Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g02380 | A08 | 1704279 | G | A | upstream_gene_variant | MODIFIER | c.-4402G>A| |
S212 |
2 | BAA08g02380 | A08 | 1705610 | C | T | upstream_gene_variant | MODIFIER | c.-3071C>T| |
S143 |
3 | BAA08g02380 | A08 | 1705767 | G | A | upstream_gene_variant | MODIFIER | c.-2914G>A| |
S263 |
4 | BAA08g02380 | A08 | 1706305 | C | T | upstream_gene_variant | MODIFIER | c.-2376C>T| |
S292 |
5 | BAA08g02380 | A08 | 1706412 | G | A | upstream_gene_variant | MODIFIER | c.-2269G>A| |
S264 |
6 | BAA08g02380 | A08 | 1708813 | G | A | missense_variant | MODERATE | c.133G>A|p.Glu45Lys |
S32 |
7 | BAA08g02380 | A08 | 1710928 | C | T | missense_variant | MODERATE | c.658C>T|p.Pro220Ser |
S28 |
8 | BAA08g02380 | A08 | 1711913 | C | T | downstream_gene_variant | MODIFIER | c.*971C>T| |
S46 |
9 | BAA08g02380 | A08 | 1712139 | C | T | downstream_gene_variant | MODIFIER | c.*1197C>T| |
S34 |
10 | BAA08g02380 | A08 | 1712263 | G | A | downstream_gene_variant | MODIFIER | c.*1321G>A| |
S190 |
11 | BAA08g02380 | A08 | 1712351 | G | A | downstream_gene_variant | MODIFIER | c.*1409G>A| |
S161 |
12 | BAA08g02380 | A08 | 1712631 | C | T | downstream_gene_variant | MODIFIER | c.*1689C>T| |
S138 |
13 | BAA08g02380 | A08 | 1713786 | C | T | downstream_gene_variant | MODIFIER | c.*2844C>T| |
S57 |
14 | BAA08g02380 | A08 | 1714306 | C | T | downstream_gene_variant | MODIFIER | c.*3364C>T| |
S295 |
15 | BAA08g02380 | A08 | 1714748 | G | A | downstream_gene_variant | MODIFIER | c.*3806G>A| |
S192 |
16 | BAA08g02380 | A08 | 1714919 | C | T | downstream_gene_variant | MODIFIER | c.*3977C>T| |
S267 |
17 | BAA08g02380 | A08 | 1715215 | C | T | downstream_gene_variant | MODIFIER | c.*4273C>T| |
S45 S78 |
18 | BAA08g02380 | A08 | 1715583 | G | A | downstream_gene_variant | MODIFIER | c.*4641G>A| |
S69 |
19 | BAA08g02380 | A08 | 1715859 | G | A | downstream_gene_variant | MODIFIER | c.*4917G>A| |
S136 |