Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g19970 | A06 | 10445618 | C | T | missense_variant | MODERATE | c.4022G>A|p.Arg1341Lys |
S236 |
2 | BAA06g19970 | A06 | 10445882 | C | T | missense_variant | MODERATE | c.3758G>A|p.Gly1253Glu |
S251 |
3 | BAA06g19970 | A06 | 10446667 | C | T | synonymous_variant | LOW | c.2973G>A|p.Glu991Glu |
S36 |
4 | BAA06g19970 | A06 | 10446828 | T | G | synonymous_variant | LOW | c.2812A>C|p.Arg938Arg |
S42 |
5 | BAA06g19970 | A06 | 10446891 | C | T | missense_variant | MODERATE | c.2749G>A|p.Asp917Asn |
S168 S64 |
6 | BAA06g19970 | A06 | 10446951 | C | T | missense_variant | MODERATE | c.2689G>A|p.Glu897Lys |
S40 S49 |
7 | BAA06g19970 | A06 | 10447572 | C | T | missense_variant | MODERATE | c.2248G>A|p.Glu750Lys |
S175 |
8 | BAA06g19970 | A06 | 10447635 | G | A | missense_variant | MODERATE | c.2185C>T|p.Pro729Ser |
S95 |
9 | BAA06g19970 | A06 | 10448874 | C | T | missense_variant | MODERATE | c.1105G>A|p.Ala369Thr |
S156 |
10 | BAA06g19970 | A06 | 10449915 | G | A | synonymous_variant | LOW | c.747C>T|p.Asp249Asp |
S130 |
11 | BAA06g19970 | A06 | 10450182 | C | T | stop_gained | HIGH | c.480G>A|p.Trp160* |
S245 |
12 | BAA06g19970 | A06 | 10453692 | C | T | upstream_gene_variant | MODIFIER | c.-3031G>A| |
S16 |
13 | BAA06g19970 | A06 | 10454537 | G | A | upstream_gene_variant | MODIFIER | c.-3876C>T| |
S209 |
14 | BAA06g19970 | A06 | 10455085 | C | T | upstream_gene_variant | MODIFIER | c.-4424G>A| |
S95 |