Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g02990 | A06 | 1731392 | G | A | synonymous_variant | LOW | c.1272C>T|p.His424His |
S144 |
2 | BAA06g02990 | A06 | 1732875 | C | T | intron_variant | MODIFIER | c.961+436G>A| |
S92 |
3 | BAA06g02990 | A06 | 1733261 | C | T | intron_variant | MODIFIER | c.961+50G>A| |
S189 |
4 | BAA06g02990 | A06 | 1733877 | C | A | intron_variant | MODIFIER | c.671-59G>T| |
S151 S263 |
5 | BAA06g02990 | A06 | 1734304 | C | T | missense_variant | MODERATE | c.554G>A|p.Gly185Glu |
S197 |
6 | BAA06g02990 | A06 | 1734526 | G | A | missense_variant | MODERATE | c.332C>T|p.Thr111Ile |
S126 |
7 | BAA06g02990 | A06 | 1734751 | A | T | intron_variant | MODIFIER | c.140-33T>A| |
S160 S270 |
8 | BAA06g02990 | A06 | 1735144 | G | A | upstream_gene_variant | MODIFIER | c.-108C>T| |
S233 |
9 | BAA06g02990 | A06 | 1736964 | G | A | upstream_gene_variant | MODIFIER | c.-1928C>T| |
S297 |
10 | BAA06g02990 | A06 | 1737096 | C | T | upstream_gene_variant | MODIFIER | c.-2060G>A| |
S130 |
11 | BAA06g02990 | A06 | 1737130 | G | A | upstream_gene_variant | MODIFIER | c.-2094C>T| |
S19 |
12 | BAA06g02990 | A06 | 1737856 | G | A | upstream_gene_variant | MODIFIER | c.-2820C>T| |
S295 |
13 | BAA06g02990 | A06 | 1737953 | C | T | upstream_gene_variant | MODIFIER | c.-2917G>A| |
S202 |
14 | BAA06g02990 | A06 | 1738269 | C | T | upstream_gene_variant | MODIFIER | c.-3233G>A| |
S230 |
15 | BAA06g02990 | A06 | 1738832 | G | A | upstream_gene_variant | MODIFIER | c.-3796C>T| |
S265 |
16 | BAA06g02990 | A06 | 1739746 | C | T | upstream_gene_variant | MODIFIER | c.-4710G>A| |
S183 S198 |
17 | BAA06g02990 | A06 | 1739948 | G | A | upstream_gene_variant | MODIFIER | c.-4912C>T| |
S42 |