Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g29720 | A01 | 18786893 | C | T | downstream_gene_variant | MODIFIER | c.*1498G>A| |
S273 |
2 | BAA01g29720 | A01 | 18787181 | C | T | downstream_gene_variant | MODIFIER | c.*1210G>A| |
S47 |
3 | BAA01g29720 | A01 | 18788697 | G | A | synonymous_variant | LOW | c.2181C>T|p.Asp727Asp |
S126 |
4 | BAA01g29720 | A01 | 18789059 | G | A | missense_variant | MODERATE | c.1819C>T|p.His607Tyr |
S151 |
5 | BAA01g29720 | A01 | 18789123 | G | A | synonymous_variant | LOW | c.1755C>T|p.Phe585Phe |
S100 |
6 | BAA01g29720 | A01 | 18789145 | G | A | missense_variant | MODERATE | c.1733C>T|p.Ala578Val |
S247 |
7 | BAA01g29720 | A01 | 18789994 | G | A | missense_variant | MODERATE | c.970C>T|p.Pro324Ser |
S257 |
8 | BAA01g29720 | A01 | 18790335 | C | T | missense_variant | MODERATE | c.629G>A|p.Gly210Asp |
S164 |
9 | BAA01g29720 | A01 | 18790747 | C | T | missense_variant | MODERATE | c.217G>A|p.Glu73Lys |
S282 |
10 | BAA01g29720 | A01 | 18790954 | G | A | missense_variant | MODERATE | c.10C>T|p.Leu4Phe |
S74 |
11 | BAA01g29720 | A01 | 18790967 | C | T | upstream_gene_variant | MODIFIER | c.-4G>A| |
S136 |
12 | BAA01g29720 | A01 | 18792099 | G | A | upstream_gene_variant | MODIFIER | c.-1136C>T| |
S298 |
13 | BAA01g29720 | A01 | 18792329 | G | A | upstream_gene_variant | MODIFIER | c.-1366C>T| |
S172 S217 |
14 | BAA01g29720 | A01 | 18792595 | G | A | upstream_gene_variant | MODIFIER | c.-1632C>T| |
S178 |
15 | BAA01g29720 | A01 | 18794615 | C | T | upstream_gene_variant | MODIFIER | c.-3652G>A| |
S289 S290 |