Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28260 | A10 | 21711655 | C | T | synonymous_variant | LOW | c.4995G>A|p.Lys1665Lys |
S104 S52 |
2 | BAA10g28260 | A10 | 21711732 | C | T | missense_variant | MODERATE | c.4918G>A|p.Asp1640Asn |
S33 |
3 | BAA10g28260 | A10 | 21712741 | G | A | synonymous_variant | LOW | c.3990C>T|p.Ile1330Ile |
S149 |
4 | BAA10g28260 | A10 | 21712822 | C | T | synonymous_variant | LOW | c.3909G>A|p.Gln1303Gln |
S247 |
5 | BAA10g28260 | A10 | 21713398 | C | T | synonymous_variant | LOW | c.3333G>A|p.Pro1111Pro |
S115 S45 |
6 | BAA10g28260 | A10 | 21713799 | C | T | missense_variant | MODERATE | c.2932G>A|p.Glu978Lys |
S8 |
7 | BAA10g28260 | A10 | 21713951 | G | A | missense_variant | MODERATE | c.2780C>T|p.Pro927Leu |
S245 |
8 | BAA10g28260 | A10 | 21714246 | G | A | missense_variant | MODERATE | c.2485C>T|p.Pro829Ser |
S43 |
9 | BAA10g28260 | A10 | 21715080 | C | T | missense_variant | MODERATE | c.1765G>A|p.Glu589Lys |
S8 |
10 | BAA10g28260 | A10 | 21715166 | C | T | missense_variant | MODERATE | c.1679G>A|p.Arg560Lys |
S19 |
11 | BAA10g28260 | A10 | 21716570 | G | A | synonymous_variant | LOW | c.360C>T|p.Val120Val |
S181 |
12 | BAA10g28260 | A10 | 21716771 | G | A | synonymous_variant | LOW | c.159C>T|p.Asn53Asn |
S278 |
13 | BAA10g28260 | A10 | 21717526 | C | T | upstream_gene_variant | MODIFIER | c.-597G>A| |
S33 |
14 | BAA10g28260 | A10 | 21718094 | C | T | upstream_gene_variant | MODIFIER | c.-1165G>A| |
S286 |
15 | BAA10g28260 | A10 | 21719434 | C | T | upstream_gene_variant | MODIFIER | c.-2505G>A| |
S292 |