Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g26740 | A06 | 18346620 | C | T | downstream_gene_variant | MODIFIER | c.*4709G>A| |
S107 |
2 | BAA06g26740 | A06 | 18347009 | G | A | downstream_gene_variant | MODIFIER | c.*4320C>T| |
S19 |
3 | BAA06g26740 | A06 | 18347899 | C | T | downstream_gene_variant | MODIFIER | c.*3430G>A| |
S296 |
4 | BAA06g26740 | A06 | 18348501 | C | T | downstream_gene_variant | MODIFIER | c.*2828G>A| |
S178 |
5 | BAA06g26740 | A06 | 18349568 | C | T | downstream_gene_variant | MODIFIER | c.*1761G>A| |
S165 |
6 | BAA06g26740 | A06 | 18351585 | C | T | missense_variant | MODERATE | c.1865G>A|p.Gly622Glu |
S260 |
7 | BAA06g26740 | A06 | 18351670 | G | A | synonymous_variant | LOW | c.1780C>T|p.Leu594Leu |
S294 |
8 | BAA06g26740 | A06 | 18352094 | C | T | synonymous_variant | LOW | c.1356G>A|p.Lys452Lys |
S17 |
9 | BAA06g26740 | A06 | 18353281 | C | T | intron_variant | MODIFIER | c.312+52G>A| |
S15 S3 |
10 | BAA06g26740 | A06 | 18353514 | G | A | missense_variant | MODERATE | c.208C>T|p.Leu70Phe |
S255 |
11 | BAA06g26740 | A06 | 18353603 | G | A | missense_variant | MODERATE | c.119C>T|p.Thr40Ile |
S19 |
12 | BAA06g26740 | A06 | 18353905 | C | T | upstream_gene_variant | MODIFIER | c.-184G>A| |
S216 S265 S39 |
13 | BAA06g26740 | A06 | 18354609 | C | A | upstream_gene_variant | MODIFIER | c.-888G>T| |
S287 |
14 | BAA06g26740 | A06 | 18354841 | G | A | upstream_gene_variant | MODIFIER | c.-1120C>T| |
S37 |
15 | BAA06g26740 | A06 | 18355184 | C | T | upstream_gene_variant | MODIFIER | c.-1463G>A| |
S107 |
16 | BAA06g26740 | A06 | 18355888 | G | A | upstream_gene_variant | MODIFIER | c.-2167C>T| |
S180 |
17 | BAA06g26740 | A06 | 18356425 | G | A | upstream_gene_variant | MODIFIER | c.-2704C>T| |
S65 |
18 | BAA06g26740 | A06 | 18358396 | C | T | upstream_gene_variant | MODIFIER | c.-4675G>A| |
S288 |