Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g33330 | A05 | 35075694 | A | G | upstream_gene_variant | MODIFIER | c.-4326A>G| |
S288 |
2 | BAA05g33330 | A05 | 35075695 | G | A | upstream_gene_variant | MODIFIER | c.-4325G>A| |
S288 |
3 | BAA05g33330 | A05 | 35075781 | C | G | upstream_gene_variant | MODIFIER | c.-4239C>G| |
S197 |
4 | BAA05g33330 | A05 | 35077234 | C | T | upstream_gene_variant | MODIFIER | c.-2786C>T| |
S9 |
5 | BAA05g33330 | A05 | 35077552 | C | T | upstream_gene_variant | MODIFIER | c.-2468C>T| |
S294 |
6 | BAA05g33330 | A05 | 35077927 | G | A | upstream_gene_variant | MODIFIER | c.-2093G>A| |
S262 S94 |
7 | BAA05g33330 | A05 | 35079224 | G | A | upstream_gene_variant | MODIFIER | c.-796G>A| |
S6 |
8 | BAA05g33330 | A05 | 35079412 | C | T | upstream_gene_variant | MODIFIER | c.-608C>T| |
S251 |
9 | BAA05g33330 | A05 | 35080116 | G | A | missense_variant | MODERATE | c.97G>A|p.Asp33Asn |
S150 |
10 | BAA05g33330 | A05 | 35080460 | C | T | splice_region_variant&intron_variant | LOW | c.216+6C>T| |
S295 |
11 | BAA05g33330 | A05 | 35080996 | C | T | missense_variant | MODERATE | c.397C>T|p.Leu133Phe |
S157 |
12 | BAA05g33330 | A05 | 35081490 | G | A | synonymous_variant | LOW | c.624G>A|p.Gln208Gln |
S270 |
13 | BAA05g33330 | A05 | 35081931 | G | A | intron_variant | MODIFIER | c.675-45G>A| |
S15 S187 S3 |
14 | BAA05g33330 | A05 | 35082410 | C | T | missense_variant | MODERATE | c.1109C>T|p.Thr370Ile |
S103 |
15 | BAA05g33330 | A05 | 35083167 | G | A | missense_variant | MODERATE | c.1615G>A|p.Asp539Asn |
S122 |
16 | BAA05g33330 | A05 | 35083861 | C | T | missense_variant | MODERATE | c.2077C>T|p.Pro693Ser |
S183 S198 |
17 | BAA05g33330 | A05 | 35083913 | C | T | missense_variant | MODERATE | c.2129C>T|p.Pro710Leu |
S58 |
18 | BAA05g33330 | A05 | 35084328 | G | A | missense_variant | MODERATE | c.2452G>A|p.Val818Ile |
S138 |
19 | BAA05g33330 | A05 | 35085907 | C | T | downstream_gene_variant | MODIFIER | c.*1325C>T| |
S194 |