Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g51370 | A09 | 53752381 | C | T | downstream_gene_variant | MODIFIER | c.*4678G>A| |
S5 |
2 | BAA09g51370 | A09 | 53757522 | C | T | missense_variant | MODERATE | c.2198G>A|p.Gly733Glu |
S225 |
3 | BAA09g51370 | A09 | 53758170 | C | T | missense_variant | MODERATE | c.1550G>A|p.Ser517Asn |
S64 |
4 | BAA09g51370 | A09 | 53758349 | C | T | synonymous_variant | LOW | c.1371G>A|p.Arg457Arg |
S295 |
5 | BAA09g51370 | A09 | 53758644 | G | A | missense_variant | MODERATE | c.1076C>T|p.Ser359Phe |
S110 |
6 | BAA09g51370 | A09 | 53758744 | G | A | missense_variant | MODERATE | c.976C>T|p.Leu326Phe |
S178 |
7 | BAA09g51370 | A09 | 53758839 | G | A | missense_variant | MODERATE | c.881C>T|p.Pro294Leu |
S167 |
8 | BAA09g51370 | A09 | 53759298 | C | T | missense_variant | MODERATE | c.422G>A|p.Gly141Asp |
S50 |
9 | BAA09g51370 | A09 | 53759436 | G | A | missense_variant | MODERATE | c.284C>T|p.Ser95Phe |
S221 |
10 | BAA09g51370 | A09 | 53760343 | C | T | upstream_gene_variant | MODIFIER | c.-624G>A| |
S66 |
11 | BAA09g51370 | A09 | 53761550 | G | A | upstream_gene_variant | MODIFIER | c.-1831C>T| |
S62 |
12 | BAA09g51370 | A09 | 53762660 | G | A | upstream_gene_variant | MODIFIER | c.-2941C>T| |
S161 |
13 | BAA09g51370 | A09 | 53763513 | G | A | upstream_gene_variant | MODIFIER | c.-3794C>T| |
S271 |
14 | BAA09g51370 | A09 | 53764712 | G | A | upstream_gene_variant | MODIFIER | c.-4993C>T| |
S240 |