATE | c.1744C>T|p.Leu582Phe |
S203 |
7 | BAA09g38070 | A09 | 46105584 | G | A | missense_variant | MODERATE | c.1333C>T|p.Pro445Ser |
S71 |
8 | BAA09g38070 | A09 | 46106267 | G | A | missense_variant | MODERATE | c.650C>T|p.Thr217Ile |
S40 S49 |
9 | BAA09g38070 | A09 | 46106331 | G | A | missense_variant | MODERATE | c.586C>T|p.Pro196Ser |
S47 |
10 | BAA09g38070 | A09 | 46106631 | A | T | missense_variant | MODERATE | c.368T>A|p.Ile123Lys |
S57 |
11 | BAA09g38070 | A09 | 46106883 | G | A | synonymous_variant | LOW | c.285C>T|p.Asp95Asp |
S270 |
12 | BAA09g38070 | A09 | 46107021 | G | A | intron_variant | MODIFIER | c.196+29C>T| |
S280 |
13 | BAA09g38070 | A09 | 46107092 | C | T | missense_variant | MODERATE | c.154G>A|p.Asp52Asn |
S267 |
14 | BAA09g38070 | A09 | 46107179 | C | T | missense_variant | MODERATE | c.67G>A|p.Gly23Arg |
S8 |
15 | BAA09g38070 | A09 | 46108084 | G | A | upstream_gene_variant | MODIFIER | c.-839C>T| |
S189 |
16 | BAA09g38070 | A09 | 46108681 | C | T | upstream_gene_variant | MODIFIER | c.-1436G>A| |
S54 |
17 | BAA09g38070 | A09 | 46108854 | C | T | upstream_gene_variant | MODIFIER | c.-1609G>A| |
S260 |
18 | BAA09g38070 | A09 | 46110095 | C | T | upstream_gene_variant | MODIFIER | c.-2850G>A| |
S140 |
19 | BAA09g38070 | A09 | 46110410 | G | A | upstream_gene_variant | MODIFIER | c.-3165C>T| |
S10 |
20 | BAA09g38070 | A09 | 46111779 | G | A | upstream_gene_variant | MODIFIER | c.-4534C>T| |
S252 |