Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g10000 | A06 | 5026416 | G | A | downstream_gene_variant | MODIFIER | c.*2581C>T| |
S117 |
2 | BAA06g10000 | A06 | 5026725 | C | T | downstream_gene_variant | MODIFIER | c.*2272G>A| |
S238 |
3 | BAA06g10000 | A06 | 5027484 | A | G | downstream_gene_variant | MODIFIER | c.*1513T>C| |
S97 |
4 | BAA06g10000 | A06 | 5028376 | C | T | downstream_gene_variant | MODIFIER | c.*621G>A| |
S60 |
5 | BAA06g10000 | A06 | 5028674 | G | A | downstream_gene_variant | MODIFIER | c.*323C>T| |
S108 |
6 | BAA06g10000 | A06 | 5030128 | G | A | splice_region_variant&intron_variant | LOW | c.1365+4C>T| |
S180 |
7 | BAA06g10000 | A06 | 5030228 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1270-1G>A| |
S61 |
8 | BAA06g10000 | A06 | 5030394 | G | A | missense_variant | MODERATE | c.1201C>T|p.Leu401Phe |
S275 |
9 | BAA06g10000 | A06 | 5030408 | C | T | missense_variant | MODERATE | c.1187G>A|p.Arg396Gln |
S296 |
10 | BAA06g10000 | A06 | 5030776 | G | A | intron_variant | MODIFIER | c.1047-12C>T| |
S218 |
11 | BAA06g10000 | A06 | 5031115 | C | T | missense_variant&splice_region_variant | MODERATE | c.967G>A|p.Asp323Asn |
S79 S91 |
12 | BAA06g10000 | A06 | 5031523 | G | A | missense_variant | MODERATE | c.736C>T|p.Pro246Ser |
S161 |
13 | BAA06g10000 | A06 | 5032176 | G | A | missense_variant | MODERATE | c.415C>T|p.Arg139Trp |
S12 |
14 | BAA06g10000 | A06 | 5034635 | C | T | upstream_gene_variant | MODIFIER | c.-927G>A| |
S23 |
15 | BAA06g10000 | A06 | 5034989 | C | T | upstream_gene_variant | MODIFIER | c.-1281G>A| |
S2 |
16 | BAA06g10000 | A06 | 5035776 | C | T | upstream_gene_variant | MODIFIER | c.-2068G>A| |
S238 |
17 | BAA06g10000 | A06 | 5035937 | C | T | upstream_gene_variant | MODIFIER | c.-2229G>A| |
S87 |
18 | BAA06g10000 | A06 | 5036494 | G | A | upstream_gene_variant | MODIFIER | c.-2786C>T| |
S112 |