Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g33570 | A10 | 23860667 | C | T | upstream_gene_variant | MODIFIER | c.-3053C>T| |
S67 |
2 | BAA10g33570 | A10 | 23860982 | G | A | upstream_gene_variant | MODIFIER | c.-2738G>A| |
S59 |
3 | BAA10g33570 | A10 | 23861484 | G | A | upstream_gene_variant | MODIFIER | c.-2236G>A| |
S265 |
4 | BAA10g33570 | A10 | 23862106 | G | A | upstream_gene_variant | MODIFIER | c.-1614G>A| |
S133 |
5 | BAA10g33570 | A10 | 23862898 | C | T | upstream_gene_variant | MODIFIER | c.-822C>T| |
S295 |
6 | BAA10g33570 | A10 | 23862913 | G | A | upstream_gene_variant | MODIFIER | c.-807G>A| |
S207 |
7 | BAA10g33570 | A10 | 23863540 | C | A | upstream_gene_variant | MODIFIER | c.-180C>A| |
S158 S168 S224 S243 S259 S270 S299 S40 S80 S81 |
8 | BAA10g33570 | A10 | 23864577 | C | T | missense_variant | MODERATE | c.775C>T|p.Arg259Cys |
S45 |
9 | BAA10g33570 | A10 | 23864691 | G | A | missense_variant&splice_region_variant | MODERATE | c.889G>A|p.Gly297Arg |
S68 |
10 | BAA10g33570 | A10 | 23864885 | C | T | missense_variant | MODERATE | c.980C>T|p.Pro327Leu |
S142 |
11 | BAA10g33570 | A10 | 23865256 | G | A | missense_variant | MODERATE | c.1096G>A|p.Asp366Asn |
S109 |
12 | BAA10g33570 | A10 | 23865951 | G | A | missense_variant | MODERATE | c.1373G>A|p.Gly458Asp |
S4 |
13 | BAA10g33570 | A10 | 23865998 | C | T | missense_variant | MODERATE | c.1420C>T|p.Pro474Ser |
S182 |
14 | BAA10g33570 | A10 | 23866891 | G | A | missense_variant | MODERATE | c.1764G>A|p.Met588Ile |
S151 |
15 | BAA10g33570 | A10 | 23868013 | G | A | missense_variant | MODERATE | c.2215G>A|p.Val739Ile |
S162 |
16 | BAA10g33570 | A10 | 23868047 | G | A | missense_variant | MODERATE | c.2249G>A|p.Arg750Gln |
S94 |