Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g33750 | A08 | 21899206 | C | T | upstream_gene_variant | MODIFIER | c.-3337C>T| |
S198 |
2 | BAA08g33750 | A08 | 21899952 | C | T | upstream_gene_variant | MODIFIER | c.-2591C>T| |
S244 |
3 | BAA08g33750 | A08 | 21900193 | G | A | upstream_gene_variant | MODIFIER | c.-2350G>A| |
S41 |
4 | BAA08g33750 | A08 | 21900993 | C | T | upstream_gene_variant | MODIFIER | c.-1550C>T| |
S173 |
5 | BAA08g33750 | A08 | 21901128 | C | T | upstream_gene_variant | MODIFIER | c.-1415C>T| |
S168 |
6 | BAA08g33750 | A08 | 21901298 | G | A | upstream_gene_variant | MODIFIER | c.-1245G>A| |
S259 |
7 | BAA08g33750 | A08 | 21905088 | G | A | missense_variant | MODERATE | c.1714G>A|p.Glu572Lys |
S219 S72 S86 |
8 | BAA08g33750 | A08 | 21905115 | G | A | missense_variant | MODERATE | c.1741G>A|p.Asp581Asn |
S15 S3 |
9 | BAA08g33750 | A08 | 21905229 | C | T | missense_variant | MODERATE | c.1855C>T|p.Leu619Phe |
S20 |
10 | BAA08g33750 | A08 | 21905821 | G | A | missense_variant | MODERATE | c.1988G>A|p.Gly663Asp |
S233 |
11 | BAA08g33750 | A08 | 21906664 | C | T | missense_variant | MODERATE | c.2750C>T|p.Ser917Phe |
S131 |
12 | BAA08g33750 | A08 | 21908157 | C | T | downstream_gene_variant | MODIFIER | c.*1435C>T| |
S59 |
13 | BAA08g33750 | A08 | 21908914 | C | T | downstream_gene_variant | MODIFIER | c.*2192C>T| |
S162 |
14 | BAA08g33750 | A08 | 21909255 | C | T | downstream_gene_variant | MODIFIER | c.*2533C>T| |
S61 |
15 | BAA08g33750 | A08 | 21909633 | G | A | downstream_gene_variant | MODIFIER | c.*2911G>A| |
S156 |
16 | BAA08g33750 | A08 | 21910242 | G | A | downstream_gene_variant | MODIFIER | c.*3520G>A| |
S165 |
17 | BAA08g33750 | A08 | 21910455 | C | T | downstream_gene_variant | MODIFIER | c.*3733C>T| |
S97 |
18 | BAA08g33750 | A08 | 21910480 | C | T | downstream_gene_variant | MODIFIER | c.*3758C>T| |
S168 |
19 | BAA08g33750 | A08 | 21910875 | G | A | downstream_gene_variant | MODIFIER | c.*4153G>A| |
S142 |