Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g11960 | A06 | 6039759 | G | A | downstream_gene_variant | MODIFIER | c.*4842C>T| |
S165 |
2 | BAA06g11960 | A06 | 6040846 | G | A | downstream_gene_variant | MODIFIER | c.*3755C>T| |
S280 |
3 | BAA06g11960 | A06 | 6040987 | C | T | downstream_gene_variant | MODIFIER | c.*3614G>A| |
S17 |
4 | BAA06g11960 | A06 | 6045331 | C | T | missense_variant | MODERATE | c.3578G>A|p.Gly1193Asp |
S80 |
5 | BAA06g11960 | A06 | 6045846 | C | T | synonymous_variant | LOW | c.3237G>A|p.Glu1079Glu |
S2 |
6 | BAA06g11960 | A06 | 6047103 | C | T | splice_region_variant&intron_variant | LOW | c.2227-4G>A| |
S80 |
7 | BAA06g11960 | A06 | 6047971 | C | T | missense_variant | MODERATE | c.1439G>A|p.Ser480Asn |
S23 |
8 | BAA06g11960 | A06 | 6048962 | C | T | missense_variant | MODERATE | c.895G>A|p.Asp299Asn |
S146 |
9 | BAA06g11960 | A06 | 6049308 | G | A | missense_variant | MODERATE | c.689C>T|p.Thr230Ile |
S179 |
10 | BAA06g11960 | A06 | 6049690 | C | T | missense_variant | MODERATE | c.307G>A|p.Asp103Asn |
S174 |
11 | BAA06g11960 | A06 | 6049906 | C | T | missense_variant | MODERATE | c.91G>A|p.Glu31Lys |
S77 S82 |
12 | BAA06g11960 | A06 | 6049952 | C | T | missense_variant | MODERATE | c.45G>A|p.Met15Ile |
S267 |
13 | BAA06g11960 | A06 | 6050505 | C | T | upstream_gene_variant | MODIFIER | c.-509G>A| |
S4 |
14 | BAA06g11960 | A06 | 6051966 | C | T | upstream_gene_variant | MODIFIER | c.-1970G>A| |
S260 |
15 | BAA06g11960 | A06 | 6052376 | G | A | upstream_gene_variant | MODIFIER | c.-2380C>T| |
S208 |
16 | BAA06g11960 | A06 | 6054812 | G | A | upstream_gene_variant | MODIFIER | c.-4816C>T| |
S305 |