Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g24400 | A06 | 16258736 | C | T | upstream_gene_variant | MODIFIER | c.-2436C>T| |
S168 |
2 | BAA06g24400 | A06 | 16259948 | C | T | upstream_gene_variant | MODIFIER | c.-1224C>T| |
S228 |
3 | BAA06g24400 | A06 | 16261049 | C | T | upstream_gene_variant | MODIFIER | c.-123C>T| |
S135 |
4 | BAA06g24400 | A06 | 16261393 | G | A | synonymous_variant | LOW | c.168G>A|p.Arg56Arg |
S170 |
5 | BAA06g24400 | A06 | 16261535 | C | T | missense_variant | MODERATE | c.310C>T|p.Leu104Phe |
S87 |
6 | BAA06g24400 | A06 | 16262073 | G | A | missense_variant | MODERATE | c.406G>A|p.Asp136Asn |
S133 |
7 | BAA06g24400 | A06 | 16263599 | C | T | missense_variant | MODERATE | c.716C>T|p.Ser239Leu |
S245 |
8 | BAA06g24400 | A06 | 16264679 | G | A | downstream_gene_variant | MODIFIER | c.*596G>A| |
S61 |
9 | BAA06g24400 | A06 | 16264759 | C | T | downstream_gene_variant | MODIFIER | c.*676C>T| |
S107 |
10 | BAA06g24400 | A06 | 16264898 | C | T | downstream_gene_variant | MODIFIER | c.*815C>T| |
S79 S91 |
11 | BAA06g24400 | A06 | 16265194 | G | A | downstream_gene_variant | MODIFIER | c.*1111G>A| |
S211 |
12 | BAA06g24400 | A06 | 16265943 | G | A | downstream_gene_variant | MODIFIER | c.*1860G>A| |
S219 S72 |
13 | BAA06g24400 | A06 | 16266667 | G | A | downstream_gene_variant | MODIFIER | c.*2584G>A| |
S257 |
14 | BAA06g24400 | A06 | 16266921 | G | A | downstream_gene_variant | MODIFIER | c.*2838G>A| |
S131 |
15 | BAA06g24400 | A06 | 16267221 | G | A | downstream_gene_variant | MODIFIER | c.*3138G>A| |
S146 |
16 | BAA06g24400 | A06 | 16267517 | C | T | downstream_gene_variant | MODIFIER | c.*3434C>T| |
S186 |
17 | BAA06g24400 | A06 | 16267903 | G | A | downstream_gene_variant | MODIFIER | c.*3820G>A| |
S65 |
18 | BAA06g24400 | A06 | 16268432 | G | A | downstream_gene_variant | MODIFIER | c.*4349G>A| |
S13 |
19 | BAA06g24400 | A06 | 16268447 | G | A | downstream_gene_variant | MODIFIER | c.*4364G>A| |
S149 |