Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15450 | A10 | 15765024 | G | A | synonymous_variant | LOW | c.2205C>T|p.Phe735Phe |
S62 |
2 | BAA10g15450 | A10 | 15765469 | G | A | synonymous_variant | LOW | c.1953C>T|p.Phe651Phe |
S157 S166 S167 S262 |
3 | BAA10g15450 | A10 | 15766598 | C | T | synonymous_variant | LOW | c.1485G>A|p.Lys495Lys |
S259 |
4 | BAA10g15450 | A10 | 15767708 | G | A | missense_variant | MODERATE | c.779C>T|p.Thr260Ile |
S293 |
5 | BAA10g15450 | A10 | 15768127 | C | T | missense_variant | MODERATE | c.532G>A|p.Glu178Lys |
S277 |
6 | BAA10g15450 | A10 | 15768311 | G | A | synonymous_variant | LOW | c.348C>T|p.Leu116Leu |
S64 |
7 | BAA10g15450 | A10 | 15768639 | G | A | missense_variant | MODERATE | c.20C>T|p.Thr7Ile |
S59 |
8 | BAA10g15450 | A10 | 15769860 | C | T | upstream_gene_variant | MODIFIER | c.-1202G>A| |
S116 |
9 | BAA10g15450 | A10 | 15770194 | C | T | upstream_gene_variant | MODIFIER | c.-1536G>A| |
S104 S52 |
10 | BAA10g15450 | A10 | 15770550 | G | A | upstream_gene_variant | MODIFIER | c.-1892C>T| |
S111 |
11 | BAA10g15450 | A10 | 15770593 | C | T | upstream_gene_variant | MODIFIER | c.-1935G>A| |
S183 |
12 | BAA10g15450 | A10 | 15771476 | G | A | upstream_gene_variant | MODIFIER | c.-2818C>T| |
S13 |
13 | BAA10g15450 | A10 | 15772287 | G | A | upstream_gene_variant | MODIFIER | c.-3629C>T| |
S40 S49 |
14 | BAA10g15450 | A10 | 15772667 | C | T | upstream_gene_variant | MODIFIER | c.-4009G>A| |
S114 |
15 | BAA10g15450 | A10 | 15773172 | G | A | upstream_gene_variant | MODIFIER | c.-4514C>T| |
S35 |
16 | BAA10g15450 | A10 | 15773337 | C | T | upstream_gene_variant | MODIFIER | c.-4679G>A| |
S161 S289 S290 |
17 | BAA10g15450 | A10 | 15773608 | G | A | upstream_gene_variant | MODIFIER | c.-4950C>T| |
S81 S85 |