Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g13900 | A06 | 6869608 | C | T | missense_variant | MODERATE | c.1027G>A|p.Asp343Asn |
S80 |
2 | BAA06g13900 | A06 | 6869657 | C | T | synonymous_variant | LOW | c.978G>A|p.Gly326Gly |
S124 |
3 | BAA06g13900 | A06 | 6869779 | G | A | missense_variant | MODERATE | c.856C>T|p.His286Tyr |
S261 |
4 | BAA06g13900 | A06 | 6870225 | G | A | synonymous_variant | LOW | c.495C>T|p.Phe165Phe |
S255 |
5 | BAA06g13900 | A06 | 6870422 | G | A | missense_variant | MODERATE | c.298C>T|p.Leu100Phe |
S165 |
6 | BAA06g13900 | A06 | 6870504 | G | A | synonymous_variant | LOW | c.216C>T|p.Asn72Asn |
S152 |
7 | BAA06g13900 | A06 | 6871903 | C | T | upstream_gene_variant | MODIFIER | c.-1184G>A| |
S146 |
8 | BAA06g13900 | A06 | 6872459 | G | A | upstream_gene_variant | MODIFIER | c.-1740C>T| |
S139 |
9 | BAA06g13900 | A06 | 6872877 | G | A | upstream_gene_variant | MODIFIER | c.-2158C>T| |
S100 |
10 | BAA06g13900 | A06 | 6872893 | G | A | upstream_gene_variant | MODIFIER | c.-2174C>T| |
S110 |
11 | BAA06g13900 | A06 | 6873139 | C | T | upstream_gene_variant | MODIFIER | c.-2420G>A| |
S215 |
12 | BAA06g13900 | A06 | 6874637 | G | A | upstream_gene_variant | MODIFIER | c.-3918C>T| |
S81 S85 |
13 | BAA06g13900 | A06 | 6875252 | C | T | upstream_gene_variant | MODIFIER | c.-4533G>A| |
S247 |