Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g02350 | A08 | 1684298 | C | T | upstream_gene_variant | MODIFIER | c.-4980C>T| |
S148 S30 S31 |
2 | BAA08g02350 | A08 | 1684307 | G | A | upstream_gene_variant | MODIFIER | c.-4971G>A| |
S34 |
3 | BAA08g02350 | A08 | 1684423 | C | T | upstream_gene_variant | MODIFIER | c.-4855C>T| |
S120 |
4 | BAA08g02350 | A08 | 1684425 | C | T | upstream_gene_variant | MODIFIER | c.-4853C>T| |
S127 |
5 | BAA08g02350 | A08 | 1685180 | G | A | upstream_gene_variant | MODIFIER | c.-4098G>A| |
S128 |
6 | BAA08g02350 | A08 | 1685496 | G | A | upstream_gene_variant | MODIFIER | c.-3782G>A| |
S288 |
7 | BAA08g02350 | A08 | 1686086 | G | A | upstream_gene_variant | MODIFIER | c.-3192G>A| |
S240 |
8 | BAA08g02350 | A08 | 1686898 | G | A | upstream_gene_variant | MODIFIER | c.-2380G>A| |
S78 |
9 | BAA08g02350 | A08 | 1687277 | C | T | upstream_gene_variant | MODIFIER | c.-2001C>T| |
S34 |
10 | BAA08g02350 | A08 | 1687351 | G | A | upstream_gene_variant | MODIFIER | c.-1927G>A| |
S181 |
11 | BAA08g02350 | A08 | 1688567 | G | A | upstream_gene_variant | MODIFIER | c.-711G>A| |
S2 S34 S4 |
12 | BAA08g02350 | A08 | 1688639 | G | A | upstream_gene_variant | MODIFIER | c.-639G>A| |
S2 S34 S4 |
13 | BAA08g02350 | A08 | 1688693 | G | A | upstream_gene_variant | MODIFIER | c.-585G>A| |
S161 |
14 | BAA08g02350 | A08 | 1689059 | C | T | upstream_gene_variant | MODIFIER | c.-219C>T| |
S157 S163 |
15 | BAA08g02350 | A08 | 1690328 | G | A | missense_variant | MODERATE | c.379G>A|p.Glu127Lys |
S158 |
16 | BAA08g02350 | A08 | 1691070 | G | A | missense_variant | MODERATE | c.1045G>A|p.Ala349Thr |
S179 |
17 | BAA08g02350 | A08 | 1691517 | C | T | missense_variant | MODERATE | c.1403C>T|p.Ser468Phe |
S12 S230 |
18 | BAA08g02350 | A08 | 1692634 | C | T | missense_variant | MODERATE | c.2053C>T|p.Pro685Ser |
S127 |
19 | BAA08g02350 | A08 | 1692883 | G | A | missense_variant | MODERATE | c.2302G>A|p.Ala768Thr |
S241 |
20 | BAA08g02350 | A08 | 1694631 | G | A | downstream_gene_variant | MODIFIER | c.*1245G>A| |
S225 |
21 | BAA08g02350 | A08 | 1694785 | G | A | downstream_gene_variant | MODIFIER | c.*1399G>A| |
S165 |
22 | BAA08g02350 | A08 | 1694991 | C | T | downstream_gene_variant | MODIFIER | c.*1605C>T| |
S1 S90 |
23 | BAA08g02350 | A08 | 1695500 | G | A | downstream_gene_variant | MODIFIER | c.*2114G>A| |
S223 |
24 | BAA08g02350 | A08 | 1695887 | C | T | downstream_gene_variant | MODIFIER | c.*2501C>T| |
S126 |