Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g40690 | A09 | 47695253 | G | A | downstream_gene_variant | MODIFIER | c.*4287C>T| |
S144 |
2 | BAA09g40690 | A09 | 47695652 | G | A | downstream_gene_variant | MODIFIER | c.*3888C>T| |
S149 |
3 | BAA09g40690 | A09 | 47695815 | G | A | downstream_gene_variant | MODIFIER | c.*3725C>T| |
S234 |
4 | BAA09g40690 | A09 | 47696273 | C | T | downstream_gene_variant | MODIFIER | c.*3267G>A| |
S213 |
5 | BAA09g40690 | A09 | 47696320 | C | T | downstream_gene_variant | MODIFIER | c.*3220G>A| |
S256 |
6 | BAA09g40690 | A09 | 47696675 | C | T | downstream_gene_variant | MODIFIER | c.*2865G>A| |
S192 |
7 | BAA09g40690 | A09 | 47697253 | C | T | downstream_gene_variant | MODIFIER | c.*2287G>A| |
S138 |
8 | BAA09g40690 | A09 | 47697372 | C | T | downstream_gene_variant | MODIFIER | c.*2168G>A| |
S262 |
9 | BAA09g40690 | A09 | 47697780 | G | A | downstream_gene_variant | MODIFIER | c.*1760C>T| |
S149 |
10 | BAA09g40690 | A09 | 47698856 | G | A | downstream_gene_variant | MODIFIER | c.*684C>T| |
S249 |
11 | BAA09g40690 | A09 | 47699609 | C | T | synonymous_variant | LOW | c.1950G>A|p.Gly650Gly |
S135 |
12 | BAA09g40690 | A09 | 47700020 | C | T | intron_variant | MODIFIER | c.1684-71G>A| |
S99 |
13 | BAA09g40690 | A09 | 47700403 | C | T | synonymous_variant | LOW | c.1611G>A|p.Gly537Gly |
S216 S241 S39 |
14 | BAA09g40690 | A09 | 47700525 | C | T | missense_variant | MODERATE | c.1489G>A|p.Asp497Asn |
S183 S198 |
15 | BAA09g40690 | A09 | 47700568 | C | T | synonymous_variant | LOW | c.1446G>A|p.Val482Val |
S267 |
16 | BAA09g40690 | A09 | 47700734 | C | T | missense_variant | MODERATE | c.1280G>A|p.Gly427Glu |
S33 |
17 | BAA09g40690 | A09 | 47700777 | C | T | missense_variant | MODERATE | c.1237G>A|p.Val413Met |
S36 |
18 | BAA09g40690 | A09 | 47700853 | C | T | synonymous_variant | LOW | c.1161G>A|p.Glu387Glu |
S234 |
19 | BAA09g40690 | A09 | 47700857 | C | T | missense_variant | MODERATE | c.1157G>A|p.Gly386Glu |
S18 |
20 | BAA09g40690 | A09 | 47700950 | C | T | missense_variant | MODERATE | c.1064G>A|p.Ser355Asn |
S235 |
21 | BAA09g40690 | A09 | 47701117 | C | T | synonymous_variant | LOW | c.897G>A|p.Glu299Glu |
S245 |
22 | BAA09g40690 | A09 | 47701308 | G | A | stop_gained | HIGH | c.706C>T|p.Gln236* |
S288 |
23 | BAA09g40690 | A09 | 47701465 | C | T | synonymous_variant | LOW | c.549G>A|p.Glu183Glu |
S292 |
24 | BAA09g40690 | A09 | 47701909 | G | A | synonymous_variant | LOW | c.105C>T|p.Ile35Ile |
S233 |
25 | BAA09g40690 | A09 | 47702351 | G | A | upstream_gene_variant | MODIFIER | c.-338C>T| |
S263 |