Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34240 | A02 | 29362010 | G | A | upstream_gene_variant | MODIFIER | c.-3910G>A| |
S51 |
2 | BAA02g34240 | A02 | 29362011 | C | T | upstream_gene_variant | MODIFIER | c.-3909C>T| |
S63 |
3 | BAA02g34240 | A02 | 29363613 | C | T | upstream_gene_variant | MODIFIER | c.-2307C>T| |
S23 |
4 | BAA02g34240 | A02 | 29363894 | G | A | upstream_gene_variant | MODIFIER | c.-2026G>A| |
S71 |
5 | BAA02g34240 | A02 | 29364969 | C | T | upstream_gene_variant | MODIFIER | c.-951C>T| |
S18 |
6 | BAA02g34240 | A02 | 29365740 | G | A | upstream_gene_variant | MODIFIER | c.-180G>A| |
S50 |
7 | BAA02g34240 | A02 | 29366308 | G | A | missense_variant | MODERATE | c.310G>A|p.Glu104Lys |
S272 |
8 | BAA02g34240 | A02 | 29366686 | C | T | missense_variant | MODERATE | c.688C>T|p.Pro230Ser |
S242 |
9 | BAA02g34240 | A02 | 29367094 | G | A | missense_variant | MODERATE | c.1096G>A|p.Ala366Thr |
S19 |
10 | BAA02g34240 | A02 | 29367339 | C | T | synonymous_variant | LOW | c.1341C>T|p.Phe447Phe |
S202 |
11 | BAA02g34240 | A02 | 29367434 | G | A | missense_variant | MODERATE | c.1436G>A|p.Gly479Glu |
S224 |
12 | BAA02g34240 | A02 | 29367487 | C | T | missense_variant | MODERATE | c.1489C>T|p.Pro497Ser |
S218 |
13 | BAA02g34240 | A02 | 29367722 | G | A | missense_variant | MODERATE | c.1724G>A|p.Gly575Glu |
S41 |
14 | BAA02g34240 | A02 | 29368028 | G | A | missense_variant | MODERATE | c.2030G>A|p.Ser677Asn |
S200 |
15 | BAA02g34240 | A02 | 29368247 | G | A | missense_variant | MODERATE | c.2249G>A|p.Arg750Lys |
S126 |
16 | BAA02g34240 | A02 | 29368474 | G | A | missense_variant | MODERATE | c.2476G>A|p.Val826Ile |
S187 |