Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g07770 | A06 | 4062394 | C | T | downstream_gene_variant | MODIFIER | c.*960G>A| |
S167 |
2 | BAA06g07770 | A06 | 4062498 | C | T | downstream_gene_variant | MODIFIER | c.*856G>A| |
S111 |
3 | BAA06g07770 | A06 | 4063407 | G | A | missense_variant | MODERATE | c.868C>T|p.Pro290Ser |
S160 |
4 | BAA06g07770 | A06 | 4063497 | G | A | missense_variant | MODERATE | c.778C>T|p.Pro260Ser |
S15 S3 |
5 | BAA06g07770 | A06 | 4063745 | C | T | stop_gained | HIGH | c.618G>A|p.Trp206* |
S171 |
6 | BAA06g07770 | A06 | 4064190 | G | A | synonymous_variant | LOW | c.390C>T|p.Cys130Cys |
S42 |
7 | BAA06g07770 | A06 | 4064689 | C | T | missense_variant | MODERATE | c.145G>A|p.Val49Ile |
S150 |
8 | BAA06g07770 | A06 | 4065256 | G | A | upstream_gene_variant | MODIFIER | c.-423C>T| |
S275 |
9 | BAA06g07770 | A06 | 4065991 | G | A | upstream_gene_variant | MODIFIER | c.-1158C>T| |
S38 |
10 | BAA06g07770 | A06 | 4066362 | C | T | upstream_gene_variant | MODIFIER | c.-1529G>A| |
S250 |
11 | BAA06g07770 | A06 | 4066566 | C | T | upstream_gene_variant | MODIFIER | c.-1733G>A| |
S30 |
12 | BAA06g07770 | A06 | 4066875 | G | A | upstream_gene_variant | MODIFIER | c.-2042C>T| |
S35 |
13 | BAA06g07770 | A06 | 4066919 | G | A | upstream_gene_variant | MODIFIER | c.-2086C>T| |
S292 |
14 | BAA06g07770 | A06 | 4066944 | C | T | upstream_gene_variant | MODIFIER | c.-2111G>A| |
S274 |
15 | BAA06g07770 | A06 | 4067045 | G | A | upstream_gene_variant | MODIFIER | c.-2212C>T| |
S202 |
16 | BAA06g07770 | A06 | 4067055 | C | T | upstream_gene_variant | MODIFIER | c.-2222G>A| |
S148 S210 S31 |