Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g05080 | A06 | 2865670 | C | T | upstream_gene_variant | MODIFIER | c.-1895C>T| |
S98 |
2 | BAA06g05080 | A06 | 2866019 | C | T | upstream_gene_variant | MODIFIER | c.-1546C>T| |
S193 |
3 | BAA06g05080 | A06 | 2867103 | C | T | upstream_gene_variant | MODIFIER | c.-462C>T| |
S136 |
4 | BAA06g05080 | A06 | 2867855 | C | T | missense_variant | MODERATE | c.205C>T|p.Pro69Ser |
S200 |
5 | BAA06g05080 | A06 | 2870369 | G | A | missense_variant | MODERATE | c.283G>A|p.Asp95Asn |
S122 |
6 | BAA06g05080 | A06 | 2870741 | C | T | missense_variant | MODERATE | c.476C>T|p.Pro159Leu |
S202 |
7 | BAA06g05080 | A06 | 2870811 | G | A | intron_variant | MODIFIER | c.489+57G>A| |
S72 S78 |
8 | BAA06g05080 | A06 | 2870853 | C | T | intron_variant | MODIFIER | c.489+99C>T| |
S211 S227 |
9 | BAA06g05080 | A06 | 2871248 | C | T | intron_variant | MODIFIER | c.489+494C>T| |
S5 |
10 | BAA06g05080 | A06 | 2875498 | C | T | missense_variant | MODERATE | c.1133C>T|p.Ser378Leu |
S239 |
11 | BAA06g05080 | A06 | 2876908 | C | T | downstream_gene_variant | MODIFIER | c.*1174C>T| |
S91 |