Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g38430 | A06 | 25190739 | G | A | upstream_gene_variant | MODIFIER | c.-2120G>A| |
S32 |
2 | BAA06g38430 | A06 | 25191246 | G | A | upstream_gene_variant | MODIFIER | c.-1613G>A| |
S206 S26 |
3 | BAA06g38430 | A06 | 25192811 | C | T | upstream_gene_variant | MODIFIER | c.-48C>T| |
S48 |
4 | BAA06g38430 | A06 | 25192880 | G | A | missense_variant | MODERATE | c.22G>A|p.Glu8Lys |
S55 |
5 | BAA06g38430 | A06 | 25192920 | G | A | missense_variant | MODERATE | c.62G>A|p.Arg21Lys |
S105 |
6 | BAA06g38430 | A06 | 25193484 | G | A | missense_variant | MODERATE | c.296G>A|p.Gly99Glu |
S53 |
7 | BAA06g38430 | A06 | 25194074 | C | T | synonymous_variant | LOW | c.816C>T|p.Ile272Ile |
S294 |
8 | BAA06g38430 | A06 | 25194699 | C | T | intron_variant | MODIFIER | c.930-74C>T| |
S178 |
9 | BAA06g38430 | A06 | 25195907 | G | A | missense_variant | MODERATE | c.1636G>A|p.Gly546Ser |
S292 |
10 | BAA06g38430 | A06 | 25196266 | C | T | synonymous_variant | LOW | c.1995C>T|p.Leu665Leu |
S84 |
11 | BAA06g38430 | A06 | 25197049 | C | T | missense_variant | MODERATE | c.2618C>T|p.Ala873Val |
S113 |
12 | BAA06g38430 | A06 | 25197106 | G | A | missense_variant | MODERATE | c.2675G>A|p.Arg892Gln |
S245 |
13 | BAA06g38430 | A06 | 25197188 | G | A | synonymous_variant | LOW | c.2757G>A|p.Leu919Leu |
S60 |
14 | BAA06g38430 | A06 | 25197819 | G | A | missense_variant | MODERATE | c.3388G>A|p.Asp1130Asn |
S60 |
15 | BAA06g38430 | A06 | 25197978 | G | A | missense_variant | MODERATE | c.3547G>A|p.Glu1183Lys |
S283 |
16 | BAA06g38430 | A06 | 25198159 | C | T | missense_variant | MODERATE | c.3728C>T|p.Thr1243Ile |
S6 |
17 | BAA06g38430 | A06 | 25202111 | G | A | downstream_gene_variant | MODIFIER | c.*3945G>A| |
S283 |
18 | BAA06g38430 | A06 | 25202203 | G | A | downstream_gene_variant | MODIFIER | c.*4037G>A| |
S250 |
19 | BAA06g38430 | A06 | 25202237 | C | T | downstream_gene_variant | MODIFIER | c.*4071C>T| |
S262 |