Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00180 | A04 | 69341 | C | T | synonymous_variant | LOW | c.2796G>A|p.Lys932Lys |
S156 |
2 | BAA04g00180 | A04 | 69641 | C | T | splice_region_variant&intron_variant | LOW | c.2503-7G>A| |
S226 |
3 | BAA04g00180 | A04 | 70646 | C | T | intron_variant | MODIFIER | c.1824+27G>A| |
S187 |
4 | BAA04g00180 | A04 | 71037 | G | A | synonymous_variant | LOW | c.1536C>T|p.Phe512Phe |
S125 |
5 | BAA04g00180 | A04 | 71137 | G | A | missense_variant | MODERATE | c.1508C>T|p.Ala503Val |
S178 |
6 | BAA04g00180 | A04 | 71695 | C | T | missense_variant | MODERATE | c.950G>A|p.Arg317His |
S35 |
7 | BAA04g00180 | A04 | 71701 | C | T | missense_variant | MODERATE | c.944G>A|p.Ser315Asn |
S286 |
8 | BAA04g00180 | A04 | 71920 | C | T | missense_variant | MODERATE | c.809G>A|p.Arg270Gln |
S69 |
9 | BAA04g00180 | A04 | 72228 | G | A | synonymous_variant | LOW | c.501C>T|p.Ala167Ala |
S151 |
10 | BAA04g00180 | A04 | 74281 | G | A | upstream_gene_variant | MODIFIER | c.-1398C>T| |
S271 |
11 | BAA04g00180 | A04 | 74822 | G | A | upstream_gene_variant | MODIFIER | c.-1939C>T| |
S190 |
12 | BAA04g00180 | A04 | 75554 | G | A | upstream_gene_variant | MODIFIER | c.-2671C>T| |
S121 |
13 | BAA04g00180 | A04 | 76228 | G | A | upstream_gene_variant | MODIFIER | c.-3345C>T| |
S82 S92 |
14 | BAA04g00180 | A04 | 77486 | C | T | upstream_gene_variant | MODIFIER | c.-4603G>A| |
S250 |