Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g24050 | A06 | 15040084 | C | T | downstream_gene_variant | MODIFIER | c.*3773G>A| |
S252 |
2 | BAA06g24050 | A06 | 15043025 | C | T | downstream_gene_variant | MODIFIER | c.*832G>A| |
S293 |
3 | BAA06g24050 | A06 | 15043093 | C | T | downstream_gene_variant | MODIFIER | c.*764G>A| |
S116 |
4 | BAA06g24050 | A06 | 15044091 | G | A | synonymous_variant | LOW | c.1455C>T|p.Leu485Leu |
S146 |
5 | BAA06g24050 | A06 | 15044114 | G | A | missense_variant | MODERATE | c.1432C>T|p.Pro478Ser |
S85 |
6 | BAA06g24050 | A06 | 15044180 | G | A | stop_gained | HIGH | c.1366C>T|p.Gln456* |
S180 |
7 | BAA06g24050 | A06 | 15044248 | C | T | missense_variant | MODERATE | c.1298G>A|p.Gly433Asp |
S93 |
8 | BAA06g24050 | A06 | 15044270 | C | T | missense_variant | MODERATE | c.1276G>A|p.Asp426Asn |
S79 S91 |
9 | BAA06g24050 | A06 | 15044393 | C | T | missense_variant | MODERATE | c.1153G>A|p.Glu385Lys |
S60 |
10 | BAA06g24050 | A06 | 15044399 | C | T | missense_variant | MODERATE | c.1147G>A|p.Glu383Lys |
S234 |
11 | BAA06g24050 | A06 | 15044870 | C | T | missense_variant | MODERATE | c.749G>A|p.Ser250Asn |
S188 |
12 | BAA06g24050 | A06 | 15045357 | G | A | splice_region_variant&intron_variant | LOW | c.338-7C>T| |
S38 |
13 | BAA06g24050 | A06 | 15045557 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.198-1G>A| |
S2 |
14 | BAA06g24050 | A06 | 15045969 | C | T | upstream_gene_variant | MODIFIER | c.-132G>A| |
S159 S243 |
15 | BAA06g24050 | A06 | 15046055 | C | T | upstream_gene_variant | MODIFIER | c.-218G>A| |
S167 |
16 | BAA06g24050 | A06 | 15046066 | G | A | upstream_gene_variant | MODIFIER | c.-229C>T| |
S228 |
17 | BAA06g24050 | A06 | 15046123 | G | A | upstream_gene_variant | MODIFIER | c.-286C>T| |
S53 |