Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g14070 | A08 | 12068810 | G | A | missense_variant | MODERATE | c.2263C>T|p.Pro755Ser |
S251 |
2 | BAA08g14070 | A08 | 12069813 | C | T | synonymous_variant | LOW | c.1776G>A|p.Val592Val |
S295 |
3 | BAA08g14070 | A08 | 12070926 | C | T | missense_variant | MODERATE | c.1238G>A|p.Ser413Asn |
S228 |
4 | BAA08g14070 | A08 | 12071237 | C | T | synonymous_variant | LOW | c.927G>A|p.Gln309Gln |
S247 |
5 | BAA08g14070 | A08 | 12071361 | G | A | missense_variant | MODERATE | c.803C>T|p.Ser268Phe |
S238 |
6 | BAA08g14070 | A08 | 12071551 | C | T | missense_variant | MODERATE | c.736G>A|p.Asp246Asn |
S51 |
7 | BAA08g14070 | A08 | 12071764 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.597-1G>A| |
S207 |
8 | BAA08g14070 | A08 | 12071962 | G | A | synonymous_variant | LOW | c.492C>T|p.Arg164Arg |
S188 |
9 | BAA08g14070 | A08 | 12072414 | C | T | missense_variant | MODERATE | c.40G>A|p.Glu14Lys |
S250 S291 S41 |
10 | BAA08g14070 | A08 | 12073080 | C | T | upstream_gene_variant | MODIFIER | c.-627G>A| |
S80 |
11 | BAA08g14070 | A08 | 12076556 | C | T | upstream_gene_variant | MODIFIER | c.-4103G>A| |
S206 S26 |