Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g28850 | A01 | 18169246 | G | A | missense_variant | MODERATE | c.968C>T|p.Ala323Val |
S124 |
2 | BAA01g28850 | A01 | 18170420 | C | T | missense_variant | MODERATE | c.409G>A|p.Asp137Asn |
S94 |
3 | BAA01g28850 | A01 | 18171141 | C | T | splice_region_variant&synonymous_variant | LOW | c.279G>A|p.Lys93Lys |
S107 |
4 | BAA01g28850 | A01 | 18171520 | G | A | upstream_gene_variant | MODIFIER | c.-101C>T| |
S296 |
5 | BAA01g28850 | A01 | 18171747 | G | A | upstream_gene_variant | MODIFIER | c.-328C>T| |
S301 S304 |
6 | BAA01g28850 | A01 | 18172182 | C | T | upstream_gene_variant | MODIFIER | c.-763G>A| |
S15 S2 S3 S34 S4 S6 S66 |
7 | BAA01g28850 | A01 | 18172302 | G | A | upstream_gene_variant | MODIFIER | c.-883C>T| |
S32 |
8 | BAA01g28850 | A01 | 18172303 | C | T | upstream_gene_variant | MODIFIER | c.-884G>A| |
S76 |
9 | BAA01g28850 | A01 | 18172376 | G | A | upstream_gene_variant | MODIFIER | c.-957C>T| |
S175 |
10 | BAA01g28850 | A01 | 18172524 | G | A | upstream_gene_variant | MODIFIER | c.-1105C>T| |
S197 |
11 | BAA01g28850 | A01 | 18172898 | G | A | upstream_gene_variant | MODIFIER | c.-1479C>T| |
S6 |
12 | BAA01g28850 | A01 | 18174319 | C | T | upstream_gene_variant | MODIFIER | c.-2900G>A| |
S28 |
13 | BAA01g28850 | A01 | 18174742 | G | A | upstream_gene_variant | MODIFIER | c.-3323C>T| |
S259 |
14 | BAA01g28850 | A01 | 18174766 | C | T | upstream_gene_variant | MODIFIER | c.-3347G>A| |
S303 |
15 | BAA01g28850 | A01 | 18174994 | C | T | upstream_gene_variant | MODIFIER | c.-3575G>A| |
S223 |
16 | BAA01g28850 | A01 | 18175033 | T | A | upstream_gene_variant | MODIFIER | c.-3614A>T| |
S20 |
17 | BAA01g28850 | A01 | 18175366 | C | T | upstream_gene_variant | MODIFIER | c.-3947G>A| |
S189 |
18 | BAA01g28850 | A01 | 18175590 | C | T | upstream_gene_variant | MODIFIER | c.-4171G>A| |
S166 S184 |
19 | BAA01g28850 | A01 | 18176114 | C | T | upstream_gene_variant | MODIFIER | c.-4695G>A| |
S111 |