Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g21290 | A06 | 11443470 | C | T | upstream_gene_variant | MODIFIER | c.-3589C>T| |
S168 |
2 | BAA06g21290 | A06 | 11443509 | G | A | upstream_gene_variant | MODIFIER | c.-3550G>A| |
S70 |
3 | BAA06g21290 | A06 | 11447744 | G | A | missense_variant&splice_region_variant | MODERATE | c.379G>A|p.Glu127Lys |
S9 |
4 | BAA06g21290 | A06 | 11447890 | G | A | missense_variant | MODERATE | c.407G>A|p.Gly136Glu |
S13 |
5 | BAA06g21290 | A06 | 11448610 | G | A | missense_variant | MODERATE | c.857G>A|p.Gly286Glu |
S213 |
6 | BAA06g21290 | A06 | 11450814 | C | T | missense_variant | MODERATE | c.2119C>T|p.Leu707Phe |
S109 |
7 | BAA06g21290 | A06 | 11451403 | C | T | missense_variant | MODERATE | c.2339C>T|p.Ala780Val |
S121 |
8 | BAA06g21290 | A06 | 11451798 | G | A | missense_variant | MODERATE | c.2578G>A|p.Glu860Lys |
S139 |
9 | BAA06g21290 | A06 | 11452303 | G | A | missense_variant | MODERATE | c.2819G>A|p.Gly940Glu |
S255 |
10 | BAA06g21290 | A06 | 11452344 | G | A | missense_variant | MODERATE | c.2860G>A|p.Glu954Lys |
S193 |
11 | BAA06g21290 | A06 | 11453771 | G | A | missense_variant | MODERATE | c.3958G>A|p.Asp1320Asn |
S161 |