Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13750 | A08 | 11904175 | C | T | upstream_gene_variant | MODIFIER | c.-2533C>T| |
S161 |
2 | BAA08g13750 | A08 | 11905213 | G | T | upstream_gene_variant | MODIFIER | c.-1495G>T| |
S139 S144 S160 S163 S164 S178 S199 S227 S238 S239 S257 S26 S268 S283 S298 S308 S55 S82 S9 |
3 | BAA08g13750 | A08 | 11905295 | C | T | upstream_gene_variant | MODIFIER | c.-1413C>T| |
S135 |
4 | BAA08g13750 | A08 | 11905681 | C | T | upstream_gene_variant | MODIFIER | c.-1027C>T| |
S280 |
5 | BAA08g13750 | A08 | 11905938 | C | T | upstream_gene_variant | MODIFIER | c.-770C>T| |
S56 |
6 | BAA08g13750 | A08 | 11906023 | C | T | upstream_gene_variant | MODIFIER | c.-685C>T| |
S67 |
7 | BAA08g13750 | A08 | 11906445 | C | T | upstream_gene_variant | MODIFIER | c.-263C>T| |
S162 |
8 | BAA08g13750 | A08 | 11907724 | C | T | missense_variant | MODERATE | c.356C>T|p.Thr119Ile |
S148 S210 S31 |
9 | BAA08g13750 | A08 | 11907780 | G | A | missense_variant | MODERATE | c.412G>A|p.Asp138Asn |
S161 |
10 | BAA08g13750 | A08 | 11908700 | C | T | missense_variant | MODERATE | c.905C>T|p.Pro302Leu |
S67 |
11 | BAA08g13750 | A08 | 11909135 | C | T | missense_variant | MODERATE | c.1340C>T|p.Ser447Phe |
S23 |
12 | BAA08g13750 | A08 | 11909476 | C | T | downstream_gene_variant | MODIFIER | c.*91C>T| |
S148 S210 S31 |
13 | BAA08g13750 | A08 | 11909699 | G | A | downstream_gene_variant | MODIFIER | c.*314G>A| |
S119 |
14 | BAA08g13750 | A08 | 11909941 | C | T | downstream_gene_variant | MODIFIER | c.*556C>T| |
S270 |