Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g17040 | A06 | 8559313 | G | A | upstream_gene_variant | MODIFIER | c.-3432G>A| |
S295 |
2 | BAA06g17040 | A06 | 8559653 | G | A | upstream_gene_variant | MODIFIER | c.-3092G>A| |
S143 |
3 | BAA06g17040 | A06 | 8559912 | G | A | upstream_gene_variant | MODIFIER | c.-2833G>A| |
S45 |
4 | BAA06g17040 | A06 | 8560163 | C | T | upstream_gene_variant | MODIFIER | c.-2582C>T| |
S62 |
5 | BAA06g17040 | A06 | 8561059 | G | A | upstream_gene_variant | MODIFIER | c.-1686G>A| |
S13 |
6 | BAA06g17040 | A06 | 8561423 | C | T | upstream_gene_variant | MODIFIER | c.-1322C>T| |
S80 |
7 | BAA06g17040 | A06 | 8562383 | G | A | upstream_gene_variant | MODIFIER | c.-362G>A| |
S1 S90 |
8 | BAA06g17040 | A06 | 8562721 | C | T | upstream_gene_variant | MODIFIER | c.-24C>T| |
S23 |
9 | BAA06g17040 | A06 | 8562975 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.148-1G>A| |
S15 S3 |
10 | BAA06g17040 | A06 | 8563882 | G | A | missense_variant | MODERATE | c.496G>A|p.Asp166Asn |
S180 |
11 | BAA06g17040 | A06 | 8567597 | C | T | downstream_gene_variant | MODIFIER | c.*2610C>T| |
S176 |
12 | BAA06g17040 | A06 | 8567873 | C | T | downstream_gene_variant | MODIFIER | c.*2886C>T| |
S183 S198 |
13 | BAA06g17040 | A06 | 8569616 | C | T | downstream_gene_variant | MODIFIER | c.*4629C>T| |
S148 S30 S31 |