Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g41650 | A06 | 27129790 | C | T | upstream_gene_variant | MODIFIER | c.-2213C>T| |
S236 |
2 | BAA06g41650 | A06 | 27130401 | C | T | upstream_gene_variant | MODIFIER | c.-1602C>T| |
S252 |
3 | BAA06g41650 | A06 | 27131000 | C | T | upstream_gene_variant | MODIFIER | c.-1003C>T| |
S148 S210 |
4 | BAA06g41650 | A06 | 27131149 | G | A | upstream_gene_variant | MODIFIER | c.-854G>A| |
S28 |
5 | BAA06g41650 | A06 | 27131330 | G | A | upstream_gene_variant | MODIFIER | c.-673G>A| |
S270 |
6 | BAA06g41650 | A06 | 27132285 | G | A | intron_variant | MODIFIER | c.29+254G>A| |
S203 |
7 | BAA06g41650 | A06 | 27133297 | C | T | intron_variant | MODIFIER | c.523-28C>T| |
S62 |
8 | BAA06g41650 | A06 | 27133976 | G | A | missense_variant | MODERATE | c.1108G>A|p.Asp370Asn |
S239 |
9 | BAA06g41650 | A06 | 27134658 | G | A | missense_variant | MODERATE | c.1703G>A|p.Gly568Glu |
S13 |
10 | BAA06g41650 | A06 | 27136314 | G | A | missense_variant | MODERATE | c.2806G>A|p.Gly936Arg |
S96 |
11 | BAA06g41650 | A06 | 27136371 | C | T | missense_variant | MODERATE | c.2863C>T|p.Pro955Ser |
S235 |
12 | BAA06g41650 | A06 | 27136954 | G | A | synonymous_variant | LOW | c.3036G>A|p.Glu1012Glu |
S64 |
13 | BAA06g41650 | A06 | 27141572 | G | A | downstream_gene_variant | MODIFIER | c.*4495G>A| |
S289 S290 |