Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g39990 | A06 | 26039518 | C | T | upstream_gene_variant | MODIFIER | c.-3063C>T| |
S241 |
2 | BAA06g39990 | A06 | 26039558 | C | T | upstream_gene_variant | MODIFIER | c.-3023C>T| |
S205 |
3 | BAA06g39990 | A06 | 26039870 | C | T | upstream_gene_variant | MODIFIER | c.-2711C>T| |
S99 |
4 | BAA06g39990 | A06 | 26039892 | C | T | upstream_gene_variant | MODIFIER | c.-2689C>T| |
S45 |
5 | BAA06g39990 | A06 | 26040806 | C | T | upstream_gene_variant | MODIFIER | c.-1775C>T| |
S144 |
6 | BAA06g39990 | A06 | 26041187 | G | A | upstream_gene_variant | MODIFIER | c.-1394G>A| |
S245 |
7 | BAA06g39990 | A06 | 26041333 | G | A | upstream_gene_variant | MODIFIER | c.-1248G>A| |
S58 |
8 | BAA06g39990 | A06 | 26043453 | C | T | missense_variant | MODERATE | c.515C>T|p.Ser172Phe |
S15 S3 |
9 | BAA06g39990 | A06 | 26043492 | G | A | missense_variant | MODERATE | c.554G>A|p.Gly185Glu |
S60 |
10 | BAA06g39990 | A06 | 26044634 | G | A | stop_gained | HIGH | c.954G>A|p.Trp318* |
S75 S81 |
11 | BAA06g39990 | A06 | 26046977 | G | A | downstream_gene_variant | MODIFIER | c.*996G>A| |
S151 |
12 | BAA06g39990 | A06 | 26047035 | G | A | downstream_gene_variant | MODIFIER | c.*1054G>A| |
S38 |
13 | BAA06g39990 | A06 | 26047195 | G | A | downstream_gene_variant | MODIFIER | c.*1214G>A| |
S98 |
14 | BAA06g39990 | A06 | 26049455 | G | A | downstream_gene_variant | MODIFIER | c.*3474G>A| |
S218 |
15 | BAA06g39990 | A06 | 26050779 | A | G | downstream_gene_variant | MODIFIER | c.*4798A>G| |
S153 |