Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g27230 | A09 | 17796355 | C | T | missense_variant | MODERATE | c.2938G>A|p.Ala980Thr |
S260 |
2 | BAA09g27230 | A09 | 17796557 | G | A | synonymous_variant | LOW | c.2736C>T|p.Asn912Asn |
S308 |
3 | BAA09g27230 | A09 | 17796924 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.2497-1G>A| |
S153 |
4 | BAA09g27230 | A09 | 17798489 | G | A | missense_variant | MODERATE | c.1774C>T|p.Pro592Ser |
S251 |
5 | BAA09g27230 | A09 | 17799018 | G | A | synonymous_variant | LOW | c.1290C>T|p.Ser430Ser |
S237 |
6 | BAA09g27230 | A09 | 17799077 | G | A | splice_region_variant&intron_variant | LOW | c.1237-6C>T| |
S8 |
7 | BAA09g27230 | A09 | 17799121 | C | T | intron_variant | MODIFIER | c.1237-50G>A| |
S174 |
8 | BAA09g27230 | A09 | 17800869 | G | A | splice_region_variant&intron_variant | LOW | c.688+8C>T| |
S189 |
9 | BAA09g27230 | A09 | 17802876 | G | A | upstream_gene_variant | MODIFIER | c.-1092C>T| |
S172 |
10 | BAA09g27230 | A09 | 17803423 | C | T | upstream_gene_variant | MODIFIER | c.-1639G>A| |
S168 |
11 | BAA09g27230 | A09 | 17803497 | G | A | upstream_gene_variant | MODIFIER | c.-1713C>T| |
S170 |
12 | BAA09g27230 | A09 | 17803701 | C | T | upstream_gene_variant | MODIFIER | c.-1917G>A| |
S204 |
13 | BAA09g27230 | A09 | 17804094 | G | A | upstream_gene_variant | MODIFIER | c.-2310C>T| |
S233 |
14 | BAA09g27230 | A09 | 17805074 | G | A | upstream_gene_variant | MODIFIER | c.-3290C>T| |
S40 S49 |