Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41890 | A09 | 48457330 | G | A | missense_variant | MODERATE | c.2254C>T|p.Pro752Ser |
S271 |
2 | BAA09g41890 | A09 | 48457555 | C | T | missense_variant | MODERATE | c.2029G>A|p.Asp677Asn |
S169 |
3 | BAA09g41890 | A09 | 48458170 | C | T | missense_variant | MODERATE | c.1414G>A|p.Gly472Arg |
S149 |
4 | BAA09g41890 | A09 | 48458577 | C | T | missense_variant | MODERATE | c.1007G>A|p.Arg336Lys |
S92 |
5 | BAA09g41890 | A09 | 48459018 | G | A | missense_variant | MODERATE | c.566C>T|p.Thr189Ile |
S271 |
6 | BAA09g41890 | A09 | 48460627 | C | A | upstream_gene_variant | MODIFIER | c.-1044G>T| |
S43 |
7 | BAA09g41890 | A09 | 48460717 | G | A | upstream_gene_variant | MODIFIER | c.-1134C>T| |
S165 S262 |
8 | BAA09g41890 | A09 | 48460726 | G | A | upstream_gene_variant | MODIFIER | c.-1143C>T| |
S221 |
9 | BAA09g41890 | A09 | 48461913 | G | A | upstream_gene_variant | MODIFIER | c.-2330C>T| |
S65 |
10 | BAA09g41890 | A09 | 48462515 | C | T | upstream_gene_variant | MODIFIER | c.-2932G>A| |
S104 S52 |
11 | BAA09g41890 | A09 | 48463168 | C | T | upstream_gene_variant | MODIFIER | c.-3585G>A| |
S90 |
12 | BAA09g41890 | A09 | 48463415 | C | T | upstream_gene_variant | MODIFIER | c.-3832G>A| |
S173 S233 |
13 | BAA09g41890 | A09 | 48463639 | G | T | upstream_gene_variant | MODIFIER | c.-4056C>A| |
S109 S255 S281 S52 |
14 | BAA09g41890 | A09 | 48464026 | G | A | upstream_gene_variant | MODIFIER | c.-4443C>T| |
S200 |
15 | BAA09g41890 | A09 | 48464273 | C | T | upstream_gene_variant | MODIFIER | c.-4690G>A| |
S100 |
16 | BAA09g41890 | A09 | 48464452 | G | A | upstream_gene_variant | MODIFIER | c.-4869C>T| |
S87 |