Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g35820 | A06 | 23854924 | G | A | upstream_gene_variant | MODIFIER | c.-2042G>A| |
S103 |
2 | BAA06g35820 | A06 | 23855134 | C | T | upstream_gene_variant | MODIFIER | c.-1832C>T| |
S177 |
3 | BAA06g35820 | A06 | 23855228 | C | T | upstream_gene_variant | MODIFIER | c.-1738C>T| |
S192 |
4 | BAA06g35820 | A06 | 23855676 | C | T | upstream_gene_variant | MODIFIER | c.-1290C>T| |
S62 |
5 | BAA06g35820 | A06 | 23856003 | G | A | upstream_gene_variant | MODIFIER | c.-963G>A| |
S219 |
6 | BAA06g35820 | A06 | 23856268 | C | T | upstream_gene_variant | MODIFIER | c.-698C>T| |
S270 |
7 | BAA06g35820 | A06 | 23856983 | G | A | synonymous_variant | LOW | c.18G>A|p.Lys6Lys |
S11 |
8 | BAA06g35820 | A06 | 23857115 | G | A | intron_variant | MODIFIER | c.66-48G>A| |
S13 |
9 | BAA06g35820 | A06 | 23857291 | G | A | missense_variant | MODERATE | c.194G>A|p.Gly65Glu |
S151 S263 |
10 | BAA06g35820 | A06 | 23857769 | G | A | intron_variant | MODIFIER | c.456+31G>A| |
S11 |
11 | BAA06g35820 | A06 | 23857897 | G | A | missense_variant | MODERATE | c.544G>A|p.Asp182Asn |
S273 |
12 | BAA06g35820 | A06 | 23859556 | G | A | splice_region_variant&intron_variant | LOW | c.1110-4G>A| |
S130 |
13 | BAA06g35820 | A06 | 23860791 | G | A | downstream_gene_variant | MODIFIER | c.*513G>A| |
S240 |
14 | BAA06g35820 | A06 | 23861452 | G | A | downstream_gene_variant | MODIFIER | c.*1174G>A| |
S157 |
15 | BAA06g35820 | A06 | 23861980 | C | T | downstream_gene_variant | MODIFIER | c.*1702C>T| |
S115 |
16 | BAA06g35820 | A06 | 23862187 | C | T | downstream_gene_variant | MODIFIER | c.*1909C>T| |
S124 S126 S127 S129 S131 S223 S57 S60 |
17 | BAA06g35820 | A06 | 23862384 | G | A | downstream_gene_variant | MODIFIER | c.*2106G>A| |
S249 |
18 | BAA06g35820 | A06 | 23862588 | G | A | downstream_gene_variant | MODIFIER | c.*2310G>A| |
S209 |
19 | BAA06g35820 | A06 | 23864274 | G | A | downstream_gene_variant | MODIFIER | c.*3996G>A| |
S67 |