Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g35700 | A08 | 22639348 | G | A | upstream_gene_variant | MODIFIER | c.-1550G>A| |
S239 |
2 | BAA08g35700 | A08 | 22639563 | C | T | upstream_gene_variant | MODIFIER | c.-1335C>T| |
S137 S215 |
3 | BAA08g35700 | A08 | 22641810 | G | A | missense_variant | MODERATE | c.296G>A|p.Gly99Glu |
S40 S49 |
4 | BAA08g35700 | A08 | 22642588 | G | A | missense_variant | MODERATE | c.854G>A|p.Gly285Glu |
S260 |
5 | BAA08g35700 | A08 | 22642872 | G | A | missense_variant | MODERATE | c.1138G>A|p.Asp380Asn |
S152 |
6 | BAA08g35700 | A08 | 22643086 | G | A | missense_variant | MODERATE | c.1352G>A|p.Arg451Lys |
S291 |
7 | BAA08g35700 | A08 | 22643224 | C | T | missense_variant | MODERATE | c.1490C>T|p.Thr497Ile |
S294 |
8 | BAA08g35700 | A08 | 22643613 | G | A | missense_variant | MODERATE | c.1879G>A|p.Val627Ile |
S80 |
9 | BAA08g35700 | A08 | 22643632 | C | T | missense_variant | MODERATE | c.1898C>T|p.Thr633Ile |
S186 |
10 | BAA08g35700 | A08 | 22643788 | C | T | missense_variant | MODERATE | c.2054C>T|p.Ser685Leu |
S202 |
11 | BAA08g35700 | A08 | 22644186 | C | T | missense_variant | MODERATE | c.2356C>T|p.Leu786Phe |
S74 |
12 | BAA08g35700 | A08 | 22644281 | C | T | synonymous_variant | LOW | c.2451C>T|p.Val817Val |
S105 S106 |
13 | BAA08g35700 | A08 | 22646201 | C | T | downstream_gene_variant | MODIFIER | c.*1374C>T| |
S100 |