Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g06600 | A04 | 4307203 | C | T | missense_variant | MODERATE | c.2431G>A|p.Gly811Ser |
S237 |
2 | BAA04g06600 | A04 | 4307514 | G | A | missense_variant | MODERATE | c.2120C>T|p.Ala707Val |
S59 |
3 | BAA04g06600 | A04 | 4308144 | C | T | synonymous_variant | LOW | c.1578G>A|p.Ser526Ser |
S100 |
4 | BAA04g06600 | A04 | 4308301 | G | A | missense_variant | MODERATE | c.1421C>T|p.Ala474Val |
S162 |
5 | BAA04g06600 | A04 | 4308673 | G | A | missense_variant | MODERATE | c.1049C>T|p.Ser350Leu |
S79 S91 |
6 | BAA04g06600 | A04 | 4309397 | C | T | missense_variant | MODERATE | c.325G>A|p.Asp109Asn |
S159 S299 |
7 | BAA04g06600 | A04 | 4309706 | A | G | missense_variant | MODERATE | c.16T>C|p.Phe6Leu |
S288 |
8 | BAA04g06600 | A04 | 4310788 | C | T | upstream_gene_variant | MODIFIER | c.-1067G>A| |
S250 |
9 | BAA04g06600 | A04 | 4310962 | G | A | upstream_gene_variant | MODIFIER | c.-1241C>T| |
S169 |
10 | BAA04g06600 | A04 | 4311403 | C | T | upstream_gene_variant | MODIFIER | c.-1682G>A| |
S209 |
11 | BAA04g06600 | A04 | 4312500 | G | A | upstream_gene_variant | MODIFIER | c.-2779C>T| |
S11 |
12 | BAA04g06600 | A04 | 4312543 | C | T | upstream_gene_variant | MODIFIER | c.-2822G>A| |
S272 S8 |
13 | BAA04g06600 | A04 | 4312692 | G | A | upstream_gene_variant | MODIFIER | c.-2971C>T| |
S190 |
14 | BAA04g06600 | A04 | 4313220 | C | T | upstream_gene_variant | MODIFIER | c.-3499G>A| |
S7 |
15 | BAA04g06600 | A04 | 4313381 | G | A | upstream_gene_variant | MODIFIER | c.-3660C>T| |
S166 |
16 | BAA04g06600 | A04 | 4313428 | G | A | upstream_gene_variant | MODIFIER | c.-3707C>T| |
S216 |
17 | BAA04g06600 | A04 | 4314119 | C | T | upstream_gene_variant | MODIFIER | c.-4398G>A| |
S180 |
18 | BAA04g06600 | A04 | 4314692 | C | T | upstream_gene_variant | MODIFIER | c.-4971G>A| |
S192 |