Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g16690 | A06 | 8373659 | C | T | upstream_gene_variant | MODIFIER | c.-4176C>T| |
S237 |
2 | BAA06g16690 | A06 | 8373708 | C | T | upstream_gene_variant | MODIFIER | c.-4127C>T| |
S80 |
3 | BAA06g16690 | A06 | 8374759 | G | A | upstream_gene_variant | MODIFIER | c.-3076G>A| |
S33 |
4 | BAA06g16690 | A06 | 8376564 | C | T | upstream_gene_variant | MODIFIER | c.-1271C>T| |
S202 |
5 | BAA06g16690 | A06 | 8377192 | C | T | upstream_gene_variant | MODIFIER | c.-643C>T| |
S136 |
6 | BAA06g16690 | A06 | 8377245 | G | A | upstream_gene_variant | MODIFIER | c.-590G>A| |
S270 |
7 | BAA06g16690 | A06 | 8377413 | C | T | upstream_gene_variant | MODIFIER | c.-422C>T| |
S239 |
8 | BAA06g16690 | A06 | 8377420 | C | T | upstream_gene_variant | MODIFIER | c.-415C>T| |
S10 |
9 | BAA06g16690 | A06 | 8380934 | G | A | splice_region_variant&intron_variant | LOW | c.2187+7G>A| |
S236 |
10 | BAA06g16690 | A06 | 8381114 | C | T | missense_variant | MODERATE | c.2291C>T|p.Ser764Phe |
S20 |
11 | BAA06g16690 | A06 | 8381191 | G | A | missense_variant | MODERATE | c.2368G>A|p.Asp790Asn |
S262 |