Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g07760 | A07 | 16947798 | C | T | missense_variant | MODERATE | c.2761G>A|p.Val921Ile |
S250 |
2 | BAA07g07760 | A07 | 16948037 | G | A | missense_variant | MODERATE | c.2522C>T|p.Ser841Phe |
S84 S93 |
3 | BAA07g07760 | A07 | 16948048 | C | T | synonymous_variant | LOW | c.2511G>A|p.Arg837Arg |
S192 |
4 | BAA07g07760 | A07 | 16948398 | C | T | missense_variant | MODERATE | c.2254G>A|p.Gly752Arg |
S18 |
5 | BAA07g07760 | A07 | 16948452 | C | T | missense_variant | MODERATE | c.2200G>A|p.Val734Ile |
S130 |
6 | BAA07g07760 | A07 | 16948587 | G | A | synonymous_variant | LOW | c.2130C>T|p.Leu710Leu |
S25 |
7 | BAA07g07760 | A07 | 16948600 | C | T | missense_variant | MODERATE | c.2117G>A|p.Arg706Lys |
S162 |
8 | BAA07g07760 | A07 | 16948965 | C | T | missense_variant | MODERATE | c.1922G>A|p.Gly641Glu |
S169 |
9 | BAA07g07760 | A07 | 16949173 | C | T | intron_variant | MODIFIER | c.1779+11G>A| |
S249 |
10 | BAA07g07760 | A07 | 16949207 | C | T | missense_variant | MODERATE | c.1756G>A|p.Glu586Lys |
S47 |
11 | BAA07g07760 | A07 | 16949278 | G | A | missense_variant | MODERATE | c.1685C>T|p.Pro562Leu |
S200 |
12 | BAA07g07760 | A07 | 16949915 | G | A | synonymous_variant | LOW | c.1230C>T|p.Asn410Asn |
S134 |
13 | BAA07g07760 | A07 | 16950394 | G | A | missense_variant | MODERATE | c.979C>T|p.Pro327Ser |
S48 |
14 | BAA07g07760 | A07 | 16952811 | A | C | upstream_gene_variant | MODIFIER | c.-864T>G| |
S222 S227 S258 |
15 | BAA07g07760 | A07 | 16953250 | G | A | upstream_gene_variant | MODIFIER | c.-1303C>T| |
S100 |
16 | BAA07g07760 | A07 | 16954787 | G | A | upstream_gene_variant | MODIFIER | c.-2840C>T| |
S129 |
17 | BAA07g07760 | A07 | 16955082 | C | T | upstream_gene_variant | MODIFIER | c.-3135G>A| |
S189 |
18 | BAA07g07760 | A07 | 16956014 | G | A | upstream_gene_variant | MODIFIER | c.-4067C>T| |
S281 |
19 | BAA07g07760 | A07 | 16956016 | G | A | upstream_gene_variant | MODIFIER | c.-4069C>T| |
S44 |
20 | BAA07g07760 | A07 | 16956134 | G | A | upstream_gene_variant | MODIFIER | c.-4187C>T| |
S292 |