Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g04880 | A07 | 4102172 | G | A | downstream_gene_variant | MODIFIER | c.*1996C>T| |
S111 |
2 | BAA07g04880 | A07 | 4102204 | G | A | downstream_gene_variant | MODIFIER | c.*1964C>T| |
S298 |
3 | BAA07g04880 | A07 | 4102241 | C | T | downstream_gene_variant | MODIFIER | c.*1927G>A| |
S8 |
4 | BAA07g04880 | A07 | 4102525 | G | A | downstream_gene_variant | MODIFIER | c.*1643C>T| |
S105 S106 |
5 | BAA07g04880 | A07 | 4102952 | G | A | downstream_gene_variant | MODIFIER | c.*1216C>T| |
S142 |
6 | BAA07g04880 | A07 | 4103068 | C | T | downstream_gene_variant | MODIFIER | c.*1100G>A| |
S195 |
7 | BAA07g04880 | A07 | 4103922 | C | T | downstream_gene_variant | MODIFIER | c.*246G>A| |
S58 |
8 | BAA07g04880 | A07 | 4104439 | C | T | missense_variant | MODERATE | c.1184G>A|p.Gly395Glu |
S133 |
9 | BAA07g04880 | A07 | 4104921 | G | A | missense_variant | MODERATE | c.860C>T|p.Pro287Leu |
S57 |
10 | BAA07g04880 | A07 | 4105856 | G | A | upstream_gene_variant | MODIFIER | c.-76C>T| |
S9 |
11 | BAA07g04880 | A07 | 4106616 | G | A | upstream_gene_variant | MODIFIER | c.-836C>T| |
S268 |
12 | BAA07g04880 | A07 | 4106698 | G | A | upstream_gene_variant | MODIFIER | c.-918C>T| |
S240 |
13 | BAA07g04880 | A07 | 4106737 | G | A | upstream_gene_variant | MODIFIER | c.-957C>T| |
S183 |
14 | BAA07g04880 | A07 | 4108290 | C | T | upstream_gene_variant | MODIFIER | c.-2510G>A| |
S128 |
15 | BAA07g04880 | A07 | 4109201 | G | A | upstream_gene_variant | MODIFIER | c.-3421C>T| |
S62 |
16 | BAA07g04880 | A07 | 4109558 | C | T | upstream_gene_variant | MODIFIER | c.-3778G>A| |
S167 |
17 | BAA07g04880 | A07 | 4109645 | G | A | upstream_gene_variant | MODIFIER | c.-3865C>T| |
S202 |
18 | BAA07g04880 | A07 | 4109891 | C | T | upstream_gene_variant | MODIFIER | c.-4111G>A| |
S294 |
19 | BAA07g04880 | A07 | 4110687 | G | A | upstream_gene_variant | MODIFIER | c.-4907C>T| |
S80 |