Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16390 | A10 | 16218033 | G | A | missense_variant | MODERATE | c.3239C>T|p.Pro1080Leu |
S132 S137 S215 |
2 | BAA10g16390 | A10 | 16218082 | C | T | missense_variant | MODERATE | c.3190G>A|p.Val1064Ile |
S60 |
3 | BAA10g16390 | A10 | 16219914 | C | T | synonymous_variant | LOW | c.2061G>A|p.Lys687Lys |
S169 |
4 | BAA10g16390 | A10 | 16220171 | G | A | missense_variant | MODERATE | c.1804C>T|p.Leu602Phe |
S59 |
5 | BAA10g16390 | A10 | 16220197 | G | A | missense_variant | MODERATE | c.1778C>T|p.Ser593Phe |
S213 |
6 | BAA10g16390 | A10 | 16220352 | G | A | synonymous_variant | LOW | c.1623C>T|p.Asn541Asn |
S125 |
7 | BAA10g16390 | A10 | 16221217 | C | T | missense_variant | MODERATE | c.758G>A|p.Arg253Lys |
S144 |
8 | BAA10g16390 | A10 | 16221389 | G | A | missense_variant | MODERATE | c.586C>T|p.Pro196Ser |
S166 |
9 | BAA10g16390 | A10 | 16221423 | C | T | synonymous_variant | LOW | c.552G>A|p.Glu184Glu |
S116 |
10 | BAA10g16390 | A10 | 16222307 | C | T | upstream_gene_variant | MODIFIER | c.-136G>A| |
S243 S298 |
11 | BAA10g16390 | A10 | 16223543 | C | A | upstream_gene_variant | MODIFIER | c.-1372G>T| |
S116 |
12 | BAA10g16390 | A10 | 16224086 | G | A | upstream_gene_variant | MODIFIER | c.-1915C>T| |
S112 |
13 | BAA10g16390 | A10 | 16224845 | G | A | upstream_gene_variant | MODIFIER | c.-2674C>T| |
S146 |
14 | BAA10g16390 | A10 | 16225097 | C | T | upstream_gene_variant | MODIFIER | c.-2926G>A| |
S249 |
15 | BAA10g16390 | A10 | 16225219 | C | T | upstream_gene_variant | MODIFIER | c.-3048G>A| |
S83 S88 |