Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g10990 | A08 | 9863180 | C | T | upstream_gene_variant | MODIFIER | c.-4489C>T| |
S60 |
2 | BAA08g10990 | A08 | 9864453 | G | A | upstream_gene_variant | MODIFIER | c.-3216G>A| |
S191 |
3 | BAA08g10990 | A08 | 9864879 | C | T | upstream_gene_variant | MODIFIER | c.-2790C>T| |
S250 |
4 | BAA08g10990 | A08 | 9866889 | C | T | upstream_gene_variant | MODIFIER | c.-780C>T| |
S44 |
5 | BAA08g10990 | A08 | 9869476 | C | T | missense_variant | MODERATE | c.1178C>T|p.Ala393Val |
S105 S106 |
6 | BAA08g10990 | A08 | 9869823 | G | A | missense_variant | MODERATE | c.1447G>A|p.Gly483Arg |
S170 |
7 | BAA08g10990 | A08 | 9869848 | G | A | missense_variant | MODERATE | c.1472G>A|p.Ser491Asn |
S221 |
8 | BAA08g10990 | A08 | 9870135 | C | T | missense_variant | MODERATE | c.1679C>T|p.Pro560Leu |
S272 |
9 | BAA08g10990 | A08 | 9870349 | G | A | splice_region_variant&intron_variant | LOW | c.1822-4G>A| |
S275 |
10 | BAA08g10990 | A08 | 9875179 | C | T | downstream_gene_variant | MODIFIER | c.*4284C>T| |
S70 |
11 | BAA08g10990 | A08 | 9875383 | G | A | downstream_gene_variant | MODIFIER | c.*4488G>A| |
S247 |