Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g09890 | A08 | 8959387 | C | T | upstream_gene_variant | MODIFIER | c.-904C>T| |
S138 |
2 | BAA08g09890 | A08 | 8960013 | C | T | upstream_gene_variant | MODIFIER | c.-278C>T| |
S76 |
3 | BAA08g09890 | A08 | 8960364 | C | T | missense_variant | MODERATE | c.74C>T|p.Pro25Leu |
S270 |
4 | BAA08g09890 | A08 | 8961270 | C | T | intron_variant | MODIFIER | c.618+362C>T| |
S226 |
5 | BAA08g09890 | A08 | 8961664 | C | T | intron_variant | MODIFIER | c.618+756C>T| |
S30 S31 |
6 | BAA08g09890 | A08 | 8961775 | C | T | intron_variant | MODIFIER | c.618+867C>T| |
S76 |
7 | BAA08g09890 | A08 | 8962547 | C | T | intron_variant | MODIFIER | c.618+1639C>T| |
S67 |
8 | BAA08g09890 | A08 | 8963527 | G | A | intron_variant | MODIFIER | c.619-999G>A| |
S257 |
9 | BAA08g09890 | A08 | 8964617 | C | T | missense_variant | MODERATE | c.710C>T|p.Ala237Val |
S5 |
10 | BAA08g09890 | A08 | 8964983 | C | T | intron_variant | MODIFIER | c.769-32C>T| |
S71 |
11 | BAA08g09890 | A08 | 8965448 | C | T | downstream_gene_variant | MODIFIER | c.*128C>T| |
S305 |
12 | BAA08g09890 | A08 | 8965992 | C | T | downstream_gene_variant | MODIFIER | c.*672C>T| |
S67 |
13 | BAA08g09890 | A08 | 8966681 | G | A | downstream_gene_variant | MODIFIER | c.*1361G>A| |
S85 |
14 | BAA08g09890 | A08 | 8967411 | G | A | downstream_gene_variant | MODIFIER | c.*2091G>A| |
S133 |
15 | BAA08g09890 | A08 | 8967544 | C | T | downstream_gene_variant | MODIFIER | c.*2224C>T| |
S150 S178 |
16 | BAA08g09890 | A08 | 8968227 | G | A | downstream_gene_variant | MODIFIER | c.*2907G>A| |
S13 |
17 | BAA08g09890 | A08 | 8968643 | C | T | downstream_gene_variant | MODIFIER | c.*3323C>T| |
S1 S90 |
18 | BAA08g09890 | A08 | 8969152 | G | A | downstream_gene_variant | MODIFIER | c.*3832G>A| |
S181 |
19 | BAA08g09890 | A08 | 8969514 | G | A | downstream_gene_variant | MODIFIER | c.*4194G>A| |
S5 |
20 | BAA08g09890 | A08 | 8969888 | G | A | downstream_gene_variant | MODIFIER | c.*4568G>A| |
S94 |