Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g11720 | A06 | 5935487 | G | A | downstream_gene_variant | MODIFIER | c.*4944C>T| |
S153 S157 S167 S236 S257 S262 S263 |
2 | BAA06g11720 | A06 | 5935559 | G | A | downstream_gene_variant | MODIFIER | c.*4872C>T| |
S33 |
3 | BAA06g11720 | A06 | 5935656 | C | T | downstream_gene_variant | MODIFIER | c.*4775G>A| |
S274 |
4 | BAA06g11720 | A06 | 5935925 | G | A | downstream_gene_variant | MODIFIER | c.*4506C>T| |
S284 |
5 | BAA06g11720 | A06 | 5936407 | G | A | downstream_gene_variant | MODIFIER | c.*4024C>T| |
S118 |
6 | BAA06g11720 | A06 | 5937359 | C | T | downstream_gene_variant | MODIFIER | c.*3072G>A| |
S84 S93 |
7 | BAA06g11720 | A06 | 5937362 | G | A | downstream_gene_variant | MODIFIER | c.*3069C>T| |
S255 |
8 | BAA06g11720 | A06 | 5937364 | G | A | downstream_gene_variant | MODIFIER | c.*3067C>T| |
S182 |
9 | BAA06g11720 | A06 | 5937435 | G | A | downstream_gene_variant | MODIFIER | c.*2996C>T| |
S131 |
10 | BAA06g11720 | A06 | 5938775 | C | T | downstream_gene_variant | MODIFIER | c.*1656G>A| |
S250 |
11 | BAA06g11720 | A06 | 5938908 | G | A | downstream_gene_variant | MODIFIER | c.*1523C>T| |
S63 |
12 | BAA06g11720 | A06 | 5939957 | G | A | downstream_gene_variant | MODIFIER | c.*474C>T| |
S42 |
13 | BAA06g11720 | A06 | 5941029 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1030-1G>A| |
S67 |
14 | BAA06g11720 | A06 | 5941221 | G | A | intron_variant | MODIFIER | c.992-74C>T| |
S186 |
15 | BAA06g11720 | A06 | 5941447 | C | T | missense_variant | MODERATE | c.982G>A|p.Glu328Lys |
S281 |
16 | BAA06g11720 | A06 | 5941599 | C | T | missense_variant | MODERATE | c.830G>A|p.Gly277Glu |
S134 |
17 | BAA06g11720 | A06 | 5941811 | G | A | missense_variant | MODERATE | c.698C>T|p.Pro233Leu |
S133 |
18 | BAA06g11720 | A06 | 5942201 | C | T | missense_variant | MODERATE | c.403G>A|p.Asp135Asn |
S13 |
19 | BAA06g11720 | A06 | 5947765 | C | T | upstream_gene_variant | MODIFIER | c.-2619G>A| |
S185 |