Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g17970 | A06 | 9175708 | G | A | missense_variant | MODERATE | c.2225C>T|p.Ala742Val |
S209 |
2 | BAA06g17970 | A06 | 9175728 | A | G | synonymous_variant | LOW | c.2205T>C|p.Asp735Asp |
S261 |
3 | BAA06g17970 | A06 | 9176045 | C | T | missense_variant | MODERATE | c.1888G>A|p.Glu630Lys |
S103 |
4 | BAA06g17970 | A06 | 9176049 | T | C | synonymous_variant | LOW | c.1884A>G|p.Glu628Glu |
S103 |
5 | BAA06g17970 | A06 | 9176179 | C | T | missense_variant | MODERATE | c.1754G>A|p.Gly585Asp |
S252 |
6 | BAA06g17970 | A06 | 9176422 | C | T | missense_variant | MODERATE | c.1511G>A|p.Cys504Tyr |
S195 |
7 | BAA06g17970 | A06 | 9177482 | G | A | missense_variant | MODERATE | c.451C>T|p.Pro151Ser |
S90 |
8 | BAA06g17970 | A06 | 9177602 | C | T | missense_variant | MODERATE | c.331G>A|p.Gly111Arg |
S291 |
9 | BAA06g17970 | A06 | 9177604 | G | A | missense_variant | MODERATE | c.329C>T|p.Thr110Met |
S275 |
10 | BAA06g17970 | A06 | 9177801 | C | T | synonymous_variant | LOW | c.132G>A|p.Lys44Lys |
S162 |
11 | BAA06g17970 | A06 | 9177845 | C | T | missense_variant | MODERATE | c.88G>A|p.Asp30Asn |
S111 |
12 | BAA06g17970 | A06 | 9177920 | C | T | missense_variant | MODERATE | c.13G>A|p.Glu5Lys |
S189 |
13 | BAA06g17970 | A06 | 9178064 | G | A | upstream_gene_variant | MODIFIER | c.-132C>T| |
S44 |
14 | BAA06g17970 | A06 | 9179110 | C | T | upstream_gene_variant | MODIFIER | c.-1178G>A| |
S46 |
15 | BAA06g17970 | A06 | 9180005 | C | T | upstream_gene_variant | MODIFIER | c.-2073G>A| |
S120 |
16 | BAA06g17970 | A06 | 9182339 | G | A | upstream_gene_variant | MODIFIER | c.-4407C>T| |
S146 |
17 | BAA06g17970 | A06 | 9182377 | G | A | upstream_gene_variant | MODIFIER | c.-4445C>T| |
S270 |