Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01480 | A10 | 743448 | G | A | upstream_gene_variant | MODIFIER | c.-3442G>A| |
S133 |
2 | BAA10g01480 | A10 | 744064 | C | T | upstream_gene_variant | MODIFIER | c.-2826C>T| |
S206 S210 S26 |
3 | BAA10g01480 | A10 | 744244 | C | T | upstream_gene_variant | MODIFIER | c.-2646C>T| |
S113 |
4 | BAA10g01480 | A10 | 744418 | G | A | upstream_gene_variant | MODIFIER | c.-2472G>A| |
S264 |
5 | BAA10g01480 | A10 | 744776 | C | T | upstream_gene_variant | MODIFIER | c.-2114C>T| |
S31 |
6 | BAA10g01480 | A10 | 745174 | G | A | upstream_gene_variant | MODIFIER | c.-1716G>A| |
S69 |
7 | BAA10g01480 | A10 | 745507 | G | A | upstream_gene_variant | MODIFIER | c.-1383G>A| |
S17 |
8 | BAA10g01480 | A10 | 745854 | G | A | upstream_gene_variant | MODIFIER | c.-1036G>A| |
S48 |
9 | BAA10g01480 | A10 | 746009 | C | T | upstream_gene_variant | MODIFIER | c.-881C>T| |
S221 |
10 | BAA10g01480 | A10 | 746450 | C | T | upstream_gene_variant | MODIFIER | c.-440C>T| |
S31 |
11 | BAA10g01480 | A10 | 746577 | G | A | upstream_gene_variant | MODIFIER | c.-313G>A| |
S211 S227 |
12 | BAA10g01480 | A10 | 747991 | C | T | synonymous_variant | LOW | c.516C>T|p.Val172Val |
S31 |
13 | BAA10g01480 | A10 | 748418 | G | A | missense_variant | MODERATE | c.757G>A|p.Asp253Asn |
S219 S72 |
14 | BAA10g01480 | A10 | 749462 | C | T | synonymous_variant | LOW | c.1479C>T|p.Thr493Thr |
S286 |
15 | BAA10g01480 | A10 | 749540 | C | T | synonymous_variant | LOW | c.1557C>T|p.Asn519Asn |
S113 |