Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g08770 | A07 | 17697449 | C | T | upstream_gene_variant | MODIFIER | c.-1573C>T| |
S187 |
2 | BAA07g08770 | A07 | 17697453 | C | T | upstream_gene_variant | MODIFIER | c.-1569C>T| |
S156 |
3 | BAA07g08770 | A07 | 17697590 | G | A | upstream_gene_variant | MODIFIER | c.-1432G>A| |
S211 S227 |
4 | BAA07g08770 | A07 | 17699414 | G | A | missense_variant | MODERATE | c.301G>A|p.Ala101Thr |
S123 |
5 | BAA07g08770 | A07 | 17699427 | C | T | missense_variant | MODERATE | c.314C>T|p.Pro105Leu |
S156 |
6 | BAA07g08770 | A07 | 17699990 | C | T | missense_variant | MODERATE | c.752C>T|p.Thr251Ile |
S216 |
7 | BAA07g08770 | A07 | 17700030 | C | T | synonymous_variant | LOW | c.792C>T|p.Asn264Asn |
S70 |
8 | BAA07g08770 | A07 | 17703595 | C | T | downstream_gene_variant | MODIFIER | c.*3176C>T| |
S192 |
9 | BAA07g08770 | A07 | 17703629 | C | T | downstream_gene_variant | MODIFIER | c.*3210C>T| |
|
10 | BAA07g08770 | A07 | 17703723 | G | A | downstream_gene_variant | MODIFIER | c.*3304G>A| |
S83 S88 |
11 | BAA07g08770 | A07 | 17703755 | G | A | downstream_gene_variant | MODIFIER | c.*3336G>A| |
S281 |
12 | BAA07g08770 | A07 | 17703902 | C | T | downstream_gene_variant | MODIFIER | c.*3483C>T| |
S179 |
13 | BAA07g08770 | A07 | 17703938 | C | T | downstream_gene_variant | MODIFIER | c.*3519C>T| |
S205 |
14 | BAA07g08770 | A07 | 17704069 | G | A | downstream_gene_variant | MODIFIER | c.*3650G>A| |
S185 |
15 | BAA07g08770 | A07 | 17704774 | C | T | downstream_gene_variant | MODIFIER | c.*4355C>T| |
S15 S156 S3 S4 S6 |
16 | BAA07g08770 | A07 | 17705107 | G | A | downstream_gene_variant | MODIFIER | c.*4688G>A| |
S262 |
17 | BAA07g08770 | A07 | 17705242 | G | A | downstream_gene_variant | MODIFIER | c.*4823G>A| |
S63 |
18 | BAA07g08770 | A07 | 17705326 | C | T | downstream_gene_variant | MODIFIER | c.*4907C>T| |
S195 |